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Questions? : Is this problem probably related to fibro?
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 Message 1 of 12 in Discussion 
From: MSN Nicknamecandypb1  (Original Message)Sent: 2/24/2005 2:17 PM
I'm going to see dr, anyway, but this is it.  I was typing, and I've been a typist forever.  I couldn't figure out where some letters were located, and I've never ever had a problem like that.  Later that day, I was working with dd on her homework.  I went to copy a word, that was on the paper, and I could not figure out how to print a "g".  I almost panicked, because it took at least a minute before I could produce it.  It came out as different scribbles.
 
I'm very concerned.
 
  


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Reply
 Message 2 of 12 in Discussion 
From: MSN NicknameSmilingSuperSmileSent: 2/25/2005 2:32 PM
I am sorry to be the one to tell you this but yes it is part of fibro.   I have forgotten how to spell words I use everyday, some as small as the letter words.  I have forgotten how to sign my name in the middle of doing so.  I have gotten lost going to my daughter's house.  I blame it on fibro fog.  The fog is the main reason I don't drive much anymore even though I have always loved driving.  I hope knowing why it happens helps.<o:p></o:p>

Mega hugs to you<o:p></o:p>


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 Message 3 of 12 in Discussion 
From: MSN Nicknamecandypb1Sent: 2/25/2005 10:51 PM
Yup - fibro.  I am waiting for a start date for physiotherapy, and a group that learns about how to live with fibro.  I also found a therapy group for fibo.  I went to the dr, and am going to have a bone scan, and some more xrays.  I even made an appt with the dentist.  I've been looking after myself, for once. 
 
I've been teaching the kids to cook, and clean (properly).  It's been working with meal preparation, but I have decided that with 6 kids, I should not have to do much around the house, when I'm in pain.  The pain has been quite intense for the last few weeks, and I'm going to make a better life for myself. 
 
 

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 Message 4 of 12 in Discussion 
From: MSN NicknameSmilingSuperSmileSent: 2/26/2005 6:35 PM
Good for you :)  You seem to have found lots of support :) Have you checked into aqua therapy?   That really helped me a lot.  Also what pain meds are you on?

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 Message 5 of 12 in Discussion 
From: MSN Nicknamecandypb1Sent: 2/27/2005 1:54 PM
I can't seem to tolerate pain meds.  I want my viox back, because it truly gave me my life back.  All anti inflamatories hurt my tummy big time.  I need to keep my mind alert, as if that will ever happen again, because all my children are classed "special needs", and there are lots of problems to avoid.  I take tylenol #1 - #3, sometimes I go on the anti inflam. with stomach meds.  I've been using melatonin, and after 3 weeks, is seems to be working finally, for sleep. 

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 Message 6 of 12 in Discussion 
From: MSN NicknameSmilingSuperSmileSent: 2/28/2005 4:46 PM
{{{{{{{{{{{{{{{{{{{{{{Candy}}}}}}}}}}}}}}}}}}}}}}}
Well there is talk that vioxx might come back.  As for the other meds I don't know them.  Right now I am taking talwin nx for pain.  I totally understand all the trouble. I used to work with special need kids I REALLY miss it.  What are their disabilities and ages?
Mega hugs always :)

Reply
 Message 7 of 12 in Discussion 
From: MSN Nicknamecatjohn1Sent: 5/2/2005 7:15 AM
I HOPE I SPELL THIS CORRECTLY...HAVE YOU BEEN CHECKED FOR ...CARPIAL TUNNEL. OR DO U EVER GET TINGLING IN YOUR ARMS OR HANDS? IF U HAVN'T TRY TO. I DID THE NUMBNESS IN THE HANDS/ARMS, FROM THE NERVES. AND YES I ACTUALLY DO HAVE A BIT OF CARPIAL. BUT WHO REALLY KNOWS. WHAT ONE OF US HAVE MANY MAY NOT. I GUESS IT'S LIKE THE MEDS///WORKS FOR SOME NOT OTHERS,IT'S JUST SO STRANGE. GOODLUCK AND TAKE CARE, CAT

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 Message 8 of 12 in Discussion 
From: MSN NicknameSmilingSuperSmileSent: 5/2/2005 6:24 PM
I have tingling in my hands and wrists and have been tested several timesfor carpal but they keep saying I don't have it.  One Dr told me that it is very possible to still have it even though the test keep saying no.  So what do you do????

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 Message 9 of 12 in Discussion 
From: MSN Nicknamecatjohn1Sent: 5/5/2005 10:46 PM
HAVE YOU GONE TO A NEUROLOGIST?? THEY DID THE TEST WHERE THEY INSERT VERY THIN NEEDLES INTO CERTAIN NERVE GROUPS FROM HEAD TO TOE. THATS WHERE I FOUND OUT I HAD CARP. BUT THIS IS MY THOUGHT ....HAVE YOU ALL NOTICED THAT IN THE GROUP///THAT HAS FIBRO/CHRONIC...AS WELL FATIGUE.ALL OF US WHO HAVE THAT SHARP UNBEARABLE PAIN AT THE BASE OF YOUR SKULL TO (C-1) WE ALL HAVE NUMBNESS PROBLEMS SOMEWHERE. I HAVE SEARCHED ON WEBMD.COM DUG WAY DEEP. I LEARNED THAT , THAT DISK IS LIKE 2 METAL WASHERS. WHAT HAS HAPPENED IS ONE OR BOTH HAVE SLIDE A BIT AND ARE UNALINED...PINCHING THE NERVES.IF ANYONE HAS ANY OTHER HELPFULL HINTS PLZ. DO TELL. I WANT TO KNOW MORE AS WELL.PAIN PAIN PAIN!!!! UGH TAKE CARE,CAT

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 Message 10 of 12 in Discussion 
From: MSN NicknameSmilingSuperSmileSent: 5/6/2005 12:15 AM
I have been to two different nueros, had the nerve tests done at least 4 times.  YUCK!!!! I had it done once with the patches and 3 times with the needles.  Still say no carpal. I do have pain at the base of my skull but it is not the worseof my pains.  The worse pains I have are in my hands, arms, legs, and feet.
 
Keep posting everything you find Cat :)  You never know who it will help or what it will click with!!!!
 
Thank you :)

Reply
 Message 11 of 12 in Discussion 
From: _still-learningSent: 5/19/2005 6:26 AM
I do the same type of thing. I take ginko biloba, it helps lots but doesn't take the loss of memory and fog away completely. Let us all know if you find something that fixes it.

Reply
 Message 12 of 12 in Discussion 
From: MSN NicknameDianaMotherGoddessSent: 6/23/2005 1:01 AM
Could it possibly be contributed to some of the meds you are on? I had terrible "fibro fog"  on tegretol, but when I went off it the fibro fog decreased dramatically.
 
 
Diana

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