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 […]
“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 […]
“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 […]
“This Too Shall Pass” – Nathan Hello again friends, thanks for taking the time to once again visit with our interesting family adventures. The past several weeks have been good […]
“Sweet William” – Jessica Hi, my name is Jessica and my son William, who just turned 5, has Creatine Transporter Deficiency (CTD). William was born in April 2011 and as first […]
“Our Salty & Sweet Life” – Nathan Welcome to what I fully expect to be a long list of random ramblings, some of which will hopefully help someone along the […]
“A Mother’s Intuition and How One Family Never Gave Up” – Whitnie Parents have a sixth sense about their children. Call it a hunch, a gut feeling or a Mother’s/Father’s […]
“Our Journey” – Kelly When Trenton was born in New York, he weighed 7 lbs 2 ounces. Before we left the hospital, he dropped to 6lbs 12 ounces, by our […]