An essential part of managing lymphedema (LE) is to wear compression garments, often for life. Most compression garments are NOT yet covered under Medicare or health insurances therefore those people having financial hardship have to go without. Without compression wear, serious medical complications may occur leading to a spiraling decline in health. Our Garment Support program will help pay for the compression garments and support bandages these people desperately need. This program was made possible using generous donations from our friends and supporters. Our funds are limited and will serve on a first come basis.
1. To provide compression garments and medical support bandages free or subsidized to the residents of Hawaii.
2. To empower people to take ownership and control of their lymphedema by providing educational classes to those enrolled in the program.
To qualify for assistance under our Garment Support program each applicant will:
1. Be assessed and measured by a Certified Lymphedema therapist (CLT),
2. Agree to enroll in our wellness program and complete a quality-of-life survey before and after the program,
3. Be living on Oahu * exceptions may be made for those living on neighbor islands, provided they are under the care of a CLT who is affiliated with LymphaCare Hawaii.
4. Have a written diagnosis of lymphedema by a medical professional requiring medical grade compression. One application / person / year.
Please contact us for further assistance with this process and find out if you are eligible. All applications will be considered, however other polices and restrictions may apply, as determined by the Board of Directors.
What is lymphoedema
Skincare
The joy of exercise
Compression garments
SLD lower limbs
SLD upper limbs
Health eating
Lipoedema
Holidays
Exercise class lower limbs
Exercise class upper limbs
Pump therapy
MLD
Have you got Genital Lymphoedema?
Men with Genital Lymphoedema
Women with Genital Lymphoedema
Surgery For Genital Lymphoedema
Filarisis
‘Lymphedema is a little-known illness, and this book will help sufferers and their carers cope – and who better to help write it than someone like Gemma Levine who is a sufferer herself.’ – Dame Judi Dench
You may download this book for free by visiting and supporting Lymphatic Education and Resource Network LE&RN. Click the link below
‘Lymphedema is a little-known illness, and this book will help sufferers and their carers cope – and who better to help write it than someone like Gemma Levine who is a sufferer herself.’ – Dame Judi Dench
You may download this book for free by visiting and supporting Lymphatic Education and Resource Network LE&RN. Click the link below to be redirected to their website and list of free resources.
Classes are generally 30-40 minutes long and are delivered as lunchtime talks suitable for the general public and clinicians alike. During classes, we provide links to research-based evidence and trusted websites for more in-depth information. Most of our classes are FREE with a suggested donation to LymphaCare Hawaii. Please contact Ellie to find out how to book a class and to inquire about possible charges for that class.
According to research, lymphedema is the No.1 complaint from breast cancer survivors. Learn non-pharmaceutical ways of managing distressing symptoms such as leaking fluid, pressure pain, and altered body image.
Discover the truth about chronic swelling and lymphedema by demystifying the facts. Learn how we can all recognize lymphedema and get medical help.
Learn how obesity is now one of the leading causes of lymphedema in the Western world. Learn about the lymphatic disease lipedema.
Learn how getting the right care for chronic leg swelling can help prevent hospitalizations, serious wound infections, and life- threatening cellulitis.
Practical session to include Tripudio Movement Systems and self-lymphatic drainage for your patients and their loved ones.
If you have a chronic swelling of a body part for more than 3 months, and your doctor has not referred you to a specialist to find out the cause, you may develop lymphedema. Lymphedema (LE) is chronic swelling (edema) caused by a buildup of fluid (lymph) that occurs when the lymphatic system is either faulty or damaged. For more information about this disease and a discussion of risk factors, please browse through our 20 short videos. If you would like to receive written information, please contact LymphaCare Hawaii.
If you are recovering from secondary LE (caused by surgery, trauma, or venous disease), there are many life changes you can make to help manage this disease. Having a fitted, comfortable compression garment is essential! Stabilizing your weight, stretching, gentle movements, and avoiding the triggers to a flare-up are key to self-management. If you need help with finding compression garments, we strongly advise you contact a Certified Lymphedema Therapist to be professionally measured and fitted.
Unfortunately, most doctors only have 30 minutes training on the lymphatic system and are not aware of best practices for treating lymphedema. LE is a progressive disease that, without treatment and self-management, can lead to life-threatening infections and hospitalizations. It is vital to find the right specialist to manage this disease. Please contact us if you need help.
The Lymphatic Education & Research Network (LE&RN) is an internationally recognized non-profit organization founded in 1998 to fight lymphatic diseases and lymphedema through education, research and advocacy. LERN has multiple information sheets to download, as well as an “ask the expert “panel for questions. There is also a local chapter in Hawaii.
Lymphedema Support Network LSN in London. This Charity has become the largest information resource for lymphedema in the UK, producing an on-going series of fact sheets, initially for patients; however, the high standard of this information has led to healthcare professionals ordering them for use in hospitals and lymphedema clinics.
Please visit their web site to discover more important educational material.
The British Lymphology Society, is a dynamic and innovative body providing a strong professional voice and support for those involved in the care and treatment of people with lymphedema and related lymphatic disorders, including lipedema. Please visit their web site for more information.
The Lymphedema Treatment Act (LTA) is a federal bill that aims to improve insurance coverage for the medically necessary, doctor-prescribed compression supplies that are the cornerstone of lymphedema treatment. To get involved on a local level.
We partner with Dolly Foley at Compression Garment Company who shares our passion to provide exceptional personal service to those people living with lymphedema. Dolly and team run a small local business dedicated to finding you the best possible solutions for compression. This web site opens up many other important education links .
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