April 2018 Surgery Support Group
I'm just following the trend of the monthly support groups. This is for those of us planning on having a surgery in April 2018. We can all get through this together.
I'm scheduled for my lumpectomy and sentinel node biopsy on the 3rd of April (right after Easter weekend). Glad that things are moving quickly here.
Who else has something planned/scheduled?
Comments
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Hi BarbMac! I have exchange surgery scheduled for April 24th. I just realized I should have probably started the thread in this fórum, but I started one for April Exchange Surgeries in Breast Reconstruction. I hope you get more responses. I had my MX last August. Surgery is hard, but waiting for surgery and results is harder, I think. I'm glad you're here looking for support, it's great!
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Hi, all,
I'm betwixt and between on which surgery I should go for. I have DCIS, grade 2, which is not invasive cancer. I have consulted with a breast specialist and a breast reconstruction surgeon. They seem to be pushing a double mastectomy. This horrifies me — a double and technically I don't have cancer. It's preventive. If I don't have the double, I will need radiation, and then have to take hormone inhibitors for 10 years. Those pills have their own risks of all kinds of sicknesses.
If I just get the lumpectomy to remove the DCIS cells, they will also have to remove my nipple because of its location. So it almost makes sense to get the single masectomy since they will be removing a about 25% of the breast anyway. But if I keep the other, they recommend the hormone pills.
This seems so radical for something that is not yet cancer. Are the ladies who have stage 1or higher being told a double mastectomy is a good way to go?
And another thing that's so annoying is the rush to surgery. I have a big family event in May and they are telling me I need to get it done before that. The lumpectomy would probably work, but not any mastectomy, because of the healing time. Jeez.
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Hi everybody!
I am having my third surgery in April. I had my bilateral mastectomy Sept 5, 2017. My exchange surgery Dec 15, 2017. I am now having my fat-grafting to finish everything up. I was supposed to have it along with my exchange surgery. But I had an infected cyst in my belly button that my plastic surgeon discovered during surgery. So that put it off until a later date. He said had he continued with the infection present we could have lost the implants and everything. I'm so thankful he discovered it and stopped the surgery when he did. I'm glad to be finally at this last stage. I had 6 rounds of Chemo and finished it in Aug prior to surgery. Then after my mastectomy I started 9 rounds of Herceptin. Tomorrow is my final treatment! I feel like I am finally coming to the end of all of this! It all started just over a year ago. My first diagnosis +/+/- was March 6 on my right breast. My left breast was diagnosed +/+/+ a year ago tomorrow.
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Hi Swee tPea and good luck with your exchange surgery. I'm still new to all of the terminology here, but I'm assuming that you mean exchanging an expander for an implant?
Hi TaraLeeOm. Wow it sounds like you have some really big decisions to make. I guess all that you can do is find out as much as you can and make the decision that works best for YOU! Try not to let anyone pressure you into something that makes you uncomfortable. I guess all of this makes us somewhat uncomfortable though doesn't it.
My surgeon left the decision of mastectomy vs lumpectomy totally up to me. He said I was luck to be 'ample' enough that a good size lumpectomy still leaves a lot to work with lol. We are going to go that route first, but I told him that when he's in there if he feels that a mastectomy better fits the situation, to go for it.
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BarbMac, you are so right. You just have to make the decision that is right for YOU. When I got my first diagnosis I was leaning towards lumpectomy. I had a Stage 1 mass that was non-aggressive and some pre-cancerous calcifications. My surgeon assured me that she could get it all with a lumpectomy. I wouldn't need chemo or radiation. She was totally on board with that decision. Then once the cancer was discovered on my left side the game plan changed totally. The left side was Stage 1 but nearly Stage 2 aggressive mass with a group of pre-cancerous nodules. It would need chemo and possibly radiation. Once she told me all of that I decided I had WAY too much going on and a bilateral mastectomy was really the only way to go. Ultimately it was my decision but my surgeon said she would highly recommend it. I haven't regretted my decision at all.
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You know, I'm leaning towards doing nothing for a few months. Since Thursday, and today is Monday, my head has been filled up with a massive amount of information.
I don't like that they are making me feel like I only have 2 weeks to decide. And that 2 weeks should be filled up with appointments with a breast reconstructor, an oncologist, bloodwork for pre-op surgery, and the decision of a lifetime.
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TaraLeeOm,
Is your initial diagnosis grade3(faster growing)? If not take your time to figure out what’s right for you. My breast surgeon promoted double mastectomy as did the first plastic surgeon I saw. If you plan for an implant reconstruction double is really the only way to get symmetry and they are thinking most women want that. My second plastic surgeon made me realize that my chance of cancer in the healthy breast was not really impacted but a double mastectomy doubled my chance of surgical complications.
Take your time to get all the information you need. Do not let anyone push you to something you aren’t ready for.
All the best to yo
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I have DCIS grade 2. There is so much information out there, and I thank you, Runrcrb, for being a voice of reason.

They are telling me that I cannot even wait 2 months, until after my only daughter gets married. My doctor actually said, “Don’t let your daughter’s wedding stop you from making a sound medical decision.” That decision being mastectomy. Seriously?
My doctor’s first words to me after the biopsy results came in were, you don’t have cancer. Her last words were, a double mastectomy means no more mammographies, no radiation, no hormone inhibiting pills.
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April 9th nuclear injection
April 10th bilateral mastectomy, sential node dissection, maybe expanders (to be determined in the next week or so) and port removal.
Never had a surgery before. Part of me is ready to just get this done! But I know I will go into anxiety mode in the days leading up to it.
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My surgery is scheduled for April 5. A bi-lateral mastectomy, sential node dissection, and expanders. I have a large mass along with my DCIS and the doctors haven't been able to find (via biopsies) anything more than DCIS. They are, however, suspicious there's something more going on. I'm very nervous about surgery, as I've never had any type of surgery in my life. Best of luck to everyone for an easy recovery. I was diagnosed in January and this is how long it's taken to get to surgery. The doctors have tried to make sure everyone (myself and them) were comfortable with our plan of action.
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Hello Everyone Good Luck to all with your surgeries. I have mine on April 11th. I will have Lumpectomy with surgical reduction lift and taking of lymphnodes. With drain tubes. I am Triple Negative Stage 2 and cancer had not gone into to lympnodes yet so this is why I chose this surgery. Is anyone else doing this type of surgery?
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Mianola- looks like we are in the same boat. I’m having a bilateral mastectomy, sentinel node dissection and expanders placed on April 4th. I also have never had surgery and don’t know what to expect. I’m scared of being knocked out. I guess it’s better than being awake. Haha.
Of course, now that I’m two weeks from surgery and can’t take any sort of medicine, I have caught a cold. Ugh! I’m hoping that TONS of vitamin C and zinc will wipe it out quickly.
Good luck everyone on their upcoming surgeries. Hugs!!!
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Hello to all, I'm grateful to have found this group as we go through this journey. My MX with DIEP stacked flap reconstruction and sentinel node biopsy is scheduled April 18. I've been undergoing test after test the last few weeks to determine if my nodes were positive, and thankfully, they are negative. I'm a single parent and most of my anxiety centers around my two sons, age 17 and 20, but so far, so good (and I will check out the family support forum). As if SAT prep weren't enough stres...!
I'm blessed to be at a world class facility in Boston, and my partner is a physician/researcher so I feel very secure with my care. However, the post-op recovery is not gong to be easy. Although the great feedback on this site has helped me prep, the unknown, especially being dependent on others for help and managing pain, is going to be tough.
Thanks to all for sharing, let's get through this together.

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Hello everyone, I was diagnosed with triple negative IDC grade 3 in November. I started chemo in December and just finished this week. Now I have bilateral mastectomy with immediate reconstruction scheduled for April 9th. Then they decide if I need more chemo or just radiation. I’m worried about surgery and getting back to good health. I’ve been reading the February surgery thread to get prepared
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I saw the surgeon today and it looks like I’ll be having surgery (lumpectomy with bilateral reduction and SNB- with SAVI spacer placed) in mid April sometime. I’m hoping to have a partial hysterectomy at the same time, but don’t know yet if the surgeons’ hospital privileges will allow for that. The radiologist told me on 2/2 that he strongly suspected cancer (official dx on 2/20), so I’m ready to move on to the next step already!
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Add us to the April Club. We met with the surgeon today and my wife will have a mastectomy on April 17th. We were told the tumor (1.3 CM) is invasive, though they think it is stage 1. It is HER2 negative. My wife has elected to not have reconstructive surgery.
The challenge will be that this is a recurrence of BC 22 years ago. They did a lumpectomy and sentinel lymph node dissection at that time, taking most of the nodes so it may be hard to get enough to check this time.
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Hi!
My next surgery will be April 5th. I was diagnosed in October 2017, exactly one month after my 40th birthday and first mammogram. Gosh- that seems like a lifetime ago already. Anyway, due to a separate diagnosis of Tourette Syndrome, an uncontrollable movement disorder, radiation was determined by the Radiation Oncologist as "too risky" so it was confirmed that a mastectomy was the right path for me. However, scheduling with the general and plastic surgeons proved to be difficult, so my general surgeon scheduled me in for a lumpectomy and SNB in November 2017 as a "staging" procedure (to figure out the stage and pathology, and as a holding pattern until I could be scheduled for the bilateral mastectomy with reconstruction). I started chemo at the end of December and had my last treatment 4 weeks ago. Finally starting to come out from the chemo haze and only have a few lingering side effects.
The plan is to have a BMX with immediate placement of TEs. Then, ultimately go back for a 3rd surgery to exchange the TEs for implants. Had the pre-op last week and left the plastic surgeon’s office in tears. I don’t like her and hate how she talks to me. I’ve been fighting my weight since I was in elementary school. Up until my diagnosis, I was the healthiest I’ve been in my life. But, I’m still considered “obese” by BMI standards. Unfortunately chemo kicked my @$$ and I haven’t been able to exercise much. Now that my appetite is back, and I’m still not exercising, I gained 5 lbs. my PS threatened to postpone my surgery until I lost 10 lbs. After looking me up and down like a piece of meat (these are my boyfriends words - he was in the room while she examined me), she agreed to proceed because I carry my weight in my hips and thighs rather than stomach and upper body.
I considered firing her and going to a trusted plastic surgeon I have used before, but he’s far away, I’d have to find a new general surgeon with rights at that hospital, and the weekly trips for fills would just be too much. And honestly, I just want to be done with treatments without any delays So, I decided to stick with her. I know her work will be amazing (referred by my trusted plastic surgeon and one of my best friends who used her as recently as 3 months ago).
I have had surgeries before, so while I am nervous about my upcoming BMX, I have some idea what to expect as far as surgeries go. I am not nearly as nervous as I was about starting chemo, but still uneasy overall.
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Hi All,
I am schedualed April 6th for a lumpectomy and sentinel node biopsy.
I was diagnosed on March 6th. I felt strong until this morning. My nerves are getting the best of me.
After meeting with my BS and hearing I will only need radiation, makes me feel guilty coming here to talk about my feelings. Reading so many brave womens stories of their BC journeys. I feel as though I should be thankful mine is just surgery, radiation and hormone therapy.
But I still have a feeling of uncertianty since my BS explained that my treatment can change depending on the surgical pathology report, or my surgery will be different if my BRCA test comes back positive. I feel alone and scared right now but also guilt beause my diagnosis could have been worse.
Thank you for reading, good luck to all of you strong brave ladies!
Xo
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Hi all,
I'm scheduled for a lumpectomy on April 13th. Figured why not do it on Friday the 13th

I was diagnosed in February and of course got the spiel about doing it within 30 days of diagnosis, I just wasn't ready yet. I'm a single mom to a 10 yr old boy and so much to figure out.
I'm waiting on results from my MRI biopsy for a second lesion that was found.
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Hi All,
I hope you don't mind if I join your group.
I am scheduled for a bilateral mastectomy with an axillary lymph node dissection and tissue expander placement on March 29. Most everyone in the March thread has had their surgeries and moved on to the next phase of recovery or treatment.
I will need radiation after surgery and can then decide if I want diep flap reconstruction or implants.
As the time gets closer I am getting more scared. Not only of the surgery but also,the pathology results.
Good Luck to everyone. Looking forward to learning of your pre and post op experiences.
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RiRi11, I'm in the exact same boat as you. My lumpectomy and sentinel node biopsy is scheduled for next Tuesday (Apr 3rd). I'm having the radioactive seen inserted tomorrow morning and the plan is radiation about a month after the lumpectomy. My doc said the same as yours....things can change, but for now it looks like no chemo.
Like you, I feel guilty. Some of our sisters here seem to have so much of a harder road ahead and I feel like I should be grateful and not really belonging here

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Hi Simbobby and welcome. What's the difference in a few calendar days between warrrior women. Glad to have you here. I try to tell myself not to be scared because it has zero impact on the inevitable outcome. Deep breaths and relax. Visualize your body defeating this.
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Hi ladies, I will have prophylactic mastectomy and Diep Flap reconstruction of both breasts next Wednesday!
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Update:
We met with the surgeon on Friday. He will do a single mastectomy with no reconstruction on Tuesday, April 17th at Kaiser Hospital in Woodland Hills, CA. Amazingly, it is day surgery there. During my wife's lumpectomy 22 years ago, she had most of her lymph nodes removed. They will do a sentinel node test this time and hope that there is no spread of the disease. He doesn't think there is, but an invasive 1.5 cm. growth is approaching a size where there could be.
On top of that, my wife's uncle passed away yesterday. Just a very tough time, but we will get through it!
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Hi all! I'm scheduled for my prophylactic bilateral mastectomies and tissue expander placement on April 16th. I'm grateful for this website, its wonderful members and volume of information, and I am cheering you all on in as you also face surgery this next month. It's getting close and I'm starting to get appropriately scared, daunted by the gauntlet I'm about to run, but I'm grateful for this opportunity to avert whatever this genetic BC thing is that I have going on. But I've already had bladder cancer and a breast lumpectomy (revealing ADH, ALH, & LCIS), so I've got some experience to lean on.
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Eugene- I’m at WH Kaiser too- my surgery is on the 5th. Who are your wife’s surgeons? My general is Tran and PS is Kim. My family and friends are all shocked the surgery is out patient. I expected it as I have had surgeries there before and all have been outpatient. Other than my PS, I’ve been incrediblly happy with the care I’ve received there.
So sorry to hear about your wife’s reoccurrence and passing of her uncle.
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Hi, LAMinders,
My name actually is Larry. I use Engine104 (Fire truck thing
) in discussion groups. Did you mean you weren't happy with the PS or that the PS was in patient?
My wife's surgeon is Dr. Kang, her internist, (Mine too) is Dr. Tallakson. We love them both.
Thanks so much. We were a bit taken aback that we are dealing with a recurrence after 22 years (With a battle with AML in between, 16 years ago), but then I heard from a friend of mine who told me that Olivia Newton John is dealing with this again after 25 years.
I pray your surgery goes easily with a great result.
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Hi Larry- Sorry about the error. I was typing on my iPhone and apparently text prediction took over and my distracted chemo brain did not catch change. So glad you like your doctors. I'm not happy with my plastic surgeon (PS), but love the rest of my medical team. I know the PS will do good work, I just don't like her bedside manner.
I hope, even with the AML battle (you two really have been hit hard!), you both got to and CONTINUE to enjoy every part of life together. Reoccurrence is my worst fear- and I am not even done with this treatment.
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I think bedside manner is very important. We've been lucky in that regard. I'm sorry that your PS is like that. I also think competence is more important than bedside manner and if a doctor could have only one, I'd pick competence every time. For example, on MASH, Charles was a big jerk, but he was a great surgeon.
Still, it's good if your doctor has both. Thanks..My wife's doctors at City of Hope felt the AML was probably a direct result of the duration of radiation she received following her lumpectomy. In those days, they did ten weeks of radiation as opposed to four now. That's a lot. My wife was in a study at City of Hope that researched a link between how radiation used to be done and AML.
I never thought after 22 years post BC and 16 years post AML that we'd be in the battle again, but here we are. It stinks, but what can you do? We just take each day and one step at a time. Please know though, that this recurrence is unusual and by far, the majority of cases result in permanent cures. Dr. Kang feels strongly that my wife's current BC is not related to the one she had 22 years ago.
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I had my seed implanted yesterday. I must admit, it took a bit longer than I had anticipated. The fact that you have to have a mammogram after all of the poking and prodding didn't make the experience any more enjoyable lol. Oh well, another step completed and now just waiting for surgery on Tuesday.
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