WE ARE THE GENESIS FOUNDATION FOR CHILDREN.
We fund programs and services that treat patients with rare diseases and genetic disorders from conception and pregnancy through childhood and adulthood.
We’re on a mission to give patients and their families access to care that’s different. Families given a rare disease or genetic disorder diagnosis can feel lost and frustrated. We fund medical care, therapy, assistive technologies, and other programs that allow doctors and staff to provide integrated, coordinated care.
We call it the Feingold Model of Coordinated Care.
The Genesis Foundation For Children provides funding for clinical, informational, and therapeutic programs for children born with physical and intellectual challenges and genetic disorders.
Through the funding of innovative programs and services, we are committed to serving and advocating for these children.
We hope you will join us in our journey to help all children reach their full potential.
Throughout the pandemic, the services provided by THE GENESIS FOUNDATION FOR CHILDREN to the rare disease community remain more critical than ever.
Our clinical staff continue to provide safe ways of finding answers for families through at home telehealth appointment and genetic testing kits. For those who need to be seen in person, by specialists, these appointments are arranged in a way that minimizes exposure to an already vulnerable population. Our grantees continue to find opportunities to move their therapeutic learning online to serve their communities, and MotherToBaby MA, our confidential information line, continues to answer the questions to those who are pregnant or breast feeding about exposures, including information about pregnancy and COVID-19.
We thank you for helping us to continue to provide this essential care to patients and families.