Living with Guillain-Barre SyndromeThis section is a place to share stories about Living with Guillain-Barre Syndrome. Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download Guillain Barre at age 13 My daughter was suddenly struck with Guillain Barre Syndrome 3 weeks ago. She is 13. She was at school and with no warning, she suddenly couldn’t move her lower extremities. She was taken to the ER and after hours going through tests, the doctors could not diagnose her. The doctors sent her home with no diagnosis; they were baffled. Even the neurologist she saw the next day was puzzled. I finally took her to see her pediatrician and she diagnosed Shannon right away. She was hospitalized immediately, had a spinal tap done upon admission, and was on immunoglobin therapy the next morning. Luckily, she did not need to be placed on a respirator. After 5 days of treatment, she was sent home. She is able to walk now, with the assistance of a walker and physical therapy It’s still painful and she is unable to walk far distances or stand too long. Gone are the days when she could walk the mall all day, run a 5K in 30 minutes, play volleyball, or join cross country. Simple things, like tiptoeing or walking up/down stairs are difficult and painful. She can no longer ride the regular school bus and needs special transportation. It has been hard for Shannon. She went from being a healthy student athlete to being a student with special needs in one day. The kids at school don’t understand what has happened to her and are sometimes cruel. Her pediatrician, God bless her, remains positive that she will fully recover. Shannon has remained positive throughout this ordeal and is optimistic that she will soon be able to start running 5Ks again. Comments
April 2009
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