dear friends :
I am opening up this blog to all those who have friends or family members who have ocular motor apraxia (oma).
our son kip Sylvester was born with it 43 years ago in new York city. at the time there was no reason given , he was the 50th person born with it and no direction was given to us to help him. his picture was placed in some medical journal up in Belleview hospital and we had follow-up visit
I did as much searching as possible in libraries and found only a little help. he drives , works and have several college degrees, however he has had a hard time getting full time work.
I will fill you in with more information. but for now I would like to hear your stories and give you
encouragement for your children etc.
love to all Charlene
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