Lymphedema Podcast

Special thank you to our loyal partners.

About AIROS Medical

Airos Medical has a team of dedicated leaders who have decades of experience in the DME world. Lymphedema pneumatic compression is what they specialize in, and they do it well. I can personally attest to the genuine hearts of the guys behind this company. To learn more about their products click the logo here. Reach out if you have any questions for them or their leadership team.

The only online store for pediatric lymphedema bandaging kits and continuing education courses. Each kit has been specially curated by a parent of a child with lymphedema and a certified lymphedema therapist. Add al la carte items as well by email bw2@pediatriclymphedema.com 

 

About medi

“I feel better.” is a promise that becomes reality with medi. With our products and technologies, our goal is to make people’s lives easier, better and more comfortable. We encompass the quality of both products and service to create the greatest possible benefit for our users, customers and partners. We foster innovation, active market development, and individualized solutions to problems both domestically and internationally.

about juzo usa

Freedom to Make the Most of Every Day Riding a bike. Working in the garden. Playing with grand kids. Taking a walk. Going to work. These are the keep moving® benefits of Juzo® compression garments, designed to improve your quality of life, not inhibit it. Family-owned since 1912, Juzo has led the compression therapy garment industry by creating high-quality products that offer you the freedom to maintain a more active lifestyle. Advancements like our FiberSoft® technology, seasonal colors, attractive styles and fun print designs ensure you move in comfort without compromising fashion.

about brylan's feat

Brylan's Feat Foundation is a non-profit 501(c)(3) organization that was started in honor of my daughter, Brylan. When she was one month old, her pediatrician noticed that her feet looked a little swollen. We did genetic testing and went through several different doctors and specialists, but no one could tell us what was wrong with our little girl. Through our own experience and hearing stories of parents struggling to afford these medically necessary garments, as well as other treatments, the idea to aid families in their fight against lymphedema was born.

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