for the a follow-up visit. She wants ds to have a 48 hour video
eeg to see what is going on. She also upped his medicine dose
which means my little boy who was just starting to smile and laugh
again will be wobby and hard to smile. It is so
frustrating. Sometimes I don't understand the medical
professionals.
Thanks for listening.
I'm sorry you got such frustrating news. Why the eeg? Why are they upping
his meds? I am curious.I am curious too..does he have seizures? We never did a eeg on Sarah but did a MRI..hope he adjust to meds quickly:)
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