Calgarians Dan Pubben and Kate Tuff join Kelsie to talk about their life since Dan was diagnosed with ALS in the fall of 2024 at 42 years old, about navigating this disease with their two young children, about how we respond when bad things happen and about the reality of living in the hopefully many years between diagnosis and -- what remains an inevitability with this disease -- death. <a href='https://www.gofundme.com/f/help-support-kate-her-family-through-the-challenges-of-als'>Support Dan and Kate here.</a> <a href='https://www.alsab.ca/donate'>Support the ALS Society of Alberta here. </a><a rel="payment" href="https://www.patreon.com/kelsiesnow">Support the show</a>

Calgarians Dan Pubben and Kate Tuff join Kelsie to talk about their life since Dan was diagnosed with ALS in the fall of 2024 at 42 years old, about navigating this disease with their two young children, about how we respond when bad things happen and about the reality of living in the hopefully many years between diagnosis and -- what remains an inevitability with this disease -- death. Support Dan and Kate here. Support the ALS Society of Alberta here. Support the show

Calgarians Dan Pubben and Kate Tuff join Kelsie to talk about their life since Dan was diagnosed with ALS in the fall of 2024 at 42 years old, about navigating this disease with their two young children, about how we respond when bad things happen and about the reality of living in the hopefully many years between diagnosis and -- what remains an inevitability with this disease -- death.&nbsp;<a href="https://www.gofundme.com/f/help-support-kate-her-family-through-the-challenges-of-als" rel="noopener noreferrer">Support Dan and Kate here.</a>&nbsp;<a href="https://www.alsab.ca/donate" rel="noopener noreferrer">Support the ALS Society of Alberta here.&nbsp;</a><a href="https://www.patreon.com/kelsiesnow" rel="noopener noreferrer">Support the show</a>

There’s No Running From It: Dan and Kate's Story

When her husband was diagnosed with Amyotrophic Lateral Sclerosis (ALS) in June 2019 and given 6-12 months to live, Kelsie Snow avoided other people's sad stories as a rule, but as time wore on she found herself seeking them out. Snow, a former sports reporter for The Boston Globe, Los Angeles Times and St. Paul Pioneer Press, began writing about her life on her website and learned there is comfort in knowing how others have loved, lost and kept going.&nbsp; Sorry, I'm Sad chronicles the Snows' story in real-time. From the desperate early days, to the hopefulness of a promising clinical trial, to heartbreaking setbacks and constant grappling with mortality, and Chris' unexpected death in September of 2023, Kelsie, along with others she has met along this path, share stories about grief, loss and the importance of hope.

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Personal Journals

When her husband was diagnosed with Amyotrophic Lateral Sclerosis (ALS) in June 2019 and given 6-12 months to live, Kelsie Snow avoided other people's sad stories as a rule, but as time wore on she found herself seeking them out. Snow, a former sports reporter for The Boston Globe, Los Angeles Times and St. Paul Pioneer Press, began writing about her life on her website and learned there is comfort in knowing how others have loved, lost and kept going.  Sorry, I'm Sad chronicles the Snows' story in real-time. From the desperate early days, to the hopefulness of a promising clinical trial, to heartbreaking setbacks and constant grappling with mortality, and Chris' unexpected death in September of 2023, Kelsie, along with others she has met along this path, share stories about grief, loss and the importance of hope.

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There’s No Running From It: Dan and Kate's Story

There’s No Running From It: Dan and Kate's Story

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