catlady
Cheer Parent
- Jun 6, 2012
- 2,797
- 6,206
Curious: has anybody else on here taken methotrexate? I've been on it for 4-5 years for my autoimmune disease, and while I know I can't stop taking it probably for a very long time, I'm still having a lot of trouble with the side effects, mainly nausea, headaches and fatigue. If anybody else on here has any experience with this yucky medicine, or better yet, any tips on how to not feel so crappy after I take it, I'd love to hear about it. It's the one thing I dread the most each week and just thinking about it while typing this is making my stomach roll.
Cp has an autoimmune disease , also (hers is ITP). Although she has not had to take methotrexate, she was on 6 mp which gave her those symptoms. Please talk to your doctor about it and have him do a blood draw just to make sure it isn't affecting your hemoglobin or liver. What may have worked for many years may not be now. If that's not the case, ask if you can take it before bedtime, sometimes sleeping will take care of the nausea part. Cp was diagnosed at 4 and is now 17, she suffers from headaches and fatigue, as well. We have been told, unfortunately, those symptoms are normal when your immune system is working 24/7 attacking whatever it is it attacks. Teenage schedules often don't make time for much sleep and it is so important with an autoimmune disease to make it a priority. Sleep and water, water, water. But, go get that blood draw if you haven't had one in awhile. Big hug from the catlady!