Hi everyone! I was recently diagnosed with psa in Nov 2024. My rheumatologist started me on methotrexate. I had pretty bad side effects such as nausea, dizziness and flu like symptoms.I couldn't function very well. The doctor cut my dosage in half in hopes that I can tolerate. Yes, it did help , not 100% , but better. Now, in addition to methotrexate, which he boosted my dosage slightly this last week. The doctor wants me on enbrel injections. Honestly, I'm super anxious about this new med. I think I spooked myself into thinking the side effects could be the same or worse. Does anyone have any suggestions on dealing with the uncertainty? This is all new to me, and I have to say I'm slightly overwhelmed.