Built by People with HS, for People with HS.

🧑 Welcome to HS Warriors

A Safe Space for People Living with Hidradenitis Suppurativa

If you’re living with Hidradenitis Suppurativa (HS) β€” or supporting someone who is β€” you’re not alone.
HS Warriors is a dedicated forum and community for real talk, real support, and real solutions.

Whether you’re newly diagnosed or have been battling HS for years, here you’ll find people who truly understand what it’s like β€” because they’ve lived it.

πŸ’¬ Start Talking. We’re Listening.

This is your space. No judgment. No shame. Just honest, supportive conversations about:

πŸ’Š Treatments that work (and don’t)
πŸ€• Dealing with pain, flares, and recovery
🍽️ Diet, skin care, supplements & self-care
🧠 Mental health, confidence & emotional support
❀️ Relationships, dating, intimacy & self-image
πŸ§β€β™€οΈ Parenting with HS and supporting loved ones
πŸ“š Latest research, medications, and clinical trials
πŸ‘š Lifestyle tips for clothing, hygiene & more

🎯 Why Join HS Warriors?

βœ… Connect with people who really get it
βœ… Ask questions, vent, share wins, or just read
βœ… Stay anonymous or build your profile β€” it’s up to you
βœ… 100% free and always will be
βœ… Moderated with care: no spam, no trolls, no shame

πŸ“’ Featured Topics

What helped your worst flare-up?
HS and sex β€” how do you cope?
Daily products you can’t live without
Has your HS changed after pregnancy?
Mental health check-in: How are you really?

πŸ™Œ Made by People with HS. For People with HS.

We’re not doctors or a pharmaceutical company β€” we’re patients, caregivers, friends, and fighters.
This is a grassroots project built out of frustration with how isolating HS can be β€” and the belief that we deserve a space to talk freely, safely, and without shame.

πŸ”’ Your Privacy Matters

Your identity and posts are always safe. You can use a nickname, post anonymously, and control what others see. HS Warriors is built with privacy and trust at its core.

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