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That is cool Tess, I have always thought that was a good day to be

born, now I know it is. Yes we will have to celebrate and hope for a

good day. Talk to you soon. Tell Em hello. in WA

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Hi ,

Remember, feeling sorry for ourselves is part of this disease and we all need

a hand to help us off the pity potty. So just ask away. We never know when

it is our turn. No two ways about it, this disease sucks at times but it has

also brought us into the lives of some of the nicest, most caring people we

would ever have the pleasure to meet. We may never meet face to face, but

our hearts are intertwined forever. You will see that some members fade away

and leave the group and you always wonder whatever happened to them. Our

founding moderator, Pat is a wonderful inspirational woman who is so busy and

has some major health problems that prevent her from posting, but all of us

" old-timers " remember her and thanks to a, she keeps us informed. Most

of us have said things on this board that we never feel comfortable in

telling our spouses, significant others, even our doctors, yet the words flow

freely here. Why? Because we all care.....truly care and most of us have

been where you are or where you have been. This disease does not behave

identical in all patients, but the paths we take to get it diagnosed, treated

and try to live a " normal " life with are often similar if not identical. We

all feel somewhat isolated from our family, friends and coworkers by this

disease and none of us WANT to be a bother to our doctors, but the truth of

the matter is that our doctors all took an oath to be bothered for the

duration of their working careers. As far as family and friends are

concerned, well they will never understand how our shoes feel on our feet and

we never really want them to ever have to try them on. But together on this

list, we all know the feelings of no validation of our symptoms, the endless

tests, the negative blood tests, the lets try another change in your

medication and see how that goes, etc. I am at a point now with most of my

family and friends that when they ask how I am, I just answer OK. OK means

to me that I am dealing with what I have on my plate and that is all I can

hope for right now. They will usually proceed with the normal " But you look

so good....you must be feeling better " . Once I am securely restrained from

putting my hands around their throats, I just smile, say thank you and walk

away! LOL. See, we have ALL been there!

Summer is here with a vengeance. Hot in the 90's and then it rains and it

feels like a sauna outside. YUK.

Hope you have a good evening with as little pain as possible. Remember we

are all just an e-mail away from you and are willing to lend a cyber ear in a

heartbeat. Just know that you are no longer alone with this disease.

Gentle, tender, angel hugs,

Debs in FL

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Guest guest

you letter in response was so beautiful. it touched on every emotion i have

had since dealing with the disease. especially about people looking at you

and seeing nothing when you know inside you are feeling the worst. i think

that is my toughest obstacle especially with my husband. i so bad just want

to yell..HEY...I'M SICK AND HURT EVERY DAY DONT YOU GET IT!!!!!!!!!!!!!!!!!!!

but i also know that will solve nothing. thank you for those beautifully

written words...love teresa

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hi

what a beautiful sentiment and expression of truths...

so so true...

hugs sam

Re: [ ] in WA

> Hi ,

>

> Remember, feeling sorry for ourselves is part of this disease and we all

need

> a hand to help us off the pity potty. So just ask away. We never know

when

> it is our turn. No two ways about it, this disease sucks at times but it

has

> also brought us into the lives of some of the nicest, most caring people

we

> would ever have the pleasure to meet. We may never meet face to face, but

> our hearts are intertwined forever. You will see that some members fade

away

> and leave the group and you always wonder whatever happened to them. Our

> founding moderator, Pat is a wonderful inspirational woman who is so busy

and

> has some major health problems that prevent her from posting, but all of

us

> " old-timers " remember her and thanks to a, she keeps us informed.

Most

> of us have said things on this board that we never feel comfortable in

> telling our spouses, significant others, even our doctors, yet the words

flow

> freely here. Why? Because we all care.....truly care and most of us have

> been where you are or where you have been. This disease does not behave

> identical in all patients, but the paths we take to get it diagnosed,

treated

> and try to live a " normal " life with are often similar if not identical.

We

> all feel somewhat isolated from our family, friends and coworkers by this

> disease and none of us WANT to be a bother to our doctors, but the truth

of

> the matter is that our doctors all took an oath to be bothered for the

> duration of their working careers. As far as family and friends are

> concerned, well they will never understand how our shoes feel on our feet

and

> we never really want them to ever have to try them on. But together on

this

> list, we all know the feelings of no validation of our symptoms, the

endless

> tests, the negative blood tests, the lets try another change in your

> medication and see how that goes, etc. I am at a point now with most of

my

> family and friends that when they ask how I am, I just answer OK. OK

means

> to me that I am dealing with what I have on my plate and that is all I can

> hope for right now. They will usually proceed with the normal " But you

look

> so good....you must be feeling better " . Once I am securely restrained

from

> putting my hands around their throats, I just smile, say thank you and

walk

> away! LOL. See, we have ALL been there!

>

> Summer is here with a vengeance. Hot in the 90's and then it rains and it

> feels like a sauna outside. YUK.

>

> Hope you have a good evening with as little pain as possible. Remember we

> are all just an e-mail away from you and are willing to lend a cyber ear

in a

> heartbeat. Just know that you are no longer alone with this disease.

>

> Gentle, tender, angel hugs,

>

> Debs in FL

>

>

>

>

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  • 1 year later...

Marla,

I moved to Vancouver, WA, which is on the south side, just over the river

from Portland, OR. I think it is beautiful here. I really like the not-so-hot

weather. I just need to get out and meet people. I am getting a bit lonely and

bored.

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Marta, Marta, Marta.....

They have been working you hard, haven't they? Elvis has left the building.

I blew that popscicle stand. I got outta Dodge. I MOVED. I am now in

Vancouver, Washington. I left at the end of July. The house that I was going to

buy

fell through a few days before the move (on the day escrow was supposed to

close) so I had to replan my stuff so that some could go to storage and some to

a 1

bedroom apartment. YUCK.

Other than that, I am generally happy, if not a bit lonesome for friends. I

like it up here. It is beautiful, the weather is nice, Tom is great, the dogs

think it is doggie-disneyland, and I get a whole new fresh start. No more

family members living with me, using me for a free/cheap babysitter, picking

through my stuff for momentos, and all that stuff. You didn't happen to notice

that

I wasn't at the second pool party...hmmmmm?

Poor dear. You need more sleep.

love ya!

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I was born and raised in Portland, Oregon and spent from 1967 until 1996 in

Washington State. I lived for 20 years half way between Portland and Seattle

in a little town named Centralia. I have a " sister-in-law who teaches in

Vancouver if you need a contact name. I also have numerous relatives if you

need some extra. If you can adjust to the rain you will really like it.

Marla

Denver

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> I miss you girl!!!!!!!!!!!!

>

> Good to hear your unpacking is going well.

What is the " unpacking " that I hear people mentioning?

Marta

Don't look in my garage or I will have to kill you.

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Marla,

Sure, pass along your sister's name, if she doesn't mind. Although a fair

amount of teaching jobs were available, because of the cutbacks in Oregon, many

teachers came over the border for jobs. At Evergreen School District the

personnel director told me that they have had upwards of 400 applicants PER

position. A real tough market.

in WA

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