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Life After. . .THAT!
Life After. . .THAT! episodes
- The David and Celia Caine Story, Part 2 of 2
Celia Caine continues sharing her and her late husband, David's, ALS journey and her insights since her husband's passed away.
31 min - The David and Celia Caine Story, Part 1 of 2
Celia Caine of Canada shares the story of her beloved husband, David, who passed away in 2022 of Amyotrophic Lateral Sclerosis (ALS). This is Part 1 of 2.
46 min - The Lee and Michael Durst Story, Part 2 -Alberta, Canada
Lee Durst continues her encouraging story of her journey with her beloved late husband Michael and her continuation of life after his death.
43 min - The Lee and Michael Durst Story, Part 1 -Alberta, Canada
Lee Durst, of Alberta Canada, shares her and husband Michael's ALS journey. This is Part 1 of 2.
1 hr 4 min - The Bobette Rose ALS Story with Daughter Kerri and Grandson Wyatt -Idaho
Bobette Rose's daughter Kerri McDonald shares her beloved mother's happy life before Amyotrophic Lateral Sclerosis and her mother's positivity and wisdom while battling ALS. Bobette's grandson Wyatt shares his thoughts on being one of his Grandma Bobby's caregivers and how she impacted his life.
37 min - The Bobette Rose Story, Part 2 with daughter Kerri and Grandson Wyatt
Join us for another heartwarming and inspirational story about an inspiring, accomplished woman, Mom, grandma, and educator, Bobette Rose. This is Part 2 of 2. Daughter Kerri and Grandson Wyatt continue their remembrance of Bobette, Wyatt's "Grandma Bobby," as well as addressing life after the ALS journey.
54 min - Part 2 - ALS - The Rachelle and Jason Gatewood Story - Idaho & Washington State
Rachelle Gatewood rejoins us this week to continue her ALS journey, particularly her "after" story and how she has continued with life, despite hardships since her young husband passed away from the disease. Rachelle's positivity will prove helpful to those needing encouragement.
35 min - ALS - The Rachelle and Jason Gatewood Story - Idaho & Washington State
Rachelle Gatewood shares the ALS story of her and her late husband, Jason, who passed away in 2018. Both young, they found positives and stuck it out together.
36 min - Part 2 of 2 - The Denise Allen and Mary DeWitt ALS Story - Gaston, Oregon
In this second of two episodes, our visit with Denise Allen of Gaston, Oregon, continues as she talks about the early difficulties after the death of her wife, Mary DeWitt, in 2015 from Amyotrophic Lateral Sclerosis. Denise also tells how she has carried on with life despite hardships and lends advice to others.
40 min - Caregiver Stress, Depression, Coping, and Suicide Risk: Carol Dean, LPC Offers Help
Forty-eight peer-reviewed journal articles, spanning low-, middle-, and high-income countries and a variety of illnesses and disabilities indicate that the proportion of caregivers experiencing suicidal ideation ranged from 2.7% to 71%, with evidence of suicide attempts, deaths by suicide, and deaths by homicide-suicide also reported. There is sufficient evidence to warrant concern for caregivers around the world and prompt action in policy and practice, but more rigorous research is required to draw clear, nuanced conclusions about risk and inform evidence-based prevention and intervention. We are grateful to Licensed Professional Counselor Carol Dean for joining us on Life After...THAT! She has helped many people cope with the challenges of caregiving. In this episode, she will talk about the importance of self-care, stress management, and mental health for caregivers who face difficult situations every day. She will also share some practical tips and strategies to help caregivers stay healthy and resilient during and after their caregiving journey. Don't miss this important episode on all major podcast platforms.
1 hr 25 min
About Life After. . .THAT!
From the publisher's feed
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.”