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In 2006, Ed and Tina McGovern discovered that their son Jack had developed a rare retinal disease in his left eye called Coats disease. They have since learned that some research has been conducted on the disease, but much, much more is needed. With three annual events per year, a growing community of supporters, and hundreds of thousands of dollars in donations for research, the JMCDF has made a dent in the work that needs to be done to cure Coats.
The Jack McGovern Coats Disease Foundation is a 501c3 and our federal ID # is 26-2439083.
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