NOA

Noa, my son, recently was diagnosed with Coats’ Disease. We don’t know much about this disease and we are pretty scared. We are from Croatia and we were told Noa is only child with Coats’ Disease in our country! Noa is fully blind in his right eye and his retina is totally detached. The doctor told us that is only matter of time before pain will start and Noa’s eye will need to be removed. I am hoping for a miracle in that he never feels any pain and I am searching for anything that could help us. We are seeking another opinion and looking to stories of other patients and families for hope.

FAQ

At the Jack McGovern Coats’ Disease Foundation, we are often contacted by anxious parents or patients who are seeking information after receiving a diagnosis of Coats’ Disease. The questions below are provided as a resource to assist you as you and your doctor decide the best approach for treatment. These questions do not constitute any form of medical advice or diagnosis. Each patient is unique. An experienced retinal specialist who has examined the patient is the best source of information for diagnosis and treatment. We always recommend getting a second opinion.

Questions to Ask Your Doctor (Download PDF)

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