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Author Topic: Reconstructive Surgery  (Read 19679 times)
vandie
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« on: July 07, 2009, 05:44:58 PM »

I will be getting a mastectomy at the end fo the month.  I spoke to a plastic surgeon today.  His plan is to put an extender in at the same time they do the mastectomy.  He will fill that every few weeks until the breast is the right size and then replace that with an implant after 2 or 3 months.

Question:  Has anyone had or known anyone that has had reconstructive surgery while being on immunosupressents?  It is my surgeon's only concern, and mine as well, because of the risk of infection.
He called my neph and is waiting for a call back, but I wanted to throw this on the board and see if anyone had any idea.
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Des
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« Reply #1 on: July 08, 2009, 03:08:11 AM »

Vandie,
My heart goes out to you and I hope everythings goes well.

I was told that I have to have my kidneys out 6 weeks before I have a tranplant because the immunosupressent medication can cause infection in the wound. But.... the doc can use certain types of antibiotics before and after the op to decrease the chance of infection.

Keep us posted.
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
rose1999
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« Reply #2 on: July 08, 2009, 05:01:58 AM »

Vandie I can't offer any advice but I just wanted you to know you are in my thoughts and I hope all goes well for you.  :cuddle;
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monrein
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Might as well smile

« Reply #3 on: July 08, 2009, 01:18:10 PM »

Sending you a truckload of hugs and good thoughts Vandie.  :cuddle;
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
paris
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« Reply #4 on: July 08, 2009, 04:28:04 PM »

Vandie,  I hate that you are going through this.  I will say, my sister in law had a double mastectomy last year, had the expanders and the reconstructive surgery.  She did well, although it is a tough thing to deal with.  Of course, she isn't dealing with the immunosupressent issues.  I hope your doctors can give you some comforting answers.  I am so sorry.  You are always so supportive and I just wish I was closer to be of some help to you.    :cuddle;    Lots of prayers   :cuddle;   :cuddle;
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vandie
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« Reply #5 on: July 09, 2009, 07:23:41 AM »

My plastic surgeon called yesterday and my neph has given his approval for the reconstructive surgery.  As soon as the two surgeons can coordinate, I will get a surgery date.

My only decision to make, and make pretty quickly, is whether or not to have a bilateral mastectomy.  Although I have no history of breast cancer in the family, I know many women who have gotten either a lumpectomy or a unilateral mastectomy only to have the cancer come back with a vengeance.  I don't want to go through this in another year or five years.  I still have a 10-year-old at home and two grown daughters who are my world, not ready to be down and out yet  Getting rid of them both at the same time seems to make the most sense. . . .logically.  Getting my emotions around losing the other breast is a whole differrent ballgame.  I know this is a kidney website, but this is my safe place.  It got me thought so much with ESRD and transplant and you are my family.

I so appreciate the support and the love I receive here.
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Life is the journey, not the destination.
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rose1999
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« Reply #6 on: July 09, 2009, 07:59:06 AM »

I can only offer you love, as you know the decision has to be yours and it will not be an easy one - but whatever you decide we will be here to love and support you. :cuddle;
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willieandwinnie
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« Reply #7 on: July 09, 2009, 08:02:50 AM »

 :grouphug; Oh vandie, I am so sorry. You need to do what you think is best for you and your future. Medicine has come a long way in treating breast cancer since 1965 when I lost my Mom and I was 11. We are your family and will be with you through this even if only in spirit. I wish I lived nearby, I'd be there in a heart beat. Keep us posted and know that we are all praying and thinking about you.  :cuddle;
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thegrammalady
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« Reply #8 on: July 09, 2009, 09:26:23 AM »

i don't dwell on this type of thing however i have thought about what i would do if it happened to me. my first though is "take both" that being said i'm not really sure that's how i would react if i needed to. but that's the direction i lean. i like the idea of not having to worry or having less worry. whatever you decide you are in our thoughts and we wish only the best for you.   :grouphug; :grouphug; :grouphug;
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paris
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« Reply #9 on: July 09, 2009, 12:55:15 PM »

Sweet Vandie, It is a very hard decision to make.  I have had lumps removed and always thought if the resutls came back as cancer, I would have both removed. Just to get it over with and not have to think about it. But, it is a huge emotional decision. We will support you in any decison you make. The only right decision is the one that is right for you.    :cuddle;   :cuddle;
« Last Edit: July 10, 2009, 07:34:12 AM by paris » Logged



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« Reply #10 on: July 09, 2009, 01:38:18 PM »


I also have thought I would do both and have reconstruction bi-laterally - but maybe that's because I like things to be symmetrical. I have not had to face the emotional challenge of this vandie, and I know it must be tough. Best wishes whatever you decide.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
glitter
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« Reply #11 on: July 09, 2009, 10:09:36 PM »

Vandie- I want you to know you  will stay in my thoughts. I think you should do whatever will keep you alive and cancer free. Whatever you decide- we will all be here to support you in any way we can.  I hope you heal beautifully and I hope the reconstuctive surgury heals swiftly.

This may be a kidney website, but its my safe place too.    Julie
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Jack A Adams July 2, 1957--Feb. 28, 2009
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paris
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« Reply #12 on: July 10, 2009, 07:35:10 AM »

You are continually in my prayers.    :grouphug;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
vandie
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« Reply #13 on: July 10, 2009, 10:17:26 PM »

I told my surgeon yesterday I would be getting a bilateral mastectomy.  He agreed and sent in the authorization today.  As soon as that is approved, we will get a date.  Probably early August.  The sooner the better for me.  Just want to start and finish this whole thing.  It's going to be a several month process from surgery to new breasts, and I just need to get it going.  I will keep you all all updated.

ps.. . . . I saw my neph yesterday too, and my kidney is still running super-duper!!

xoxo
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rose1999
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« Reply #14 on: July 10, 2009, 10:31:41 PM »

You are a brave and sensible lady but it can't have been an easy decision.  I am truly in awe of the way you are dealing with this.  I hope you have a successful surgery and heal well, I will keep you in my prayers.  Fantastic news on the kidney. :thumbup;
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Zach
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« Reply #15 on: July 11, 2009, 06:46:02 AM »

Sending my love and prayers.
 
:-*
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
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No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
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lola
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« Reply #16 on: July 11, 2009, 07:06:28 AM »

Good luck Vans, xoxoxoxo :cuddle;
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kitkatz
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« Reply #17 on: July 11, 2009, 06:55:32 PM »

HEy Sweetie! I hope things go good for you.
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Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
donnia
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me and my donor Joyce

« Reply #18 on: July 12, 2009, 06:18:47 PM »

Hugs and Prayers Vandie! 

I'm not sure what immunosuppresents you are on, but when I had my hip surgery they took me off of Rapamune and switched me to Prograf for a while because Rapamune hinders healing.  If you are on Rapamune and they do decide to switch you to Prograf, I would suggest you switch at least 2 weeks ahead of time.  I switched only a few days before and it played havoc on my tummy and umm....  and bowels.  Wish I had gotten over that before I had the surgery.... instead I was trying to recover from surgery and had a double hard time with my bowels. 

Hope everything goes well and I will continue to keep you in my prayers!!!!   :flower;
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Born with one kidney 1972
Ureter re-constructured 1975 (reflux had already damaged the kidney)
Diagnosed and treated for high blood pressure 2000
Diagnosed ESRF October 2006
Started dialysis September 2007
Last dialysis June 4, 2008
Transplant from my hero, Joyce, June 5, 2008
monrein
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« Reply #19 on: July 12, 2009, 06:45:12 PM »

It must feel good to have come to a decision and it will feel even better when it's all behind you.   :flower; :cuddle; :flower;
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #20 on: July 12, 2009, 08:32:38 PM »

You are amazing.  Thinking of and praying for you at this time.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
paris
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« Reply #21 on: July 16, 2009, 05:08:33 PM »

I have shared your story with my sister in law who was down this road 2 years ago.  You're in her prayers too.  She is now glad she opted to have both removed.  You are a very brave and strong woman. We are here for you, especially during the next few weeks.  Sending you much love   :cuddle;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Jill D.
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« Reply #22 on: July 16, 2009, 05:27:07 PM »

Sending you love, hope, strength and support. I'm glad you posted the question about surgery and immunosuppressants as I have always wondered about that as well with any type of surgery.

It sounds like you have very good doctors and surgeons that are looking out for you and listening to your concerns. Oh Vandie, I will keep you in my prayers!!!
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Diagnosed with FSGS in1990.
Started hemodialysis in April 2006.
Received a new kidney from my sister on Dec. 5, 2006.
Transplant rejection in March, 2009
Approved for second transplant in May 2009
Sister-in-law approved as donor in Dec 2009
vandie
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« Reply #23 on: July 17, 2009, 08:46:11 PM »

We have a tentative date of August 14th for surgery.  The surgeons are coordinated.  Just have to confirm with the hospital.

I will tell you that this has been the craziest of rides.  When I was diagnosed with kidney disease, I came to this board and I realized that my job is to meet every challenge head on because my daughters deserve all that I have to give.  They have been through so much, as I know you all understand having to deal with ESRD and what it does to your family, I want easy for them.  I don't want them to worry again or hurt again because their mama is sick.  That is the most heartbreaking of things when I hit a hurdle like this.

I love my IHD family and am so appreciative that I have you in my corner.

xoxo







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Life is the journey, not the destination.
_________________________________________
I received a kidney transplant on August 4, 2007.
okarol
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« Reply #24 on: July 17, 2009, 08:58:56 PM »


You are a great example for your girls Vandie - and you will get through this fine.
 :grouphug; :grouphug; :grouphug;
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
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