Ulcerative Colitis questions: Confused and frustrated

I have pancolitis too. It has only been a few years but I started with proctitis, which has evolved into full blown pancolitis! The mesalamine (oral and rectal) only helped for a few months and then I tried my first biologic (Entyvio) which worked beautifully for 13 months until I stopped responding. After that was Stelara, which didn’t do much at all. Finally I was prescribed Remicade which worked somewhat and then my GI doc fought to get insurance authorization for a higher dose of Remicade and every 4 weeks at that! So far, so good. For 16 months I was flaring horribly, several hospitalizations, malnourished, under 100 pounds and on mega doses of IV and oral prednisone. Fecal calprotectin was 1280 and I had met with a colorectal surgeon and scheduled a proctocolectomy. The higher dose of Remicade seems to be working and I am cautiously optimistic… Pancolitis is the most severe form of UC, so you may want to think about biologics or one of the newer orals that have been approved over the past year or so (Rinvoq, Zeposia, Xeljanz). There are others and they have different mechanisms of action. Talk to your doctor and decide which one you’re comfortable with… I was thrilled with Entyvio- it has a decent safety profile and it worked for me for over a year. The Remicade is one of the older biologics (TNF inhibitor) but I needed a higher dose for it to work completely. You and your GI doc can decide what is best for you! I wish you the very best of luck and a long remission!

I have been dealing with my UC for almost 2 years now I started on Remicade and it was the miracle drug I believed. It took away all my pain in my stomach also stopped my constant diarrhea and nausea. After being on the Remicade infusions for a year I started to have a lot of pain in my joints and bones and I was getting blurry vision so my doctor did some tests . They said the Remicade gave me drug induced lupus! So they took me off of it and started me on and Entyvio I have had four infusions and so far nothing I am back to the beginning severe stomach pains severe diarrhea severe nausea. Have you had any trouble with the Remicade I keep asking my doctors to please put me back on it I never felt so great as is when I was on the Remicade. All I do is cry and that's not good.

I’m so sorry for what you’re going through and sadly, I understand. I must have shed a million tears over what this illness has cost my family and me… The only issue I have had with Remicade was a few patches of psoriasis and that was only a couple weeks when they started the higher dose. If you have drug induced lupus, you have no choice… I know how you feel because early on, my first line of treatment was oral mesalamine and it was working beautifully until it caused drug induced pancreatitis and I had to discontinue it immediately. The next year was hell with the flaring and mega doses of steroids!!! They did have me on Stelara for a couple months and that did nothing! These drugs all have different mechanisms of action and target the inflammation differently. Remicade is a TNF inhibitor and if that worked for you, maybe Humira would work- that’s a TNF inhibitor too. If your doctor says you can’t take that kind of drug, they have recently approved a couple others - Zeposia, Rinvoq. Xeljanz has been out a few years, so there is some hope… and these are all oral medications. Again, I am so sorry and I understand all too well!! The best thing you can do is work closely with your doctor on choosing the next line of treatment. This disease is a relentless bitch and we have to stay on top of it with our doctors. I wish you the very best of luck and strength!! Please feel free to reach out if you have any questions or if you just need someone that understands the roller coaster of hell that you’re on….

Hello dval,
Your post is from nearly 4 years ago, and I certainly hope you are improving.
Which Visbiome do you take: Visbiome GI Care 225 billion per 2-capsule dose? Or Visbiome Extra Strength 900 billion per extra strength packet?
Thank you for your recommendation!
With kindest regards,
tmh

I take the capsule and have been for years! I am still on the higher dose of Remicade (10mg/kg) IV infusion every 6 weeks. He started me at that dose every 4 weeks, then after a year and a half, every 5 weeks and now, every 6 weeks. GI doctor does therapeutic drug monitoring to check trough levels and antibody titers, which determines what is in my system and if it is effective, based on inflammation markers, which have been in a normal range, and for all of this I am extremely grateful!!! Thank you for asking. I wish you a long remission and for all of us, ultimately a cure!! 🙏🏻

I also live in central NJ. Red Bank area. My drs are in NYC , looking for a dr closer to home for my UC. Could you share your dr’s name please?

Of course! Since this posting, much has happened! I developed antibodies to the Entyvio and was switched to Stelara, which did NOT do anything for me. I had 16 months of pure hell, flaring, 5 hospitalizations, lots of prednisone (both oral and IV) and finally, a higher dose of Remicade (infliximab) infusions (10 mg/kg) every 4 weeks got me back into remission. Once again my brilliant GI doc had to battle my insurance company to get authorization for the higher dose, as I was barely 100 pounds. While waiting, I had scheduled a proctocolectomy and was able to cancel that less than 2 weeks before it was to happen. The colorectal surgeon is at the same hospital. I have been in remission over 2 years and get the Remicade infusions every 6 weeks now. My GI doc does therapeutic drug monitoring to test inflammation markers, trough levels and antibody titers every few months to make sure the levels are adequate and that I have not developed antibodies. I am blessed to have this brilliant caring doctor! His name is Anil Balani, MD and he is with Capital Health. Good luck to you!!

Thank you! I’m presently on Humira weekly ( just started weekly) . Only have had 3 weekly doses and hasn’t helped. Dr wants me to continue for a few more weeks -(even though been on it every 2 weeks since November). Making me feel so nauseous and tired. I’m looking forward to changing meds and feeling better.

I’m so sorry and I understand the frustration and devastation! This is a life altering disease, a roller coaster of hell, if you will… Remicade was my first and only TNF inhibitor and I’m grateful it is working, but the fear never goes away…. The one positive for all of us is that several newer drugs have been developed, with different mechanisms of action. They scare me, too, but my doctor taught me to focus on benefits vs. risks. So I take it one day at a time and try to be grateful that the good days now outnumber the bad ones… and my GI doc stays on top of it should things get bad again… 🙏🏻. I wish you the best and a very long remission!

I have ulcerated colitis and had colon cancer removed and now have an ostomy bag. Can I eat salads, or Italian food?