During these uncertain times, how can we help?
See below to access our COVID-19 Resource Hub, and to explore our growing directory of COVID-19-specific and virtual volunteering opportunities.
Children and young adults from around the world have been diagnosed with a rare and incurable Chromosome 8p disorder. This disorder is hard to diagnose and can affect every cell in a person’s body. Project 8p is a nonprofit organization raising research funds, building a family support network and designing standards of care for the medical community.
Being new, we have work to do, and grant writing is too heavy a lift to do alone. We've identified some amazing opportunities, but need help crafting requests.
No additional volunteer opportunities at this time.
600 3RD AVE FL 42, NEW YORK, NY 10016, US
Creating a path to treatment for chromosome 8p disorders through research, community, and intelligent information.
Project 8p Foundation is a 501(c)(3) nonprofit organization that is researching 8p disorders to find treatment options and give meaningful answers to those affected and their families. We are patient-led. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment. Project 8P is the only organization dedicated to funding research to uncover treatment for chromosome 8p disorder. Chromosome 8p is a rare genetic condition with approximately 350 patients around the world and counting. A chromosome disorder typically impacts every cell in your body, not just in one organ of your body, but often your entire human system. Right now, science does not have the means to treat this condition. The good news is that the scientific community is making substantial progress and together with Project 8p, we are going to do everything we can to help.
We'll work with your schedule.
This is a Virtual Opportunity, with no fixed address.
December 10, 2020