June 20, 2012
Foundation for Angelman Syndrome Therapeutics is an amazing organization! It's founder Paula Evans is a mom who saw a need for a focus on development of treatments and an eventual cure and began a mission to do just that. She has stopped at nothing to raise funds and has made a current treatment trial happen. Along with Paula the entire board has worked tirelessly to ensure that the organization stays on a path that will meet the treatment needs of all individuals with AS. Without them the current trial simply would not be happening. Thank You FAST!!!
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