Providing Education, Support and Hope to Families Living With Autism | TACA Now!
A Letter From Lisa Ackerman, Founder
In September 1999, the word “autism” rang through my ears like a cannon shot across the bow. My husband and I knew something was not going well with our son Jeff, but we would have never guessed it was autism.
Following that fateful visit with the neurologist, we visited many other professionals, including medical doctors, speech pathologists, audiologists, and behaviorists. The list seemed endless. The common message we were given; Autism has no hope, no cure. In fact, the first three medical doctors recommended that my family find “institutional placement” for Jeff who was the ripe old age of 2½ years at the time.
Refusing to give up on our son, my husband and I spent hundreds of hours talking to any and all parents of a child diagnosed with autism, reading dozens of recommended books, watching countless hours of educational videos, and of course, surfing the internet constantly. We were determined that our beloved son would grow far beyond his label and that he would have a future that was wonderful and amazing despite his autism diagnosis. Early on, the most important step for us was to GET BUSY. It was up to us, HIS PARENTS, to make a difference for his future.
TACA’s goal is to provide education, support, and information to parents to help their children diagnosed with autism be the very best they can be, with the hope of recovery and or independence.
I wish all families treating and caring for their children with autism the very best possible outcomes for their children as they continue forward on the autism journey.
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