lymphadema!
 

My lymphadema is getting worse! I'm almost 6 years out now. I'm trying PT and going to go learn some water excercies. My husband is also going to learn some tech. to help the swelling with massage.(i just hope he doesn't expect something in return everytime! Ha) Does anyone have any ideas on garments to wear to bed? The sleeve is useless. I need it more under my arm and top of arm. I'm looking for something that fits like a tank top and has a sleeve attached to it. Can't find anything like that out there. My arm is always tingly now

Dear Michele,

I am sorry to hear about your lymphadema. I really do not have any thing else to recomend but the pressure sleeve which seems not to work to good for you. I know the massages are the best that you can get for treatment. I am sure that some of our sisters here could recommed something like Caya for example. Hope somebody can suggest something good for you very soon. Keep us posted how do things develop.

Paty

Hi Michele,

Just saw your post... sorry the lymphedema is so bad for you. My lymphedema is mild, mostly contained to my right hand, and both my breast surgeon and the therapist at the lymphedema clinic at the hospital I go to for treatment think it will be completely reversible.

That being said, I did get referred to an RMT (registered massage therapist) who specializes in lymphedema massage. Here in Ontario the therapist has to take about 140 extra hours of instruction/practicum to get the lymphedema certification. I'm sure you could find a lymphedema massage expert in your area - it is well worth the money, you may even have health coverage for it. Sofia, my masseuse, told me to bring my hubby next time to learn the massages.

I have an appointment tomorrow at the Lymphedema Clinic at PMH (Princess Margaret Hospital, in Toronto) for another assessment and massage. I will ask the therapist if she knows of any other garments to wear to bed like the one you are describing.

all the best
Caya

Michele - I've had lymphedma for several years in my right arm following mastectomy. I've been able to control it well with lots of persistence. In the beginning I bandaged every night; now I don't do that unless I have a flair up. At night I have 2 garments I use alternatively - something called a tribute, and a different one that has velcro straps I can't think of the name of. I looked up on-line and found a site lymphedemaproducts.com. If you go to the custom garments tab it shows examples of each. I don't recomment the reidsleeve - it's very still and uncomfortable.

During the day I always where the sleeve and sometimes a gauntlet if my hand is puffy. The sleeve is always custom fit; the gauntlet I get off the shelf.

I go to a therapist who has had all the certification for lymphedema therapy - that's all she does. She says bandaging at night is the very best to get it under control. Also manual lymph drainage therapy has helped me - I try to go 2 times a month & my insurance pays for it. To get the garments I go to someone my therapist recommends who is trained to do proper measuring/fitting of the garments. My insurance also pays for them.

My therapist also said the under armour compression shirts can be helpful to wear. Not all of the underarmour things are compression, but it will say on the tag. Offers a little bit of support & you can buy them at most sporting wear stores.

Hope this helps.

OK, this will probably be a really stupid idea! Maybe it should go on the keeping your mind off bc forum...

How about getting a wetsuit and cutting it to "fit" where you want it?

lymphadema!
 

I think the water exercise is worth a try. When we do water exercises we get the benefit of the exercises without tiredness and aches and pains we can sometimes get from regular exercise. Let us know how it goes.

Hi Michele,

I had lymphedema massage therapy today at PMH. The therapist gave me a few sheets of exercises to do, if you want to PM your address I would be happy to mail you a copy.

I asked her about the type of garment you described, she said a good custom fitter should be able to make you whatever you want, but she does not advise sleeping in it. She also recommended swimming as excellent for lymphedema management - the breast stroke and back stroke especially because the arms move so broadly so that the lymph system gets a good work out.

all the best
Caya

I don't know if this will help or not...I did not have Lymphedema (don't yet I think) but I did have painful "cording" down my arm. I was sent to a lymphedema massage therapist as they also address cording (webbing) and loss of range of motion. One of the things they did do was to teach me how to do my own massage...said I should do it indefinitely. Maybe this is something you already do. If not it might be an idea. I notice that small cuts and insect bites on my one arm take longer to heal (by days) than on the other. The massage seems to help the healing process. Whether it would help with swelling is something I do not know (though I suspect it could).

Melanie

PS: The whole idea of things getting worse six years down the road is sobering to me. Probably in a good way. I hope the water exercises help.

I never thought about the underarmour. That is a very good idea!! thanks for all your help.

Hey Michele,
Sorry to hear your lymphedema is getting out of hand. I got mine about 6 months after dx.

When I was at MDAnderson this week a Bc survivor volunteer told me a story of a women who had bad lymphedema that had surgery and it was fixed. She said there is one Dr. there who does this surgery. The Dr. is a woman but she couldn’t remember her name.

My PT told me about Underarmer too.

Have a great Saturdary.

The Doctor that Alice is referring to is Dr Marga Massey,MD,FACS.( She is double board certified in plastics and general surgery)
"Dr Massey has been interested in lymphadema for 15 years.During her residency at Duke a senior cardiac surgeon assigned her the topic. With the initial study of the historic "Charles Procedure" and lymphovenous bypass,a plastic surgeon was born."
Vascularized Lymph Node Transfer (VLNTx) is a novel approach where normal lymphatic tissue us transferred from one area of the body to another.
Dr Marga has trained in Paris under the mentorship of Dr Corrine Becker which has resulted in a collaboration extending to the US Brazil and Egypt.
Dr Massey recently joined forces with the Center for Restorative Breast Surgery (Drs DellaCroce and Sullivan) in New Orleans (which thrills me no end!).. What a step up for us BC survivors to have a facility of this calibre available to us!

http://www.drmarga.com/stats.html

Marcia

certified LANA lymphedema therapist
 

The lymph node transfer is very interesting. I emailed Dr. Massey some questions. we'll see if she responds

I got mild swelling and pain/tingling overdoing some house construction and my chiropractor resolved it in 2 visits. Maybe you could explore that option.

Dr Vodder's School
 

This was the website I went to to make sure I was going to a certified practitioner http://www.vodderschool.com/
On the website you can find a qualified therapist in your area. I found a wonderful woman and she knew everything I needed to know and had references to all the places in town for fitting garments. If you are interested in a book that outlines the physical massage you can do at home e-mail me and I will dig it out for you.

Re: lymphadema!
 

I used a tribute sleeve by Solaris for several years and it worked wonderfully. It was prescribed by my lymphedema therapist and she did the measurements. It is a made-measure-garment. I wore a garment at night and also a garment during the day and can say that my lymphadema is now under control and I don't need to wear anything. I continue to get monthly massages from a massage therpist that I believe help me out as well.

Good luck to you!

Re: lymphadema!
 

http://www.bio-con.com/lymphedema.html

These guys make awesome custom made sleeves, good quality and very durable. I have used them since 2007 and they wear well and are comfortable. If I swell really bad then go back to wrapping at night. I also found at that after weekly herceptin since 3/06, my cardiologist put me on low dose of diovan and hctz which helped dramatically as well.

Goodluck

Darita

Re: lymphadema!
 

http://www.breastcenter.com/news/20090803_wwl.php

Michelle, I thought you might want to see this segment from WWL-TV in New Orleans on the VLNT procedure...
Marcia

Re: lymphadema!
 

I am so happy to learn about this procedure. I almost did not have the recommended radiation treatments even though I had 21 of 21 lymph nodes removed from my left arm test positive. My left arm is my "good" arm that performs all of my daily living tasks due to the fact that as a small child I had Polio that caused me to have very limited use of my right arm. I cannot lift anything, feed myself, write, etc. with my right arm. When the radiation oncologist told me that there would be a 30% increase in the chance of the lymphadema occurring, I almost bolted and ran for the hills. I did go ahead since I had so many positive lymph nodes and completed 5 weeks therapy in April this year. So far I have had only very mild swelling problems and I do have a compression sleeve, gauntlet and the therapist has taught my husband to do the massages. Knowing there is this procedure in case it progresses and causes problem using my only operative arm brings me much relief!!!

Sandra
_________________________________________
Diagonosed: August 2008 ERPR- HER2+ (3+), 3 cm tumor Stage III with lymphatic and vascular invasion, 21/21 nodes positive. No spread to other areas of the body
Surgery: Double mastectomy R-Prophylactic with reconstruction of R brst begun; 21 lymph nodes removed from left arm
Chemo: A/C began in Sept. 2008 every other week X's 4
Nov. 2009 began Tykerb daily along with Taxol and Herceptin given weekly for 12 weeks (this stretched to 14 weeks because of low WBC and temp on two occasions).
Now taking Herceptin once every 3 weeks and daily oral Tykerb until middle of Nov.

In a phase II study of the cardiac safety and tolerability of Herceptin and Tykerb added to adjuvant chemotherapy at Mayo Clinic in Jacksonville, FL for early stage treatment.

Re: lymphadema!
 

oh my, this is awful! after 6 years...I still have large ares of numbness and some puffy skin flaps left over from surgery and I wonder about them. And no one seems to get it that if one has had both breasts removed, and some lypmh nodes on both sides that blood pressure cuffs should not be used. And I am usually such a weenie that I let them do it anyway. Well, Michele, you have inspired me to say "NO" to more blood pressures!!! It is the least I can do!!! Good luck to you!!! Hey, do you think the altitude where you live has any bearing on any of this???