What bad thing can happen to implants if you do weight training?

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  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    I know what you mean....physicalilty and going back to my previous activites was super important to me.  I cannot speak to the question re: contact sports... I'm a weightlifter and runner.  All I can "add" to your decision making process, is that I have had bilateral mastectomies, and I am very pleased overall.  I did not require radiation, since I had two spots of DCIS without any microinvasion....so the mastectomies took care of it.  I am back to running and weightlifting at my pre-cancer condition.   My fitness lifestyle was very important to me.

    Each women has to weigh her options with consideration to the full scope of her lifestyle.

    Do what will enable you to resume to the optimum, the life you enjoy.

    Praying for your wisdom and discernment in your decision making process.

    xo,

    Sue

  • TeresaD
    TeresaD Member Posts: 7
    edited June 2010

    Many Thanks for the reply, OnEaglesWings. When I was first diagnosed with BC I never realized the complexity of the decision-making process.

  • 1WonderWoman
    1WonderWoman Member Posts: 2,065
    edited June 2010

    OnEagles( and everyone else)-

    I really need your advice.   I have been weightlifting for years and did body build some years ago.   I still love lifting etc... and am really, reallly concerned about my upcoming bilateral and the potential I might not regain upper body strength.  I have, all over the net, read horror stories of women who never get strength back.   Unfortunately I have not been able to ascertain what their level (s) of activity were before surgery.  

    Do you feel that you previous working out *helped* your resiliency relative to post-surgery strength regaining?  Also, do you feel your implants "slip?"   Furthermore, how long was it before you were strong again?   Isn't it the lymph node removal that really negates the strength in the affected side?  When one has a bmx, strength is only affected in the cancer side, correct?  I am 40 years old and don't want to start living like I am 80.  As I said, I have been recently reading information where women who had mx/bmx have had to ask people to open doors for them.   Pre-dx I was benching 115 which was light for me.  I am so perplexed and consummed by all of this.   No matter which way you go, the potential for the most dreadful side effects is evident. 

    Everyone wants to make the right decision and try to bring recurrence low, thereby hopefully putting this mess in the rear view, but the roads are all paved with sand. 

     Any information on personal experience is welcomed.   I need to know what I can expect after surgery and the doctors, who I have already consulted with, can only tell me so much.   A collective reasoning is far more pertinent than what a doctor can tell me at this point.

    Thanks-

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    Hi Lizzymack,

    I hear your concern.  I can only speak from my experience, but if you scroll up on this thread to see my response dated March 22, 2010 (includes a progress pic)  you will see that the bilateral mastectomies I had almost two years ago have not detrimentally affected me in ANY way. 

    My cancer was purely  DCIS, and I only had 4 sentinel nodes taken on each side (no chemo, no radiation), plus I would consider myself to have been in excellent health pre-surgery....so I believe all those factors have contributed to being back to my pre-cancer condition.  I do not have ANY limitations.  The only thing I avoid doing is flat bench presses, (though I do incline without a problem), because I was told that it might put undue pressure on the implants in the pockets that were created.

    My PS used alloderm "sling" to also secure the implants in place (sutured to the pectoral/chest muscle as well as the serratus muscle at the side of the breast area....so my implants are very "secure" and held nicely in place.  I have had absolutely NO problem with implants slipping.  I do push ups, pull ups, incline presses, all back work (lat pulldowns, etc...) without any problem.

     I would HIGHLY recommended you check out this link: 

    http://www.fitnessreinvented.com/aboutDorelle.html

    Dorelle Laffal is a woman who had bilateral mastectomies (even nodes taken and radiation on one side!) and went on to become a certified fitness trainer and champion bodybuilder!  You will be greatly encouraged.

    She has a contact number on that site.  I actually called her soon after my Bmx.  She welcomed my call, gave me some great instruction about returning to weights post surgery, and all for FREE!

    I think she would be of encouragement to you!

    Find out all you can and that which pertains to your particular medical breast ca history and treatment, stay positive, and with your previous fitness lifestyle, it sounds like you will do great!

    xo,

    Sue

  • Debwa100
    Debwa100 Member Posts: 59
    edited June 2010

    Wow, you are my inspiration. You look great!!  Actually you all are amazing.  I just had Bmx 4 weeks, ago. I walked 5 miles the other day, and every muscle in my lower body is sore.  lol  - I used to run 5 miles. I had back problems earlier in the year, and had some pain management, blah blah, I started taking yoga and got some relief, and was just starting to get it back together when I got the diagnosis (BC).  I have TE's and my doc wants me to take it easy, it's just hard when you are used to being fit, and now I'm a blob.  At least I know you guys are getting it back together.  I feel so much better now.  Thanks for sharing. 

  • 1WonderWoman
    1WonderWoman Member Posts: 2,065
    edited June 2010

    Hi Sue!

    Thank you so very much for your informative response. I really appreciate it. I found your March 22 post...thank you for that also. I am very glad to hear you have not been detrimentally affected by the bmx. I am just riddled with trepidation that at 40 I could lose upper body strength but I think perhaps the people who's horror stories I read maybe were not into building their muscles prior to bmx? My feeling is my muscles are a jacket for my bones and the better the developed they are, the less trauma can come to my bones.

    You are so fortunate it was DCIS. Mine is invasive. Preliminary "touch" from my surgeon concluded my nodes feel the same on both sides which is nothing short of a very good sign. I am so hopeful for no node involvement. Unlike you, however, I don't consider myself to be in excellent shape pre-surgery. I wish I was. In fact, most recently I am starting to feel a little short of breath like walking up a hill (very odd) and, needless to say, I am concerned it has mets to my lungs. I think my mental concern is causing a physical response (hopefully anyway) but what can you do? Simply hope and that is about it. \

    My PS declared I definitely have well-developed pecs. I will miss benching, however! I am stunned that you can do incline press and flies. Are you doing smith inclines or free? Just wondering. BTW, that alloderm "sling" business sounds like a fantastic way for you to be in the best shape possible post-surgery. Your docs really seemed to reflect on your situation and did what was very much in your absolute best interests.

    Speaking of lat pulldowns are you coming to the back of your neck, including your traps or to the front, engaging your pecs? I also noticed when I was doing trap work with an Olympic bar the other night I did engage my pecs. It is unbelievable how much pecs are engaged in resistance training for other body parts. I have been working my tri's and bi's overtime. Is it because, on the affected side, they cut muscles getting to the lymph nodes that causes weakness or it is weakness with both arms because of the pec cutting to put the te's in? Did you, post bmx, have weakness in both arms, just the affect side arm or in both but to a lesser extent in the unaffected side? Just wondering.

    I am definitely going to check the link and thank you so much for that. I am so looking forward to checking it out and trying to reach out to her this weekend. I am kind of upset that we have such paltry options with this dx...no matter which way you go there is so many considerations. Endless considerations. I just am thankful I don't' have BRCA genes. That was good news.

    Have a great weekend and thanks for the all the information. I appreciate it more than you will ever know-

    Liz

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    Hi Liz,

    I know, the whole prospect of mastectomies and the "unknown" can bring great fear and trepidation.  Like you, I am in my "fab forties" (48 to be exact).  I think the key, regardless of what shape you go into surgery in, is to work with your surgeon re: your particular cancer history, and in terms of appropriate healing times so you can safely be guided in return to normal function as possible.  For me, I didn't have TE's put in, until week #3 post op (they were waiting for my pathology, to see if I had any invasive component.)  During those three weeks where I just had the mastectomy, I did the recommended stretching exercises and by week 3 was having a pretty good range of motion.  My doctor also allowed me to ride my bike at 2 weeks post op, and I had no problem with any chest issues.  For me, the limitations came after, at week 3, I had the left prophylactically taken off, and then had temporary expanders put in on both sides.  It was quite uncomfortable, and I was limited mostly due to pain early on.  It just felt very uncomfortable to open tight lids so I would have my husband help me open jars (amazing how opening jar lids engages your pecs!).  Also, opening heavy car doors felt a bit uncomfortable for awhile -- all because of the pressure of the TE's under my pec muscles.  As things went along (after week 7-8 I began to feel MUCH better in terms of function) I was doing pretty well.  I followed instruction re: range of motion exercises.  I did not return to any weightlifting until my switch to permanent implants.....even then, my plastic surgeon had me wait the 6 weeks (the time frame for tissue healing.  the breast tissues as well as scar tissue reaches about 80% it's original strength by week 6-8; so most surgeons release you back to normal activities by then)  But for all intents and purposes, my plastic surgeon said to return to whatever I was used to, but just let pain be my guide.

    I returned to weight lifting very slowly and progressed slowly.  Using as little as 5# for chest and upper body.  Just to get my muscles used to it, and gradually progressed from there.  By 6 months, I was back to my pre-cancer condition and weight lifting routine.  I'm not an extremely heavy lifter.  I typically just use dumbells for chest with incline presses at 20-25 pound dumbells maximum.  On lat pulldowns, I pull to the front toward the collarbone (I heard it is much more safer this way for the shoulder girdle).  I usually pull around 50-65 pounds. 

    Dorelle (on that link) could really give you guidance after your surgery.  I've heard other BC overcomers hiring a personal trainer specializing in BC recovery to oversee their return to working out.  If you have lymph node involvement and removal, it would be wise to work with a physical therapists that are trained to work with BC women (lymphadema certified therapist a plus - for education and training on avoiding issues with that), particularly if they have had any lymph nodes removed.  Many studies have shown the benefits of guided weight lifting in preventing and reducing lymphadema.  Often, a compression sleeve is recommended as an added precaution when exercising, if a woman has had a lot of lymph nodes taken out.  Since I only had 4 sentinel nodes taken on each side (and you have about 30 lymph nodes under each armpit), my surgeon and BC nurse coordinator said I did not require a sleeve).

    Are you planning on having reconstruction?  If so, what kind?  That will also determine your post op guidance on return to physical fitness.

     To answer your question about weakness.  I don't have ANY weakness due to my surgeries. 

    And about the Alloderm sling - if you are planning on having implants, most plastic surgeons now do this as standard procedure.  You should ask your doc about that if you are going with implants. 

    Let me know if you have a problem with the link I sent you.  I know that Dorelle had mastectomies with lymph node removal and radiation, and she is a professional lifter.

    I'm sure she could really encourage you, and answer you questions.  Since she is also a personal trainer who specializes in working with women post BC surgery, I'm sure she would have a WEALTH of experience and wisdom to share with you.

    In my heart, I really feel like you need to believe that you will come back strong.  Fight those negative thoughts.  Be wise and educated in your recovery period, but stay positive.  You are courageous!  You are a warrior woman!  You will overcome all those threatening voices that scare you with the "what if's" and the unknowns.  I know.  I've been there.  You will come through stronger on the other side.

    God bless you RICHLY with peace and comfort and strength as you journey through this.

    We are all here to support you!

    xo,

    Sue

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    p.s.  I meant to tell you, that I used speed walking as my primary form of exercise during all the recovery times when I was unable to lift.  With a sensible diet and the walking, I was able to maintain a healthy lifestyle.

    To aid with tissue healing, make sure you eat plenty of fruits and veggies.  Get some good quality protein in your diet, since protein is the essential building block of all tissues.  I actually supplemented with vit. C - 5oo mg. during my recovery phases.  I believe it really helped with my tissue healing.

     A GREAT book resource (covers everything about return to fitness, and adapted to various BC scenarios and reconstructive options, etc) is:  THe Breast Cancer Survivor's Fitness Plan by Carolyn M. Kaelin, MD, MPH.   The author is an MD and a breast cancer survivor, too.  It's a really helpful book.  You could probably order it through Amazon.com for inexpensive.  They sell used copies for reallly cheap!

    xo,

    Sue

  • Debwa100
    Debwa100 Member Posts: 59
    edited June 2010

    Made an appointment with a physical therapist today (funny, I am a physical therapist, but I specialize in pediatrics).  I'm hoping to get some advice on how I'm doing with my strength and range of motion Ii think pretty good).  But, also how to progress my program.  I'm walking 3-5 miles a day, but that's it for now.  I'm still in the expanding process so I'm sure there will be limitations.  I'm also hoping to get some information on lymphedema prevention, and if I should be wearing any specific garments for flying.  Anyway, that is my progress in the exercise department.

  • Estel
    Estel Member Posts: 3,353
    edited June 2010

    Wow!  I've been looking for information like this since my diagnosis in September.

     I did Body Pump at Gold's gym 3x a week and Pilates at another gym 2x a week before my diagnosis.  And speedwalked about 4 miles a day.

     When first diagnosed I was sure I didn't want to do the reconstruction b/c I wanted to get back to my 'normal' activities as quickly as possible.  After consulting with a plastic surgeon he assured me I could do what I was doing before.

     Since my DMX, I've doubted him!  But what you're saying gives me hope.  I will definitely check out that link. 

    Oh, you have no idea how relieved I am.  THANK YOU!  It's so helpful to know that there are others out there who gone thru it and are doing what they were doing before.  The softening of my arms and my belly has been difficult.  I have my exchange surgery on July 19.  I had my DMX on Feb 25th.  Woo hoo!  Something to look forward to.  thanks again!!

  • ktym
    ktym Member Posts: 2,637
    edited June 2010

    I get a bit defensive when people assume my weakness post op is because I wasn't working out hard pre op.  I do still do aerobic activity and weight lift now just like I did previously and I do have strength deficits.  I went to pub med and searched pectoralis muscle and reconstruction.  Most of what is done deals with pectoralis muscle flaps, but there is a small body on breast reconstruction.  Most of them show a small but significant decrease in pectoralis muscle strength.  It has taken me a year to get even close to the level of weights I did before.  My PS didn't tell me not to flat bench press so I'm still doing it and haven't noticed any difficulties. I had expander and sentinel node.  I do have lymphedema and a lot of neuropathy from chemo so it is hard to know how much that is contributing.  Plus, with the lymphedema I am very careful to not overtrain weight lifting.  Even with that, it has been very slow progress.  Personally I'm suspicious part of it is muscle flexibility.  I have to work at stretching constantly.  But, think about it.  They take all the fascia off the muscle doing the mastectomy, they mobilize the pectoralis insertion to do the sentinel node, then, they mobilize the pec and stretch it and cut into it twice by the time they do the implant exchange.  How could there not be scar tissue that you need to work with?

    I too found it frustrating pre treatment to know what would happen post treatment.  Personally I found that the physicians who worked out didn't know breast cancer, and the ones that knew breast cancer didn't work out so getting straight answers was impossilble.  One nurse told me I wasn't allowed to break a sweat after my surgery--for weeks.  Thankfully my Onc intervened on that one.  At least my Onc got that there weren't enough psych meds invented that did as much for me as yoga and a treadmill during the whole treatment experience.   So, my personal experience is that yes, mastectomies and recon can hurt your strength, but they won't keep you from weight lifting and being active.

  • 1WonderWoman
    1WonderWoman Member Posts: 2,065
    edited June 2010

    Hi Sue!

    Thanks so much for responding. I like the fact that you refer to us as being in the "fab forties!!!!!!" I am having prophylactic removal of the right breast and I, too, am having te's, on TUESDAY, JUNE 22 to be exact (woe is me!) so I will be joining you all on this magic carpet ride! Thanks for the info on the tight lids...I keep trying to forecast what I will have a problem with..perhaps relaxing?! Where did you sleep after surgery? Were you a stomach sleeper?

    I do plan to listen to the docs and I actually bought 5lb hand weights the other night. I have checked out the Dorelle link and will continue to use that as a reference. You see, I think I am wonder woman and will be downstairs in my gym using my Weider Pro double station and doing all my workouts in no time flat! No, I did not start my post-operative meds yet!!!!!!

    My surgeon also remarked, and thereby concurred with you, on the value of weight lifting when staving off lymphedema.

    Question: why were nodes taken on the left and right when the left was a prophylactic removal? I was surprised to learn how many lymph nodes are under each arm. Wow...I did not know.

    I do feel I will come back strong and, to be honest, I am tired of these big, old boobs! I am not lamenting the loss of them. I would never have elected such a ludicrous surgery if it weren't for bc but I am looking forward to smaller boobs that don't move and no more bras. I know it sounds silly but we should be able to look forward to some parts of this, after all!

    Yeah, I got the idea when perusing these boards that a lot of women use power walking as a way to recover. I do have a recumbent bike and an upright in my gym and have been wanting to get a treadmill so perhaps now is the time! It is summer in CT and I don't love humidity.

    Thanks for the reference on the Vitamin C. I already loaded the freezer with pre-made, protein-heavy meals and Boost with protein. I don't have much of an appetite these days and I know I won't eat hospital food so I need to ask my surgeon to order those high protein drinks and cranberry juice. Just reminded myself!

    I will check out the Breast Cancer Survivor's Fitness Plan book. Certainly I do need some guidance.

    Debwa: That is so odd that you, a PT, had to go to a PT! I know you are in pediatrics...isn't it funny how life comes at us. I am sure you never really reflected on having to hire a PT as a PT! I will be joining all of my BMX w/recon TE sisters on Tuesday so I will definitely be posting my progress especially where working out is returned. I do believe, if you have lymphedema, there is a sleeve to wear. Check around the boards. There are posts on that topic.

    Dawn-Hope:

    It seems a lot of people get back to there normal activities so soon you too shall put this all behind you. I will be thinking of you on July 19th when you get your permanents and congratulations ;)

    KMMD: My company was nothing short of a pain in the ___ when I got your post on my blackberry. I was surrounded with those "what if you die/it spread/blah blah" well-meaning types but they failed to mention the "and then you won't see us again" bonus!!!!! In any case, it helped me to take a little STAYCATION from that madness! Don't listen to what jackass people say because they don't know what a "hard workout" is for you and unless they were tracking you, how do they know what you were doing pre surgery? I would encourage you to double check on the flat bench press b/c I was told by more than one PS when I was interviewing them that is off the menu after surgery. Just letting you know. I agree with you on the potential for scar tissue and the need to work with it but I don't know exactly what that means.

    I am totally with you on the frustration pre-treatment to know what would happen post-treatment. My BMX w/te's is Tuesday, June 22 and I kind of gave up trying to figure out what life was going to be like after because cancer is in my breasts, trying to kill me and I really don't have a choice. In fact, I am going through all this, as most of us have, to bring recurrence as low as possible. My reason for doing it has nothing to do with my being satisfied with regaining strength but to try to save my life. I don't know what the definition of my life is going to become over this next year but I am just grateful it was found early enough and that hopefully they can remove it all, it has not spread, and they can save my life.

    I know there are a ton of nervous nellies (like the nurse that told you not to break a sweat) who think they are helping but we are all different. I totally agree with you: If you want to be strong again, to bike, to run, to windsurf, you will do it. Nothing held us back before and certainly nothing will hold us back going forward.

    Best of luck on all of your continued progress-

    Liz

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    Hey Liz,

    Just to answer the two questions you put out on your last post: the first being about where I slept after TE's were put in:   After I had the temporary expanders put in, I was most comfortable sleeping on our couch.  We have a really soft couch with a puffy armrest.  It kept me upright at about a 40 degree angle, and kept alot of the pressure off of my chest.  Lying flat really bothered me.  Fortunately, I'm a back sleeper, so it was easy to continue to sleep on my back.  If I'm remembering correctly, my plastic surgeon recommended avoiding sleeping on the side for at least 3-4 weeks post TE placement, to allow for tissue healing in the pocket that was created.

    I finally returned to my normal bed by week 7.  (Again tissue healing takes about 6-8 weeks, so looking back, it makes sense that I started to feel markedly improved by around then.).

     Your second question had to deal with why I had sentinel nodes taken on the left, which was a prophylatic mastectomy.  I had sentinel nodes taken because I had already had numerous biopsies on the left breast as well, though they all came back benign....my "microcalcification" clusters that were biopsied on the left breast, exactly mirrored the pattern that was cancerous on my right.  So, it was simply a precautionary measure, because if for some unforseen scenario that they missed any cancer in my breast on the left, and it showed up in my lymph nodes, they would go ahead and take out the nodes while I was under anesthesia then, vs. having to come back for another trip. 

    They were being very precautious, because when my right cancerous breast was removed, they found a SECOND spot of cancer in it, that none of the tests had shown.....so they were concerned my left breast could potentially have cancer that the biopsies had missed.

    sorry for the longwinded answer.  ;-)

     Stay strong ladies.

    You all are awesome!

    xo,

    Sue

  • speech529
    speech529 Member Posts: 337
    edited June 2010

    Wow

    What an amazing thread!  I loved reading about all of you STRONG ladies and your athleticism.  It is encouraging to me.  This is a long post...but it helps to tell my story.

    I am 51 years old and in March I found out I needed a hysterectomy; then a week later my breast biopsy results came in--DCIS.  So my docs said we will do it all at once.  I had a vaginal hysterectomy with BSO and a lumpectomy on 6/2.  I ramped up my training from early April to June  with a combination of weights, aerobics and hiking.  My surgeries went very well, I feel wonderful!  No pain, only slight discomfort on hyster and docs attribute that to my health and vigor.  

    Unfortunately margins were not wide enough and BS wanted to go in and get more tissue out but due to size of 1st excision (lesion 1.9 cm and they removed a 5x4 cm segment) and my tiny breast, I opted for a uniMX.  So, I am going to have a one step MX with alloderm/implant on Monday (6/28); I will have implant on L also for symmetry. 

    I am very active--hiking is my sport.  I live in Phoenix and I hike from Sept to May--lots of mountains and foothills here.  Every year I hike to Phantom Ranch in the Grand Canyon with a group of hiking ladies.  We go again in Jan '11. Can't wait!!

    Some of the training hikes we do involve upper body moves to climb up over large boulders.  I do very moderate weight lifting to keep muscle strength for hiking and the climbing.  I know that I am losing upper body strength daily although I am doing some light lifting now.  Due to the hysterectomy I am limited on what I can do--no running, lunges, swimming, biking, or standing and lifting until mid July.  Basically I can walk.

    Today is 3 weeks since surgery and I walk daily and have worked up to fast walking 2+ miles.  I know this next surgery is going to be harder but I am ready to do what I need to do to regain strength.

    You ladies are an inspiration!

  • vmudrow
    vmudrow Member Posts: 846
    edited June 2010

    Just got back from the PS, it's been 8 weeks, still have TEs in, asked again and he said no push ups, bench pressing or flies - ever.  I can do anything else, waterski, bike ride, weights (just not the above as they could cause implants to shift). 

  • trigeek
    trigeek Member Posts: 916
    edited July 2010

    well it has been quite a while since I went through this but I remember going back to my personal trainer to do weights about 4 months after bilateral mastectomy during chemo before exchange.

    Now I am lifting and  did crossfit for a while too with no restrictions, except the weird feeling of muscles pressing on implants. I am definitely back to where I was and even stronger.

    Now I had alloderm added to my chest muscles because they were not big enough to accomodate the expanders ( I have a narrow torso) ... and one of them i think did not patch properly and I have a double chin on my prophylactic mx side (revenge of the innocent boob) .. other than that all is good. So I guess I also have patched chest muscles.. anyone else have that ?

    And that is not noticeable unless I do a wet t-shirt contest with a white t-shirt lol...

    Keep on liftin' !

  • whitedove
    whitedove Member Posts: 292
    edited July 2010

    Hi All:

    I am in the same boat as vmudrow. Had TEs put in for BMX and for 8 weeks none of the exercises she mentioned + many, many, many more restrictions, NO driving, lifting, pulling, using arms, dishwashing, anything repetitive. I am a former gym fanatic and have had to patiently wait to exercise.  Why such wide variation of what folks are told what they can/cannot do?

  • Estel
    Estel Member Posts: 3,353
    edited August 2010

    whitedove - I don't know and it is sooo frustrating.  I don't know if it is because active women are getting diagnosed younger and younger and the research is behind.

     I'm going to check out the book posted above. 
    Diagnosis: 9/2009, DCIS, Stage 0, Grade 2, 0/2 nodes, ER+/PR+, HER2-

  • ktym
    ktym Member Posts: 2,637
    edited January 2011

    Hoping to bump this up.  (hoping lizzymack is still posting) if you read above we had discussed the question of flat bench pressing after implants because some PS warned against it, but, no one seemed to give a good reason why.  Well, I tried it, resounding not good idea. Did fine until I got up to about 80 lbs (far less then I was pre BC, so its not like my chest hadn't trained harder before).   About that same time I ended up doing a lot of pushing/pulling/lifting/upper body things at work where it was impossible to control position and muscle use.  I really ended up screwing up my pecs.  Have been in PT for the last several weeks and not been able to use them at all for lifting.  Still not back to normal, but, the pain is less.  Funny thing though.  I had never had the implant drop and "fluff" after the exchange. My PS was even discussing more surgery which I deferred.  I was happy enough and didn't want to go through another forced recuperation nonactive period.  Well, the stupid thing seems to be dropping and fluffing.  Looks better now then anytime in the last almost year and a half. 

    So, I'm interested in hearing if anyone else has had any problems.  I'm not sure I can blame it on the lifting, like I said, I used to lift much more and the weightlifting was more controlled then the other physical activity, but, pec work is sure off the table for awhile.  Anyone have anything similar, or, anyone doing flat bench pressing without problems?

  • DiDel
    DiDel Member Posts: 1,329
    edited January 2011

    KMMD. My PS is a weightlifter so he didnt really put me on any restrictions of lifting other than no more than 20lbs for the first 6 months after exchange. I had some cording issues so had to lighten the load to no more than 10 lbs until cording issue resolved. I went to PT to discuss cording issues and what exercises I should be doing etc. My PT said absolutely NO chest presses push ups or butterflies for at least a year and no more than 5lbs on exercises in repetition. Which is fine for me for now as I am just getting back into the groove after 4 surgeries in a year. My PT just said it takes a long time for your pec muscle to heal from surgery. I told my PS what my PT said and he agreed on waiting to do chest exercises but everything else he was fine with since I just had hopefully my last surgery. I had some scar tissue build up and my pec on my mx side felt strange when I did chest presses and push ups. So I don't want to strain anything.

    Diane

  • ktym
    ktym Member Posts: 2,637
    edited January 2011

    Thanks Diane.  I could deal with the strange feelings and implant distortion, the pain and inability to exercise I don't want to go through again

  • ktym
    ktym Member Posts: 2,637
    edited January 2011

    I have to say the 5 lb thing, uggh.  The PT didn't get why I'd want to do pec and lat lifting, "those muscles are strong alredy" getting across to someone who doesn't lift why you like doing it is hard.  This is also impacting power yoga (planks to upward dog, etc) which is killing me too

  • Gran
    Gran Member Posts: 104
    edited January 2011

    Hi kmmd,

     I had bilateral mastectomies at the end of March 2010 and then had silicone implants placed below the pec muscles in July 2010.  I have alloderm supporting the inferior part of the implants (Mentor moderate plus profile cohesive silicone gel 400cc implants)  Not gummy bears.

    I am a former bodybuilder and started back to the gym in October.  I have torn rotator cuffs so I have been doing physical therapy for that, but have also been working my pecs.  I have been doing incline flies and bench with only 2/3 of my normal weight for flies and a much less for my incline benches (I am using dumbells instead of a bar because I feel more in control with the dumbells).  When I do these exercises my implants distort quite a bit and they become more lateral.  I am afraid that if I lift too much weight or try flat benches, etc I will push an implant out of my lateral pec area.  I know it is possible to dislocate an implant in this way because I spoke with a woman who took up bodybuilding after mastectomy and she did end up needing surgery to put the implant back where it belonged.  So...out of fear I am going very slowly. 

     I have not tried push-ups because even the hint of that motion makes the implants distort greatly and they feel extremely vulnerable to dislocation.  I have also not tried dips.  Lat pulldowns with a moderate amount of weight also cause the same distortion. 

    The good news is that my "iron bra syndrome" sensation has gone away completely now that I am lifting and stretching at the gym.  It came back only when I was on vacation and unable to lift, so I know it's the lifting that is making the difference. 

    Overall, my pecs and implants feel better now that I am lifting.  The implants feel less prone to distortion with simple, everyday activities now, and my mood in general is much better.  I think slow and steady is the key (although I brought in a bundle of firewood the other day that had to have weighed at least 50 pounds.  I couldn't help myself -- I am so used to doing that). 

    Anyway, no ill effects from the firewood or the lifting.  And I am getting used to the feeling of the implants distorting so it does not bother me as much as it did in the beginning.  I am wearing very tight sports bras, though, in an effort to keep the implants from being pushed too laterally.  If I were going to increase my weights or try dips/push-ups, I would probably wear an ace wrap to ensure that the implants would not dislocate.  Especially at first, until I knew what my limits were.

    I hope this helps.  Let's keep in touch as we get back to bodybuilding.

    Gran

  • ktym
    ktym Member Posts: 2,637
    edited January 2011

    Gran, it helps a lot, thank you.  It is so valuable to hear from a body builder living through this. I had noticed the pull down issue too and tried to limit the weights

  • ktym
    ktym Member Posts: 2,637
    edited January 2011

    anyone used an incline pulldown bench lide the "total gym"?

  • Gran
    Gran Member Posts: 104
    edited January 2011

    Hi kmmd,

    The woman I mentioned who displaced her implant while bodybuilding is Dorelle Laffal.  Go to Google Images and take a look -- she looks incredible and she did win some contests with her 'foobs' so there is hope for us!  She lives in the Washington, DC area.  You should be able to find her contact info on the internet -- I don't have it handy.  I spoke with her by phone a few months back and will be going to DC at some future point to train with her for a few days.  She is such an inspiration.

    Gran

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

    My bilateral Mastectomies were in '08.  I have the alloderm sling as well that I understand helps to hold them in place.

    I have been told to avoid FLAT bench presses... but I do INCLINE presses using dumbells.  I don't usually go higher than 20-25 pound dumbells, because I do not feel the need to press the issue (no pun intended. ha!) 

    I have been pleased with being able to do pushups and lat pulldowns without problems.  I am choosing to avoid tricep dips..just because, for me, I feel it would place to much strain on my pecs and shoulder girdle, due to the abnormal way the pec has to lie over the implants.

     I pull around 65# on the lat pulldowns without any issue.  On chest presses, they temporarily compress and may look funky, but go back to normal afterwards. 

    I've been very grateful that I do not feel any limitations due to the surgery.  I'm not into serious bodybuilding, but like a firm, muscular, athletic body.... and I have been able to achieve that, thankfully!

     Best wishes to all of you lovely ladies....and HAPPY and HEALTHY NEW YEAR!

    :-)

    Sue 

  • Mel22125756
    Mel22125756 Member Posts: 10
    edited March 2011
    I'm interested in hearing more from anyone that has information about implant displacement. I had TE exchange surgery with a saline implant in June 2010. I couldn't have been happier with both the comfort and aesthetics of my implant. Six months later I was exercising (stretching my pec muscle, yoga and some easy push-ups etc.) and I noticed a major change over the course of two days. At the time, I thought it had ruptured. It seems as though it shifted down and out and became flatter. Now, I have an increased tingling sensation toward my armpit, increased rippling of the implant and every time I flex my pec, the implant is uncomfortably 'jumpy' and wrinkles in the cleavage area.I saw my PS about this right away and he simply said that everything looks normal to him. I have a follow-up with him this week and would like to be more informed when I talk with him. I had done more vigorous exercise involving my pec muscle with the tissue expander, without having any problems. I was careful to ease into exercising for several months after my final implant surgery. I don't know why this would happen after six months.I do not have Alloderm and do not wear bra while sleeping (I always wear a very supportive bra while working out). Are these factors important to keeping the implants in place? I'd love to hear about any similar experiences. Somehow, I need to convince my PS that my implant isn't 'normal'.Thank you,Mel 
  • sweetie2040
    sweetie2040 Member Posts: 817
    edited March 2011

    Mel22-You have to be careful about what type of exercises you do when you have implants. Some pec exercises can push them to the sides causing lateral displacement. It sounds like you may have the that. The jumpy part you are talking about could be the movement of your pec muscles. Since the implant is under them and we have no breast tissue this will show up as a distortion when you flex those muscles. It's very normal after a MX although odd looking. If  Youd don't agree with your PS  I would seek out a second opinion to be sure.  I would wear a supportive sports bra when sleeping as well to hold them in laterally. My implants fall to the side when lying down and I have worn a bra when sleeping since I got them. I am going for a revision due to severe rippling and my PS is also going to put stitches laterally to hold them more in place. The thing is to really keep them supported. Also I would specifically ask you PS about what exercises you can and can't do. Unfortunately I have steered away from most exercises the engage my pec muscles. I think you can still do many types of exercises and work outs you just have to be extra careful with implants or they could displace. Get a second opinion if something doesn't feel right. It's always better to at least have peace of mind about what is normal and what is not. Wish you the best. Keep us posted.

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

    Just to add my two cents:  You know your body.  You know that it is not the same.  you noticed changes after that lifting episode.  The tingling would seem to suggest that it has shifted and maybe touching on a sensory nerve in the area. 

    In re: to your comment about not having issues with the tissue expanders -- the tissue expanders are textured.  That is so they stay lodged in place.  Of course the saline implants are smooth (which would make them more prone to slippage).  The alloderm sling is designed to hold them more securely in place.  If you do not have that, it is very possible that it has shifted.  If this is the case, I guess the question now would be, are you discontent with the look?  Is the tingling problematic or limiting you in any way?  Options would be to continue as is, or if troublesome to you (cosmetically, or due to the tingling) and you want more future "security"...... you could consider an implant revision with alloderm.

    since you don't have alloderm, I would ask your PS to be VERY specific about exercises to avoid.  I'm thinking anything that causes agressive compression or stretching of your chest muscles might put you at risk.

     I do have alloderm, and I think that does make a big difference in terms of the implants being held more firmly in place.  Typically, 12 weeks is a safe zone to resume previous activity.  For me, I was able to cautiously resume weightlifting, etc..

    I think about 8 months out I was back to pull ups, push ups, and chest exercises (always on an incline.  I had a physical trainer who also had BMX say never to do flat bench presses, because of too much pressure on the pectoral muscles that could dislodge the implants.) 

     I never sleep with a bra....it hasn't caused any issues. ( 3 years now since surgery).

    Best wishes to you.  Let us know what you find out.

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