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Confident in your skin.

Your daily companion for living well with Lichen Sclerosus.

Developed with the support of the Dutch Lichen Sclerosus Foundation and Startup Incubator UtrechtInc.

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Navigate LS with confidence and care

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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 for life with LS: daily support, more insight and less uncertainty. Follow your treatment plan, track your symptoms, learn what works for your body, and find reliable information in one place.

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

Free beta now open. A completely renewed version is on its way.
Be part of the journey.

Built together with the LS community

We work closely with the Dutch Lichen Sclerosus Foundation. They help us test new features and share our mission within their community, so that everything we build is rooted in the real, lived experience of people with LS.

Our partnerships are built on shared commitment. This photo was taken at the National LS Information Day, where we were invited by the Dutch LS Foundation to connect with the community. We are deeply grateful to the women who spoke with us there so openly. Your vulnerability and trust were incredibly moving; your stories are the foundation of everything we are building.
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National LS Information Day, Netherlands 2025

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

Set up your own treatment plan and get gentle reminders, so you don't have to keep it all in your head. Consistent treatment is important with LS.

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

Clear, easy-to-read articles about LS and links to trusted organizations, whether you're newly diagnosed or years in.

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 grow through partnerships with national LS organizations and healthcare experts. This way, local recommendations and resources can be added for each country, without rebuilding the app each time.​

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

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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.

Living with LS?

Try the free beta and help shape the app.

Working in healthcare or with an organization?

Healthcare professionals, patient organizations, researchers and partners: let's work together.

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