By Holly Bortfeld For 16 years, I’ve watched government agencies say nothing useful and do nothing to help my kids. For as long, I’ve seen autism orgs fight a regimented system who doesn’t care, for money they don’t want to spend on a diagnosis that no one can agree on the cause, treatment,... Continue Reading →
16 years later
By Holly Bortfeld My son Max was diagnosed with autism 16 years ago today, May 4, 1998. I have been mulling around in my head for a few weeks how I wanted to mark this anniversary of autism entering our lives and had drafted a blog but I didn’t like it. I kept poking at... Continue Reading →
Hindsight and the evolution of ASD treatment and recovery
By Holly Bortfeld I went to the IACC meeting in Washington DC on April 8, 2014 (1) to testify in front of the committee about my family’s autism journey. I took my son with me, as I am a single parent and have never had respite care. Standing over 6 feet tall, my... Continue Reading →
DSM-5, the fall out begins
By Holly Bortfeld TACA has been reporting on the potential effects that the proposed DSM-5 changes, which eliminated PDD, PDD-NOS, Asperger’s Syndrome, Childhood Disintegrative disorder and others, from the DSM since 20111. Now, we see the first tangible proof2 that the new diagnostic criteria will reduce the number of those diagnosed with autism spectrum disorder... Continue Reading →
Max Goes to the Neurologist – Part Two of Three
Part Two: Surviving the Hospital Stay and Testing By Holly Bortfeld Catch up - see Part One: Max goes to the Neurologist https://tacanowblog.com/2013/08/14/max-goes-to-the-neurologist-part-1-of-3/ *Disclaimer, I am a parent, not a doctor. This is not intended to be used as medical advice. If your child has a seizure, please contact a licensed physician. Please remember... Continue Reading →
Max goes to the Neurologist – Part 1 of 3
By Holly Bortfeld *Disclaimer, I am a parent, not a doctor. This is not intended to be used as medical advice. If your child has a seizure, please contact a licensed physician. On the 4th of July, my son Max had a grand mal seizure. For background purposes, he’s never had seizures before. Max has... Continue Reading →
Autism and the Holidays…
Guest Blog By Holly Bortfeld I am a single parent of two teenagers with ASD. I live 3000 miles from everyone I grew up with, and my family. My ex lives 1000 miles away and has no contact with our children. I live hours away from friends. I live here because autism services are tremendous,... Continue Reading →