The Michael J. Fox Foundation Parkinson's Podcast

The Michael J. Fox Foundation for Parkinson’s Research

Subscribe for coverage and analysis of current neurology/brain research, patient and caregiver profiles, drug development strategy, pioneering nonprofit management and other topics of interest in a wide-ranging series of conversations that include the voices of those affected by Parkinson's as well as clinicians.

  1. 19 AOÛT

    Ask Us Anything About Parkinson’s and Relationships

    How do I tell my children about my Parkinson’s disease (PD) diagnosis? How do I explain a tremor to my grandkids? How can I support my parent with Parkinson’s from a distance? How can my spouse and I communicate around a symptom of apathy?  Every year our community submits thousands of questions online and at in-person events. Many are about Parkinson’s symptoms, treatment options and the latest research, but we’re also asked questions about relationships and how to maintain connection with loved ones with Parkinson’s in the picture. In this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast, our expert panel tackles questions on relationships and shares their personal experiences and advice.  To connect with others for support and community, join the Parkinson’s Buddy Network. https://parkinsonsbuddynetwork.michaeljfox.org/  Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0  The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi Mentioned in this episode: The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.

    40 min
4,1
sur 5
200 notes

À propos

Subscribe for coverage and analysis of current neurology/brain research, patient and caregiver profiles, drug development strategy, pioneering nonprofit management and other topics of interest in a wide-ranging series of conversations that include the voices of those affected by Parkinson's as well as clinicians.

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