u/SelfSignificant6204

Just wanted to introduce myself. I was just diagnosed with RA on May 8th. I had a feeling it could be but then again I felt like it probably wasn’t because all my other tests for autoimmune were coming back normal. So I joined this group to get familiar with RA in case I did get a positive result. While waiting for results, I was on Prednisone but it didn’t help much except more energy. Now I’ve started methotrexate but was told it can take 2 to 3 months to kick in. All she offered me was Prednisone again and I want nothing to do with steroids because of side effects. I only took it because I wanted my hand and wrist pain to go away along with the swelling. My hand is still swollen with no change. I am on Tramadol with my PCP. I asked her if we can increase it because I’ve been on 50 mg for over 8 yrs. Idk if she will now that I have RA diagnosis and if she will direct to my Rheumatologist. Anyone have experience or suggestions with this? The pain I had recently was unbearable! I tried to call my rheumatologist office but they didn’t call me back. There was no option to leave a brief message but I should have! I asked another question in the portal so idk if they assumed that’s what I wanted. I had no idea RA pain could get that bad so quickly. My symptoms started in December and it seemed slow but then it started to migrate to other areas and then into really bad constant pain with throbbing at times. I couldn’t use my hands at all for those few days other than the real necessities like eating, bathroom etc. but with lots of pain trying to do that. I can’t write or text without pain so I use the voice text now. Trying to adapt to all the new changes and it’s so hard. Some days I’m good and other days I feel like I’ve lost my independence and will it come back?? I was so relieved when those few days passed and I could use my hands again. Any tips would be greatly appreciated adjusting to RA changes.