Re: Response to Sue

[Guest guest]

--- PAT HARRAH wrote:

> Hi Sue,

>

> Yep....sure sounds like you're a member of this

> unique club we have! I feel

> just as you do. IS THERE NO END TO SYMPTOMS AND

> PROBLEMS ASSOCIATED WITH

> FMS/CFS????? Just when I think it can't do any more

> damage, sure enough,

> along comes something else. I suppose it keeps life

> exciting just trying to

> guess what will be next....haha.

>

> Perhaps we should all invest in companies that make

> lotion! Sure would help

> those of us who can no longer work!...hahaha.

>

> Pat Harrah (aka AliveAgain1951)

>

>

>abraxis3@...

Here, here!!!! Great idea!!!!!!!

Why didn't I think of that?

Have a great day!

Sue

>

>

> Tami and Pat,

>

> Oh, my gosh! I've had that, too, but I never

> associated it with my fibro. I just keep coming up

> with more and more stuff! WOW! I thought my dry

> mouth was because I can't drink alot at a time. I

> have to sip all day...I had my stomach stapled in

> 1986. I have the bumps and the red tongue, and I've

> had sores, but not all of the time. It comes and

> goes. I guess I just thought they were like pimples

> in my mouth. In fact, I had one this past week! Is

> there no end to the symptoms this illness has?!!!

>

> I'm not on medication, so I can't blame it on that.

>

> I have the driest skin and scalp, too, but I also

> thought that came from my stomach surgery, because

> I've had this since then. My skin soaks up lotion

> like

> a sponge

> ...slurp!...slurp!

> I should have stock in the company for all the

> lotion

> I buy!

>

> Thanks for the info. I know not to bother wasting

> money going to the doctor!

>

> Have a great day

>

> Sue

>

>

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