Again! HEW Honored by Sonia Chasteen Memorial Fund - Community Foundation

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    • Home
    • About Us
    • news
    • All Things Lymphedema
    • Compression Garment Fund
    • in thanks
    • contact
    • how you can help HEW
    • Events
    • COVID 19
    • HEW on YouTube - TBA

  • Home
  • About Us
  • news
  • All Things Lymphedema
  • Compression Garment Fund
  • in thanks
  • contact
  • how you can help HEW
  • Events
  • COVID 19
  • HEW on YouTube - TBA

Educate - Encourage - Empower

All Things Lymphedema

Making Wisconsin History

Wisconsin's first and only financial aid program helping Lymphedema survivors obtain their medically needed compression garments.     


Since 2019, more than $100,000.00 in compression garments provided to those in need.


  • Medicare provides no coverage
  • Health insurance may not provide adequate or any coverage
  • Healthcare systems do not provide financial assistance for compression garments.

Learn more about The Fund

Advances in Lymphedema Care Conferences

Premiering in 2018, Wisconsin's first and only Lymphedema conference for Lymphedema survivors, their supporters, and the healthcare community, all under one roof.  Providing unprecedented direct access to noted Lymphedema experts, and national manufacturers of Lymphedema products.

The Shellie Stellrecht Award

Wisconsin's first and only award recognizing excellence in Lymphedema advocacy.


Educate. Encourage. Empower.

All Things Lymphedema

Advances in Lymphedema Care Conference

Advances in Lymphedema Care Conference

Jennifer sits down with Hayley Tenpas of WHBY to talk about "All Things Lymphedema"

Listen Here

Advances in Lymphedema Care Conference

Advances in Lymphedema Care Conference

Advances in Lymphedema Care Conference

Thanks to Amanda Sharon at 91.1 The Avenue Radio for talking to us about the November 23 Lymphedema conference!

Listen to the interview

The Science Behind the Need for Compression Therapy for Lymphedema - It Can Save Your Life

The Science Behind the Need for Compression Therapy for Lymphedema - It Can Save Your Life

The Science Behind the Need for Compression Therapy for Lymphedema - It Can Save Your Life

Find out more

Study finds cellular processes controlling the formation of lymphatic valves

The Science Behind the Need for Compression Therapy for Lymphedema - It Can Save Your Life

The Science Behind the Need for Compression Therapy for Lymphedema - It Can Save Your Life

Read about it

Scenes from our Advances in Lymphedema Care Conferences - Wisconsin's First and Only

HEW's youngest volunteer.

    lymphdema fund wisconsin's first

    All Things Lymphedema

    An estimated 10 million Americans live with Lymphdema –  more than the combined total of Americans living with ALS, AIDs, Alzheimer’s, Parkinson’s, MS, and Muscular Dystrophy.  Yet, the disease remains little known amongst the general population, and often misunderstood within the medical community.    

    Learn more

    What is Lymphedema?

    Photo courtesy of Northwest Lymphedema Ctr.

    A Potentially Life Threatening Disease of the Immune System

    • Lymphedema occurs when a person's lymphatic system (part of our immune system) doesn't function properly.   
    • Lymphedema can affect any part of the body, head, neck, torso, arms, legs, etc.  This photo depicts Lymphedema of the leg.   
    • There is no cure for Lymphedema.  Once you have it, you have it for life.

    How Lymphedema Develops

    Categories of Lymphedema

    • Primary Lymphedema occurs when people are born with this disease.  
    • Secondary Lymphedema can occur after physical trauma, or from surgery or cancer treatments, such as radiation therapy.   An estimated 5 - 40% of breast cancer patients experience some form of Lymphedema.   Those who have lymph nodes removed and/or have radiation are at an even higher risk of developing this disease.

    Why a Turquoise Butterfly?

    The turquoise butterfly is the international symbol for Lymphedema.

    What You Can Do

    • You've already made a great start - by being aware
    • Learn all you can about Lymphedema - we've provided access to great information and resources
    • Join us at our Advances in Lymphedema Care conferences
    • Come and join us - volunteer, donate, contribute - be a part of our important work!

    how you can help us

    Additional Lymphedema Resources For You

    Treatment of Lymphedema

    Lymphatic Education and Research Network (LE&RN)

    Lymphatic Education and Research Network (LE&RN)

     Treatment of Lymphedema should be provided by a Certified Lymphedema Therapist (CLT), who has undergone specialized training in Lymphedema care. 

    What you need to Know

    Lymphatic Education and Research Network (LE&RN)

    Lymphatic Education and Research Network (LE&RN)

    Lymphatic Education and Research Network (LE&RN)

    LE&RN more

    National Lymphedema Network

    National Lymphedema Network

    National Lymphedema Network

    click for nln

    Lymphedema Treatment Act

    National Lymphedema Network

    National Lymphedema Network

     Currently, many policies, including Medicare, do not cover the medically- necessary compression supplies used daily in lymphedema treatment. As a result, many patients who cannot afford compression supplies suffer from recurrent infections, progressive degradation in their condition and eventual disability.

    Why It’s Important
    Netgiver Candid Platinum Seal Cancer Lymphedema Nonprofit Donation
    • Netgiver Candid Platinum Seal Cancer Lymphedema Nonprofit Donation
    • Netgiver Candid Platinum Seal Cancer Lymphedema Nonprofit Donation
    • Netgiver Candid Platinum Seal Cancer Lymphedema Nonprofit Donation

    Proud to be Located in Appleton, Wisconsin

    Health, Education & Welfare is an all volunteer 501(c)(3) nonprofit. Contributions are tax deductible as provided by law. EIN #82-5171301

    Copyright © 2024 Health, Education and Welfare - All Rights Reserved.

    All Things Lymphedema, Healing Through the Arts, and Artful Healing are HEW registered trade names. 

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