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RSD Intro's : New member Jean here and my story
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 Message 1 of 3 in Discussion 
From: Jean  (Original Message)Sent: 9/3/2008 2:57 PM
 
Hi there,
 
My name is Jean, I live in Australia, and I have had rsd for 22 years.
It started in the right arm and hand, travelled to the left arm, down both sides of torso and up into my neck, left ear and left side of the face.  I have also developed fibromyalgia in the rest of my body.  Great.  This has ruined my life and dreams also.  I have trouble typing as well, my arms feel heavy and like they are not mine.  I get burning in the backs of my hands and pins and needles as well.  I am on a few meds which have helped but of course all this has caused nerve damage (not the meds).  I have a lot of pain in my legs and hips ((fibro).
 
I am on Lexapro and Lyrica.  They have helped me a lot and I have no side effects, the pain I still have I can cope with.  The pain in my face and ear have disappeared, and so my legs.  My rheumatologist is great. 
 
I put up with the pain without meds for years, trying all sorts of things.  Back in the 80's I feel I was a guinea pig.  Back then too it was called RSI.  Going to physios who stretched my neck, manipulated my shoulder blades which spasmed violently, put me on light duties...hah...repititive duties which only made it worse.  I don't think they knew what to do with me.  I went to a chiropractor but to no avail.  Had acupuncture which helped the headaches.  I finally joined a support group cried for 2 hours because I finally found other people who were going through the same thing.  The topic of the day was "My frightened arms".  That really scared me, because I couldn't do anything with my arms.  Workcover sent me to there doctors who said it was in my head, or because I got divorced...after a while you begin to believe them.  Went to a pain specialist who used to hynotise me...which worked to a certain degree...but most times she hynotised herself.
 
I left work in 1996 after fighting for a payout which I finally got on Jan 3 1996.  I was immediately marched out of the office, not being allowed to speak to anyone and it was all very humiliating.
 
I didn't go to another rheumatologist until 2003 because I found it so tiresome of trying to justify my pain.  How surprised I was when he was very sympathetic and very helpful and understanding.  It wasn't a workcover doctor.  He changed all my meds and changed my life.  I was seeing light at the end of the tunnel.
 
I will have to stop now...I'm seizing up....
 
It's great to be here and I look forward to getting to know you all.
Jean.


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Reply
 Message 2 of 3 in Discussion 
From: MSN NicknamefranknberrieSent: 9/4/2008 5:50 PM
Hello Jean,
 My Gosh, another person wha has been thru what I have! I have RSD in my upperbody,hands,arms,mid back and neck! I noticed you called the Drs there Work Cover, here we call them work comp Drs.....they all must have went to the same medical school! LOL! I too went for almost 3 years before I went to a neuroligist outside the Work Compensation system,  my RSD started with a work related carpal tunnel surgery. I never was able to go back to work, previous to the left hand surgery that started things I had 5 other nerve surgeries on my hands and elbows....I was able to go to work after those but surgery #6 finished me off. I have been on all the drugs they normally try and nothing worked, I ended up taking an opiate and getting spinal blocks every 4 to 6 months now. It very hard for me to type but thats easier than using a pen or pencil...no grip!
 Well Jean, welcome to our group! A while back I posted a question as to where people in our group live, it was unbelievable how spread out we are yet so close! That post is still up and you are welcome to add Austraila to the long list.
 
Again Welcome,
Frank (asst manager)

Reply
 Message 3 of 3 in Discussion 
From: MSN Nicknamekunzite2Sent: 9/13/2008 1:38 PM

Hey Jean, how are you sorry to hear that you have had rsd for so long anyway?<o:p></o:p>

I was just wondering if I could have an email contact to you as I live in <st1:country-region w:st="on"><st1:place w:st="on">Australia</st1:place></st1:country-region>, in Vic<o:p></o:p>

And have had rsd for three years now and was just wondering if I could ask you a few things<o:p></o:p>

As you are the 1st Person I no that’s not my age that has had a lot of experience with rsd so if you could please email <o:p></o:p>

Me on this email address which is kunzite69@ hotmail.com to get back to me as I would love to have a chat please<o:p></o:p>

As im on my own in this and would like to talk to people around <st1:country-region w:st="on"><st1:place w:st="on">Australia</st1:place></st1:country-region> who have rsd and how they manage it as im having a really hard time with <o:p></o:p>

It im 21 years old and they have no clue how I got it as a lot of things went wrong that year when it all started happening they think it was from when I hurt myself when I fall of an 8 foot bridge so it would be great to hear from you thank you hope you are doing well take care<o:p></o:p>

Yours truly Brie<o:p></o:p>

<o:p> </o:p>

P.s sorry if this email doesn’t make sense but I have rsd in the right are all the way up and in the left leg so for some know reason the brain doesn’t work with <o:p></o:p>

My arms if that makes sense. I know the feeling with rsd affecting your life as it has affected mine big time even through year 12 and tafe. So at the moment I can’t study or work because of it im not even aloud to drive I hate it cya thanks hope to hear from you <o:p></o:p>



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