Experiences with

Colitis

I wondered do either of these drugs make Chrons or Colitis worse at all? I noticed sometimes they make me feel abit worse. Thanks

Hi, has anyone been prescribed Budenofalk 2mg rectal foam for Ulcerative colitis? I have been given this at my hospital appt to help with the inflammation/ diarrhoea/ bleeding. Just wondering if it caused anyone any side effects or if it helped in anyway?

Does anyone on here have firsthand experience of ulcerative colitis? If yes what were your symptoms and how did you get a diagnosis (if you have a diagnosis) please? Many thanks in advance.

Information but comment: I have ulcerative colitis. My specialist nurse told me that some people with IBD also suffer with RLS. As high as 20%. I have an appointment with my GP next week, I will see if she was aware of this relationship.

Yep it's colitis following colonoscopy biopsy results. They are of the impression it is microscopic colitis (associated to auto immune diseases) but not 100% sure. So the handle is unspecified colitis which is a common saying. Treatment is steroids.

I have ulcerative colitis and its kicking in big time. Any one else had this?

I have decompensated cirrhosis of the liver, Addison disease, colitis, and just had a stroke 3 weeks ago.

hi, I’m due to start an 8 week trial of Bendenofalk (Budenoside) in the sachets/granules form for recently diagnosed Microscipic Colitis I’m worried about side effects, particularly related to mental health as I am prone to depression and anxiety although managed currently . Thanks Claire

If I had crohns or colitis, would the colonoscopy had shown it? What else could it be? Or what other tests should I push for? I was so convinced that it was going to be Crohns, Colitis or worse, but now I’m not sure. Of course I’m happy the test was normal but unsure what to do next.

I have PSC, Cirrhosis (due to PSC - tea-total), Ulcerative Colitis, etc. so already have a messed up immune system and low platelets. Would like to make sure I am well informed before my next dental visit.

Hello lovely people just wanted to find out if anyone has experienced abdominal pain linked to inflammation of the bowel/colon and a possible diagnosis of colitis.

I have colitis that began to present in December of 2023.

After that I had about 4 or 5 flare ups over the course of the next 50 years, not having been officially diagnosed with Ulcerative Colitis until 12 years ago. Mostly I tried fasting or Chinese herbs for those flare ups and largely, it worked.

All good and after a recent flexible signoidscopy no sign of ulteratuvr colitis yay. However, after the injection sometimes I get a slight rash / bump on my thigh (especially after a shower) and this time slight swelling on my thigh. I’ve taken anti pesimines and it goes away.

What hasn't helped matters is that I was taking cholesterol for colitis which has also inhibited absorption. I've stopped taking them now. I've asked for years for referral to endocrine but as my tsh levels are medically ok they have refused.

Trihexyphenidyl (Artane)Chemotherapy and hormonal medicines: Antiandrogens (Casodex, Flutamide, Nilutamide) Busulfan (Myleran) Cyclophosphamide (Cytoxan) Ketoconazole LHRH agonists (Lupron, Zoladex) LHRH antagonist (Firmagon) Other medicines: Aminocaproic acid (Amicar) Atropine Clofibrate (Atromid-S

I had improved my symptoms greatly about a week prior to diagnosis via dietary changes, but since ibd diagnosis and starting octasa things have gotten much worse despite maintaining the same diet. Is it likely the fault of the medication or would it be too soon to tell (I have only been taking it for

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Hi, my husband was diagnosed with PSC 2 years ago and has since been further diagnosed with colitis, IBD, early stage crohns and is also type 2 diabetic (a lot going on!) has anyone tried spirulina?

Damage from op for kidney stone, colitis, hormones/hrt? Before operations apart from gallbladder attacks I was fine. Any ideas or similar experiences?