Good luck to you Shazia. For me, mestinon makes my symptoms disappear. I am lucky and gr8ful that it works since I know it doesn't help everyone.

Now I'l ask a really naive question: I believe you Shazia, but it makes no sense that a drug like mestinon (with zero abuse potential) could be prohibited for those who need it. Is this a matter of high cost, or is there really no way for a person with MG to find this drug in your country?

I don't mean to get political but rather am at a loss for what I would do if I couldn't get this drug. Is this a common situation across the world?