Resources
Lymphedema resources from all around the world
please email me if you have a resource link to add to this database
Social Media is a great tool to build a community of support.
Visit any of these link for clinical information, research updates, surgical options, lymphedema education, and opportunities to attend in person (or virtual) sessions.
looking for a clt?
Search the school directories for a therapist near you.
Juzo Blog
Relatable stories from others with Lymphedema as well as helpful information.
Lower Extremity virtual/home fitter guide from Juzo is FREE and linked below!
Upper Extremity virtual/home fitter guide from Juzo is FREE and linked below!
pediatric lymphedema nonprofit
Brylan’s Feat Foundation is the only organization in the world dedicated to helping children with Lymphedema. Contact Brittany or visit the website to learn more.
Lymphedema blog
Joachim Zuther is the Lymphedema Guru who shares his expertise on his blog, Lymphedema Blog. Visit the blog to learn more on specific topics of interest.
pediatric lymphedema
“The Lymphedema Program in the Department of Plastic Surgery at Boston Children’s Hospital offers individuals of all ages with lymphedema interdisciplinary care. Staffed by plastic and reconstructive surgeons with expertise in the management of lymphedema, the program provides consultation, diagnostic services, treatment options, and research opportunities.
Patients have access to specialists in plastic surgery, nuclear medicine, radiology and rehabilitation. With these resources, the program provides evaluation, diagnosis and treatment options. The team also is working to develop improved treatments for lymphedema through clinical and basic science research.”
- 617-355-8415
- plasticsurgery@childrens.harvard.edu
Lymphie Life blog
As a Primary Lymphedema patient herself Alexa shares a special insigt on her blog, Lymphie Life. Follow Lymphie Life on social media as well.
international lymphedema resource
“A dedicated platform for the lymphoedema community to improve the management of the condition and related disorders worldwide.”
- +45 7020 0305
- info@lympho.org
Is no longer listed as a resource as a direct result of their changes to unperson hands on training changes.
medi education
As a leader in compression garments medi USA is here to help you say “I feel better.” Learn more on their website.
“Lymphedema changes lives. The chronic disease is a constant companion in all aspects of life. But what is the best way to deal with the disease symptoms? Which therapy is best suited for you? How can you live a normal life despite lymphedema? The film “Living with Lymphedema – Education, Therapy, Quality of Life“ from medi gives concrete answers as well as practical tips for everyday life.”
- +1 800-633-6334
- info@mediusa.com
vodder school
“The Dr. Vodder School International is the training program to take if you are looking for the source of the original Dr. Vodder Method of Manual Lymph Drainage (MLD®) and Combined Decongestive Therapy.”
- (250) 598-9862
- 1-800-522-9862 (USA & Canada)
- info@vodderschool.com
ALFP
“Improve the management of lymphedema and related disorders in the United States while contributing to global international advancement.”
published articles
Published Medical Journals for reference and sharing with your medical team. Click any link below for more information.
nln
“National Lymphedema Network’s mission is to empower our community of lymphedema practitioners and patients by providing educational opportunities, networking opportunities, and interventional resources. We aim to inspire clinicians to provide world-class care for people with lymphedema by promoting best practice guidelines and standards of care.”