If you are a Facebook user and are about to complete another trip around the sun, we hope you will consider choosing our affiliated organization, the Lymphedema Education & Awareness Project (LEAP) for your birthday fundraiser! These easy-to-follow instructions will walk you through the set-up (https://lnkd.in/dsFsYmX). It only takes a couple of minutes and can be done up to one month before your birthday. And don’t forget to like and follow the LEAP Facebook page (https://lnkd.in/gbTT-mps).
关于我们
The Lymphedema Advocacy Group is a nationwide, all-volunteer organization of patients, caregivers, healthcare professionals and industry partners. Our mission is to advance lymphedema care in the United States by advocating for improved insurance coverage for the diagnosis and treatment of the disease. For this purpose we work to increase awareness of and education about lymphedema amongst lawmakers, insurance providers and other relevant entities. We support attempts to improve coverage at both the state and federal levels and encourage all members of the lymphedema community to become active participants in this process.
- 网站
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https://lymphedematreatmentact.org
Lymphedema Advocacy Group的外部链接
- 所属行业
- 医院和医疗ä¿å¥
- 规模
- 11-50 人
- 类型
- éžè¥åˆ©æœºæž„
- 创立
- 2010
Lymphedema Advocacy Group员工
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Abbe Buck Hann
O/O ABPR, LLC; Advocate at Lymphedema Support Group, Obesity Advocacy Coalition.
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Lois Tiemann
Marketing Director at Accu Rate Mortgage Express, Inc.
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Adam Van Essen
Director of Research & Development | Innovating Medical Solutions | Passionate About Patient-Centered Solutions
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Lindsay Ryback
Director of Lymphology & Phlebology
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For more information about the new Lymphedema Treatment Act coverage please visit our website (https://lnkd.in/dEnHjsPq).
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On May 3, 2025, the National Lymphedema Network will be hosting an in-person patient lymphedema summit. Details are available in our newsletter (https://lnkd.in/gwCdm55q).
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Way to go, Gavin! If you are interested in purchasing this book, it is available at Barnes and Noble (https://lnkd.in/gWwxmB94) and elsewhere. https://lnkd.in/g5zTji_r
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For more information please visit our website at https://lnkd.in/dEnHjsPq
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We are always looking for ways to improve access to care, and that's why we've recently created an Insurance Coverage Reporting Form https://lnkd.in/gf9tgbGs The information submitted will assist us in better understanding the overall insurance coverage landscape for lymphedema treatment supplies and services. Responses will be kept confidential and results will only be shared in aggregate, to assist lymphedema patients in choosing insurance policies that provide the best coverage. Read the full update in our newsletter - https://lnkd.in/gVBj-bN5
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In recognition of World Lymphedema Day, we are excited to share our redesigned information cards! This item and others are all available on our Educational Materials page (https://lnkd.in/gN8Zp5EW). #worldlymphedemaday #lymphedema
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March is Lymphedema Awareness Month and we are thrilled to announce the launch of the Lymphedema Education & Awareness Project! Learn more in our newsletter. (https://lnkd.in/gCnqyVse)
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15 years ago yesterday, on February 23, 2010, the Lymphedema Treatment Act was introduced into Congress for the very first time. It would take more than 12 years for the bill to become law, but we persisted and we prevailed! In honor of the last 15 years of advocacy, and because there's more work to be done, we hope you will show your support by donating to our 15th Anniversary Fundraising Campaign.?(https://lnkd.in/dSwhiJNm) Every dollar you contribute fuels our mission to close coverage gaps, advocate for fair policies, and empower patients. Together, we can continue to improve access to care for the millions of men, women, and children in America who are affected by lymphedema!
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