I met a lady that worked in NY with the Dystrophy Association for over 30 years and she sent me the info by email. At first I had no idea that MG was in the list of diseases from the Dystrophy Association. It was some way depressing that is a dystrophy too... but in the positive side they are a big Association that can help you or I. I already called and they already gave me an appointment for the beginning of nov, which I was very surprise. I know the doctor that would see me and is a great neurologist. I am not sure all the support I would get but I will find out on the first visit. They have over 400 places in USA where you can get help and support. In Puerto Rico they do have an office and service at different points of the island. The link of the USA SITE is http://www.mdausa.org