This web site was constructed personally for the individuals who have Agenesis of the Corpus Callosum (ACC) and their families. Hoping it would be a help for them concerning to ACC.
Also professionals will be welcome.
The cause of ACC is not clear yet and the prognosis is various.
My daughter Maki has ACC and CP
(Cerebral Palsy). I am feeling anxiety
for her future, but information on ACC is very poor as for as I know.
Now I am contacting to 'The ACC Network'
in U.S. and I am getting information about ACC.
I would like to introduce to you
the content of a packet I've got from The ACC
Network.
If there should be incorrect writings, please let me know because I am
not a professional writer nor a doctor.
The ACC Network
5749 Merrill Hall, Room 18
University of Maine
Orono, ME 04469-5749
(207) 581-3119
Fax(207) 581-3120
Email: um-acc@maine.maine.edu