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Hi all!

Since living with CMT I have always ran into people who have never heard of

it.My wife and I have been involved with other fundraisers such as MS society

and the MDA.

We now want to start to raise awareness and a non profit organization us

CMTers.I have searched for groups in southern California (thats where we

live)and

they had one at the MDA clinic in San Diego but it faded off.Because we live

in So.Cal and have some connections,we want to go big with this taking it to

the stars of Hollywood

We were wondering if any of you have started anything like this in your state

or hometown and how did you get it off the ground.Any helpful tips would be

much appreciated.

Thank you ,

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