
Check out Marcy's new blog at:
You'll need to register to view, but once you do you'll be able to view and comment on her blogging. Thanks.
This summer, we held our annual fundraiser at the Geffen Playhouse. The full house that attended the bio-play/musical "Monsieur Chopin" were welcomed by a special greeting... + Play the Video
Madisons Foundation is dedicated to improving the quality and quantity of information available to parents of children with rare, life-threatening diseases, and to facilitating effective communication among parents, physicians and medical experts through:
We are the only website in the world that connects parents whose children have the same rare disease. We understand how important it is to have access to medical information and to get in touch with other parents dealing with your same issues.
Click this link: howtobeadoctor
...for a video preview of...
How to be a Doctor for Kids
by Madison Smith
Empower yourself with knowledge about your child's rare disease. Together with a team of medical specialists, we have created a library of rare pediatric disease write-ups. We compile and post current medical facts, information, support groups, and web links to explore.
