~ ~ This site is for individuals who have or deal with Charcot-Marie-Tooth Disease. ~ ~
Here at CMTLIST2, members feel safe to share their experiences & knowledge of living & surviving with CMT. * Each member has a story to tell & we encourage each one to join in & share their life story with CMT (the good & the bad). * It is important to ask questions, & it is just as important to respond to another members questions. (Just because your a new member doesn't mean you wouldn't be able to help by adding your input to a question). Please share your knowledge (experience). You can help make a difference to someone who is reaching out for support. * Don't be surprised when you realize that you have found both support & friendship from people that know what CMT is.
In order to join a yahoo group you will need to have a yahoo user ID. You should already have one since you have gotten to here. After you add your e-mail address into the SUBSCRIBE box you should be sent a form from asking specific info. If you don't get it you need to contact us, because without this info you will not be approved for membership.
This CMT group cares about you. If you need someone to listen to you, you have found the correct group for CMT support.
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