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

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/givingtuesday

Additional Resources:

• Learn more about LSSN's programs and resources: https://lssupportnetwork.org
• Join LSSN's online community: https://lssupportnetwork.org/membership
• Attend LSSN's Giving Tuesday live events: https://lssupportnetwork.org/givingtuesday

Thank you for listening and for your support!