About Hope for PDCD
Our mission is simple: to find a cure for Pyruvate Dehydrogenase Complex Deficiency. 1 in 41,138 children is born with PDCD; gene therapy will give them a fighting chance. Our work will help advance research for gene therapy, which is currently the best hope for PDCD and other neurodegenerative diseases. 100% of donations go to research, treatment, and ultimately, a cure for PDCD. Currently, Dr. Bedoyan at UPMC is completing a natural patient history study and adding PDCD to the newborn screen. In addition, the Gray Lab at UTSW is conducting a proof of concept study in mice models, but they need a surge in funding to continue their work. We are completely parent powered and run by volunteers. Not a single penny goes to overhead or salaries. We are planning to feature different families, educate our followers on rare disease statistics, and use the social media graphics provided by the Rare Disease day organization. I will also put a call out to post family photos with lights on Feb 28.