Association for Creatine Deficiencies
Cure Creatine Deficiencies
The Association for Creatine Deficiencies (ACD) was established in 2012 by dedicated parents of children diagnosed with Cerebral Creatine Deficiency Syndromes (CCDS). This non-profit organization plays a pivotal role in the fight against CCDS, a group of three rare diseases often overlooked and misdiagnosed due to symptom overlap with other conditions. ACD's mission is threefold: to educate the public and medical community, to advocate for early intervention through newborn screening, and to fuel research for treatments and cures. ACD's commitment is to transform the CCDS diagnostic journey from a seven-year odyssey to a rapid seven-day route to effective treatments. In striving towards its future vision - a world where effective treatments and newborn screening for CCDS are the norm - ACD passionately supports the potential of every CCDS patient, serving as a voice for those who cannot speak and ensuring research is moving at lightning speed.
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