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occupational therapy

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

Boy pointing to a word on the white board in school.
CCDS Family Stories

“Obtain, Maintain, Sustain” – Regina

Byacd_master February 14, 2019October 8, 2025

“Obtain, Maintain, Sustain” – Regina Immediately following Caiden’s birth, we knew he was facing many struggles. We had a lot…

Read More “Obtain, Maintain, Sustain” – ReginaContinue

CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“A Day in the Life” – Amy

Byacd_master August 26, 2017October 27, 2022

“A Day in the Life” – Amy I thought it would be beneficial to share a profile of our four,…

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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 | 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…

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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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