ADALIMUMAB-BWWD vs INFLIXIMAB-DYYB

I just had a follow up with my gastrointerologist and the majority of our conversation was about all or most insurances not covering Abbvie’s Humira. He told me Abbie has been preparing to stop servicing Humira for a few years now and with the patent expiring, this is the year they have done it.

First, I would just love to say that I am so excited I found this. Newer to Reddit. But the amount of information that I have read in this has helped me tremendously. I was diagnosed a year and a half ago. Been through methotrexate and prednisone and unfortunately, I have been in a flareup for most

I just wanted to share my recent experience with recapturing remisson if it helps. I had been in Hadlima induced remission for 11 months and experienced the worst flare of my life the week before I started my new job. I was bed bound three full days and continued to suffer an additional three week

Hi all, I have been taking Humira auto-injector pen for Chron's and hidradentritis supprativa for several years now. i have had almost no issues. January this year, I received a letter that my insurance no longer covers Humira. my doctor said they would submit a prior authorization for me to try

Hello everyone. I was diagnosed almost a year ago. my flair ups have been reduced thanks to Hadlima, but I still experience frequent flair ups. I have a mostly desk job but I find myself in such incredible paid from looking down at paperwork I sometimes have to leave mid day. I was recently contacte

Just an informative post for those in Canada, but more specifically Ontario. My dermatologist, when I first met with her regarding HS, put me on an oral antibiotic (Amoxycilin) and a topical (clindamycin). Personally, the topical did not work for me, but after a few months, she recommended I try a

I'm an ex-junkie (8 years clean this past december) and I started hadlima a few months ago and I swear to God, for like 2-3 days after I take my shot, I feel vaguely like I'm going through withdrawal like sweaty, a little manic, jittery, rapid temperature shifts, and just like my whole body feels of

I’m a hospital worker so I was able to get the vaccine (Pfizer brand) today. I wanted to share my experience with everyone as I had a lot of fear and doubts about getting it myself. Everything went extremely well, so far I have no side effects at all and it’s been about 4 hours. My arm doesn’t even

I’m bored and have a funny story, so I thought I’d share. I’m in the worst Crohn’s flare up thing of my life, which was brought on by a series of traumatic experiences. Inflectra/Remicade/Infliximab doesn’t work on me anymore apparently and neither do steroids, so my doctor changed me to Entivio re

Hi everyone, I had the idea of putting together a community developed survey for those of us diagnosed with Crohn's disease. The survey could allow us to gain insights into many different aspects of the Crohn's community. I am curious if anyone has some questions they would like to be included, if

Long of the short I was diagnosed with UC in 2020. Took mesalamine until December of 2025. Two flares one in October 2024 (lost 30 lbs) second and ongoing flare July 2025-present. I can’t gain any weight back. I started Inflectra in Feb of 2026 and just had my second dose. I am currently in a flare

I'm starting on Inflectra on Friday, and I'm a bit nervous, wondering: what might I expect? What I can bring to make the experience better? I have Crohn's and perianal disease (with two draining setons from a recent surgery). Planning on bringing some audiobooks, my donut pillow, and some snacks, bu

QUICK BIO: Was first diagnosed with UC in 2015. Was fairly moderate until 2020, when worsening symptoms led me to starting infusions of Inflectra. Was on that steady for nearly three years until my GI took me off of it because my inflammation markers still weren't looking good enough. I was on zero