• Life After. . .THAT!

  • 著者: Jan W Murray
  • ポッドキャスト

Life After. . .THAT!

著者: Jan W Murray
  • サマリー

  • What was THAT? This podcast will focus on survival and pushing forward after life events, tragic or not. Life after illness, Life after abuse, Life after a career, Life after whatever else happens! Season 1 focuses on the survivors of Amyotrophic Lateral Sclerosis (ALS)--widows, widowers, partners, friends, siblings, children, etc. Each of our participants will have 2 episodes, the first being their story--Life AFTER the diagnosis, the onslaught of the changing dynamics of the disease, and how it changed relationships, and life. The second episode for each story will focus on Life After THAT monster and how they are moving on or not and what might help themselves and others. In other words, how are they now carrying on? ALS is considered rare, yet it kills tens of thousands in the United States annually and many more worldwide. Most ALS patients live 2-5 years from diagnosis, but not all. Regardless, the body movements die off while the mind usually stays vibrant. Most of those affected wouldn’t wish the disease on their worst enemy and would actually prefer cancer over ALS...because except in rare cases, there’s at least a chance to survive with the other. In either case, loved ones are changed forever, and suffer from PTSD, depression, etc. The importance of spreading awareness of the disease is important, but so is acknowledging what the caretakers and loved ones have been through. This season provides that opportunity, a sounding board if you will, and hopefully what my late husband, also a victim of ALS, encouraged...”Keep on keepin’ on because being sad or mad will not do you any good. Be happy.”

    Jan Murray 2022
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あらすじ・解説

What was THAT? This podcast will focus on survival and pushing forward after life events, tragic or not. Life after illness, Life after abuse, Life after a career, Life after whatever else happens! Season 1 focuses on the survivors of Amyotrophic Lateral Sclerosis (ALS)--widows, widowers, partners, friends, siblings, children, etc. Each of our participants will have 2 episodes, the first being their story--Life AFTER the diagnosis, the onslaught of the changing dynamics of the disease, and how it changed relationships, and life. The second episode for each story will focus on Life After THAT monster and how they are moving on or not and what might help themselves and others. In other words, how are they now carrying on? ALS is considered rare, yet it kills tens of thousands in the United States annually and many more worldwide. Most ALS patients live 2-5 years from diagnosis, but not all. Regardless, the body movements die off while the mind usually stays vibrant. Most of those affected wouldn’t wish the disease on their worst enemy and would actually prefer cancer over ALS...because except in rare cases, there’s at least a chance to survive with the other. In either case, loved ones are changed forever, and suffer from PTSD, depression, etc. The importance of spreading awareness of the disease is important, but so is acknowledging what the caretakers and loved ones have been through. This season provides that opportunity, a sounding board if you will, and hopefully what my late husband, also a victim of ALS, encouraged...”Keep on keepin’ on because being sad or mad will not do you any good. Be happy.”

Jan Murray 2022
エピソード
  • The Cynthia and Billy Snyder Story, Part 2 - Philadelpha, PA
    2023/11/28
    In this Part 2 of the Snyder story, Cynthia makes important observations about how to carry on after decades with her "person", Billy, who passed away from ALS. She shares about finding new love, but a different love, in a different era of life.
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    32 分
  • The Cynthia and Billy Snyder Story, Part 1 - Philadelpha, PA
    2023/11/21
    Welcome to Part 1 of the Cynthia and Billy Snyder Story. Cynthia discusses life before and during Billy's life with ALS, as well as what caregivers, professional healthcare workers and others need to know.
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    48 分
  • The Beth and John Reed Story, Part 2 - Pennsylvania
    2023/12/27

    Beth Reed continues to share her journey through memories of caring for husband John and explaining how she is carrying on now.

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    44 分

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