Nystagmus Research Funding
Dr. Hertle has touched many of our lives and the lives of our loved ones, and many of us view him as the best hope in developing successful treatments of and eventually a cure for Nystagmus. Dr. Hertle has also been a great friend of ANN over the years, having volunteered a considerable amount of his time to ANN through personal appearances at our bi-annual conferences and making himself available whenever requested to assist our organization and its members. Dr. Hertle notes that Government funding for biomedical research, including Dr. Hertle’s research in Nystagmus, has almost disappeared. As a result, The Children’s Hospital of Pittsburgh and The Eye and Ear Foundation of Pittsburgh have developed an ambitious program to set up a foundation that will help long-lasting research to help children with Nystagmus and related disorders. The following links will take you to a letter from Dr. Hertle and a flyer for the Right to See Foundation.
If anyone knows of an individual or organization that might be able to support this effort, please pass along this link or provide them with copies of the documents referenced above.
ANN, Inc. Caveat: Though discussions on specific problems are permissible and expected, remember that no posting here shall constitute professional health care or medical advice, and you should never rely on any contribution to this, or any, Internet discussion forum on important medical or professional health care questions. Indeed, no Internet discussion forum is a substitute for the careful advice and treatment of a competent professional health care provider or doctor.
ANN, Inc. is a volunteer, nonprofit organization for persons and families involved with nystagmus. ANN, Inc. does not diagnose or treat, or provide professional counseling. It is involved in self-help, while trying to promote research and education, among other goals contained in its mission statement.
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