Tag Archives: support stockings

Lymphedema = Pain = More Pain = Avoidance = Get Educated = Get Fit

 

Lymphedema = Pain = More Pain = Avoidance = Get Educated = Get Fit  

National Lymphedema Network – Educating Patients Online 

Part 3b of 3b 

Exercise and Compression Garments:

Lymphedema Remedial Exercise as a part of CDT requires compression garments or bandages.3-5 There are no studies on the use of compression garments when performing stretching or flexibility exercise alone.

Our visiting young cousin from Norway rode her first recumbent trike in Silverdale and wore "What is COPD" tee shirt while she was here.
Our visiting young cousin from Norway rode her first recumbent trike in Silverdale and wore “What is COPD” tee shirt while she was here.

My young cousin, Malin from Norway is included here because COPD (Chronic Obstructive Pulmonary Disease) began in 1997 for me and led into my long ride into medical conditions – one after the other and my gathering weight attracted lymphedema as surely as fresh bread and butter sticks to peanut butter and strawberry jam. 

“The NLN Medical Advisory Committee (MAC) recommends using the guidelines for aerobic and resistance exercise to guide use of compression during flexibility exercise since flexibility exercises may be combined with other forms of exercise. 

The amount and type of compression for exercise should be decided with input from a professional knowledgeable about lymphedema. There is no strong evidence basis for the use of compression garments during exercise; however, most experts in the field of lymphedema advise the use of compression during vigorous exercise for people with a confirmed diagnosis of lymphedema.

Melissa showing me the latest fast, protective lower leg support
Melissa showing me the latest fast, protective lower leg support

Melissa Mercogliano, Center for Orthopedic & Lymphatic Physical Therapy in Port Orchard, WA. recently showed me a new and easy way to add support stockings…easy except for we Tub’ettes.

“One study suggested that individuals with lymphedema who do resistance exercise without compression may increase swelling. 

20 Resistance exercise may reduce limb volume when used as an adjunct to compression therapy in people with confirmed lymphedema.

8 One study showed that aerobic and weight-lifting exercise was safely performed without compression in women at risk for breast cancer-related lymphedema.

9 That study showed patients who developed lymphedema could continue to exercise with compression garments. Compression garments should be measured by an individual trained and experienced in fitting compression garments for lymphedema and should be at least Class I compression for upper extremity. Higher classes may be required for more severe lymphedema and for lower extremity lymphedema.

 1-IMG_29033-IMG_29074-IMG_2909

Custom sized, each leg. This pair is old...notice the crinkles below the rubber dotted band. The replacement compression stockings are black.This pair is about one year old.
Custom sized, each leg. This pair is old…notice the crinkles below the rubber dotted band. The replacement compression stockings are black.
This pair is about one year old.

I throw the stockings in a little zippered mesh cloth bag and into the washer on a short cycle, regular soap, extra rinse – cold water and smooth out and let them hang to dry.

I prefer the toe less stocking so my toes don’t get scrunched up and have two different kinds. The little rubbery tips around the tops of both help them from sliding on down my leg and cutting off circulation.  Ask your doctor. 

“A hand piece (gauntlet or glove) is recommended when exercising with a sleeve to avoid causing or exacerbating hand swelling. 

Definition of Individuals At Risk for Lymphedema:

Individuals at risk for lymphedema have not displayed signs and symptoms of lymphedema but may have sustained damage to their lymphatic systems through surgical lymph node removal or radiation therapy.

Additionally, individuals at risk may have surgical incisions in the vicinity of lymph transport vessels.

Individuals who have family members with hereditary lymphedema may also be at risk.

An individual’s risk of lymphedema may change over time depending on factors such as weight gain, age, and changes in medical condition. 

It is the position of the NLN that:

Exercise is a part of a healthy lifestyle and is essential for effective lymphedema management

Before starting any exercise program, individuals should be cleared for the program of activity by their physician.

Lymphedema Exercises (also known as Remedial Exercises) are specific rhythmic muscle and breathing exercises used as a part of lymphedema treatment in Phase I and Phase II

Complete Decongestive Therapy (see the NLN Position Paper on Diagnosis and Treatment). http://www.lymphnet.org/pdfDocs/nlntreatment.pdf 

In Phase II lymphedema maintenance, these exercises can be combined with or integrated into a regular exercise program.

After intensive treatment with CDT, the person with lymphedema should work with the certified lymphedema therapist or qualified lymphedema specialist provider (MD, NP) to adapt their remedial exercises into their fitness and weight management program at the time they are moving from Phase I (treatment phase) to Phase II (self-management).

Individuals with or at risk for lymphedema can and should perform aerobic and resistance exercise in a safe manner.

The individual with or at risk for lymphedema may benefit from working with an Exercise Physiologist and/or Personal Trainer. The person with lymphedema should inquire if the trainer or exercise physiologist has experience working with lymphedema and other medical conditions. Certification for personal trainers varies. Patients who are unsure of about the qualifications of a community exercise practitioner should work with a certified lymphedema therapist or health care provider to assist them in finding a community exercise program or professional.

In general, individuals with a confirmed diagnosis of lymphedema should utilize compression garments or compression bandages during exercise.

Individuals at risk for lymphedema may or may not utilize compression garments during exercise; this is an individual decision to be made with guidance from a care provider and/or therapist based on risk, activity, and conditioning level.

Individuals at risk for lymphedema will benefit from most forms of exercise tailored to their individual needs.

Individuals at risk for or with a confirmed diagnosis of lymphedema should avoid repetitive overuse of the affected part. Sudden increase in an individual’s usual exercise duration or intensity may trigger or worsen lymphedema. It is likely that a program of slowly progressive exercise for the affected body part will decrease the potential for common daily activities to result in overuse.

Exercise should be started gradually, increased cautiously, and stopped for pain, increased swelling, or discomfort.

The risks of exercise for the individual with or at risk for lymphedema must be balanced against the risks of deconditioning that undoubtedly results from not exercising. A deconditioned body part with or at risk for lymphedema can do progressively less without risk of overuse. As a result, exercise is recommended for those with and at risk for lymphedema.

The NLN cannot specifically determine the safety of exercise for any individual. The guidelines in this Position Paper provide general principles, but do not substitute for medical evaluation and recommendations from a health care professional. It is the responsibility of all individuals with or at risk for lymphedema to consult with their health care provider regarding their own specific needs. 

References:

1. Tidhar D, Katz-Leurer M. Aqua lymphatic therapy in women who suffer from breast cancer treatment related lymphedema: a randomized controlled study. Support Care Cancer. 2010;18(3):383-392.

 2.Moseley AL, Piller NB, Carati CJ. The effect of gentle arm exercise and deep breathing on secondary arm lymphedema.Lymphol. 2005;38(3):136-145.

3.Boris M, Weindorf S, Lasinski B, Boris G. Lymphedema reduction by noninvasive complex lymphedema therapy. Oncol (Williston Park). 1994;8(9):95-106; discussion 109-110.

4.Földi E, Földi M, Weissleder H. Conservative treatment of lymphoedema of the limbs. Angiol. 1985;36(3):171-180.

5.Földi M, Földi E, eds-in-chief. Foldi’s Textbook of Lymphology for Physicians and Lymphedema Therapists, 2nd ed. Munchen, Germany:Urban & Fischer; 2006.

6.Bergmann A, Mendes VV, de Almeida Dias R, do Amaral E Silva B, da Costa Leite Ferreira MG, Fabro EA. 

Incidence and risk factors for axillary web syndrome after breast cancer surgery [published online ahead of print October 17, 2011].

Breast Cancer Res Treat. doi:10.1007/s10549-011-1805-7.

7.Fourie W, Rob KA. Physiotherapy management of axillary web syndrome following breast cancer treatment: discussing the use of soft tissue techniques. 

Physiotherapy. 2009;95(4):314-320. 

 

NLN • 116 New Montgomery Street, Suite 235 • San Francisco, CA 94105

Tel: 415-908-3681 • Fax: 415-908-3813

Infoline: 1-800-541-3259 • Email: nln@lymphnet.org •

Online: www.lymphnet.org 

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Several years ago, I called Harrison Medical Center and asked if non-cancer patients with lymphedema could attend their support group meetings.  At that time, it was limited to cancer patients.

Yesterday I called the following number to be certain it was still up to date.  It is and the closest Lymphedema Support Group I know about.

If anyone knows of more, let me know – I can post it here.

 

Kitsap County Closest Support Group 

Northwest Lymphedema Center

Kent, WA (24.11 miles * Meeting times: Date varies  Phone: (206) 575-7775 

 

Tub’etts! 

I’d like to be part of a support group of fatties who NEED to lose weight for their health’s sake – with or without current medical issues. No dues – a scale and occasionally health professionals willing to talk to us – to educate us – to motivate us – guest speakers. 

I have been told that I’m not a good candidate for bariatric surgery…so, before I push that particular button – is there anyone beside me, who wants to be part of an obese/tubby support group to work together for weight loss and good health? 

To lose weight through good nutrition and exercise is my goal. 

We are dying of too much fat, fellow Tubby Ones.

Will you join me in our battle to shed the fat and live healthy?  Let me know…

 

Thanks for reading… Sharon O’Hara familien1@comcast.net

Kitsap County Library System has educational Lymphedema books for the layperson – just ask.

Lymphedema Risk Reduction Practices Part 2 of 3

  Greetings!  Part 2 of 3 is the, “Summary of Lymphedema Risk Reduction Practices”

Note that “Obesity” is mentioned as a risk and I’ll have more to say about it in part 3. 

A reminder to ask your doctor – I’m a patient who believes in patient education.  Talk to your doctor.

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“Summary of Lymphedema Risk Reduction Practices

Please refer to the complete Risk Reduction document for details.

 

I. Skin Care – Avoid trauma / injury to reduce infection risk

Keep extremity clean and dry.

Apply moisturizer daily to prevent chapping/chafing of skin.

Attention to nail care; do not cut cuticles.

Protect exposed skin with sunscreen and insect repellent.

Use care with razors to avoid nicks and skin irritation.

If possible, avoid punctures such as injections and blood draws.

Wear gloves while doing activities that may cause skin injury (e.g. washing dishes, gardening, working with tools, using chemicals such as detergent).

If scratches/punctures to skin occur, wash with soap and water, apply antibiotics, and observe for signs of infection (i.e. redness).

If a rash, itching, redness, pain, increased skin temperature, increased swelling, fever or flu-like symptoms occur, contact your physician immediately for early treatment of possible infection.

II.

Activity / Lifestyle

Gradually build up the duration and intensity of any activity or exercise. Review the Exercise Position Paper.

Take frequent rest periods during activity to allow for limb recovery.

Monitor the extremity during and after activity for any change in size, shape, tissue, texture, soreness, heaviness or firmness.

Maintain optimal weight. Obesity is known to be a major lymphedema risk factor.

 

III. Avoid Limb Constriction

If possible, avoid having blood pressure taken on the at-risk extremity, especially repetitive pumping.

Wear non-constrictive jewelry and clothing.

Avoid carrying a heavy bag or purse over the at risk or lymphedematous extremity.

IV. Compression Garments should be well-fitting.

Support the at-risk limb with a compression garment for strenuous activity (i.e. weight lifting, prolonged standing, and running) except in patients with open wounds or with poor circulation in the at-risk limb.

Patients with lymphedema should consider wearing a well-fitting compression garment for air travel. The NLN cannot specifically recommend compression garments for prophylaxis in at-risk patients.”

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In part 3,  I’ll show you the two kinds of leg support stockings I use and why I like them.  There are many other support stockings out there – ask your doctor what she/he recommends.   Also, I’ll show you several tools that aid in putting them on.

Thanks for reading… Sharon O’Hara, familien1@comcast.net

Suquamish – Re: COPD – the beginning. Pain – the end.

Thank you for taking the time to write, Suquamish – and you are young at only 52 to have COPD.  I’m sure there are other young ones with COPD who live to be retired and ancient without adding more diseases.  They keep moving as best they can, get good medical care, an exercise program and good nutrition too can overcome almost anything.

What does your doc say about the x-rays?

The pain is in my lower legs – not lungs and I’m one of those COPDers who gathered all these other medical conditions after COPD.

Venous Stasis Dermatitis – Lymphedema – Cellulitis – when I’m not careful enough about sodium and wearing support stockings.  This time though, thanks to Mellissa’s teaching and my husband’s help they didn’t swell, crack open and leak for about a year and a half.  The condition is chronic but I learned more good lessons to keep this from happening again through checking labels more carefully on everything I eat or drink.  Moreover, this too will pass – so will the pain.

The neat thing Suquamish – you gave me another idea.  You are young.  There have to be other people out there who would gladly give living with COPD and heart worthy tips to other COPDers.  Working full time, you probably aren’t able to attend the monthly afternoon Harrison Medical Center/Better Breathers educational classes at Harrison Silverdale.  However ….

Would you be interested in an evening support group of like-minded people who not only have lung or heart disease they are living life to the fullest in spite of it and want to share what has worked for them?

We should have such a support group in Silverdale. No gloom & doom – no cost – just patients sharing what works for us.

What do you think?  Would Tuesday evenings from 7 – 8 pm work for you?  Occasionally we could have speakers willing to donate their time to help educate us too.

Suquamish – Thanks for reading my posts and hope they haven’t been gloomy and doomy for you or anyone – I didn’t meant them to be.  This pain will pass when my lower legs get ‘normal’ again and I take proper care of them – including the support stockings and no more high sodium diet sodas.

I’m open to any suggestions for a meeting place that will allow COPDers (lung and heart folks) to meet on a monthly basis in the evening for an hour…

BTW:  I may be moaning and groaning about pain from my legs but it doesn’t change my plans to make a recumbent trike trip next summer from here to the other Washington for COPD.

Thanks… Sharon

One Response to “COPD – the beginning. Pain – the end”

  1. Suquamish Says:
    November 2nd, 2011 at 4:11 am

I am sorry Sharon, I guess I am following in your footsteps. The VA gave me a chest x-ray and it had a white spot on my lung. They told me to see my health provider (Group Death) I mean Group Health. They put a clip on my nipple to rule out the phantom shadow on the lung. Too bad the clip and the white spot both showed up in different areas. Group Health never diagnosed it at COPD. But a couple weeks ago when I went in Urgent care and underwent a breathing treatment the noted COPD in my health chart. I had another chest xray because of the pain you stated in your post. I guess it is just the muscles that got strained. I guess there weren’t any fractures or they would have been noted. I hope you take care of yourself Sharon, I enjoy reading your post on Kitsapsun.com. I would like to learn more about COPD from someone affected by it. I wonder how much longer I will be able to work. I am just a young guy at 52.
Read more: http://pugetsoundblogs.com/copd-and-other-stuff/2011/11/01/copd-the-beginning-pain-the-end/#ixzz1cbDldPN6