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.

by 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.
Language
🇺🇲
Publishing Since
6/10/2021
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June 2, 2026
<p>We spoke to Zubyda Azzam, who is a Psychotherapist at Rareminds, all about carers resilience. </p><p><br></p><p>We discussed:</p><ul><li>Common challenges that families and carers face</li><li>What signs to look out for when carers resilience is being stretched </li><li>Lots of practical ways to help your family members and resources you can access</li></ul>

April 30, 2026
<p>We spoke to Peggy Newton, PSPA Helpline and Support Services Manager, all about the different kinds of financial support that is available for people living with PSP & CBD and how the Helpline can support you.</p><p><br></p>

April 9, 2026
<p>This podcast features a discussion between Helen Chapman, PSPA Communications Manager and Chloe Cripps, Speech and Language Therapist all about communicating whilst living with PSP & CBD. </p><p>Chloe shared how she supports people with neurological conditions as their speech changes, the practicalities of attending an appointment, useful tips and more information around Voice Banking. </p>
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Dr Bicky Marshall
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Paul Johnson
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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.
This podcast updates bi-weekly.
This podcast is available on 7 platforms including Apple Podcasts, Spotify, and more. You can also use the RSS feed directly.
Information about guest appearances is not available.
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