GUSELKUMAB vs LEFLUNOMIDE

It's not every day you find a promising pennystock before it pops, and if you've been looking for one then you're gonna want to read this. I've been wanting to write a definitive DD post for this stock for a while but haven't had the time until now. There's been a few good posts about it but none ha

Hi everyone, first, just want to thank everyone for sharing in this forum, for the courage to reveal and be vulnerable, for providing a sense of community and connection when its easy to feel alone in what we're struggling with, and for the encouragement and support. About me: 51yo male with recen

I use the biologic in the photo. My doctor gave me the first injection, and today I have to do the second injection by myself. I wanted to ask if you inject yourself? Is it easy? I

My gf has been prescribed to get Secukinumab (Scapho) for 5 weeks, then monthly after, and Guselkumab (Tremfya) once a month (afaik this is conditional to her response to Scapho in the first 4 weeks). She's being charged 32k for Secukinumab and 82k for Guselkumab per session. Are there any availabl

So..we don't exactly know for sure even whether the injection had a direct effect or was merely acting on the gut microbiome which then quenched the inflammation. # Compositional Alteration of Gut Microbiota in Psoriasis Treated with IL-23 and IL-17 Inhibitors [Yu-Huei Huang](https://pubmed.ncbi.nl

Hi All, I was able to join a clinical trial for Guselkumab and had my first dose 3-4 weeks ago. Just wondering if any of you had experienced an onset of Migraine as a side effect of the medicine? Also, maybe more acne? Thanks!

***EDIT: I am in the US. I have my next GI follow up to likely begin Tremfya on 10/7. I did my labs today for calprotectin, TB, HIV, CBC, CMP, Hepatitis, and TPMT activity. Hi everyone, I stopped into my GI today and got copies of my colonoscopy, biopsy, and follow-up visit note with my GI from las

I was diagnosed with Psoriasis last March 2024. 3 months later, I started Guselkumab (Tremfya). Since then, my skin really cleared up. No flares. I feel normal and back with my old self except that I have hyperpigmentation on some areas but not really a big problem. Been taking this biologic for 8 m

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