The Rainbow Connection is a Non-Profit Organization founded in 1985 that offers the opportunity for a child (Ages 2 to 18) with a life-threatening or terminal illness to have a wish granted, academic scholarships, cancer family events, and case managers.
Pickles Group’s mission is to provide free peer-to-peer support and resources to kids affected by their parent or guardian’s cancer. Having a parent with cancer can be a lonely, isolating experience. Pickles Group creates thriving communities of kids supporting kids through and beyond their parent’s cancer journeys. Pickles kids strengthen resilience, have fun with friends […]
The Make-A-Wish Foundation of Michigan is a Non-Profit Organization founded in 1984 that offers the opportunity of having a wish granted to a child with a life-threatening medical condition who is between the ages of 2 and 18.
St. Jude Children’s Research Hospital, founded in 1962, is a pediatric treatment and research facility focused on children’s catastrophic diseases. Consistent with the vision of the founder Danny Thomas, no child is denied treatment based on race, religion or a family’s ability to pay.
Stupid Cancer’s mission is to help empower everyone affected by adolescent and young adult (AYA) cancer by ending isolation and building community. Stupid Cancer offers a lifeline to the adolescent and young adult cancer community by providing age-appropriate resources to help navigate treatment and survivorship on your own terms.
The Wigs 4 Kids is a Non-Profit Organization founded in 2010 that offers hair replacement, support services, counseling, and fieldtrips for children ages 3-18, living in Michigan and suffering from hair loss as a result of illness.
Young Adult Cancer Connection provides a rare opportunity for young adults (18-39) and their caregivers to come together and work through the issues unique to our age group, discover emotional and clinical resources, and ultimately know that we’re not alone in our cancer experience.
The Bright Spot Network provides young cancer survivors who are parents of small children with a safe space for individual and familial healing, recovery, and reconnection. They focus on young parents and guardians caring for young children at the time of diagnosis, including those diagnosed during pregnancy.
The American Childhood Cancer Organization, established in 1995, provides information, resources, books and support for parents, children, and adolescents with cancer to provide grassroots leadership through advocacy and awareness, and to support research leading to a cure for all children diagnosed with this life-threatening disease.
Young adult cancer survivors often face fertility challenges. Our mission is to ease the burden for young adult cancer survivors pursuing parenthood by providing financial support for fertility treatments, adoption and surrogacy.