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This page contains a list of some informative web site links about lymphedema. Please note that we do not endorse any of the content on these sites; the list is provided for your reference only. Please see our Privacy Policy for further information.

If you know of a website that may be helpful for the lymphedema community, please send an email to and let us know.

Patient Information & Support

http://www.oncologypt.org/presrc.cfm
The Oncology Section of the American Physical Therapy Association website offers several very useful links. In addition to a “Lymphedema Fact Sheet”, there is also a new “Peripheral Neuropathy Fact Sheet".

http://www.caringbridge.org/index.htm
CaringBridge.org is a non-profit organization that supports families facing serious illness by allowing them to create free web pages to help family and friends stay in touch.

http://www.bcaction.org
The motto of Breast Cancer Action is “Do something besides worry…educate, agitate, organize”. BCA is an activist political group whose aim is to “compel the changes needed to end the breast cancer epidemic”. The group is known particularly for its “Think Before You Pink” critique of the commercialization of Breast Cancer Awareness Month.

http://www.mylymphedema.com/lymphedema_garments.htm
Juzo offers compression garments for the entire body. Visit the link above for information on all of Juzo's compression garments. The MyLymphedema.com site also provides useful general information on the management and treatment of lymphedema.

http://www.cancersupportivecare.com/lymphedema.html
Once a person has been given a diagnosis of cancer, supportive care becomes the fifth therapeutic dimension, and a vital complement to surgery, radiation therapy, chemotherapy, and immunotherapy. We hope by reading and using www.cancersupportivecare.com, you will be able to better cope with the myriad of challenges that accompany the diagnosis and treatment of cancer.

http://www.educareinc.com
Although the Educare site does not discuss lymphedema, it provides excellent, compassionate information about the symptoms and treatment of breast cancer, including a locator tool for finding a breast health specialist in your area. It also contains useful information for therapists and other professionals, including guidance on starting and growing breast health programs.

http://listserv.acor.org/archives/lymphedema.html
The Lymphedema Online Support Group.

http://www.shopwellwithyou.org
Shop Well with You is a not-for-profit organization that uses clothing to help cancer patients and survivors improve their body image and quality of life. The Shop Well with You site contains a number of useful resources, such as listings for shops and boutiques that carry specialty items, and a one-on-one personal shopper service. One of the most useful features of the site is the information it offers about how to be both comfortable and fashionable while coping with various medical conditions, including lymphedema. A great site for women seeking to renew their sense of style and self after illness.

http://www.bcrfcure.org
Established in 1993 by Evelyn Lauder, the mission of The Breast Cancer Research Foundation is to achieve prevention and a cure for breast cancer in our lifetime by providing funding for innovative clinical and genetic research, and by increasing public awareness about good breast health.

http://www.lifeabc.org/
Life After Early Breast Cancer provides information on what happens in the years after initial treatment for breast cancer. The site is designed to be used by patients, caregivers, health care professionals, and advocates. Particularly useful are checklists for women to use when talking with their health care providers.

http://www.womenshealthresearch.org
The Society for Women’s Health Research raises awareness of the need for more research into conditions that affect women disproportionately, predominately, or differently than men. (Currently, it’s the only non-profit in the US that does this.) Through research, education, and corporate and legislative advocacy, the Society works for increased funding for women’s health issues and for the inclusion of women in major medical research studies.

http://www.Y-Me.org
The Mission of the Y-Me National Breast Cancer Organization is to decrease the impact of breast cancer; create and increase breast cancer awareness; and to ensure through information, empowerment, and peer support that no one faces breast cancer alone.

http://www.dol.gov/ebsa/publications/whcra.html
Your Rights After a Mastectomy…Women’s Health and Cancer Rights Act of 1998
A very useful page on the website of the US Department of Labor Employee Benefits Security Administration. You’ll find valuable information on the laws relating to health care coverage for mastectomies and reconstructive surgery – a real boon to anyone struggling to navigate the complexities of our health care system.

Click here for an explanation of how the Women’s Health and Cancer Rights Act applies to coverage for breast lymphedema patients.

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Information on Lymphedema and Treatment Products

Preventing and Treating Arm Lymphedema

http://www.lymphedemazone.com/Lymphedema.html
The Lymphedema Zone is an excellent reference site, full of useful basic information on lymphedema's causes and symptoms, as well as information about therapeutic methods, compression products, and therapist training.

http://www.jovipak.com
JoVi PAK lymphedema treatment. Ready-made and custom products.

http://www.klosetraining.com/
The goal of Klose Training & Consulting, LLC is to provide the highest quality Manual Lymph Drainage (MLD) and Complete Decongestive Therapy (CDT) training available in the U.S.

http://www.nortonschool.com/
The Norton School of Lymphatic Therapy is the premier educational institution for training medical doctors, physical therapists and their assistants, occupational therapists and their assistants, registered nurses, and nationally-certified massage therapists to become expert in the treatment of pathologies related to the lymphatic system.

http://www.lymphaticresearch.org
The mission of the Lymphatic Research Foundation is to find improved treatments and cures for lymphatic disease, lymphedema, and related disorders.

http://www.lymphaware.org
The mission of the Lymphedema Awareness Foundation is to be a LOUD voice in the promotion of lymphedema awareness and to establish referral networks and outreach programs for health care professionals and lymphedema patients.

Check out the Lymphedema Awareness Foundation’s online magazine, eLymphNotes, at http://www.elymphnotes.org. The "first e-zine on lymphedema", eLymphNotes is primarily geared toward therapists, but may also have some articles of interest to patients.

http://www.lymphedemacircleofhope.org
The Circle of Hope Lymphedema Foundation, Inc, is an organization dedicated to promoting education, awareness, research, assistance, and support for lymphedema patients and their doctors.

http://www.lymphnet.org
Bellisse is a supplying sponsor to the National Lymphedema Network (NLN) which is an internationally recognized non-profit organization founded in 1988 by Saskia R.J. Thiadens, R.N. Its mission is to provide education and guidance to lymphedema patients, health care professionals and the general public by disseminating information on the prevention and management of primary and secondary lymphedema.

http://www.lymphnotes.com
Lymph Notes is the information resource and online support group to serve those who are affected by lymphedema, the health care professional who treat them, and the suppliers who provide for their specialized needs.

http://www.acols.com/
Academy of Lymphatic Studies
11632 High Street, Suite A
Sebastian, FL 32958
772-589-3355
 
The primary objective of the the Academy of Lymphatic Studies is to provide the highest quality education in Manual Lymph Drainage and Complete Decongestive Therapy (MLD/CDT) and to advance the availability, quality, use and support of lymphedema management techniques through standard settings, terminology, education and research.

http://www.clt-lana.org
LANA
The Lymphology Association of North America (LANA) is a non-profit corporation composed of health care professionals, including physicians, nurses, massage therapists, physical therapists, and occupational therapists experienced in the field of Lymphology and lymphedema. They have acknowledged the need for a national certification examination for lymphedema therapists, to test knowledge considered fundamental in the treatment of lymphedema.

http://www.vodderschool.com
Dr Vodder School-North America
To provide the highest quality educatio in the Dr. Vodder method of Manual Lymph Draiage and Combined Decongestive Therapy and to ensure the continuing competence of practitioners trained by the Dr. Vodder School

If you know of a link or article that you think should be in this section, or you would like to contribute a story or case study, please email us at .