“Less Than One Percent” – Kelly I would have never guessed in a million years that I would have a child who has CTD. I mean, who has even ever […]
“Bravery” – Beth I woke up this morning with anxiety. We needed to change my daughter’s g-tube today. Through the course of treatment for GAMT, it became clear that she needed […]
“Time” – Janet Sometimes, as a parent you get sucked into the daily grind of routines and chaos. It’s life with kids. And this life and its fast-paced schedule zooms […]
Creatine Transporter Deficiency – Judith Miller, PhD By Judith Miller, PhD, and Rebecca Thomas, MA – The Children’s Hospital of Philadelphia Creatine Transporter Deficiency (CTD) – work presented at the […]
“Amazing Kids” – Nathan Greetings again friends! I hope this post finds everyone well as we move headlong into the fall season. Last month I had the opportunity to celebrate […]
“How this GAMT Dad Deals” – Jerry I recently came across an organization that, when I took a look at their mission and what they based their mission on, really resonated […]
“William’s Big School Journey” – Jess My son William (5), has CTD, and started big school for the first time this year. William has always been very passive, largely due to […]
“Meet Max” – Mikelle Meet Max. Six years ago (almost seven), my life changed when he was born. He was my first child and the most amazing gift to me […]
“Those Who ‘Get It’” – Janet My 7 year old son has CTD and Autism. He was diagnosed with CTD January 2012 and then Autism, September that same year. At […]
“Blessed to Have Her Here” – Sarah So this is my second post about Ella, who is 7 in a few weeks’ time! It’s scary how quickly they grow. In […]