What causes your LE flares?

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carol57
carol57 Member Posts: 3,567
edited June 2014 in Lymphedema
What causes your LE flares?
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  • carol57
    carol57 Member Posts: 3,567
    edited November 2011

    I've been trying to figure out LE swelling cause and effect (I'm new to LE).  It would be so helpful if everyone posts their most common flare triggers, which would give me some good ideas of what to watch for.  Now when I have swelling, I'm not sure if it was triggered by something I just did, or something I did several hours ago. Or could it possibly be something I ate or drank...recently or some hours ago?  Maybe my swelling was triggered by something obvious, or maybe not so obvious--not sure I would know!  So...what triggers your flares, and how how much time usually passes between trigger and flare?

    Thanks so much!  Everyone here is incredibly helpful!

    Carol

  • NatsFan
    NatsFan Member Posts: 3,745
    edited November 2011

    I have Stage I LE so I'm lucky.  For me, arm flares are rare and I can trace them to some carelessness on my part, like overdoing it and not wearing compression.  I'm still trying to figure out my truncal flares, but these are my prime suspects so far:

    • Salty meals, especially if I indulge on 2 consecutive days (Mexican and Chinese food are my downfalls)
    • Lack of hard aerobic exercise for a few days
    • Failure to do Lebeds for a few days
    • Failure to do MLD  for a few days


    It seems I can get away with these things once, but not two or three times in a row.  Or I can get away with it if I only allow one of these things to happen, but if I allow 2 or more of them to happen at the same time, I tend to flare.

    I'm still experimenting with other suspects, like certain bras, not wearing my UnderArmor for compression for some period of time, etc.  But the 4 above I've pretty much figured out are my main "bad guys". 

  • BeckySharp
    BeckySharp Member Posts: 935
    edited November 2011

    I have not yet had a flare.  Mine has been under control since July.  I just got LE in March.  I am having a lot of trouble with cording but it has not yet affected my arm or trunk dimensions.  I have religiously followed all that my therapist has told me to do.  I don't skip anything.  I do not eat salty food.  I have also lost 42 lbs since surgery in Feb and she said weight loss will help tremendously.  I do an hour or two of aerobic daily.  I also do Lebed daily and MLD twice daily.  I only take off my sleeve for showering and MLD.  I wear a night sleeve. 

    From all I have read here each person probably has different triggers. 

    Becky

  • kira66715
    kira66715 Member Posts: 4,681
    edited November 2011

    Becky, may I just say that you're amazing: so compliant and the 42 lb weight loss is great. I'm feeling guilty as I read your post.

    Early on, I was more compliant--but have started to skip some of the MLD at times, but always wrap at night.

    Carol: my flares have been caused by increased activity--I swelled when I started a new job in 2009 that involved a lot of writing, heat, flying, not being hydrated enough, and early in the the course of my LE there was this sense of horror as new swelling just appeared no no reason--in my finger, my palm.

    It's been a year since I broke my LE hand: and the cast did me no favors. But it's much, much better now.

    I still get the occasional cord--had one two weeks ago--I emailed Jodi Winocour in disgust, but some stretches and skin lifting and it's better.

    Oh, and hormones--still perimenopausal.

    Totally agree with everything Mary wrote (as always)--aerobic exercise is so good for LE. 

    Kira 

  • carol57
    carol57 Member Posts: 3,567
    edited November 2011

    Wow, these are great (well, not so great cause they're making you swell, but you know what I mean). I'm trying to keep a journal to figure this out. Thanks for suggesting some additional items to make note of. Becky, wish I could shake those pounds! One hour of aerobics is my normal routine unless traveling for business, but it still doesn't help me drop the weight. Sigh. Could lose 20 for sure. Only thing that makes me wish for my 40's again--used to be able to lose!

  • vlnrph
    vlnrph Member Posts: 1,632
    edited November 2011

    I am blaming Beethoven for my LE: the final movement of the 5th Symphony to be exact. My first orchestra rehearsal since the surgeries and there it was a few days later (I'm a violinist - using the bow arm under tension seemed to be the trigger because light, gentle playing during the summer was no problem).

    Yard work that same week did not help the situation. We will need to hire tree and shrub maintenance people in the future. 

  • Leah_S
    Leah_S Member Posts: 8,458
    edited November 2011

    Carol, I can't help since I had only one flare since I was dx with LE and I can't figure out what caused it. No change in diet, no change in activities, and it was at the end of the summer after the weather wasn't as hot as it had been.

    I suspect general trauma to your body can have an effect, also. After my mx I had numbness in the back of my upper arm for about 2 years. Then I had an ooph and noticed swelling and a feeling of "holding a pillow under my arm". I know my arm wasn't used during the surgery since I already had the IV and BP cuff on my unaffected arm before I was put under. After the surgery I started to feel it more & more so I think the combination of now feeling that arm and the trauma of surgery caused a flare that I was aware of.

    Hope all goes well for you with your tx.

    Leah

  • BeckySharp
    BeckySharp Member Posts: 935
    edited November 2011
    Hey I am just so compliant because you all have scared the heck out of me about flares.  I lost a lot of weight several years ago and gained some back.  I was so mad at myself.  Plus I read on the hormonal therapy section that I would gain weight on tamoxifen.  I was bummed out.  But I am losing weight much easier being on tamox than off.  The only good side effect I have had.  Laughing LE maintenance is very time consuming Carol.  Becky
  • sushanna1
    sushanna1 Member Posts: 764
    edited November 2011

    My lymphedema is in my right hand.  (Needless to say, I am right-handed.) Had one serious flare 6 years ago--painted part of an apartment in hot, humid weather. The lymphedema has been under control since 2006 to the point I don't have to wear a glove and sleeve every day.  However, humidity seems to aggravate it.  That, and packing.  I try to spread out packing and put my suitcase on the bed instead of the floor.    

  • kira66715
    kira66715 Member Posts: 4,681
    edited November 2011

    Leah: there's a lot of research on LE and inflammation--so it makes complete sense that any inflammation/trauma/illness can cause a flare.

    Becky: it really helps to hear how compliant you are--I let the second MLD slide, but I was right in there with you for the first two years. My LE therapist says that when we get good control, then we experiment with what we can get away with.I think I just pooped out a bit. She thinks I'm the most compliant person in the world, but you are much better than me. I wish I did an hour of exercise a day, and could lose the pesky weight that has crept up on me.

    Sushanna--my LE is in my left, dominant hand. Saw my ob/gyn yesterday, and she's one of the few doctors in my "treatment group" who actually examines my hand carefully and can see that darn residual puff in the web space between the first and second fingers. Repetitive motion is such a trigger: we got a new ceramic cooktop and I have to be careful with the cleaning of it.

    Kira 

  • NatsFan
    NatsFan Member Posts: 3,745
    edited November 2011

    Kira - your LE therapist sounds very wise about our "experimentation" - when I read that I realized that's exactly what I've been doing lately.  I guess we'd all like to figure out the minimum amount we have to do to maintain, but we don't want to go to far.  I guess it's all part of the learning process.   

    Geez, when I was younger, "experimentation" had a whole 'nother meaning and was a lot more fun!! Cool

  • olearca
    olearca Member Posts: 215
    edited November 2011

    Wow, great thread. Carol, I'm new to this also and have been trying to figure out what makes the swelling more or less. I've not had a true flare yet, but I do notice lack of hydration (I'm really bad at drinking enough especially when the weather is cooler), salty food (Asian especially, drats) and not doing MLD religiously. I still can't tell if the daily sleeve helps or not. And I get truncal which was definitely exacerbated by TEs and now by various shelf camis, or surg bra. I have yet to find a bra that supports my implants but doesn't cause swelling. I'm continuing to experiment.



    Mary and Kira, good to hear that you both think aerobic exercise helps. I can't wait to get back to it.



    Becky, you are inspiring me to be more diligent. Way to go on the weight loss.

  • Binney4
    Binney4 Member Posts: 8,609
    edited November 2011

    Becky, you are an inspiration -- thank you! Back to the daily Lebed for me!

    My lymphedema is really affected by barometric changes. But I also have trouble when I don't get enough sleep. The barometric pressure thing makes physiologic sense, but I have no idea why sleep should affect it. I just know when I don't sleep enough I have to spend extra time doing Lebed, clearing nodes, and wearing extra compression.Frown As if losing sleep didn't make me grumpy enough!

    Yes to experimenting!Cool But there are parameters. First, we need to have the "tools" to fix any problems that may develop (like knowing how to wrap, self-MLD, having the compression garments and aids we need). Then we need to be in GOOD control before we try anything, and we need to try only one thing at a time -- like the good scientists we've all had to become to treat this stupid LE.Kiss 

    Be well!
    Binney

  • Cori221
    Cori221 Member Posts: 21
    edited November 2011

    Interesting discussion. I was diagnosed with LE in July of 2010.  At that time my arm was 10.2% (with the overall measurements and computer calculations they do) than my non LE arm. After 2 days of wrapping by the LE therapist my arm was down to 2%.  My therapist taught me how to do self massage, taught my daughter how to bandage and take measurements, and had me fitted with a daytime compression sleeve and glove. My daughter took measurements weekly and over the next nine months my measurements went down and then stayed pretty steady.  I was faithful about doing my daily massage and wearing my garments and taking the general precautions we are taught.  Starting in May my measurements started slowly going up with most of the swelling in my forearm. It was before it got hot, I don't know of anything I did differently , it just started swelling and getting hard. I was in touch with the therapist and tried massage twice a day.  My daughter bandaged a couple of times but we didn't see much progress.  I went back to therapy and was now 18% larger, it took two weeks of bandaging to get the measurements down to 6% and I now wear a night sleeve nightly adding extra compression (the jacket over the Solarius Tribute ) twice a week and bandaging twice a month. My therapist is hoping that these steps will help maintain or even decrease the swelling.

    What I learned from this last experience is that I can't always control what happens with my LE.  I can do everything possible to prevent flares and I admire all of you who have really disciplined yourselves with exercise and diet and other precautions. I have a number of tools that my therapist has armed me with and a game plan that we can keep modifying if necessary. My therapist doesn't know why I may have flared.  She has said in her experience it just can happen.Everyone is different and experiences this disease so differently. I guess for me since it is a life long chronic condition the sense of control comes from knowing that I have the support I need to manage this awful disease.  I may not be able to prevent flares but I have confidence that I will be able to manage them and find a new normal as I had to do recently.  I feel very blessed to have a wonderful daughter who helps with measuring, bandaging and giving me moral support, a therapist who is very skilled, empathetic, and makes herself very available, insurance that pays part of the cost for the things I need and this wonderful discussion forum where I gain so much knowledge, support and inspiration.

    Thank you all for sharing. It helps make living with this double whammy  of breast cancer and LE possible.

    Best wishes to all,

    Cori

  • Springtime
    Springtime Member Posts: 5,355
    edited November 2011

    I have one trigger, inversions. Going upside down. Yoga: shoulder stands, down dogs. Anything that dumps the blood upwards. I wear compression top (under armour) and sleeve - I have breast / tructal LE. When I lift weights or do aerobic activity, I wear these things but I never get a flair from those activities. I still get a flare from inversions, no matter what I do!!!! 

    I miss doing inversions in yoga. I sometimes try them agian, but I pay for it.. :((( 

  • carol57
    carol57 Member Posts: 3,567
    edited November 2011

    The rhyme/reason factor in LE surely is not obvious!  The last few weeks, I was SURE that flying (even wearing a compression shirt) had caused the swelling on my side, under my SNB arm. Yesterday I got home from another trip--four flights in two days--and no unusual swelling during the trip, nor last night nor this morning.  Go figure.

    Thanks to everyone for sharing all the cause/effect.

    Carol

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2011

    kira, I have to jump in now without reading all the posts!! Cleaning your smooth top stove should be easy. I am an appliance expert and the first thing I tell people when they buy a smooth top is how to clean it. Your old pots have crud on the bottom that cannot be scrubbed off. BUT when you put them on the glass of a smooth top - they transfer to the glass!!! They are very hard to clean off, but once gone off your pots you shouldn't have that problem again. Solution? Buy new pots when you buy the new stove.

    Many people think the white creamy cleaner is to clean off that crud. It isn't!! It's like wax for a car AFTER the car is clean. It is just a film that makes it easier to clean your stovetop later. First you have to get your stovetop clean.

    The stovetop is just glass. That's it! The more expensive models have the imprint of the burner UNDER the glass and they come with a fancy razor to scrape the crud off the glass when it happens. Most models have the imprint on the top so using a razor will scrape them off.

    What you should use is the green scrubbies that you find in Walmart or your local grocery store. Or, if you have $$$$, buy the Vileda ones that are two coloured. When a pot boils over it leaves crud. If you let it dry it hardens. When you are doing your clean-up use your dishcloth to wipe your stove. Something is left there? Squeeze your dishtop on the crud and turn the burner to low. Come back and scrape the crud with a plastic spatula and wipe it all clean. Turn the burner off and ta da!!!

    It is REALLY easy to keep a smooth top stove clean. MUCH easier than a coil burner with the aluminum food/grease traps. Let me know how it goes. Do NOT let the stove top intimidate you!!

    As for LE triggers, I have truncal LE so I avoid:

    lugging or holding something heavy (purse, luggage (is lugging why they call it luggage?) groceries and grandchildren) I use my non-LE side

    humidity affects me and there's not too much I can do but up my MLD (which I do not perform religiously anyway, but DO have my DH do my back which I can't reach)

    I don't even have a salt shaker in my house and haven't for over 20 years (high blood pressure) but do notice that if I have pizza or something I do retain fluid (even on a diuretic!!!)

    I don't elevate my arms as that drains to my torso, I guess you have to know where your LE originates to know the positions to avoid

    Good luck, sweetie!

  • sushanna1
    sushanna1 Member Posts: 764
    edited November 2011

    Kira--Funny that you should mention ceramic stove tops.  I started to clean my friend's and half way through realized that it was a really bad idea.

    Barbe--Thanks for the tips re: ceramic stove tops.  I had no idea! 

  • lionessdoe
    lionessdoe Member Posts: 780
    edited November 2011

    We took a poll on this once before. I think Binney was collecting the examples for some researcher. The answers were great. But I can't find it now.

    Reaching

    Pushing

    Pulling

    Carrying

    Anything repetitive (even if it's just my hand)

    The weather, the weather, the weather

    Sleeping the wrong way (sometimes it's just out of my control)

    Being outside when it's too hot and the same when it's too cold. Humidity .......... GEEZ I just stay in cotrolled environments. There are days I am still using AC in the Fall, just to get the humidity out!

    The worst is when I'm having a 'good day', seems I still want to just act normal and end up paying for it later!

    Oh and Doctors who want to deny you even have it because they examine and measure you during the day. I would just love to see a parade of lymphedemers get measured around 9- 10 PM! No diagnosis = no script for massage! No early intervention, which is crucial for management, control, and prevention of a later stage.

    Best thing I discovered this past summer are those anti-mosquito whirly fans that you clip on to your clothing. I spent twice as much time outside last summer because of them! Great invention! They really worked for me! I love summer! :-)

  • Suzybelle
    Suzybelle Member Posts: 920
    edited November 2011

    RE: Ceramic stovetop - I have the best way to clean mine - can't remember where I read this, but it really works.  Just sprinkle baking soda on it, spray some white vinegar (it will bubble) and let it sit a few minutes.  Then wipe off with a damp towel.  It WORKS.  And you don't run the risk of scratching the glass or flaring your LE arm.  Cool

    Things that make me flare -

    Flying without being wrapped in bandages.

    Not bandaging twice a week.

    And I hate bandaging.  Yell

    Going without my nightsleeve (solaris tribute) for more than 2 days a week.

    Not walking at least 5 days a week.

    Salty food.

    Repetitive motion - like playing the guitar for more than an hour.  Yellor working on the computer for more than 3-4 hours, which is what I get paid to do.  YellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYellYell

    Putting lots of weight on the arm/lifting too much weight.

    That's all I can think of now...I hate flares.  YellYellYellYellYellYellYellYellYell

    I really love that mad little man.  He is sooo cute.

  • Nordy
    Nordy Member Posts: 2,106
    edited November 2011

    I LOVE the tips on cleaning a ceramic stove top! Now... if I ever own a ceramic stove top again, I know where to go to remember how to clean one! (We have a gas stove... I need tips for that one - Barbe???)

    Flares:

    Going without my sleeve, hot weather, hot humid weather, zumba (still do it - just pay), step class,  not drinking enough water, hot baths, wrapping too tightly, sometimes cycling - sometimes not... Actually - sometimes there seems to be no rhyme or reason to why my arm does what it does... sometimes I think it has a mind of its own... 

  • carol57
    carol57 Member Posts: 3,567
    edited November 2011

    I guess we can say that what is predictable here is that cause/effect is not predictable.  I have been so hopeful of figuring out what to avoid so my very early LE stays that way. The growing list of what causes trouble is not encouraging, because much of this is simply not avoidable. I guess it's better to know than not!

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2011

    Carol, I guess it's like trying to figure out what gave us bc in the first place! Just a crap shoot.

    Suzy, great tip on the baking soda!! Nordy, I'd run with that one. I did it years ago and have totally forgotten about it!! Vinegar alone is an amzing cleaner as well. When you switch out a faucet there is horrid crud left on the sink. Pour vinegar on it and it cleans it right up. Also leaves a good smell as the vinegar breaks down nicely.

  • kira66715
    kira66715 Member Posts: 4,681
    edited November 2011

    Barbe, the woman who cleans my house pretty much only uses vinegar, and the previous woman used all the smelly cleaners, and wondered why her asthma was always acting up. The house feels so much better after the vinegar cleaning...

    Back to flares: there are obvious precipitants and the ones that come out of the blue when you're doing everything right. Those are the ones that are REALLY frustrating.

    I once went to a meditation workshop and had to sit on a mat for hours and clasped my hands around my knees, as I actually didn't find that sitting comfortable, and came home with pitting edema on the inside of my wrist. Didn't do wonders for my mental state....

    Kira 

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2011

    Kira, was that for Mindfulness Meditation? I'm taking that course and we had a 6 hour class one day on a classroom floor! I got permission to bring my DH as he had to help me up and down. It's not a pretty sight when I have to get on my knees to get helped up...sigh. I lay flat with a pillow under my knees for most of it and took a lot of extra pain meds.

  • kira66715
    kira66715 Member Posts: 4,681
    edited November 2011

    Barbe, it was for a contemplative studies course, and it was a special instructor who taught on the west coast and did a 7-8 hour meditation session, and it was focused on expectations and forgiveness. I went with a colleague who is a psychologist and was very involved in the contemplative studies department.

    But, the room was full of undergraduates, and these mats and little butt pillows, and I found the sitting very, very uncomfortable. Some people sat in chairs, and I should have joined them.

    Jon Kabat-Zin who started the Mindfulness Meditation for medical patients at U Mass has a fellowship program, and I called them, and they said they required a regular practice of meditation and having done a 7 day silent retreat, before you could even apply to be trained in the program.

    I liked his books and heard him talk, but that was too much for me.

    Kira 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2011

    Unfortunately, I have to concur with ALL of the things everyone has listed. They have caused flares for me at one time or another, usually within an hour or two. Heat, humidity and not drinking enough water are my main culprits.



    Two other things that definitely cause a flare are stress or alcohol. Alcohol two or more days in a row affects me, even when I drink lots of water to compensate. It messes with my sleep cycle and quality of sleep, so that may be why. As far as stress goes, an argument with my husband will often set me off. I try and remember to breathe, but there is something about the tension my body holds that is a trigger. I try and do Lebed or deep breathing after to remedy. Going back to the lack of sleep, that also effects my ability to deal as well with stressful situations, so I think sometimes a flare can often be a culmination of things that occur throughout a day.



    Today. Me. My oncologist. 3 1/2 yrs cancer free! Yippee!! Don't have to show my face for another year.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2011

    Oh! I forgot to ask you guys a question. In my ongoing quest for a wardrobe that supports going form free, I have become obsessed with skinny legged jeans and boots. I have gained a few pounds (around the middle, naturally) which has caused my clothes to be a smidge tighter than I'd like. I'm working on shedding but was just away on vacation and let things slide. Anyhow, my question is: Could a muffin top limit lymphatic flow and set you up for a possible flare? Please say no!

  • carol57
    carol57 Member Posts: 3,567
    edited November 2011

    OMG Tina, that muffin-top question has to be the most critical one I've ever read on the forum!  I cannot wait to hear everyone's perspective on that one!  My LE therapist has a drawing of a person in very tight panties, with a big X on the photo--I suspect wearing tight enough clothing to  mush that muffin up there causes the same kind of effect.  You have given me a whole new wardrobe worry...

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2011

    I would think that JEANS would be way worse than leggings!!! That's MY story and I'm sticking to it!

    Kira, our medical care pays for the course it's so respected up here!! I am enjoying it very much as I took the Hoffman Quadrinity Program about 20 years ago and find the thinking very similar.

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