ADALIMUMAB-BWWD vs Etanercept

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

Hey there! I’m coming up on 30 years living with RA. I was diagnosed as a young woman - only 22 years old! I was originally diagnosed seronegative RA, but am now seropositive. I’ve been on biologics over 25 years. I’ve managed to lead a full life after diagnosis: corporate career, two kids, world tr

hi guys, I recovered from long Covid, it started beginning 2022 for me and I relapsed many times, because any time I recover I’d get Covid again and bam another 3 months in bed. I’ll probably get it again, if I get Covid again. But I really pray and take all precautions to not get it. I know it’s di

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Hi everyone, I'm writing on behalf of my partner, because we’re both overwhelmed and could really use some advice and support. After nearly **8 years of pain and being misdiagnosed**, he was finally diagnosed with **Ankylosing Spondylitis (AS)**. For years, doctors said it was just stress, posture,

Edit: some folks brought up the very good point that you need to balance effects of any treatment against the effects of doing nothing. I was only focusing on the side effects of TNFi bc that's what I received a bunch of good (published) shareable info from my doc on, but we have had previous conver

I have been doing a lot of AI deep searches to find a way to reduce PD progression by using various supplements. Below is the extract of the findings. I suspect that for people at the early stages of PD might benefit from the effects and potentially slow down PD progression. If we have enough peo

I just switched insurances (new job), and my new insurance won't cover Enbrel for psoriatic arthritis, preferring one of 3 other TNF blockers. I've been on Enbrel for the last 5 years, and would really rather not switch away from something that's working so well, especially since I work in healthcar