GetttDunkedOn 3 points 1y ago
Hi! My grandmother had this in both eyes. She still has it in one, as due to other issues doctors can’t operate on it. She experienced those symptoms you described rapidly, and became unable to read. They normally do a cornea transplant, as that’s what it affects. She had a trial surgery, a partial cornea transplant using a synthetic cornea and has recovered her vision in that eye.
It’s hereditary, and children have a 50/50 chance of developing it, usually after 40. Sometimes it stays dormant but make sure those related to them get tested regularly at that age to catch it early.
Your family member should get looked at by a cornea specialist if possible!
loonling 1 points 1y ago
I know this is an old thread, but I have been diagnosed with this recently and will soon be getting a partial corneal transplant.
My vision became increasingly blurry over the summer, and I chalked it up to needing a new prescription as I'd skipped a year due to COVID. My biggest issue is low-light or high contract situations. I am by no means severely impaired, but if I tested for a driver's test right now, I might not pass. And since my diagnosis in the fall, I have stopped driving at night.
I wish your family member the best.