MGers are greatly affected by heat. Muscles work best when they are cold. I start feeling the effects at 70 degrees. I can barely go outside if it is above 85 degrees.

some people are affected more by the heat than others.

Good luck with your treatment and don't get too stressed. There are a lot of nice people here on this forum to help you through.

I was evaluated for MS and MG. I use to pray to God, please let it be MG and not MS. I read a lot on line on MG and it appears to be more manageable and there are some treatment that can lead to remission.

I am newly diagnoses too - just 6 months. I am on Mestinon and 40 mg pregnisone. My neuro is trying to get me approved for IVIG.

Please keep us updated,
kathie