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Re: new list for FUN

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Hi Ladies,

I think this is a marvelous idea; as 10 minutes worth of laughter per day is

equal to something significantly positve, yet I can't remember what it is!

AHa! How many of us have this problem? I have now been " on the sofa " for 2

full months recovering from, what was originally, a minor leg surgery.

Just these minor set-backs can have a terrible effect of depression, as you

lay there thinking about all the things you need to be working on with this

issue, not to mention the things for your family. Once I get 'comfortable'

with the pain, etc. I just have to stay where I am, although I worry about

what I should be doing -- my lazy butt, just doesn't want to take the chance

of getting up and doing something for fear of another episode of pain taking

over! I honestly think this is God's and our body's ways of telling us when

to 'stop' & rest!

For what it's worth, with blessings,

MM / NSIF

Martha Murdock, Director

National Silicone Implant Foundation

Dallas, Texas Headquarters

-----Original Message-----

From: Peggy Allgauer Eckl <allgauer-eckl@...>

< >

Date: Sunday, February 11, 2001 5:54 PM

Subject: new list for FUN

>Hi guys:

>

>I started a list for those of us affected with chronic fatigue. It is a

>list for folks with fibro, lupus, arthritis, depression, disease from

>implants, etc. - anything that causes dipillitating fatigue. My plans

>are not to compete with this list at all - my hopes are to bring

>folks together from many different disease processes for FUN - if

>we can't laugh, we'll never get through this.

>

>If you're interested, here's instructions & info:

>Subscribe: LazyButts-subscribe

>URL to this page: LazyButts

>

>Now - to the name ---- my husband and I joke that I have LBS

>(lazy butt syndrome) on those days when I just can't get off the

>sofa. And, if someone asks why I'm not at a certain function, my

>husband will seriously explain to them that I have LBS & need

>my rest, LOLOLOL. Since there are so many diseases using

>acronyms, nobody even asks -- they act like they know exactly

>what it is, giggle.

>

>That's my story, and I'm sticking to it! :-)

>

>Peg in Springfield MO

>silicone/saline double-whammy double-lumen implants

>implanted 8/88

>explanted 1/01

>

>

>

>

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