Understanding Lymphedema Webinar

We’re truly grateful for this new collaboration with the National Lymphedema Network and for the opportunity to share trusted resources on Turner syndrome and lymphedema with our community.

Turner syndrome and lymphedema are typically related to a genetic lymphatic response. Topics of particular interest to our audience include:

• How lymphedema may present in infant patients with Turner syndrome
• Causes of lymphedema
• Short-term and long-term treatment approaches
• Whether lymphedema can progress or resolve over time
• Long-term impact of the condition
• Health-related and insurance considerations
• Strategies to manage and cope with lymphedema
• Any relevant medical advancements or research developments
• Resources for compression

Who Should Attend & What You’ll Gain

This webinar is highly relevant not only to professionals, but to the general public—because nearly everyone has a family member, friend, colleague, or community connection who experiences lymphedema. Whether you work in education, healthcare, counseling, or simply want to be more informed and inclusive, this session offers knowledge you can immediately apply.

About the Presenter
Lauren Brown, MSOT, OTR/L, CLT-LANA
Rocky Mountain Lymphedema and Cancer Rehab 

Lauren Brown represents the National Lymphedema Network and operates a private practice dedicated to providing individualized lymphedema care, having transitioned from corporate healthcare. Since 2018, she has specialized in lymphedema services and oncology rehabilitation, working with patients across the lifespan—from infancy through end of life—with and without cancer diagnoses.

Recognizing the limited availability of lymphedema therapy resources, Lauren has forged an independent path, using a highly personalized, trial-and-response approach to adapt treatments based on each patient’s needs. She has successfully delivered care both in person and through telehealth consultations worldwide, creating meaningful outcomes for individuals with primary and secondary lymphedema. Lauren is also actively developing standardized care protocols for pediatric lymphedema, advancing the field and expanding access to specialized treatment.

Who Should Attend:
Patients, caregivers, allied health professionals, clinical researchers, health administration, policymakers, and philanthropists

Event Link:
Check the email you provided to receive the webinar link.

Cost:
Free. Donations are appreciated.