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Topic: Lift/Reduction to radiated breast?

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  • Posted on: May 27, 2009 04:23 pm, edited May 27, 2009 04:27 PM by Boo307
Joined: May 2008
Posts: 38
Boo307 wrote:

Has anyone had a lift/reduction to a radiated breast?  I had bilateral lumpectomies in March 2008 and bilateral re-excision in April 2008.  I had two different cancers (IDC and DCIS), two different locations, two different surgeries leaving me with two different looking breasts.

I am now debating a lift/reduction to my right side to give some symmetry under clothes, but am worried about the risk of surgery to the radiated tissue. 

Does anyone have experience with this procedure after surgery and radiation?

Thanks. Betsy 

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Posts 31 - 60 (89 total)
tkone
Seattle, WA
Joined: Jul 2008
Posts: 293
Jun 14, 2009 11:21 am tkone wrote:

I am doing well.  I went in on Thursday to see if I could have my stitches removed and my PS thought it was just a tad early, so they are staying in until Tuesday.  I definitely have swelling and some fluid retention, but honestly, I have more in the non-radiated side than the radiated side.  At the Post-op appointment they removed my dressings and I got to get a good look at the results and I'm pretty happy with it overall.  She said that because one side has been radiated, it may "unswell" differently than the other one so I may end up slightly unsymmetrical.  Although it doesn't look that way now-they look very symmetrical.  She did say if they end up uneven, it is pretty easy to fix by use of a little liposuction instead of full blown surgery again.

So far so good!

Tracy

Tracy http://tracy-breastcancerandme.blogspot.com/
Dx 5/7/2008, IDC, 2cm, Stage II, Grade 3, 0/4 nodes, ER+/PR+, HER2-
HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 14, 2009 12:01 pm, edited Jun 14, 2009 12:03 PM by HollyHopes HollyHopes wrote:

ugh - Mainer...that is a scary story....the PS told me to scrube the wond areas vigorously and i have been avoiding that because it is so creepy and unsettling and it hurts...but your hurt was far, far wrose...so i guess i'll start scrubbing away...thank you for sharing a cautionary tale....

Tracy - glad that you are doing well...I didn't have to get any stiches removed - I guess they are the dissolving kind....

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
tkone
Seattle, WA
Joined: Jul 2008
Posts: 293
Jun 14, 2009 03:46 pm tkone wrote:

Hollyhopes-the stitches that I have are for the lift part.  I have internal stitches as well, but the ones for the lift are pretty heavy duty.  I guess it takes quite a bit to hike a breast up from hanging out on top of your stomach to actually putting it on your chest where it belongs!

Tracy http://tracy-breastcancerandme.blogspot.com/
Dx 5/7/2008, IDC, 2cm, Stage II, Grade 3, 0/4 nodes, ER+/PR+, HER2-
HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 14, 2009 04:07 pm HollyHopes wrote:

hey tracy -  i had a major lift too...but no external stiches...hmmmm

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 14, 2009 09:39 pm Boo307 wrote:

Tracy, I'm glad to hear you are doing well so far. 

Native Mainer, Thank you for your story.  That is horrible and gives some real perspective to the challenges of healing radiated tissue.  Could you email me, I have some questions, bpchapman@roadrunner.com

Holly, Good to hear you are still making progress. 

I don't understand why this issue of complications with future surgery isn't talked about as a side effect of radiation therapy.  I thought that if I had a lumpectomy, later had a local recurrence, I could just have a mastectomy/reconstruction at that time.  Little did I know that it is possible, but has unpredictable results.  There doesn't seem to be much information about the second or more times cancer returns and the impact of your earlier decisions on your later options.  Maybe that will be the next information phase that breastcancer.org will cover in the future as they fill out their material.   

Betsy

DX 3-18-08: Bilateral BC - IDC, 1.8 cm, Stage 1, Grade 3, 0/1 nodes, ER-/PR-, HER2+

                                             DCIS, high nuclear grade, ER+/PR-

WarriorJenn…
Conifer, CO
Joined: Jun 2009
Posts: 20
Jun 14, 2009 10:19 pm WarriorJenn wrote:

Plainjane64, the Center for Restorative Breast Surgery has a success rate greater than 99%.  I believe they've only lost one or two perforator flaps since they began doing them--they can confirm the exact number for you if you ask them.   As they've done over 3000, you can see that their success rate is pretty much 100%, including women who've had radiation.

Boo307
Joined: May 2008
Posts: 38
Jun 15, 2009 09:22 pm Boo307 wrote:

WarriorJenn,  Thanks so much for the information.  I had heard about the doctors in New Orleans, but didn't know who they were.  Their website is impressive.

Betsy

carolynf
So Berwick, ME
Joined: Dec 2007
Posts: 248
Jun 16, 2009 07:19 am carolynf wrote:

I am really interested in the website for the highly trained docs in New Orleans...I guess I really didn't know the issues that can surround surgery w/a radiated breast!  It is not very comforting.  I know everyone heals differently but there must be some kind of surgery where it heals w/out huge issues.  It's scary to think that if I cut myself (somehow) on that radiated breast that it will not heal up quickly.  I am almost 2 yrs out from my lumpectomy and i still have booby pain.  How unfair is that?  I am wondering if I get a recon will that pain be diminished or will it be worse?  Anyone else w/the same thing?

Carolyn
Dx 10/26/2007, IDC, 1cm, Stage I, Grade 3, 0/7 nodes, ER-/PR-, HER2-
HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 17, 2009 03:59 am HollyHopes wrote:

Just to update you... I am feeling much better in the past few days...but the radiated breast is still having a hard time healing...now that most of the swelling has subsided I can see that the radiated breast is larger than the other side.  My original reduction and lift was to make both breast more equal and to revise the scars....so, rather than the 'good' breast being bigger than the 'bad' one...I have the opposite effect...ah well...I will live my life unbalanced I guess...probably the physical  reality is a reflection of my internal state!!  LOL...I want to hear how everyone else is doing....

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 18, 2009 11:03 pm Boo307 wrote:

Carolyn,

Here are some items that I found informative.

Reconstructing the Radiated Breast This type of surgery includes all of the pitfalls of any breast procedure

by Jane Petro, MD http://www.plasticsurgerypractice.com/issues/articles/2009-02_03.asp

Asymmetry correction in the irradiated breast: outcomes of reduction mammaplasty and mastopexy after breast-conserving therapy.
Chin MS, Brooks GS, Stueber K, Hadaegh A, Griggs J, Johnson MA.
Tufts University School of Medicine, Boston, MA, USA.

BACKGROUND: There is relatively scant evidence concerning radiation effects on reduction mammaplasty and mastopexy, two procedures which are often used in the irradiated breast to restore symmetry following breast-conserving therapy (BCT).

OBJECTIVE: The purpose of this study is to further examine outcomes of reduction mammaplasty and mastopexy in breast cancer patients previously treated with BCT and radiation.

METHODS: A retrospective search at Baystate Medical Center (Springfield, MA) identified 12 patients who had received external beam radiation and either reduction mammaplasty or mastopexy. Overall radiation doses, including tumor bed boost, ranged from 5000 to 6600 cGy. The mean time between completion of radiation therapy and asymmetry correction was 63 months (range, 5 to 169 months). An overall average of 910 g of tissue was removed from the irradiated breast (range, 180 to 2925 g). The average length follow-up after asymmetry correction was 9 months (range, 1 to 44 months).

RESULTS: In our patients, there were no major complications such as flap loss, tissue necrosis, heavy scarring, infection, or severe deformity. Minor complications in the irradiated breast occurred in 25% of patients and included prolonged edema (n = 1), delayed wound closure (n = 1), and minor scarring (n = 1). Histopathology was unremarkable except for one patient who was found to have recurrent ductal carcinoma in situ.

CONCLUSIONS: In the cases reviewed, we did not observe any complications commonly associated with operating in an irradiated field. Good cosmesis and acceptable symmetry were achieved in all patients. Our data suggest that reduction mammaplasty and mastopexy after radiation therapy are relatively safe procedures with risks not significantly higher than either operation performed in patients without radiation.

http://www.ncbi.nlm.nih.gov/pubmed/19371840?dopt=Abstract

Betsy

HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 19, 2009 12:08 pm HollyHopes wrote:

Hi Betsy - great info...I can attest that I am fitting into all the remarks in the "Results and Conclusion" sections.  My wounds are healing slower than in the normal breast.  the scars will consequently be larger - but over all...I am very pleased and I know that six months from now I will be very happy that I chose this option!

 Hugs to all,

Holly

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
tkone
Seattle, WA
Joined: Jul 2008
Posts: 293
Jun 19, 2009 12:16 pm tkone wrote:

I don't know why this is the case, but I am just the opposite.  I still have a little bit of discharge from the non-radiated side and much more swelling.  The radiated side is great so far.  Normal swelling, my scars all look fine.  I don't know if it makes much difference but I had very few skin problems with radiation.  In fact I didn't even turn pink until about 5 weeks into it.

Interesting!

Tracy http://tracy-breastcancerandme.blogspot.com/
Dx 5/7/2008, IDC, 2cm, Stage II, Grade 3, 0/4 nodes, ER+/PR+, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 19, 2009 03:44 pm Boo307 wrote:

Holly, I'm so glad to hear things are going well.  Maybe the radiated side still has edema and will 'shrink' as the months go by to give better symmetry. 

Tracy,  Didn't you have your surgery just two weeks ago?  It sounds like you are doing great.  I wonder what is up with the non-radiated side.

I have my surgery scheduled for December 1st, right after I get back from walking the BC 3 Day in San Diego.  I walked 18 miles last Thursday!  I'll either be in great shape or totally exhausted for surgery. 

Best to all.  Betsy

HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 20, 2009 07:24 pm HollyHopes wrote:

18 miles!  wow - that is amazing...i am a total slug....good luck in December Betsy!

you are lucky Tracy.... I'm glad one side is 'behaving' and hope hte other does too!

xoxox

Holly

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 21, 2009 06:03 pm plainjane64 wrote:

Gosh, haven't been on in a while but read thru all...

Holly, hope things continue to go well, slowly or quicker...at least it's going the right direction-and since I'm playing catch up I just want to say I am so glad you're rid of the loser who had the nerve to seek out someone 'unscarred'.....excuse me but what an #@%!!!!  You're better off w/o him!

WarriorJenn:  yes, I feel more comfortable by the minute and am leaning heavily to NOLA. They've operated on plenty of irradiated tissue, have awesome resuts have been fabulous w/ every phone contact-and as an RN myself who is famiiar w/ complications/risks, etc -I grilled them and they are still making A's in my book.

I know at my teaching facility/ breast center the whole topic/side effects, future considerations of radiation was discussed in depth.  The risks and fact that you are forever altering your tissues by radiating them was made pretty clear to me.She also radiated me prone because I was a good candidate for that. I am going into this next surgery (when I can)knowing that side may/may not have issues.

I'd actually appreciate any good vibes, thoughts, prayers for my current issue!  seroma in my lumpectomy/MRI guided biopsy site....grrr.  Has been taking forever to go away but this week right at the surg site red/hard warm and I've had a low grade fever....and I'm 7 mos from surgery and 4 mos out of rads and praying this will clear w/ antibiotics-they needled and sent off cultures friday and I follow next week.  Trying not to freak or read anything else about IBC...scary stuff. 

Carolyn, re: the booby pain-yeah.....I'm really hoping mine will go away when I take out all the badness....I think the seroma has just been there tho since nov and that that is the culprit......I just hope they can remove all the scarring etc and the new tissue from elsewhere won't give me any issues.

Betsy sounds as if all is progressing! cool,

thanks ladies-ps.......my avatar is a painting of St. Agatha-she's the patron saint of breast cancer(and multiple other causes)-you know how we catholics are!


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 21, 2009 08:59 pm Boo307 wrote:

PlanJane,  I'm sorry to hear that the seroma still isn't healed.  Don't you hate waiting for test results?

You wouldn't want to suggest that BC.org add information about the permenant change to tissue caused by radiation in their "Ten Key Points About Radiation Therapy"?  I've made suggestions to fill out the radiation information and they added an item under Lump vs. Mast pros and cons.  They need to explain more about radiation.  It isn't really a side effect when all tissue is permenantly changed.  It is a consequence of that therapy. 

Betsy

plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 22, 2009 02:08 pm plainjane64 wrote:

No...I think it's a great idea. Guess I didn't realize the lack of info since I read and read from multiple sources.  Sorry being a nurse may have given me a bit of a leg up.....or maybe more like I'm obsessed!   I think it's lousy people don't know more...I was glad I knew....I feel the nasty secret kept from me was unresolved seroma/lymphedema being a pretty common side effect/complication? following breast surgery.   And the lack of attention to it/patronizing comments by the people whose work caused it.  SORRY to drone on!  My breast is less red but still lumpy/uncomfortable, ugly.  Think the fever is gone and by god I don't miss that keflex every 6 hrs.  Have been on the phone all a.m. trying to line up a lymphedema therapist  so that when I return to surgeons office I'll ask for an official referral.  I also have a compressure bra on the way.  Ok, enough about me!  Thanks for listening!


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 22, 2009 07:56 pm Boo307 wrote:

PlaneJane, I developed lymphodema also.  My oncologist sent for a consult to get a glove because I was flying and the therapist found my left arm was larger that the right.  I went to the therapist for three months and we got it down to normal and I've been able to keep it there with manual lymph massage.  I hope yours can also get under control.

At least you don't have the infection and it seems to be getting a little better. 

I finally figured out how to get my diagnosis profiled, although there is no option to add the full bilateral diagnosis.  And I figured out how to add my photo! 

Betsy


Dx 3/18/2008, IDC, 1cm, Stage Ib, Grade 3, 0/1 nodes, ER-/PR-, HER2+
plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 22, 2009 09:17 pm plainjane64 wrote:

Good job Betsy...I could have sworn bilateral was an option?  hmmm,...anyhoo,

Actually I do have an infection and the lymphedema I have is not in the arm...it's in the breast.But YES!  I DO believe it is improving!  I have thought all along that I had truncal edema and should have asserted myself more but it just wasn't ever obvious until I was red feverish, etc.  It's going to be OK tho!  This too shall pass, live and learn!


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-
Boo307
Joined: May 2008
Posts: 38
Jun 23, 2009 10:47 am Boo307 wrote:

PlainJane,  I have read that losing some weight and exercise reduces the severity of lymphodema.  Of course that must be in relation to where you are currently at or below normal weight and/or exercising an ample amount now.  No easy answers, but just some ideas to manage the situation.

Tracy, How are you doing since having surgery on the 5th?  I hope all went well. 

Sirsmom, Are you still scheduled for July 7th?  We will be pulling for you. 

Betsy 


Dx 3/18/2008, IDC, 1cm, Stage Ib, Grade 3, 0/1 nodes, ER-/PR-, HER2+
HollyHopes
North Hollywood, CA
Joined: Feb 2007
Posts: 494
Jun 23, 2009 03:26 pm HollyHopes wrote:

Hi Jane and all....Jane - I had tons of problems with a seroma all of which seem to have disappeared since the reduction surgery.  Maybe that will happen for you too...and I will be sending lots of good energy your way for healing....

...treatment completed 8/31/07...reconstruction surgery 5/14/09
Dx 2/7/2007, IDC, 1cm, Stage II, Grade 3, 0/3 nodes, ER-/PR-, HER2-
NativeMaine…
ME
Joined: Mar 2007
Posts: 766
Jun 23, 2009 07:35 pm NativeMainer wrote:

plainjane--

you are so lucky.  When I had my radiation consult the doc told me the normal cells completely recover from radiation, that only any bc cells left behind would be damaged.   A bald-faced lie, like much of the other info I was given, as evidenced by the truncal lymphedema, severe pain syndrome, recurrent abscesses, and hyperbaric treatments that led to a mastectomy last summer.  At this point I don't believe anything a provider tells me without making them back it up with research.  I've gotten a reputation for being a "difficult" and "suspicious" patient.  Not that I care what they think of me, I'm paying them, not the other way around.  You'd think there would be some sort of standard of information that has to be given to women before getting radiation, just like all the potential complications and side effects of sugery or a medicine. 

dx 3/07, Stage 2, Grade 2 IDC, 2.8cm, ER+PR+, Her2(-), SN-, lumpectomy & rads, mastectomy 8/15/08
plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 23, 2009 09:43 pm plainjane64 wrote:

WOW

Native mainer...........I am Soooo sorry that happened.....eeeks recurrent abscess! and hyperbaric!  ....OK, I'm sorry, so sorry....BUT.......if you don't mind me asking, did you reconstruct?  Sheesh after all that-and my new education on LE....yikes...I am definitely rethinking and will be doing some serious grilling in regards to seroma/abscess/LE that I might expect.........Perhaps I'm delusional in my expectations for truthfulness from the docs....BUT....I'm trying to also get a feel via LE therapists and people who have done similar to what I'd like to do....to see if I really want to do it.  I might PM you...feel free to pm me...ok...so sorry for what you had to go thru.

Holly, that is awesome news!  where was your seroma?...And did they aspirate yours?.mine is in a very difficult lateral L breast area....after my first f/u mammo in may that was normal I discussed what I thought I wanted to do w/ my BS....when I asked if I could still do skin sparing she did indicate that my scar which is L lateral and horizontal....(.but you can't see it unless I turn sideways) she'd probably extend to areola.......since the nipple is removed and moved up(if it is deemed clean).....of course if there is any suspicion of ca or the ca was withinn I think 2 cm-depending on who is doing your work they may just replace w/ another at the final stage....ok, sorry I'm droning on here.  Holly thanks for the good wishes.

Betsy, I believe you are right....and I'd love to drop a few lbs .......I'm a big fan of exercise just am at a bit of an impasse.  Pretty restricted and will resume and hopefully get back to where I was. I've been in pretty good shape most my life, strength train/aerobic dance, cardio and circuit training, etc, etc.....ever since I've tried to get back into it...even going slowly I have to back off because I start having pain/swelling....this most recent issue is the only time tho I've had redness/fever.  So...I see an LE hopefully next week and will very carefully and compliantly proceed again but this time by someone else's direction/time table....I get a little overenthusiastic.


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-
carolynf
So Berwick, ME
Joined: Dec 2007
Posts: 248
Jun 23, 2009 09:47 pm carolynf wrote:

Betsy: Thanks for the great info.  I will need to take some time and review the info.  I think I will also need to look at a PS w/all the quals for working on a Rad Breast.  I need to find out if its better to wait a longggggggg time or does it matter how long after radiation you have the surgery done.  TOOO many questions.

 Holly:  Sounds like things are moving on.  You sound like things are moving on for the good.  Kudos to you.

NativeMainer:  I am curious as to what hospital you went to because I think I want to stay away from there!  My onc. is in York.  I feel very comfortable with him.  He's a smart cookie and has been up front with me thru everything.  He may not totally agree w/what I say but he listens.

PlainJane:  My girlfriend only had rads and ended up w/lymphedema in her arm and breast.  She gets a massage 2x a week and insurance pays.  She also swears by wearing a compression shirt.  I had lymphedema in my arm and had PT 2x a week which really helped.  Good luck.

Carolyn
Dx 10/26/2007, IDC, 1cm, Stage I, Grade 3, 0/7 nodes, ER-/PR-, HER2-
plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 23, 2009 10:24 pm plainjane64 wrote:

Carolyn,

Thanks, Re the how long after radiation.  I think and have heard the longer, more time that passes the better...BUT...My BS specifically said 6 mos after rads I could have lift/realign if I wanted.  Considering my current issues......I doubt they'd do surgery w/ active infection.  I read on the bresatcenter.com  website you should be 4 mos out of rads to have perforator recon surgery.

per the 2-3 LE therapists I've spoken w/ here is a LOT of post RADS truncal LE that they are seeing and apparently it is the topic of frequent discussions at their conferences. Yet the MD's just don't admit to it...and don't really know what to do about it.

So it is 100plus humidity here in TX...what is it like in Maine so I can live vicariously?


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-
tkone
Seattle, WA
Joined: Jul 2008
Posts: 293
Jun 24, 2009 01:20 am tkone wrote:

Had my last two anchor stitches out today.  I have a couple of spots in my scar that aren't completely closed, but otherwise, everything looks good.  The swelling is going down much better on the radiated side than on the other side.  So far, so good!

Tracy http://tracy-breastcancerandme.blogspot.com/
Dx 5/7/2008, IDC, 2cm, Stage II, Grade 3, 0/4 nodes, ER+/PR+, HER2-
carolynf
So Berwick, ME
Joined: Dec 2007
Posts: 248
Jun 24, 2009 07:57 am carolynf wrote:

Plainjane,

That's good to know at least how long to wait before the recon surgery. I think i need to talk to some therapist here to see if they are seeing the same thing. That's very interesting and esp if the docs aren't admitting to something that is affecting a bunch of us which should be told.

Sounds like the weather down in TX is better here! We have been having rain for the past 2 weeks or it might be most of the month of June. It's very depressing! My plants are not doing to good w/all this rain and no sunshine. Looking at the long range forecast, we should be seeing some of the sun on Friday! I hope the weatherman are wrong as usual and it comes out before that. I have to go out and inspect a house lot in the pouring rain and am not looking forward to that!

Carolyn
Dx 10/26/2007, IDC, 1cm, Stage I, Grade 3, 0/7 nodes, ER-/PR-, HER2-
NativeMaine…
ME
Joined: Mar 2007
Posts: 766
Jun 24, 2009 03:37 pm NativeMainer wrote:

I got radiation at MaineGeneral Medical Center in Waterville.  Dr. Glen Healey was the doc that told me that normal tissue recovers completely from radiation.  I was seeing a med onc there, too until they "lost" my records in the move to their new, "state-of-the-art" buidling in Augusta. I was never comfortable at MaineGeneral, but I couldn't afford to go anywhere else at the time, and was so freaked out by all the delays up to that point (found the lump in Jan, didn't get mammogram results from my primary until 4 weeks later, didn't see surgeon until March, couldn't get in to see med onc and rad onc until May, couldn't start radiation until June) that I didn't dare take any more time to look for a center where I would feel like a human being and not like a piece of meat on an assembly line.   I finally found a medical oncologist, Nicolette Erikson, in Lewiston who is fantastic.  The office staff there are great, too, always returning my calls the same day, haven't yet had the wrong chart when they call me in for my appointments, and treat me like a real human being. 

I am planning reconstruction next June.  I'm taking this summer "off" from surgeries, complications, and living my life around cancer appointments.  This is also giving me enough time to thouroughly think through everything and be sure that I know all my options before making a final decision and committment.  No more nasty surprises for me!  Not to mention that I am now so afraid of needles that I have to be sedated before they try to start an IV (it usually takes 4 or 5 tries to get one in).  I'm going to make sure that I'm not treated like a child or suffer needlessly during the recon process.  I'm going to find docs and hospitals that will do what I want and need,not just plug me into "the system." "This is how we usually do this" isn't going to cut it with me this time through. 

dx 3/07, Stage 2, Grade 2 IDC, 2.8cm, ER+PR+, Her2(-), SN-, lumpectomy & rads, mastectomy 8/15/08
Roya
Paris
Joined: May 2008
Posts: 338
Jun 24, 2009 05:03 pm Roya wrote:

I am planning a lift in February.  I had a lumpectomy last June, chemo Aug-Dec, rads Jan.-Feb.

I was told that it was recommended to wait one year from the last rads tx to do surgeries such as lifts etc in order to allow the skin and breast tissues to completely heal.  There are possible hindrances to proper healing if surgeries are performed too soon past radiation.  Even now I notice that my radiated breast remains slightly darker than the other.  It is also still slightly larger than the other. It takes a while for the tisues to settle.  When I went for my 1st post op mammo last week the tech told me that rads make the breasts more thicker and more  dense than previously.  They had to do a magnifying mammo along with the routine one because ot these changes.

Believe!
Dx 5/2008, IDC, 2cm, Stage II, Grade 3, 0/5 nodes, ER-/PR-, HER2-
plainjane64…
Irving, TX
Joined: Jan 2009
Posts: 435
Jun 24, 2009 06:18 pm plainjane64 wrote:

I do....think sure- a year is probably better....as opposed to 6 mos....and may even decide to wait longer.....nonetheless.......part of me feels I've waited long enough....and honestly HATE waiting for the other shoe to drop.  Part of me would do whatever ot takes to get this monkey off my back....the thing is.............. it just isn't that easy!  I see my md for f/u re; last weeks infection/cellulitis and appt w/ PS  number 1 on monday following appt w/ LE and fit for compression bra............I view all this as good....I know now EXACTLY what to ask about in regards to post op/complications in general......I remain positive yet informed.  I'll let you guys know!  ps....all my cultures came back negative, per md phone call/check in w/ me today.  I'm going back to work tommorrow.  Still a teeny bit pink/swollen but able to tolerate some compression and 4-5 more days antibiotics...pretty sure the fever gone...I really need to go buy a thermometer.  Have a fab wed.  Rain cooling the 100 plus summer day here............jealous of all you mild temp area folks. 


Dx 10/18/2008, IDC, <1cm, Stage I, Grade 1, 0/4 nodes, ER+/PR+, HER2-

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