<description>&lt;p&gt;Join us for an insightful conversation with Dr. Jill Krapf, a leading expert in vulvar lichen sclerosus (LS), as we discuss the challenges and opportunities in LS care and introduce the Provider Continuous Education Program (PCEP).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Why Provider Education Matters:&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;LS is often misdiagnosed or diagnosed late, leading to years of unnecessary suffering for patients.  &amp;nbsp; &lt;/li&gt;&lt;li&gt;Many healthcare providers lack the knowledge and training to properly diagnose and manage LS.  &amp;nbsp; &lt;/li&gt;&lt;li&gt;The PCEP will equip providers with the tools and resources they need to provide effective, patient-centered LS care.  &amp;nbsp; &lt;/li&gt;&lt;/ul&gt;&lt;br/&gt;&lt;p&gt;&lt;strong&gt;How the PCEP Will Make a Difference:&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The PCEP will provide comprehensive education on LS, covering diagnosis, treatment, and patient communication.  &amp;nbsp; &lt;/li&gt;&lt;li&gt;It will feature expert-led training by experienced LS specialists.  &amp;nbsp; &lt;/li&gt;&lt;li&gt;It will focus on evidence-based practices and patient-centered care.  &amp;nbsp; &lt;/li&gt;&lt;li&gt;It will create a network of knowledgeable healthcare providers who can support each other and share best practices.  &amp;nbsp; &lt;/li&gt;&lt;/ul&gt;&lt;br/&gt;&lt;p&gt;&lt;strong&gt;Call to Action:&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;Support the PCEP and help us transform the future of LS care. Your donation will directly impact the lives of those affected by this often-misunderstood condition.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Donate to LSSN's Campaign:&lt;/strong&gt; https://lssupportnetwork.org/givingtuesday&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Additional Resources:&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Learn more about LSSN's programs and resources: https://lssupportnetwork.org&lt;/li&gt;&lt;li&gt;Join LSSN's online community: https://lssupportnetwork.org/membership&lt;/li&gt;&lt;li&gt;Attend LSSN's Giving Tuesday live events: https://lssupportnetwork.org/givingtuesday&lt;/li&gt;&lt;/ul&gt;&lt;br/&gt;&lt;p&gt;&lt;strong&gt;Thank you for listening and for your support!&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;Mentioned in this episode:&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Finally Get Clear Answers About LS, Menopause, and Your Treatment&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;If you’ve ever found yourself listening to this podcast searching for answers…
trying to figure out why your body feels different…
why your treatment isn’t working…
or whether this is menopause, lichen sclerosus, or something else entirely…

You’re not alone.

And more importantly—
you’re not the problem.

Most people with LS are left trying to piece together a care plan from short appointments, conflicting advice, and hours of searching like this.

That’s exactly why we created the Wholistic Healing Summit.

This free, live event (May 11–15, 2026) brings together 12+ leading specialists to help you finally connect the dots between your symptoms, your treatment, and your next steps.

Inside the summit, you’ll get answers to questions like:

Why does my treatment stop working?
Is this LS progression… or hormonal change?
What order should I actually be using my medications?
How do I navigate intimacy, pain, and changing skin?

And if you choose to upgrade, you’ll also get access to exclusive Q&amp;A sessions,
where you can hear real questions from people just like you…
and get expert answers you’d normally wait months (and pay hundreds) for.

This is where the guessing stops.

👉 Register here: https://lssupportnetwork.org/whs

If you’re tired of second-guessing your care… this is your next step.

P.S. If you’ve ever wished you had more time with a specialist or left an appointment with unanswered questions, the All-Access Pass gives you direct access to expert Q&amp;As you can revisit anytime.&lt;/p&gt;</description>

Lichen Sclerosus Podcast

Kathy Ruiz-Carter

The Future of LS Care: A Conversation with Dr. Jill Krapf

DEC 9, 202454 MIN
Lichen Sclerosus Podcast

The Future of LS Care: A Conversation with Dr. Jill Krapf

DEC 9, 202454 MIN

Description

Join us for an insightful conversation with Dr. Jill Krapf, a leading expert in vulvar lichen sclerosus (LS), as we discuss the challenges and opportunities in LS care and introduce the Provider Continuous Education Program (PCEP).Why Provider Education Matters:LS is often misdiagnosed or diagnosed late, leading to years of unnecessary suffering for patients.   Many healthcare providers lack the knowledge and training to properly diagnose and manage LS.   The PCEP will equip providers with the tools and resources they need to provide effective, patient-centered LS care.   How the PCEP Will Make a Difference:The PCEP will provide comprehensive education on LS, covering diagnosis, treatment, and patient communication.   It will feature expert-led training by experienced LS specialists.   It will focus on evidence-based practices and patient-centered care.   It will create a network of knowledgeable healthcare providers who can support each other and share best practices.   Call to Action:Support the PCEP and help us transform the future of LS care. Your donation will directly impact the lives of those affected by this often-misunderstood condition.Donate to LSSN's Campaign: https://lssupportnetwork.org/givingtuesdayAdditional Resources:Learn more about LSSN's programs and resources: https://lssupportnetwork.orgJoin LSSN's online community: https://lssupportnetwork.org/membershipAttend LSSN's Giving Tuesday live events: https://lssupportnetwork.org/givingtuesdayThank you for listening and for your support!Mentioned in this episode:Finally Get Clear Answers About LS, Menopause, and Your TreatmentIf you’ve ever found yourself listening to this podcast searching for answers… trying to figure out why your body feels different… why your treatment isn’t working… or whether this is menopause, lichen sclerosus, or something else entirely… You’re not alone. And more importantly— you’re not the problem. Most people with LS are left trying to piece together a care plan from short appointments, conflicting advice, and hours of searching like this. That’s exactly why we created the Wholistic Healing Summit. This free, live event (May 11–15, 2026) brings together 12+ leading specialists to help you finally connect the dots between your symptoms, your treatment, and your next steps. Inside the summit, you’ll get answers to questions like: Why does my treatment stop working? Is this LS progression… or hormonal change? What order should I actually be using my medications? How do I navigate intimacy, pain, and changing skin? And if you choose to upgrade, you’ll also get access to exclusive Q&A sessions, where you can hear real questions from people just like you… and get expert answers you’d normally wait months (and pay hundreds) for. This is where the guessing stops. 👉 Register here: https://lssupportnetwork.org/whs If you’re tired of second-guessing your care… this is your next step. P.S. If you’ve ever wished you had more time with a specialist or left an appointment with unanswered questions, the All-Access Pass gives you direct access to expert Q&As you can revisit anytime.