“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 […]
“The Happiest Person I Know” – Kyle A couple of months ago, I was asked to write a blog about having a brother with CTD. I promptly dragged my feet […]
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 […]
“Run” – Nathan Greetings again friends! While I had a post all written about expectations for this week, I just felt like this topic weighed heavier on my heart, so […]
“The Seizure Battle” – Heidi When Samantha was five, she began having absence seizures. The quick, least scary type of seizures (still scary) where she would seem to look up […]
“The One in the Middle” – Beth With the GAMT diagnosis of two of our children, our unaffected middle child immediately became the odd man out. Even my husband and I, […]
“Raising Reid” – Whitnie They say it takes a village to raise a child. I believe that to be true. If left up to me alone, I’m not sure I’d survive […]