🧠 Thank you, @frontiersin.bsky.social! We’re excited to share this peer-reviewed article on efforts to accelerate diagnosis & develop treatments for Creatine Transporter Deficiency.

🔗 Read here: tr.ee/aJQy6V

#CreatineResearch #ACDResearch #RareDisease

CTD dad, Jeff Allen, sat down with The Iced Coffee Hour to give a behind-the-scenes look at his experience on Beast Games! 🏆🔥

Catch the interview: tr.ee/S2pLKc

#CreatineHeroes #CreatineInfo #CreatineResearch #ACDResearch #RareDiseaseAwareness #RareDisease #Ruck4Rare #IceCoffeeHour

📢 Community Chat!
🗓 Friday, March 7th | 3 PM EST
Topic: Creatine Deficiency - Diagnosis, Inheritance, & Mosaicism - Your Questions Answered
Speakers: Dr. Sarah Young & Jenny Goldstein

📌 Register: creatineinfo.org/chat-series

#FuelingHope #CreatineInfo #CreatineResearch #ACDResearch #RareDisease

Save the Date!
ACD’s annual Walk for Strength is back on June 21, 2025.

🚨 Start your team today! It’s easy-we’ll support you every step of the way from now until June. Sign up here: www.creatineinfo.org/walk

#FuelingHope #CreatineHeroes #CreatineResearch #ACDResearch #RareDisease #WalkForStrength

CCDS Day 2025 Our Hopes for a Treatment. Our hope is that a treatment for Xavier would allow him to bathe and use the toilet independently, so he could do more activities that typical teens can do.

#CCDSDay #FuelingHope #CreatineDeficiencyResearch #CreatineHeroes #CreatineInfo #CreatineResearch #ACDResearch #RareDiseaseAwareness #RareDisease