The PNH Research and Support Foundation

The PNH Research and Support Foundation is dedicated to funding research to find a cure and new treatments for Paroxysmal Nocturnal Hemoglobinuria (PNH disease) and to helping PNH patients in need with funding for disease-related expenses not covered by insurance.

NEWS + ANNOUNCEMENTS:

The 6th annual Walk for PNH took place in New York City and in LA (Long Beach) on September 25, 2011.  We raised $40,000 this year and had an amazing time.  In 2012 we are planning to hold walks in New York, LA and Chicago and are setting our fund raising goal at $60,000!

 Support the Foundation and join the fight against PNH Disease by making a tax-deductible donation today!

Thank Thank you Lon Larson, for this great photo of "Team Minnesota"!