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 […]
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 […]
“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 […]