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Association for Creatine Deficiencies

Q&A With Dr. Ton DeGrauw— New Board Member

Byacd_master March 23, 2019December 5, 2022

Q&A With Dr. Ton DeGrauw— New Board Member The Association for Creatine Deficiencies (ACD) welcomes Dr. Ton DeGrauw as part…

Read More Q&A With Dr. Ton DeGrauw— New Board MemberContinue

Beth with Jerry and Benny at birth
CCDS Family Stories | GAMT Deficiency

“Picturing the Future” – Beth

Byacd_master January 15, 2018October 15, 2025

“Picturing the Future” – Beth During the winter break, we undertook the daunting task of organizing digital photos from the…

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Sawyer in hospital bed
CCDS Family Stories | GAMT Deficiency

“What Are the Odds?” – Laura

Byacd_master August 19, 2017October 15, 2025

“What Are the Odds?” – Laura GAMT is really, really, rare. We all know that! I am sure quite a…

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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“Getting Better” – Amy

Byacd_master July 6, 2017October 27, 2022

“Getting Better” – Amy Ben’s recent Creatine Transporter Deficiency (CTD) diagnosis has hit me hard emotionally, so I thought that…

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Kelly and Toby sticking out his tongue with a lollipop
CCDS Family Stories | GAMT Deficiency

“What About Me?” – Kelly

Byacd_master May 29, 2017October 15, 2025

“What About Me?” – Kelly I’ve made no secret that our family life is somewhat different from the norm. Our…

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CCDS Family Stories | GAMT Deficiency

“Travel Supplements” – Laura

Byacd_master May 27, 2017October 27, 2022

“Travel Supplements” – Laura We recently returned from a very fun and needed vacation to Disneyland! It was magical with…

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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“The More Things Change…” – Nathan

Byacd_master May 9, 2017October 27, 2022

“The More Things Change…” – Nathan Greetings friends! Well, it is that time again as I am once more honored…

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Young Levi on a scoot along toy
CCDS Family Stories | GAMT Deficiency

“1% Chance” – Laura

Byacd_master February 23, 2017October 15, 2025

“1% Chance” – Laura GAMT is so rare, just getting diagnosed seems to be quite an ordeal. I like hearing…

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Isaac Sitting on Holly's Lap
CCDS Family Stories | GAMT Deficiency

“Why Getting a Diagnosis Is So Much More Than a Label” – Kelly

Byacd_master February 17, 2017October 15, 2025

“Why Getting a Diagnosis Is So Much More Than a Label” – Kelly My daughter Holly (9) & son Isaac…

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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“On Valentine’s Day” – Nathan

Byacd_master February 14, 2017October 26, 2022

“On Valentine’s Day” – Nathan Well, it’s here friends, February 14th , and according to the automatic reminder on my…

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