Monday, May 11 @ 2pm, my son was seen by the paediatric neurologist, I am some-what relieved that she was able to give us some insight on the past 3.5 years and brings much of it into perspective, as well as gives us hope for the future.
The results of the first EEG came back fine but we have to go back for another in hopes that he will sleep this time. The Dr. wants to see if he is possibly having seizures while he is sleeping. Apparently something not uncommon. We also have some other tests to be completed and therapy's to begin which will help our situation dramatically.
A diagnosis is not going to solve anything... we just need someone to help show us how to help this little boy so that he is given the chance to succeed in life and develop to his full potential. I am hopeful that he will get through this and he will live a happy life.
Passing The Baton
10 months ago
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