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Re: ROGENE & everyone

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ROGENE

thanks for the advise. I have been talking to my hubby about finding a way to

make it work and he said that we will manage. he would rather I stayed home to

get better anyways. it is just a matter of actually doing it and finding a

doctor who will write that letter. FM an CFS are hard to diagnose (and for

others to believe in)although I have been offically diagnosed with them. I am

not sure if these illnesses along with the depression would qualify for long

term disability. do you have any ideas on that? i know plenty of the girls

here are on disability but I am not sure what the grounds are and where i would

fall in. would I get this letter from the rhuemmy or the pain doc or ??? I

don't know where to go with this. has anyone else here gotten disability for FM

and CFS?Who knows, after my appt. w/ doc Vasey Friday he may say that I have

Lupus or MS, too. I know that I am too sick to work but nobody else here (at

work) really knows the extent of my problems. am scared of getting fired as

you were saying so I try to keep it to myself but it is getting so hard to hide

my sadness and pain. I am making more and more mistakes as the brain fog is

really becoming a problem with my job and I am at the point of writing

everything down that I do so I can remember from day to day so details don't

fall through the cracks. this is all so confusing. I guess if worse came to

worse we could file bankruptcy but i can't imagine getting to that point. this

is so sad as I have always prided myself of having perfect credit and a good

job. I have paid my dues and worked my way into a good paying position

(although it is a high stress job). At least then maybe we could keep our

house. thanks for your help. any additional details on how to get this started

would be appreciated. (and what I shouldn't do to avoid screwing my benefits

up).

I have been doing the coconut oil, raw garlic, black walnut, & finished a round

of fungal defense. I have cut way back on sugar-no breads, etc.

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