Tag Archives: GAMT

“On Valentine’s Day” – Nathan Well, it’s here friends, February 14th , and according to the automatic reminder on my phone, that means it is time to stop at the […]

“My little guy” – Jane My little guy is now 8 years old and was diagnosed with Creatine Transporter Deficiency (CTD) at 19 months of age – well before we […]

“The Three P’s” – Beth My husband likes tattoos.  Really likes them.  I do not have one spot of ink on my body.  An indecisive person like myself is not […]

“Five Years… Then and Now” – Janet When my son Spiro was first diagnosed with CTD, I thought it would mean better management, a quick fix, and a real turn […]

“Levi” – Laura My name is Levi. I am 5 years old and ALL boy. I love everything life has to offer me. I am an easy going, BUSY, happy, […]

“Our Gifts” – Nathan Happy New Year friends! Have you made your resolutions yet? To be honest I don’t do resolutions, I plan for contributions. So, with that in mind, […]

“Strongest Kids God Created” – Sarah I thought this post I would write about some of the things I guess us parents all go through, at some point or other. […]

“Asking for Help” – Beth I broke my arm about two months ago. I’m 41 and I tried to ride a skateboard. It didn’t work out. It seemed like a […]

“CTD Workshop Recap” – Whitnie When they say Paris is magical, it’s true. The ACD was honored to attend the CTD workshop, organized by Dr. Aurore Curie, Dr. Vincent des […]