On Nov. 23, 2010, when my firstborn, Cammy, was 20 months old, a physiatrist clinically diagnosed her with Rett…
Jackie Babiarz
When Jackie Babiarz’s daughter, Cammy, was diagnosed with Rett syndrome at age 2 in 2011, Jackie became a point person for newly diagnosed Rett syndrome families across the country by providing guidance for marketing and fundraising, and by advocating for families with IEP meetings and transitions. Jackie also created a social media page with over 12,000 followers. She speaks to classes and schools about special needs, inclusion, and anti-bullying. Jackie is dedicated to helping families and strengthening communities. She and her family reside in Wheaton, Illinois. "The IncRETTibles" is her family's journey with Rett syndrome.
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Articles by Jackie Babiarz
My husband, Billy, met his best friend, Aaron, while playing golf at high school. Aaron began dating his wife, Joy,…
I vividly remember reading an article about the late Boston Marathon icon Dick Hoyt. It was 2005, and I…
As my two girls finished up fifth and seventh grade, I completed my coursework in special education. My firstborn, Cammy,…
Everyone remembers their first concert — who came along, where it was at, and most importantly, who performed. I went…
Our family hosts an annual fundraiser on behalf of our 13-year-old daughter, Cammy, who has Rett syndrome. This year’s…
Some of my pet peeves in the typical world in which I live are people who incorrectly use the word…
It’s no wonder that Cammy, my 13-year-old daughter with Rett syndrome, is a superhero. She comes from a…
Our nearest and dearest friends, George and Lisa Karavas, have been with us through every step, twist and turn, and…
When I was in middle school, I had sleepovers with my friends every weekend. My 11-year-old neurotypical daughter, Ryan,…