mastectomy, radiation and reconstruction
Anyone else faced this? I hear of so many women having reconstruction at the same time as the mastectomy. I hate the thought of having all that time pass and them enduring another major surgery. Wish I could do it all at once.
thanks,
maddie
Comments
-
I did have the same situation. My rad onc and my plastic surgeon were opposed to having implants at the time of mastectomy, but my plastic surgeon agreed to do it anyway. As it turned out my plastic surgeon got sick on the day of my surgery and I didn't have them. For me it turned out to be lucky. I also had 22 nodes and had a lot more radiation than I expected. After my surgery I developed seromas and had to have them drained weekly for quite awhile. I've also developed lymphedema in my arm and trunk. So, as it turns out that even though I'm dissappointed that I can't consider surgery until next summer, (finished all treatments in July) I'm glad not to be dealing with implants now. I also saw a new plastic surgeon (mine was really sick). She will not do simple implants because of the amount of radiation, so my only option is Latisimus flaps (I won't do TRAM flap. A lot of surgery so I don't know if I'm going to do anything.
I hope this isn't too discouraging, but the day of my mastectomy my plastic surg and I agreed there must be a reason for this and as it turned out there seemed to be.
I know how tough it is making all these decisions and wish you the best.
She0 -
Why won't you do the TRAM flap? Too much surgery and recovery? That's what worries me.3cbrca said:I did have the same situation. My rad onc and my plastic surgeon were opposed to having implants at the time of mastectomy, but my plastic surgeon agreed to do it anyway. As it turned out my plastic surgeon got sick on the day of my surgery and I didn't have them. For me it turned out to be lucky. I also had 22 nodes and had a lot more radiation than I expected. After my surgery I developed seromas and had to have them drained weekly for quite awhile. I've also developed lymphedema in my arm and trunk. So, as it turns out that even though I'm dissappointed that I can't consider surgery until next summer, (finished all treatments in July) I'm glad not to be dealing with implants now. I also saw a new plastic surgeon (mine was really sick). She will not do simple implants because of the amount of radiation, so my only option is Latisimus flaps (I won't do TRAM flap. A lot of surgery so I don't know if I'm going to do anything.
I hope this isn't too discouraging, but the day of my mastectomy my plastic surg and I agreed there must be a reason for this and as it turned out there seemed to be.
I know how tough it is making all these decisions and wish you the best.
She
I saw your post about your lymphedema - sounds horrible. I wish you the best with that.
-maddie0 -
I've heard too many stories about the damage to the abdominal muscles. I'm fairly active and have arthritis in my lower back so I need to hang on to those muscles. I think the Tram and the LAT flap sound about the same in terms of recovery-both more than the implants. I have a friend who has had one of each. She was really excited about the TRAM and it turned out that she was more satisfied with the LAT, although she has no real problems with her Abdominal muscles..maddie0908 said:Why won't you do the TRAM flap? Too much surgery and recovery? That's what worries me.
I saw your post about your lymphedema - sounds horrible. I wish you the best with that.
-maddie
Thanks for your thoughts
She0 -
All these decisions are tough, with so much variation between individuals and no guarantees. I ony had one lump (chemo has broken it up, just some suspicous dark clouds left on ultrasound) and about 4 nodes (I think, not many). I will be done with chemo November 26 and have mastectomy Dec. 21, with reconstruction. In my case I was told the best option would be to have a device which has a real name, but the plastic surgeon said they are like "placeholders"...sort of a temporary implant (but not called implants, I just cant remember the name). That will keep the skin from shrinking up while the body heals from the mastectomy and it will allow adjustments during the radiation. She said the radiation turns the skin to cardboard, and that has to heal up before the reconstruction process can continue. In any event, reconstruction seems to be a long process (about a year). I was disappointed that it wasn't an "instant" fix either, but if it takes one year of work to have many more years of health and happiness, why not? You probably already know this, but I would say talk to your Doctors and ask questions, ask questions, ask questions. If you don't get answers from your Drs, ask others. I believe the best defence we can have against the fear and uncertainty is knowledge. Arm yourself and go forward.
Best wishes, seof0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.8K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 397 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 61 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 539 Sarcoma
- 730 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards