Kelly
mother of 3 year old Kate with Angelman Syndrome
I am the mother of a 3 year old girl named Kate. Kate has a severe disability called Angelman Syndrome, which makes it difficult for Kate to walk, talk and learn. It’s a hard diagnosis and hard to accept, but Kate has taught me a lot of things I never understood before.
Being a parent, I just love my child and want to do right by her. I have searched desperately for the “right” therapy that matches Kate’s needs and personality. We’ve tried intense physiotherapy, CME, and ABM with Judy.
We have observed that Kate hits major developmental milestones after her ABM sessions with Judy, the biggest being her transitions in and out of sitting.
Judy is calm, understanding, reassuring, caring and a wonderful therapist. Our Kate trusts Judy and enjoys her sessions immensely. Even our golden retriever loves a mini ABM session with Judy!
Judy has become a part of our family and an integral member of Kate’s “team” and success! We’d be lost without her!
