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I put a link to the outline on the website at www.MyotoniaCongenita.org.
I was exited when I saw in Quest that you were looking at doing a documentary. There is so much information that is not correct on the disease. It is frustrating at the way you can be treated by health care proffessionals at times.
I look forward to hearing about the progress of this journey you are looking to embark on. Thank you.
Hi Kristie - Be sure to post what state or country you are from, so if it isn't already on the list, it can be added... we want to know how many places this forum reaches! The documentary project is so exciting - Jim is biting off A LOT!!! lois
I hope they're interested in your subject, it would make such a change to see something positive on MC; in fact it would make a change to see SOMETHING on MC!
Jim I think this is great! One of the most frustrating things about this disease is all the efforts to hide it or when we reveal it then we are misunderstood. This has been bottled up inside us for too long...it is time to feel understood or at least feel like there are efforts made toward this. Awesome!!
Type of Myotonia: Beckers
Country: United States of America