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Has anyone with UC stopped responding to Entyvio?

Digestive Health | Last Active: Jan 26 2:41pm | Replies (48)

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@msgtrebholtz

Of all the drugs I was put on (all that you list plus more) none worked except Entyvio , in fact I had bad reactions to most.

Entyvio worked well for about 6 months then tapered off and started the worst flare I ever had.

So what's my advice? In my experience when something didn't work or stopped working I said done, next! Only you can decide when that happens.

Another suggestion I have is Never, EVER think a second opinion is wrong or will hurt someones feelings. It's your body. Each time I got a second opinion I got the answers and information I needed to make an informed decision on my next course of treatment.

For me the battle was lost so I opted for a total proctocolectomy, which was absolutely the best medical decision I have ever made. I got my life back and no drugs. It wasn't all rainbows and unicorns, but looking back at where I was in the summer of 17 to now, I pick now.

Please ask if you have questions. I'll go back through my records and help you with anything I can.

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Replies to "Of all the drugs I was put on (all that you list plus more) none worked..."

TY so much @msgtrebholtz for your encouragement. May I ask more info about your proctocolectomy? With an autoimmune disease, once the colon is removed, will it now just start attacking something else? I’ve had the ‘last resort’ in my mind from the beginning & the more I hear about it the more it doesn’t sound SO bad. I will say I’m truly scared about being on 6MP (if it even does work) for long term. I’ve been on prednisone for an 11 month yo-yo & back on another yo-yo since mid June (+ possibly another 5 months). I see GI for “next step” on Monday.