Madisons Foundation - Moms And Dads In Search Of Needed Support
Connect
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.
Ms. Smith Goes To Washington
LOCATION: WASHINGTON, DC DATE: September, 23, 2011 -- Marcy Smith, founder of Madisons Foundation, addresses a press conference as part of National Childhood Cancer Awareness Month on Friday, September 23rd at the U.S. Capitol Visitor Center in Washington D.C. CREDIT: Jay Premack/Hyundai Hope on Wheels Jay Premack, All Rights Reserved
Ms. Smith Goes To Washington-Video
Watch the video of Marcy speaking in Washington at the 2011 Childhood Cancer Summit, Washington D.C.
CoRDS
Here at Sanford Research, we are committed to finding cures and advancing therapies into rare diseases. To further this mission, we established the Coordination of Rare Diseases at Sanford (CoRDS) – a national rare disease registry designed to accelerate research into these rare conditions.
m-Power® Database
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.
Tom Hanks Greeting
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Champagne Tasting Fund Raiser
WALLY'S WINES AND SPIRITS is holding their 21st ANNUAL GRANDE MARQUE CHAMPAGNE TESTING on June 2, 2013 at Le Merigot Hotel in Santa Monica. A portion of the proceeds will benefit MADISONS Foundation! A big thank you to Wally's Wines and Spirits! For ticket information, please call 310-475-0606.
Chronic Complex Diseases of Childhood
Marcy Smith's mission to educate parents about their child's rare disease, inspired us to create a text book dedicated solely to the care of children with complex and chronic diseases.
Quick Links
to other parents with your child's disease
explore the rare pediatric disease database
to help support Madisons Foundation
Our Mission
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: