Tag Archives: slc6A8 Deficiency

“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 […]

“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 […]

“Seasons” – Nathan Well friends, the end of summer is again upon us.  Children are heading back to school and hopefully, soon the cool air of fall will again give […]

“Oops, Sorry!” – Jess Today I am writing about one of William’s favourite phrases – “Oops, sorry!”. He is 5 and has Creatine Transporter Deficiency (CTD).