Rare Connection

Rare Connection Episode 4: Pyruvate Dehydogenase Defiecency (PDCD)

April 07, 2024 Joanna
Rare Connection Episode 4: Pyruvate Dehydogenase Defiecency (PDCD)
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Rare Connection
Rare Connection Episode 4: Pyruvate Dehydogenase Defiecency (PDCD)
Apr 07, 2024
Joanna

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In this episode I talk with Layna (parent and advocate with Hope for PDCD https://www.hopeforpdcd.org/) .  PDCD is a inherited metabolic condition that has to do with Carbohydrate metabolism.  They follow the Keto diet.  Layna is responsible for fundraising, education, social media, education, and advocacy.  She has a youtube channel of her own https://www.youtube.com/@laynaoconnor5382 You can donate to Hope for PDCD with the link above.  In addition to being a leader with Hope for PDCD, she is also a parent of a child (Piper) who has PDCD.  

Listen as we talk to Latna about her piper's story and how she was diagnosed,as well as her role with Hope for PDCD and other tools that may be helpful if you are a parent of someone with PDCD or have it yourself.  Most die before they reach adulthood or are severly disabled unfortunately.  

This like all other episodes are originally filmed on YouTube Live and transfered to buzzsprout who then transfers them to other podcasting stations.  This can take up to 24 hours.  They are also posted to Linkedin, Facebook, X, and later turned into shorts for TikTok, and YouTube.  


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Send us a Text Message.

In this episode I talk with Layna (parent and advocate with Hope for PDCD https://www.hopeforpdcd.org/) .  PDCD is a inherited metabolic condition that has to do with Carbohydrate metabolism.  They follow the Keto diet.  Layna is responsible for fundraising, education, social media, education, and advocacy.  She has a youtube channel of her own https://www.youtube.com/@laynaoconnor5382 You can donate to Hope for PDCD with the link above.  In addition to being a leader with Hope for PDCD, she is also a parent of a child (Piper) who has PDCD.  

Listen as we talk to Latna about her piper's story and how she was diagnosed,as well as her role with Hope for PDCD and other tools that may be helpful if you are a parent of someone with PDCD or have it yourself.  Most die before they reach adulthood or are severly disabled unfortunately.  

This like all other episodes are originally filmed on YouTube Live and transfered to buzzsprout who then transfers them to other podcasting stations.  This can take up to 24 hours.  They are also posted to Linkedin, Facebook, X, and later turned into shorts for TikTok, and YouTube.  


Support the Show.

Pyruvatt Dehydrogenase Complex deficiency diagnosis
PDCD VS Diabetes
challenges
initiatives and impact
symptoms and and manifestations
Medical formula
emotional toll and careiving for a child with PDCD
education and awareness
education and awareness
advancements and developments in research
advice for parents