TACA’s Doctor Appreciation Day

  By Jackie Moore On March 30th, 2016 TACA will hold the first TACA Doctor Appreciation Day in partnership with Houston Enzymes to recognize physicians who have dedicated their practice to help children with autism. This past summer, the autism community lost Dr. Jeff Bradstreet. The first couple of days after he died, I read... Continue Reading →

#Presidential Candidates Let’s Talk #Autism Plan

WHY HAVE A PLAN IN THE FIRST PLACE? As a country, we need to address this important health issue affecting 1 in 68 every US Children (1.) A more recent parent survey shows the number even higher at 1 in 45 (2.) Candidates need to know this should be a front-of-mind issue affecting many families living with autism. They also need to know we need help.

Meet Me at the National TACA #Autism Conference

  Janice Kern TACA National Conference Coordinator   TACA hosts events every week somewhere in the country. There are coffee talks, family picnics, TACA Meetings, Autism Learning Seminars, Family Hikes, TACA Birthday Parties and the list goes on. It’s a fact that TACA has some of the most creative volunteers you’ll ever meet. If they... Continue Reading →

From #autism to skateboard star

By Jacqueline Garza Hi I am a TACA mom and I have an amazing, incredible 9 year old superhero son named Mason. Mason began receiving early intervention at 17 months and was formally diagnosed with autism at 2.5 years old. In April 2014, Mason participated in Volcom Autism Awareness Day brought to us through TACA... Continue Reading →

Girls have #autism too

    By Jackie Moore – TACA Georgia   Every autism journey is different. This is our family’s journey with autism. Thirteen years ago, I gave birth to my daughter, Jordyn. At that time, I knew very little about autism. If you would have asked me what I knew, I think my response would have... Continue Reading →

15 years later, ready for #autism answers

By Melanie Sanchez - TACA Mom My son Andrew is 15 1/2 years old.  He is non verbal, has autism, and a lovely contagious smile.  He had a brief "sleep deprived" EEG done right after diagnosis when he was around 3 years old.  It lasted  less than an hour and hardly seemed worth the time and effort.  At the... Continue Reading →

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