Mississippi Metabolics Foundation
Hi, I am Shannah, mom to Emmalyn, who has a rare genetic metabolic disorder, Glutaric Aciduria/Acidemia Type 1. Mississippi Metabolics Foundation's (MMF) was founded with the primary mission to raise awareness, educate, and provide support to those living or caring for someone with genetic metabolic disorders/Inborn Errors of Metabolism. We advocate for the continued expansion and implementation of Newborn Screening Programs and access to available resources for caregivers/patients. MMF promotes and supports further advancements in research, studies, and treatments for Metabolic Disorders/IEM. We are increasing the community involvement in MS for rare genetic Metabolic Disorders and helping families navigate their rare disease journey.
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Mississippi Metabolics Foundation Our Mission Mississippi Metabolics Foundation MMF was founded to raise awareness educate and provide support to those living or caring for someone with genetic metabolic disordersinborn errors of metabolism IEM. We advocate for the continued expansion and implementation of Newborn Screening Programs and access to available resources for caregiverspatients. MMF promotes and supports further advancements in legislation research trials and studies therapies targeted treatments and eventual cures for metabolic disorders IEMs and all rare genetic diseases. We are committed to increasing community involvement in Mississippi for rare genetic metabolic disorders and support families as they navigate their rare disease journey.
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