Welcome to the Klose Training & Consulting Blog

January 4, 2011 at 2:31 pm | Posted in Klose Training & Lymphedema Care | 3 Comments
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We provide the highest quality Lymphedema Therapy Certification Courses in the U.S.

Dedicated to our students, we provide individual attention to each participant during the initial training and offer ongoing support and education throughout your career.

Please feel free to subscribe to our blog updates and follow us on facebook, twitter, and Linkedin by clicking the buttons on the top right of this page. And please feel free to comment or ask questions anytime—welooking forward to serving you.

Ethel Foldi and her Impact on Lymphedema

August 17, 2011 at 12:02 pm | Posted in Certified Lymphedema Therapist, Klose Training Continuing Education Courses | Leave a comment
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As we continue to prepare for the Lymphedema conference in October, we get more and more excited about our keynote speaker, Professor Ethel Foldi, MD.  Dr. Foldi has quite a “resume” and is considered one of the world’s top experts in Lymphedema treatment.

Dr. Foldi is very special to Klose Training & Consulting for many reasons but of most importance: our director, Guenter Klose, received his training at the Foldi Schools years ago.

We recently came across one more article Dr. Foldi was featured in- in a German newspaper. We apologize that the words are written in German. However, it excites us that her knowledge and expertise continues to get more publicity.

We can’t wait for her keynote speech at the Klose Lymphedema Conference!

Professor Ethel Foldi to Lecture on Chronic Lymphedema at Klose Lymphedema Conference 2011

August 1, 2011 at 8:05 am | Posted in Lymphedema, Lymphedema Education | Leave a comment
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Professor Ethel Foldi is one of the premier pioneers in Lymphology. Her devotion and dedication to the field for over 40 years has helped thousands of patients, as well as trained hundreds of professional Lymphedema treatment experts.

We at Klose Training are very pleased and honored that Professor Foldi will be the keynote speaker at the Klose Lymphedema conference this October in Estes Park, Colorado. Professor Foldi will be lecturing on Inflammatory and other Skin Changes in Chronic Lymphedema: Etiology and Treatment.

Professor Foldi’s lecture will inform and educate participants on some very important things about etiology and treatment of chronic lymphedema. Dr. Foldi is extremely knowledgable and is one of the world’s leading experts on this topic.  Past participants of her lectures have been amazed by her knowledge and skill.

Several Lymphedema professionals and treatment practitioners recently had the opportunity to hear Professor Foldi lecture on Lipedema and were able to ask questions regarding the topic. The lecture was part of Klose Training’s Advanced & Review course in Hinterzarten, Germany.

The lecture was very well liked and received. Many of the attendees commented on Prof. Foldi’s knowledge and skills. Some of the comments included:

“What an honor for us as practitioners to have someone like professor Foldi take the time to lecture us.”

“Excellent to have a chance to hear from professor Foldi on this [topic].  Really enhanced my understanding on this topic which I had been unclear on.”

“I could sit and listen to Dr. Foldi at all times. She is obviously extremely intelligent, but at the same time so down to Earth.”

To have Professor Foldi speak at our Lymphedema Conference is truly a gift that any Lymphedema professional will enjoy. We hope that you will attend and take advantage of the opportunity to be part of the world’s leading experts in the field of Lymphedema.  If you are interested in learning more about the conference this October, please visit the Lymphedema Conference website.

Klose Training and the Foldi Clinic Make the German Newspapers

July 26, 2011 at 3:53 pm | Posted in Lymphedema Therapy Advanced & Review, Lymphedema Therapy Certification | Leave a comment
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Last month, Klose Training collaborated with the Foldi Clinic, in Hinterzarten, Germany, to provide Advanced and Review trainings for Lymphedema Professionals. Lymphedema Therapists from all over the world participated in the trainings.

Here is an image from the write up in the Dreisamtaler newspaper. We apologize that the article is not transcribed in English.

Lymphedema Training and Breaking Down Common Myths

July 11, 2011 at 10:40 am | Posted in Lymphedema Education, Lymphedema Training | Leave a comment
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A recent article written by Jan Hasak lists six commonly mistaken myths about Lymphedema. We’ve reposted it here to help bring more awareness to Lymphedema education.  If you have any questions regarding the content of the article, please ask Jan directly by visiting her website, which is http://www.janhasak.com/.

Dispelling Myths About Lymphedema

Lymphedema is the swelling of a human body part caused by an abnormal accumulation of fluid, proteins, and cellular waste in the tissues under the skin. It occurs when there is a problem with the lymphatic system caused by one of the factors below:

-The failure of lymph vessels to develop properly

-Damage to lymph vessels by trauma, surgery, or infection

-Removal or destruction of lymph nodes, usually during treatment of cancer

Most of the advancements made in the understanding and treatment of lymphedema result from research on those who acquired lymphedema as a complication of breast cancer treatment.

Here are some common misconceptions about lymphedema:

Myth 1: It is a curable condition. While it can be managed, lymphedema is a lifelong condition that will not go away over time. In fact, because it is a chronic progressive condition, even mild cases can eventually escalate and have serious consequences if not properly treated.

The gold standard for lymphedema treatment is complete decongestive therapy, which consists of two stages: a clinical phase where a lymphedema therapist performs manual lymph drainage and bandaging, and a self-care phase where the patient or caregiver performs the daily massage and bandaging. The clinical treatment may only take 4-6 weeks, but managing lymphedema is an ongoing process.

Myth 2: It will only develop within the first five years after surgery and radiation. Although we wish this were true, people can develop lymphedema at any stage in life. I have heard of a cancer survivor who 30 years after her treatment developed lymphedema after reaching up to pull down a garage door. It may be uncommon, but it can happen.

Myth 3: Lymphedema will make one’s arm huge. One-size-fits-all is not true for lymphedema. Like cancer, lymphedema has various stages. Stage I is mild, Stage II moderate and Stage III severe. I’ve seen pictures of a lymphedemous leg grossly misshapen, and I’ve seen cases where I could hardly tell the person had lymphedema.

Myth 4: The sentinel node biopsy that only removes a few lymph nodes stops lymphedema from happening. The procedure, while reducing the incidence of lymphedema, has not eliminated it. Genetic predisposition to any disruption of lymphatic flow may tip the scales.

Myth 5: A person at risk for lymphedema or who has it should not carry heavy objects. This has recently been disproven. In fact, gradual lifting of weights with a compression garment helps with lymphatic flow.

Myth 6: If your limb starts to swell you can wait a while to get therapy. If you notice any swelling in a limb after removal of lymph nodes, even after a sentinel node biopsy, see a surgeon right away. The earlier you catch it, the better. If the doctor does not listen, go to another M.D. who will. And if you are diagnosed, insist that you get a prescription for lymphedema therapy.

To reduce the risk of developing lymphedema, many therapists advise patients to have their arm fitted for a compression sleeve to be donned during plane rides longer than four hours. But newer findings indicate that cabin pressure at high altitudes may not make a difference in swelling. In addition, survivors may wish to wear the sleeve when lifting heavy objects with that arm. One should consult the National Lymphedema Network or Step-Up, Speak Out to get current, reliable doctor-approved advice on risk-reduction practices.

While certain triggers have been found anecdotally to bring on lymphedema (such as long plane rides or repeated puncture wounds), many experts in lymphology now surmise that those who develop lymphedema do so because of a genetic predisposition. Also, some people are born with more lymph nodes than others, providing a more protective effect.

Notwithstanding myriad myths and misconceptions about lymphedema, my main advice is never to despair. You can lead a normal life after lymphedema. Some patients turn the anger they feel toward their surgeon in not informing them of lymphedema into legislative and other action to ensure more research is directed toward this under-served condition. Others start Web sites and blogs to provide needed information to patients at risk and those with lymphedema. Still others go on to live their lives without fanfare. All of these responses are valid.
Article Source: http://EzineArticles.com/6406336

NALEA: A New Organization For Lymphedema Teaching Standards

June 7, 2011 at 11:09 am | Posted in Custom Lymphedema Therapy Courses, Klose Training & Lymphedema Care, LANA | Leave a comment
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Klose Training is now part of the North American Lymphedema Education Association (NALEA). The organization administers training standards for lymphedema therapists.

NALEA is currently an alliance of the four lymphedema therapy certification schools
responsible for training the majority of Certified Lymphedema Therapists (CLTs)
in North America according to standards set forth by the Lymphology Association
of North America (LANA). In addition to Klose Training, the three other schools inculde the Academy of Lymphatic Studies, Dr. Vodder School International, and Norton School of Lymphatic Therapy.

The NALEA doesn’t offer individual memberships to Lymphedema professionals. However, if you have feedback or comments on how to more professional standards, we at Klose Training welcome your feedback.

If you would like to read the Mission statement of the NALEA, please follow this link:

NALEA’s Mission

Jodi Winicour’s “Painful Cording of the Arm” Article in the National Lymphedema Network Newsletter

May 31, 2011 at 10:34 am | Posted in Breast Cancer Rehabilitation, Certified Lymphedema Therapist, Klose Training & Lymphedema Care, Klose Training Faculty, NLN | 1 Comment
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The article below was published in the NLN’s May-June newsletter. References and other information regarding this article can be found on the NLN website.

Painful Cording of the Arm
by Jodi Winicour PT, CMT, CLT-LANA

If you have upper extremity lymphedema caused by breast cancer surgery or treatments, you may have experienced a painful and bothersome condition called axillary web syndrome, or AWS. [Figure 1] Unfortunately, most lymphedema certification programs do not have the time to teach the treatment of AWS, which leaves lymphedema patients well treated for their swelling conditions but inadequately cared for regarding their cording. As few as 6% [1] to as many as 72% [2] of women who have had lymph nodes removed from their armpit (axilla) will develop AWS. Considering the pain it causes along with its frequent relationship with lymphedema, knowledge of its characteristics, onset and treatment is necessary to provide safe, holistic care for breast cancer survivors.

AWS characteristics:

AWS has certainly been around since the first radical mastectomies of the early 1900s, but the phrase “Axillary Web Syndrome” was coined in 2001 by Alexander Moskovitz, MD et al. [1] He describes painful cords of tissue that originate in the axilla, run along the inside of the upper arm to the elbow, and sometimes even to the wrist or the base of the thumb. These cords are made more taught by reaching out to the side and frequently can be seen as well as felt. Painful cording typically limits overhead and forward reaching along with elbow and forearm movements which makes activities such as cooking, cleaning, exercise, reaching and dressing difficult or impossible during the more painful stages.

How and when does AWS happen?

Typical onset of cording is 2 to 4 weeks after axillary node removal. [1, 2, 4, 5] Some with AWS have so much pain that it is difficult to use their arm while others feel that stretching and massage techniques are very helpful. Studies consistently report that the AWS will resolve on its own between 3 and 4 months after onset, but therapists who treat AWS have noted it lasting up to 1 year or longer without treatment. Untreated AWS may cause problems during the planning period for radiation therapy in those not needing chemotherapy. If unresolved, the cording can make CT scanning for radiation planning a very painful procedure which can delay the start of radiation therapy. It is much less common to see AWS after chemotherapy is completed, which is typically 3 to 6 months post surgery, but it does occur.

What is the stuff called AWS?

Although there are few tissue samples of AWS that have been looked at under the microscope, we do know that AWS can be hardened and enlarged lymphatic vessels that are filled with lymphatic fluid. This fluid cannot exit the arm normally through lymphatic pathways to the axilla due to lymph node removal. [1, 5, 10] AWS may also be small veins near the skin that are clotted or hardened. [1] In some cases, the webbing is hardened and clotted lymphatic fluid that causes inflammation of the vessels and makes them stick to the fatty tissues of the arm resulting in pain when moving or stretching the arm.

What increases my risk of having AWS?

While weight gain [11,13], obesity [11,13] & higher Body Mass Index (BMI of 25-26 kg/m2 [2,12,13]) have been associated with the onset of lymphedema, a lower BMI of 23[2] and 25.1 [ 3]) have been associated with the onset of AWS. These are confusing findings especially considering that both lymphedema and AWS seem to be caused by the axillary node removal and tissue scarring. Thinner women have both the increased risk of AWS and difficulties with shoulder movement after lymph node surgeries for breast cancer, while their risk for lymphedema should be lower than heavier women. [2, 11, 13]

What can I do about AWS?

While studies written by physician researchers state that AWS will resolve on its own, therapists around the world who frequently treat AWS agree that gentle massage, manual lymphatic drainage techniques and range of motion exercise can accelerate pain relief and tissue healing. Physical therapy may shorten the natural course of AWS to 6-8 weeks. [3] In some cases, the AWS presents with a mild lymphedema of the forearm. While traditional CDT (Complete Decongestive Therapy) techniques may reduce the lymphedema, it may become a chronic condition unless the AWS is treated.

Soft tissue techniques for cording include very gentle tissue “bending” or “traction” techniques applied along the taut cord in a comfortable position of stretch. Localized thumb and whole handed MLD techniques along the cording is also useful. Do combine active stretching with massage techniques to further improvements and do not be surprised if a “pop” is heard along the cording during your gentle treatments or during stretching. This “pop” will usually ensure immediate pain relief during movement but can also lead to lymphedema on rare occasions. Please avoid being overly aggressive (causing pain) during your treatments as this can cause an inflammatory reaction that may increase the lymphedema risk of your affected arm.

Knowledge of safe and effective techniques to hasten the resolution of AWS is necessary in the treatment of those recovering from breast cancer treatments and arm lymphedema. Hopefully reading this article will help to ease you or your patients’ discomfort and increase your awareness of the treatments that are available.

Jodi Winicour PT, CMT, CLT-LANA
Longmont United Hospital, Longmont, Colorado.
Jodi is a full time clinician specializing in the treatment of lymphedema and cancer related dysfunction. She also is a Lymphedema Certification and Breast Cancer Rehabilitation Course instructor for Klose Training & Consulting.
Contact her at: Jodi@KloseTraining.com

Guenter Klose’s Therapist Review of My Sassy Sleeve

May 20, 2011 at 11:45 am | Posted in Certified Lymphedema Therapist, Lymphedema Certified Therapist, NLN | Leave a comment
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In the most recent e-newsletter from the National Lymphedema Network, Guenter Klose, Founder and Director of Klose Training, reviewed the products from My Sassy Sleeve. In the commentary below, Guenter describes not just the physical benefits of the garment used for Lymphedema treatment, but also the emotional benefits.

Therapist Review:

by: Guenter Klose, MLD/CDT Certified Instructor, CLT, founder of Klose Lymphedema Care in Lafayette, CO., Executive Director of Klose Training and Consulting.

When Monica (co-founder of MySassySleeve) introduced me to her decorative coverlets and brought several samples in to our office, I was happy to see such a fresh and innovative product offered for people with lymphedema. It is exciting that patients who wear compression garments to manage their lymphedema now have a design choice with these interchangeable, non-medical sleeves.  Instead of feeling like they need to hide their compression sleeve under a jacket or long-sleeved shirt, they can wear these light-weight, stretchable coverlets over their garment to add a bit of light-hearted fun.

I often hear from many of my patients that having to wear a medical garment is not only unattractive but makes them feel self-conscious. We immediately saw emotional benefits in patients who wear the MySassySleeve coverlets. By drawing attention to the colorful, tattoo designs and away from the medical looking therapeutic compression sleeve, my patients have rediscovered their self-esteem and self-confidence. They feel good about themselves and that has empowered them.

While MySassySleeve is only decorative and does not manage lymphedema, it certainly provides an emotional, feel-good benefit that medical garments alone cannot provide. Congratulations on a wonderful and beneficial product.

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