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hello i'm a twentyfive year old women. i was just recently told i have

fibro. i wasnt told much about it. all i know i'm always in pain it is

so fusterating cause it seems like no one beleived me even the dr's

they ran every test possable and still found nothing .it wasmt till i

went to see a bone dr. for my shoulder and they tested me for ruma

arth and i tested possitive for that. then was told to see a arthir

specilist and he told me it was fibro with all the things i had

expland to him.so now what????

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Welcome . The diagnosis is very confusing to many of us at first.

You're so young, and then to find out you have this life-long chronic condition

can be overwhelming(sp?). If you check out the files and links on the website,

it will lead you to lots of excellent places to learn stuff.

I hope by joining our group you realize that you are not alone in your

suffering and confusion. We are here to help and support you. My 14 yr. old

daughter also has FM.

Take care.

Jeanne in WI

hello i'm a twentyfive year old women. i was just recently told i have fibro.

i wasnt told much about it. all i know i'm always in pain it is so fusterating

cause it seems like no one beleived me even the dr's

they ran every test possable and still found nothing .it wasmt till i went to

see a bone dr. for my shoulder and they tested me for ruma arth and i tested

possitive for that. then was told to see a arthir specilist and he told me it

was fibro with all the things i had expland to him.so now what????

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Hi yes I agree you are so young but then again I was younger

once upon a time ago too when I first got Diagnosed. I was Diagnosed

back in 98 and I am now today 42 yrs old. There is a lot to learn

about Fibro on the net just go to your favorite search engine and look

it up. But the best place to look is like the Fibromyalgia Network

(Based out of Tucson AZ.) or like the National Fibromyalgia

Association - these few places you will learn a lot of what you have.

Do you have a support group in your area that you can attend too? They

are always nice because you can get the support that you need

there.Plus you get to meet people that have the same as you do or

more. You should look into this - I have come to know that they do

help offline and I have made many friends through this and we call

each other a lot during the week to see how we are all doing. The Best

thing about OUR support group at the end there is ALWAYS a HUG before

you walk out that door. So try to look for one in your area.

Fibro Friend,

Lauri

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, first of all ((((((Hugs))))). Sorry you have this

condition. My name is Tammi. I'm 36, married and stay at home mother

of two teens. I was dxed at 31 but had chronic pain since 22 and

symptoms since 18. I have a son who also has fibro. He's not as sever

as most and is fairly " normal. " I had never heard of fibro until a

couple weeks before dx. The internet is very helpful. I found this

group only recently and they are very supportive and helpful with

figuring out some of stuff that goes with this illness. I hope you are

seeing a good doctor. Don't be afraid to ask the doctors about your

condition. The more you know the better your care and treatment. Ask

anyone here anything you want, they know so much about so much.

Tammi

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