ACD History

The Association for Creatine Deficiencies (ACD) was established in 2012, by parents with children diagnosed with a Creatine Deficiency Syndrome.

Because Creatine Deficiency Syndromes (CDS) mimic symptoms of other medical conditions, patients are often misdiagnosed. Proper diagnosis and early intervention are critical to establish treatments needed to improve life quality and longevity of the CDS patient.

The ACD was established to raise awareness and education of CDS among the medical community, as well as the general public, and to advocate on behalf of families and patients living with Creatine Deficiency syndromes.


Learn more about our Board of Trustees HERE