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>

> A friend sent me this, thought you'd all like it.

>

>

>

>

> FIBROMYALGIA TALKS TO YOU

>

>

>

> Hi! My name is Fibromyalgia and I'm YOUR invisible chronic illness. I

> am now velcro'ed to you for life. Others around you can't see me or

> hear me, but YOUR body feels me. I can attack you anywhere and

anyhow I

> please. I can cause you severe pain or, if I'm in a good mood, I can

> just cause you to ache all over. Remember when you and Energy ran

> around together and had fun? I took Energy from you and gave you

> Exhaustion (the chronic fatigue that I send to follow you with this).

> Try to have fun now! I also took Good Sleep from you and, in its

place,

> gave you Brain Fog (when you can't remember what you were talking about

> 5 minutes before). I can make you tremble internally or make you feel

> cold or hot when everyone else feels normal. Oh, yeah, I can make you

> feel anxious or depressed too. If you have something planned, or are

> looking forward to a great day, I can take that away too.

>

>

>

> You didn't ask for me. I chose you for various reasons: that virus

you

> had that you never recovered from, or that car accident, or maybe it

was

> the years of abuse, trauma or stress. Well anyway, I'm here to

stay! I

> hear you're going to see a doctor who can " get rid " of me. I'm rolling

> on the floor, laughing. Just try! You will have to go to many, many

> doctors until you find one who even BELIEVES I EXIST. You will be put

> on pain pills, sleeping pills, energy pills or shots, told you are

> suffering from anxiety or depression, given a TENs unit, get massaged,

> told if you just sleep and exercise more, I will go away, told to think

> positive, poked, prodded, and MOST OF ALL, laughed at when you tell the

> doctor I am debilitating.

>

>

>

> Your family, friends and co-workers will all listen to you until they

> just get tired of hearing about how I make you feel, and that I'm a

real

> disease. Some of them will say things like, " Oh, you're just having a

> bad day, " or " Well, remember, you can't do the things you use to do 20

> YEARS AGO, " not hearing that you said 20 days ago. Some will just

> start talking behind your back, " All she does is whine, " or " She

sure is

> a hypochondriac. " Slowly you will feel that you are losing your

dignity

> trying to make them understand, especially, when you are in the middle

> of a conversation with a " normal " person, and can't remember what you

> were going to say next! Eventually most of them will be like all the

> doctors who say, " It's all in your head. "

>

>

>

> In closing (I was hoping that I kept this part a secret), but I guess

> you already found out...the ONLY please you will get any support and

> understanding in dealing with me is with other people with Fibromyalgia.

>

>

> OMG isn't that the truth!!!!!! Where did you get that? and can you

send it to my e-mail so I cna forward it to other people? thanks Leanne

>

>

>

>

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Drug Approved. Is Disease Real? - AOL News look what my b/f found these people

are so full of crap

Re: Sharing

Leanee,

you can find a copy of that letter at teh following website also:

http://www.fms- help.com/ mnif.htm

The author's name is Terry Been and she is from Colorado.

lisa n.

________________________________________________________________________________\

____

Never miss a thing. Make Yahoo your home page.

http://www.yahoo.com/r/hs

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  • 2 weeks later...

For the first time I opened up to the group and shared things about my

life when I can't even tell my friends. I don't know if I will ever

feel free to do that again.

The answer I got from djgraves9497@... taught me not to

share. I certainly don't care to be made fun of when I am on the edge.

It won't happen again.

Little

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Go ahead and share....that person isnt to bright or

important.

--- lilbit_sunnygirl

wrote:

> For the first time I opened up to the group and

> shared things about my

> life when I can't even tell my friends. I don't

> know if I will ever

> feel free to do that again.

> The answer I got from djgraves9497@...

> taught me not to

> share. I certainly don't care to be made fun of

> when I am on the edge.

> It won't happen again.

> Little

>

>

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Please lilbit,

Do not judge us by one persons very unkind remarks. This is a wonderful

group and are willing to help you in any way they can. I am a Group Moderator

so if you need anything please feel free to email me personally.

Again I apologize if you think anyone was making fun of you that is " NOT

SOMETHING WE DO IN THIS GROUP " EVER! Please give us another chance?

Lori H

Moderator

lilbit_sunnygirl wrote:

For the first time I opened up to the group and shared things about my

life when I can't even tell my friends. I don't know if I will ever

feel free to do that again.

The answer I got from djgraves9497@... taught me not to

share. I certainly don't care to be made fun of when I am on the edge.

It won't happen again.

Little

---------------------------------

Never miss a thing. Make Yahoo your homepage.

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