top of page

Confident in your skin.

Your daily companion for living well with Lichen Sclerosus.

Developed with the Dutch Lichen Sclerosus Foundation and supported by UtrechtInc.

IMG_8036.PNG

Navigate LS with confidence and care

IMG_8198.PNG
IMG_8041.PNG
Living with Lichen Sclerosus can be overwhelming — especially when answers are hard to find and support feels out of reach.

myLSCare is your personal companion app, designed to help improve your quality of life with LS — through daily support, better insights, and less uncertainty. Track your symptoms, follow your treatment plan, learn what works for your body, and access expert-reviewed guidance you can trust.

We’re building it with care — and with you in mind.

Launching in 2026.
Be part of the journey — as a user, partner, or supporter.
IMG_8042.PNG
We’re co-creating myLSCare with the Dutch Lichen Sclerosus Foundation, following the official national care guidelines in the Netherlands. Every insight, tool, and feature is built on clinical knowledge and deep, lived experience.

Built with experts, backed by trusted partners

IMG_8039.PNG

What myLSCare helps you do

Made for your daily life with LS — physical, emotional, and everything in between.

Symptom tracking

Understand your whole health story

Track symptoms, emotions, and lifestyle in one place. Over time, you’ll see patterns — helping you and your doctor make clearer, more informed decisions.

Treatment reminders

Stay on track, with less stress

Get gentle, personalized reminders so you never miss a treatment. Staying consistent can reduce flare-ups and long-term complications.

Data insights

See what’s working — and what’s not

Turn your daily tracking into insights. Visualize how your treatments, habits, and wellbeing connect — so you can make confident choices.

Trusted information

Learn about LS

Browse resources reviewed by LS experts — whether you're newly diagnosed or years in, you'll find answers you can rely on.

Research contribution

Support better care for everyone

By using the app, you can choose to anonymously share data to help researchers better understand LS — and help shape the future of care.

Shaping the future of LS care — together
 

We're building carefully, in partnership with patients, specialists, and organizations.

Our vision extends beyond the app itself — toward a future where every person with LS has access to the care, understanding, and confidence they deserve.

Here’s what’s next on our roadmap:

A private, moderated community space

Personal LS-health reports to share with your doctor

Localized app versions (starting with DE, US)

A clear, expert-reviewed FAQ for daily LS questions

Secure image upload and annotation for visual symptom tracking

Tools to connect patients with LS-informed specialists

LS care should reflect local needs — globally

Lichen Sclerosus care may look slightly different from country to country, but the need for clarity, confidence, and trusted guidance is universal.

That’s why myLSCare will expand through partnerships with national LS organizations and healthcare experts, ensuring that local recommendations and resources reflect each region’s needs — without reinventing the app each time.

Are you part of an LS organization or support network elsewhere? Let’s talk.

IMG_8039.PNG
IMG_8041.PNG
IMG_8043.PNG

Join the Movement

Whether you're living with LS, caring for someone who is, working in healthcare, or advocating for better support — we’d love to hear from you.
Sign up for early access, updates, or opportunities to collaborate.

Leave a message if you'd like — we're listening.

This helps us build support where it’s needed most.

bottom of page