A YOUNG LADY WHO LIVES IN ISRAEL WAS STRUCK WITH TM AS A VERY YOUNG GIRL.  HER 
NAME IS NETTA GAYNOR.  TO THIS DAY, SHE REMAINS A QUAD AND USES A POWER 
WHEELCHAIR FOR MOBILITY.  SHE IS NOW A VERY ACCOMPLISHED ARTIST AND PLYS HER 
CRAFT BY HOLDING A PAINT BRUSH IN HER MOUTH.

YOU CAN VISIT HER WEB SITE AT http://gnetta.cabspace.com/

YOU CAN READ HER STORY AND SEE WHAT SHE HAS AND IS DOING.

THERE ARE MANY YOUNG LADIES THAT HAVE ACCOMPLISHED LOTS, ALTHOUGH THEY HAVE TM 
OR ADEM OR OTHER PHYSICALLY LIMITING DISORDERS.
AND, YES, THERE ARE OTHER PARENTS OUT THERE WHO HAVE CHILDREN WITH TM AND ADEM, 
WHOM I HOPE WILL RESPOND TO YOUR INQUIRY SOON. THE ORIGINATOR AND FOUNDER OF 
THE TMA HAS A DAUGHTER AFFECTED MY TM AT THE AGE OF 18 MONTHS WHO IS NOW A 
TEENAGER.

I WISH YOU AND THE FAMILY WELL.

BOB COOK
TM CLASS OF ' 94 = T-1 PARA
SPRING, TEXAS


----- Original Message ----- 
From: Moses, Anna S 
To: tmic-list@eskimo.com
Sent: 2/2/2007 7:42:41 AM 
Subject: [TMIC] new to list


I’m new to this list and wanted to do a quick introduction. I am Anna Moses and 
live in Little Rock, Arkansas. My daughter was ill with ADEM about 3 years ago 
and is still recovering. She was up to the point of walking some with quad 
canes, but had surgery for scoliosis in October and is back in the wheelchair 
98% of the time. She seems to have lost the hope of walking and only tries to 
walk when she goes to physical therapy. She seems to have a good attitude for 
the most part, but just doesn’t seem to want to spend the time trying to walk. 
She is 14 now and has the typical teenager attitudes. I get very frustrated 
with her and with myself. I try to live my life with a good attitude, but 
sometimes it all gets to me. My daughter’s illness has really affected our 
whole family.
 
John’s story really touched me. You must have been really frightened when you 
woke up and couldn’t walk. I remember that moment clearly with my daughter. She 
had been to the hospital and had been diagnosed with spinal meningitis and sent 
home after a short stay. She was sleeping with me since she was ill. She got up 
early in the morning to go to the bathroom and couldn’t walk. I tried to help 
her to the bathroom, but we both ended up on the floor. She looked at me and 
said, “Mom, what’s happening to me?” My husband rushed her to the ER while I 
got my son up and off to Grannie’s. She spent 10 days in ICU, most of it 
unconscious and another 6 weeks in the hospital getting to the point where she 
could feed herself and sit up in a wheelchair. She was on steroids, so didn’t 
look like herself for several months. It was a scary time for her and for us.
 
Thanks to John and others for sharing their stories.
 
Are there any parents out there with children that have been ill with ADEM or 
TM? 
 
Anna Moses

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