When can you have DIEP after IBC treatment?
Just wondering what everyone's timeline was for DIEP surgery after treatment ends. I ended chemo on 4/2/13 & rads on 7/15/13. I will finish herceptin at the end of Oct. I want to get this surgery behind me ASAP! My oncologist had said before - 1 year. I will see him in 2 weeks to get clarification on this - 1 year from chemo? 1 year from when rad treatment ended (mid-July) & why? Before he had mentioned because of a recurrence, but even if I would recur in a year or two, I would still want to have this done soon. He also said that he could treat me for a recurrence right after I had the DIEP surgery, if needed. So I am not sure why...
Comments
-
Donna,
Do check out the surgery thread here. I did implants after bmx. Diep will take a lot more recovery time and I assume more painful. Check it out carefully.
Terri -
Hi, Donna. I wasn't diagnosed with IBC, but it was semantics only...I had a red patch of skin on my breast that was about 3" in diameter that was positive for dermal lymphatic invasion, but didn't involve 1/3 of the breast, as is required by IBC criteria.
Anyway, you're almost exactly a year behind my treatment. My radiation oncologist, who is the most conservative doctor on the planet, wanted me to wait two years after my last radiation treatment, and I believe it was because he was concerned about recurrence. I mentally told him to stick it. My plastic surgeon wanted me to wait at least six months from the end of rads, to let the tissue settle down and heal after the radiation damage.
My rads ended July 17, 2012, and I had DIEP on April 15, 2013. Nine months wait. I'm thrilled with my recon. No, the noobs aren't as pretty as God makes, but they're soft, warm, me, and something to hold out a bra! For the first time since my umx in April 212, I feel beautiful again.
Blessings as you move forward with these decisions! -
sbelizabeth -
My plastic surgeon said 6 months would be ok. It is the oncologist that says 1 year.
I obviously don't want to do anything to jeopardize my health - that is way more important than having reconstruction done earlier! However, I just feel like I have this "hanging over me" & want to be done with it all! -
I was told had to wait a year. ALL of my Drs (Surgeon, Chemo, Rads and my PA) gave the same time frame. So I waited to look into recpn. When the time came to look into recon, spring was coming amd there was no way I wantd to potentially loose part of my summer activities with recovering from elective surgery. I never went ahead with recon and have never regretted my decision. Actually it was our Son (adult) who put things in prospective for me. Hubby had been very surportive of me getting recon because HE thought I felt I needed to do it. A big part of why I was thinking of doing it was it was because I thought he wanted me to. (For those of us who are older, there is an O'Henry Story about long hair and a comb that fits.) So my final decision was to go with no recon and I could not be happier with my decision.
-
Less than a year out from rads. Definitely do it if you want, definitely don't if you don't. Whatever is right for you, is right.
My DIEP recon was absolutely the correct thing to do for me, personally. Made me feel much better in ways that I didn't realize were bothering me until they were gone. I also wanted to wait the least amount of time, just to get it over with. Happy to say cancer in no way dominates my life anymore, and I'm happy with my appearance again (for a middle aged lady, anyway, hah!). -
What is important to DIEP healing/success is the amount of tissue damage from rads. I believe the further out from rads, the better the end result. I was 11 & 8 years past rads and the 8 year side DIEP didn't completely heal for almost 6 months. I'm very fair skinned and rads damage for me was considerable. The end result is amazing. We're all different, and you know best how your body heals. -
8 & 11 years - wow! Much longer than I thought. I was under the impression that 6 mos after rads things would be healed enough for diep.
How does the radiated skin generally look when it has healed adequately? I am 3 mos out from rads and my skin is still tight and darker in color than my non-radiated skin. Also, I just finished herceptin this week. Should I expect my skin to improve much more? Did the herceptin slow the healing?
Thanks -
Hello I am 48 years old and recent was diagnose with IBC in early September. I am presently, having chemo going on 6th treatment next week. (Taxol) . I am stage IV with mets in the bone.I am having a problem with my oncologist at slogan she tells me that having a mastectomy according to her is a clinical trail and she is not sure for me to have it. After during intense research with other cancer centers including Md. anderson survival rate goes up when the primary tumor is remove. My question is has anyone with IBC been told that surgery is not option?
Thank you,
Mercy NJ -
Donna, I was 11 months out of radiation and healed up with no issues. The radiated side took perhaps about a week longer to heal than the non-radiated side (I had a bmx with bilat DIEP recon). Everyone is different. My oncologist also said 1 yr after end of rads and a month after stopping Herceptin. Yes, your skin will get lighter and softer in time - I do think at about 6 months mine really started changing back to normal. My radiated skin doesn't feel rough, dry, or hard anymore but I don't know if the "tan line" ever completely fades. -
Donna, I was that far out from rads and had a third primary hence the time gap until bmx/DIEP.
Sherlocked, my tan lines eventually disappeared. -
I was told at least 1 year & for a long time I didn't want it. But I kept having infections in my arm on the bc side so I decided to go ahead with it. I had a Bi-lateral D.I.E.P and I am so glad I did. My doctor was able to remove a lot of damage caused by the rads & I am in less pain than I was in before the surgery. It's a personal choice so do what is best for YOU!!!! NJ -
Thanks, She, it's a comfort to know that it will match the skin around it better in time.
MrsNJBand, I had a similar experience - not with infection, but with lymphedema which can lead to infection. I pretty much swelled up like a balloon on my cancer side right after mastectomy from lymphedema, and the reconstruction helped with that problem by replacing some lymph nodes in the breast. Also had a considerable amount of pain at the mx site that went away when I healed up.
But it's a painful surgery, no doubt about that. The results are amazing - you have breasts that look and feel natural, and a flat stomach again if you're like me and gained weight in treatment. It's not so much pain but just discomfort from the pulling feeling in your stomach. It's odd and annoying and lasts a few months - or did in my case. To me, it seemed like there was so much trauma in my life (other stuff in addition to IBC) that what the heck, get it all over with at once and recover at your own pace. But, everyone's different psychologically too. Such a surgery is trauma. If you want reconstruction, you have to consider: are you one who wants to get it over with and be done, or one who wants to regain stability and come to terms with the crappyness of breast cancer let *alone* IBC before dealing with yet more invasive physical crap? That's probably the most important consideration, as the right answer is different for everyone. -
My oncologist gave me the "go ahead" for January. I have been thru a lot in the past year, and do feel as if this is "hanging over me". Just want to get it done so I can move on with life... I am early 40s and know that I definitely want reconstruction, so not having it done is not a consideration for me.
I am working hard at getting in great shape and eating well. I figured that if I went into surgery being a good weight, that I would probably have a better outcome (physically & cosmetically). I am now at my ideal weight - took me since June to get here. I am now just working on toning and building lean muscle.
I am always open to ideas - so if anyone else has any suggestions/advice for me, I want to hear it all!
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team