Myasthenia Gravis Community Group
Pretty simple: I would love to engage/communicate with those dealing with the daily struggle of having Myasthenia Gravis. My world as I knew it, no longer existed when I was diagnosed with MG in 2013 ( it took a year to get diagnosed). Sometimes, I feel like no one truly understands this limiting, unpredictable chronic autoimmune disease.
When I was recovering from sepsis, I had a lot of trouble sleeping. My doctor gave me amitriptylene. It's a 1970s era anti-depressent which makes the patient sleepy, and it seems to clear the system quickly. You might try that. It helped to get me back on track, with normal sleep habits. Beyond that, try sleeping with the TV on. It just helps to keep your mind in check.
I even tried THC, with marginal results. Seemed like you had to take a lot of it.
Hope this might steer you in a direction that works.