Rebuilding Relationships and Reconnecting with Lichen Sclerosus

Topics:

• What is the LSSN Wholistic Healing Summit?
• Importance of addressing relationships affected by Lichen Sclerosus (LS)
• Summit focus: Partners, Caregivers, and Disclosure
• Sessions for patients, partners, and caregivers
• Wellbeing activities for stress management
• Opportunities to connect with other attendees

Key Points

• LSSN is a non-profit patient organization providing education and support for those with LS.
• LS impacts all aspects of life, including relationships.
• The summit helps patients, partners, and caregivers discuss LS, manage sexual health, and build intimacy.
• Free, Value, and All Access ticket options are available.

Time Stamps

00:00:00 - Introduction to Holistic Healing Summit

00:02:36 - Challenges in Talking About LS

00:04:38 - Disclosing LS to Partners

00:08:45 - Supporting Caregivers of LS Patients

00:10:07 - Managing LS Symptoms and Well-being

00:15:18 - Ticket Options for the Summit

00:16:09 - All Access Pass Benefits

00:17:18 - Partnership Meetup

00:18:48 - Exclusive Summit Benefits

00:20:55 - Summit Evolution and Community Impact

Mentioned in this episode:

Demystify LS with Dr. jill Krapf

Whether you're personally affected by LS, care for someone who is, or simply want to learn more about vulvar health, this event is for YOU.

Join renowned LS specialist Dr. Jill Krapf for a FREE interactive learning experience that will demystify LS and empower you with knowledge.

In this engaging session, you'll:
* Gain a deeper understanding of LS: Dr. Krapf will guide you through two fascinating case studies, sharing her expertise on symptoms, diagnosis, and treatment options.
* Test your knowledge: Participate in live polls and quizzes to see how much you know and learn from others' experiences.
* Get your questions answered: Dr. Krapf will host a live Q&A session, giving you the opportunity to get your questions answered.
* Become an advocate for vulvar health: Learn how to break the stigma and support those affected by LS.

This event is perfect for:

* People with LS who want to take control of their health.
* Caregivers seeking to better support their loved ones with LS.
* Healthcare professionals who want to expand their knowledge of LS.
* Anyone curious to learn more about vulvar health and contribute to a more informed and supportive community.

Don't miss this opportunity to:
* Learn from a leading expert in LS care.
* Engage with real-life case studies and test your knowledge.
* Connect with others who are passionate about vulvar health.
* Become an advocate for breaking the stigma around LS.

This event is part of our "Year of the Vulva: Breaking the Stigma" campaign. We believe that knowledge is power, and by learning more about LS, we can break down barriers and create a more supportive and understanding environment for everyone.