We’ve been waiting for you.
You have Lichen Sclerosus, right?
You’re looking for information on what this is and what it means for your life, right?
You've mostly been going it alone and you're ready for that to change, right?
I thought so!
Relax. Release the tension you’ve been holding in your neck, shoulders, back, PELVIS.
What if I told you there is a way to reclaim your life from LS? Yes, your sex life too.
What if I told you there was a path toward acceptance and resilience.
Don’t believe me?
I can prove it.
My name is Kathy and I host Lichen Sclerosus Podcast and Lichen Sclerosus Support Virtual Meetups. I’ve spoken to many people who have found acceptance, resilience, and live happy normal lives. Yes, including sex lives.
I am one of those people. And I want to help you become one of those people too.
Now I’m not saying it’s going to be easy. As a matter of fact, it’s going to be hard work, both mental and physical. But if you’re truly ready to take back your life, like I know you can, we’re here to support you every step of the way.
Are you ready?
LSSN was originally built as a way to support people with Lichen Sclerosus. It's grown into something so much bigger. LSSN is a nonprofit who's mission is to empower people with LS to get diagnosed earlier.
Education, Information, and Resources
Do you have a burning question and you need a quick answer? You've come to the right place. Check our growing FAQ page to see if we've got you covered.
Can't find what you're looking for? No problem drop us an email with your question and we'll get back to you as soon as possible.
Who knows? If we get the same question enough times we'll add it to the page.
Interested in Lichen Sclerosus research? Coming soon a searchable database of up-to-date Lichen Sclerosus studies, trials, and research papers for you to read and provide for your medical professional.
We're always looking for more information. Have a research paper you would like to submit to the database?
Click the link below, fill out the form, and tell us about it. We'll check it out as soon as possible. Thanks!
Are you having a hard time finding quality care? Would you like someone knowledgeable about LS? Also coming soon a database of medical professionals referred by people with Lichen Sclerosus. So you can be confident you're going to the right place.
Want to recommend your medical professional? Click the link below and submit their information.
So you don't have to fight alone anymore
We've got you covered. Choose the amount of support you need.