ASHLEY LOVES TO GO SURFING
In June of 2019, at 15 years old, Ashley was diagnosed with Coats’ Disease in her right eye by Dr. R. Sisk at the Cincinnati Eye Institute. Ashley has undergone four laser surgery procedures. After her last procedure in November 2019, her test showed she has lost the far peripheral vision on the nose side. Her pupil has becomes unresponsive to light so it remains dilated. Prior to her diagnosis, Ashley had 20/20 vision the entire time, making her discovery unique.
As of today, there are no leaks. Ashley continues to attend classes at her high school, play club and high school soccer, and go surfing whenever she can get to the beach!
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.
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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.
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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?
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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?