MS and myasthenia


Does anyone else out there have both MS and myasthenia?
Having been diagnosed with both of them I find it so difficult to work out what symptoms to attribute to which! Started with RRMS 33 years ago but now SPMS and then myasthenia diagnosis about 5 years ago. Now wheelchair user full time. Also just been diagnosed with B12 anaemia, so it feels like my body is set on attacking itself! Not sure what it all means for me.

saw that you had no replies so here’s a bump up to the top


Hi Kate, just googled the condition. Mmm, I can see how MS and MG can be so similar in effect. Poor you.


Having googled the combination of MS and MG I thought it would be a long shot to find anyone else who had the two conditions, but thought it was worth a try! However, thanks for the interest.