Weight Training Post Lymph Node Removal
Ladies...guidance required. I had a lumpectomy with lymph node removal Nov 2008, finished chemo mid Feb and rads the end of Apr 2009. While I started back with walking and slow running, I really want to get back to my weight training. What I want to avoid is potentially developing lymphedema. Does anyone know if I need to restrict the amount of weight I use, reps, etc? Any advice?
Comments
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PurpleMe: I've been doing it, and I have had difficulty with mild LE. Weight limits, reps etc are good questions. Unfortunately, what I have found is that every LE therapist, website, etc has a different opinion and the literature is scant. Actually, good literature on lymphedema is scant, information on getting truly active women back to doing what they want to do even more scant. Opinions abound, good research scarce. The good news is, most recent info seems to agree that if you've already been active and lifting you should be able to get back to it. Less clear if those that never lifted will be able to heavy lift.
So, I can only tell you what I decided, when I realized how little guidance there was. I started with low weights, (e.g. 5 lbs when it used to be 25) and 2 sets of 8 reps. I then went up a couple of reps in each set each time I lifted. When I get up to 18 reps and I'm not having any swelling, I go up on the weight and start down at 8 reps in each set again. As far as going up on the weight, it has depended on what I was doing. 2.5 on things like biceps or delts, closer to 7-10 on pull downs. I also only go up on weight on one "station" a day.
I just watch closely, if I get arm tingling, heaviness, etc. some of those symptoms they now think may be early signs, I back down again. I've just tried to take it slow and easy and be happy I was lifting. It can be very frustrating. I do have a sleeve, but as I said I have had some mild LE that did get better and I'm trying to keep from worsening. There was just a lot of back and forth on another thread about the wisdom of wearing a sleeve to prevent LE developing if you haven't had it. Can't remember the thread.
Good luck, do me a favor and let me know how you do and what works for you.
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Purple, I second what kmmd said about le and activity. I did not lift weights before I was dx with bc, but I did climb regularly. I was able to resume climbing after I had a mx, despite mild le. I started slowly, wearing a sleeve and a compression shirt. When I got measured after I started climbing again, both arms went down in size.
I think being systematic about resuming an activity is key. As kmmd describes, watch how your body reponds and let that be your guide.
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I wondered the same thing....a fellow bc sister and I have the same onc and they work out at the same gym...anyway she asked our onc about lifting weights, and was told anything 10 lbs are lower is fine.
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Kari, exactly what I was mentioning. You are so right, the contradictory advise is amazing. I've always assumed that only a doc who has never lifted could give that advice with a straight face.
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I had a bilateral mast with reconstruction and chest wall patch( had to have patch cause they could not stretch it ) had 6 nodes removed and have finally worked up to my pre-surgery weights I am not a weight lifter but am pretty strong. It has been 2 years, so it was a slow process I took it easy.
Heard that swimming is good to encourage proper lymph drainage too..
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kmmd, lisa-e, kfinnigan, trigeek thank you all so much for your replys.
kmmd, you are so right about all of the conflicting and practically non-existing information. Perhaps it's time the medical community did a properly controlled study to see if they can come up with a difinitive answer. Then again maybe I am wishing in technicolour...LOL
I will definitely start slow with the weights and see how it goes. I will post how things are going, what weight, exercises etc I am doing.
Thanks again...must say that this site has been so helpful through this entire process.
Love you all ladies,
Carol
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IvoryMom, would you mind popping in now and then and let us know how it is going? For all of the info out there about how important exercise is for breast cancer patients, I have to say, good information, not dogma or what happened to one patient, but good information about running/yoga etc. with TE's, running with implants, weight lifting and lymphedema etc is almost non-existent. It is all anectdotal and no way it is good or we wouldn't have so many different answers depending on who our doc is. Came across something about never doing downward dog pose in yoga because its bad for LE. Can not see any anatomic or physiologic reason that is worse then heavy weights, which obviously some are doing.
So, we're really dependent on each other for information when it comes to getting back to what we did before.
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ivorymom...great info. Thanks, this really does help.
kmmd: I also do yoga once a week and downward dog is one of my favorite poses LOL.
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Awesome ivorymom...this makes me very happy! I love doing weights
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Thanks IvoryMom. Sad the largest study was of 45 women, but great to have one
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Actually that study was preliminary and the results of the more extensive study that grew from it have just been published this year--more study subjects for this one. You can read the abstract here:
http://www.journals.elsevierhealth.com/periodicals/concli/article/PIIS1551714409000020/abstract
The safe practices y'all have already mentioned are important in this study as well -- progressing slowly; stopping and elevating your arm when you sense achiness, tiingling, heaviness or just "odd" feelings. It can be especially helpful for your future well-being to insist on a referral for an evaluation by a fully-trained lymphedema therapist, who can do baseline arm measurements for future reference, teach you a gentle prophylactic lymph massage, give you personalized risk reduction tips, and fit you for compression garments to use prophylactically.
Downward dog adds a dimension of gravity to the weight issue that can flood and overwhelm a compromised lymph system. Your call, of course, but there is a good deal of anecdotal evidence about that one. (Naturally it would be everybody's favorite!
)
Be well,
Binney -
KM,
I row in a crew boat.. and carry that beast with 7 other people from the boathouse and it almost crushes me but the arm is ok.
I have been doing downward dogs and actually for the first time was able to do low planks !!! with no problem. Bridge pose was mentally challenging but happened after a couple of tries.
Sculling was one of my favorite pastimes.. I can do that too with no problem.
No power loss in my erg workouts I could still pull 1000 pieces at 2:15 as I did before.
Just winged a half ironman at 8.5 hours..
So all is good.. but like I said it has been 2 years.
Come to think of it I think the reconstruction messed me more than the lymph removal as I had to rebuild the chest muscle that had been dissected and patched up with a graft. There is a cosmetic defect which the PS wants to fix but I really do not want to go through the whole recovery process again..
Basically if you were moving before s!@#$ hit the fan.. continue chugging along
but do listen to your bodies signals diligently.
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Thanks Binney4 and trigeek. I was absolutely moving before the s*** hit the fan - running, weights, yoga. Binney4 - good suggestion about a referral to a lymphedema therapist.
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Hey gang...started the weights about a week ago..5 lbs for my shoulder workout, bicep/tricep work out, chest and lats. Doing 2 sets of 8 reps, Mon/Wed/Fri. Am keeping a close eye on the how surgery side feels and so far so good. Continue to build up my running.
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Awesome, I've been able to go up on the weights too. Being careful, but recovering from that last surgery and now being able to do things without having the next phase of treatment hanging over my head makes me feel so good, I keep wanting to do more
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Hello everyone - this is a really useful thread. I am going in for surgery on 17 June, and to date this is the most useful thread I have found for those of us into weight training.
I am very interested in the rowing possibilities; a good friend of mine coaches well known teams and I hadthought about doing a bit of rowing before I got diagnosed on May 9th.
I will post any info I come across regardingvarious exercises.
Does anyone know if it would be ok to use a Powerplate at all?
good to meet you all and much love for continued good progress -
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Hey London, I used to scull before !@#$ hit the fan now I have bumped it up and am rowing in an 8 ( will be racing in the women's 4 in sunshine states this weekend I am sooo psyched !!)
There also might be dragon boating possibilities ... I will be doing that too they are in the process of getting one up and running here in Orlando ! Dang the problem with bc diagnosis is one tries to squeeze in soo many activities once over the hump it is a bit hard to work !! hehe..
Let me know if you have any questions on rowing I had heard that Harvard did a study on bc patients who had surgery rowing and the studies were very promising did not lead to lymphedema.
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Thanks for this thread girls. I got the go ahead for weights in moderation from my oncologist today. Michele Obama arms here I come;)
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I recently joined a gym. My trainer tells me I shouldn't do any of the resistance machine with weights that work on the pectoralis major because it will tighten the muscle too much over my implant from my reconstruction. Has anyone else heard of this? I'm doing other things for my triceps and biceps.
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becky1955, I've been training my pecs all along before this, after TE, and now after the exchange. My PS mentioned I had huge pec muscles when she did the exchange, but was fine with all the lifting and what it did to the muscles.
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Hi Gang..just wanted to report that I have upped my weights to 10 lbs - still keeping the reps low - 2 sets of 8 reps. Doing shoulder work, bicep, triceps, lats, chest and am doing some of the work on an exercise ball. So far so good!
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Upped my reps from 2 x 8 to 2 x 10, still using 10lbs for most exercises and 20lbs for things like bent over row, good morning, squats, etc. Unfortunately, I have had to put my running - okay more like slow jogging - on hold for a couple of weeks because I broke my toe the other day. Go figure. Wonder if the universe is telling me to slow down...LOL
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Hi ladies! I am so glad I found this thread. I am still going through chemo but am trying to work out as I feel up to it. I was so frustrated about the lack of info on weight training guidelines after surgery. I'm really not trying to build strentgh right now but your tips will be great once I'm cut loose from restrictions. My left side, surgery side, is so much weaker than the right that I'll just be happy to have it catch up at this point!
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Hi greytmom_17...first, it's to bad you are on this train (BC) however, glad you found this thread. I still find that my right side (my surgery side) is still weaker, however, it is getting stonger. Definitely start slowly when you are ready to start with the weights and really listen to your body. Best of luck with the chemo!
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Purple me - thanks for the well wishes. So far the chemo is going well. Very minimal side effects, mostly just fatigue, and within a few days I fell almost normal.
Question for the group - are you wearing a compression sleeve while working out? Where is the best place to get one? Thanks!
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Greytmom_17...good news on your chemo!
I plan to call my oncology nurse for recommendations on therapists who deal with lymphodema (which I don't have...hopefully won't develop it either). Hopefully some of our US sisters have more info. The other option would be to hop on over to one of the threads dealing with lymphodema and see if the ladies there have any info for you. Good luck!
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I had started out going to a specialist for a lymphodema sleeve - then (for a variety of reasons) decided to check out the local pharmacy - and I mean, one of the old-fashioned ones, not just another CVS or Rite-Aid. They had one with light compression for less than 1/2 of the specialist's price - and no fancy insurance claims - I just used my Flex Account.
Today was the first day that I used dumbbells outside of physical therapy, and I didn't even think about a sleeve until after the class was done. However, I used much lighter weights than I'd ever used before. No problems, so far!
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asedge...question for you...do you have lymphodema or did you get the sleeve to help prevent while doing weight workouts?
Plan to call my oncology nurse today to get a recommendation to a lymphodema specialist so I can find out about possible ways to prevent it from happening.
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PurpleMe -
My onc suggested I wear the sleeve when flying - I had a conference in Fla and a mini-vaca with friends in Colorado in the same 2-3 week period. Because each flight was more than an hour, he suggested that I wear the sleeve. He pointed out that it was easier to find out that I don't need it than to end up in a hospital away from home. . . participarly if my arm started sweling while I was on the side of a 12,000 foot mountain and 2 hours from a major hospital center.
I hadn't thought seriously about using the sleeve during exercise until this week when 1) I read this thread and 2) I started using dumbbells again.
My physical therapist and most of my docs suggested that I probably wouldn't need it just becuase I was lifting weights, since I'd been doing that regularly before the surgeries. They also suggested that I work my way back up to the 10 and 15 pound weights I'd been using before, and start with bands and 2 or 3 lb dumb bells on the affected side.
I got cocky this week and jumped up to 8 lb bells, after more than a year of irregular lifting. So far, so good. I'm going todo some research or check with my docs again before I use the heavier wts, though, to see if I should be wearing the sleeve for working out. It's so hard to tell how much of the lumphadema warnings are things we should be scared of - those fears kept me from doing ANYTHING exercise related for almost a year!
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thanks ivorymom and asedge for the info...every little bit helps. Left a msg with my oncology nurse on Thursday morning and will follow up with her this week.
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