BRAYDAN

My son, Braydan, is nine months old. When he was just four months old, our world came to a screeching halt. At two months old, our pediatrician referred us to PT for what she thought was torticollis. After three sessions with the PT, she referred us to an ophthalmologist following a hunch that something “was up” with his eye, despite the fact that he was hitting his milestones and tracking objects well. We followed her advice and the appointment that I thought would be for lazy eye quickly turned into a parent’s worst fear – the local ophthalmologist called in his partners and phoned a specialist from New York Presbyterian, which resulted in him sharing that he was concerned Braydan may have a retinoblastoma.

In that moment, I felt as if I could pass out with my baby in my lap and could not comprehend how this was happening. He was too little and seemingly fine! A long five days later, we saw Dr. Lopez at New York Presbyterian, who recommended we see another specialist that day. Five hours later, we met with Dr. Marr who examined Braydan and stated that he felt it was not a retinoblastoma, but wanted to perform a sediated exam to make sure. While it felt we could take a breath for a moment, the fear of “what if” lingered endlessly. Braydan underwent his exam at Morgan Stanley Children’s Hospital with Dr Marr and two hours later we learned Braydan had Coats’ Disease in his right eye.

Following that exam, Braydan has since had two surgeries to laser the mass in an effort to keep it away from the retina. Thanks to the medical team at Morgan Stanley, both surgeries have gone well. Bryadan continues to be “Braydan Brave” and, at nine months old, is crawling, standing, and talking away. There are still moments where I fear the things that may be hard for him, but then I look at what he has already done and I am refocused on all that is possible.

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)

  • Ahead of any treatments or procedures, it is important to ask yourself and the doctor the following questions:

    • How do you know that this is Coats’ Disease?

    • Has your doctor treated other patients with Coats’ Disease?

    • Have you sought a second opinion? If not, please consult our Doctor Directory for knowledgeable doctors in your area.

    • What Stage of Coats’ Disease is he/she in?

    • Will his/her vision get worse over time?

    • Will the eye have pain?

    • Will his/her eye start to turn out? Is muscle corrective surgery an option?

    • Are cataracts likely?

    • How likely is glaucoma? (due to retinal detachment)

    • Is there calcification?

    • What is the anticipated disease progression?

    • Is there a thorough vision exam available?

    • Where is the vision affected? (central/peripheral/distance)

    • Does he/she have depth perception? (3D visibility)

    • What about the non-Coats’ eye?

    • To what extent is his/her vision affected?

    • Will we be able to use this as a baseline to measure progress/decline?

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