PSPA Podcast – Details, episodes & analysis

Podcast details

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Podcast PSPA Podcast

PSPA Podcast

PSPA

Business

Frequency: 1 episode/63d. Total Eps: 30

Hosting podcast Spotify for Podcasters
The PSPA Podcast will provide discussions and information for people caring for someone living with rare brain diseases, PSP or CBD. This podcast is brought to you thanks to the kind support of the Pavers Foundation in memory of Mary Youll.
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Recent rankings

Latest chart positions across Apple Podcasts and Spotify rankings.

Apple Podcasts

  • 🇬🇧 Great Britain - nonProfit

    25/06/2026
    #80

  • 🇬🇧 Great Britain - nonProfit

    01/06/2026
    #85

  • 🇬🇧 Great Britain - nonProfit

    12/05/2026
    #83

  • 🇩🇪 Germany - nonProfit

    15/04/2026
    #75

  • 🇬🇧 Great Britain - nonProfit

    10/04/2026
    #92

  • 🇬🇧 Great Britain - nonProfit

    04/04/2026
    #94

  • 🇬🇧 Great Britain - nonProfit

    03/04/2026
    #79

  • 🇬🇧 Great Britain - nonProfit

    02/04/2026
    #63

  • 🇬🇧 Great Britain - nonProfit

    01/04/2026
    #56

  • 🇬🇧 Great Britain - nonProfit

    30/03/2026
    #24

Spotify

    No recent rankings available

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RSS feed quality
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Score global : 28%

Publication history

Monthly episode publishing history over the past years.

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Latest published episodes

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Episode 6: Research update with Dr Ed Jabbari

mercredi 7 août 2024 • Duration 21:15

In this episode, PSPA Research Coordinator, Megan Hodgson talks to Dr Ed Jabbari.

Dr Jabbari has been working in the field of PSP & CBD research since 2016, when he became the Sara Koe Research Follow.

Ed talks about his different research projects, study outcomes and hopes for the future.

Episode 5: PSP & CBD Awareness Week with Rebecca Packwood and Mark Jackson

lundi 17 juin 2024 • Duration 21:06

In this episode, CEO Rebecca Packwood talks to PSPA's new Director of Policy and Influencing, Mark Jackson.

Mark shares what his role is and the launch of the #WeCare campaign and how people can help amplify our voice in PSP & CBD Awareness week, and beyond.

PSPA Podcast Episode 10 - Support for Carers

Season 1 · Episode 10

vendredi 29 avril 2022 • Duration 21:41

In this episode we speak to PSPA’s Director of Engagement, Carol Amirghiasvand, about PSPA’s new carers support groups. PSPA Volunteer Caroline Woodcock also joins us to speak about how her granny inspired her to volunteer for PSPA and host carer pamper sessions.

PSPA PodCast Episode 9 - Taking on a challenge with Katy Butterill

Season 1 · Episode 9

vendredi 11 mars 2022 • Duration 23:08

Katy Butterill joins us for this episode to share why she chose to take on a walking challenge in honour of her mum, who is living with PSP.

PSPA Podcast Episode 8 - Advance Care Planning with Ewan Phillips

Season 1 · Episode 8

mardi 1 mars 2022 • Duration 44:16

Ewan Phillips joins us to share his experience of Advance Care Planning with her mum, who was living with a diagnosis of PSP.

PSPA Podcast Episode 7 Home Adaptations

Season 1 · Episode 7

vendredi 26 novembre 2021 • Duration 42:36

OT Julie Cummins joins us for the seventh episode of the PSP podcast to advise about making adaptations in your home. Julie draws from her experience as an OT but also from her personal experience of PSP too.

PSPA Podcast Episode 6 Voice Banking

Season 1 · Episode 6

mercredi 27 octobre 2021 • Duration 22:24

Samanta and Chris join us to chat about their experience of voice banking with SpeakUnique.

PSPA Podcast Episode 5 - Explaining PSP to friends and family.

Season 1 · Episode 5

lundi 27 septembre 2021 • Duration 15:27

In this episode we chat to Sue Wilsea who shares details about her husband Mike, his PSP diagnosis and how they explained the condition to their friends and family.

PSPA Podcast Episode 4 - Caring for a parent

Episode 4

mardi 17 août 2021 • Duration 33:20

In our fourth episode we talking about caring for a parent. Claire Wells joins us to share her experience of her mum’s CBD diagnosis, her care routine with her mum and gaining Essential Care Giver status after her mum moved into a care home.

PSPA Podcast - Episode 3

vendredi 9 juillet 2021 • Duration 38:39

In our third episode we talk about delayed diagnosis. Denise Hunt and Navin Sewak share their experiences of their mums receiving a delayed diagnosis, the impact this had on the family and the care they received. They also share why raising awareness is so important.

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