Registration Information

Topic Overview

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

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.

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.

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WE- Understanding Lymphedema

By TURNER SYNDROME FOUNDATION INC

WE- Understanding Lymphedema

Donations and sponsorships make learning events such as this WE LEARN webinar activity provided freely and accessible to everyone. Please support today!