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Welcome to the Cody Foundation. The aim of our organization is to educate people about Duchennes (DMD) and to assist Cody and other children affected by DMD and similar life threatening illnesses. Please contact us with any questions or comments and thank you for your interest and support. Click here for a message from the President of the Cody Foundation, Nina Cobia.
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100
years from now, it will not matter what my bank account was, the
sort of house I lived in, or the kind of car I drove: but the world
may be different because I was important in the life of a child. |
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