Wow its so nice to find a place where people ‘get me’!!!
Ive had this problem most of my life, but it had become exceedingly bad in the last 7 or so years (Im 30 now).
I live in australia, restasis is not available but I recently found out about cyclosporin. My hospital pharmacy makes me a months supply at a time (0.05%).
What baffles me is that opthamoligists did not tell me about this! They would just prod and probe my eyes, put dyes and all kinds of foreign objects in them, do blood tests, salivary glad biopsys (to check for autoimmune conditions) yaddi yadda, Im sure I don’t need to go into detail with you guys coz Im sure you’ve been round the traps (eastern/western/alternative medicine – the lot!).
In any case Im grateful I now my eyes are less red and a bit better hydrated (altho Im still waking up between 2 and 6 times a night to put eye drops in coz they get so dry I can barely move my eyes).
Keep in touch!
Ive had this problem most of my life, but it had become exceedingly bad in the last 7 or so years (Im 30 now).
I live in australia, restasis is not available but I recently found out about cyclosporin. My hospital pharmacy makes me a months supply at a time (0.05%).
What baffles me is that opthamoligists did not tell me about this! They would just prod and probe my eyes, put dyes and all kinds of foreign objects in them, do blood tests, salivary glad biopsys (to check for autoimmune conditions) yaddi yadda, Im sure I don’t need to go into detail with you guys coz Im sure you’ve been round the traps (eastern/western/alternative medicine – the lot!).
In any case Im grateful I now my eyes are less red and a bit better hydrated (altho Im still waking up between 2 and 6 times a night to put eye drops in coz they get so dry I can barely move my eyes).
Keep in touch!
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