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MitoCast

Hosted by Mito Foundation · health · EN-AU

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About this Podcast:

MitoCast by Mito Foundation shares clear, reliable information for people living with mitochondrial disease (mito), their families, and the wider community. Each episode takes trusted Mito Foundation resources and presents them in plain-language audio, giving you another way to learn and feel supported.All content is created by the Mito Foundation. AI tools are used only in production, helping us turn trusted resources into audio that’s accessible for more people.Subscribe wherever you get your podcasts, and stay supported, informed, and connected on your mito journey.

Pitch Analysis

Required Pod Score for this podcast. PitchCentric checks your profile against host openness, topical fit, and audience signals before you generate a pitch.

Contact path

Verified email

Booking probability

31%

Guest openness

Selective

Verified email on file
80/100
Required Score

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Questions about MitoCast

What is MitoCast about?

MitoCast by Mito Foundation shares clear, reliable information for people living with mitochondrial disease (mito), their families, and the wider community. Each episode takes trusted Mito Foundation resources and presents them in plain-language audio, giving you another way to learn and feel supported. All content is created by the Mito Foundation.

Who hosts MitoCast?

MitoCast is hosted by Mito Foundation. The show has published 26 episodes to date.

What has MitoCast covered recently?

Recent episodes include "Let's talk TK2d" (30 August 2026, 24 minutes), "Let's talk ADOA" (24 August 2026, 21 minutes), and "Let’s talk NARP" (21 June 2026, 33 minutes).

How often does MitoCast publish?

MitoCast publishes roughly every two weeks, with episodes averaging 23 minutes across 26 episodes.

How hard is it to get booked on MitoCast?

Booking probability for MitoCast is 31%, and the host is rated Selective on guests. MitoCast requires a Pod Score of 80 or higher. MitoCast's contact route on record: verified email.

Who should pitch MitoCast?

The strongest fits for MitoCast are Health & Wellness Services. MitoCast has a health audience.

About the host

Mito Foundation hosts MitoCast, a health podcast with 26 episodes published.

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Recent episodes

Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

  • Episode #10

    Let's talk TK2d

    Aug 30, 202624 minS3

    Thymidine kinase 2 deficiency , or TK2d, is a rare type of mitochondrial disease that mainly affects the muscles and can impact movement, swallowing, speech and breathing. Symptoms can begin in infancy or childhood, but...

  • Episode #9

    Let's talk ADOA

    Aug 24, 202621 minS3

    Autosomal dominant optic atrophy , or ADOA, is a rare inherited condition that affects the optic nerves and can lead to gradual changes in vision. It is one of at least 350 known types of mitochondrial disease. In this...

  • Jun 21, 202633 minS3

    Neurogenic weakness with Ataxia and Retinitis Pigmentosa, also known as NARP, is a rare type of mitochondrial disease, mito for short. It affects mitochondria, the parts of our cells that make energy, and it commonly...

  • Jun 7, 202643 minS3

    Leigh syndrome, sometimes called Leigh’s disease, is a rare type of mitochondrial disease, mito for short. It mainly affects the brain, nervous system and muscles, and it can also impact things like vision, hearing...

  • May 24, 202636 minS3

    Myoclonic epilepsy and ragged-red fibres, or MERRF, is a rare type of mitochondrial disease (mito). It most often affects the brain, nerves and muscles. Signs and symptoms usually begin in late adolescence through...

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  • May 10, 202643 minS3

    Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, or MELAS, is a rare type of mitochondrial disease, mito for short. MELAS most often impacts the brain and muscles, and it can also affect things...

  • Episode #3

    Let's talk LHON

    Apr 26, 202647 minS3

    Leber hereditary optic neuropathy, or LHON, is a rare type of mitochondrial disease, mito for short. LHON most often affects central vision. In this episode, we talk through what LHON can look like in everyday life...

  • Episode #2

    Let's talk KSS

    Apr 12, 202635 minS3

    Kearns–Sayre syndrome, or KSS, is a rare type of mitochondrial disease, mito for short. It usually starts before the age of 20. KSS often affects the muscles around the eyes. It can also affect the back of the eye...

  • Mar 29, 202648 minS3

    Chronic progressive external ophthalmoplegia, or CPEO, is a type of mitochondrial disease (mito) that most often affects the muscles around the eyes. Some people only have eye symptoms. Others may also have things like...

  • Mar 15, 202611 minS2

    This episode shares key tips from Dr Shanti, a metabolic geneticist. She explained why regular checks help people with mito stay safe and supported. Main points: Check hearing, heart and eyes often. Check vitamin levels...

  • Mar 1, 202610 minS2

    This episode shares key points from Dr Isabelle Adant, a paediatrician and metabolic fellow who supports people living with mito. She explained simple ways food can help with energy, muscles, bones and gut comfort. Her...

  • Feb 27, 202613 min

    Momentum in mitochondrial disease (mito) research is building, and this episode brings you the February Mito Community Newsletter in a clear, listener-friendly way, from progress in clinical studies and approvals, to...

  • Feb 15, 202613 minS2

    This episode shares updates from Dr Serge Geara, neurologist and mito fellow at NeuRA. He explained why mito is hard to treat and what new research is happening. Key points: New treatments like elamipretide, BIO101...

  • Feb 4, 20268 min

    From advocacy and research to practical supports, this episode shares the key updates shaping the year ahead for the mito community. In this episode, we walk through highlights from the January community newsletter...

  • Feb 1, 202612 minS2

    This episode shares key points from a panel led by Clare Stuart, with speakers Lani Quirk, Jessica Stevenson, Dr Sebastian Lush and Monique Alves. They explained how trials work and what they mean for people living with...

  • Jan 18, 202612 minS2

    This episode shares key points from Dr Christina Liang, a neurologist who supports people living with mito. She explained what we know about supplements, what we don’t know yet, and how to make safe choices. Her main...

  • Dec 21, 202514 minS1

    Living with mito means looking after your whole self — your body, your relationships, and your mind. This episode explores how mental health and wellbeing are part of that balance. It covers simple, practical ways to...

  • Dec 14, 20257 min

    This episode gives you an overview of the key updates from Mito Foundation’s November newsletter. We touch on global progress in new treatments, early steps in mitochondrial donation, highlights from the Mito Community...

  • Dec 7, 202517 minS1

    Exercise can help your body make and use energy more efficiently. But knowing where to start can be tricky. In this episode, we talk about how movement supports your mitochondria, ways to begin safely, and tips to make...

Recent guests

Recent guests on MitoCast. Study who booked and why before you pitch.

M

Monique Alves

D

Dr Isabelle Adant

Mito Foundation

D

Dr Serge Geara

NeuRA

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