Ixekizumab vs LEFLUNOMIDE

Came up as an ad on Reddit. We’re doing BOGO on injectables now?

I was diagnosed with Ankylosing Spondylitis when I was 20, I’m now 28. My medication journey has been nothing short of annoying. I’ve tried nearly all TNF blockers and they help my symptoms, but the injections themselves are horrific for some, or my insurance won’t cover them. Humira: injection site

I have been living with psoriatic arthrisis for almost 2 years. I am 23yo. I caught covid in December 2021 and I started feeling pain in my back out of nowhere. I let a couple of months pass by before the pain worsened and one day I couldn't stand on my left leg without feeling atrocious pain. Went

In a couple of weeks I'll be starting on Taltz (ixekizumab). Is anyone one it? Has anyone been on it? Was it effective? What side effects should I expect? Anything I should know going in?

Tldr - Been through Methotrexate (DMARD) , Humira / Adalimumab (Anti-TNF) , Taltz / Ixekizumab (IL-17A), and currently on Cosentyx / Secukinumab (IL-17A), Sulfasalazine (1000mg) and Ibuprofen (1600mg) I’m thinking of switching to a Jak inhibitor. But all the risks involved are ma

Hi all, My now-4 year old son has ILVEN that I described in [my initial post here](https://www.reddit.com/r/ilven/comments/swimto/what_has_been_your_ilven_experience/). Since then, it's grown significantly across the entirety of the left side of his body, from head to foot. It seems to have progress

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