Mommys Little Girl
Posted: Mon Sep 26, 2011 11:32 pm
In November it will be 3 years since Brachial Plexus Neuropathy affected my daughter at the age of 2 due to a virus.
Although I took her to the hospital immediately, had numerous tests done including MRI's, Nerve Graphs, etc. The neurologist would not admit that she had a brachial plexus. She has lost all of her muscle in her right arm from her neck to her wrist. She also has little to no nerve activity.
The problem is that since I live in Canada, there seems to be no doctor in this country that will look at her numerous MRI's and say that we can see the actual injury.
It frustrates me to no end that this beautiful little girl, could have actually had a chance and regaining some of her arm back, had the specialist had taken the time over the year that he say her and said.."this is what she has and we are going to send her somewhere that specializes in this". But instead he ignored her.
It wasnt until I took her to the Mayo Clinic in Minnnesota, where someone actually gave me a name. Within 5 minutes of the doctors there meeting with her, they knew exactly what was wrong and scheduled her for surgery the following morning. However Canada refused to finance the surgery since it could have been done here all along.
SInce then I have to fly her once a year to Toronto, so that she can be assessed. Our last visit they started talking about performing a Free Muscle Transfer. This scares me because she is only 5.
How does a parent make that decision? After all this time, can it be successful? What do I do?
Is there anyone that has any advice.
So Scared
Although I took her to the hospital immediately, had numerous tests done including MRI's, Nerve Graphs, etc. The neurologist would not admit that she had a brachial plexus. She has lost all of her muscle in her right arm from her neck to her wrist. She also has little to no nerve activity.
The problem is that since I live in Canada, there seems to be no doctor in this country that will look at her numerous MRI's and say that we can see the actual injury.
It frustrates me to no end that this beautiful little girl, could have actually had a chance and regaining some of her arm back, had the specialist had taken the time over the year that he say her and said.."this is what she has and we are going to send her somewhere that specializes in this". But instead he ignored her.
It wasnt until I took her to the Mayo Clinic in Minnnesota, where someone actually gave me a name. Within 5 minutes of the doctors there meeting with her, they knew exactly what was wrong and scheduled her for surgery the following morning. However Canada refused to finance the surgery since it could have been done here all along.
SInce then I have to fly her once a year to Toronto, so that she can be assessed. Our last visit they started talking about performing a Free Muscle Transfer. This scares me because she is only 5.
How does a parent make that decision? After all this time, can it be successful? What do I do?
Is there anyone that has any advice.
So Scared