CALEB

Caleb’s Story:

My son lost his left eye on March 8, 2018 after being diagnosed with Coats’ Disease on January 12, 2018. Below is his video we made for local news channels of Caleb’s story when they learned he was the first boy in Florida to lose his eye to a disease that is too rarely spoken of! I feel if I had known earlier about this I, as his mother, could have changed the outcome!!! Bottom line – if Caleb’s story finds and save one eye, it was worth the video and please, please have your child’s eyes checked every year!

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)

Find a Doctor