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1 of 20 Podcast
Jonathan Cappiello
53 episodes
6 days ago
Jonathan Cappiello was diagnosed with a rare genetic disorder that only 20 people in the world have. The condition is called 3 hydroxyacyl coa synthase deficiency, which in short compromises his immune system and his body cannot process fats. Each week, he will discuss his lifestyle, his diet, and how he adapted to his condition. Additionally, he has a variety of guests to talk about their conditions. If you’re interested in genetics, rare disorders, medicine, and healthy living-- this is the podcast for you!
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Medicine
Health & Fitness
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Jonathan Cappiello was diagnosed with a rare genetic disorder that only 20 people in the world have. The condition is called 3 hydroxyacyl coa synthase deficiency, which in short compromises his immune system and his body cannot process fats. Each week, he will discuss his lifestyle, his diet, and how he adapted to his condition. Additionally, he has a variety of guests to talk about their conditions. If you’re interested in genetics, rare disorders, medicine, and healthy living-- this is the podcast for you!
Show more...
Medicine
Health & Fitness
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MECP2 Duplication syndrome - Natalia Cordero
1 of 20 Podcast
29 minutes 28 seconds
6 months ago
MECP2 Duplication syndrome - Natalia Cordero
  • Season 5, Episode 11: In conversation with Natalia Cordero

    → Who?: Natalia Cordero is a rare disease mom, advocate, and podcast host. She started in Dylan's world, a space for medical families to get information about grants in Georgia, resources, events, recommendations, and more all in one place. Additionally, she Co-Hosts the Medical Momma Drama podcast, where she and her co-host Jen, talk about the challenges and victories of being Mommas of special needs children. Join them as they share personal stories, learning moments, and the experience they've gained through the drama of being a medical momma.

    → Rare Disease Connection: Natalia is the mom and caregiver to Dylan, who has MECP2 duplication syndrome.

    → What is MECP2 duplication syndrome?: MECP2 duplication syndrome is a condition that occurs almost exclusively in males and is characterized by moderate to severe intellectual disability. Most people with this condition also have weak muscle tone in infancy, feeding difficulties, poor or absent speech, or muscle stiffness (rigidity). Individuals with MECP2 duplication syndrome have delayed development of motor skills such as sitting and walking. 

    → Where to find Natalia?:

    @imnataliacordero_
    @medicalmommadrama

    https://www.indylansworld.org/ 


    #RareDiseaseAwareness #FightForACure #RareButReal #InvisibleIllness #RareDiseaseCommunity #RareDiseasePodcasts #ListenToRareVoices #RareStories #RareDiseaseAwareness #PodcastLife #PodcastsToListenTo #PodcastRecommendations #PodcastCommunity #MECP2 #Neurogenetics #GeneticResearch #RareDiseaseAwareness

  • 1 of 20 Podcast
    Jonathan Cappiello was diagnosed with a rare genetic disorder that only 20 people in the world have. The condition is called 3 hydroxyacyl coa synthase deficiency, which in short compromises his immune system and his body cannot process fats. Each week, he will discuss his lifestyle, his diet, and how he adapted to his condition. Additionally, he has a variety of guests to talk about their conditions. If you’re interested in genetics, rare disorders, medicine, and healthy living-- this is the podcast for you!