My Nonprofit Reviews
Review for LGS Foundation, New York, NY, USA
My son was dx was LGS at age 2 and we went over twenty years not knowing others, it is such a terrible disease and no know ones what your going through, it really is so hard to deal with. but the lgs foundation helped me when i needed them most and helped me meet other families. they also keep me updated of news and information thoruhg there website and newsletters. i hope to go to there conference in november it looks fantastic.