Build the Future of LS Care

Your gift helps launch the first LS Specialist Training and changes what happens next.

Every gift is matched until we reach $24,000.

🎁 Unlocks the December 17 Whole Body LS Q&A.

🎁 Gifts of $100+ receive lifetime access to the Best of WHS Replay Series.

👆 Give now and unlock the Q&A + match

Too many people with LS wait years for answers. Many are dismissed, misdiagnosed, or told to “give it time.” By the time they find help, their symptoms have worsened and their confidence is gone.

No one should have to live this way.

The Provider Continuous Education Program (PCEP) is the first LS Specialist Training designed to fix the root problem: providers are not trained. Your support helps finish:

The PCEP course
The provider resource library
The clinical tools providers will rely on for years

Your gift builds the future of LS care.

If we reach our $24,000 goal, we unlock access to a 90-minute live Q&A with:

✨ Heather Cooan, Integrative Oncology and Autoimmune Nutrition Specialist and LS thriver
✨ Christine Myers, Functional Nutrition Practitioner for Autoimmunity, MCAS, Histamine Intolerance, and LS Warrior

Donors receive:
• The live session
• Replay access
• Early question submission

This is the kind of whole-body LS guidance most people never receive in a medical appointment.

👆 Give now and unlock the Q&A + match

Your gift brings clarity to someone still searching for answers.

Your gift does more than open the event. It moves the Provider Continuous Education Program into its next phase of development:

✔️ Finish the PCEP course recordings

✔️ Build the provider resource library

✔️ Finalize the clinical tools clinicians will use

✔️ Prepare for the first LS Specialist Training launch

This is how we shorten the years-long diagnostic delay.
This is how we improve care from the first appointment.
This is how we build the future of LS care together.

⭐ More Voices You Helped Lift

“My life changed when I finally understood what LS was.”
“If someone had recognized this years earlier, my life would look different.”
“I finally understood what was happening to my body.”

Read More Patient Stories

Your gift ensures providers have the training to prevent stories like these.

👆 Give now and unlock the Q&A + match

You can help build the future of LS care.
Your matched gift helps unlock the Q&A and completes the next phase of PCEP.

👆 Give now and unlock the Q&A + match

About the LSSN

The Lichen Sclerosus Support Network (LSSN) is the only English-based organization providing easy-to-understand, evidence-based education for patients and providers. It also offers global patient support through a connected community that understands the challenges of living with LS.