LSSN's Mission
Every person affected by Lichen Sclerosus deserves accurate and thorough information. This allows them to make sound decisions on their health.
We also believe every provider who treats a patient with or possibly with Lichen Sclerosus should be well-informed on diagnosing, treating, and caring for that person.
That is why Lichen Sclerosus Support Network's mission is to provide accurate and evidence-based education to patients and providers.
Our Vision
LSSN's vision is a world where those affected by lichen sclerosus are informed, educated, and get diagnosed early.
LSSN will empower vulva owners to take an active role in their vulvar health. Programs such as the “Check Your Vulva” program will create an appreciation and knowledge of the vulva. These programs will allow people to advocate for themselves better, leading to earlier diagnosis.
On the other hand, the more Lichen Sclerosus specific education we can provide medical providers, the earlier they can diagnose people. Hence, our second program, the provider education program.
By targeting the problem from both sides, we will reduce the current wait time of 5-15 years for an LS diagnosis.
Company Details
- Employees
- 2
- Founded
- -
- Address
- Chicago, Il, Us
- Industry
- Non-Profit Organizations
- Keywords
- Lichen Sclerosus Awareness, Lichen Sclerosus Support, Women's Health Advocate, Lichen Sclerosus Education, Lichen Sclerosus Provider Directory, Lichen Sclerosus Patient Advocate, Lichen Sclerosus Advocate, Lichen Sclerosus Evidence-Based Research, Lichen Sclerosus Support Network.
- HQ
- Chicago, IL
- Competitors
- Verein Lichen Sclerosus, Sitz in der Schweiz, aktiv und engagiert mit Aufklärung n ganz Europa, Stichting Lichen Sclerosus, TLLC (The Lost Labia Chronicles), Scleroderma & Raynaud's UK, The Lavender Woman Foundation, Berufsverband der Frauenärzte e.V., PoTS UK, INSTITUTE FOR LICHEN SCLEROSUS & VULVAL HEALTH INC, TRANS-IT FOUNDATION, Feeding Charlotte.
Lichen Sclerosus Support Network Questions
Lichen Sclerosus Support Network's website is https://lssupportnetwork.org/about-lichen-sclerosus-support-network/
Lichen Sclerosus Support Network's LinkedIn profile is https://www.linkedin.com/company/lichen-sclerosus-support-network
Lichen Sclerosus Support Network has
2 employees.
View email and phone details for 2
employees at Lichen Sclerosus Support Network.
Lichen Sclerosus Support Network's industry is
Non-profit Organizations
Lichen Sclerosus Support Network's top competitors are
Verein Lichen Sclerosus, Sitz In Der Schweiz, Aktiv Und Engagiert Mit Aufklärung N Ganz Europa,
Stichting Lichen Sclerosus,
Tllc (The Lost Labia Chronicles),
Scleroderma & Raynaud's Uk,
The Lavender Woman Foundation,
Berufsverband Der Frauenärzte E.v.,
Pots Uk,
Institute For Lichen Sclerosus & Vulval Health Inc,
Trans-It Foundation,
Feeding Charlotte.
Lichen Sclerosus Support Network's categories are Non-profit Organizations
Lichen Sclerosus Support Network's founding year is 2021
