PSPA Podcast

Por: PSPA
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.
24 episodios disponibles

Latest episodes of the podcast PSPA Podcast

The benefit of movement 02/09/2025
Understanding support and care 10/06/2025
Dealing with diagnosis 24/02/2025
Living with PSP 19/12/2024
Episode 6: Research update with Dr Ed Jabbari 07/08/2024
Episode 5: PSP & CBD Awareness Week with Rebecca Packwood and Mark Jackson 17/06/2024
Episode 4: Becoming a PSPA volunteer with Lavonne McCormack and Sally Reynolds 14/06/2024
Episode 3: PSPA's 30th Anniversary with CEO Rebecca Packwood 02/01/2024
Episode 2: Diagnosing PSP & CBD with Dr Boyd Ghosh 30/11/2023
Episode 1: Living with CBD 07/11/2023
Episode 14 - How the Helpline can help 30/09/2022
PSPA Podcast Episode 13 - Support for Young People 11/08/2022
PSPA Podcast Episode 12 - Carers Week with Jacqui Ede 08/06/2022
PSPA Podcast Episode 11 - Relaunching Ed’s Lace with Scott Smith 23/05/2022
PSPA Podcast Episode 10 - Support for Carers 29/04/2022
PSPA PodCast Episode 9 - Taking on a challenge with Katy Butterill 11/03/2022
PSPA Podcast Episode 8 - Advance Care Planning with Ewan Phillips 01/03/2022
PSPA Podcast Episode 7 Home Adaptations 26/11/2021
PSPA Podcast Episode 6 Voice Banking 27/10/2021
PSPA Podcast Episode 5 - Explaining PSP to friends and family. 27/09/2021
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