
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.
Please reach us at lymphladyhawaii@gmail.com if you cannot find an answer to your question.
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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