ADALIMUMAB vs USTEKINUMAB

Hey everyone! I've been on a deep dive into understanding the immune system, particularly in relation to psoriasis. Consolidating information like this really helps me grasp it better. While there's a wealth of knowledge out there, I've highlighted both natural and conventional methods that I've per

Hi all, have had worsening psoriasis and PsA since 2014 and finally today my dermatologist saw me and has put me forward for Adalimumab! I am so happy to finally get approved for a biologic. Fingers crossed it will be the treatment that finally works for me!

Started Skyrizi on Sunday and things are changing. As the old adage goes "Changeable, Curable" I've had one small area of persistent psoriasis clear completely - I'd given it a friction burn from rubbing through clothes on Saturday. On Monday it was red and sore. Tuesday it had dried. Wednesday it p

I’m 23M with psoriasis. I’ve used methotrexate before, then Apremilast for 6 months (stopped working). Now my doctor wants to put me on Tofacitinib, but also asked me to check with insurance about biologics. Shes recommending Ixekizumab (Taltz), but it’s super expensive (₹3–4.5 lakh first year, then

If you'd all humour me while I vent, I'm very much an emotional wreck atm 😅 I've had Plaque Psoriasis since 2012, started on my forehead and then spread to cover my entire face, big patches on my legs, arms, back torso, scalp, ears... You get the drift. After Ciclosporine in 2019 I took a break wit

Welcome back to this week's newsflash 1. Surgery for UC can be a major life change, but it is often a necessary step when medications fail. Understanding the adjustments to diet and daily life afterward is crucial for recovery and long-term well-being. This guide explores what patients can expect re

#The Effectiveness of Medications for Ulcerative Colitis *This post was last revised September 19, 2019.* Here I have compiled data on the effectiveness of medications used to treat ulcerative colitis, as compared to placebos or to other medications. ###Risk Ratios (RRs) All values here are shown as

Since eternacept started to wear off over the years my docs gave me the choice to switch to Ustekinumab. The 3 months injection rhythm sounds pretty unreal when coming from 3-day-interval Eternacept jabs, but well.. you could call it progress in medical science. I am now 3 weeks in after my first do

I wanted to follow-up on a previous post I made regarding starting Stelara. https://old.reddit.com/r/Psoriasis/comments/yjhr6z/plaque_psoriasis_after_a_covid_vaccine/ I have now be on Stelara for 7 months and it has nearly cleared my Psoriasis. I stopped applying Clobetasol some months ago and each

I’ve been on biologics for about a year now, i started in December 2024. About 45ml shot of Ustekinumab every 3 months as prescribed by my dermatologist. Problem is, it is losing its efficacy. Since August, every time it clears up about 70%, the same thing happens, it comes back worse even with topi

Phase 3 trials to commence. Possibly another biological option. http://www.medscape.com/viewarticle/878838

Sulforaphane Protects from T Cell–Mediated Autoimmune Disease by Inhibition of IL-23 and IL-12 in Dendritic Cells [https://www.jimmunol.org/content/192/8/3530](https://www.jimmunol.org/content/192/8/3530) **Ustekinumab,** sold under the brand name **Stelara** is a [monoclonal antibody](https://en.wi

Hi everyone, i went through a lot of derms(atleast) from hand eczeme to funghus .. it is everything but nothing helps… my newest diagnose is pustulare psoriasis.. I aplied Winxory for 2weeks where my hands got „fine“ and then it happend again. my derm wants to put me on Ustekinumab?? just wante