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Kelsie is back with an update on the Snow family and to read her most recent blog post, which can be found on her website, www.kelsiesnowwrites.com.
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After a tough fall season for Chris' health, Kelsie offers short update on how the Snows are doing and when Sorry, I'm Sad will be back with new episodes.
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In the Season Three opener, Chris and Kelsie talk about the loneliness of longterm illness, about the difficulty of watching your person grieve losses and grapple with profound sadness, about feeling isolated and alone in rooms full of people or even next to the person you love most, and about how to let people know you see their struggle and that you care.
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In this season two finale, Chris and Kelsie answer questions submitted by followers on Twitter and Instagram about life, marriage, illness and work three years removed from Chris' ALS diagnosis.
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Steve Gleason, the former NFL safety who has been living with ALS for 11 years and been totally paralyzed for eight of those, joins Kelsie and Chris for a conversation about how he and his family are flourishing in a life most people would find impossible thanks to radical acceptance, deep compassion for themselves and each other and abiding love.
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Photos of ESPN SportsCenter anchor Nicole Briscoe’s family look like a dream life, but infertility and the isolation and shame it causes are an all-too-common nightmare. Nicole and her husband, professional race-car driver Ryan Briscoe, worked for 10 years to make their picture-perfect family. The end result was two beautiful little girls. The path to that point involved seemingly endless cycles of hormones, needles, IVF treatments, never being diagnosed with a disease that can directly impact fertility despite being seen by countless fertility doctors and miscarriages so numerous you lose track of exactly how many there were.
Now, only two months removed from a hysterectomy, Nicole talks about it all – the complicated and conflicting emotions, the guilt, the anger, the shame, the isolation, the resulting grief from 10 years of thinking constantly about getting pregnant and staying pregnant and losing pregnancies – in an effort to help other women going through the same thing know that they are not alone.
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One year after her first appearance on Sorry, I'm Sad, Sandra Abrevaya joins Kelsie to talk about her life over the last 12 months, their friendship and their husband's shared illnesses.
Sandra cofounded I Am ALS and Synapticure with her husband, Brian, after he was diagnosed with ALS about five years ago. More than an interview, this is a conversation between two friends, two women, two mothers, two wives, trying to make sense of lives they never envisioned for themselves, trying to find a way to find joy and luck and gratitude and hope in a world that sometimes feels dark and filled with sadness. This is about finding a way to still ask, in spite of the odds -- what if it all works out?
Listen to Sandra's first Sorry, I'm Sad episode.
Learn more about I Am ALS.
Learn more about Synapticure.
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The pandemic that never ends is still disrupting our daily lives and killing many, many people no matter how tired of it we are. Darren Markland is an ICU doctor at the Royal Alexandra Hospital in Edmonton, Alberta, Canada, and has been in the trenches since the pandemic started. His twitter account, @drdagly, has swelled to more than 55,000 followers since he began recounting raw, broken-down stories of patients he has treated. He joins Sorry, I'm Sad to talk about the state of the pandemic, how he has managed his own mental and physical wellbeing during the last two years and where he finds hope.
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Four years removed from her stroke, Kelsie and Chris talk about how it happened, the physical healing required in the weeks and months after her six-day hospital stay in 2018 and the emotional healing that they realize is still unresolved.
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In March 2018, Jessie Ravnsborg was diagnosed with ALS. She was just 35 years old. She died just before her 37th birthday. In today's episode, our second about Medical Assistance in Dying (MAID), you’ll meet Jessie through her mom, Heather Lucier. This is a story about choosing joy, about wringing out all the good from life that you can for as long as you can and, when the joy can no longer compete with the darkness of a most insidious disease, choosing to say goodbye. It's about facing your mortality, about knowing what matters to you in life and about the bravery of understanding what it means when those things move beyond your reach.
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From the publisher's feed
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…

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