Hi all. Glad I found this place.
Wednesday night I just rubbed my left eye. I felt like something was in it, maybe some mascara. Both my eyes got dry which is what happens when something is in them. I got into see the opthalmologist who I had just seen 2 weeks prior when something really was stuck to my eyelid.
The bad news is there is nothing in my eyes. Some minor swelling maybe from me looking for something in my eye.
I left with some Systane drops to try instead of the Optive which lasts 10 minutes maybe and some durozol which I don't want to use. She was getting authorization for plugs. (I knew nothing of these). I left with no instructions and no information and no diagnosis. No tests either.
So I need to educate myself because I have discovered she is not very forthcoming with information. I need to know what to ask. (I'm on medicare so don't have a lot of options for doctors). I know nothing about this "condition".
I ordered some Omega-3 so waiting for that. Meantime I'm using my drops and trying to just figure out what works for me. I'm going to get several drops and see what works best for me.
It seems that there are options less invasive than plugs before I go that route. Like Lacrisert. I am very sensitive to medications so try to do things with a more natural approach, but this is miserable.
I have been living with Myalgic Encephelomyelitis for almost 16 years. I would say I'm about 90% housebound. My life was/is watching tv and being on the computer. Now I have to figure this all out.
Love to hear from you. Just one favor. Please put lots of paragraphs in your replies. I have problems with too much text, my brain just shuts off. Thanks again!
Wednesday night I just rubbed my left eye. I felt like something was in it, maybe some mascara. Both my eyes got dry which is what happens when something is in them. I got into see the opthalmologist who I had just seen 2 weeks prior when something really was stuck to my eyelid.
The bad news is there is nothing in my eyes. Some minor swelling maybe from me looking for something in my eye.
I left with some Systane drops to try instead of the Optive which lasts 10 minutes maybe and some durozol which I don't want to use. She was getting authorization for plugs. (I knew nothing of these). I left with no instructions and no information and no diagnosis. No tests either.
So I need to educate myself because I have discovered she is not very forthcoming with information. I need to know what to ask. (I'm on medicare so don't have a lot of options for doctors). I know nothing about this "condition".
I ordered some Omega-3 so waiting for that. Meantime I'm using my drops and trying to just figure out what works for me. I'm going to get several drops and see what works best for me.
It seems that there are options less invasive than plugs before I go that route. Like Lacrisert. I am very sensitive to medications so try to do things with a more natural approach, but this is miserable.
I have been living with Myalgic Encephelomyelitis for almost 16 years. I would say I'm about 90% housebound. My life was/is watching tv and being on the computer. Now I have to figure this all out.
Love to hear from you. Just one favor. Please put lots of paragraphs in your replies. I have problems with too much text, my brain just shuts off. Thanks again!
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