Constipation caused codeine by
Could these symptoms be caused by Crohn's?
2024.05.23 11:45 LionUnusual23 Could these symptoms be caused by Crohn's?
Hello, I am 22, female, 5'2", and weigh 115 lbs. I have bouts of reocurring cramps in my lower abdomen that are as painful if not more so than kidney stones which I have also had in the past. The pain comes in waves of around 30-seconds to a few minutes and then goes away for a few minutes before returning. This pattern lasts anywhere from an hour to several hours. During the cramping periods I have diarrhea, sweat horribly, become nauseous, and get chills where the hair on my arms stands up. I've taken my temperature after having one of these episodes and it was normal so I don't believe that they cause a fever. Recently I've also become dizzy during these episodes which has made me a bit more concerned than usual.
I have had these cramps since I was 16. They happen once or twice a month but sometimes disapear entirely for a full month or two. What I eat doesn't seem to affect the severity or quantity of episodes. I buy the same food every week and only go out and eat something different once a month or less. I've even had a cramping episode after a full day of not eating. If I remember correctly they started a few months before my first kidney stone so I attributed them as a side effect of that. I have since solved that problem (parathyroidectimy) but the cramps have continued. My leading theory is that they are caused by Crohn's. I found a post where a lady diagnosed with Crohn's had a specific symptom similar to one of mine. That being an abdominal mass. I have a lower right abdominal mass that comes and goes and that doctors attributed to extreme constipation and not a hernia which they originally thought. They didn't request a follow up so I figured it was not a problem. I've had the abdominal mass for around two years now.
Does this sound like Crohn's or like something else? I have researched extensively online but I am far from a medical professional. I am hesitant to go to my doctor as she takes a very passive approach to health. She thinks all my symptoms are normal and doesn't provide reasons for or solutions to stop them besides excersize and sleep. I've asked for various tests after trying to research symptoms myself but they always come back negative or find some new minor problem. Either way I am not sure if it is worth going to her at all as I am sure that she would not prescribe anything or suggest any helpful life changes unless I was in immediate need for surgery. As it is I am unsure of what can even be done to lesson Crohns Disease symptoms.
submitted by LionUnusual23 to DiagnoseMe [link] [comments]
I have had these cramps since I was 16. They happen once or twice a month but sometimes disapear entirely for a full month or two. What I eat doesn't seem to affect the severity or quantity of episodes. I buy the same food every week and only go out and eat something different once a month or less. I've even had a cramping episode after a full day of not eating. If I remember correctly they started a few months before my first kidney stone so I attributed them as a side effect of that. I have since solved that problem (parathyroidectimy) but the cramps have continued. My leading theory is that they are caused by Crohn's. I found a post where a lady diagnosed with Crohn's had a specific symptom similar to one of mine. That being an abdominal mass. I have a lower right abdominal mass that comes and goes and that doctors attributed to extreme constipation and not a hernia which they originally thought. They didn't request a follow up so I figured it was not a problem. I've had the abdominal mass for around two years now.
Does this sound like Crohn's or like something else? I have researched extensively online but I am far from a medical professional. I am hesitant to go to my doctor as she takes a very passive approach to health. She thinks all my symptoms are normal and doesn't provide reasons for or solutions to stop them besides excersize and sleep. I've asked for various tests after trying to research symptoms myself but they always come back negative or find some new minor problem. Either way I am not sure if it is worth going to her at all as I am sure that she would not prescribe anything or suggest any helpful life changes unless I was in immediate need for surgery. As it is I am unsure of what can even be done to lesson Crohns Disease symptoms.
2024.05.23 11:11 idkwhatidek Why are discredited medical practices still practiced?
In around 500BCE there was this guy — Alcmaeon of Croton — who coined a branch of natural philosophy known as humorism. So humorists believe there are 4 essential fluids in the body — blood, black bile, yellow bile and phlegm — and disease is caused by an imbalance of these 4 fluids.
Treatments to remove excess fluid became popular (Charles II of Spain being a notable example) such as phlebotomy (aka blood-letting) which involved methods such as leeching, cupping, and cutting. For yellow bile, treatments that would cause a patient to vomit were used. In short — blood, mucous, poop and vomit were believe to be the source of most maladies.
Phlebotomy is still practiced all over the world; however, it is primarily used for sampling blood to find specific levels, and for donations. That's the important point: donations. When people donate blood; they are removing 10% of their blood. If humorism was real it would cause an imbalance in the 4 humors — it obviously does not cause any illness so why are treatments such as fire cupping, wet cupping, incisions, enemas (specifically when abused i.e., when there is no impaction, constipation or surgery to prepare for), laxatives, foods that will make you vomit (e.g, milk and honey) used so often? I understand this is "alternative medicine" and it is scoffed at, but it doesn't stop it from being somewhat popular.
On a side-note: I have noticed on tiktok that phrenology has been trending for quite some time. For example: those gridlines that show how close your face is to Phi.
submitted by idkwhatidek to NoStupidQuestions [link] [comments]
Treatments to remove excess fluid became popular (Charles II of Spain being a notable example) such as phlebotomy (aka blood-letting) which involved methods such as leeching, cupping, and cutting. For yellow bile, treatments that would cause a patient to vomit were used. In short — blood, mucous, poop and vomit were believe to be the source of most maladies.
Phlebotomy is still practiced all over the world; however, it is primarily used for sampling blood to find specific levels, and for donations. That's the important point: donations. When people donate blood; they are removing 10% of their blood. If humorism was real it would cause an imbalance in the 4 humors — it obviously does not cause any illness so why are treatments such as fire cupping, wet cupping, incisions, enemas (specifically when abused i.e., when there is no impaction, constipation or surgery to prepare for), laxatives, foods that will make you vomit (e.g, milk and honey) used so often? I understand this is "alternative medicine" and it is scoffed at, but it doesn't stop it from being somewhat popular.
On a side-note: I have noticed on tiktok that phrenology has been trending for quite some time. For example: those gridlines that show how close your face is to Phi.
2024.05.23 11:05 GuiltlessMaple Best Dandelion Herbal Supplements
 | submitted by GuiltlessMaple to u/GuiltlessMaple [link] [comments] https://preview.redd.it/biajivh8652d1.jpg?width=720&format=pjpg&auto=webp&s=006ed4f6662d49cf0d81f74152817f60225ea6e3 Explore the world of Dandelion Herbal Supplements with us as we delve into the top products available in the market. Dandelion, a powerful herb, is known for its diverse health benefits, which range from digestive support to liver detoxification. Our roundup will give you an in-depth look at some of the best dandelion supplements available, guiding you towards the perfect option for your healthcare routine. The Top 7 Best Dandelion Herbal Supplements
Reviews🔗Organic Roasted Dandelion Root Tea for Liver Supporthttps://preview.redd.it/f8tfj0s8652d1.jpg?width=720&format=pjpg&auto=webp&s=f0e3fd6b31104855d914b0ca93b547d83ae45bdf Dandelion Herbal Supplements by Traditional Medicinals are just what I needed to maintain a healthy liver and promote better digestion in my daily life. As a regular tea user, I appreciate the quality and potency that this organic Roasted Dandelion Root Tea offers. Its earthy aroma and pleasantly bitter taste create a cozy, grounding experience that has become a staple in my daily routine. One thing I particularly love about this product is its versatility. The caffeine-free nature allows me to enjoy it at any time without worrying about sleepless nights or caffeine jitters. Additionally, I find the taste perfect for sipping on during my late afternoons as a gentle pick-me-up before dinner. As an added bonus, dandelion root is known for its detoxifying properties, which have helped me maintain a healthier liver and digestive system. However, one minor issue I've encountered with this product is that some teas can be a little inconsistent in terms of flavor. There have been occasions where the taste wasn't as potent as I preferred, but overall, the quality and benefits of Traditional Medicinals' Dandelion Herbal Supplements make them a worthy addition to my tea collection. In summary, I wholeheartedly recommend Traditional Medicinals' Organic Roasted Dandelion Root Tea for anyone looking to improve their liver function and promote healthy digestion. Its blend of quality and versatility make it a standout choice among other herbal tea options, and its numerous benefits make it a worthwhile investment in your wellness routine. 🔗Dandelion Herbal Supplement Capsules (2,250mg, 200 Capsules)https://preview.redd.it/islunza9652d1.jpg?width=720&format=pjpg&auto=webp&s=841f021be43c9ae5d97fd96799c51cec42b82873 Earlier this year, my mom got me started on Nusapure's Dandelion Extract capsules, and it's been a game-changer for my digestive health. . I've had issues with minor constipation, and these powerful capsules have helped smooth things out, no pun intended. . The best part? . They're made from pure, potent Dandelion Root Extract, packed into one pill, and they're so easy to take. . Plus, knowing they're Non-GMO and Gluten-free gives me extra peace of mind. . If you're looking for a trustworthy and effective Dandelion supplement, look no further than Nusapure. . While the capsules are a bit large, they are still manageable even for someone like me with a sensitive gag reflex. . Overall, it's a fantastic product that has significantly improved my health and lifestyle! . 🔗GNC Herbal Plus Dandelion Root 550mg Capsules, 100 Eahttps://preview.redd.it/yxanumf9652d1.jpg?width=720&format=pjpg&auto=webp&s=ea8a67ca99d3499ac171ee409179e25f6a5d1ee7 As an avid user of GNC's Herbal Plus Dandelion Root supplements, I can vouch for their effectiveness firsthand. I started taking these capsules after a friend recommended them to relieve my ankle inflammation, and I must say, I've been pleasantly surprised by the results. The whole herb approach, in which the dandelion root is dried and processed without any additives, guarantees a potent and natural solution. One of the features that stood out to me is the convenience of consuming the capsules. Unlike traditional dandelion tea, there's no bitter taste or preparation required – just a quick swallow with water. Additionally, the daily dosage of one capsule helps maintain a balance in my body, without leaving any unpleasant aftertastes. However, everyone's body reacts differently to supplements, and some users have reported that the Dandelion Root made their stomach feel worse. It's essential to listen to your body and adjust your dosage or consult a healthcare professional if you experience any adverse effects. Overall, these capsules have been a game-changer in managing my inflammation, and I feel more energetic since I started taking them. If you're looking for a natural and potent supplement to improve your health, GNC's Herbal Plus Dandelion Root capsules are definitely worth considering. 🔗Herbal Liver Detox Supplement with Milk Thistle, Artichoke, Dandelion, and Spinach Extracthttps://preview.redd.it/11qzw1s9652d1.jpg?width=720&format=pjpg&auto=webp&s=14419513fd116ce9aab4a9566c160c9a5b06387f I've been using this herbal liver detox supplement for a few weeks now, and I must say, it's been quite the journey so far. The Siberian Green Herbal Liver Detox, as I like to call it, is a blend of well-tested and potent herbs like Milk Thistle, Artichoke, and Dandelion. These herbs have been used in traditional Siberian practices for centuries and are known for their liver-protecting properties. The Milk Thistle, in particular, is rich in Silymarin, which helps maintain liver cell health and supports normal liver function. Additionally, the Artichoke aids in the digestion process by stimulating blood flow from the liver. The Dandelion, on the other hand, boasts polysaccharides that reduce stress on the liver, empowering it to filter out harmful chemicals from your food. Furthermore, the Solarplast—a unique complex derived from spinach leaf extract—harnesses the power of its micronutrients to provide a rich source of antioxidants. It also offers a lipid protective coating, bolstering the overall well-being of your liver. What resonated with me most about this supplement is that it's based on old Siberian formulations and incorporates globally recognized herbal traditions. Plus, it's manufactured in the USA at a facility that adheres to the highest cGMP standards, ensuring superior quality assurance. I take three capsules daily, usually with my meals, as recommended by the healthcare professionals. At approximately $20 per bottle, which includes 60 capsules, this liver detox supplement is quite affordable. However, it's worth mentioning that I've only been using it for a month, so it's still early to gauge the long-term effects. So far, I've experienced a slight improvement in my overall energy levels and general well-being. I've also noticed that it has helped regulate my bowel movements without causing any stomach discomfort, which is a definite plus. To sum up, the Siberian Green Herbal Liver Detox is a potent natural formulation that brings together globally recognized herbal traditions to support, protect, and nourish your liver. While the results are promising, I'm excited to see how my body adapts to this supplement in the coming weeks. As a cautionary note, I would recommend consulting with your healthcare professional before starting any new supplement, especially if you have pre-existing medical conditions or are on prescribed medication. Pros:
🔗Nature's Answer Dandelion Root Liquid Extract - 1 fl oz (Gluten Free, Low Alcohol, Organic)https://preview.redd.it/3wblutea652d1.jpg?width=720&format=pjpg&auto=webp&s=d2b4fb869dcd54e35c48ec109a5f9f6b48ce6ae7 Dandelion Root from Nature's Answer has been a game-changer for me. As someone who's conscious about their well-being, I've always been drawn to natural remedies and supplements. When I came across this product, I was intrigued by its use of dandelion, a plant that's rich in vitamins and minerals. Firstly, I love how they've managed to capture all the goodness into a small bottle. The fact that there are 2000 mg of dandelion root extract in every drop makes it incredibly potent. And the best part? It doesn't contain alcohol, which is a plus for those who prefer avoiding it. Secondly, the packaging is super practical. The compact design makes it easy to carry around and discreetly take the liquid extract wherever I go. Plus, the dropper that comes with it helps me measure an accurate dose. One of the standout benefits is how it aids in digestion, liver health, and overall wellness. Dandelion root has a long-standing reputation for promoting digestive well-being and supporting liver functions. I've noticed a significant improvement in my digestive health since incorporating this into my daily routine. It's like my body is operating on a more balanced rhythm now. Another pro is its suitability for vegetarian diets. There are no animal-based ingredients, which is a big win for those who follow a plant-based lifestyle. However, I do wish that this bottle would last longer. It's just 30 ml, which can be consumed quite quickly if you're taking it daily. But given its concentrated potency and the noticeable benefits, I suppose it's understandable. In conclusion, Nature's Answer Dandelion Root Liquid Extract is a fantastic addition to any natural wellness arsenal. It offers a myriad of health benefits and is truly aligned with Nature's Answer's commitment to providing holistic support to the entire body. So, if you're looking for a reliable and effective health supplement, this could be your perfect match! 🔗Dandelion Root Infusion for Herbal Supplementshttps://preview.redd.it/o0dgs9ra652d1.jpg?width=720&format=pjpg&auto=webp&s=32174b4c61854f3e7c441b7fea0c66c64194bc36 As a coffee lover, I never thought I'd switch to dandelion root tea, but oh boy, was I in for a surprise! Just Herbs' Dandelion Root is as close as it gets to a morning pick-me-up. I add a hint of date syrup and Ceylon cinnamon to make a delicious infusion that's perfect for starting my day on a healthy note. I was a bit skeptical about trying an herbal supplement, but this miraculous root has been a game-changer for my mom, who suffers from chronic health conditions. The combination of dandelion root, palo d'arco, and muellin flowers has worked wonders in reducing inflammation and fluid retention. It's now a staple in her daily routine, and the difference in her overall health is evident. The taste of this dandelion tea is rich and unique, but it's definitely an acquired taste. If you're not a fan of the natural bitterness, adding some sweetener or pairing it with other ingredients can help make it more palatable. But honestly, I think it's worth trying at least once to see if it's something you'll enjoy. While I'm not a health expert, I can say that I've noticed a difference in how I feel since incorporating dandelion root tea into my routine. The natural diuretic properties help keep bloating at bay, and I find myself feeling more energized than ever. Plus, the fact that this product is sourced from a trusted online store makes it even more appealing. In conclusion, I highly recommend giving Just Herbs' Dandelion Root a try if you're looking for a natural way to support your overall health and well-being. Just remember to give your taste buds a little time to adjust if you're not used to the unique taste! 🔗Dandelion Root 180 Capsuleshttps://preview.redd.it/jxe1fj1b652d1.jpg?width=720&format=pjpg&auto=webp&s=b9253c7711643672c63b9c1a9387d4817027c2d9 As a health enthusiast, I've tried countless natural remedies and supplements. One such supplement that has been a game-changer for me is the Solaray Dandelion - 180 Capsules. This isn't just another weed in your lawn; it's a potent ingredient that has been proven to support healthy liver and kidney function. The Solaray Dandelion Root capsules are easy to consume and digest. I take two capsules twice a day with meals, as recommended on the bottle. The whole root is included, ensuring I get all the nutrients contained in the plant. One of the things that I've noticed since incorporating this supplement into my routine is improved digestion, especially of fats and maintaining water balance in my body. It's a trusted brand, manufactured in their own facility with non-GMO and vegan ingredients. However, not everything about this product is perfect. It does have a mild diuretic effect, which might be a problem for some individuals. Also, it's worth mentioning that while the capsules do not have a strong taste, there are other brands on the market that offer slightly better quality Dandelion extracts. In conclusion, if you are looking for a natural remedy to support your liver and kidney function, the Solaray Dandelion Root capsules are definitely worth trying. They are easy to use, packed with nutrients, and have helped me maintain a healthier lifestyle. Just remember to start with a lower dosage to see how your body reacts before increasing it. Buyer's GuideImportant Features of Dandelion Herbal Supplementshttps://preview.redd.it/h2qyc2eb652d1.jpg?width=720&format=pjpg&auto=webp&s=ef5a8472e9d407fe6a83c9bbd44950e2666141ec Dandelion herbal supplements are natural remedies derived from the dandelion plant. These supplements consist of various active compounds such as taraxacin, taraxasterol, and inulin, among others. Typically, they come in the form of tablets, capsules, or liquid extracts. Key features include:
Considerations When Buying Dandelion Herbal SupplementsIt's crucial to consider several factors before purchasing dandelion herbal supplements. These include:
General Advice When Using Dandelion Herbal SupplementsWhile dandelion herbal supplements generally have a good safety profile, it's always best to follow these general guidelines:
https://preview.redd.it/1gc59nxb652d1.jpg?width=720&format=pjpg&auto=webp&s=67073b93780187a4d3d5a854a0943228308bbc99 FAQWhat are the potential health benefits of dandelion herbal supplements?Dandelion herbal supplements are believed to offer several health benefits, such as improving digestion and liver function, promoting urinary health, supporting healthier skin, and helping to maintain blood sugar levels within a normal range.How do dandelion supplements work?https://preview.redd.it/jengk96c652d1.jpg?width=720&format=pjpg&auto=webp&s=8c6f381756aadf3e5e03a64dd397e6639525355f Dandelion herbal supplements contain various active ingredients like taraxacin, inulin, sesquiterpenes, and triterpenes. These compounds work together to help support the healthy functioning of the liver, kidneys, and digestive system. What are some potential side effects of dandelion herbal supplements?Although generally considered safe, some people may experience side effects such as minor stomach upset, diarrhea, or skin irritation. Persons with specific health conditions should consult their doctors before using dandelion supplements.Is it safe to take dandelion supplements while pregnant or breastfeeding?It is best to consult with your healthcare provider before taking any herbal supplements while pregnant or breastfeeding since they may affect hormones and potentially interact with other medications or herbal products you are taking. https://preview.redd.it/y569fsgc652d1.jpg?width=720&format=pjpg&auto=webp&s=fb111bddbafb9b23d4ade94495e1722d5154f872 How do I choose the best dandelion herbal supplement for my needs?To choose the best dandelion supplement, look for products made by reputable brands, with high-quality ingredients and free from added artificial ingredients and fillers. Also, consider the dosage strength and whether it's suitable for your specific health goals and needs.How long does it take for dandelion herbal supplements to work?The effects of dandelion supplements may vary depending on the individual, but some may notice improvements in digestion, energy levels, and overall well-being within a few weeks of starting the supplement. However, it is essential to give your body time to adjust and to keep consistent with your dosage recommendations.What is the recommended dosage for dandelion herbal supplements?Recommended dosages for dandelion herbal supplements can vary depending on the product, but typically range from 500-1500 mg per day, divided into two or three doses. Always follow the instructions on the product label and consult your healthcare provider if you have any questions or concerns.Can I take dandelion supplements with other medications or herbal products?It is essential to consult your doctor before combining any herbal supplement with prescription or over-the-counter medications. Dandelion may interact with certain drugs, such as diuretics, blood thinners, and lithium. Be sure to disclose any medication or supplement use to your healthcare provider for proper guidance.How can I store dandelion herbal supplements?To maintain the freshness and effectiveness of dandelion herbal supplements, store them in a cool, dry place away from direct sunlight, excessive heat, or moisture. Keep the container sealed to prevent contamination and oxidation.What should I do if I accidentally overdose on dandelion herbal supplements?If you suspect you have taken too much dandelion, contact your local poison control center or seek medical attention immediately. Overdose symptoms may vary, but it is crucial to seek professional help to assess the situation and provide appropriate treatment.As an Amazon™ Associate, we earn from qualifying purchases. |
2024.05.23 10:33 Toothlessenjoyer ULPT request: How can I deal with a flatmate with inconsiderate bathroom antics?
Hello, I'm looking for some advice on how to deal with my flatmate over his extremely inconsiderate bathroom antics.
He leaves his hair in the bathroom, EVERYWHERE, especially after a shower there's hundreds of what look like pubes all over the shower tray.
He spends ages (30-90 minutes) in the bathroom at a time, just sitting on the toilet scrolling tiktok. We've talked to him many times about this and he doesn't care. I recently have been getting him out by turning off his wifi with parent privileges but it seems he's now using mobile data.
He's a fat Pakistani slob that only eats Weetabix and instant noodles, so any constipation is his own doing.
Please give me suggestions, I'm from the UK and dont want to do anything illegal like using a cellphone jammer (also expensive). I am considering removing the locks from the door but we share the bathroom with a female flatmate and that isn't fair on her, though she does 'side' with me over having to do something.
I move out in 3 weeks so anything drastic will likely be done right at the end, but I have exams and this guy is causing me to delay my days activities by hours sometimes as he times his bathroom adventures to be exactly right when I'm about to use it myself.
Please help me
submitted by Toothlessenjoyer to UnethicalLifeProTips [link] [comments]
He leaves his hair in the bathroom, EVERYWHERE, especially after a shower there's hundreds of what look like pubes all over the shower tray.
He spends ages (30-90 minutes) in the bathroom at a time, just sitting on the toilet scrolling tiktok. We've talked to him many times about this and he doesn't care. I recently have been getting him out by turning off his wifi with parent privileges but it seems he's now using mobile data.
He's a fat Pakistani slob that only eats Weetabix and instant noodles, so any constipation is his own doing.
Please give me suggestions, I'm from the UK and dont want to do anything illegal like using a cellphone jammer (also expensive). I am considering removing the locks from the door but we share the bathroom with a female flatmate and that isn't fair on her, though she does 'side' with me over having to do something.
I move out in 3 weeks so anything drastic will likely be done right at the end, but I have exams and this guy is causing me to delay my days activities by hours sometimes as he times his bathroom adventures to be exactly right when I'm about to use it myself.
Please help me
2024.05.23 08:27 wtfizthiss Help with complex health issues, most recent labs & overall declining health?
Female, 134, 5’5”, 120lbs
I am in desperate need of any kind of help as I’m declining in health, and it took a sharp fall off the cliff 2 years ago. I’ve been in and out of every specialist’s office you can think of, and done so many tests that I feel like a lab rat; no answers, no effective care plans, and some doctors just telling me they don’t know what to do and they can no longer help me. Only thing is do get is new symptoms every couple of months. My most pressing issue is my inability to gain weight/strength - I’m a shell of my former self. Started at 160lbs and dropped to 140lbs in 2 months, then 140 to 130 in 1 month. I hovered between 128-133 for about a year, then dropped to 119-123, and have been there since; all of this has been without trying. Since the first sudden drop, I began tracking caloric intake to try to maintain my weight. Since getting into the 120s, I began, and currently have and have a caloric intake which should have me gaining 2-3lbs/ day, given my TDEE, but it’s not working. I’m throwing back around 2,000 (sometimes more) calories/day of all types of food; both healthy and horrible, to the point where I’m grocery shopping 2-3x/wk. The only results I’ve gotten are constipation, pain, and abdominal distention.
I am folate deficient w/macrocytic anemia, have been for years, and my doctors have tried pushing me to eat more folate - spoiler, doesn’t work, as my diet is already high in folate. I also had a severe reaction to taking 1mg of folic acid - I’m talking drug allergy type of reaction. The first time I’d ever had my folate tested, it was at 2.5 mg/dL - and this was while I’d already been taking prenatal vitamins for years, for the biotin, and eating an extremely high-folate diet. I am concerned for my health, given everything I’ve mentioned, and listed below. I’m especially concerned since I now take AEDs, is a contraindication of my MTHFR polymorphism (undermethylation) and can impact my kidneys. Nothing is helping, I’m concerned, and my family and friends are concerned, telling me I need to eat more (how much more can I eat?!), and I just need some input from a broader audience.
I’ve included my current health summary, most recent labs, and relevant test findings. As I am a data analyst, I have all my labs for the last 10 years tracked, and all my H and L values have been creeping more and more out of range every year. Please let me know if there is any additional pertinent data/info you need to give some insight as to what is going on. I’ll try to put my previous bloodwork in the comments, as photos.
Shooting into the dark here - TIA.
Coagulation - Prothrombin Time 14.0 - INR 1.1 - Partial Thromboplastin Time 28
Routine Chemistry - Sodium Level 141 - Potassium Level 4.1 - Chloride Level 110 High - CO2 24 - Alk Phos 50 - AST 13.0 - ALT 12 - BUN 7 - Glucose Level 99 - Creatinine Level 0.76 - BUN/Creat Ratio 9 - eGFR AA 105 - eGFR Non-AA 87 - Calcium Level 8.60 - Protein Total 5.9 Low - Albumin Level 3.8 - Globulin 2 - A/G Ratio 2 - Bilirubin Total 0.4 - Anion Gap 7
Thanks again
Edit: formatting
submitted by wtfizthiss to AskDocs [link] [comments]
I am in desperate need of any kind of help as I’m declining in health, and it took a sharp fall off the cliff 2 years ago. I’ve been in and out of every specialist’s office you can think of, and done so many tests that I feel like a lab rat; no answers, no effective care plans, and some doctors just telling me they don’t know what to do and they can no longer help me. Only thing is do get is new symptoms every couple of months. My most pressing issue is my inability to gain weight/strength - I’m a shell of my former self. Started at 160lbs and dropped to 140lbs in 2 months, then 140 to 130 in 1 month. I hovered between 128-133 for about a year, then dropped to 119-123, and have been there since; all of this has been without trying. Since the first sudden drop, I began tracking caloric intake to try to maintain my weight. Since getting into the 120s, I began, and currently have and have a caloric intake which should have me gaining 2-3lbs/ day, given my TDEE, but it’s not working. I’m throwing back around 2,000 (sometimes more) calories/day of all types of food; both healthy and horrible, to the point where I’m grocery shopping 2-3x/wk. The only results I’ve gotten are constipation, pain, and abdominal distention.
I am folate deficient w/macrocytic anemia, have been for years, and my doctors have tried pushing me to eat more folate - spoiler, doesn’t work, as my diet is already high in folate. I also had a severe reaction to taking 1mg of folic acid - I’m talking drug allergy type of reaction. The first time I’d ever had my folate tested, it was at 2.5 mg/dL - and this was while I’d already been taking prenatal vitamins for years, for the biotin, and eating an extremely high-folate diet. I am concerned for my health, given everything I’ve mentioned, and listed below. I’m especially concerned since I now take AEDs, is a contraindication of my MTHFR polymorphism (undermethylation) and can impact my kidneys. Nothing is helping, I’m concerned, and my family and friends are concerned, telling me I need to eat more (how much more can I eat?!), and I just need some input from a broader audience.
I’ve included my current health summary, most recent labs, and relevant test findings. As I am a data analyst, I have all my labs for the last 10 years tracked, and all my H and L values have been creeping more and more out of range every year. Please let me know if there is any additional pertinent data/info you need to give some insight as to what is going on. I’ll try to put my previous bloodwork in the comments, as photos.
Shooting into the dark here - TIA.
Current Health Summary
- Celiac Disease
- compliant w/GF diet since 2012
- Macrocytic Anemia
- consistently low folate
- consistently High MCH, MCV
- consistently Low RBC
- consistently low Immunoglobulin A, qn, serum: 65 mg/dL (most recent)
- Elevated Homocysteine
- 48.9 umol/L before starting AEDs
- hEDS
- Primary Generalized Myoclonic Epilepsy
- sudden onset with rapid progression over 4-6 months
- controlled on meds
- negative panel for cancerous cause of sudden onset of epilepsy
- 2 abnormal EEGs
- Convulsive Pre-Syncope/Syncope
- Multiple swollen lymph nodes
- 3 occipital, one behind jaw/under ear, 2 in groin region
- all present for over 1 year
- hard, not painful
- neck/head US: “likely correspond to benign/reactive lymph nodes”; Pending US for others
- ADHD
- Generalized Depression
- Mild Scoliosis
- Bilateral trochanteric bursitis
- Sudden-onset vertical diplopia
- 02/16/2024
- Migraines with Aura
- Frequent heart palpitations
Test Findings
- Genetics
- Comp-Het. MTHFR variations: C677T/A1298C; clinically significant
- HCN4 Gene Variation: heterozygous
- PMS2 Gene Variation: heterozygous
- KCNH2 Gene Variation: heterozygous
- HLA Typing, DQA1*05 - Positive
- Gastroenterology
- EGD: “Active granulation tissue with exudate, consistent with erosion/ulcer”
- Colonoscopy: Unremarkable
- Small Intestine MRI: Unremarkable
- Rheumatology
- was told that eventually I’ll almost certainly be dx’d with Sjögren’s, but bloodwork just wasn’t there yet (2020)
- Anti-la (ss-B) Ab (rdl): Positive 52 units
- Anti-nuclear Ab by ifa (rdl): Positive
- ANA Speckled Pattern: 1:320
- Sjogren’s anti-ss-B High: 1.8 ai
- Antinuclear antibodies, ifa, serum: Pos.
- ANA Speckled Pattern, serum: 1:80
- Neurology
- Chiari 1 Malformation (05/31/2023)
Current Medications
- Lacosamide: 100mg BID
- Clobazam: 10mg BID
- AdderallXR: 30mg Capsule, daily as needed (taking maybe 2x/wk)
Lab Results
CBC and Differential (5/4/24) - WBC 5.0 - RBC 3.74 - Hgb 12.9 - Hct 36.7 Low - Platelets 251 - MCV 97.9 High - MCH 34.6 High - MCHC 35.3 - RDW 12.1 Low - MPV 7.2 Low - Neutro Auto 47.0 - Lymph Auto 40.0 - Mono Auto 6.9 - Eos, Auto 4.9 - Basophil Auto 1.1 - NRBC Auto 0.1 - Neutro Absolute 2.4 - Lymph Absolute 2.0 - Mono Absolute 0.4 - Eos Absolute 0.2 - Baso Absolute 0.1 - NRBC Absolute 0.01Coagulation - Prothrombin Time 14.0 - INR 1.1 - Partial Thromboplastin Time 28
Routine Chemistry - Sodium Level 141 - Potassium Level 4.1 - Chloride Level 110 High - CO2 24 - Alk Phos 50 - AST 13.0 - ALT 12 - BUN 7 - Glucose Level 99 - Creatinine Level 0.76 - BUN/Creat Ratio 9 - eGFR AA 105 - eGFR Non-AA 87 - Calcium Level 8.60 - Protein Total 5.9 Low - Albumin Level 3.8 - Globulin 2 - A/G Ratio 2 - Bilirubin Total 0.4 - Anion Gap 7
Thanks again
Edit: formatting
2024.05.23 08:06 KonoKayStarDa What Else Can I Do To Ease My Stomach Problems?
I'm (F21) going to start off by saying I'm not a 100% sure I have IBS, but I'm fairly certain I have it. My mother has IBS, but I don't know if that can be passed down to children.
For starters, this all started around Spring of 2023 when I was under intense stress. I noticed I was having constant stomach pain, flatulence, bloating, and constipation. That summer I went to the ER and had some tests done, and the doctor quite literally said I had about 10 pounds of poop backed up. In addition, I went to another doctor, and he said I had constipation along with GERD. Okay, so, I did around 2 or 3 colon cleanses with Miralax, Senna, Magnesium gummies, Enemas, and a laxative mixed with lemonade.
My stomach was, at most, okay-ish after that, I think. I still had various bouts of feeling bloated, flatuence, and problems pooping. To combat this, my grandma started giving me the herb, Slippery Elm (400 mg), to take. I took 1-3 capsules each day ever since, and the herb has been effective!
Fast forward to now, things have slowly started getting a bit problematic. Recently, I've been feeling full and bloated after about every meal. It's uncomfortable and feels like I will vomit, but I never do (severely happy about this because I have the strong fear of vomiting). As for bowel movements, they've been happening every other day, or it takes around two days for me to poop. My stool is still hard but is sometimes like average pebble size. I can feel the gas inside my stomach moving and shifting around, which causes discomfort and feels like I'm going to explode.
I've noticed it takes around 15-30 minutes before I start burping or passing gas after a meal, which eases the bloated feeling slowly. When I exercise, the gas comes out rapidly in short bursts. Right now, it feels like I need to poop, but it won't come out.
In addition, my stomach will sometimes feels acidic I think, which is where it feels like there's gas building up, so I usually combat this by eating something.
My diet isn't the healthiest right now. I start off the day with eating 4 Van's Gluten Free waffles and two patty sausages. For dinner and/or lunch, I eat some type of meat (chicken, spaghetti with ground beef in it, or tortillas stuffed with ground beef) and some of Cybele's Gluten Free and Vegan Confetti Cookies. I eat vegetables every other day. I drink around, at least, two bottles of water daily. I eat spearmint throughout the day a whole lot (I go through three bags in a week).
So, I'm mainly asking for advice on how to combat this. The bloating makes me feel like I'm going to burst after about every meal, and I just want any advice for the rest of my stomach issues. Tips, feedback, advice, and etc are welcomed! I apologize if this was long! This has been an on-going problem, and I didn't want to leave anything out that may be important :).
submitted by KonoKayStarDa to ibs [link] [comments]
For starters, this all started around Spring of 2023 when I was under intense stress. I noticed I was having constant stomach pain, flatulence, bloating, and constipation. That summer I went to the ER and had some tests done, and the doctor quite literally said I had about 10 pounds of poop backed up. In addition, I went to another doctor, and he said I had constipation along with GERD. Okay, so, I did around 2 or 3 colon cleanses with Miralax, Senna, Magnesium gummies, Enemas, and a laxative mixed with lemonade.
My stomach was, at most, okay-ish after that, I think. I still had various bouts of feeling bloated, flatuence, and problems pooping. To combat this, my grandma started giving me the herb, Slippery Elm (400 mg), to take. I took 1-3 capsules each day ever since, and the herb has been effective!
Fast forward to now, things have slowly started getting a bit problematic. Recently, I've been feeling full and bloated after about every meal. It's uncomfortable and feels like I will vomit, but I never do (severely happy about this because I have the strong fear of vomiting). As for bowel movements, they've been happening every other day, or it takes around two days for me to poop. My stool is still hard but is sometimes like average pebble size. I can feel the gas inside my stomach moving and shifting around, which causes discomfort and feels like I'm going to explode.
I've noticed it takes around 15-30 minutes before I start burping or passing gas after a meal, which eases the bloated feeling slowly. When I exercise, the gas comes out rapidly in short bursts. Right now, it feels like I need to poop, but it won't come out.
In addition, my stomach will sometimes feels acidic I think, which is where it feels like there's gas building up, so I usually combat this by eating something.
My diet isn't the healthiest right now. I start off the day with eating 4 Van's Gluten Free waffles and two patty sausages. For dinner and/or lunch, I eat some type of meat (chicken, spaghetti with ground beef in it, or tortillas stuffed with ground beef) and some of Cybele's Gluten Free and Vegan Confetti Cookies. I eat vegetables every other day. I drink around, at least, two bottles of water daily. I eat spearmint throughout the day a whole lot (I go through three bags in a week).
So, I'm mainly asking for advice on how to combat this. The bloating makes me feel like I'm going to burst after about every meal, and I just want any advice for the rest of my stomach issues. Tips, feedback, advice, and etc are welcomed! I apologize if this was long! This has been an on-going problem, and I didn't want to leave anything out that may be important :).
2024.05.23 06:28 comicallylarge_rat Did psych meds and anxiety cause my IBS?
22F here looking for any sort of advice regarding IBS-M, mostly diarrhea symptoms. When I was 12 I was diagnosed w anxiety, depression, and ADHD and was put on a cocktail of meds. Right around that time, I noticed worsening of symptoms I’d always had, mainly diarrhea. That was also when my anxiety symptoms first seriously took over my life.
All doctors I see tell me my IBS symptoms are “just side effects” of my meds. I find that hard to believe as I’ve been on dozens of meds and endless combinations and never noticed changes (other than slight improvement when I stopped taking a stimulant). I am bipolar so going off of meds is out of the question for me, I need them for maintenance and to stay out of jail. I’m currently on 4, one of which is lithium, which notoriously causes GI issues.
In addition to a fascinating array of mental illnesses, I have fibromyalgia, POTS, migraines, some kind of mentrual disorder (debilitating cramps and insane flow), and chronic knee and back injuries that hurt just about always. I feel like somehow, someway it’s all related.
I usually “go” 3-8 times a day, followed by a day or two of constipation and being so bloated I can’t do anything comfortably. I’m gassy and tired.
I also know coffee, dairy, red meat, anything processed, things high in sugafat, and any stimulant including coffee is a trigger, but avoiding those never helped much. If I avoided everything that gives me diarrhea I would perish of starvation.
Any advice is appreciated. I’ve tried probiotics and fiber supplements, I was vegan for years, and I even went a gastro who only wanted to stick a camera up my butt. I was tested for celiacs and it’s not that. I’m tired of living in fear of my next meal, traveling, and potentially mortifying bathroom experiences. Help!
submitted by comicallylarge_rat to IBSHelp [link] [comments]
All doctors I see tell me my IBS symptoms are “just side effects” of my meds. I find that hard to believe as I’ve been on dozens of meds and endless combinations and never noticed changes (other than slight improvement when I stopped taking a stimulant). I am bipolar so going off of meds is out of the question for me, I need them for maintenance and to stay out of jail. I’m currently on 4, one of which is lithium, which notoriously causes GI issues.
In addition to a fascinating array of mental illnesses, I have fibromyalgia, POTS, migraines, some kind of mentrual disorder (debilitating cramps and insane flow), and chronic knee and back injuries that hurt just about always. I feel like somehow, someway it’s all related.
I usually “go” 3-8 times a day, followed by a day or two of constipation and being so bloated I can’t do anything comfortably. I’m gassy and tired.
I also know coffee, dairy, red meat, anything processed, things high in sugafat, and any stimulant including coffee is a trigger, but avoiding those never helped much. If I avoided everything that gives me diarrhea I would perish of starvation.
Any advice is appreciated. I’ve tried probiotics and fiber supplements, I was vegan for years, and I even went a gastro who only wanted to stick a camera up my butt. I was tested for celiacs and it’s not that. I’m tired of living in fear of my next meal, traveling, and potentially mortifying bathroom experiences. Help!
2024.05.23 05:29 Forward_Part4638 Need help 🙏
Not looking for diagnose, looking for help🙏
(Made a throw away for privacy) Pre diagnose :
Background : M/23 , 76 kgs and 6’2 regular in gym for last 3 year . Fittest person I have met in my life never had a flu or stomachache more than 2-3 in my entire life.
January 2024 Started having stomach pain, bloating, constipation and diarrhoea and tingling sensation in stomach everywhere like small knifes cutting my insides.
Went to a GI 1 : Test 1 : Calprotectin fecal test : Came negative, given ibs meds for 2 weeks to no avail.
Changed to G1 2 :
He ordered ultrasound and a blood and liver function test, thyroid function test(as I was going through very anxious period of life).
Ultrasound: All normal except fecal loaded bowels i.e. constipation.
Blood test : All normal except few nutrophiles and lymphocides here and there not my much.
Liver function test : All normal exceptionally high alkaline phosphate.
Thyroid : TSH = 7.5 (normal range reference 0.4-4) ; checked for anti tpo bodies which were 400+ diagnosed with Hashimoto thyroid and asked for a thyroid function test after a month , which came elevated so on 12.5 mg of levo.l recommended by an endo mentioned later.
Coming back to GI issues , so GI had no more answers so he suggested a Fibroscan and a endoscopy which I went with here the story gets interesting.
Fibroscan normal .
Endoscopy with 4 biopsy samples taken from D2.
D1 : normal visually.
D2 : Scalloping of folds , malabsorption , erosion observed in stomach.
Biopsy : normal lymphocytes and villi so verdict was “Chronic duodentis “. Given IBS meds and asked to ” exercise” lmao! Also my anxiety and stress was very high during this period cause of thyroid diagnose, new job and stomach pain not going away.
Had a colonoscopy for my peace of mind too on my expense which came out negative too.
Went to a Endocrinologist for thyroid recheck: He was the one who put me on levo and I asked him about my stomach concerns and ordered a ttg-iga test which came at 20U/ml with range as >13 negative and 13-18 equivocal and <18 as positive.(attached picture) and immediately put me on gluten and dairy free diet.
Post diagnose : 22 May
Symptoms still there stomach pain occasional under left and right rib, very clay like stool with undigested food.
On strict gluten free diet from past 1.5 month which is very strict except had a bite of sandwich cause this thing is new to me and almost forgot about diet.
Losing weight now am only 70kg which makes me cry when I look in the mirror.I just want to cry cause it feels like everything this is falling apart my body, job and relationship.
Question: Why didn’t the celiac show up on endo? Could it be anxiety and stress which caused this? Is celiac raised by hashimoto’s? Or I am just a new celiac dealing with denial and need to be gluten free for a lot more.
(Yes , I know these questions are for my health provider but looking for some guidance here thanks🙏)
Will be seeing my GI and a new GI this weekend.
submitted by Forward_Part4638 to AskDocs [link] [comments]
(Made a throw away for privacy) Pre diagnose :
Background : M/23 , 76 kgs and 6’2 regular in gym for last 3 year . Fittest person I have met in my life never had a flu or stomachache more than 2-3 in my entire life.
January 2024 Started having stomach pain, bloating, constipation and diarrhoea and tingling sensation in stomach everywhere like small knifes cutting my insides.
Went to a GI 1 : Test 1 : Calprotectin fecal test : Came negative, given ibs meds for 2 weeks to no avail.
Changed to G1 2 :
He ordered ultrasound and a blood and liver function test, thyroid function test(as I was going through very anxious period of life).
Ultrasound: All normal except fecal loaded bowels i.e. constipation.
Blood test : All normal except few nutrophiles and lymphocides here and there not my much.
Liver function test : All normal exceptionally high alkaline phosphate.
Thyroid : TSH = 7.5 (normal range reference 0.4-4) ; checked for anti tpo bodies which were 400+ diagnosed with Hashimoto thyroid and asked for a thyroid function test after a month , which came elevated so on 12.5 mg of levo.l recommended by an endo mentioned later.
Coming back to GI issues , so GI had no more answers so he suggested a Fibroscan and a endoscopy which I went with here the story gets interesting.
Fibroscan normal .
Endoscopy with 4 biopsy samples taken from D2.
D1 : normal visually.
D2 : Scalloping of folds , malabsorption , erosion observed in stomach.
Biopsy : normal lymphocytes and villi so verdict was “Chronic duodentis “. Given IBS meds and asked to ” exercise” lmao! Also my anxiety and stress was very high during this period cause of thyroid diagnose, new job and stomach pain not going away.
Had a colonoscopy for my peace of mind too on my expense which came out negative too.
Went to a Endocrinologist for thyroid recheck: He was the one who put me on levo and I asked him about my stomach concerns and ordered a ttg-iga test which came at 20U/ml with range as >13 negative and 13-18 equivocal and <18 as positive.(attached picture) and immediately put me on gluten and dairy free diet.
Post diagnose : 22 May
Symptoms still there stomach pain occasional under left and right rib, very clay like stool with undigested food.
On strict gluten free diet from past 1.5 month which is very strict except had a bite of sandwich cause this thing is new to me and almost forgot about diet.
Losing weight now am only 70kg which makes me cry when I look in the mirror.I just want to cry cause it feels like everything this is falling apart my body, job and relationship.
Question: Why didn’t the celiac show up on endo? Could it be anxiety and stress which caused this? Is celiac raised by hashimoto’s? Or I am just a new celiac dealing with denial and need to be gluten free for a lot more.
(Yes , I know these questions are for my health provider but looking for some guidance here thanks🙏)
Will be seeing my GI and a new GI this weekend.
2024.05.23 05:25 1cecream4breakfast Surgical menopause, HRT, and constipation?
37, had my ovaries both removed by age 30 due to cancer.
Was on OCP for several years for HRT, but the last couple years I’ve had quite a lot of unpredictable bleeding for weeks at a time. Multiple hysteroscopy and a colposcopy were normal. I finally caved and got an IUD and switched to an estrogen gel on my thigh. I have high BP so the gel is better as it lowers my risk of a blood clot compared to OCP. (I also have T2 diabetes but it’s very well managed, and I don’t smoke).
Anyhoo, I have had a lot of belly pressure lately. I thought I had a recurring umbilical hernia, but CT scan only noted a “tiny defect” which would not explain the feeling that my stomach feels like it’s about to pop. It WOULD explain why such a tiny defect feels so large. I’ve noticed the last 3 weeks or so that I poop less often. i usually go once a day but lately it’s once every 2-3. I don’t feel like I have to go—I feel like everything just takes forever to work its way down. I take stool softeners to help and I’ve already been taking a fiber supplement and adding fiber to my diet. I feel like I stay pretty well hydrated but I could probably do better. But out of curiosity I googled whether estrogen gel could cause this and apparently it can. Has anyone experienced this? Did it resolve after a while? I’m wondering if I should get my estrogen levels checked by OBGYN or just ask her to reduce my dose or just not use the whole packet (with her blessing). I was just in a couple weeks ago for my IUD 1-month check but I hadn’t noticed constipation yet at that point so I didn’t bring it up. I wonder if my estrogen might be too high though. Or maybe I’m getting more from the gel than I did from the pill and my body needs a minute?
submitted by 1cecream4breakfast to Menopause [link] [comments]
Was on OCP for several years for HRT, but the last couple years I’ve had quite a lot of unpredictable bleeding for weeks at a time. Multiple hysteroscopy and a colposcopy were normal. I finally caved and got an IUD and switched to an estrogen gel on my thigh. I have high BP so the gel is better as it lowers my risk of a blood clot compared to OCP. (I also have T2 diabetes but it’s very well managed, and I don’t smoke).
Anyhoo, I have had a lot of belly pressure lately. I thought I had a recurring umbilical hernia, but CT scan only noted a “tiny defect” which would not explain the feeling that my stomach feels like it’s about to pop. It WOULD explain why such a tiny defect feels so large. I’ve noticed the last 3 weeks or so that I poop less often. i usually go once a day but lately it’s once every 2-3. I don’t feel like I have to go—I feel like everything just takes forever to work its way down. I take stool softeners to help and I’ve already been taking a fiber supplement and adding fiber to my diet. I feel like I stay pretty well hydrated but I could probably do better. But out of curiosity I googled whether estrogen gel could cause this and apparently it can. Has anyone experienced this? Did it resolve after a while? I’m wondering if I should get my estrogen levels checked by OBGYN or just ask her to reduce my dose or just not use the whole packet (with her blessing). I was just in a couple weeks ago for my IUD 1-month check but I hadn’t noticed constipation yet at that point so I didn’t bring it up. I wonder if my estrogen might be too high though. Or maybe I’m getting more from the gel than I did from the pill and my body needs a minute?
2024.05.23 05:01 sabbyyanks Symptoms
Hey all! My mom is going for a gullbladder removal tomorrow, and just praying everything is taken care of. She’s been dealing with this since about Mid Feb! She first went in after constant throwing up all day and then threw up blood after so much throw up. ER said kidney stones, and the throw up was caused by an excess throwing up all day. Then she didn’t feel well again, went to a different ER and was said to believe she has ulcers, and gave her some stomach medicine. She went to her primary doctor which had her do a cologuard test, and said he also thinks it’s ulcers. She was throwing up the next morning, so i told her to go in and not leave until she can see a specialist or they run every test in the book. It was scary. They referred her to a general surgeon, and which they have led us to the conclusion it’s her gullbladder. She had her HIDA scan before vacation, and now surgery tomorrow AM. I’m just so worried due to her symptoms. She has lost weight, looks pale, looks always fatigued, can’t eat much and when she does she may get constipated, diarrhea etc…and also has the upper right pain under her lung area. I am a worried son, and just want some other perspectives!!
submitted by sabbyyanks to gallbladders [link] [comments]
2024.05.23 04:35 renegade455 MBD or just a birth defect/ old injury?
 | Hey guys this here is Mr. Chile. He has a bit of a wonky spine as you can see in the pictures. I was just curious and wanted to get your guys opinions. I purchased him from a breeder (unfortunately do not remember the name) at a reptile expo back in April. He was in a tank with two other beardies piled on top of him. I was enamored by his color and felt bad for him because he was in an obvious losing battle for resources. He was constipated when i got him and uninterested in food. I got him back up to speed and he now loves his greens and insects. He gets plain calcium dusted on his insects every feeding and calcium with d3 every other feeding. He is alert and active, loves running around. He is in a 40 gallon with paper towels as substrate and a T5 10.0 ZooMed above him. His spine doesn’t cause him and obvious discomfort and it doesn’t keep him from moving around. Thanks in advanced guys! submitted by renegade455 to BeardedDragons [link] [comments] |
2024.05.23 00:40 RegainingMe Help please
Hi, so I’m usually a very sensible person, who researches everything to the nth degree.
Well not this week, after all lifetime of being unhappy about my weight, I stumbled across something about Mounjaro on Tuesday. Decided it’s now or never and placed an order that day, it was approved today and I think my first pen might be arriving tomorrow.
I’ve created a new account for this so that no one knows about this unless I want them to. I have tried to read some of the recent posts and identify with many comments. I’ve never felt slim. I’ve had 3 babies and 12 miscarriages between babies 2 and 3 which took its toll, along with losing a parent during that. In the recurrent miscarriage journey, I was told I have PCOS. I only have to look at food to put on weight, it’s always been the same. I also have hyper-mobility and 3 C sections have left me with a back that is prone to going. Knees aren’t great either and I’ve never enjoyed exercise and I just don’t do anything anymore. I just want to lose weight and feel better about myself, stop avoiding photos with my children, be happy to go out for a meal without feeling like others are judging what I order, be more active and fun as a Mum. Be the person I was when I met my husband. He tells me all the time he loves me and he does so much to show me that, but I just hate what I look like.
So I’m 47, 5’1”, 14st 6lb. I would love to get to 10 stone, the charts would say I need to be less than that but as I haven’t seen that weight since I met my husband, I think that’s a more than optimistic target for now!
What I need help with is guidance over what to eat. I’m a fussy eater which won’t help matters!
So far I’ve seen lots of comments about drinking water, I drink no added sugar squash, I’m hoping that will be ok?
I don’t eat breakfast. Currently I usually have 2 slices of white toast for lunch with chicken dripping on (so collagen is good but the little bit of fat on the top may cause problems? How much fat can be tolerated?) and then I have a glass of semi-skimmed milk and a small packet of crisps from a multi pack, and then either a nectarine or a clementine or some grapes or strawberries. Our children eat hot meals at school and so they have cold teas, and we’ve got out of the habit of bothering to cook a proper meal for ourselves at night. I sometimes have a bowl of cauliflower with gravy and then a slice of bread to soak into the leftover gravy. I sometimes have some Itsu gyoza dumplings. Sometimes I might have a fish finger sandwich. Or some prawns on a plate with beetroot and cherry tomatoes and a slice of edam. Sometimes just a bowl of crunchy nut cornflakes or a couple of dippy eggs. Fridays I cook for us at lunch as I don’t work then, so we usually have bavette steak with 3 hash browns each and then babycorn that i microwave and then finish in a pan with a little butter and salt. Weekends I properly cook for us all. I eat caramel snack a jacks and I’m partial to a mini caiipo in warm weather.
What should I be aiming at eating each day? My biggest worry is the side effects and doing what I can to minimise the chances of sickness or trouble with constipation or diarrhoea. I want to lose weight but I want to try and be healthy if I can, so I’m not having my hair fall out which I saw one person mention. I’m also hoping I can lose weight without having to much exercise at least for now, because I’m just not ready to go there right now.
Also, I have an afternoon tea booked 4.5 weeks from now and I need to go. Sandwiches, scones and fancy desserts. How bad will it be being on the injections to do that? It’s booked for 1pm, if I don’t eat anything until then, might I be able to appear normal to the others there in terms of volume? Or should I be saying that I’m not feeling well and asking for a doggy bag…Or if I time my first injection so that I’m due to inject the day after the afternoon tea, would that lessen the effects by the day I go?
PS sorry for how long this ended up being, I think I’m slightly panicking as I really want this to work and to lose weight like you have all done, but scared about getting it wrong and making myself ill!
submitted by RegainingMe to mounjarouk [link] [comments]
Well not this week, after all lifetime of being unhappy about my weight, I stumbled across something about Mounjaro on Tuesday. Decided it’s now or never and placed an order that day, it was approved today and I think my first pen might be arriving tomorrow.
I’ve created a new account for this so that no one knows about this unless I want them to. I have tried to read some of the recent posts and identify with many comments. I’ve never felt slim. I’ve had 3 babies and 12 miscarriages between babies 2 and 3 which took its toll, along with losing a parent during that. In the recurrent miscarriage journey, I was told I have PCOS. I only have to look at food to put on weight, it’s always been the same. I also have hyper-mobility and 3 C sections have left me with a back that is prone to going. Knees aren’t great either and I’ve never enjoyed exercise and I just don’t do anything anymore. I just want to lose weight and feel better about myself, stop avoiding photos with my children, be happy to go out for a meal without feeling like others are judging what I order, be more active and fun as a Mum. Be the person I was when I met my husband. He tells me all the time he loves me and he does so much to show me that, but I just hate what I look like.
So I’m 47, 5’1”, 14st 6lb. I would love to get to 10 stone, the charts would say I need to be less than that but as I haven’t seen that weight since I met my husband, I think that’s a more than optimistic target for now!
What I need help with is guidance over what to eat. I’m a fussy eater which won’t help matters!
So far I’ve seen lots of comments about drinking water, I drink no added sugar squash, I’m hoping that will be ok?
I don’t eat breakfast. Currently I usually have 2 slices of white toast for lunch with chicken dripping on (so collagen is good but the little bit of fat on the top may cause problems? How much fat can be tolerated?) and then I have a glass of semi-skimmed milk and a small packet of crisps from a multi pack, and then either a nectarine or a clementine or some grapes or strawberries. Our children eat hot meals at school and so they have cold teas, and we’ve got out of the habit of bothering to cook a proper meal for ourselves at night. I sometimes have a bowl of cauliflower with gravy and then a slice of bread to soak into the leftover gravy. I sometimes have some Itsu gyoza dumplings. Sometimes I might have a fish finger sandwich. Or some prawns on a plate with beetroot and cherry tomatoes and a slice of edam. Sometimes just a bowl of crunchy nut cornflakes or a couple of dippy eggs. Fridays I cook for us at lunch as I don’t work then, so we usually have bavette steak with 3 hash browns each and then babycorn that i microwave and then finish in a pan with a little butter and salt. Weekends I properly cook for us all. I eat caramel snack a jacks and I’m partial to a mini caiipo in warm weather.
What should I be aiming at eating each day? My biggest worry is the side effects and doing what I can to minimise the chances of sickness or trouble with constipation or diarrhoea. I want to lose weight but I want to try and be healthy if I can, so I’m not having my hair fall out which I saw one person mention. I’m also hoping I can lose weight without having to much exercise at least for now, because I’m just not ready to go there right now.
Also, I have an afternoon tea booked 4.5 weeks from now and I need to go. Sandwiches, scones and fancy desserts. How bad will it be being on the injections to do that? It’s booked for 1pm, if I don’t eat anything until then, might I be able to appear normal to the others there in terms of volume? Or should I be saying that I’m not feeling well and asking for a doggy bag…Or if I time my first injection so that I’m due to inject the day after the afternoon tea, would that lessen the effects by the day I go?
PS sorry for how long this ended up being, I think I’m slightly panicking as I really want this to work and to lose weight like you have all done, but scared about getting it wrong and making myself ill!
2024.05.22 23:37 TeeefWeeef Cavernous Smooth Muscle
I got hard flaccid in 2021 after jelqing with an oil called gres cacao. It came after i squeezed too hard while jelqing and i believe i injured my cavernosa muscles causing hypertone. Subsequently I got lower back pain, soft glans, constipation, extremely tight scrotum,as well as trouble urinating. My flaccid penis is so hard that I can literally feel the two cavernosa tubes by touching which i never have been able to before. When i urinate, i never get a splatter because the cavernosa muscles are so hard. Finding a way to fully relax the cavernosa muscles is what I think will solve the hard flaccid condition I have. I no longer have constipation, my back pain has improved but has not fully gone away. If anyone has any advice let me know. I believe this condition has relation to the parasympathetic nervous system.
submitted by TeeefWeeef to hardflaccidresearch [link] [comments]
2024.05.22 23:31 morgiek8 1 week post op. If you were terrified like me, read this lol
Hey friends! Just wanted to share my story in hopes it might make one person out there feel better. I’m 30F with 2 kids for context.
Backstory:
I’ve been having terrible attacks since January, although at that time I had no idea what was happening to me. The attacks were lasting anywhere from 1.5-4 hours and the only thing I could do was lay in bed in fetal position with a heating pad on my stomach. The attacks would always happen in the evening and my husband would have to put the kids to bed at night because I could hardly move. They went away for a few weeks and then came back with a vengeance in February which resulted in me going to the ER (still had no idea what was going on) and after multiple tests and a CT scan—sent home with some strong ibuprofen because everything came back clear. To be honest, I felt like I was going crazy. My husband had no idea what to do for me (I didn’t know what to do for myself either lol) but the attacks and soreness went away after a couple weeks.
Fast forward to beginning of May and they started up again—this time, they were hella angry. I was staring to throw up after everything I ate until I reached the point I was too afraid to eat at all. I became Super irritated and had a short fuse and basically felt like the worst mother on the planet. I knew something was really wrong so I did a bunch of research that eventually led me to this sub, and let me tell ya, I FOUND MY PEOPLE haha! Everything that I was experiencing was validated by people in this sub, so I scheduled an appointment with my primary doctor and told her I have suspicions it could be my gallbladder. She absolutely agreed and ordered me a HIDA scan for the following day. The HIDA came back with a 10% ef and I finally felt validated. It pays to advocate for yourself!! In the meantime, I did try to do a gb flush, but felt like it just irritated it more. That was a wicked 24 hours on the toilet lol
Met with the surgeon the following day after my HIDA scan and she told me she thinks I should get it out asap. Surgery scheduled for 5/16. Did an ultrasound and didn’t have any stones. I’m going to be honest, I have major white coat syndrome. I rarely ever go to the doctor for anything, so I was really going back and forth on this decision. I felt that there maybe could be some way to “save” it because I’m a very naturopathic minded person, but that could be a long process with no guaranteed results. After a lot of back and forth, I decided to move forward with the surgery. I just couldn’t live with this pain and irritability. The part that was killing me the most was that I couldn’t be fully present for my children and be the best I could be for THEM.
Surgery day (5/16) rolls around and I’m nervous as hell. I know I’m going to feel like garbage after and who wants that? Hahaha! But my surgeon and her team of nurses were SO amazing. The surgery went great and I woke up in the recovery room a couple hours later and had a lot of nausea and gas. They gave me some ice chips and sprite to sip on which helped. All and all—they took excellent care of me.
Post op day one:
Pretty nauseous on the way home from the anesthesia but never did puke. I was feeling pretty rough. Took the oxycodone and stool softener that was prescribed and zombied out for a bit on the recliner with a heating pad on my back and ice pack over the incisions. I had quite a bit of gas pain, but not unbearable. I got up and walked often, drank Sprite to burp and took GasX which really helped. Surprisingly I was able to lay in bed and fall asleep for the night on my back.
Day two:
Still quite a bit of gas and incision site pain, but surprisingly felt pretty good. Continued to walk as much as I could and snacked on some crackers and toast throughout the day. Took some ibuprofen for the day and an oxy at night to help me sleep. (I always took a stool softener with the oxy because it tends to make a person constipated) The heating pad and ice pack has been a lifesaver throughout this whole process.
Day three:
Woke up feeling pretty dang good. Took a shower and a couple naps. Ate more and even had the guts to try a piece of pizza that evening with no repercussions. Felt amazing! I quit taking the oxy this day, but it dawned on me that I still hadn’t had a bowl movement since the day before surgery, so I took mirilax morning and night.
Day four:
This was a turning point day. I felt markedly better and was able to have my first poop lol! Incisions weren’t as sore and I was even able to hold my 10 month old baby when the grandparents brought the kids back home. (Thank god I was able to rest at home kidless for a few days, but I missed them terribly!) I also didn’t feel the need to take any sort of pain meds this day and haven’t since.
Days five and six:
Holy it’s truly amazing how fast the body can heal itself. I’ve woken up each day feeling stronger. I’ve been able to lift my baby a few times throughout the day, but still not pushing it too far. Thank god for my retired Mother In Law who’s been here to help with the kiddos! I’ve still been using the ice pack and heating pad throughout the day when I start to feel a little sore and tired but the past couple days I’ve put in over 3500 steps doing odd jobs (slowly) and some playing outside with the kids. I’ve been able to have consistent bowl movements and been able to eat whatever I want without any sort of pain or upset.
Some unexpected GOOD side effects from this surgery:
submitted by morgiek8 to gallbladders [link] [comments]
Backstory:
I’ve been having terrible attacks since January, although at that time I had no idea what was happening to me. The attacks were lasting anywhere from 1.5-4 hours and the only thing I could do was lay in bed in fetal position with a heating pad on my stomach. The attacks would always happen in the evening and my husband would have to put the kids to bed at night because I could hardly move. They went away for a few weeks and then came back with a vengeance in February which resulted in me going to the ER (still had no idea what was going on) and after multiple tests and a CT scan—sent home with some strong ibuprofen because everything came back clear. To be honest, I felt like I was going crazy. My husband had no idea what to do for me (I didn’t know what to do for myself either lol) but the attacks and soreness went away after a couple weeks.
Fast forward to beginning of May and they started up again—this time, they were hella angry. I was staring to throw up after everything I ate until I reached the point I was too afraid to eat at all. I became Super irritated and had a short fuse and basically felt like the worst mother on the planet. I knew something was really wrong so I did a bunch of research that eventually led me to this sub, and let me tell ya, I FOUND MY PEOPLE haha! Everything that I was experiencing was validated by people in this sub, so I scheduled an appointment with my primary doctor and told her I have suspicions it could be my gallbladder. She absolutely agreed and ordered me a HIDA scan for the following day. The HIDA came back with a 10% ef and I finally felt validated. It pays to advocate for yourself!! In the meantime, I did try to do a gb flush, but felt like it just irritated it more. That was a wicked 24 hours on the toilet lol
Met with the surgeon the following day after my HIDA scan and she told me she thinks I should get it out asap. Surgery scheduled for 5/16. Did an ultrasound and didn’t have any stones. I’m going to be honest, I have major white coat syndrome. I rarely ever go to the doctor for anything, so I was really going back and forth on this decision. I felt that there maybe could be some way to “save” it because I’m a very naturopathic minded person, but that could be a long process with no guaranteed results. After a lot of back and forth, I decided to move forward with the surgery. I just couldn’t live with this pain and irritability. The part that was killing me the most was that I couldn’t be fully present for my children and be the best I could be for THEM.
Surgery day (5/16) rolls around and I’m nervous as hell. I know I’m going to feel like garbage after and who wants that? Hahaha! But my surgeon and her team of nurses were SO amazing. The surgery went great and I woke up in the recovery room a couple hours later and had a lot of nausea and gas. They gave me some ice chips and sprite to sip on which helped. All and all—they took excellent care of me.
Post op day one:
Pretty nauseous on the way home from the anesthesia but never did puke. I was feeling pretty rough. Took the oxycodone and stool softener that was prescribed and zombied out for a bit on the recliner with a heating pad on my back and ice pack over the incisions. I had quite a bit of gas pain, but not unbearable. I got up and walked often, drank Sprite to burp and took GasX which really helped. Surprisingly I was able to lay in bed and fall asleep for the night on my back.
Day two:
Still quite a bit of gas and incision site pain, but surprisingly felt pretty good. Continued to walk as much as I could and snacked on some crackers and toast throughout the day. Took some ibuprofen for the day and an oxy at night to help me sleep. (I always took a stool softener with the oxy because it tends to make a person constipated) The heating pad and ice pack has been a lifesaver throughout this whole process.
Day three:
Woke up feeling pretty dang good. Took a shower and a couple naps. Ate more and even had the guts to try a piece of pizza that evening with no repercussions. Felt amazing! I quit taking the oxy this day, but it dawned on me that I still hadn’t had a bowl movement since the day before surgery, so I took mirilax morning and night.
Day four:
This was a turning point day. I felt markedly better and was able to have my first poop lol! Incisions weren’t as sore and I was even able to hold my 10 month old baby when the grandparents brought the kids back home. (Thank god I was able to rest at home kidless for a few days, but I missed them terribly!) I also didn’t feel the need to take any sort of pain meds this day and haven’t since.
Days five and six:
Holy it’s truly amazing how fast the body can heal itself. I’ve woken up each day feeling stronger. I’ve been able to lift my baby a few times throughout the day, but still not pushing it too far. Thank god for my retired Mother In Law who’s been here to help with the kiddos! I’ve still been using the ice pack and heating pad throughout the day when I start to feel a little sore and tired but the past couple days I’ve put in over 3500 steps doing odd jobs (slowly) and some playing outside with the kids. I’ve been able to have consistent bowl movements and been able to eat whatever I want without any sort of pain or upset.
Some unexpected GOOD side effects from this surgery:
- I don’t remember the last time I’ve felt so clear minded. I’ve struggled with brain fog for years and chalked it up to pregnancy/having small children. The brain fog is completely gone.
- For the past two months, I’ve had terrible IT band and soreness in my right butt cheek. I was doing daily stretches and using a massage gun on it multiple times a day, even up to the night before surgery. After the surgery—completely gone. My literal pain in the ass is nonexistent. What in the actual f hahaha
I don’t regret the decision to yeet this gallbladder out. It was basically dead inside my body and causing a lot of havoc. It makes me wonder how long my gb has been having issues and I didn’t really notice it until the attacks but I’m finally starting to feel like myself again and it’s such a burden lifted from my shoulders. I’m going to continue to take it easy for a while, which sucks because I need to constantly be moving and keeping busy AND 3 days away from my 30th birthday. I was planning on getting really drunk for my 30th, but the universe had other plans I guess hahahah! If you’re feeling super nervous and uneasy like I was—it’s going to be okay. I got nervous reading some horror story posts here, but my experience hasn’t been a bad one. I’m expecting it to take time for my body to adjust without a gb, so I guess that will be a bit of a journey. So far so good! If you have any questions or need some words of encouragement, I’m here for ya. ❤️✌️
2024.05.22 18:05 LectureSorry6338 Mailbox~adlerneve@gmail.com
submitted by LectureSorry6338 to NursingStudent [link] [comments]
2024.05.22 18:03 Ok_Entertainment4946 Fleet enema WORKS!
Okay so this is my first reddit post so idk how to go about this. (I find this embarrassing to type out but I hope others who are dealing with this can relate and feel comfort.) But I, 21 female, have been dealing with on and off constipation since I was a child. I'm not dealing with constipation every time I have poop, however every once or twice every 2-3 months or so I get constipated.
So I have been constipated for the past 3 days. (I was constipated about 2 weeks ago also and although it hurt like hell to get out I was able to do it) Once again it had been stuck and hard to get out. This time is hurt about 50% more than before and I just couldn't push it out. I essentially had to leave it, as straining hurt my anus and was just draining.
I started getting horrible stomach pain and it had been hard to sleep at night. It got so bad that I bought multiple medications to help: Ducolax stool softener, milk of magnesia, and fleet laxative saline enema. (I had not taken stool softener for constipation since I was about 10 years old, when I had been prescribed medication by my family doctor) I took 1 Ducolax tablet and waited. I managed to push out one tiny piece the night of taking it, and was able to strain out 2 smaller pieces today.
The Ducolax had only worked so much and I had felt like I needed to poop however it was still stuck and hurt. It was to the point where I couldn't sit and had horrible stomach pain. So with no other options I decided to use the Fleet Saline enema. I was nervous to use it but had no issue getting it up there. (It will only sting a little bit if you tense up and clench or angle it wrong, just move slow and you can push it up futher as you squeeze the solution out)
So after inserting all the solution I laid on my side and set an alarm for 15 minutes. However I felt I wouldn't be able to hold it in, but I manged at least 5 minutes which is like the minimum amount to time to hold it. And after struggling to hold it in and I got to the toilet and at first struggled to push, only pushing some of the solution out at first. Then it kicked in...and Holy shit it works.
I didn't think it would even work tbh when trying it, but I had no other options so I just tried to trust the process. But omg when I tell you it was like a damn bursting. Everything I was straining to push out came flowing out in a matter of seconds. Along with the saline solution as well. And I swear I've never felt such painless relief in my life.
Fleet saline enema is a 10/10 product fr. If you're genuinely struggling and straining on the toilet I would recommend you use it. (And no this isn't an ad unfortunately) You would be saving yourself time and pain. And yes you will probably have to stay on/around the toilet for 15 mins to possibly an hour cause more might come out depending on how much build up you have.
submitted by Ok_Entertainment4946 to Constipation [link] [comments]
So I have been constipated for the past 3 days. (I was constipated about 2 weeks ago also and although it hurt like hell to get out I was able to do it) Once again it had been stuck and hard to get out. This time is hurt about 50% more than before and I just couldn't push it out. I essentially had to leave it, as straining hurt my anus and was just draining.
I started getting horrible stomach pain and it had been hard to sleep at night. It got so bad that I bought multiple medications to help: Ducolax stool softener, milk of magnesia, and fleet laxative saline enema. (I had not taken stool softener for constipation since I was about 10 years old, when I had been prescribed medication by my family doctor) I took 1 Ducolax tablet and waited. I managed to push out one tiny piece the night of taking it, and was able to strain out 2 smaller pieces today.
The Ducolax had only worked so much and I had felt like I needed to poop however it was still stuck and hurt. It was to the point where I couldn't sit and had horrible stomach pain. So with no other options I decided to use the Fleet Saline enema. I was nervous to use it but had no issue getting it up there. (It will only sting a little bit if you tense up and clench or angle it wrong, just move slow and you can push it up futher as you squeeze the solution out)
So after inserting all the solution I laid on my side and set an alarm for 15 minutes. However I felt I wouldn't be able to hold it in, but I manged at least 5 minutes which is like the minimum amount to time to hold it. And after struggling to hold it in and I got to the toilet and at first struggled to push, only pushing some of the solution out at first. Then it kicked in...and Holy shit it works.
I didn't think it would even work tbh when trying it, but I had no other options so I just tried to trust the process. But omg when I tell you it was like a damn bursting. Everything I was straining to push out came flowing out in a matter of seconds. Along with the saline solution as well. And I swear I've never felt such painless relief in my life.
Fleet saline enema is a 10/10 product fr. If you're genuinely struggling and straining on the toilet I would recommend you use it. (And no this isn't an ad unfortunately) You would be saving yourself time and pain. And yes you will probably have to stay on/around the toilet for 15 mins to possibly an hour cause more might come out depending on how much build up you have.
2024.05.22 15:43 rua0020 Calcified fibroid entangled in nerves post UFE - Reason for 9 months of chronic pain
Hi all, apologies in advance as this is a thesis!!
Just sharing my story as it's a little unique, and I'm all for sharing everything we have to add to our collective bank of anecdotal info and insight. Hoping this might just help someone out there in the future.
Context:
I (27f) was always healthy, with the exception of very heavy periods starting at age 9. Thought nothing of it as my mum and sister were the same. At age 25, I decided to get a full women's health check up privately before TTC planning. A 5cm pedunculated fibroid was found swinging beside my right ovary, as well as a few small intramural pests. I was advised that due to it's location, it may cause pregnancy risk, and that addressing it now while it was a manageable size would be best. They told me UFE would be best for me, a myo would be more risky due to it's posterior location (I now know that this advice was based on the limited skill of the Gynae who would have performed the myo at this hospital).
Lesson 1: Ask ALL the questions. It is their job to educate you on what will happen to YOUR body.
I had UFE last summer, one year later. In hindsight, there were several red flags, unfortunately, with this particular hospital. They never explained to me that UFE is known to be a potential risk to fertility. I learned this later, when my current Gynae (different hospital) was shocked that they did not do an AMH blood test prior to the procedure - as UFE is known to affect egg count. He ordered one, and lo and behold, the results were rather low (c. 11 pmol). I will never know if this was affected by the UFE.
The IR actually told me he would do a "75% blast" "just to lower any risk" during the embolization. Yeah, red flag. You'll see later how this decision panned out.
I posted here before about the level of pain I experienced after this procedure, so I'll just highlight that it was simply the worst state I have ever found myself in, and nothing short of living hell.
Lesson 2: Advocate for yourself. Be the CEO of your health.
Fast forward 3 months, they do the follow up MRI, I'm told that all fibroids were successfully devascularlised. Insert another red flag (this was not the truth). Now from about this exact time onwards, I began waking up in pain every day, and finding myself in unbearable pain after eating. This was my constant state within a few weeks - day and night, I was in 8/10 pain, genuinely reaching 10/10 after eating anything. I also developed a weird abdominal rash (also posted about this here I think) during this time, it would not go away and is still with me to this day. I slipped a disc in my neck three times during this time, I was told by the A&E doc that it was due to postural strain - my being hunched over in pain constantly, led to a herniated cervical disc that I will now have to look after forever.
I resigned from my job in early November, after having taken 2 months plus of sick leave. There was no hope for me at this point; my health was aggressively deteriorating and I saw no light at the end of the tunnel. Nobody would help me.
During this time, I was trying to get into contact with the IR about the both rash (which was getting sorer and spreading) and pain. I was ignored and told to "go back to the referring Gynae for aftercare". I sent countless emails to the Gynae department, all ignored, I called every day but was told each time (if they answered) that I should follow up with my GP.
With the help of my GP, I finally got an appointment for end November, 3 months into my chronic pain and inability to eat. They did a TV US and assured me the pedunculated fibroid had indeed shrunk a little and that I "just need the coil". I refused, stating that my whole reason for doing all of this in the first place was to prepare myself for TTC.
I told them I just felt like something wasn't right with the fibroid, that maybe my body was freaking out after the UFE , that maybe it was more of a foreign body now that it was dead and my body was treating it as such. They laughed. And once I refused the coil/pill "solution", they totally gave up on me and fobbed me off to Gastro, insisting it must be a stomach issue.
By this time I had lost 10kg from not being able to eat because of the exacerbated pain. I was eating a couple of slices of dry toast and plain yogurt every day. The pain also seemed to be "spreading", up in and under my ribs, my flank area, and upper back - as did the rash! The rash followed the pain. Just so weird!
Lesson 3: Trust your gut, you know your body.
I spent 2 weeks in hospital over Christmas under the care of the GI consultant who ruled out Crohn's (his first theory), Coeliac disease, UC, H Pylori, ulcers, and even tested me for kidney malfunction, pancreatitis and gallstones. I was lucky that this doc was very caring, and although he dismissed my fibroid " UFE reaction" theory, he did refer me to an Endo specialist (my current Gyna), saying it must be extensive Endo. Something my previous Gynae never mentioned btw... I didn't really know anything about endo sobstarted educating myself immediately. Although I had the textbook endo symptoms, my gut stopped me from fully resonating with all the anecdotes and stories I was reading. It just didn't feel like this was what was going on in my body. It didn't feel like my story.
Lesson 4: You are not crazy.
I had the consultation with the Endo specialist end March, who actually turned out to be a gynaecological oncology surgeon who also dealt with fibroids. Finally, the universe looking out for me!! I told him that I really thought I was having some sort of systemic reaction to the UFE/fibroid. He however, was very confident that I had Endo, saying that it would explain the terrible pain - "a fibroid wouldn't cause this much chaos". But he said he would remove the pedunculated fibroid while they were in there. The fibroid was very much a secondary concern.
So I had my first lap this Sunday for the suspected endo. Alas, there was no Endo!! He told me that the fibroid was "more complex than anticipated". It was a lot larger than shown on any imagery, and was not in fact entirely devascularized as it had definitely grown since the UFE. However, it had been cut off enough from its blood supply to start calcifying. The calcification process led to the pedunculated fibroid lodging itself in a fixed position between my spinal cord and bowel, heavily pressing and impacting on both. Upon removal, the fibroid was actually found to be pressing on, and entangled in nerves.
This explains everything. This "spreading", non cyclical, constant, intrusive, relentless pain - my nerves were being irritated! This was why I was suffering with extreme constipation and zero appetite - my bowel was being bullied! There was a reason for it after all. It was not in my head. I was not crazy. And neither are you!!
Lesson 5 - one for the medical field: fibroids are NOT "just fibroids".
Fibroids are not taken as seriously as they should be. Fibroids are tumours. Fibroids are foreign bodies that grow, and take up space in our bodies that is meant for our vital organs. Fibroids mess up our hormonal system and have the ability to take complete control of it.
Fibroids took my dream job, my financial security, my confidence, my mental health, my whole entire life and my sense of control and trust of my body.
Stop telling us how common they are, how normal they are, how they can be managed with hormonal intervention. Fibroids are not normal and we should not be expected to live with them.
Edit: spelling and grammar.
submitted by rua0020 to Fibroids [link] [comments]
Just sharing my story as it's a little unique, and I'm all for sharing everything we have to add to our collective bank of anecdotal info and insight. Hoping this might just help someone out there in the future.
Context:
I (27f) was always healthy, with the exception of very heavy periods starting at age 9. Thought nothing of it as my mum and sister were the same. At age 25, I decided to get a full women's health check up privately before TTC planning. A 5cm pedunculated fibroid was found swinging beside my right ovary, as well as a few small intramural pests. I was advised that due to it's location, it may cause pregnancy risk, and that addressing it now while it was a manageable size would be best. They told me UFE would be best for me, a myo would be more risky due to it's posterior location (I now know that this advice was based on the limited skill of the Gynae who would have performed the myo at this hospital).
Lesson 1: Ask ALL the questions. It is their job to educate you on what will happen to YOUR body.
I had UFE last summer, one year later. In hindsight, there were several red flags, unfortunately, with this particular hospital. They never explained to me that UFE is known to be a potential risk to fertility. I learned this later, when my current Gynae (different hospital) was shocked that they did not do an AMH blood test prior to the procedure - as UFE is known to affect egg count. He ordered one, and lo and behold, the results were rather low (c. 11 pmol). I will never know if this was affected by the UFE.
The IR actually told me he would do a "75% blast" "just to lower any risk" during the embolization. Yeah, red flag. You'll see later how this decision panned out.
I posted here before about the level of pain I experienced after this procedure, so I'll just highlight that it was simply the worst state I have ever found myself in, and nothing short of living hell.
Lesson 2: Advocate for yourself. Be the CEO of your health.
Fast forward 3 months, they do the follow up MRI, I'm told that all fibroids were successfully devascularlised. Insert another red flag (this was not the truth). Now from about this exact time onwards, I began waking up in pain every day, and finding myself in unbearable pain after eating. This was my constant state within a few weeks - day and night, I was in 8/10 pain, genuinely reaching 10/10 after eating anything. I also developed a weird abdominal rash (also posted about this here I think) during this time, it would not go away and is still with me to this day. I slipped a disc in my neck three times during this time, I was told by the A&E doc that it was due to postural strain - my being hunched over in pain constantly, led to a herniated cervical disc that I will now have to look after forever.
I resigned from my job in early November, after having taken 2 months plus of sick leave. There was no hope for me at this point; my health was aggressively deteriorating and I saw no light at the end of the tunnel. Nobody would help me.
During this time, I was trying to get into contact with the IR about the both rash (which was getting sorer and spreading) and pain. I was ignored and told to "go back to the referring Gynae for aftercare". I sent countless emails to the Gynae department, all ignored, I called every day but was told each time (if they answered) that I should follow up with my GP.
With the help of my GP, I finally got an appointment for end November, 3 months into my chronic pain and inability to eat. They did a TV US and assured me the pedunculated fibroid had indeed shrunk a little and that I "just need the coil". I refused, stating that my whole reason for doing all of this in the first place was to prepare myself for TTC.
I told them I just felt like something wasn't right with the fibroid, that maybe my body was freaking out after the UFE , that maybe it was more of a foreign body now that it was dead and my body was treating it as such. They laughed. And once I refused the coil/pill "solution", they totally gave up on me and fobbed me off to Gastro, insisting it must be a stomach issue.
By this time I had lost 10kg from not being able to eat because of the exacerbated pain. I was eating a couple of slices of dry toast and plain yogurt every day. The pain also seemed to be "spreading", up in and under my ribs, my flank area, and upper back - as did the rash! The rash followed the pain. Just so weird!
Lesson 3: Trust your gut, you know your body.
I spent 2 weeks in hospital over Christmas under the care of the GI consultant who ruled out Crohn's (his first theory), Coeliac disease, UC, H Pylori, ulcers, and even tested me for kidney malfunction, pancreatitis and gallstones. I was lucky that this doc was very caring, and although he dismissed my fibroid " UFE reaction" theory, he did refer me to an Endo specialist (my current Gyna), saying it must be extensive Endo. Something my previous Gynae never mentioned btw... I didn't really know anything about endo sobstarted educating myself immediately. Although I had the textbook endo symptoms, my gut stopped me from fully resonating with all the anecdotes and stories I was reading. It just didn't feel like this was what was going on in my body. It didn't feel like my story.
Lesson 4: You are not crazy.
I had the consultation with the Endo specialist end March, who actually turned out to be a gynaecological oncology surgeon who also dealt with fibroids. Finally, the universe looking out for me!! I told him that I really thought I was having some sort of systemic reaction to the UFE/fibroid. He however, was very confident that I had Endo, saying that it would explain the terrible pain - "a fibroid wouldn't cause this much chaos". But he said he would remove the pedunculated fibroid while they were in there. The fibroid was very much a secondary concern.
So I had my first lap this Sunday for the suspected endo. Alas, there was no Endo!! He told me that the fibroid was "more complex than anticipated". It was a lot larger than shown on any imagery, and was not in fact entirely devascularized as it had definitely grown since the UFE. However, it had been cut off enough from its blood supply to start calcifying. The calcification process led to the pedunculated fibroid lodging itself in a fixed position between my spinal cord and bowel, heavily pressing and impacting on both. Upon removal, the fibroid was actually found to be pressing on, and entangled in nerves.
This explains everything. This "spreading", non cyclical, constant, intrusive, relentless pain - my nerves were being irritated! This was why I was suffering with extreme constipation and zero appetite - my bowel was being bullied! There was a reason for it after all. It was not in my head. I was not crazy. And neither are you!!
Lesson 5 - one for the medical field: fibroids are NOT "just fibroids".
Fibroids are not taken as seriously as they should be. Fibroids are tumours. Fibroids are foreign bodies that grow, and take up space in our bodies that is meant for our vital organs. Fibroids mess up our hormonal system and have the ability to take complete control of it.
Fibroids took my dream job, my financial security, my confidence, my mental health, my whole entire life and my sense of control and trust of my body.
Stop telling us how common they are, how normal they are, how they can be managed with hormonal intervention. Fibroids are not normal and we should not be expected to live with them.
Edit: spelling and grammar.
2024.05.22 15:10 reee9000 I am slowly seeing a change - finally!
Let me start by saying I came here when I was EXTREMELY constipated (before almost going to the ER and after getting an abdominal CT scan from Gi) I saw many of you posting different things.
For me, I did NOT want to get addicted or my body used to to ANY laxatives/softeners/suppositories, I DID NOT want to mess up my insides with anymore enemas etc, and I DEF DIDNT want to get on ANY medication.
So out of sheer desperation, I began doing a few things that I now believe have helped me to become more regular. I decided to share here as it’s almost been one month, that I’m going every other day to every 2-3 days which I now realize might be my “norm” by tracking everything I now saw my poop pattern … 🧐
I’ve also tracked EVERY meal and poop type and color since I started the experiment April 23rd. Though, I didn’t change my mainly already whole food clean diet significantly, but I made a point to religiously ADD slowly item by item in the following things & tbh in less than 2-3 weeks of this change; I’m regularly pooping again and I do believe that I will/can keep trying this for as long as finances will allow.
First; I had to take the contrast stuff from the CT scan (so they could check me for the any bad colon issues since i hadn’t gone in a week +) so I did have stool softeners and a 1 laxative before drinking 2 bottles of contrast /the prep white stuff drink for that first time.
Once that was all out tho (that was4/30 to 5/3 ... it was up to me from there!😱😖 … I started first with more water and walking:
drinking 32-64 oz water daily (I made a special jug for keeping count with cute saying that’s inspire me each oz)
drinking 8 oz 100% prune juice (no sugars!) 1 or 2 times a day
drinking 4 oz pedialyte sugar free (I now do every other day (not daily) tho to replenish any electrolyte or hydration imbalance I may have/had after laxative/softener?)
I ate/eat more salads 2-3 cups at lunch (with kale and Brussels)
added in 1/2c-1c lentils (for 1 or 2 meals)
I began forcing myself to walk just around my block (no matter what I feel like even tired); walking 1-2 mph 5k-7k steps OR .5 mile to 1 whole mile (2-3x a week) (I can’t walk too much)
1 magnifical supplement at night/am
1 probiotic digestion 1x a day
added in 1/4 c sauerkraut (to any meal or alone) as prebiotic
added in 1/4 avocado daily (to any meal) as a healthy fat
added in 1-3 raw radishes (*I do not like them but I like pooping and that’s what I focus on while I eat a few radish pieces lol)
1 c oatmeal (but with adding 1 tbsp chia and cinnamon)
random carrots as a snacks or celery sticks (no peanut butter!)
I changed my wastebasket to be the height I can add my feet to in front of toilet (raises my legs in squat position) but ONLY when I really feel like I may need extra positioning.
I also really realized I prob wasn’t chewing certain foods as much as I could have been so I started eating more slowly and making sure my food was chewed.
That’s it. ☺️ Those were my changes that seem to have caused major differences.
I will keep you posted as I increase my protein or as my diet shifts etc. I plan to keep doing this for as long as I can as all of this slowly added in has helped me a ton and my poops are all a perfect type 3-5 :)
No more hard pushing. No more forcing it. No more type 1 pellets which is such a big W for me!
Wishing the best for you all! I know how tough it can be and make you want to just give up all hope! Not to mention the added headaches, stress, pains, bloating and much more!! 🫂💕Now if I can just find a way get rid of these constant migraines, I can quit Excedrin!
submitted by reee9000 to Constipation [link] [comments]
For me, I did NOT want to get addicted or my body used to to ANY laxatives/softeners/suppositories, I DID NOT want to mess up my insides with anymore enemas etc, and I DEF DIDNT want to get on ANY medication.
So out of sheer desperation, I began doing a few things that I now believe have helped me to become more regular. I decided to share here as it’s almost been one month, that I’m going every other day to every 2-3 days which I now realize might be my “norm” by tracking everything I now saw my poop pattern … 🧐
I’ve also tracked EVERY meal and poop type and color since I started the experiment April 23rd. Though, I didn’t change my mainly already whole food clean diet significantly, but I made a point to religiously ADD slowly item by item in the following things & tbh in less than 2-3 weeks of this change; I’m regularly pooping again and I do believe that I will/can keep trying this for as long as finances will allow.
First; I had to take the contrast stuff from the CT scan (so they could check me for the any bad colon issues since i hadn’t gone in a week +) so I did have stool softeners and a 1 laxative before drinking 2 bottles of contrast /the prep white stuff drink for that first time.
Once that was all out tho (that was4/30 to 5/3 ... it was up to me from there!😱😖 … I started first with more water and walking:
drinking 32-64 oz water daily (I made a special jug for keeping count with cute saying that’s inspire me each oz)
drinking 8 oz 100% prune juice (no sugars!) 1 or 2 times a day
drinking 4 oz pedialyte sugar free (I now do every other day (not daily) tho to replenish any electrolyte or hydration imbalance I may have/had after laxative/softener?)
I ate/eat more salads 2-3 cups at lunch (with kale and Brussels)
added in 1/2c-1c lentils (for 1 or 2 meals)
I began forcing myself to walk just around my block (no matter what I feel like even tired); walking 1-2 mph 5k-7k steps OR .5 mile to 1 whole mile (2-3x a week) (I can’t walk too much)
1 magnifical supplement at night/am
1 probiotic digestion 1x a day
added in 1/4 c sauerkraut (to any meal or alone) as prebiotic
added in 1/4 avocado daily (to any meal) as a healthy fat
added in 1-3 raw radishes (*I do not like them but I like pooping and that’s what I focus on while I eat a few radish pieces lol)
1 c oatmeal (but with adding 1 tbsp chia and cinnamon)
random carrots as a snacks or celery sticks (no peanut butter!)
I changed my wastebasket to be the height I can add my feet to in front of toilet (raises my legs in squat position) but ONLY when I really feel like I may need extra positioning.
I also really realized I prob wasn’t chewing certain foods as much as I could have been so I started eating more slowly and making sure my food was chewed.
That’s it. ☺️ Those were my changes that seem to have caused major differences.
I will keep you posted as I increase my protein or as my diet shifts etc. I plan to keep doing this for as long as I can as all of this slowly added in has helped me a ton and my poops are all a perfect type 3-5 :)
No more hard pushing. No more forcing it. No more type 1 pellets which is such a big W for me!
Wishing the best for you all! I know how tough it can be and make you want to just give up all hope! Not to mention the added headaches, stress, pains, bloating and much more!! 🫂💕Now if I can just find a way get rid of these constant migraines, I can quit Excedrin!
2024.05.22 10:30 Significant_Ice856 RN ATI PHARMACOLOGY 2023 Exam(70 Questions) DM! nyalandojulian@gmail.com
submitted by Significant_Ice856 to NursingStudent [link] [comments]
2024.05.22 10:28 Significant_Ice856 RN ATI PHARMACOLOGY 2023 Exam(70 Questions) DM! nyalandojulian@gmail.com
submitted by Significant_Ice856 to NursingStudent [link] [comments]
2024.05.22 06:33 Roleynicoley Need Advice (Kind of Long Story)
Sigh. Please read if you can.
So let's start the journey back in July 2021. I was getting horrible stomach pain. The cramping would last a few hours. After the third night in a row, I went to the ER. They told me it was gas and sent me home. It continued to happen the next couple of weeks on and off, so I saw my gastroenterologist. He told me I had IBS. Believing this, I started eating more fiber and changing my diet (this was now around January 2022). Of course, this was killing my stomach more. The pain increased during my stomach cramps. I also gained other symptoms such as non-stop nausea all day, throwing up multiple times a day, constipation no matter how much fiber I ate. I went to my doctor again and told him I think it's more than IBS. He refused to run anymore tests but gave me a 3 anemias and a colonoscopy instead (around March 2022- This was okay although the colonoscopy liquid nearly killed me) hoping this would "clear me out." Of course, this did not help. I still went through this pain for another year. Trying to get my doctor to do more tests but he refused. He told me that my problem was mental. He gaslighted me into thinking that if I healed "psychological" then my IBS would be cured. On another note, I was diagnosed with diabetes by my main provider. They told me to "eat right and exercise" and put me on basic diabetic meds." In May 2023, I got a new doctor and changed insurances (I was finally able to change insurances and get a new doctor due to job change).
This was the doctor who actually finally listened to me. The first appointment she assigned me to nearly every test (including gluten and the gastroparesis test which I had been asking my old DR about). My tests showed that I had severe gastroparesis. By this point, my symptoms had gotten so bad. Throwing up so much I couldn't keep food down. The cramping would last nearly all day. It would keep me up at night. I wasn't sleeping. I started having intense food aversions. Foods I used to love were now making me nauseous just by smelling them. The bloating would cause so much pain. I developed heartburn which I never had before. I had lost 100 pounds since last year. I was almost immobile because any walking/extensive work longer than 15 minutes would give me cramps. This was around the same time that my diabetic meds kicked in and my blood sugar would go SUPER low, and I started feeling sick. Ultimately, I stopped taking my diabetic meds because the doctor assumed that my blood sugar was messed up because of my gastroparesis. Then the worse thing happened and my doctor left.
Now I finally found a new doctor who wants me to start taking diabetic meds again. Although my symptoms have not changed. No one is willing to address my gastroparesis. And the diabetic meds are AGAIN making my blood sugar super low. I told her that this happened last time and what the doctor had said, but my current doctor ignored it, and put me on Ozempic. Now I'm feeling so sick. Not only my gastroparesis but low sugar- my doctor is insisting that I have diabetic gastro (which may be true but it's not been handled well).
I'm just so lost. No one is listening to me anymore. And I'm feeling sicker and sicker. My symptoms are getting worse. I am actually starting to LOOK sick. And that has been super hard for me.
submitted by Roleynicoley to Gastroparesis [link] [comments]
So let's start the journey back in July 2021. I was getting horrible stomach pain. The cramping would last a few hours. After the third night in a row, I went to the ER. They told me it was gas and sent me home. It continued to happen the next couple of weeks on and off, so I saw my gastroenterologist. He told me I had IBS. Believing this, I started eating more fiber and changing my diet (this was now around January 2022). Of course, this was killing my stomach more. The pain increased during my stomach cramps. I also gained other symptoms such as non-stop nausea all day, throwing up multiple times a day, constipation no matter how much fiber I ate. I went to my doctor again and told him I think it's more than IBS. He refused to run anymore tests but gave me a 3 anemias and a colonoscopy instead (around March 2022- This was okay although the colonoscopy liquid nearly killed me) hoping this would "clear me out." Of course, this did not help. I still went through this pain for another year. Trying to get my doctor to do more tests but he refused. He told me that my problem was mental. He gaslighted me into thinking that if I healed "psychological" then my IBS would be cured. On another note, I was diagnosed with diabetes by my main provider. They told me to "eat right and exercise" and put me on basic diabetic meds." In May 2023, I got a new doctor and changed insurances (I was finally able to change insurances and get a new doctor due to job change).
This was the doctor who actually finally listened to me. The first appointment she assigned me to nearly every test (including gluten and the gastroparesis test which I had been asking my old DR about). My tests showed that I had severe gastroparesis. By this point, my symptoms had gotten so bad. Throwing up so much I couldn't keep food down. The cramping would last nearly all day. It would keep me up at night. I wasn't sleeping. I started having intense food aversions. Foods I used to love were now making me nauseous just by smelling them. The bloating would cause so much pain. I developed heartburn which I never had before. I had lost 100 pounds since last year. I was almost immobile because any walking/extensive work longer than 15 minutes would give me cramps. This was around the same time that my diabetic meds kicked in and my blood sugar would go SUPER low, and I started feeling sick. Ultimately, I stopped taking my diabetic meds because the doctor assumed that my blood sugar was messed up because of my gastroparesis. Then the worse thing happened and my doctor left.
Now I finally found a new doctor who wants me to start taking diabetic meds again. Although my symptoms have not changed. No one is willing to address my gastroparesis. And the diabetic meds are AGAIN making my blood sugar super low. I told her that this happened last time and what the doctor had said, but my current doctor ignored it, and put me on Ozempic. Now I'm feeling so sick. Not only my gastroparesis but low sugar- my doctor is insisting that I have diabetic gastro (which may be true but it's not been handled well).
I'm just so lost. No one is listening to me anymore. And I'm feeling sicker and sicker. My symptoms are getting worse. I am actually starting to LOOK sick. And that has been super hard for me.
2024.05.22 04:07 magnusrushesin_ potential cushings?
hey! ive been concerned about the possibility of cushings for about a year, and i thought i would come here to ask for advice or opinions as spaces such as this have always been the most helpful in figuring out the next steps.
i first found out about cushings not too long after i was put on prednisone at a dose considered to be high (50mg) for a few months to help handle my indeterminate IBD which i was diagnosed with at the same time. the tapering of my dose was rushed right at the end due to extreme constipation caused by the medication, but i had also experienced weight gain of about 60 pounds that has not budged since. i went from 130 to 190, and most of the weight went to my midsection, as well as my thighs and upper arms, and the rest of my legs and arms are quite muscular but still much thinner in comparison with no additional growth there, and i developed a hump on my neck that is quite solid. the hump was my first sign that pushed me to look into cushings as i noticed it when trying to lay my head back, it blocks most motion, which i typically would have a lot of in that area as i have EDS, which also complicates this even more as all of the skin symptoms from cushings other than the purple stretch marks are also caused by that. we never really looked into cushings during that time as it was pure chaos trying to get my IBD and other gi issues under control after prednisone, and i was in the hospital for treatments, scans, or tests almost constantly for a few months. even now things are still crazy, but its been sitting in the back of my mind for so long.
i am happy to provide more details if needed, but i’d like to know if people think this is reasonable to look into still, and where to go from here if so?
submitted by magnusrushesin_ to Cushings [link] [comments]
i first found out about cushings not too long after i was put on prednisone at a dose considered to be high (50mg) for a few months to help handle my indeterminate IBD which i was diagnosed with at the same time. the tapering of my dose was rushed right at the end due to extreme constipation caused by the medication, but i had also experienced weight gain of about 60 pounds that has not budged since. i went from 130 to 190, and most of the weight went to my midsection, as well as my thighs and upper arms, and the rest of my legs and arms are quite muscular but still much thinner in comparison with no additional growth there, and i developed a hump on my neck that is quite solid. the hump was my first sign that pushed me to look into cushings as i noticed it when trying to lay my head back, it blocks most motion, which i typically would have a lot of in that area as i have EDS, which also complicates this even more as all of the skin symptoms from cushings other than the purple stretch marks are also caused by that. we never really looked into cushings during that time as it was pure chaos trying to get my IBD and other gi issues under control after prednisone, and i was in the hospital for treatments, scans, or tests almost constantly for a few months. even now things are still crazy, but its been sitting in the back of my mind for so long.
i am happy to provide more details if needed, but i’d like to know if people think this is reasonable to look into still, and where to go from here if so?