The Williams Syndrome Association is a non-profit organization that strives to enrich the lives of individuals and families affected by Williams syndrome and similar conditions through support, research and education.
United Cerebral Palsy of Michigan connects people with disabilities to the opportunities and resources needed to live productive and independent lives.
The Tourette Association of America Michigan Chapter is a volunteer led, nonprofit organization supporting the needs of individuals and families affected by Tourette Syndrome and Tic Disorders. We are committed to raising public awareness and fostering social acceptance; advancing scientific understanding, treatment options and care; educating professionals to better serve the needs of children, adults and families challenged by Tourette and Tic Disorders through advocacy.
The M.O.R.G.A.N. Project is a national, community-based organization of volunteers whose mission is to promote awareness and facilitate support of parents caring for their children with special health care needs, and to enhance the Quality-of-Life for these special families.
We are a nonprofit tax exempt 501c3 organization that advocates for children and young adults who have syndromes without a name. We offer support, advice and information on the challenges that families face when there is no diagnosis. We also advocate for changes in the medical community that will benefit undiagnosed individuals.
PWSA-MI is a Michigan Chapter of PWSAUSA the National Organization. We give families information and support to handle the problems associated with PWS through education, advocacy and research.
Parent to Parent USA defines parent to parent support as the intentional connection between a trained volunteer Support Parent and a parent seeking information, resources, guidance, and support from an experienced parent. Parent to Parent programs facilitate parent “matches” and provide follow-up support to assure the matched relationship meets peer expectations.
Parent Leadership in State Government (PLISG) connects parents and professionals to build stronger families and communities across the state of Michigan. The PLISG initiative provides training and support to parents in using their voice to impact local, state, and federal program planning and policy development. Parents are given the knowledge and skills to participate on advisory boards, committees, and other decision-making bodies.
Disability Rights Michigan is the independent, private, nonprofit organization designated by the governor of the State of Michigan to advocate and protect the legal rights of people with disabilities in. Disability Rights Michigan services include information and referral, short-term assistance, selected individual and legal representation, systemic advocacy, monitoring, and training.
Michigan Parents of Children with Visual Impairments is an affiliate of the National Association of Parents of Children with Visual Impairments (NAPVI.) We strive to help families with support, information, advocacy, and events that are fun, educational, and practical. MPVI is a group of families, members of the blind community, and professionals who have or work with children who are blind or visually impaired.