Who hosts Let’s talk about epilepsy?

Let’s talk about epilepsy is hosted by Young Epilepsy. They have published 19 episodes. The show covers health, with a fitness focus.

What has Let’s talk about epilepsy covered recently?

Recent episodes include "Harder to manage epilepsy: moving into adult healthcare", "Venting", and "Harder to Manage Epilepsy: Could VNS Therapy Help?". The latest went out on 9 Sep 2026 and ran about 51 minutes. These are from season 2. Reading two or three of these before pitching is the fastest way to see what the show actually books.

How often does Let’s talk about epilepsy publish?

Let’s talk about epilepsy publishes every couple of weeks, a median of 18 days between episodes. Episodes average about 50 minutes. The back catalogue stands at 19 episodes. A show on this cadence plans ahead, so pitch earlier rather than closer to the date you want.

How hard is it to get booked on Let’s talk about epilepsy?

For Let’s talk about epilepsy, Booking Probability sits at 29/100, Listen Score at 18/100, and the guest bar is around 80/100. The show has not signalled guest openness recently, which raises the bar on relevance. A verified contact is on file.

Who should pitch Let’s talk about epilepsy?

Let’s talk about epilepsy covers epilepsy, mental health, support, childhood epilepsy, so guests who can speak to those specifically fit best. The show carries an audience score of 11/100 and 5,860 YouTube subscribers. Lead with a specific result you can describe in numbers rather than a job title, and tie it to something the show has already covered.

health

Let’s talk about epilepsy

Q: What is Let’s talk about epilepsy about?

Welcome to, Let’s Talk about Epilepsy - your podcast to hear real stories, expert insights, and honest conversations about life with epilepsy. It is listed as a health show, with a fitness focus.

Hosted by Young Epilepsy · health · EN · 19 episodes

Audience: 11~5.9k on YouTube

Apple Podcasts Website

About this Podcast:

Welcome to —Let’s Talk about Epilepsy - your podcast to hear real stories, expert insights, and honest conversations about life with epilepsy. Whether you’re living with epilepsy, supporting a young person who is, or just want to understand more, we’re here to help you feel informed, empowered, and connected. We bring together the voices that matter—young people, families, and experts—to share experiences, tackle challenges, and celebrate wins. Tune in and be part of something bigger!

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Contact path

Verified email

Booking probability

29%

Guest openness

Selective

Verified email on file

80/100

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What is Let’s talk about epilepsy?

Let’s talk about epilepsy is a health podcast hosted by Young Epilepsy, with 19 episodes on record and a Required Pod Score of 80.

About the host

Young Epilepsy hosts Let’s talk about epilepsy, a health show with 19 episodes published.

Verified host email: ████████@████.comSign in to unlock →

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 #8
Harder to manage epilepsy: moving into adult healthcare
Sep 8, 202651 minS2
In this episode of the Young Epilepsy Podcast, we explore the transition from children’s to adult services for young people with harder-to-manage epilepsy. Host Joe Paternoster, Assistant Psychologist at Young Epilepsy, is joined by Neil Williamson, Safeguarding Trustee at Dravet Syndrome UK and former children’s epilepsy nurse; Nicky Heenan, Children’s Neurology Nurse and joint lead on the transition section of the NHS England Epilepsy Bundle of Care; and Denise Murphy, whose daughter Lucy has Dravet syndrome. Together, they discuss what a good transition should look like, why families can encounter gaps between children’s and adult care, and how early planning, clear information and the right professional support can make a difference. Denise also shares her family’s experience of navigating specialist healthcare, funding and supported independent living. Whether you’re a young person preparing to move into adult services, a parent or carer supporting someone with complex needs, or a professional involved in transition planning, this episode offers practical information and lived experience to help you prepare. NOTICE: Epilepsy is a highly individualised condition. The information, experiences and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice. Always consult a qualified healthcare provider for personalised support. If you’re feeling sad, worried or lonely, text ‘PURPLE’ to 85258 to start a conversation with Shout. More information: Shout | Support Service for Young Epilepsy Support and signposting If you’re preparing to move from children’s to adult services, these resources offer further information and support: Epilepsy transition booklets: Includes resources for teenagers, Easy Read versions and booklets for parents of young people with additional needs: https://www.youngepilepsy.org.uk/blog/young-voices-shape-nhs-transition-booklets Contact’s Preparing for adult life guidance: Important information for families supporting young people with complex or additional needs, including planning, mental capacity, benefits, health and social care, housing and independent living: https://contact.org.uk/help-for-families/information-advice-services/preparing-for-adult-life/ NHS continuing healthcare: Information about eligibility, assessments and NHS-funded support for adults with long-term complex health needs: https://www.nhs.uk/social-care-and-support/money-work-and-benefits/nhs-continuing-healthcare/ SCN1A/ Horizons Natural History Study: Information about research involving people with Dravet syndrome and other SCN1A-related epilepsies: https://www.dravet.org.uk/healthcare-professionals/insight-articles/article-scn1a-horizons-natural-history-study/ National Hospital for Neurology and Neurosurgery at Chalfont: Information about its specialist epilepsy services: https://www.uclh.nhs.uk/our-services/our-hospitals/national-hospital-neurology-and-neurosurgery/NHNN-chalfont Follow Young Epilepsy: Facebook: http://facebook.com/YoungEpilepsy Instagram: https://www.instagram.com/youngepilepsy/ YouTube: https://www.youtube.com/user/youngepilepsy LinkedIn: https://www.linkedin.com/company/young-epilepsy/ TikTok: https://www.tiktok.com/@youngepilepsy
Listen Show Notes
Episode #19
Venting
Aug 18, 20260 min
What really frustrates young people about living with epilepsy? In this honest and unfiltered episode of Let's Talk About Epilepsy, host Cam is joined by members of Young Epilepsy's Youth Voice Network: Hattie, Sophie and Spike. Together, they create a safe space to vent about the realities of living with epilepsy and the challenges that often go unseen. From lack of understanding in schools and workplaces to navigating friendships, dating, independence and public transport, the conversation shines a light on the barriers, misconceptions and frustrations that many young people with epilepsy face every day. Our guests share personal experiences of being excluded from activities, struggling to access the right support, managing medications, dealing with stigma, and fighting for their voices to be heard. They also discuss the importance of good support networks, self-advocacy and connecting with others who understand what life with epilepsy is really like. While some of the topics discussed are challenging, this episode is full of humour, resilience and encouragement for other young people living with epilepsy. ⚠️ Trigger warning: This episode contains discussion of seizures, discrimination, mental wellbeing challenges, medication side effects and SUDEP (Sudden Unexpected Death in Epilepsy). NOTICE: Epilepsy is a highly individualised condition. The information, experiences, and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice. Always consult a qualified healthcare provider for personalised support. If you’re feeling sad, worried, or lonely, text ‘PURPLE’ to 85258 to start a conversation with Shout. More info: https://www.youngepilepsy.org.uk/shout Support and signposting Information about epilepsy: https://www.youngepilepsy.org.uk/about-epilepsy Youth Voice Network: https://www.youngepilepsy.org.uk/get-involved/youth-voice-network Support for young people and families: https://www.youngepilepsy.org.uk/support-and-services The Channel - A space for young people, aged 13+, who are living with epilepsy, for them to share, learn and find support: https://www.youngepilepsy.org.uk/i-have-epilepsy/the-channel Follow Young Epilepsy: Facebook: http://facebook.com/YoungEpilepsy Instagram: https://www.instagram.com/youngepilepsy/ YouTube: https://www.youtube.com/user/youngepilepsy LinkedIn: https://www.linkedin.com/company/young-epilepsy/ TikTok: https://www.tiktok.com/@youngepilepsy
Listen Show Notes
Episode #18
Harder to Manage Epilepsy: Could VNS Therapy Help?
Jul 21, 202633 min
In this episode of the Young Epilepsy Podcast, we explore Vagus Nerve Stimulation (VNS) therapy and how it can help children and young people with harder to manage epilepsy. Host Kirsten McHale, Head of Healthcare at Young Epilepsy, is joined by Dr Das, Paediatric Consultant Neurologist at Great Ormond Street Hospital, and Hattie, a member of the Youth Voice Network who has been living with a VNS device for several years. Together, they explain how VNS works, who it might be suitable for, and what life is really like with the device. Whether you're considering VNS therapy yourself, supporting a young person with epilepsy, or simply want to understand more about treatment options, this episode provides expert information alongside real-life experience. NOTICE: Epilepsy is a highly individualised condition. The information, experiences, and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice. Always consult a qualified healthcare provider for personalised support. If you’re feeling sad, worried, or lonely, text ‘PURPLE’ to 85258 to start a conversation with Shout. More info: https://www.youngepilepsy.org.uk/shout Support and signposting If you'd like to learn more about VNS therapy or other treatment options for epilepsy: Visit the Young Epilepsy website for trusted information and support: https://www.youngepilepsy.org.uk/about-epilepsy/treatments Find out more about Young Epilepsy Youth Support: https://www.youngepilepsy.org.uk/what-we-do/support-inclusion/youth-support Join the Youth Voice Network: https://www.youngepilepsy.org.uk/youth-voice-network Follow Young Epilepsy: Facebook: http://facebook.com/YoungEpilepsy Instagram: https://www.instagram.com/youngepilepsy/ YouTube: https://www.youtube.com/user/youngepilepsy LinkedIn: https://www.linkedin.com/company/young-epilepsy/ TikTok: https://www.tiktok.com/@youngepilepsy
Listen Show Notes
Episode #5
Hear Her Voice 2026 – Exploring the impact of epilepsy on women and girls
Jun 30, 20261h 23mS2
PLEASE NOTE: Epilepsy is a highly individualised condition, and each person’s experience can vary significantly. The information, experiences, and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider for personalised medical advice and support tailored to your specific needs. ⚠️ Please proceed with care: This episode discusses SUDEP (Sudden Unexpected Death in Epilepsy) and includes references to bereavement and loss, which may be distressing for some listeners. For more information: https://www.youngepilepsy.org.uk/about-epilepsy/sudden-unexpected-death-in-epilepsy-sudep If you’re feeling sad, worried or lonely, text the word ‘PURPLE’ to 85258 to start a conversation with Shout. More info: Shout support service: https://www.youngepilepsy.org.uk/shout/ In this special live episode, actress and Young Epilepsy supporter Ellie Henry and broadcaster Jennie Gow host a series of powerful conversations bringing together women, young people and families to share their experiences of epilepsy. We hear deeply personal stories from Young Epilepsy ambassador Sam Bailey and autism and epilepsy advocate Holly Steer, who open up about the reality of supporting children with epilepsy, from diagnosis to navigating complex needs and daily life. The conversation continues with young people sharing their own journeys. Youth Voice Network member Elina reflects on growing up with epilepsy and the pressures of feeling different, while Olivia speaks about independence, education and managing epilepsy through key life milestones. In a powerful mothers’ panel, Nicole Ronson Allalouf, Clare Scheckter and Emma O’Brien share honest and emotional accounts of caring for children with complex epilepsy, highlighting the challenges families face across healthcare, education and wider support systems. Throughout the episode, we explore the emotional realities of epilepsy, the importance of being heard, and the strength that comes from shared experience and community. Hear Her Voice centres the voices of women and girls living with epilepsy and shows just how impactful it can be when those voices are heard. ________________________________________ Useful Links: Young Epilepsy website: https://www.youngepilepsy.org.uk/ SUDEP information: https://www.youngepilepsy.org.uk/about-epilepsy/sudden-unexpected-death-in-epilepsy-sudep Information about epilepsy: https://www.youngepilepsy.org.uk/about-epilepsy Youth Voice Network: https://www.youngepilepsy.org.uk/youth-voice-network Young Epilepsy Youth Support Services: https://www.youngepilepsy.org.uk/youth-support ________________________________________ Social Media: Facebook: https://www.facebook.com/YoungEpilepsy/ Instagram: https://www.instagram.com/youngepilepsy/ YouTube: https://www.youtube.com/young%20epilepsy LinkedIn: https://www.linkedin.com/company/young-epilepsy/ TikTok: https://www.tiktok.com/@youngepilepsy Spotify: https://open.spotify.com/show/0Rd6NvABed0T1gvQGYju0x?si=ddb31e5b7a774664 Contact: communications@youngepilepsy.org.uk
Listen Show Notes
Episode #17
Brain Surgery: Harder to Manage Epilepsy
Jun 2, 202625 minS0
In this episode, host Dr Lara Carr is joined by Professor Helen Cross and Tanisha from the Youth Voice Network to talk about epilepsy brain surgery. They explain when surgery might be considered, what the process involves, and how it can change a young person’s life, alongside real reassurance and support for families. NOTICE: Epilepsy is a highly individualised condition. The information, experiences, and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice. Always consult a qualified healthcare provider for pe...
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Guest Appearances

Recent guests on Let’s talk about epilepsy. Study who booked and why before you pitch.

Chris McCarthy

Fractional Chief Marketing Officer for Ecommerce Stores

Mark Richardson

business consultant, author and leader in the remodeling industry, New England Botanic Garden at Tower Hill

Nicky Heenan

NHS England

Neil Williamson

Dravet Syndrome UK

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Episode #8

Harder to manage epilepsy: moving into adult healthcare

Sep 8, 202651 minS2

In this episode of the Young Epilepsy Podcast, we explore the transition from children’s to adult services for young people with harder-to-manage epilepsy. Host Joe Paternoster, Assistant Psychologist at Young Epilepsy, is joined by Neil Williamson, Safeguarding Trustee at Dravet Syndrome UK and former children’s epilepsy nurse; Nicky Heenan, Children’s Neurology Nurse and joint lead on the transition section of the NHS England Epilepsy Bundle of Care; and Denise Murphy, whose daughter Lucy has Dravet syndrome. Together, they discuss what a good transition should look like, why families can encounter gaps between children’s and adult care, and how early planning, clear information and the right professional support can make a difference. Denise also shares her family’s experience of navigating specialist healthcare, funding and supported independent living. Whether you’re a young person preparing to move into adult services, a parent or carer supporting someone with complex needs, or a professional involved in transition planning, this episode offers practical information and lived experience to help you prepare. NOTICE: Epilepsy is a highly individualised condition. The information, experiences and views shared in this podcast may not reflect those of Young Epilepsy and are not intended to replace professional medical advice. Always consult a qualified healthcare provider for personalised support. If you’re feeling sad, worried or lonely, text ‘PURPLE’ to 85258 to start a conversation with Shout. More information: Shout | Support Service for Young Epilepsy Support and signposting If you’re preparing to move from children’s to adult services, these resources offer further information and support: Epilepsy transition booklets: Includes resources for teenagers, Easy Read versions and booklets for parents of young people with additional needs: https://www.youngepilepsy.org.uk/blog/young-voices-shape-nhs-transition-booklets Contact’s Preparing for adult life guidance: Important information for families supporting young people with complex or additional needs, including planning, mental capacity, benefits, health and social care, housing and independent living: https://contact.org.uk/help-for-families/information-advice-services/preparing-for-adult-life/ NHS continuing healthcare: Information about eligibility, assessments and NHS-funded support for adults with long-term complex health needs: https://www.nhs.uk/social-care-and-support/money-work-and-benefits/nhs-continuing-healthcare/ SCN1A/ Horizons Natural History Study: Information about research involving people with Dravet syndrome and other SCN1A-related epilepsies: https://www.dravet.org.uk/healthcare-professionals/insight-articles/article-scn1a-horizons-natural-history-study/ National Hospital for Neurology and Neurosurgery at Chalfont: Information about its specialist epilepsy services: https://www.uclh.nhs.uk/our-services/our-hospitals/national-hospital-neurology-and-neurosurgery/NHNN-chalfont Follow Young Epilepsy: Facebook: http://facebook.com/YoungEpilepsy Instagram: https://www.instagram.com/youngepilepsy/ YouTube: https://www.youtube.com/user/youngepilepsy LinkedIn: https://www.linkedin.com/company/young-epilepsy/ TikTok: https://www.tiktok.com/@youngepilepsy

Listen Show Notes

Every question we get asked before
someone starts their trial.

If you have a concern about deliverability, AI quality, data privacy, or whether this will actually work for your specific situation, it's probably answered below.

What is the difference between Founder Solo and Founder Pro?

How do agency tiers work?

What is a talent profile?

Can I switch plans later?

Yes, at any time. Upgrades take effect immediately; downgrades apply at the end of the current billing period. Contact support if you need help migrating between plan families.

Do you offer a free trial?

Every paid plan includes a 15-day free trial. Your card is saved at signup but you will not be charged until day 16. Cancel any time from your dashboard.

What happens if I cancel?

You keep access until the end of your current billing period. No charges after that. Your data is retained for 30 days in case you reactivate.

Is the 20% annual discount automatic?

Yes. Select Annual on the pricing toggle and the discounted price is applied automatically at checkout. The annual price shown is the full year cost.

What if I have more than 50 profiles or 20 clients?

That is our Enterprise tier. Contact our sales team and we will build a custom plan with volume pricing, a dedicated account manager, and SLA guarantees.

Let’s talk about epilepsy

About this Podcast:

Pitch Analysis

What is Let’s talk about epilepsy?

About the host

Recent episodes

Harder to manage epilepsy: moving into adult healthcare

Venting

Harder to Manage Epilepsy: Could VNS Therapy Help?

Hear Her Voice 2026 – Exploring the impact of epilepsy on women and girls

Brain Surgery: Harder to Manage Epilepsy

Guest Appearances

Chris McCarthy

Mark Richardson

Nicky Heenan

Neil Williamson

Advertisers on this show

Best industries to pitch Let’s talk about epilepsy for

Podcasts like Let’s talk about epilepsy

Every question we get asked beforesomeone starts their trial.

Let’s talk about epilepsy

About this Podcast:

Pitch Analysis

What is Let’s talk about epilepsy?

About the host

Recent episodes

Harder to manage epilepsy: moving into adult healthcare

Venting

Harder to Manage Epilepsy: Could VNS Therapy Help?

Hear Her Voice 2026 – Exploring the impact of epilepsy on women and girls

Brain Surgery: Harder to Manage Epilepsy

Guest Appearances

Chris McCarthy

Mark Richardson

Nicky Heenan

Neil Williamson

Advertisers on this show

Best industries to pitch Let’s talk about epilepsy for

Podcasts like Let’s talk about epilepsy

Every question we get asked beforesomeone starts their trial.

Every question we get asked before
someone starts their trial.

Every question we get asked before
someone starts their trial.