Parents of 4p- Support Group
The 4p- Support Group is a membership owned and operated 501(c)(3) organization. Membership is free.
Only parents and legal guardians of children with 4th chromosomal abnormality are eligible for membership.
Membership Benefits
- Opportunities to participate in research
- The Wolf-Hirschhorn Syndrome, 4p-: A Guidebook for Families (digital format). This is a wonderful resource for doctors, therapists, and family members
- E-newsletters and organization updates
- And more!
Links to Parent’s Personal Pages
Here you will find links to Personal blog sites created for their children, poems, and stories. The pages linked here are listed only with the permission of their creators.
These pages are for the parents to express themselves on whatever topics seem appropriate to communicate about our children.
