The journey is easier when you don’t walk it alone. Hear from those who know best — other people in your health community — as they share intimate personal stories, relatable experiences, and the everyday tips and advice that make each day living with a condition a little better than the one before.
Finding communities online … made me feel like I have hope. We’re all dealing with something. Even if it’s not visible to the outside world, we all could be struggling with
something.
something.
Sydney Jenkins, living with atopic dermatitis

I hope when I share my story, it helps you to want to share your story. Then there’s a domino effect … and another person is empowered to tell theirs. Then we have this beautiful tapestry of stories being told, and people are feeling less and less alone.
Asha Miller, breast cancer veteran

When I was first diagnosed, I felt very alone. ... I wanted to share my experience in hopes that other people would feel less alone.
Kody Green, living with schizophrenia

It’s really about connecting with other people. That’s what broke me out of my shell. So, I’m really grateful for meeting people [who] confirm I’m not alone in this disease.
Alisha Bridges, living with psoriasis

Tippi
These community-sourced tips can help you — and others — live well every day. Join the exchange of tips, advice, and aha moments.
Before today I had never met anybody with MASH. … This has been incredibly helpful to meet you. Better than that, it’s been hopeful.
— Jeff Beckley, diagnosed with MASH in 2024

Susan Jara
Parent of child with anaphylaxis
“You carry around the device and you watch the videos, and you know that it's there to help. But, you know, when push comes to shove and it's time to use it, it's very nerve wracking.”
Transcript Available

Monique
Heart disease survivor
“The physician said, ‘You know, I have some really important news to share with you. You're very sick.’”
Transcript Available

Jayme Kelly
Stroke survivor
“My doctors only focused on my physical health. They focused on the fact that I can talk again. The fact that I can walk again. No one focused on my mental and emotional health at all.”
Transcript Available

Nicole Gillen
Caring for a daughter with schizophrenia
“[I created] a series of 10 things that she has to do basically every day. ... This [was giving] her structure for the first time, really, in five years.”
Transcript Available

Thomas
Living with multiple myeloma
“I was completely shocked when I was diagnosed with myeloma … and finding out that it was most common in African Americans, I was shocked even more because I'd never heard of it.”
Transcript Available

Harmon
Living with Crohn's disease
“If I don't sleep correctly … my body doesn't have a chance to heal and recover. Everything is harder.”
Transcript Available
Most of the people I saw did not look like me. … And the interesting fact about seeing only a handful of people who look like me is I tend to gravitate towards those people because I want to talk to them and see what's happening.
— Josephine Dakers-Brathwaite, diagnosed with multiple myeloma in 2017
Stories of Breast Cancer
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Breast Cancer
‘There’s No Manual’: Intimacy After Breast Cancer Treatment
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Breast Cancer
'I Could Just Show Up as Myself'
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Breast Cancer
Being Black With Metastatic Breast Cancer: ‘It’s a Disadvantage’
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Breast Cancer
Feel for Yourself
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Breast Cancer
Redefining ‘Why Me?‘ When Living With Metastatic Breast Cancer
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Breast Cancer
Talking to Kids About Mom's Breast Cancer Diagnosis
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Our top priority is making sure our community is informed. Knowledge is power — and it’s often our first line of defense.
— Tari Hanneman, Human Rights Campaign







