116 episodes

WeHaveAFace.org Inc. has created "WeHaveAVoice" Radio for the Huntington's and Juvenile Huntington's disease community. It is time for the community to speak out...speak up! We must openly share what all of us in the Huntington's community experience on a daily basis! Removing the stigmas and broadening social awareness and acceptance is paramount!
Visit: www.WeHaveAFace.org/Radio for more information.

WeHaveAVoice WeHaveAVoice

    • Education
    • 5.0 • 4 Ratings

WeHaveAFace.org Inc. has created "WeHaveAVoice" Radio for the Huntington's and Juvenile Huntington's disease community. It is time for the community to speak out...speak up! We must openly share what all of us in the Huntington's community experience on a daily basis! Removing the stigmas and broadening social awareness and acceptance is paramount!
Visit: www.WeHaveAFace.org/Radio for more information.

    Rare Disease Day

    Rare Disease Day

    Host, Kevin Jess, talks about Rare Disease Day which is just around the corner

    • 12 min
    New Guidelines to Revolutionize Care for Huntington's Disease Patients

    New Guidelines to Revolutionize Care for Huntington's Disease Patients

    Kevin Jess talks about recent papers published and about to be published concerning changing the diagnostic criteria for HD

    • 13 min
    Bunny Clark and the 10th Annual Huntington's Heroes Walk

    Bunny Clark and the 10th Annual Huntington's Heroes Walk

    Bunny Clark talks about The Walk for Huntington's Disease May 28th

    • 13 min
    Erin Paterson - Huntington's Disease Heroes

    Erin Paterson - Huntington's Disease Heroes

    • 22 min
    WeHaveAFace! What's next?

    WeHaveAFace! What's next?

    Kevin Jess announces charity closings and discusses what's next for WeHaveAFace.

    • 20 min
    Worthlessness

    Worthlessness

    Kevin Jess talks about the feeling of worthlessness and how the media may drive this feeling.

    • 21 min

Customer Reviews

5.0 out of 5
4 Ratings

4 Ratings

WeHaveAFace ,

Huntington’s disease awareness

We will never stop talking about HD until the world knows that we are here!

Emily Nana ,

Great show!

I’m so happy that this show exists. We need to educate the world about Huntington’s disease!

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