VISIBLE SIGNS OF LYMPHEDEMA - A PICTORIAL
Comments
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Thank you so much for posting and for the pictures..they are very informative...
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I think what you did, showing all different signs of swelling in your hand and arm is great info. I just had partial mastectomy on Friday the 16th and will be watching for signs like these shown. Thank you again
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Thank you so much for all of your information and photos.
This Summer I woke up with puffiness on the top side of my hand along with my index finger swollen. My arm sleeve that I wore the day before while I was doing some gardening I think may have caused it. The sleeve being too tight at the wrist and also using the hand too much.
Anyway, I found a great therapist that works weekends. She turned me on to Kinesio Tape. Applied it while my hand was flexed with fingers pointed up. Starting above the wrist crease and made a split down the middle like two legs. one stretched a little past my first knuckle on the finger and the other down my thumb.It"s stretchy but tight and It seems to force the lymph fluid back up the arm. I've been wearing it everyday and am having great results. Of course I am also doing self LDM. Top of hand and finger shows no visible signs since I've been using the tape. It stays on for a couple of days then I have to reapply a new one.
Just want to let you ladies know to check out Kinesio Taping and lymphedma.
Tina
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Thank you so much, I am in Australia and struggling after a preventative bi-lateral mastectomy 10 weeks ago, i have huge truncal swelling and mild left arm and chronic right arm LE. I have just purchased a sleeve and am about to be fitted for a full garment. Your photos prove without a doubt I am not imagining whats happened to me. Thank you again..
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I developed lymphedema on the 1 year anniversary of my last radiation treatment. I was going to cardiac rehab due to having 95% blockage of my LAD, due to radiation. One week after starting using the weights (only 3 pounds) my hand swelled up. I had a ring on and could not get it off. Went to physical therapist that helped me with cording and getting my shoulder back to normal. She did some manual decompression so we could get my ring off. WHEW! It was my Mother's ring my husband bought me after my 3rd baby. We went through many different sleeves/gloves/wrapping and nothing helped. She lent me a compression pump and had to pump for an hour a day and that is only thing that helps. Now I have a fitted sleeve/glove and also a night one that looks like a huge oven mit. Funny thing. My physical therapist (specializes in breast cancer patients) had never saw lymphedema present in the hand before me (in 20 years), but she has since seen 3 more patients with it. Your pictures lindalu53 look alot like my hand. I have to have a little padding on back of hand, under the glove/sleeve so there is a better flow of the fluid. If I didn't have that, my hand looks like those surgical gloves blown up. Between the Neurapathy that I have and the Lymphedema, I don't know which is worse. But, I am ALIVE. 2 year survivor of Inflammatory Breast Cancer.
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I have Axillary Web Syndrome with cording. BMX 6/10 ..had 6 weeks of LE/PT....the cording is much better after myofascial release. I am at risk for LE, and am getting fitted this week for a sleeve/ glove. Mainly advised to wear it for flying..... I still have some upper chest swelling right next to my shoulder anteriorly/ upper pecs on both sides r >l and am advised to wear jovi packs for my chest wall edema.
I still note I have engorged veins on my problem side with the AWS mainly my hand.
Any advice on the chest jovi pac as I see the fitter on wed? My fitter did not seem to know about them? But was well versed in the lyphedema sleeves/gauntlets.
And Lastly..... any thoughts on getting a dental cleaning and antibiotics in this sitchy?
Thank you for your great info..... esp in all these unchartered waters I swim of late.
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Brazos, hello!
The JoviPac chest garments are very helpful, at least for nighttime use. They're relatively comfortable, machine washable, and they come in a bunch of colors. But there are other options to consider too. Here's a page with a whole lot of other chest/breast garment suggestions, some much easier to tolerate for daytime wear (scroll down the page and you'll see the links):
http://www.stepup-speakout.org/breast_chest_trunckal_lymphedema.htmLet us know what you discover!
Hugs,
Binney -
Hi Brazos,
Binney gave you good info on the JoviPaks and chest garments.
Regarding the need for antibiotics when you get dental cleanings, I am not aware of that being routine protocol for patients with lymphedema alone, unless you have a history of infections following dental procedures. Persons with a history of rheumatic heart fever, heart murmurs or valve replacements are often advised to take oral antibiotics before any dental procedure including cleanings. If you do not fit into any of those categories though, I am not aware that preventive antibiotics would be necessary for lymphedema in the absence of a current infection.
I have had routine dental cleanings every 6 months in addition to fillings and crowns replaced without requiring prophylactic antibiotics. Of more personal concern to me is that I have been on IV Zometa for over 4 years which carries a low risk of degenerative bone disease of the jaw following dental procedures....totally unrelated to lymphedema by the way.
Discuss your concerns with your dentist before your next cleaning.
Best wishes!
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Hi,
I just had a radical unilateral nipple sparing mastectomy (with 12 nodes removed) & immediate tissue expander reconstruction on Friday the 15th. I am experiencing swelling on my upper arm specifically the tricep/bottom portion. It feels almost numb or strange sensations when I touch it. I have been stretching and have really good range of motion for only 1 week post surgery. Should I be worried about lymphedema so soon or let things settle down first. I think the drain is not draining exactly right considering it leaks on under my arm a bit and the pain in my tricep seems to be more pronounced since the leaking increased. My doctor says the leaking is normal and its not swollen but I clearly know it is as- well as my torso on the side of the surgery.
Paranoid and confused...
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binney, thank you for your thoughts re: the Jovi Pak.... I saw the fitter and have a chest pad one waiting to come in. Do you find it best to wear at nite or during the day?. They look like they would offer some much needed chest wall protection from hypersensitivity....
lindalou many thanks to you as well. I did ask my Dentist and LE/ PT re antibiotics and it was not an issue at all.
I have hopped over to the GGGGrrrrr thread, reading some in there.... starting to learn.
ladygrey, get well wish's to you. I had/ have swelling under my arms and armpits on both sides following my bilateral Mx/ prophy in 6/10. Esp in the area you describe as well as my back. Also have numbness and strange tingling, vibrational feelings. Sounds like post op swelling .Not all of this has quieted down to normal yet either....I measured my upper arm circumfrence and my wrist as well to monitor it. If your drain is leaking at the insertion site, that is not normal and you may have a clot in the drain.Sounds like your drain is having an issue more than likely. I would only expect a tiny bit of that.But then I am not familiar with Nipple sparing sx with node removal.... Do you have Visiting Nurses seeing you? I always follow my instinct,,,, if I feel something is not right, and the answer I get from the Dr. does not feel right.....I press on for answers until its clear.
We always have to keep a heads up on lymphedema b/c of our surgery, we need to learn about it, and see a Lymphedema/ PT for evaluation and monitoring....
I am sure LindaLou will be along to answer your questions as well.
Best of Luck to you and keep asking questions.
Ease for your mind and clarity!
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Brazos, I do wear my Jovi vest during the day when I have pain or sensitivity. It's gentle and it just feels better. Otherwise I wear a WearEase Slimmer cami or a WearEase compression bra, both of which do a good job of covering the areas near the front of the axilla and on my back where I have swelling. And I always wear the Jovi at night. In the summer I put it in a plastic bag and store it in the refrigerator during the day so it's cool to put on in the evening -- the foam holds the cool for a few hours. Just don't put it right next to the onions...
Abrazos!
Binney -
Binney thank you for guiding me so much today. I cant wait for the jovipak...and I love the idea of chillin it down with all these hot flashs. Note to self about the onions.
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Linda,
I can't thank you enough for putting up your pictures. If you had not, I NEVER would have understood that I have LE. Mine is in the metacarpals, and I had been watching it ever since I saw your pics, then I watched it get worse when I fell on my arm last week. I was devastated, not knowing how bad my injury was. I know I have a lot of learning to do, and have been spurred on to action by other's stories. I did see the LE PT yesterday, and have begun my exercises. I start at Stage 0, and have already begun to re-route my LE most likely due to swimming. This was her assessment. She felt it could have been much worse. So I will go and get my sleeve and glove, and start the work of getting this under control.
So I wanted to introduce myself, and I'm sure I will have more questions.
Thanks so much,
traci
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Linda-- because I am getting Zometa every six months, both my onc and my dentist are being super-cautious and having me take two Ertyhromisin (sp?) forty five minutes before my teeth cleaning.
They both think of it as insurance, since I have implants and have had lots of dental work in the past, and neither of them wants to even think about any possibilities of infections in my jaw.
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Wonderful job. I am actually going to go to a therapist tomorrow. My new onycologist referred me. Had not had such a great response about this slight issue until I changed doctors. I thought that I was with a great ony doc, but when he kept sending my reports to my regular physician and he said I should continue seeing the breast surgeon....when I had clearly been telling him I had no breasts. Go figure. I didn't have a clue until my primary dr told me all this. Guess that is a good reason to change onycologist.
Thanks again for the pics.
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Thank you very much for posting those pictures, LindaLou. This is incredibly helpful!
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AWESOME thread... not that I am excited to be here, but learning from you ladies! I have the tuncal lymphedema... I am 2 years post treatment, etc... I went to a LE therapist for most of the first year and then it seemed to get better.. I travel a lot for work and have noticed it again in my back. Do I need to go back to the LE therapist? Or should I continue to try and maneuver the fluid, which does not seem successful?
Nicole
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LINDA YOU ROCK!
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Nicole, hello!
I'm really sorry you're having further problems.
Bummer! But yes, by all means do make an appointment with your therapist to get everything back in control. Not sure if you've been using any breast compression, but there are a lot of options available now that are both effective and comfortable. If you're not familiar with them, use the links at the bottom of this StepUp-SpeakOut page to see what's out there:
http://www.stepup-speakout.org/breast_chest_trunckal_lymphedema.htmKeep us posted on your progress!
Gentle hugs,
Binney -
just wanna say bc dx 2/3/10/Stage IIB, 3.5 cm, rt breast/lump/2 lymph nodes/rad/on Anastrazole since 10/1/10
only swelling lymphedoma & ITCHING in my legs,ankles & feet---some itching in the breast area, but not near as bad as my legs----every day of the rads (completed 9/15/10), every day after----last 2 days I think it's getting better, the itching, that is, stell have swollen calves, some swelling in ankles in ankles & feet----all medical professionals said it is lymphedema
numbness in feet & fingertips, some days stronger than others
no swelling in hands, fingers, wrists, arms
the odd thing that happens to me is anything the least bit fitted will leave indentations in my skin, i.e., leggings, most socks (even so-called "sof" diabetic socks, I've discovered one brand, Keds, aren't as bad as all the others I've tried
I stay as far away from chemicals as I can, very little makeup (eyeliner/eyeshadow/lipstick used as rouge & also part of the eyeshadow, pink color, that is), sometimes, actually lipstick. I never did like foundation makeup (too greasy), but I did try the mineral powder, it seems ok.''
NO nailpolish & I quit wearing my rings 'cause they leave "blue" marks on my fingers, & itch, besides!
Another question I have---what is meant by being "in remission??" Does that mean having made it through the treatments? Is it the same as "cancer survivor?"
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Linda Lou: God bless you for this thread. It was on BC.Org that I read about it WAY before I ended up with it. Had a BLM in July of this year and as soon as I had the first syptmom, I was on my way to a therapist. I have been getting the massage and wrappings for two weeks with visable results. All you ladies, this just proves that we have to be are own advocates. Good Luck to all. and Thank you again for your postings. The more that are aware, the more that will seek help. Onward
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I had sentinel node surgery on 12/2. I had the lumpectomy 6 weeks prior so this surgery was by itself. 3 nodes were removed and all were neg. I was swollen and in pain for the first 3 days or so. Then I backed off to just Tylenol for pain and did ok the next 3 days. About the 6th day after surgery the numbness across my back (shoulder blade area) and shoulder wore off and the area hurt. If you touched it, no matter how light it felt severely bruised. I looked at it in the mirror and saw nothing. There was very mild swelling but that could have been my imagination because my husband didn't see it. The surgery area was still swollen which I expected. I went for a 1 week follow up to the doctor and she said I may need to have a seroma drained. I wish she would have drained it then now that I have been through this but didn't know at the time. As the overall swelling went down, the giant egg remained and hurt. My breast on the outside also starting hurting and my back continued to be very painful. My breast was almost a full cup size bigger. By day 9 I was taking 4 Advil every 6 hours and getting no relief from it. So on day 13 I had the seroma drained. There was 20 cc's. I immediately felt better since I could now put my arm down at my side. The next day it filled right back up and I didn't call the dr. since I was busy at work. I found a tight camisole that came up high under the arm and wore that for 3 days straight. The large painful area across my back started to shrink to a smaller area and the seroma filled up a little less each day. Most mornings it was almost gone. On day 20 I went back and had it drained again since it hurt to put my arm at my side and I had stopped wearing the camisole. She drained only 5 cc's but it made a huge difference since now it didn't hurt and I could put my arm down. I wore the camisole days 21 and 22 but then didn't on 23 and 24 and did fine those days without pain. Day 25 the pain was back but the amount of fluid in the seroma I'm sure is less than 5 cc's. I could feel an area of pain and heaviness on my back by my armpit and down the back of my arm. I wore the camisole yesterday and today and the pain area goes away except for a very small area of the seroma (like the size of a penny rather than an egg). My breast is nearly normal sized now but it is still painful on the outside edge. So my question is, do I have truncal lymphedema or is this all normal 3 1/2 weeks after surgery and I'm just impatient. I know many of did not have sentinel node surgery by itself so your recovery was probably expected to be longer than mine, but for some reason I thought after 2 weeks I should be back to 90% normal. My doctor doesn't seem concerned and doesn't seem to believe me about the back pain. She said maybe I pulled a muscle. But that's not possible since I hardly use that arm. Also, I started radiation last week so I would love to be done with this pain so I can move on to radiation pain. Thanks for any advice you can give me!
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Cincilady--your post got over-looked because this thread tends not to be too active.
What you're describing could be fluid trapped in the trunk--truncal lymphedema, or at this point so close to surgery--a seroma.
I'm going to put a couple of links here, but I'd recommend getting evaluated by a lymphedema therapist, and if that camisole works--by all means, wear it! I'll also put up a link to truncal lymphedema.
Hope you check back.
http://www.stepup-speakout.org/Finding_a_Qualified_Lymphedema_Therapist.htm
http://www.stepup-speakout.org/breast_chest_trunckal_lymphedema.htm
Kira
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Hi Lindalou. I just came homr from seeing a specialist doctor or therapist in my area. I was a little blown away with the limitations and effects of having just one lymph node removed from under my arm.I had a Matectomy of my right breast done on Nov 22nd 2010. They took one lymph node from under my right arm. My surgeon told me that I would possibly suffer some swelling after the surgery. I was not aware that it would be a lifetime possibility of swelling occuring from this procedure. It is taking a little getting use to since my job is housekeeping and pushing my somewhat heavy cart and what my job consists of,I may need to rethink my job potition. As I am going to apparently put myself at risk of getting lymphedema or swelling of the arm or hand.I am on a sick leave at the moment and plan on returning to work soon.I did not opt to get reconstructive surgery of my right breast and am also about to get a protisis.I was going to wait to get a glove,but now that I saw the reality of what can happen if precations are not taken I think it may be wize for me to rethink this too. What is your opinion on the compression bandage if I have no swelling yet?Thanks very much for taking the time to post your pictures. You to me were more informative with those pictures than any doctor visit.I am true testimony to that. thnx again Angel1960
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i have made several unsuccessful attempts to "Start A Topic"----I want to know if ANYONE out there has ongoing swollen legs/ankles/feet, especially if you wear socks----the tops "dig trenches" in my legs, then the rest of my leg from calf to ankle really swell out----it's frightening. Of course, when I remove my socks, the "trench/swelling" eventually go away.
I even ordered some "soft socks" online----you guessed it, 2 deep trenches at the end of the day right there where the top of the sock just dug a hole all around my calf (they were crew-length).
I don't know what to do. So far, by the grace of God, NO swelling of arms/hands/fingers, though I have read LE can happen years from now....how do I prevent it?? HELP!!!
I even
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nancy I do but I'm still doing Taxotere which can make some retain fluid. When I take the steriods just before treatment Iose 4lbs overnight! My legs are shiny which is a sign of edema. My stomach wells etc. My mom had lymphedema in her legs but I think my issue is the chemo.
For risk reduction: http://www.stepup-speakout.org/riskreduction_for_lymphedema.htm
BTW I am going to the lymphedema specialist MD today. Took me a month to get an appointment!
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Regarding prevention, this new study showed that lifting weights actually helps prevent lymphedema. The risk can be reduced by 70% if you had more than 5 nodes removed. But you have to start very slowly and build up. In my case I used therabands before I graduated to free weights. During rads treatment I exercised my arms 1-2 hours everyday with dance movements (no resistance). My rad onc was very pleased to hear it. Please ask your doctors.
http://www.sciencedaily.com/releases/2010/12/101208201012.htm
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It is almost a year later and your pictures are still most helpful. Thanks for taking the time and effort to post them.
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I noticed puffiness in my hand several weeks ago, and then noticed I could not see the veins in my wrist last night. Then I found this thread this morning and found out it could be lymphedema.
I am half way through chemo and looking into reconstruction this summer. What should be my next step? My arm is not really bothering me, although I do have numbness in my upper arm.
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Get this looked at right away. This sounds like lymphedema. The earlier it's treated the better off you will be. I didn't start to have the issue till 1/2 through chemo too. It did get a little worse but I'm in therapy now.
I retain a lot of water on chemo so I think it aggravated the condition. I'm hoping it will flare up less once this chemo is out of my system. I'm only 2 weeks out from my last tx.
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