ADALIMUMAB vs MELOXICAM

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

I am absolutely going to scream! I had a vacation recently with friends where on the last day my meloxicam got packed into the bag, was unreachable and I hit a flareup mid morning. Not proud of it but I had a meltdown at some point because everything was too much and they wanted to discuss everythin

My pain doctor increased my hydrocodone from 3 a day to 4 a day. My pharmacist refused to fill the prescription. The prescription was sent to them on 10/6. They didn’t fill it. So my Dr sent it again on 10/22. Now I have 2 pills left, and the pharmacist said he needs the Dr to write out his detail

I had to tag this as funny, in a very sarcastic way. Talk about feeling unseen. I am on meloxicam, cymbalta and Humira for my RA. Stretching, Epsom salts baths, plant based diet just in case, meditate, starting therapy, limit my caffeine, medical marijuana. I know what I forgot, ibuprofen!

Hey, all. I have chronic pain due to ehlers danlos, fibromyalgia, carpal and ulnar tunnel in both arms, osteoarthritis in my lower back, and what I think are some other issues that haven't been diagnosed. I've had pain for years and have tried everything over the counter as well as Celebrex, Meloxic

After struggling for years with doctors that either don't take me seriously, try stupid solutions that dont work or just help me learn to "cope with it" instead of working on a diagnosis i got a new primary doctor THAT ACTUALLY LISTENS!!!! I mentioned a few different things i think i could have, she

First, this is a rant and basically nothing but a rant. I'm new here and I've been reading through a lot of posts that might apply to me. I just turned 40 in Feb of this year. Memorial day weekend of 2023 my car got totaled on a drivers side impact, and I've been in excruciating pain ever since. I'v

What’s up with Pain management drs not giving out pain killers to people who actually need it? Not everyone has addictive behaviors! I just had shoulder surgery was given a script of 30 OxyContin 5s that’s it and when I asked surgeon to get it refilled I was told to go to pain management. So I go to

Today i saw the new NP at pain management, i expressed how much pain ive been in, what it feels like, how it affects my daily life. She said “you’re only 40 and thats young, we already increase 1.5 times ( went from hydrocodone 5/325 to oxycodone 5 IR) i don’t want to change anything cause your “you