4P Support Group

Our Story

Founded in 1984 by Becky Richardson, the 4P Support Group began as a grassroots effort to connect parents of children with a deletion of the 4th Chromosome. Through newsletters, national gatherings, and support networks, this organization has united families and professionals to promote awareness and research of 4p- syndrome and Wolf-Hirschhorn Syndrome.

Impact

The 4P Support Group has successfully created a supportive community for families affected by 4p- and Wolf-Hirschhorn Syndrome, facilitating national conferences and providing essential resources.

Why Donate?

Your donation helps provide vital resources, support networks, and educational materials for families, ensuring they receive the care and information they need to thrive.

Get Involved

Join the mission to support families affected by 4p- and Wolf-Hirschhorn Syndrome. Donate cryptocurrency or cash today to make a difference in their lives!