Hemophilia Center Scholarships for Blood Disorders

Hemophilia Center Scholarships

Individuals who suffer from the bleeding disorder hemophilia, and who are looking for money for college can benefit from the Hemophilia Center scholarships for blood disorders. Each year, approximately $2,000 in disability related scholarships are awarded by the center to assist college-bound students and their families with the cost of a higher education.

The Bob Hersh Scholarship for blood disorders

In 2009, the Hemophilia Center introduced an additional scholarship in memory of Bob Hersh. The Bob Hersh Scholarship is named in memory of Robert Hersh, Ph.D. Dr. Hersh served as a psychologist at Finger Lakes Developmental Disabilities and was also an associate professor at Monroe Community College. In addition, he served as a board member for the Hemophilia Center Board. One scholarship is available. The recipient will receive a $1,000 scholarship to be used toward educational expenses.

Along with the Bob Hersh Scholarship, the center also offers another scholarship opportunity for the bleeding disorder community. The Mary M. Gooley Hemophilia Center Scholarship makes a $2,000 scholarship available to students each year.

Eligibility requirements for the Hemophilia Center scholarships

To be eligible for hemophilia scholarships from the Hemophilia Center, scholarship candidates must be directly or indirectly affected by Von Willebrand Disease, hemophilia, hemochromatosis, or a hereditary bleeding disorder. All application materials must be received by no later than March 30th to be considered for the scholarships.

The Mary M. Gooley Hemophilia Center is located in Rochester, New York. The Center was originally established by Mary M. Gooley in 1959 along with help from the Rochester Chapter of the National Hemophilia Foundation. The Center became one of the first chapters of the National Hemophilia Foundation to be chartered outside of New York City and the first freestanding comprehensive care clinic in the entire country.

Following the establishment of the clinic in Rochester, Mary Gooley continued to serve as the first executive director of the center until her retirement in 1986. Throughout the next several decades, the Center remained at the forefront of national hemophilia care. Eventually, programs were also established in Albany, Syracuse, Buffalo, and the Southern Tier in an effort to provide comprehensive hemophilia care throughout the region. The Center has retained a goal of providing compassionate, comprehensive care that will lead to wellness and independence among patients affected by bleeding disorders.

Today, the Center remains one of the few combined treatment chapters and centers in the nation. The Center continues to focus on the provision of research, advocacy, and treatment to individuals and families affected by a variety of inherited diseases, including iron overload and blood clotting conditions. One of the ways in which the Center does this is through the provision of hemophilia Scholarships from the Hemophilia Center. The Center focuses on treating the entire person and their family instead of just the disease. Along with the underlying medical problem, the Center also addresses social issues, insurance needs, and psychosocial needs as well as financial challenges, including those that might otherwise prevent individuals affected by bleeding disorders from completing their college education. In this regard, the Center is able to fulfill their mission of treating the person, not just the disease.

The Hemophilia scholarships from the Hemophilia Center are one way that this organization trys to help help students towards a higher education and they do a great job of it.