VISIBLE SIGNS OF LYMPHEDEMA - A PICTORIAL

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  • Binney4
    Binney4 Member Posts: 8,609
    edited April 2012

    Bummer, StarWish!Frown Really sorry you've had to join our "swell" sisterhood, but glad you found us here. Please tell us how we can help.

    Gentle hugs,
    Binney

  • newksmom100
    newksmom100 Member Posts: 55
    edited May 2012

    Question for all:  After getting a consult to a PT for tightness in my underarm and breast I was told yesterday that I have cording.  Does this mean I also have LE?  I can't find much info on it.  Thanks for your help.

  • lago
    lago Member Posts: 17,186
    edited May 2012

    Newksmom there is much they don't know about cording but NO cording doesn't mean you have LE. It is thought that you have a higher risk by some but not others.

    That said I had cording in my right arm (4 nodes) but no cording in my left/cancer side (10 nodes). I have LE in my left arm but none in my right.

    So unless your PT said specifically you have LE, cording does not  mean an automatic diagnosis for LE.

    You can read more about it here: http://www.stepup-speakout.org/Cording_and_Axillary_Web_Syndrome.htm 

  • Adey
    Adey Member Posts: 3,610
    edited May 2012

    LindaLou-  Old news but thanks very much for the pix!  They helped me know what to look for.

  • journey4life
    journey4life Member Posts: 517
    edited May 2012

    Hi ladies,

    I think I've developed lyphedema. Over the past few days, I've experienced pain in my forearm, especially when flexing my wrist. Yesterday, I noticed swelling and I have pitting.

    Should I call my MO in the morning or wait until my infusion on Wednesday? Is there something I can do now to reduce the swelling? I don't have a sleeve and have not been given any instruction on wrapping.

    I am so disheartened and sick of all this crap that comes with BC... 

  • lago
    lago Member Posts: 17,186
    edited May 2012

    Baldeagle I would call on Monday because you will go crazy waiting till Wednesday. Try to keep the arm elevated ( over the heart). Also don't get too sweaty but walking might get the fluids going. Keep away from salty, water retaining foods. Drink fluids.

    Most of all don't freak out or get bummed (like I did). Right now it sounds like you have a very manageable case (like mine). I have never wrapped. I could give you exercises but I feel you need to get these from a PT to make sure you are doing them correctly.  I think it was weeks before I got to see the MD for my LE because he was on vacation. Then another week before PT. It really didn't make a difference for me.

    I had a feeling I had it after my 2nd chemo. After my 4th chemo was when I noticed the swelling. 

  • kira66715
    kira66715 Member Posts: 4,681
    edited May 2012

    Bald Eagle: Yes, it does stink--but early detection and treatment leads to the best outcome.

    Here are some suggestions on what to do while waiting--on the web page there's a link on how to find a qualified therapist:

    http://www.stepup-speakout.org/How_You_Can_Cope_with_Lymphedema.htm#while%20waiting

    What to do While Waiting for Your First Appointment with a Qualified Lymphedema Therapist


    DO NOT try and treat this yourself!!! Proper professional treatment is essential to getting control of lymphedema and preventing its progression. Treatment can be expensive and inconvenient, but this condition is life long, potentially disfiguring, disabling and possibly life-threatening (if you get an infection known as cellulitis) so professional evaluation and treatment as soon as possible is essential.
     

    1) Get evaluated promptly by your doctor to rule out other causes for the swelling in your hand/arm, and get a referral to see a well-trained lymphedema therapist;
    2) Drink plenty of fluids -- staying well hydrated helps dilute lymph fluid and keep it moving freely;

    3) Elevate the swollen arm or hand as much as possible during the day and on pillows at night; support the arm well so that it doesn't tire;
    4) Several times a day pause and do some deep breathing -- this helps stimulate the largest lymph vessels in your body;

    5) Raise hands over head as high as is comfortable for you, three times a day, and pump fists 20 times;
    6) Call for medical help immediately if you have severe pain, redness, fever or feel ill;

    7) You can try mild compression gloves by either Sammons Preston or Isotoner® Fingerless Therapeutic Gloves if your hands and/or fingers are swollen until your appointment with your lymphedema therapist. Be sure to bring them along to your appointment;
    8) Do NOT use ACE wraps or any other wraps without the advice of your lymphedema therapist after your evaluation and your treatment plan is scheduled.

    An aside: is thread no longer pinned?

    Kira

  • Binney4
    Binney4 Member Posts: 8,609
    edited May 2012

    About pinning this thread: yesterday the moderators took all of our pinned threads and put links to them together in a single category at the top of the board, called "Key Lymphedema Threads (former stickies)". It's a resource for newbies so they have somewhere to start looking for information and asking questions. There are links there to the following three threads:

    Visible Signs of Lymphedma

    MBCS: Tool Predicts Arm Swelling in Breast Cancer

    Instruction on How to Wrap Your Hand and Arm

    They had also included the RIBP thread, but kindly removed that one when requested, so the RIBP ladies can more easily find their thread, and so that newbies don't think it's early LE information.

    I don't know about the rest of you, but I think the MBCS prediction tool is extremely flawed and shouldn't be part of anyone's self-assessment process. It's a nice stab at trying to predict risk, but the science just isn't there yet to support such an attempt. There are still many factors we can't account for, so I for one would like that removed.

    How to the rest of you feel about that?
    Binney

  • 1Athena1
    1Athena1 Member Posts: 6,696
    edited May 2012

    LindaLou,

    Thank you so much for your hard work, courage and generosity in sharing these pictures with us. I don't have LE, but as a former BMX and AND patient, I will always be at risk of developing it and it's hard to know what to look for if one has never seen it before. Thank you, again!

  • journey4life
    journey4life Member Posts: 517
    edited May 2012

    Thanks for the information. This has really upset me and I feel so defeated. I am right handed and all I can see right now is a lifetime of dealing with this. I hate FBC

  • lago
    lago Member Posts: 17,186
    edited May 2012

    Baldeagle I have it in my left but it really hasn't been a  huge issue. I was diagnosed in Dec 2010. I'm back to strength training… and I've surpassed my pre-diagnosis level. I do wear my sleeve. I also carry antibiotic ointment, bandaids and antibacterial cleanser (sample sizes) in my purse now but everything else is really the same.

    The problem with the MBCS tool is it doesn't predict for those of us who had just level I or less our risk of getting LE. Guess 10 nodes wasn't supposed to get LE, but I did.

  • Binney4
    Binney4 Member Posts: 8,609
    edited May 2012

    Baldeagle, this is another hard-to-digest elephant, but you can do this -- one bite at a time!Tongue out We all sure hear you on how distressing this is, but I want to assure you it really does get better--honest.Smile

    First bite is getting an appointment with a well-qualified lymphedema therapist. Start tomorrow. Any doctor on your team can write you a referral. Please let us know how it goes. We're here for you.

    Tell us how we can help! Gentle hugs,
    Binney

  • carol57
    carol57 Member Posts: 3,567
    edited May 2012

    Binney, I agree with Lago that the prediction tool is not a good fit for those of us with few nodes removed. When I gave it a try, I remember I had to overstate the number of nodes removed...no choice for my 5 lost to SNB. I can no longer recall the risk % the tool returned, but I do remember thinking it was a very strange result.

  • journey4life
    journey4life Member Posts: 517
    edited May 2012

    Thanks, Binney. I plan to call my MOs office in the morning. Its hard to fathom right now that this will get better, so soon after my surgery and right in the middle of tx. I feel like I've done almost everything I was supposed to do (i.e. pay attention to what I lift, no repetitive motion like sweeping, vacuuming or raking) and it still happened.

    Any suggestions on transitioning from right-handed to left? :)

  • Binney4
    Binney4 Member Posts: 8,609
    edited May 2012

    Lisa, you most likely won't need to transition from right-handed to left except on a very temporary basis, while in treatment. The point of lymphedema therapy is to return our arms to usable condition and teach us how to keep them that way.

    While waiting for treatment, though, I found it easy to avoid over-using my right arm, because I was so worried about it. You can certainly use it, even while waiting -- just be careful about straining it. Most of us are careless of simple body mechanics, like holding heavier loads with both hands and keeping them close to our bodies instead of extended outward where they strain our arms more. So just being thoughtful about those things is usually enough to get you through until you can find your way to a good lymphedema therapist. If you're doing something that is repetitive (knitting, say) just plan to take a break now and then and do something else for a while, then return to it later.

    If in the long term you find you need to modify your right-arm use, there are loads of simple and effective ways to do that, but for now it shouldn't be an issue. And hopefully never!Smile

    Hugs,
    Binney

  • carol57
    carol57 Member Posts: 3,567
    edited May 2012

    Lisa, I see bald eagles out my window most days, and they are a very focused bunch of birds!  You, too will find you can zero in on a few good strategies to understand LE and craft a strategy to move forward.  Along the lines of Binney's comments, I have become very aware that I use my nondominant hand for lots of the brute-force work that we all do in daily life. My LE is in that arm, so I've had to remind myself all the time to transfer the heavy load to my right hand and let the LE hand do some of the finer work.  All of which to say--I wonder if in your case, you are already letting your non-LE limb do the heavy lifting, which is a good policy and can only help you here.  I will admit to getting frustrated when I try to type wearing my compression gauntlet, but then I just remind myself that it's slowing me down, and that means (glass half full) that I'm taking more time to think about what I write instead of just dumping thoughts!  You will find ways to look at the glass half full, I promise.  And a good measure of that comes from all the amazing support you'll find in the LE forum here.  Having LE PO's every single one of us...so we're a good group to dump frustration on, because we've all been there in some degree or another.

    Do keep us posted!  And if you find that walking or any kind of exercise is a sanity strategy for you while under stress, consider joining the kick-LE's-butt thread.  We would love to see you there!

    Carol 

  • Galsal
    Galsal Member Posts: 1,886
    edited May 2012

    any chance of pictorial of truncal?

  • BeckySharp
    BeckySharp Member Posts: 935
    edited May 2012

    Lisa--I have LE in my right arm and I am right handed.  I was wrapped for 3 mos and now wear a sleeve and gauntlet.  I was so clutzy with my left hand and always said I could never become left handed.  But with some loss of tactile sense with gauntlet I realized I was using my left hand/side more and more.  I often do something with my left hand when I could have used my right.  I was told recently that I was lucky I was left handed since my LE was on the right!  My left hand automatically reaches out.  It was a gradual phasing in.  I now use both and no longer baby my right as much unless it is heavy lifting.  Good luck to you!

  • lago
    lago Member Posts: 17,186
    edited May 2012

    I hated the gauntlet. The glove works much better for me especially when typing. Granted I can wear an off the counter glove. Gloves are more expensive than gauntlets especially if you need them custom made.

  • journey4life
    journey4life Member Posts: 517
    edited June 2012

    Hi Ladies - Just checking in with an update. Its hard to believe it has almost been a month since I was here last! I have been going to an LE therapist for two weeks now. She wanted to see me daily for 2 weeks but I couldn't afford to take that much time off work and would also have to pay my insurance co-pay of $20 at every visit. So, we agreed on a MWF schedule.

    I have Stage 1 LE and early stage cording. I've been fitted for a sleeve and gauntlet and will probably order them on Monday. Did anyone purchase from LympheDIVAS? Some of the designs are so not me but I've narrowed my choices down to a couple. I'm not seeing a tremendous difference yet in swelling reduction but I can tell the range of motion in my arm is better. I can certainly tell I'm doing the correct exercises - I can "feel" each of them!

    Hope you all are doing well. Again I thank you for the advice and support. LE has become an added feature to my new normal and I'm going to make the best of it. TGIF!

  • lago
    lago Member Posts: 17,186
    edited June 2012

    I tried a lymphediva sleeve at my LE MD's office. He had a sample that happened to be my size. I felt the fabric was thinner than what I'm wearing now but the compression was not the same. I'm sticking with the medi 95 sleeve.

    Note that LympheDivas does have 2nds. They are just misprints but cheaper. If you need an extra set or on a limited budget (especially after all those co-pays) you might want to consider. I also found this site to have decent prices (they sell Lymphedivas too) brightlifedirect.com

  • journey4life
    journey4life Member Posts: 517
    edited June 2012

    To anyone who's been wrapped - I was wrapped today and I'm already having some discomfort in my elbow, mostly on the inside and underside. Is this normal? I can feel constant pressure on the rest of my arm but the elbow area is painful when I bend it.  Also because of the way it feels, I want to shove something under the wraps and scratch! Most of my work involves a computer so bending is a must! What can I do?

  • BeckySharp
    BeckySharp Member Posts: 935
    edited June 2012

    baldeagle--I was having trouble with irritation in my inner elbow when I was wrapped.  My therapist started putting a piece of foam in the area.  Plus she doubled the wrap before the bandage in that area.  It helped a lot.

  • kira66715
    kira66715 Member Posts: 4,681
    edited June 2012

    Baldeagle, pain isn't good: if it really starts to hurt--consider taking it off, or calling your therapist. You don't want a bad chafe.

    The elbow area is tough: my therapist cut me a piece of gray foam to go over the elbow on the outside, and I wrap over it with artiflex and we apply the bandage to go above the elbow, around the arm and then criss cross back over it.

    It's crucial that a wrap allows freedom of motion at the wrist and elbow. 

    I've had therapists wrap me too tight, and it hurts. My LE therapist doesn't put much stretch on the bandage, but adds layers for compression, and it's actually, comfortable.

    Give the therapist a call, if it's bothering you.

    Kira

  • journey4life
    journey4life Member Posts: 517
    edited June 2012

    Becky and Kira - thanks. I will give her a call in the morning and see what she suggests. It didn't appear that she put much stretch on the bandages and she did add layers. I'll see how it does tonight; as long as I keep my arm straight, it doesn't bother me. Its just that I can't do that all the time.

    Lisa 

  • sas-schatzi
    sas-schatzi Member Posts: 19,603
    edited June 2012

    reposted with permission of Dunes:

    An hour ago dunesleeper wrote:

    Here is something for you all to pass around to the various groups you belong to:Please join us on Monday, June 25th or Tuesday, June 26th for an important free webinar: Take Back Our Genes: Ending the Patent on Breast Cancer Genes to learn about how one company's control of the "breast cancer genes" creates barriers to research and testing that could endanger your health and compromise the healthcare of hundreds of thousands of women.

    In 2009, Breast Cancer Action signed on as a plaintiff in the lawsuit challenging Myriad Genetics' patents on our genes. The lawsuit, filed by the American Civil Liberties Union (ACLU) and the Public Patent Foundation, challenges the legality of the patents that grant Myriad Genetics control over the BRCA1 and BRCA2 (the "breast cancer") genes.

    Myriad's monopoly prevents anyone else from so much as examining the genes, and creates barriers to scientific research and medical care relating to breast and ovarian cancer. It also limits women's ability to get second opinions when they receive ambiguous test results, which happens disproportionately to women from ethnic minorities, including African-Americans, Hispanics and Asian-Americans.

    Breast Cancer Action is the only national breast cancer organization named as a plaintiff in the lawsuit. We are able to take this stand because we have no conflicts of interest: we don't take money from companies that profit from or contribute to cancer, and because our work demands that patients must always come before profits.

    The webinar will be presented by BCAction's executive director Karuna Jaggar, Sandra Park, Staff Attorney for the Women's Rights Project at the ACLU and Runi Limary, breast cancer survivor and plaintiff. Topics we'll cover include:

    Why BCAction opposes gene patenting and why the issue is important for women
    The impact of gene patenting on underserved communities
    The current status of the ACLU's lawsuit challenging the legality of patents on human genes
    Real stories of women's experiences with gene patenting
    How you can get involved

    Join us on Monday June 25th 3pm PDT/6pm EDT or Tuesday June 26th 10am PDT/1pm EDT for this free one-hour webinar to hear the real story about the effects of gene patents on women's health and to join us in opposing corporate control over our bodies, our genes, and our health.

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    For your convenience, we are offering the webinar at two different times. Click on the links above to register for the time and day that works for you.

    Sincerely,


    Sahru Keiser
    BCAction Program Associate of Education and Mobilization

  • momx3
    momx3 Member Posts: 161
    edited July 2012

    Is anyone having issues with swelling throughout the night??? My arm and my foobes are feeling HUGE when I get up in the morning.

  • Binney4
    Binney4 Member Posts: 8,609
    edited July 2012

    Momx3, are you using any compression on arm and foob at night?
    Binney

  • lago
    lago Member Posts: 17,186
    edited July 2012

    Momx3 I actually have just the opposite

  • kittyabc3
    kittyabc3 Member Posts: 1
    edited July 2012

    thank you so much for sharing your information. education is so important.

    educating ourselves as we travel down "unknown" paths gives us light and understanding.

    i learned many things that i did not know about lymphedema. i recently had my left breast removed and 14 lymph nodes also removed. i can feel areas that seem "not quite right" in the healing process. now i know what to look for...i had a wonderful doctor and staff to help and support me through this surgery. but, few see the importance to educate one on the "out-skirts" of what to look for after surgery and also in the area of preventive care. this has help me out tremdously and i will certainly pass this on to others. thank you also for the pictures, visual aides are so helpful. i go to my doctor in August for a follow-up visit. i do keep swelling in my shoulder, arm and hand on the left side...and there has recently been a low consistant pain under my arm and on my left side. this i know, after reading your article needs to be addressed when i go to see my doctor. thank you again, for helping me.

    terrie daniel

    adrian, ga.  

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