Tag Archives: creatine deficiency syndrome

“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 […]

“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).

“Warning: Rant Up Ahead” – Beth I feel like my previous entries have been thoughtful and reflective, and admittedly, very therapeutic for me. This one is a little rough around the […]

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 […]

“Spiro and I” – Janet My Creatine Transporter Deficiency journey began September 5th, 2009 with the birth of my son Spiro. Although I didn’t know it at the time, our […]