I was a Little more active a while ago. Then I got my rheumatoid arthritis diagnosis and it seems like everything went to hell for me. I’m not currently taking a DMD because my MRIs are “stable” according to my MS specialist. I’m actually getting a second opinion from a local neurologist that my mom sees for her MS.
I am, however, taking methotrexate for my rheumatoid arthritis. I took steroids for about a month, and that did help. But now I’m suffering from ridiculous joint pain and swelling at times. It could take up to 3 to 6 months for my methotrexate to kick in full speed and at the two month mark. The fatigue has been absolutely devastating.
All that being said, I am still reading posts and keeping up with everyone and learning more about MS every day. This community has been so accepting and wonderful for me, I’m sorry I’ve been mostly lurking!!
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Qt314grl
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So sorry you are in pain Qt314grl. I’m glad you are going to get a second opinion regarding the DMTS. I took Copaxone for 12 years and stopped and am ok. I went to Europe for 2 weeks and came home with tendonitis and arthritis in my knee! But things are looking up, I myself have been lurking but we are lucky to find acceptance in this chat room. Take care my friend 😀❤️
Oh bless u hun you've got a lot going on 🤔🤔🤔 . Really hope u will start to feel better soon with the arthritis as if MS isn't enough for u. Big hugs xxx
My wife has arthritis and Chron’s. She has been on Remicade since last October and Chron’s has really improved. Also the Remicade has helped with her arthritis also 🙏👍. The weather changes really effects her arthritis 😕. Now her pain doctor is talking about a pain pump. Good luck and keep us posted how you are doing 🤷🏼♂️. 🙏👍🐾😉. Ken
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