A Place of Yes | A Grief Podcast

She’s buried 4 members of her immediate family. Only she and her mom are left. In part 2 of this devastating conversation, Heather sits down with Kelly Talbot to talk about the most recent two losses—her brothers Jason & Sean. We thank Kelly for sharing her story, and being so deeply vulnerable with our audience. We hope her story has inspired you ❤️‍🩹 Find Heather and Jake's Help from Heaven: ❤️ APOY Instagram: htt...

She’s buried 4 members of her immediate family. Only she & her mom are left.

In part one of this devastating conversation, Heather sits down with Kelly Talbot to talk about the first two losses—her brother Ryan, killed in a hit-and-run murder, and her father, who died after a long battle with cancer.This is just the beginning of a grief story that’s almost too much to comprehend. Find Heather and Jake's Help from Heaven:

Leah Stern was more than just a daughter—she was her dad’s best friend. When he died of glioblastoma, her world broke open. In this emotional and raw conversation, Leah shares how she’s navigating life without him, the jealousy she feels when others still have their dads, and how grief doesn’t always look like tears—it can show up as rage, loneliness, and quiet resentment. This episode explores what it really means to lose a paren...

This week’s episode is sponsored by Freedom Concepts, creators of custom adaptive tricycles, Chill-Out Chairs, and early intervention equipment that help individuals of all ages and abilities experience mobility, comfort, and dignity. Heather shares the powerful stories of two families whose children’s lives changed dramatically after being matched with Freedom Concepts equipment. From new levels of independence to moments of pure...

This week’s episode is a special live recording from Northshire Bookstore in Saratoga Springs, where Heather sits down with author Casey Mulligan Walsh to talk about her deeply moving memoir, The Full Catastrophe. Orphaned by twelve, the only surviving sibling, and later a mother navigating divorce and the unraveling of her family, Casey opens up about the grief that shaped her life—and the unimaginable loss of her firstborn son, ...

At just 19 years old, she lost her mom to Alpha-1 Antitrypsin Deficiency—a rare genetic disorder that went undiagnosed until it was too late. In this episode, she shares what it was like to watch her mom suffer without answers, and how the grief of that experience changed everything: her family, her future, and her sense of self.

Dr. Al Freedman knows firsthand what it’s like to be a parent in the rare disease world—his son Jack lived with Spinal Muscular Atrophy for 26 years. In this conversation, he joins Heather to talk about the deep grief and isolation that comes with rare parenting, and what it means to lose a child to a disease no one else seems to understand. As both a psychologist and a rare disease dad, Dr. Freedman brings a unique perspective—sh...

Aubrey Ide was only 18 when she lost her best friend Olivia Allen to cancer. In this episode, Aubrey sits down with Heather to share what it’s been like to grieve so young—how the loss changed her, what she misses most, and the milestones that feel so different without Olivia there. She talks about the things they didn’t get to do together, the deep loneliness of losing a friend at that age, and what healing looks like nearly a ye...

Grief doesn’t come with a roadmap—and it definitely doesn’t fit into a 3-day leave policy. In this episode, Heather sits down with Rebecca Feinglos, founder of Grieve Leave, to talk about what it really looks like to take time to mourn. After losing both of her parents and going through a divorce, Rebecca quit her job in 2021 to dedicate a full year to grieving—and she documented every step. That journey grew into Grieve Leave, a ...

When Amelia Lawrence’s son Leo was born with limited mobility, she didn’t know if he’d ever experience the simple joys other kids take for granted—like riding a bike or sitting comfortably at school. But everything changed when Leo was introduced to adaptive equipment designed specifically for his needs.

When Maria Quiban Whitesell’s husband, Sean, was diagnosed with glioblastoma—a deadly and aggressive brain cancer—her world fell apart. Eighteen months later, she found herself a widow and a solo parent to their young son, Gus. In this powerful conversation, Maria shares the raw truth about navigating her husband’s illness, the impossible grief that followed, and how she learned to keep moving forward when it felt impossible.

Gabby Petito’s name is known around the world—but behind the headlines is a family still living with unimaginable grief. In this powerful conversation, Heather sits down with Gabby’s mother and stepmother to talk about what life has been like without her: the milestones she’s missed, the memories they hold close, and the heartbreak that lingers on birthdays, holidays, and especially Mother’s Day.

Jake’s birthday is coming, and it still hurts just as much as it did that first year. In this solo episode, Heather opens up about what it really feels like to face another year without her son—the lead-up, the dread, the heartbreak that anniversaries bring when someone you love is gone.

Jessica Patay is a full-time caregiver to her son with Prader-Willi syndrome—and the founder of We Are Brave Together, a global support network for caregiving moms. In this episode, she joins Heather to talk about the emotional toll of rare parenting, why self-care isn’t a luxury, and what it really takes to show up for yourself when you're constantly showing up for everyone else.

They get honest about burnout, identity loss, an...

After losing her daughter Kelsey, Debbie Waffle was left with a grief that didn’t fade—but she also felt a quiet pull toward purpose. In Part 2 of her conversation with Heather, Debbie shares how she began to live for Kelsey—writing her book My Grief Jar and training Kelsey’s beloved dog, Brody, to become a therapy dog, just as Kelsey had dreamed.

This episode is about the healing that happens in motion, the love that continues ...

Debbie Waffle built a life filled with joy, purpose, and hope—but nothing could prepare her for what came next. Her daughter Kelsey’s medical challenges grew more complex over time, leaving Debbie desperate for answers and overwhelmed with fear. And when Kelsey died, the grief nearly consumed her.

On what would have been Kelsey’s birthday, Debbie speaks with Heather about the deep unraveling that comes with losing a child—the gu...

Being a rare disease parent means living in a world of unpredictability—and in this powerful follow-up episode, Jessica Troiano shares what that really looks like. From a terrifying recent emergency surgery to the countless difficult decisions she’s had to make over the years, Jess opens up about the emotional and mental toll of parenting a medically complex child.

She talks about the weight of advocacy, the fear of the unknown,...

Losing a sister at 15 changes everything. Sophia Allen opens up about the heartbreak of losing Olivia—her sister, her best friend, her constant.

She shares what people don’t understand about sibling grief, the loneliness of navigating loss at such a young age, and the trauma that shaped her teenage years. This raw and honest conversation gives voice to the kind of grief that often goes unseen but never goes unfelt.

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Three years after losing her daughter Dalia to a rare disease, Jessica Fein embarked on a powerful journey to Guatemala—Dalia’s birthplace—to reconnect with her spirit.

In this episode, she shares the emotional experience of returning to the country, the rituals her family performed to feel Dalia’s presence, and the deep, unexpected ways grief and love intertwine. This is a story of remembrance, connection, and the unbreakable ...