| Subject: Re: fibromialga |
Author:
Judy Brigman
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Date Posted: 17:26:36 01/06/03 Mon
In reply to:
tammy
's message, "Re: fibromialga" on 22:47:47 11/05/02 Tue
Tammy,
Thankyou for your information, I am not sure if I have it but the symptoms add up...I am in the process of having to be tested for it. Thankyou again
Warm Christian Love,
Judy
>>>might have fibromialga and was wondering for those
>>>people who have been confirmed to have it if they can
>>>give me any advice or information that might ease the
>>>pain. I'm to young to have it but I do. Can any one
>>>help?
>>Hello: I have had fibro for 10yrs I was also to young
>>I was 29 when i was told I had fibro. My best advice
>>is to excercise and keep your muscles in the best
>>possible shape.Stay away from the msg's msg are
>>additives in foods. Chinese food is a nono I have it
>>as a treat once in awhile. My other advice to you is
>>to find a good caring pain managment doc and I pray
>>you have support from your family and hope you don't
>>have to go what we went threw 10 yrs ago. We were all
>>told it was all in our heads. Keep your chin up never
>>loose faith and when the pain is bad do some stretches
>>and find something to keep your mind off of it.
>>
>>Hope this helped some. Feel Free to e-mail me and Good
>>luck hon.
>>Rhonda
>>hello, my nane is tammy, and i thought i would reply
>to >your message! i feel so bad for you, ive had
>fibromialga >for 6 yrs, i was diagnosed by many
>doctors, i am now 35yrs >old and am suffering in very
>intence pain, its almost like >nothing will make the
>pain go away!especially when i have >real bad flare
>ups, i am totaly bed ridden, with all my >pills, that
>they put you on for fibromialga,some for sleep
>>disorder, some for anxiety, and deffenatly some for
>pain, >dont get me wrong they do help me !! some days
>alot , but >others hardly at all, on those days i feel
>like i have the >worst flu in the world, and nothing
>helps at all,my legs >are the worst with this, so
>every morning i cant barley >get out of bed cause im
>so stiff, once i get them working >i do what i can
>through out the day, sometimes nothing at >all just
>lying in a chair, and i have 2 babies to look >after,
>wow sometimes it gets real hard for me! but i >manage
>to make it day by day! exersise is the best thing >for
>you but not to vigarus, anything like stair steppers
>>or riding a bike , only causes me more pain, and i
>dont >need that,and either do you! eating the right
>foods, and >taking your vitamins,pluss drink lots of
>water that is the >best! they used to say it was all
>in your mind , but >obviously they have proven this
>thery WRONG, although u >can do alot with your mind,
>by thinking positive, and >saying this illness will
>not get the best of me! i am to >young and want to
>live my life to the fullest! i will try >every day, to
>ignor this pain and get on with my life!but >most of
>all do not whatever you do complaine about this
>>terrible pain to others they will get sick of hearing
>it!! >sucks i know but the truth,just rest when you
>need to on >bad days, and do what you can on better
>ones, and >deffenatly find a pain manegment doctor who
>has compassion >for this illness , to help with the
>pain, longterm, word >to the wise do not take viox for
>inflamation it is no good >for you!hope i helped you
>in some way, about how this >illness workes,and what
>to do for yourself to make life
>>liveable..... feel free to leave me a message if you
>would like tamfloo11@aol.com sincerly, tammy
>>
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