“Blessed to Have Her Here” – Sarah
“Blessed to Have Her Here” – Sarah So this is my second post about Ella, who is 7 in a…
“CTD in Everyday Terms” – Sean
“CTD in Everyday Terms” – Sean I went to college with the intention of becoming a scientist. With that in…
“Oops, Sorry!” – Jess
“Oops, Sorry!” – Jess Today I am writing about one of William’s favourite phrases – “Oops, sorry!”. He is 5…
“Warning: Rant Up Ahead” – Beth
“Warning: Rant Up Ahead” – Beth I feel like my previous entries have been thoughtful and reflective, and admittedly, very…
“The Happiest Person I Know” – Kyle
“The Happiest Person I Know” – Kyle A couple of months ago, I was asked to write a blog about…
GAMT Newborn Screening Update – Kim
GAMT Newborn Screening Update – Kim In May, the ACD met with the Advisory Committee on Heritable Disorders in Newborns…
“Spiro and I” – Janet
“Spiro and I” – Janet My Creatine Transporter Deficiency journey began September 5th, 2009 with the birth of my son…
“Run” – Nathan
“Run” – Nathan Greetings again friends! While I had a post all written about expectations for this week, I just…
“The Seizure Battle” – Heidi
“The Seizure Battle” – Heidi When Samantha was five, she began having absence seizures. The quick, least scary type of…
“The One in the Middle” – Beth
“The One in the Middle” – Beth With the GAMT diagnosis of two of our children, our unaffected middle child…