Insights from recent episode analysis
Audience Interest
Podcast Focus
Publishing Consistency
Platform Reach
Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Total monthly reach
Estimated from 4 chart positions in 4 markets.
By chart position
- 🇦🇺AU · Non-Profit#35100K to 300K
- 🇬🇧GB · Non-Profit#1925K to 30K
- 🇿🇦ZA · Non-Profit#1830K to 100K
- 🇮🇪IE · Non-Profit#2710K to 30K
- Per-Episode Audience
Est. listeners per new episode within ~30 days
73K to 230K🎙 Weekly cadence·14 episodes·Last published 3mo ago - Monthly Reach
Unique listeners across all episodes (30 days)
145K to 460K🇦🇺65%🇿🇦22%🇬🇧7%+1 more - Active Followers
Loyal subscribers who consistently listen
44K to 138K
Market Insights
Platform Distribution
Reach across major podcast platforms, updated hourly
Total Followers
—
Total Plays
—
Total Reviews
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
Recent episodes
Driving and getting about after a diagnosis of PSP or CBD
Feb 10, 2026
Unknown duration
The benefit of movement
Sep 2, 2025
Unknown duration
Understanding support and care
Jun 10, 2025
Unknown duration
Dealing with diagnosis
Feb 24, 2025
Unknown duration
Living with PSP
Dec 19, 2024
Unknown duration
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 2/10/26 |  Driving and getting about after a diagnosis of PSP or CBD | Following a diagnosis, people commonly question how their day to day life will be affected. This can include how they might get about and whether they are still able to drive.Helpline Care Navigator, Dionne Ward, talks to us about what people should consider following a diagnosis, and help that maybe available in your community to help with transportation. | — | ||||||
| 9/2/25 |  The benefit of movement | In episode three of the PSPA Podcast, we talk to Laura Douglas from Neuro Heroes. Laura highlights what you might expect from any physiotherapy appointments you are referred for. And how movement, big and small, can help people who are living with PSP & CBD maintain functions and wellbeing. | — | ||||||
| 6/10/25 | Understanding support and care | In episode 2 of series 3 of the PSPA Podcast, we speak to Dr Bicky Marshall, Consultant Neurologist at Queen Elizabeth University Hospital in Glasgow. Dr Marshall helps to answer questions from the PSP & CBD community related to accessing support and care for a loved one living with the conditions, ensuring they remain at the centre of discussions and enough time is allocated to discuss everything you might want to know. | — | ||||||
| 2/24/25 | Dealing with diagnosis | In the first episode of series three of the PSPA Podcast, we speak to Anna from Rare Minds. Anna helps us to unpick the complexities of coming to terms with a diagnosis of PSP or CBD, for both the person diagnosed, and their carer. As well as looking at the different emotions you may experience, Anna also provides some insight and tips to help you understand and process your feelings. | — | ||||||
| 12/19/24 | Living with PSP | Paul Johnson shares an insight into his first PSP symptoms, his diagnosis and how his interests have changed since his diagnosis. | — | ||||||
| 8/7/24 | Episode 6: Research update with Dr Ed Jabbari | 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. | — | ||||||
| 6/17/24 | Episode 5: PSP & CBD Awareness Week with Rebecca Packwood and Mark Jackson | 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. | — | ||||||
| 6/14/24 | Episode 4: Becoming a PSPA volunteer with Lavonne McCormack and Sally Reynolds | PSPA Volunteer Coordinator Lavonne McCormack speaks to volunteer Sally Reynolds. Sally shares details of how she become a Support Group volunteer ten years ago. And also how she increased her volunteering support to include being a Link Volunteer. | — | ||||||
| 1/2/24 |  Episode 3: PSPA's 30th Anniversary with CEO Rebecca Packwood | 2024 is a milestone year for PSPA - it marks 30 years since the charity was registered. In this episode of the PSPA Podcast, CEO Rebecca Packwood shares an insight into what we have planned for this important year. Highlights of the year include: Telling 30 stories for 30 years of PSPA in our interactive timeline – new stories will be released each month. Circulating four themed editions of our magazine, PSPA Matters Enabling you to share special moments and dates via our Celebration Wall Opening the PSPA 30th Anniversary Awards nomination period Launching our 30 for 30 challenge with PSPA supporter Kelly Hooper Holding a 30th Anniversary Party in London Building the biggest Walk of Hope to date And much, much more. | — | ||||||
| 11/30/23 |  Episode 2: Diagnosing PSP & CBD with Dr Boyd Ghosh | As rare diseases, we know diagnosing PSP & CBD can be difficult. In the second episode of series two of the PSPA Podcast, we talk to Dr Boyd Ghosh about how PSP & CBD are diagnosed, what the challenges can be and what he hopes are for the future to improve diagnosis of the conditions. | — | ||||||
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| 11/7/23 |  Episode 1: Living with CBD | In the first episode of our second series of the PSPA Podcast, we talk to Gilda who has been diagnosed with CBD. Gilda talks about her symptoms, her diagnosis and how she has adapted her home and hobbies to ensure she remains active and independent, for as long as possible. Tune into Gilda's personal experience and planning tips today! | — | ||||||
| 9/30/22 | Episode 14 - How the Helpline can help | Today we’re joined by Jules Brown, PSPA Helpline Manager to talk about the support we can offer to your and your family. | — | ||||||
| 8/11/22 | PSPA Podcast Episode 13 - Support for Young People | In our 13th episode we speak to Kathryn Embree, the PSPA volunteer who runs our Youth Support Group. Here Kathryn talks about the importance of peer support and the benefits of the group. | — | ||||||
| 6/8/22 |  PSPA Podcast Episode 12 - Carers Week with Jacqui Ede | PSPA Carers Support Group facilitator, Jacqui Ede joins us as we celebrate Carers Week and our podcast being live for one year! Jacqui also shares a ten minute relaxation session with listeners at the end of the podcast. | — | ||||||
| 5/23/22 | PSPA Podcast Episode 11 - Relaunching Ed’s Lace with Scott Smith | In this episode we talk to Scott Smith about the inspiration behind his Ed’s Lace Awareness campaign and how he feels about it relaunching in 2022. | — | ||||||
| 4/29/22 | PSPA Podcast Episode 10 - Support for Carers | 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. | — | ||||||
| 3/11/22 | PSPA PodCast Episode 9 - Taking on a challenge with Katy Butterill | 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. | — | ||||||
| 3/1/22 | PSPA Podcast Episode 8 - Advance Care Planning with Ewan Phillips | Ewan Phillips joins us to share his experience of Advance Care Planning with her mum, who was living with a diagnosis of PSP. | — | ||||||
| 11/26/21 | PSPA Podcast Episode 7 Home Adaptations | 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. | — | ||||||
| 10/27/21 | PSPA Podcast Episode 6 Voice Banking | Samanta and Chris join us to chat about their experience of voice banking with SpeakUnique. | — | ||||||
| 9/27/21 | PSPA Podcast Episode 5 - Explaining PSP to friends and family. | 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. | — | ||||||
| 8/17/21 | PSPA Podcast Episode 4 - Caring for a parent | 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. | — | ||||||
| 7/9/21 | PSPA Podcast - Episode 3 | 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. | — | ||||||
| 6/10/21 | PSPA Podcast Episode 2 - Getting support | In our second PSPA Podcast we talk to Julia Tickridge. Julia shares details of caring for her husband Laurie who is living with a diagnosis of evolving PSP. Julia also talks about where she has found support in her role as a carer. | — | ||||||
| 6/10/21 | PSPA Podcast Episode 1 - An introduction with Beth Morgan-Henderson from Pavers. | Find out more about Beth’s personal experience of PSP and how support from the Pavers Foundation for the podcast came about. | — | ||||||
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Chart Positions
4 placements across 4 markets.
Chart Positions
4 placements across 4 markets.