Today, January 17, is a special day for all women affected by lichen sclerosus vulvae. Vulvar lichen sclerosus (VLL) as it is (LSV) as we celebrate World Vulvar Lichen Sclerosus Day 2025.
On this occasion, I am writing to you as president of the Nixarian Foundationand to invite you to join this very necessary cause.
Together we can break the silence and eliminate the taboo that so often prevents women from seeing a specialist.
It is exciting to see how this day is having repercussions in national media such as Infosalus y Telecinco. I want to thank these platforms for their help in making this disease visible.
Early diagnosis can change lives and prevent serious complications such as vulvar cancer.
At the Nixarian Foundation we are driven by three fundamental principles:
Research: Promote studies for early diagnosis and effective treatment of LEV.
2. Outreach: Raise public awareness and train health professionals.
3. Access to treatment: Offer innovative solutions such as treatment with stem cells from the patient’s own fat to women in vulnerable situations.
As a woman, surgeon and scientific researcher, it fills me with hope to know that we have a treatment such as the Liquenia TreatmentTreatment, which has already restored the quality of life to hundreds of women affected by Lichen Sclerosus Vulvaris (LSV).
World Vulvar Lichen Sclerosus Day 2025
Talking about LEV is one way to help. Don’t give up: help exists, and it’s within your reach. And World Vulvar Lichen Sclerosus Day 2025 is the perfect time to take action!
I also invite you to read the articles published today in our blog of the Nixarian Foundation and to share this information in your social networks.
Together we can make a difference.
And remember that the hashtag for today is: #DiaLEV2025
Thank you from the bottom of my heart!





