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Re: Life for FMS/CFS Sufferers

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RAB>>

I am new to the group and already have started to feel better

knowing that there is someone out there that knows about some of the

feelings and things that I have that no one that I have contact with

has a clue. I hurt, my skin hurts, I want to cry for no reason!! I

still work but some days is just more than I can bear. The only med

that I take now is Cymbalta, I was on alot especially zanax 3 a day

at .5, and I took them at nite to sleep. I just take tylenol PM at

nite now (3 of them) and am sleeping several hours. I find that I am

not a very nice person sometimes, my temper and mouth seem to get me

in trouble!! I also know my gall bladder is bad and right now having

to deal with that. And I have had alot of personal crisis in my life

and that is also causing alot of stress. It is one of those things

that you don't know where the fibro starts and the other " stuff "

starts. Thanks for listening..

-- In Fibromyalgia_Support_Group , raburtongdyr@...

wrote:

>

> Group I would like you honest opinion/thoughts on what kind of life

you lead and what your biggest setbacks are due to the above

diagnosises and the meds you take daily. Most of all what drives you

day to day. If you prefer you may email me privatly.

>

> Thank you and gentle hugs,

>

> RAB

> Sent from my Verizon Wireless BlackBerry

>

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