Small, Important Victories: Living Actively with ALS

著者： The Joe Martin ALS Foundation & Neil Cottrell
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  • A podcast from The Joe Martin ALS Foundation, where we equip people living with ALS (amyotrophic lateral sclerosis, or Lou Gehrig's Disease) to live actively amidst this challenging diagnosis. The Joe Martin ALS Foundation's mission is to empower families as they face the challenge of living actively with ALS by providing home care and other services at no cost. We believe that with the help of family and a caring community people with ALS can live with purpose, with joy, and with hope. This philosophy drives us to empower families with the knowledge and tools to navigate this progressive disease. Learn more and support our mission by visiting www.joemartinalsfoundation.org
    The Joe Martin ALS Foundation 2022
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あらすじ・解説

A podcast from The Joe Martin ALS Foundation, where we equip people living with ALS (amyotrophic lateral sclerosis, or Lou Gehrig's Disease) to live actively amidst this challenging diagnosis. The Joe Martin ALS Foundation's mission is to empower families as they face the challenge of living actively with ALS by providing home care and other services at no cost. We believe that with the help of family and a caring community people with ALS can live with purpose, with joy, and with hope. This philosophy drives us to empower families with the knowledge and tools to navigate this progressive disease. Learn more and support our mission by visiting www.joemartinalsfoundation.org
The Joe Martin ALS Foundation 2022
マネジメント 個人的成功 経済学
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エピソード
  • 15 Years Fighting ALS - with Joe B. Martin

    15 Years Fighting ALS - with Joe B. Martin
    2022/09/29

    In our first episode, we explore how we've made it 15 years as a nonprofit that people said "wouldn't work!" The Rev. Dr. Joe B. Martin, son of our namesake Joe Martin, shares the story of how we came to be a leading provider of free ALS-specialized care, and the key to our success: building a caring community that surrounds every person living with ALS (amyotrophic lateral sclerosis) who we help. Have a look at our logo, the embracing hands, which were inspired by this caring community as we take you on a 15 year journey (in just 19 minutes!).

    Joe Martin lived actively with ALS for 12 years. One year after his passing, The Joe Martin ALS Foundation was founded according to his vision and instructions for an organization that would provide free care to everyone facing this challenging diagnosis. Today we have served over 800 families with free care and extensive support including free transportation, loaner equipment, travel planning, caregiving workshops, and Joe's Camp, a camp for kids who have a parent or grandparent with ALS. To learn more, visit: www.joemartinalsfoundation.org and follow us on Instagram, Facebook, or Twitter.
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    20 分

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