We are a 501(c)3 organization, a member of the National Hemophilia Foundation. We serve families in South Texas dealing with genetic bleeding disorders, such as hemophilia and von Willebrand disease. We provide support programs for newly-diagnosed families, Family Camp, advocacy efforts at both state and national level, and a legal hotline giving information relating to job and insurance claims. Treatment for hemophilia is well over $150,000 a year, and we offer financial assistance to many of our families.
10500 Northwest Freeway Suite 226 Houston, TX 77092