waxing underarms
If you are at risk for lymphedema but don't have it is it safe to get underarm waxing done?
Comments
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I would think it was not a good idea. You don't want to do anything that might cause swelling, irritation or infection.
If I had know what I know now I would have had laser hair removal on my underarm before surgery and radiation if that's possible.
I was shaving with a razor until I developed lymphedema. My LE therapist was surprised that I was doing that. Now I used one of those little electric trimmers they advertise for use on facial hair. It works OK but with the LE, I never go without sleeves so it doesn't matter all that much anymore.
Anything you can do to avoid getting LE is well worth it. -
Any advice on the following question would be appreciated. I have skin tags in my armpits that I want to get removed. One is on the side that I had 20 lymph nodes removed. I think they usually freeze them off or remove with scalpel. I don't have LE but am afraid of getting it.
Thanks for you replies. -
Hi, Annie,
You might want to talk to your doctor about a prophylactic antibiotic Rx for the procedure, as infection is more likely in an area where the lymph system has been compromised, and any infection is very likely to lead to lymphedema. Do scrupulous wound care following, and watch it carefully for any signs of infection (redness, heat, swelling, pain) so you can act quickly to treat it. Also, don't use heat for treating any discomfort, as heat can also encourage lymphedema.
Hope it goes well!
Binney -
Thanks for the advice Binney. I will talk to my dr about the proph. rx
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FYI, my daughter is in cosmotology school currently and since I her mom developed LE she has researched and discovered that people with LE should not wax armpits or wear acrylic or fiberglass nails because of what they do to the nailbed for bonding, it breaks the surface integrity leaving opportunity for infection, ie bacteria to get in there. I also wouldn't wax the groin area for example, my right arm is where LE is so that set of nodes is not working properly so I need to rely on the area in groin to let that fluid out that gets brushed down. Its more work, but what is our health worth, if it wasn't worth it, we would not be such warriors on this subject.
love and light, sherry -
Hi Binney,
A couple of questions for you. :-)
After my mastectomy and removal of 14 nodes on April 11th, my surgeon mentioned that if I got a cut or scrape on the affected side, I should go to the ER. I wondered after I got home if he meant to go immediately or can I watch it closely and use an antibiotic ointment. (What would they do for a new cut in the ER, I wonder.)
I am gardening and try to remember to wear gloves, however yesterday I did get a thorn in one finger and that worried me a little. I guess what I REALLY want to know is: do the remaining nodes handle some inflammation and mild infections?
Has anyone experienced minor cuts etc. without problems?
Such a steep learning curve we find ourselves on and it never seems to end!!
Thanks anyone for some information~~
Speth -
Sherry, I am interested in your comment about relying on the nodes in your groin.
A friend of mine says she massages the glands in her groin when she has a bath and she believes very strongly that it increses the lymph drainage throughout her body?
Is this what you meant?
Thanks :-)
Speth -
I did a very stupid thing not all that long ago. I grabbed a pan of boiling water accidentally spilled it and got a pretty good burn on my hand on the mast side. I was so worried. I don't know if i was lucky just that one time or not as nothing happened. I try to be carefull but sometimes forget.
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Hi, Speth, and welcome,
I think what your doctor meant was to watch it closely and to get to the ER or Critical Care at the first sign of infection. Some of us with LE carry antibiotic ointment with us, and that might make sense for anyone at risk for LE too. Even a paper cut is a potential problem. (Once we have LE, though, we also keep a Rx or a bottle of oral antibiotics on hand.)
Of course many women post bc cut, nick, burn, or even break their affected arms without developing LE. There has not been enough research to determine what any one person's risk factors for LE might be, so you sometimes see women who take no particular precautions and never have problems, and others who are careful but still run into difficulties. As Rhymeee suggests, a single incident of injury to an at-risk arm does not necessarily result in LE disaster. Unfortunately, that is one reason why so many women ignore precautions. But any number of near-misses do not in any way protect us from later developing LE. It can happen at any point for the rest of our lives after bc treatment. It is a very strange condition, and there just isn't enough known about it. The prevention guidelines at www.lymphnet.org are fairly simple ways to protect yourself from the most common "triggers," so that's one way to take an active role in protecting yourself.
Here are some of the questions that researchers are posing about LE risk: Is there a genetic link that makes some people more susceptible than others? Is the dominant hand/arm at higher risk than the other? Does a woman's physical condition before LE make a difference? Can arm-strengthening exercises after treatment help prevent LE? Can LE massage following bc treatment prevent LE from developing?
I hope we get better answers soon!
Binney -
Great informative reply Binney! Thank you.
I have been reading all the web sites recommended by you and others and I do think I have a better understanding of the risks,etc.
The one thing I can't seem to get an answer to is this:
Is the other arm,(non-surgical side) at risk for lymphedema as well as the mastectomy side? Please tell me I don't have to baby that arm as well!
Binney, I have a feeling you should have the title "Lymphedema Expert" ---- I have read all your posts and responses on the subject. Good job!
Rhymeee, we better get you some heavy duty elbow high oven mitts! You be careful.
Thanks again,
Speth -
Okay, Speth, happy to oblige: you don't have to baby the other arm! In fact, if your affected arm is your dominant arm, you might want to challenge yourself to use your non-dominant arm more than you did before.
Where the lymph system is concerned, our bodies are divided into quadrants, kind of like chicken quarters. The quarters divide at the waist and straight down our center line. The only quadrant at risk is the one that was treated with surgery and/or rads. Our "wing" quarters drain into the nodes under our arms, our leg sections into the two sides at our groin. So the one wing quarter where you had surgery is the only one at risk. All unaffected quadrants will just keep on draining happily. Yes!
Binney -
Thanks so much for your quick and helpful replies.
Operative site is on my left and I am right handed. ( Good thing, I guess,)
All the best~
Speth -
Why do you say to use your affected arm less? Is it to decrease the risk of cuts leading to infection, or does just the movement of the arm increase risk? I would have thought that movement would be a good thing.
I'm so terrified of getting this. I asked my doc how many nodes he removed, but I didn't get an answer. He said something about them being in some sort of a cluster and you can't really tell exactly how many? I didn't really understand. I think I should call the drs. office and ask them again. Surely it's documented somewhere? It would help my comfort level if I knew how many. -
Hi, jbc,
I'm sorry I left that confused impression. Yes, you're right that movement is a very good thing. What I meant (and should have said more clearly) is that things like jerking suitcases off luggage carousels or hefting heavy loads up into cupboards, or even hard, repeitive things like vacuuming would be better done with an unaffected arm. Movement that strains or stresses the affected arm can be damaging. But building strength, flexibility and range of motion are helpful and can be done slowly and gently.
I sure do understand your concern about developing LE, and it's really wise to be aware of ways you can protect yourself, but I really hope you won't live in fear of this. It's not worth wasting good and satisfying days worrying about something that may never happen. And even if it does, there's help for it, so please don't be afraid of it.
All best,
Binney -
Thanks for the clarification and the advice. Your posts are all very helpful.
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I am still a little confused (sometimes doesn't take much !!) over the lymphedema risks and how much is required of us to prevent it from happening.
Benny, it makes so much sense to always use the non-affected arm to lift heavier objects, grab overhead luggage etc. BUT, what does a person do if they have had a bilateral?
I have read all the interesting posts here and am shocked to find out that a prophylactic mastectomy will put both arms at risk. ( For the first time, I am now second guessing my choice to have, what I call, my good breast removed. Wish I knew what to do as I meet with my surgeon today for 6 week check-up and was going to tell him my decision.)
Would you say there is less risk on the side where there was no underarm node removal...or are both arms at equal risk?
One more thought: I am someone who seems to always develop small infections after abrasions and scratches and am very allergic to wasp stings with immediate cellulitis following any sting. Maybe because of this I am becoming a little paranoid.
Back to my thought, lol---
I find it interesting that so few ladies mention any infections following the procedures such as the injection for the dye prior to SNB, the wire placement for tumor localization, the node dissection incision, the lumpectomy or mastectomy incision, often a later injection for fluid removal etc. I realize the instruments are sterilized but there are still tiny openings left for invasion of bacteria. Is it just luck, or are those compromised nodes still able to handle things in a reduced way?
Sorry to make this so long. I had a bad night dreamimg about lymphedema and the risks/rewards of a prophylactic mastectomy. Goodness, I don't have either as yet so aren't I a mess??
Thanks for listening and any answers to my "way-out-there" questions are so much appreciated.
Speth -
Speth, LE is NOTHING like cancer. It is not nice, true. But it is not going to cost you your life. No contest.
Being bilateral is a bit trickier to handle, but not impossible, and I don't regret my decision to have a prophylactic mastectomy at all. In my case it's a tremendous relief and safe-guard. My path uncovered some LCIS in the "unaffected" breast, and my onc did a happy little jig that we'd made the decision to remove it. He likes happy outcomes a lot. I use both hands together to lift especially heavy items, don't lift them at all if they're too much for me, and am actively engaged in arm-strengthening exercises, working my way up sloooowly. I already have LE, obviously, so I always wear gloves and sleeves, but you can be fitted for sleeves and gloves to wear prophylactically when you're going to be doing something unusually stressful for your arms (or traveling by air). You might also want to see a LE therapist for base-line measurements so you'll have something to check later on, and for prevention education. Your tendency to develop infections easily just means you'll want to act quickly whenever something happens that could result in infection. I carry antibiotic cream with me and use it promptly for anything suspicious.
Even with sterile instruments, you're right that infection does happen following the procedures you mention, especially aspiration of fluid post-surgery. The compromised lymph system is definitely able to handle things in a reduced manner, or else every one of us would develop LE directly. Unfortunately, nobody knows enough about all the factors involved to make accurate predictions about who will or will not have problems, but there is research evidence that fewer nodes taken reduces the risk in a general way, so a prophylactic is less likely to cause problems than one with multiple nodes removed. Other factors that up the risk are diabetes and overweight, but those aren't guarantees either.
Don't be afriad, Speth. Do what you need to to beat the bc, and then expect only the best to follow. You're not alone!
Binney -
Speth, my comment about relying on the groin lymph nodes for draining is because my armpit or axillary nodes are compromised so its important to open the groin nodes on that same side. Your friend is correct in her opinion. Hope this clears things up. Sherry
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Just curious as how ladies are managing underarm hair. I have always waxed. Is laser an option?
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Laser is pretty risky in this area after surgery.
Some of us have very little underarm hair to worry about following treatment
, others use shavers of various kinds. There's a section on this page about some shaver alternatives:
http://www.stepup-speakout.org/How_You_Can_Cope_with_Lymphedema.htm
You need to be really careful shaving. Do it while your skin is warm from a shower, use a good shaving cream or soap, and use a mirror, especially if the area is numb from surgery. Of course try your darnedest to avoid nicks, but if you get a nick or scratch treat it promptly with antibiotic cream and keep a close eye on it for redness, swelling or other signs of infection. Clean your shaver on the super-hot cycle in your dishwasher between uses.
Hope some of that helps. Be well!
Bonnie -
I'm glad I read this subject--I have LE--both arms so they can't be used for anything (BP.Blood draws--whatever) But that must be why my scratches never heal right. my legs swell also and I have forever scratch marks on them. I really didn't ask why My Dr. told me to watch them, my fault never asked. I never got an infection and as far as shaving--I don't need to but a little every so often, but your right, both arms are totally numb so I do watch charefully, Thank u for all the info
.
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Babysammy - I had a bmx and I use a razor, but as Binney said, (and YES, she is the expert!!!!!
) I am very careful when I do it. I tried the electric razor and hated it.
Since I had a bmx, I'm very careful with both arms, but do get blood taken from the left. My right has LE. I talked with my LE therapist and it's just not worth it for me to get blood draws/ivs from the foot and my onco. uses the wrist blood pressure cuff.
Having LE in the wake of BC is just a big drag but it has gotten easier. I don't think about it that much anymore other than the occasional 'oh, crap' moments that come up (hello, cellulitis).
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thanks for the info.
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