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 5 - Explaining PSP to friends and family.

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

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

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