Etanercept vs LEFLUNOMIDE

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

In the UK it's known as Humira, Trudexa, Amgevita, Hyrimoz, Idacio, Imraldi and Yuflyma. After about two years on Methotrexate and one year on leflunomide I was really worried about starting Adalimumab. The other two drugs ravaged my body for a long time and made me feel like less of a person. They

RA is unapologetially kicking my ass both directly and indirectly lately. It makes my life so inconvenient in so many creative ways that it's almost funny. So to both vent some frustration and hopefully give you all a chuckle, here are some of the downright ridiculous things that are pushing me to t

Hey, just going to share my story as a warning for others. I’ve been on mtx for years, with good effect and usually prepare my meds in a dispense pack so I’m not getting a bunch of tabs out every morning. Ironically, a big part of the reason I do this is to minimise the risk of accidental incorrect

I’m honestly feeling lost and scared for my mom right now. She was diagnosed recently with seronegative rheumatoid arthritis after suffering from joint pain for almost a year. Her rheumatologist started her on the following medications: 1. Methotrexate 15 mg (once a week) 2. Folvite 5 mg (daily exce

I'm in SO MUCH PAIN right now. Preface. Ha. Saw rheumatologist yesterday for follow up. On Rinvoq & Leflunomide. Rinvoq isn't the miracle I'd hoped it would be but I'm so tired of switching meds and I need a break from injectables. Trying to make it work. Using Celebrex/celecoxib as needed. So r

hi yall! 23yrs, seropositive & 2.5 years into diagnosis here! this is my first real post in the sub! i wanted to share some positivity that has finally come my way!!! after cycling through a plethora of treatments - methotrexate (which put me in the er & resulted in nearly 70lbs of weight lo