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Making a Difference The SSADH community is made up of families scientists and doctors from around the world working together to make a better life for this very special patient population. Join Our Registry Donate Today Fundraise With Us Our Mission The SSADH Association is a voluntary notforprofit 501c 3 organization dedicated to helping children and families affected by an ultrarare neurometabolic disorder known as Succinic Semialdehyde Dehydrogenase Deficiency or SSADH. The SSADH Association is committed to those affected with this neurotransmitter disease through education advocacy and research. News Updates Celebrating Rare Disease Day Wisconsin mother creates SSADH Association after her son is diagnosed with neuro disorder.