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TO MEET THE PHYSICAL, EMOTIONAL AND SPIRITUAL NEEDS OF THE CHILDREN IN OUR CARE, DEVELOP PERSONAL, FAMILY AND COMMUNITY RELATIONSHIPS THAT WILL CONTRIBUTE TO HEALTHY OPPORTUNITIES FOR THE CHILDREN TO REACH THEIR FULLEST POTENTIAL, AND TO ADVOCATE ON BEHALF OF ALL CHILDREN.

ALS of Michigan is dedicated to helping people with ALS (pALS), their families and caregivers live life as fully as possible. We also support research into the cause, treatment, and cure of ALS. Services are provided throughout Michigan

They provide compassionate care in the later stages of life and support through the grief experience for individuals and families.

Their mission is to provide high quality, compassionate care at the end of life.

Empower, educate, and enhance the lives of individuals impacted by vision loss through all of life's transitions.

PROVIDE QUALITY CARE FOR CHILDREN WHO HAVE BEEN SEPARATED FROM THEIR HOMES BECAUSE OF DEATH, DIVORCE, SEPARATION, NEGLECT, ABUSE, OR INABILITY TO ADJUST TO THEIR PRESENT LIVING SITUATION. THE HOME SEEKS TO PROVIDE AN ENVIRONMENT OF LOVE, SECURITY, AND ACCEPTANCE WHERE A CHILD CAN GROW AND DEVELOP AS AN INDIVIDUAL.

The Mission of Children's Respite Care Center is to provide comprehensive services and family support to medically fragile, developmentally delayed, physically challenged, and behaviorally disordered children and their families by providing services that evoke maximum potential and foster the development of intellectual and social competence.

The mission of the Noah's Hope – Hope4Bridget Foundation is to raise funds in support of scientific research, and inform the community about Batten Disease. Batten Disease is a rare, fatal autosomal recessive neurodegenerative disorder that begins in childhood.

The purpose of the Spiritus Project is to provide various forms of direct, need-based financial assistance to adult cystic fibrosis patients in an effort to reduce stress and provide an improved quality of life. The initial focus of the Spiritus Project is to assist North Carolina-based cystic fibrosis patients. Through Q3, 2020, your support has allowed us to touch patient lives over 1,500 times in five years through financial assistance and/or hospital admission and refill bags. This means that roughly every day since we started, we have impacted a patient’s life in some meaningful way. Some impacts were large, some were small, but all helped us to achieve Jessica Link’s vision to improve the lives of adult cystic fibrosis patients.

Cure CMD’s mission is to advance research for treatments and a cure for the congenital muscular dystrophies. Cure CMD will also improve the lives of those living with CMD through engagement and support of our community.

The KAT6 Foundation supports people and their families who are living with KAT6A and KAT6B syndromes around the world. We advance scientific research aimed at developing treatments and spread awareness of KAT6 syndromes so they can be more easily identified, treated and studied.

Peggy Lillis Foundation is building a nationwide clostridium difficile awareness movement by educating the public, empowering advocates, and shaping policy.