There are a couple of newer foundations that have formed in the US over the last few years who are also dedicated to supporting SMS.
Taylor Bug Kisses Foundation is dedicated to providing funding for medical research, educating, and providing financial assistance and emotional support for families who have a child with Smith-Magenis Syndrome.Taylor Bug Kisses Foundation.
The Smith-Magenis Research Foundation supports research to improve the knowledge and understanding of Smith-Magenis Syndrome so that viable therapeutic options can be developed to improve the quality of life of those with SMS.
Smith-Magenis Syndrome Research Foundation.
Smith-Magenis Syndrome Research Foundation.
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Smith-Magenis Syndrome Fact 27
