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@kenyalama

Hello RA friends,
I have been taking Humira pen every two weeks and methotrexate eight tablets weekly for my RA, RF borderline. It was out of control. Swelling in every joint, knuckles, knees, tendinitis, periferal neuropathy, it was so painful to type! Attacks of Raynaud’s, Sjogren’s. Vasculitis.
My rheumatologist and neurologist were at odds with my treatment. Finally about a month ago my PCP consulted the rheumatologist in adding Prednisone 5mg daily to my meds regime. I am even allowed to take 10 mg if needed. Docs were reluctant to give me steroids but decided the benefits outweighed the risks in my case.
After one month I feel like something like a miracle has happened. I almost feel in remission. I hope this story is useful for many RA patients dealing with unsuccessful treatments. It takes a combination of drugs to do the trick. And yes, be prepared for flares. It’s part of the deal. Good luck to all from my heart
Anny Rapoport

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Replies to "Hello RA friends, I have been taking Humira pen every two weeks and methotrexate eight tablets..."

@kenyalama this is so wonderful to hear!!!! Your doctors are really working together, aren’t they. I am so glad you saw this discussion and decided to get involved. Thank you
Have you noticed any problems since you added in the prednisone?

Methatrexate really did the same for me. I changed to injectable and it made the days easier. However, changing my diet to non processed, avoiding sugar, potatoes, tomato and moderating dairy and whole wheat as well as adding a daily walk to my lifestyle worked well with it. PT referral for chronic joint ills is great. At retirement I was able to go off of MTX. I have been on Plaquenil for years; going to half dose this year to see if that will do. Apparently, I am elderly now. Of course, I have to pace myself and do the ice/heat, lidocaine patches, epsom salt baths etc, but resting without daily movement is toxic.