ADALIMUMAB-AQVH vs Etanercept

$995 for a carton of 2 auto injectors vs Humira's $6922, good news for the patients. We can hope for more price reductions as the market is expecting at least 11 Humira biosimilars to be released.

This is my first time posting in this community, although I’ve lurked ever since I was diagnosed a little over a month ago. About 3 years ago I woke up with insane elbow pain out of nowhere. That was the only joint that hurt, but it was super intense considering when I went to bed the night before

My employer switched insurance companies at the beginning of the year. I am now on WPS and use SmithRx and Costco Speciality Pharmacy to get my meds delivered to my house each month. I am on Zeposia and have been since January 2023 without any relapses and no side effects. I got a letter from Smith

I have Crohn's disease and I'm trying to narrow down what health plan I wish to go with. I used to be on Humira, but my old insurance in the private sector moved me to a biosimilar named Yusimry. Based on my research, none of the Federal plans cover or supply this drug, so I'm willing to move to a b

Hey chat, has anyone switched to Yusimry from Humira? Or experiences with other biosimilars? I’m considering making the jump due to insurance reasons so plz lmk your experiences with Yusimry or other products.

Hi, I'm totally new to this subreddit, so please bear with me! I was diagnosed with Juvenile Idiopathic Arthritis (However, it's Rheumatoid in my jaw) in October of 2021. I've been on Humira for 4 year now since then and it has worked pretty well (besides irritation at my injection site, handled wit

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

​ [Stockhead Image - https:\/\/stockhead.com.au\/health\/incannex-has-positive-pre-ind-meeting-with-us-fda-on-ihl-675a-for-treatment-of-rheumatoid-arthritis\/](https://preview.redd.it/1h5zxr69o6ib1.png?width=2338&format=png&auto=webp&s=91dc29b8a14eea7ea69d1cf39265915cf2107e9d)

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