Blog
How 2 Families Found Hope in Adaptive Equipment
“When we first got the trike, he couldn’t stop smiling. It was like he realized for the first time that he could move on his own terms—and he hasn’t stopped since.”
The Full Catastrophe: Losing a Son and Learning How to Live Again
“You don’t think your life can fall apart more than once—but mine did. And then I lost my son. The only way I’ve survived it is by telling the truth, and trusting that love could still lead me somewhere worth living.”
A Late Diagnosis: Losing My Mom to Rare Disease
“We kept asking doctors what was wrong. No one had answers. And then, just like that, I was 19 years old and saying goodbye to my mom.”
Losing a Son to Rare Disease: Parental Isolation & Grief
“When you’re a rare parent, it’s not just the disease—it’s the loneliness, the constant feeling that no one really gets it. And when your child is gone, that grief is even more complicated. Jack taught me so much. I want other parents to know they’re not alone.”
What It’s Like to Lose Your Best Friend at 18
“She was supposed to be here for the birthdays, the firsts, the little moments that feel big. But she’s not—and that’s the part that never stops hurting.”
Why I Quit My Job to Grieve My Parents’ Deaths
“I realized I’d never actually stopped to grieve. Not after losing my mom, my dad, or my marriage. So I quit my job and took a year to do it. That time changed everything—and now I’m helping others do the same.”
How Adaptive Equipment Changed My Son’s Life
“It wasn’t just a bike—it was the first time Leo could ride alongside his siblings. That moment changed everything. With the Chill-Out Chair, he’s comfortable at home, at school, everywhere. These tools gave him more than mobility. They gave him a way to be part of the world.”
What Life Looks Like After Losing My Husband to Brain Cancer – Maria Quiban Whitesell
“When my husband was diagnosed, I felt completely lost. I wasn’t prepared for the caregiving, the fear, or the grief that came after. I wrote You Can’t Do It Alone because I learned the hardest way possible—none of us should have to walk through this kind of loss alone.”
Gabby Petito’s Moms on “Surviving” Mother’s Day
“The world knows Gabby’s name, but they don’t know what it’s like to wake up every day without her. Birthdays, holidays, Mother’s Day—nothing feels the same. We miss her laugh. Her light. Everything. And there are things we wish we’d said, things we’ll always carry.”
How I Cope with My Son’s Birthday Now That He’s Gone
“His birthday is coming, and my whole body feels it. People think grief fades with time, but these days—birthdays, anniversaries—they hit just as hard. I should be planning a party. Instead, I’m learning how to survive another year without him.”
Self-Care Sounds Nice, But Who’s Watching My Kid?
“Self-care sounds great until you realize there’s no one else to watch your kid. When you’re a full-time caregiver, even basic things—like rest, a walk, or five minutes alone—feel impossible. But if I don’t take care of myself, I can’t show up for my family. That’s not selfish. That’s survival.”
What I Did After My Daughter Died: Grief, Purpose & Carrying Her Legacy
After Kelsey died, I blamed myself. I replayed every decision, every appointment, every moment. I thought I was prepared to fight for her—I wasn’t prepared to lose her. Grief didn’t just touch my life, it unraveled it. And for a long time, I didn’t know how I’d ever come back from that. This is the part of motherhood no one talks about.
I Couldn’t Save Her: Losing My Daughter Changed Everything
After Kelsey died, I blamed myself. I replayed every decision, every appointment, every moment. I thought I was prepared to fight for her—I wasn’t prepared to lose her. Grief didn’t just touch my life, it unraveled it. And for a long time, I didn’t know how I’d ever come back from that. This is the part of motherhood no one talks about.
What No One Tells You About Parenting a Child with Rare Disease – Emergency Surgeries & Advocacy
When Jude needed emergency surgery, there wasn’t time to process—just to act. That’s the reality of parenting a medically complex child. It’s not just the big surgeries or diagnoses—it’s the constant decisions, the fear of missing something, the exhaustion of always being on alert. But somehow, through it all, there’s still joy. There’s still love. And there’s a strength I never knew I had until I became Jude’s mom.
Losing My Sister at 15 – One Year Later
When my sister died, I felt like the world kept moving—and I didn’t. I was only 15, and suddenly everything changed. No one talks about how isolating it is to lose a sibling, especially that young. People asked how my parents were doing, but no one ever really asked me. I had to figure out how to grow up with a kind of grief that didn’t have a place. This is what it’s really like to lose your sister when you’re still just a kid.
I Traveled to Guatemala to Honor My Late Daughter | Losing Her to a Rare Disease
After losing her daughter Dalia to a rare disease, Jessica Fein embarked on a deeply personal journey to Guatemala—Dalia’s birthplace—to honor her memory and reconnect with her spirit. In this episode, she opens up about the rituals her family performed, the signs she received, and the profound ways grief and love intertwine.
How One Tragic Loss Changed a Family Forever: Grieving a Husband & Father
Losing someone suddenly leaves you with more questions than answers. One moment, life feels normal, and the next, everything has changed. When Robert Bolton Best passed away in 2018, his family was forced to navigate grief in ways they never expected. Lisa lost her husband, Aly and Tyler lost their father, but each of them experienced that loss in a different way. In this episode, they open up about the shock, the trauma, and the long road of healing after sudden loss—because grief doesn’t look the same for everyone, even when you’re mourning the same person.
The Doctors Were WRONG: A Mother’s Fight for Her Son with 15 Diagnoses
When we were told halfway through my pregnancy that our baby wouldn’t survive, our world shattered. But Jude had other plans. Now, at 13 years old, he’s living proof that the doctors were wrong. With 15 medical diagnoses, including the rare PHGDH deficiency, our journey has been anything but easy—countless surgeries, hospital stays, and moments of uncertainty. But through it all, there’s been love, resilience, and a strength I never knew we had. This is our story.
A Year Without Olivia Allen: Her Mom, Sister & Best Friend Share Their Story
Nearly a year after Olivia Allen lost her battle with leukemia, her mother, Mellissa, her sister, Sophia, and her best friend, Aubrey, share what life has really been like without her. From the milestones she’ll never reach to the moments that still feel impossibly heavy, they open up about the ways grief changes with time—and how Olivia’s presence is still deeply felt, even in her absence.
How a 3,288-Mile Run Sparked a NATIONWIDE Fight Against Multiple Sclerosis
Ashley Schneider grew up watching her mother, Jill, battle multiple sclerosis with quiet strength. Determined to take action, she founded MS Run the US from her childhood bedroom in Wisconsin, turning her love of running into a mission to raise awareness and funds for those affected by MS.
In 2010, she took it to the next level—running 3,288 miles across America to bring national attention to the cause.
But her journey didn’t end there. She built a nonprofit that now unites runners nationwide to continue the fight.