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The Association for Creatine Deficiencies (ACD) is the only patient advocacy group devoted to the three known Cerebral Creatine Deficiency Syndromes (CCDS), individually referred to as GAMT, AGAT and CTD.

We are committed to meeting the goals set forth by our mission statement, which are to provide patient, family, and public education, to advocate for early intervention through newborn screening, and to promote and fund medical research for treatments and cures for these three rare disorders

ACD’s PatientStrong™ funds these mission programs, benefitting CCDS patients and allowing ACD to continue to drive progress for GAMT, AGAT, and CTD.

The Association for Creatine Deficiencies is a charitable 501c3 organization and contributions are tax deductible. EIN#46-2133007

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