Hope for Pdcd Foundation

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Fundraising for a cure for Pyruvate Dehydrogenase Complex Deficiency (PDCD) & advancing research for rare diseases. Collaboration and research for genetic medicine for Pyruvate Dehydrogenase Complex Deficiency. Support and fund the development of life-saving treatment for patients with pyruvate dehydrogenase complex deficiency and related genetic diseases.

Founded

2022

Facebook

1400

X (Twitter)

43

Address

Folsom

Address: 1106 Buckbrush Dr, FolsomWeb: Sign in to see organisation websiteFacebook: hopeforpdcdX (Twitter): hopeforpdcdRevenue: 426280ICO: 920361943

Hope for PDCD Foundation Accelerating Research to Cure Pyruvate Dehydrogenase Complex Deficiency No cure is not an answer. Our mission is simple to find a cure for PDCD. 1 in 40000 children is born with PDCD genetic medicine combined with standards of care small molecule therapy and early diagnosis will give them a fighting chance1. Our work will help advance research for AAV9 genetic medicine which is currently the best hope for PDCD and other neurodegenerative diseases.

News & Updates XX

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News about from their social media (Facebook and X).

Hope for Pdcd Foundation

πŸ“’ Register today. Please join us for the next community webinar. Saol Therapeutics will present information about the Sodium Dichloroacetate clinical trial for PDCD, the decision from the FDA, and what comes next for DCA.

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Vera

Absolutely on board with this mission! Fundraising and research are crucial for turning hope into reality for those affected by Pyruvate Dehydrogenase Complex Deficiency. Together, we can find that cure! πŸ™Œβœ¨ #HopeForPDCD

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Hope for Pdcd Foundation

Attention: please note the new title for our community webinar with Saol Therapeutics next week. Please also submit your questions ahead of time at the registration link. We know our community has a lot to discuss so let’s make the most of our time by submitting questions ahead of time.

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Zoe

1. What innovative fundraising strategies can NGOs implement to raise awareness and support for rare diseases like Pyruvate Dehydrogenase Complex Deficiency?

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Andrea

2. How can collaborations between patient advocacy groups and research foundations accelerate the development of treatments for genetic disorders such as PDCD?

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Terry

So inspiring to see the hope and dedication behind the Hope for PDCD Foundation! Every step taken in research brings us closer to a cure for PDCD. πŸ’™ #LetsMakeADifference

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Data about organisation

Birth Defects, Genetic Diseases Research Category

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Tax ID 46-5088936 DONATE TODAY.

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