Celebrating Lymphedema Awareness Month

by | Mar 4, 2024 | Lymphedema, News

What is Lymphedema Month

Lymphedema Awareness Month in March does more than signal the arrival of spring; it marks a pivotal period for raising awareness about lymphedema, a condition impacting millions globally. This month serves as a crucial reminder of the challenges faced by those living with the condition, emphasizing the importance of community support, education, and advocacy. Let’s take a moment to delve into the significance of this month and discuss how we can all contribute to this essential cause.

Understanding Lymphedema

Lymphedema is a chronic condition characterized by swelling in body parts, often in the arms or legs, due to a blockage in the lymphatic system. Consequently, this can lead to discomfort, mobility issues, and emotional distress. Moreover, despite its significant impact, lymphedema remains underrecognized and underdiagnosed, highlighting a gap in awareness and understanding within both the general public and the medical community.

The Importance of Awareness

  • Educate the public about the signs, symptoms, and treatment options available for lymphedema.
  • Support individuals and families affected by lymphedema through community-building and resources.
  • Advocate for better healthcare policies, research funding, and insurance coverage for lymphedema treatments.

How You Can Get Involved

  1. Spread the Word: Use your voice on social media to share information about lymphedema. Hashtags like #LymphedemaAwareness and #MarchingForward can help your message reach a broader audience.
  2. Participate in Events: Many organizations host events during March to support lymphedema awareness. Look for virtual walks, webinars, and fundraisers to join.

Join the Movement Against Lymphedema: Empower, Educate, Advocate!

Click the links below for more information:

Additional Ways to Support

  • Educate Yourself and Others: Take the time to learn more about lymphedema. Sharing accurate information can help dispel myths and encourage those undiagnosed to seek help.
  • Support Lymphedema Research: Consider donating to organizations focused on lymphedema research or advocating for better treatment options. Your support can make a significant difference in advancing the understanding of this condition.
  • Wear Teal and Turn Your Social Media Profile Picture Teal: Teal is the color of lymphedema awareness. Wearing teal ribbons, teal clothing or turning your social media image teal can spark conversations and show solidarity with the lymphedema community.

    Stories of Hope and Resilience

    This month, we additionally share inspiring stories of individuals living with lymphedema. Importantly, these narratives underscore the strength, resilience, and hope that epitomize the lymphedema community. Furthermore, by attentively listening

    Amanda Sobey

    About the author

    Amanda Sobey is a certified personal trainer, certified nutritionist, and lymphedema coach with over 20 years of personal experience battling lymphedema.

    She is the creator of the 16-Week Ultimate Lymphedema Journey program, which combines fitness, nutrition, and self-care to empower those with lymphedema, lipedema, or lipolymphedema.

    Recent posts

    Manitoba Legislature Shines in Teal for World Lymphedema Day

    Amanda Sobey’s battle with lymphedema began over two decades ago, stemming from a mosquito bite followed by a traumatic event that led to abnormal swelling in her right leg. Faced with a condition that is incurable, she turned her life around from despair to advocacy. Now a personal trainer, nutritionist, and lymphedema coach, Sobey’s journey from patient to president of the Lymphedema Association of Manitoba is a testament to her resilience and dedication to making a difference.

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