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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“How Gio’s Diagnosis Affected Us” -Sylvia

Byacd_master February 1, 2024September 30, 2025

“How Gio’s Diagnosis Affected Us” –Sylvia In 2019 I was planning to have a hysterectomy due to my endometriosis, but…

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Conferences

“CCDS Seizures” – Denise Morita, MD

Byacd_master December 22, 2018October 28, 2022

“CCDS Seizures” – Denise Morita, MD Our son Dylan, who is 5 and was diagnosed with CTD earlier this year,…

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CCDS Family Stories | GAMT Deficiency

“A Boy and His Dog” – Laura

Byacd_master October 24, 2017October 27, 2022

“A Boy and His Dog” – Laura Trevor and I both grew up with dogs as family pets. We knew…

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CCDS Family Stories | Creatine Transporter Deficiency (CTD)

“Franco’s Journey” – Lisa

Byacd_master April 20, 2017October 27, 2022

“Franco’s Journey” – Lisa This is our story and our journey that led to our son’s diagnosis of CTD. It…

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CCDS Family Stories | GAMT Deficiency

“An update – 4 months on from the GAMT deficiency bombshell” – Kelly

Byacd_master March 25, 2017October 27, 2022

“An update – 4 months on from the GAMT deficiency bombshell” – Kelly If someone told me at the beginning…

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