Megan R
Chantelle Parra2024-07-11T15:38:46-07:00At the time of filming, Megan had been using a CAYA iPad with TouchChat for about one year. In this video, her CAYA SLP, Tiffany, [...]
At the time of filming, Megan had been using a CAYA iPad with TouchChat for about one year. In this video, her CAYA SLP, Tiffany, [...]
My name is Al Daly. I have ALS, a progressive neurological disease, and can no longer communicate with my own voice. During the earlier stages [...]
Hi there, this is Abby’s communication story. Before we met with the team from CAYA, we were using the Picture Exchange Communication system and had [...]
Hi, my name is Jan Bruce. In 2012 I diagnosed with a progressive degenerative neurological disease. I was referred to CAYA in 2013 when my [...]
AAC users from across the Okanagan gathered at Spirit Square on Peach Orchard Beach in Summerland in June to celebrate being together again with food, [...]
Hello, I am writing to share a recent experience with CAYA services. My daughter uses an Accent communication device. Throughout her adult life we have [...]
Our Poem about Fall Fall is… once a year. Fall feels… breezy and cold. Fall smells… nice and stinky. Fall brings… mushrooms, rainpants and Halloween. [...]
Dear Jan and Rheanne and William, Thank you for all of your assistance to Jenny and me through these four difficult years. As the ALS [...]
“For years, regional CAYA teams have hosted local, monthly communication groups. When most of us started to go virtual in 2020, we asked ourselves, what [...]
Hi, my name is Sara, and I live in Kelowna. I was diagnosed with ALS in late January 2020 after noticing that my speech was [...]