HS Brotherhood
🔥 Welcome to the HS Brotherhood Podcast 🔥
Hosted by Joey Torre & Parish Armstead
👊 Real Talk. Raw Stories. Unbreakable Brotherhood.
Living with Hidradenitis Suppurativa (HS) as a man can feel isolating—but it doesn’t have to. Join Joey Torre (HS advocate and resilience coach) and Parish Armstead (patient warrior and community builder) as they smash the stigma around men’s health and HS.
What You’ll Hear:
✅ No-BS Conversations: From flare-ups to fatherhood, mental health to manhood myths.
✅ Expert Insights: Dermatologists, therapists, and researchers break down treatments and hope.
✅ Brotherhood Wins: Stories of men thriving with HS—in the gym, at work, and beyond.
✅ Your Voice: Listener Q&As, shoutouts, and uncensored lived experiences.
Why Listen?
- “We’re not just surviving HS—we’re rewriting what it means to be strong.”
- For guys tired of silent suffering: This is your mic drop moment.
🎧 Subscribe now on [Apple Podcasts/Spotify/etc.] and join the tribe that’s turning pain into power.
New episodes drop every Tuesday. Tag a brother who needs this crew. 💪
HS Brotherhood
Why Your Story Matters in Rare Disease Research
Welcome to Season 2, Episode 1 of HS Brotherhood! Your hosts Joey Torre and Parish Armstead are back and kicking off this season with a powerful conversation you won’t want to miss. This week, they’re joined by Stacey Haines, Patient Outreach and Social Media Manager at Rare Patient Voice — a company dedicated to empowering patients and caregivers from rare disease communities to make their voices heard.
In this episode:
- Stacey opens up about her personal journey — from caregiver to patient-advocate — and how that experience shaped her work at Rare Patient Voice.
- She shares how Rare Patient Voice connects patients and caregivers with research opportunities (including paid surveys and interviews), helping bridge the gap between lived experience and medical development.
This episode brings fresh perspective on giving voice to underserved communities. With Stacey’s lived perspective and Rare Patient Voice’s mission to uplift patient opinion in research, you’ll walk away with a deeper understanding of both the human side of rare disease and the strategic implications for ethical engagement.
Connect & engage
Check out Rare Patient Voice (https://rarepatientvoice.com) to learn more about how patients and caregivers can contribute to research and influence change.
Stay tuned for the rest of Season 2 of HS Brotherhood - subscribe so you get all the latest episodes.
This podcast was made possible by Moonlake.