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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“Are You a 21st Century Pioneer?” – Nancy

Byacd_master September 2, 2020September 30, 2025

“Are You a 21st Century Pioneer?” – Nancy Pioneer. Verb. A person who is among the first to develop or…

Read More “Are You a 21st Century Pioneer?” – NancyContinue

Man running in a race.
CCDS Family Stories

“IRONMAN Lake Placid Recap” – Jerry

Byacd_master August 7, 2019October 15, 2025

“IRONMAN Lake Placid Recap” – Jerry My fourth Ironman is in the books. Lake Placid, New York is a beautiful place…

Read More “IRONMAN Lake Placid Recap” – JerryContinue

“The Paradox of an Aging Special Needs Child” – Beth
CCDS Family Stories | GAMT Deficiency

“The Paradox of an Aging Special Needs Child” – Beth

Byacd_master March 26, 2019October 8, 2025

The Paradox of an Aging Special Needs Child” – Beth Standing in front of my kitchen sink in the cold,…

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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

Parents and son in a field with a red tractor behind them.
CCDS Family Stories

“WHO’S GOING TO PROTECT HIM WHEN I’M GONE?” – Nancy

Byacd_master March 5, 2019October 8, 2025

“WHO’S GOING TO PROTECT HIM WHEN I’M GONE?” – Nancy Over-protective. Controlling. Helicopter Mom. Whatever you call it, that’s who…

Read More “WHO’S GOING TO PROTECT HIM WHEN I’M GONE?” – NancyContinue

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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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“The Long and Winding Road” – Amy

Byacd_master May 24, 2017October 27, 2022

“The Long and Winding Road” – Amy Not having a diagnosis for your child when you know something is wrong…

Read More “The Long and Winding Road” – AmyContinue

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…

Read More “The More Things Change…” – NathanContinue

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…

Read More “1% Chance” – LauraContinue

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…

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

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