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!