I've noticed lately that people have been coming to this blog using the search engine tag "children with cerebral palsy" or something to that effect. I thought it would be good to create a page here for those people so that you can easily find out information about cerebral palsy as well as how it affects my son. But first a little disclaimer… I am attempting to put what I have learned about cerebral palsy over the years into laymen’s terms but please keep in mind that I am not a doctor, a nurse, or a trained professional who deals with cerebral palsy. I’m simply a mother wanting to educate others about her son's condition. For more information on cerebral palsy, please see the "CP Links" section at the bottom of this page.
What is Cerebral Palsy? (I will refer to Cerebral Palsy as CP from now on.) CP is a condition caused by injury to the brain resulting in loss of oxygen right before, during, or after birth. More and more often, CP is being linked to negligence on the medical professionals part. It can often be very common in premature babies as well. What are the effects of CP? CP affects each person differently. It can affect their speech, motor control, ability to walk, and the ability to do everyday things - even eating! It can affect their whole body or it can affect just certain aspects of their functioning.
How many children have CP? According to UCP, about 8,000 babies/children are diagnosed with CP each year.
Does the condition get worse over time? No! CP is considered a "static" condition - meaning it does not get worse. With therapy and hard work, people with CP can overcome their obstacles.
Since each child with CP is different, I thought I would take a moment and walk you through 
how CP has affected Noah. Eager to see the world, Noah arrived 6 weeks early weighing 4 lbs and 12 oz. After I was given the epidural, he lost oxygen which resulted in CP. We did not know he had CP at the time. After an attorney did an investigation as to what caused the CP, I firmly believe that Noah's CP is the result of my reaction to 
the epidural and the doctors not responding quick enough to that reaction.
how CP has affected Noah. Eager to see the world, Noah arrived 6 weeks early weighing 4 lbs and 12 oz. After I was given the epidural, he lost oxygen which resulted in CP. We did not know he had CP at the time. After an attorney did an investigation as to what caused the CP, I firmly believe that Noah's CP is the result of my reaction to the epidural and the doctors not responding quick enough to that reaction. Noah was a happy baby, but we did begin to notice that he was not on target with some of his milestones. At about 8 months old, a CT scan was done and it was then determined that Noah did have CP. 
Noah had surgery at Shriner's Children's Hospital in November of 2002 to lengthen his heel cords and to put steel plates in his hips. It was a long process - he was in a cast from the waist down for a month and then in "boot" casts from the knees down for another month. The surgery has helped some and Noah is able to walk short distances in a walker.
Noah had surgery at Shriner's Children's Hospital in November of 2002 to lengthen his heel cords and to put steel plates in his hips. It was a long process - he was in a cast from the waist down for a month and then in "boot" casts from the knees down for another month. The surgery has helped some and Noah is able to walk short distances in a walker. Noah's speech is also delayed by CP - although he comprehends and understands so much! He is now communicating with sign language and a communication device. Noah goes to a very good local school for children with special needs. He is in a class room setting, but receives occupational, physical, and speech therapy and learns life skills at school as well. He is doing well in school and enjoys school - especially riding on the school bus! 
Noah continues to amaze us with his zest and love of life. Noah is a very happy and loving boy who enjoys making others smile and laugh by doing silly little things. He plays Miracle League baseball (baseball program for children with special needs), loves the Clemson tigers, and enjoys reading and going places. He is a curious learner and a bit of dare devil at times - especially when it comes to roller coasters. People have asked me if I wonder what Noah's life would be like if he did not have CP, but that is hard for me to imagine.
Noah is who he is - CP and all.
Cerebral Palsy Links:
UCP Support Community for Parents of Children with CP Noah continues to amaze us with his zest and love of life. Noah is a very happy and loving boy who enjoys making others smile and laugh by doing silly little things. He plays Miracle League baseball (baseball program for children with special needs), loves the Clemson tigers, and enjoys reading and going places. He is a curious learner and a bit of dare devil at times - especially when it comes to roller coasters. People have asked me if I wonder what Noah's life would be like if he did not have CP, but that is hard for me to imagine. Noah is who he is - CP and all.
Cerebral Palsy Links:
Links to things I have written regarding CP:
Cerebral Palsy Awareness Month
What Do You Call Someone with a Disability?
Defining Noah
My sister sent this blog to me. I am Gary Lynn's mother. It was an honor for Gary to be one of the All Stars and recognized by the President's of the US.
ReplyDeleteGary is working with one of the world's greatest neurologists to raise funds for the research and cure of CP. She is dedicated to finding a cure and we cannot rid anyone of any disease without research. Cerebral Palsy International Research Foundation, as far as we know, is the only CP group working on research for cerebral palsy.
Gary will continue his events to raise funds until every child is out of a wheelchair and for for those that cannot speak, they will be heard.
Thank you for recognizing Gary .
www.thegaryjlynnfoundation.org
Andrea Lynn