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Help Advocate for ALS with Amanda Stevens, Mayuri Saxena, & Sandra Abrevaya

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Manage episode 332085033 series 3323162
Content provided by Caitlin McHugh Stamos. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Caitlin McHugh Stamos or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

ALS, also known as Lou Gehrig’s disease, is a neurodegenerative disease that attacks the cells of the nervous system and the brain. Most people who get diagnosed have a life expectancy of only 2-5 years on average. There are currently promising treatments in late trial stages that give hope to patients suffering from this horrific disease, but most people cannot access these treatments. Advocates, including my guests in this episode, are fighting to get medicine in bodies and increase funding for research. We’ll learn the personal stories and struggles of a couple people battling ALS and how we can help advocate on their behalf.

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24 episodes

Artwork
iconShare
 
Manage episode 332085033 series 3323162
Content provided by Caitlin McHugh Stamos. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Caitlin McHugh Stamos or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

ALS, also known as Lou Gehrig’s disease, is a neurodegenerative disease that attacks the cells of the nervous system and the brain. Most people who get diagnosed have a life expectancy of only 2-5 years on average. There are currently promising treatments in late trial stages that give hope to patients suffering from this horrific disease, but most people cannot access these treatments. Advocates, including my guests in this episode, are fighting to get medicine in bodies and increase funding for research. We’ll learn the personal stories and struggles of a couple people battling ALS and how we can help advocate on their behalf.

Links:

  continue reading

24 episodes

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