I've had relatively mild dry eyes for years. No one ever examined them, they just put me on simple eye drops (hypromellose). My eyes are now worse, and in particular it's getting on my nerves that they will randomly sting and swell shut when I'm in the shower, purely from the steam. Since I have severe ME/CFS and get very dizzy in the shower, this just isn't safe. Anyway, I spoke to my optometrist about ten days ago, and he suggested using the eye drops every hour. He said it should take a week or two to kick in, and if it didn't, then come and see him for a proper examination. It's been ten days, and it doesn't feel like my eyes are any better. Should I see him as soon as I can arrange an appointment, or should I wait a bit longer? And secondly, should I use the eye drops just before the appointment, or let him see my eyes as they are in their natural state?
Background: the ME, of course. Suspected Postural Orthostatic Tachycardia Syndrome, Ehlers Danlos Syndrome, and/or mast cell disorder. (Referral for those is taking forever.) I'm on antihistamines for, well, they haven't really said what for, but if there's a mast cell disorder in there, it would explain why they help so much. Anyway, the antihistamines don't seem to coincide with my eyes getting worse. I'm 35. My mother has map dot fingerprint epithelial dystrophy, but my optometrist said it's not inheritable and that I'd know by now if I had it. The ME causes neurological and muscular problems with my eyes, such as intolerance of fluorescent light and difficulty reading.
Background: the ME, of course. Suspected Postural Orthostatic Tachycardia Syndrome, Ehlers Danlos Syndrome, and/or mast cell disorder. (Referral for those is taking forever.) I'm on antihistamines for, well, they haven't really said what for, but if there's a mast cell disorder in there, it would explain why they help so much. Anyway, the antihistamines don't seem to coincide with my eyes getting worse. I'm 35. My mother has map dot fingerprint epithelial dystrophy, but my optometrist said it's not inheritable and that I'd know by now if I had it. The ME causes neurological and muscular problems with my eyes, such as intolerance of fluorescent light and difficulty reading.
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