For many, a world without bleeding disorders is simply a dream. Thousands of kids and adults affected face internal bleeding, costly treatments and lifelong infusions.
Our 2 year-old son Oliver has severe hemophilia A. We have witnessed first hand just how new therapies and support from hemophilia treatment centers impact quality of life. We are looking forward to participating in our second walk!
Every dollar is put back into the bleeding disorder community. Your contributions will support critical initiatives such as research funding, educating medical providers, and ensuring that families effected by bleeding disorders have access to healthcare and better resources.
Thank you for your support and please join us on October 10th for the virtual walk.
The National Hemophilia Foundation is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. "Coming together is a beginning. Keeping together is progress. Working together is success."