Has anyone been misdiagnosed with RA? I was diagnosed 10 years ago (mri of my wrists) and was on methotrexate 10 yrs. I never had a flare up and thought the drug must be doing wonders. I recently moved and a new rheumatologist said he thinks i was misdiagnosed - I have no markers for RA. I am off of methotrexate now 3 weeks and so far so good. How often does this happen that people are wrongly misdiagnosed with RA?
Awful that it took that long to diagnose you correctly. I’m very disappointed in doctors. I didn’t think I had RA but the blood tests show I do. It affected my big joints not small and I never got the swelling. I guess I’m lucky that way. I went for a second opinion and I was told the same. 😟
Thank you. The information was quite helpful. I guess it jmakes we wonder why some rheumatologists don't routinely check for markers every few years as standard protocol. Either way, I'm happy to be feeling good and that's what counts.
That is awful and I feel they do misdiagnose RA and you took methotrexate all those years for nothing I had a bad reaction to that medication. Sometimes I feel I am misdiagnosed because RA doesn’t run in my family on either side. My mother had multiple sclerosis. I always feel like do I have RA or am I misdiagnosed. I was diagnosed with hypothyroidism way before RA. Makes you think 🤔 I’m glad you found out and you feel good!