Showing posts with label DIEP flap failure. Show all posts
Showing posts with label DIEP flap failure. Show all posts

Monday, October 25, 2010

Pictures from Surgery

Here are some pictures from before and after my surgery. I think this one worked pretty decently and I actually have a lot more symmetry.


Just before the surgery on October 11, 2010
Waiting for surgery


About a week after the surgery.
The Good Morning America segment about the Penguin Cold Caps has been changed to Thursday October 28th. They said it should be on sometime between 8 and 8:30. I hope it actually airs.
Today is the 29th anniversary of my Mother's death. Its a long time but it certainly doesn't seem like it. RIP MOM.

Tuesday, June 22, 2010

More Surgery Tomorrow

I am having more surgery tomorrow. Of course I am pretty stressed out about it because it is causing me to go back to zero again. They are going to replace the tissue expander with an implant. They are also going to take some fat out of my hip and add it to the right breast to give it a more breast like shape. He told me it wouldn't be enough fat removal to make any noticeable difference. I advised Dr. Keller that I was ok with him taking out more and wasting it was fine with me. He laughed about that but I don't think he is going to do it. Bummer.

There is a big dent in the top of the right breast. That is because they used fat from my abdomen. That fat has a breast like feel but it is not shaped like a breast. It is not supposed to be. They have to do revisions to make it more normal. They would have had to do that and it is not due to error.

The left side is an expander because of the errors. The expander has to come out because it is not made to be in there long term. The other problem with it is that the fill has metal components and it is blocking my MUGA (heart) scan. They have to do the heart scans on me every three months because the herceptin I get every three weeks can be cardio toxic. They want to make sure the drug is not having toxic effects. When I had the MUGA scan with the expander in they had a great deal of difficulty because the metal fill is directly above my left ventricle. The left ventricle is the area they need to see because that is what would thicken if the herceptin is causing congestive heart failure. The expander needs to come out because that scan is essential.

As much as I would like reconstructive success I would almost leave it for now because I am so sick of surgery and treatment in general. I can't because of the scans.

I am biting the bullet and putting some pictures on here. I am doing it because I have received a lot of email from other women who have done theses procedures or are about to do it and they want an honest account of what its like. It is not so great but I wish I had some real honesty when I was getting ready to go there.
This is how it looks right now. There is about a four inch difference in height. Its hard to really see it in the picture. I have looked this way since October.


This is how it looked after the second surgery when they had to remove the transplanted tissue.
I would never put these pictures on here if I actually felt like they were breasts. I don't feel like they are. The tissue feels essentially dead. There is really no sensation because they cut the nerves when they do the mastectomies. I can feel pain to the area but the skin itself really has no sensation. They say that may change but they are not sure. It is different for everyone.
I am hoping that I will have more symmetry after surgery tomorrow. I am hoping that I will not have drains. Dr. Keller said I am not likely to need drains but he couldn't guarantee it.
Julianna is going to Grandma and Pop-Pop's house until Friday morning. After that she is going to go to the O'Brien's house and on Sunday my friend Vanna is going to take her. I am really lucky that she can go be with people she loves and is comfortable with. I am truly grateful to have so many awesome people in my life. Thanks for all the good thoughts, prayers and positive vibes!!!!

Monday, October 12, 2009

Misery and Hope

Everyone, I am sorry I had no chance to update you earlier today. I have been at the hospital all day long.
Mary Ellen had a vein blockage in the transplanted flap tissue on the left side. The surgeon was unable to save the flap.
The worst part is that Mary Ellen told the resident on duty overnight again and again that she thought it was encapsulated, engorged, and without vein function. She told him this very clearly and she was in great pain, The details of this is a long story, but basically she was discounted by a man who had less medical knowledge than Mary Ellen herself. When the surgical people arrived in the morning, she was rushed to the OR stat.
Writhing in pain, frightened and angry, Mary Ellen pushed a random button on her phone and got her friend Colleen. Colleen mobilized. She called Cathy, who ran red lights en route to the hospital in her pajamas, and was able to see Mary Ellen before surgery. I rushed to the hospital, but arrived after she was in surgery.
Several hours later, Dr. Keller came out to tell me they had lost the flap. I waited to see her in recovery, but I did not want to be the person to tell her the flap was lost. The recovery room nurse told me that she already knew, but she was in a lot of pain, and while I was there I just kept advocating for more medication, letting the nurse know that Mary Ellen is particularly tough with a strong constitution and a high pain tolerance, and that she did require more pain killers. They finally relented.
Colleen came in, and as a breast surgery recovery room nurse herself, she quickly discovered that Mary Ellen's drain was full and elevated above her incision. As politely as she could muster, Colleen asked the nurse to empty and lower the drain. The nurse did this, but then kicked Colleen out of recovery.
Colleen and I waited four hours in ME's room, being told she would be brought up "any minute." When she finally came up, we were deep in discussion with the nursing manager about what had gone wrong in the night. An investigation is underway, and Mary Ellen has requested a formal copy of that report.
I told the nurse manager to be absolutely sure that neither the night nurse nor the resident would set foot in Mary Ellen's room or she was sure to bludgeon them with her IV pole and strangle them with the tubes. She agreed to have both of them reassigned.
After quite a while, we finally got some big-picture good news: Dr. Kostroff, the first breast surgeon, who did the mastectomy phase, came in to the room, still in evening clothes, having recently heard of the setback. When ME asked her "how are you?" she said she was almost as devastated as Mary Ellen. She said that although she rarely gives preliminary pathology results, she had to bring ME the early good news:
The cancer might be only stage zero, and there may be no need for chemo. Now, before you all get your hopes too high, there will be more tests done to look for any other cancer that has emerged from the ducts, but so far they have not found any except very small bits of cancer, and the sentinal nodes are negative, so there may be an excellent overall prognosis!!!!
That news helped, but Mary Ellen is still devastated at losing her chance of cosmetic success to a resident's negligence.
Vanna and I helped ME get to the bathroom and then resettled comfortably, and Vanna was going to guard her quiet space so she might sleep, and I left the hospital finally.
I will see her first thing tomorrow. I'm sorry I can't update through the day, but I have no computer access until I get home.
Pray for Mary Ellen to see the big picture, be relieved from pain, and to refrain from justifiable homicide.
More tomorrow, Kathleen