Noonan Syndrome Foundation

The mission of the Noonan Syndrome Foundation is to support, educate and advocate for those diagnosed with Noonan's Syndrome by supporting research for the development of effective treatments, and ultimately, a cure for the syndrome. Noonan's Syndrome is identified by a genetic mutation in the RAS/MAPK pathway and is expressed in many ways, over numerous systems in patients. The Noonan Syndrome Foundation supports patients and families by providing information online and in regular publications, holding regional events, conferences and support groups. Connecting patients and families to caregivers familiar with Noonan Syndrome is of the utmost importance ot the Foundation as well. Another goal is to increase public awareness of Noonan Syndrome to allow for accurate diagnosis by medical providers and to allow for those not affected by the syndrome to understand the challenges of those affected and to increase financial support

The rasopathies foundation is dedicated to saving the lives of, and providing a better quality of life for, persons living with a genetic mutation in the ras/mapk pathway, by leading the way to effective treatments and ultimately cures for all. The mission of the rasopathies foundation is to: bring together all individual rasopathy sydrome organizations. Together, support research for the deveopment of effective treatments and ultimately cures for all. Together, support persons with a rasopathy syndrome, families and caregivers by providing readily accessible information online, regional events, conferences, and support groups. Together, expand public awareness of the rasopathies to promote earlier and accurate diagnoses by the medical community, increase the non-affected population's understanding of the challenges facing persons with a rasopathy syndrome and encourage financial support from public and private sources.