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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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Ehlers-Danlos syndrome, Mast Cell Activation and Gastroparesis - Carter Hemion
1 of 20 Podcast
49 minutes 32 seconds
10 months ago
Ehlers-Danlos syndrome, Mast Cell Activation and Gastroparesis - Carter Hemion

Season 5, Episode 1: In Conversation with Carter Hemion

→ Who?: Carter Hemion, a trailblazing advocate in the rare disease, disability and immunocompromised spaces.

→ Rare Disease Connection: Carter is an individual living with Ehlers-Danlos syndrome, Mast Cell Activation and Gastroparesis.

→ What is Ehlers-Danlos Syndrome: Defined by the National Organization of Rare Diseases (NORD) Ehlers-Danlos syndrome (EDS) is a group of related disorders caused by different genetic defects in collagen. Collagen is one of the major structural components of the body. Collagen is a tough, fibrous, protein, and serves as a building block essential in both strengthening connective tissue (e.g. bones) and providing flexibility where needed (e.g. cartilage).

→ Where to find Carter?:

@carter_cricket

—


#RareDiseaseAwareness #FightForACure #RareButReal #InvisibleIllness #RareDiseaseCommunity #RareDiseasePodcasts #ListenToRareVoices #RareStories #PodcastForACause #RareDiseaseAwareness #PodcastLife #PodcastsToListenTo #PodcastRecommendations #PodcastCommunity #EhlersDanlosSyndrome #EDS #ChronicPain #HypermobileEDS #InvisibleIllness #MastCellActivation #MCAS #ChronicIllness #AllergySymptoms #InvisibleDisability

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!