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Lipedema Awareness Month: Raising Awareness and Advocating for Proper Diagnosis and Treatment

Lipedema Awareness Month: Raising Awareness and Advocating for Proper Diagnosis and Treatment

June is a significant month for the Lipedema community as it marks Lipedema Awareness Month, with World Lipedema Day celebrated on June 11. This month is dedicated to increasing awareness about lipedema, a chronic condition that affects millions of women worldwide. Despite its prevalence, lipedema remains underdiagnosed and misunderstood. At Lipedema Surgical Solutions, we are committed to spreading awareness, educating the public, and supporting those affected by lipedema.

Understanding Lipedema

Lipedema is a chronic condition characterized by the abnormal and symmetrical accumulation of subcutaneous adipose tissue  [fat]  in the legs, arms, and sometimes other body parts. Unlike ordinary obesity, the fat deposits in lipedema are painful or tender and do not respond well to conventional diet and exercise, often remaining unchanged even as other body fat decreases. The condition typically progresses through stages, from mild enlargement of the limbs to more severe cases where mobility is significantly affected. Lipedema is also marked by a tendency to bruise easily and may include symptoms such as fibrosis, which is a thickening and hardening of tissue. While it is believed to have a genetic component, lipedema almost exclusively affects women and is often linked to hormonal changes associated with puberty, pregnancy, or menopause. Coexisting conditions such as lymphedema, swelling due to lymph fluid buildup, and venous insufficiency are common.

Why Lipedema is Under-diagnosed

Lipedema is often misdiagnosed as obesity or lymphedema due to its similar appearance. This misdiagnosis can delay proper treatment and exacerbate symptoms. The lack of awareness among healthcare professionals and the general public contributes to the underdiagnosis of lipedema. Many women struggle for years without receiving a correct diagnosis, leading to frustration and worsening health outcomes. 

Awareness and recognition of lipedema is poor in the public and among medical professionals, which leads to some women who have lipedema not being diagnosed with lipedema.  The opposite can occur.  Not everyone with large legs and ankle cuffs and who appears to have lipedema disease suffers from it. Several other conditions and diseases can mimic the appearance of lipedema, making accurate diagnosis essential for effective treatment.  Misdiagnosis of lipedema leads to improper treatment, so it is important to be careful and thorough. 

Spreading Awareness and Advocating for Proper Diagnosis

Women with lipedema can take several steps to spread awareness and advocate for themselves:

  1. Educate Yourself and Others: Learn about lipedema and share information with friends, family, and healthcare providers. Utilize resources from reputable organizations such as Lipedema Surgical Solutions and Lipedema UK.
  2. Seek Specialist Care: If you suspect you have lipedema, consult a specialist experienced in diagnosing and treating the condition. In St. Louis, MO, Dr. Wright is a leading expert in lipedema treatment.
  3. Join Support Groups: Connect with others affected by lipedema through support groups and online communities. Sharing experiences can provide emotional support and valuable information.
  4. Participate in Awareness Events: During Lipedema Awareness Month, engage in events to learn more about the condition and support the community.

Attend Dr. Wright’s Speaker Series

Join Dr. Wright this June for informative events to foster a greater understanding of lipedema and its treatment. These events are an excellent opportunity to learn from experts and connect with community members.

  • June 5th at 7 PM CST via Zoom: Dr. Wright and Tactile Medical discuss how improper diagnosis leads to improper treatment. Special guest Connie Boyer, a lipedema patient, will share her experiences. Link to join.
  • June 11th at 6:30 PM CST via YouTube Live: Dr. Wright will discuss lipedema and lymphatic function, lipedema, and gait changes, followed by a Q&A session. Submit questions ahead of time at or join live. Join on YouTube.
  • June 12th at 12 PM CST via YouTube Live: Dr. Wright and Lipedema UK will cover topics on lipedema, lymphatic function, and gait changes. View on YouTube.
  • June 13th from 5:30 PM to 7:30 PM CST via YouTube Live: Dr. Wright will discuss the benefits of lipedema reduction surgery and knee mechanics at the LE&RN event. Join via livestream or attend in person at The Lodge in Des Peres, 1050 Des Peres Road, Des Peres, MO 63131. Join on YouTube.
  • June 26th via Zoom: Time and link coming soon! Join Dr. Wright and the Lipedema World Alliance to discuss Lipedema and Lipedema Awareness Month. Details will be added to our socials soon. Your Primary Information Hub is a comprehensive resource for anyone seeking detailed information about lipedema. The website features:

  • Educational Articles: In-depth coverage of lipedema’s stages, symptoms, and management strategies.
  • Treatment Information: The latest advancements in both surgical and non-surgical treatment options.
  • Patient Resources: Guides and tools to help patients manage their condition effectively.
  • Medical Research: Updates on new research publications related to lipedema and its treatment.

Dr. Wright’s YouTube Channel: Visual Learning and Community Engagement

Dr. Wright’s YouTube channel, Lipedema Info, offers:

  • Informative Videos: Covering basics to complex treatment procedures.
  • Patient Testimonials: Stories from those who have undergone treatment.
  • Q&A Sessions: Regular sessions addressing common questions and concerns.
  • Conference Updates: Presentations from national and international medical conferences.

Lipedema Group – A Facebook Community

The Lipedema Group – on Facebook is a supportive community offering:

  • Peer Support: Engage with others who understand the challenges of living with lipedema.
  • Latest News and Research: Stay informed about the latest findings.
  • Advice and Tips: Practical daily advice on managing the condition.

Instagram: A Glimpse into Real-life Experiences

Dr. Wright’s Instagram page, @lipedemasurgicalsolutions, provides:

  • Before and After Photos: Visual evidence of treatment effectiveness.
  • Daily Tips and Motivation: Regular posts to inspire and guide those living with lipedema.
  • Community Interaction: Engage with a supportive community.

Pinterest: Educational Resources and Inspiration

Dr. Wright’s Pinterest page, Laser Lipo Vein, offers:

  • Informative Pins: Links to articles, research papers, and treatment information.
  • Inspiration Boards: Showcasing success stories and positive affirmations.
  • Community Engagement: Connect with others on a similar journey.

Join Our Lipedema Community – You Aren’t Alone!

Living with lipedema can be challenging, but with the right resources and support, managing the condition becomes significantly easier. From comprehensive information hubs like to engaging social media platforms, numerous avenues exist for education, support, and community. Dr. Wright’s dedication to providing resources highlights the growing awareness and support for those battling lipedema.

Remember, while online resources are invaluable, they should complement, not replace, professional medical advice. Always consult with healthcare professionals for personalized medical guidance and treatment plans.

Contact Lipedema Surgical Solutions

If you or someone you know is struggling with symptoms of lipedema, don’t hesitate to seek help. Contact Lipedema Surgical Solutions online for guidance on understanding lipedema, obtaining a proper diagnosis, and exploring treatment options. Our team, led by Dr. Wright, is dedicated to providing comprehensive care and support for women with lipedema.

Keywords: Lipedema, Lipedema Treatment, St. Louis MO Lipedema Specialists, Dr. Wright St. Louis, Lipedema Awareness Month, World Lipedema Day

By spreading awareness and advocating for proper diagnosis and treatment, we can improve the lives of those affected by lipedema. Let’s work together to make a difference this Lipedema Awareness Month and beyond.