“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 […]
“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 […]
“CTD in Everyday Terms” – Sean I went to college with the intention of becoming a scientist. With that in mind, I studied biology and chemistry. While I never ended […]
“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).
GAMT Newborn Screening Update – Kim In May, the ACD met with the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC). GAMT was nominated for inclusion on the […]