Etanercept vs USTEKINUMAB

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

Even though several of these medications are manufactured in the USA, it doesn't mean it's cheaper in the USA. "Socialised healthcare" negotiates in a free market outside the USA. No wonder travel insurance costs a fortune in USA. Detailed story..... https://www.msn.com/en-au/health/other/doctors-

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