Hello, I am searching for a safe diet that a person with an ileostomy can go on. No matter what I do, I cannot lose the extra weight that I have gathered around my stomach since having my most recent surgery in 2018. It is very difficult to do exercise outside now due to my knee being replaced and the heart condition that was graciously given to me by Covid. All the diets I have seen include raw vegetables that I cannot eat. I am down to one meal a day now. Also, my Hashimoto's Thyroiditis is causing total chaos, causing my Hypothyroidism to go rogue. The doctors are having a very difficult time regulating it, which causes the symptoms to go out of control. It seems that when they put me on a higher dose, I am OK for a short time and then I am getting too much TSH. Then, they lower the dose and I end up not getting enough. There is no in-between with 175mg and 150mg. It has literally been a nightmare!! When I go low, my other two immune disorders attack and I break out with the sores from Prurigo Nodularis and the blisters from Bullous Pemphigoid. On top of that, my hair starts to fall out, the weight packs on, and the fatigue sets in. It's one thing after another and it is so depressing!! I have gone to a dietitian but they really cannot help because regular diets don't work well. I cannot take diet pills as they don't stay in my system long enough to do anything. Things fly through the ileostomy very quickly. I do take gummy vitamins so I am getting some useful nutrients. I am seriously thinking of having liposuction done since all the muscles in my stomach area have been damaged from 2 Cesareans, several abdominal surgeries, and a full hysterectomy. I worry about intimacy with a partner because my body is so beat up and ugly. Please, if any of you have found a diet that works, please tell me what it is. Any advice will be greatly appreciated. Thank you.
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Geekyjen,
Thanks for the reply. I will be seeing my doctor on Friday and mention Entyvio. I did not remain paralyzed for more than 2 days, but it was terrible and I was so scared. The doctors just used alot of xanax and other drugs like that to UN paralyze my joints that were being attacked by the remicade. Turns out I have been diagnosed with LUPUS. It is attacking my nervous system. I had ulcerative colitis in 1996 and they had to remove my colon. Had a J pouch for 10 years, until it started failing. I then got a permanent iliosomy, and I suffer from severe chronic diareha, and I dehydrate frequently. I recently had a proctectomy, and that is when the new autoimmune disorder, Lupus, appeared. I have had two hospital stays now because of the blisters and the paralyzing incident. I will be dealing with this forever now. I have just been working on acceptance.
I love this website because of wonderful people like you!
Betty
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