Hemi_1
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- Dec 25, 2003
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I have never really said much here regarding my Boy Brady.
He was diagnosed 4 years ago with APRAXIA
It is a nuerological dissorder effecting the strength of his tounge along with control as well. So, short story is he struggles badly with speech.
Outrageously talented little man and motor skills well beyond his years.
We recently had an Brain MRI to check his frontal Lobe. He was born in Norwood Mass in 2002. An April baby.
The MRI did not show any deformity in his frontal lobe. ( the Doctor told me there would be and it would likely be both sides of his frontal lobe because, when we struggle with speech which is developed in the right side of the frontal lobe the left side of the FL takes over and assist with this development to prevent issues)
What we did find was a Cyst on his right FL.
More than 1.
We will have another MRI done in 90 days. If conditions worsen or at that time if the Cyst grows or changes we will take action. If nothing changes than his doctor said we should just monitor it.
CKA and SM kind of inspired me to share my issues with you guys.
Prayers are welcomed, I will tell Bradys mom tonight when she gets home. Especially now that I have told the rest of the world.
He was diagnosed 4 years ago with APRAXIA
It is a nuerological dissorder effecting the strength of his tounge along with control as well. So, short story is he struggles badly with speech.
Outrageously talented little man and motor skills well beyond his years.
We recently had an Brain MRI to check his frontal Lobe. He was born in Norwood Mass in 2002. An April baby.
The MRI did not show any deformity in his frontal lobe. ( the Doctor told me there would be and it would likely be both sides of his frontal lobe because, when we struggle with speech which is developed in the right side of the frontal lobe the left side of the FL takes over and assist with this development to prevent issues)
What we did find was a Cyst on his right FL.
More than 1.
We will have another MRI done in 90 days. If conditions worsen or at that time if the Cyst grows or changes we will take action. If nothing changes than his doctor said we should just monitor it.
CKA and SM kind of inspired me to share my issues with you guys.
Prayers are welcomed, I will tell Bradys mom tonight when she gets home. Especially now that I have told the rest of the world.