August 2013 Surgeries

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  • poodle_mum
    poodle_mum Member Posts: 83
    edited May 2014

    Thanks Pam.  Right now, anything that will get me through the next three weeks is helpful.  It really is.

  • wrenn
    wrenn Member Posts: 2,707
    edited May 2014

    No tips here poodlemum, I am "flat", which means lumpy with wings under my arms so can't help but I wish you the best for your upcoming surgery. Take care of yourself.

  • VintageGal1111
    VintageGal1111 Member Posts: 705
    edited May 2014

    Hi Poodle Mum

    I had no choice so didn't give it much thought. But I will say my teeny breasts were never a BIG part of me LOL I always wore a padded bra, never had cleavage so didn't wear revealing clothing & honestly they weren't a major part in sex play. 

    I guess we just accept things as they are. Ya know, that old "it is what it is". I don't like what I see in the mirror naked. Specially now with my chest burned to a crisp & peeling & leathery from rads. I don't like how my sternum sticks out like a skinny old chicken & both my sides cave in. But with my little soft foobs in my stretch bra I looked just as I did before when I am dressed. 

    Maybe this is a good time to seek help from a therapist. Maybe it isn't the actual loss of nipples that is bothering you. Perhaps it is more but right now that is your focus? 

    All the best to you.

  • KBeee
    KBeee Member Posts: 5,109
    edited May 2014

    Poodlemum, I am sorry that you are struggling with this.  My tumor was very close to my nipple, so I had no choice.  It really did not bother me; I just wanted all traces of the cancer gone, so I was fine with seeing them go.  I have reconstructed ones now, and though I have had some complications with their healing, they look decent now.

  • poodle_mum
    poodle_mum Member Posts: 83
    edited June 2014

    Hi everyone - 

    I just wanted to give you all an update.  I went in May 27th and found out I had to have a total mastectomy.  Last August I had the nipple sparing.  

    I had surgery June 20th. I had a fast growing mass that at the time of surgery was over 5cm and had a break-away section.  She was able to get everything out.  She said it was a lot of work but there is absolutely nothing there now.  Thankfully no nodes were affected, but she wants yearly scans of my nodes.

    I also need to be tested for BRCA.  I have drains and she will remove them on Wednesday.  Her method is to go topless (open to air) and never leaves drains in longer than 5 days.

    If I have any waves or anything I'm not comfortable with 6 months from now, she will go in and clean that up.  I'm not a candidate for reconstruction and I don't want it either.

    I am home with nursing care and extremely lucky. Who knew I'd go in for preventative surgery and end up with low grade DCIS and 10 months less 2 days I would be in surgery for invasive cancer?  Oh well, it is what it is.  I hope all of you ladies are doing well and I thank you for everything over the past 10 months.

    All the best to you.

  • KBeee
    KBeee Member Posts: 5,109
    edited June 2014

    Poodlemum, I am so sorry that you've had to go through all of that.  I hope BRCA comes back negative. Hope you get those dang drains out soon. I am sorry you had to have them, but glad that you are on top of things and got this quick-growing beast removed.

    Lili, How are you doing?

    Wren, Feeling any better?

    Babs, Healing OK?

    Everyone else???? How's everyone doing?????

    I had follow up today with BS today about the lumps that came after fat grafting. He explained his rationale for not ordering ultrasound based on the fact that the fat cells in the lump would look like other fat cells on ultrasound. He first said that the lumps were fat necrosis and that the biopsy showed lipocytes. I politely corrected/questioned him (since I had asked for copy of my biopsy results and knew it said lymphocytes).  He did go and double check my biopsy results and said that they were in fact lymphocytes and not lipocytes, and said that since I am thin, maybe my lymph nodes are more on the surface. Um.....just on one side???!!!   He still did not see a value in an ultrasound, but said he would send a note to MO and have him make the final call. Moral of the story is if you do not have a copy of all of your biopsy results, get them in your hands!!!!! I now will have to work on MO to see if he'll order the ultrasound. I think he may do that. He'll see more value in having a baseline than the surgeon, who said we could always remove them if they are bothersome, but did say it was better to wait and see. I tried to explain that I was not wanting it to rule out anything now since the fine needle aspiration was negative, but so that we have a baseline, so if there are changes over the course of the next 6 months or so, we have something to which to compare it. Since there are several lumps, I do not trust my fingers to remember which are new and which are not. He thought we'd be able to.  He thought that based on my tumor stats and treatment, my risk of recurrence was really low. I wanted to scream...my risk of BC was even lower than that statistically, but here I am! I didn't...by that time I decided that I would see what MO has to say..................I think (hope) he will be more open minded to it, especially since his PA asked if he had ordered one previously..........I see him on Wednesday.  Wish me luck!

  • wrenn
    wrenn Member Posts: 2,707
    edited June 2014

    Karen, I can't imagine what you are going through. The frustration must be horrible. I am so glad you are pushing and able to keep on top of it but sorry you have to struggle. Sometimes I wonder if some docs are still living in the 50s....blind to anything new and just reciting what they learned in school. My MO is like that but my GP listens.

    Good luck and keep us posted on the outcome. Again sorry this is happening to someone who doesn't deserve it.

    Poodlemum, sorry for what you are going through too. It is endless isn't it?  Hang in there. You still sound strong.

    All good here except for the damned neuropathy. Take care everyone. xo

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited June 2014

    sorry Poodlemum-- what a long year for you! At least it was caught and removed, and can now carry on. Hope your recovery is a smooth one...

    I just had my 2d exchange (smaller, diff shape, with lipo), and think Im about done with it. Taking arimidex, got lucky no chemo or rads...maybe some tatts instead of nipples!

  • Jo6202
    Jo6202 Member Posts: 372
    edited June 2014

    Poodlemum, All I can say is wow! You are living my fear...that breast cancer is just going to keep on taking and taking. I have to have another mammo in three months because there is something showing that I hope is just a Seroma but who knows. Hope your drains come out soon and that your testing goes well.

    Karen, how frustrating to have to push for testing. Seems like they (doctors) would want to be sure too. I can't see why they wouldn't just order an ultrasound. Good thing you were on top of things with your biopsy report. 

  • KBeee
    KBeee Member Posts: 5,109
    edited August 2014

    How 'bout a 1 year check-in???  How are all of our Aug 13 ladies doing???

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited August 2014

    I'm good. Onco score of 2, no chemo or rads.  Reconstruction has been ok tho one revision done and will have one more in November...just to adjust one size, finish Lipo and fix a thick scar.  I'm still on the birds, try to give encouragement to newbies.

  • jbdayton
    jbdayton Member Posts: 700
    edited August 2014

    it has been a wild year.  

    I did radiation during October and November.  I lost my mother 2 days before finishing radiation.  Had a gastric flair up Thanksgiving and was given meds to resolve those issues.  Husband said he thought it was gallbladder but doctors said no. 

    In March I did a bilateral DIEP reconstruction.  Woke up with only one breast reconstructed, luckily the radiated one. Had some minor healing issues with my belly incision and a small area on the breast.

    In June I did a Ruben's flap for my other breast.  Had major complications, lower incision opened back up after the staples were removed.  Had to do wet/dry packing for 8 weeks then decided to hook up a wound vac to assist in healing, had that for 3 weeks.  Got the pump off off on Friday then on Sunday started having bad gastric pains.  Took all the gastric meds I got at thanksgiving.  By Friday not getting better, so I went to my GP and he had tests run and said gallbladder was ripe and I needed to go get checked in to the hospital and get it removed immediately.  That was August 17.

    I have a followup appointment this afternoon with the surgeon.  Too many surgeries this year.  I think I am just going to heal and maybe start finishing revisions next year.  I did not anticipate all these hick ups.  Oh well, could have been worse.  

    Hope everyone else is moving along nicely.

    Hard to believe it was a year ago we were all going through our mastectomies.

  • VintageGal1111
    VintageGal1111 Member Posts: 705
    edited August 2014

    What a difference a year makes! So many mixed emotions looking back. At times I hought I'd never get through it all, the bald chemo sick Winter lasted forever. Then at times I cannot believe it has been a year, time does flies.

    I am doing well. A year tomorrow I had what I thought would be a fairly mundane lumpectomy. Then have rads. But I ended up waking from surgery to be told there was lymph node involvement and a port was placed for chemo. And the report came back no clean margins. So...A&C, (ugh!) then 12 weeks of Taxol/Herceptin. Then BMX in March (no recon!) quick trip next day back to OR for re-incision & evacuation of blood, then radiation for 6 weeks & now finally just have 3 more Herceptin infusions to go!

    Life is good. It's good because I am alive. We only have today, nothing else is guaranteed. I may only have 1.5" of hair growth after 7 months post chemo, I may have more wrinkles & more sags (at age 60) and I may have a concave scrawny flat chest but I also got my lashes & brows back, I healed well, got back to the gym, am enjoying being on the motorcycle, going in the motor home, still buying & selling other people's old stuff, painting furniture & just loving family, pets & home.

  • KBeee
    KBeee Member Posts: 5,109
    edited August 2014

    I healed fine after BMX.  I did 4 rounds of TC chemo, then had exchange surgery over the winter and nipple reconstruction and fat grafting in early spring.  I have healed well from everything, but developed lumps after fat grafting.  One was biopsied and is inflammation.  Others that have developed since were assessed by ultrasound and since there's some cortical thickening of 2 lymph nodes, they will be reassessed in November and biopsied if still enlarged.  I am thinking it is just more inflammation.  My body seems to like making inflammation...developed carpal tunnel, cubital tunnel (elbow) and trigger thumb in the months that followed chemo.  I am back to work now and trying to just enjoy life and not think about cancer all the time!  Hard to believe it's been a year.  Time stood still in the 3 weeks between diagnosis and BMX and also during chemo, but it has flown by since!

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited August 2014

    the best part is we are here to tell our stories.

  • jbdayton
    jbdayton Member Posts: 700
    edited August 2014
  • ndgrrl
    ndgrrl Member Posts: 741
    edited August 2014


    My one year anniversary was on August 19.  I had my first MRI yesterday , it was good news!!  I have been fretting wanting one for a year. I just have a cyst I have been watching every 6 months and that seroma being watched.  I had a lumpectomy with 7 lymph nodes removed and they were all negative so I was lucky. I qualified for high dose internal radiation so that was done twice a day for 5 days and then a trip to the ER and a couple days in the hospital for dehydration.  My sister was diagnosed with breast cancer the day I went to the ER, but she is also doing well. Along with my cousin and neice also diagnosed in 2013.  I returned to work with my doctors note stating I was well enough to return only to find out my job was eliminated but after a few months I found another part time job as an advocate with domestic violence and as the county victims advocate.

    As I look back I realize how nothing is cut and dry- everyone is different and every decision has to be made quickly for what you want for yourself. No one can tell us what to do. I have had people come up to me and say why didn't you just cut them off?  Then you would be done. and I just say that is not what I wanted. if I need to at some point then I will decide that now.

    Its been one learning year for sure!!

    I wish everyone well!! :)

  • wrenn
    wrenn Member Posts: 2,707
    edited August 2014

    I can't believe it's been a year. So glad to see you folks doing well. It has been an eventful year for sure. I had surgery August 16th and had homecare coming daily or every other day until boxing day. I still feel weird getting in the shower without wearing plastic bags. It is so freeing. I had a BMX and 6 clear nodes removed. I am triple neg so should have started chemo earlier than the date I started (Nov 25th). I developed diverticulitis so was cut off chemo and saw onc in 4 months and now see him every 6 months.

    I am about to have a D&C to biopsy my thickened uterine lining. I was spotting and cramping (not good at age 67) and am not looking forward to another anesthetic but for some reason I am not worried about outcome.

    I have peripheral neuropathy which shouldn't happen from one infusion of taxotere/cytoxan but I think that combined with the cipro/flagyl for the diverticulitis the same week is what caused it. I am having trouble walking but still really feel pretty good especially when I read what other's endure.

    The weirdest chemo side effect is my curley hair. I had really straight hair before and now I look like I got an old lady perm. It is growing very slowly but picked up some after starting on synthroid. I became hypothyroid in the spring and the meds seemed to make my hair grow faster.

    I guess my post seems to have a lot of complaints but really I feel lucky and am happy to be here. I hope more of the woman check in. This was a nice idea to start this thread.

    Take care everyone. xoxo

  • babs6287
    babs6287 Member Posts: 2,021
    edited September 2014

    Hello to all my wonderful brave friends.  So happy we're all here 1 year later!!!!  We rock!!!!!!!!!!!!!!!

    Poodlemum so sorry for all you've been through!  Karen, praying everything turns out to just be inflammations.

    I can't believe it's 2 years since my Ca diagnosis (8/17), 2 years since my first mastectomy (8/24) and 1 year since my prophylactic mastectomy (8/29).  I go back to my PS next week to discuss and finalize my next surgery.  Hoping it's my last!!!!  I had my second FG on 5/22 and for the first time, I did NOT get an infection.  I think the first FG worked and improved the integrity of my skin- at last.  The next surgery is an exchange on the right with a reduction and a lift and a small implant on the left (my compromised side).  I am tired from all of this.  If the implant doesn't work, then I'll just be a uni-boober.  I don't mind because the FG gave me some upper pole fullness so I'm no longer concave in tanks and bathing suits.  

    My MO recently wanted to move me from visits every 3 months to every 6  months visits but I declined-just too nervous.  I think we all get nervous easily now.  

    Please all be well and take great care of yourselves,

    Babs

  • poodle_mum
    poodle_mum Member Posts: 83
    edited September 2014

    Hello ladies!  Here's my update.

    As you know I had DCIS last August, nipple sparing.  A growth came up in November that they thought at first was scar tissue due to the complications of my seromas.  I went on chemo, the growth continued. In March they canned the chemo since it was an obvious growth, scar tissue doesn't grow! :-)

    I was too sick to have surgery so they had to wait it out.  IDC so continual x-rays, etc to make sure it wasn't spreading into the ribcage. Ultimately I had surgery June 20th. 4.5x5x4cm - she had to go slightly under the ribcage.  Pathology reports came back three weeks later - she got it all.  She seriously wasn't sure she was going to get it - but it's all gone - I'm cancer free!!! I joined Flat and Fabulous on Facebook and I love it. No complications from this surgery. Drains came out in 5 days. Small seromas on each side near drain sites.  The left one has almost totally reabsorbed.  The right one is still on its way to reabsorbing but it will do fine. She's going to see me in March (she "accidentally got pregnant" so my 6 month check up had to be postponed).  She will decide at that time if she or I want to go back in for some minor clean up of any extra skin that may not flatten out completely. I go in January for my BRCA assessment.

    So all in all, I'm doing great.  Slowly getting back into my normal routine. I have to remember to slow down a bit and not do too much since I have to do everything with my arms and I tend to forget until "after the fact" that I'm still healing. I'm using pure coconut oil on the incisions and area to loosen it up - the tightness in the morning was awful.  So once the incisions were clear and free and fully healed up, I started using the coconut oil twice a day and it's really helped a lot.  My porcupine is totally untamed, it's coming in thicker than it was before the chemo, sadly the grey still decided to return, but that's alright.

    I lost my grandma 4 weeks after surgery. We thought we were going to lose her last summer and against the advice of my family, I told her I had breast cancer and would be having surgery, she hung on and went home to her apartment.  In and out of the hospital over the year. She had gangrene in her legs that was spreading throughout her body.  In May they told us she would probably be gone within 3 weeks.  A week or so later I found out I would be having my surgery and showed her the tumour which was quite prominent.  She held on.  She was in the hospital shortly after I had my surgery but came home and celebrated her 93rd birthday July 3rd.  She was back in the hospital the following week and then I had my follow-up on the Tuesday two weeks later.  She asked Mum how I was doing and if I was well enough to "officiate" her funeral.  Mum said yes and my grandma went home the following day and passed away almost exactly 24 hours after she heard that I was fine.  She was more of a parent to me than a grandmother and she fought to stay here this past year until she knew I was ok.  It did set me back a bit - developed the right seroma (very small) on the right side because I had to use my crutches for the time of funeral, etc. But here I am!

    I haven't tried using my manual chair yet because of the movement and I want to ease into it and not do anything stupid. 

    I also signed up for the CIBC walk again this year and I've raised over $2,030 (I raised $1,030 last year) and I'm still raising more for the next month.  So, as crappy and hard a year as it has been - I'm pleased to say - I'm healthy, I'm happy and I'm alive and here to stay! :-D

  • wrenn
    wrenn Member Posts: 2,707
    edited September 2014

    what a nice post poodle um.  I knew you would kick it and be back in good shape.  Good to see you too Babs.  Hopefully soon you will be finished with all the surgeries as well. it is a long haul this stuff.  Take care everyone. 

  • ndgrrl
    ndgrrl Member Posts: 741
    edited October 2014


    Hi past August surgeries , we are all a year out now :)  I have a question does anyone else still have pain where the incision was if you had a Lumpectomy?  I still do and its actually sunk in some. My bra rubs the spot so that doesn't help either I am sure. I do see my radiologist this week for I hope my final checkup as its been a year since internal radiation.

  • jbdayton
    jbdayton Member Posts: 700
    edited October 2014

    Sorry you are still having pain.  I would check with the PS and ask for some fat grafting.  I just had fat grafted this past Monday.  I am pleased with the looks so far.

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited October 2014

    I have about a 3 inch area on one side that is scar that alternately hurts and itches, off and on. It is still raised more than the rest of my scars. Technically its a scar from the lumpectomy/oncoplasty that was done. I have a (final?) surgery coming up in November, Ive asked him to see what he can do about it. Its not infected, but just oddly hasnt settled down like the rest of the scars.

  • babs6287
    babs6287 Member Posts: 2,021
    edited February 2015

    Hi All my August sisters,

    I just read my last post here-so ironic. I wrote in it that my onco wanted to move me from visits every 3 mos to visits every 6 but I wouldn't let her do that. Good thing. In October all was fine. In Jan at my visit both my cancer markers were high-more than double. She had me retested and they were still high. Had a PET/CT scan-nothing lit up but there were some lymph nodes that were "enlarged." I had a biopsy of one on my right (non-cancer side) side first and it was benign. Had another on my left clavicle lymph node and I have BC again! I really don't know very much at this point. The onco is waiting for more test results and then we meet on Tuesday-scared but I will deal-what choice do ANY of us have!

    BC really does suck!

    Babs

  • wrenn
    wrenn Member Posts: 2,707
    edited February 2015

    I'm so sorry to hear this news Babs. It seems like such a long time ago but I will always remember that I wouldn't have got through it all without the August surgery sisters. I had complications and although all of us were experiencing the nightmare of discovering and starting on this cancer journey I still felt supported by everyone.

    It is doubly hard to watch sisters struggle through treatment and reconstruction (which I was lucky to avoid) and still not be done with this stuff.

    I guess we know from this forum that it is not a death sentence but really seems to be a life sentence when it comes back. I hope you have lots of support dealing with this and that it can be resolved. Take care. You are in my thoughts.

  • babs6287
    babs6287 Member Posts: 2,021
    edited February 2015

    Thanks so much Wrenn- I am lucky to have a wonderful family (except for my dumb son) and great friends who have all been there 100% throughout all my trials and tribulations-plus all of my BC sisters on line!!!! Even my drs have been amazing. I saw my recon PS for a regular check up a few hours after I found out about my recurrence and he has been amazing. He lives near me and offered to come to my house to talk if needed, hold my hand if needed or to even dop off food for me and my husband if needed. And he called me the next day to just touch base and to make sure I was doing ok. I am blessed with all the support I have. Just really scared.

    Babs

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited February 2015

    so sorry to hear that Babs. I agree-- my August 13 sisters really have helped me thru. Ive had a lucky journey but am still here getting, and hopefully, giving support.. Hang in there girl!

  • babs6287
    babs6287 Member Posts: 2,021
    edited February 2015

    Thanks s much Aviva- these boards do keep me strong!

    Babs

  • KBeee
    KBeee Member Posts: 5,109
    edited February 2015

    Just PM'd you Babs. I am dealing with a recurrence too. I just found out on Monday. I know will know the plan next week.

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