May 2013 surgeries
Comments
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Ann thats awesome that you are handling the tes that well. Great that you are almost filled. Why did they delay your diep?
Ck, spider bites can be serious so I wouldnt blow it off. Im surprised your doctor didnt require you to go in and get it checked out. Hope it gets better and Bugspray is your friend. I live outside with my plants especially now that its 90°. I always forget to put bugspray on too. I should know better.I have had 1 le occurrence that lasted about 3 months before I was able to get it under control.
Hope everyone has a blessed day. -
ck, I found a tick on my leg earlier this week, and it left a bruise too. I put some hydrogen peroxide on it, and showed it to the nurse at RADS that morning and she said as long as there was no swelling, no problem. I'm noticing odd bruises here and there on my body, too, so don't worry about the bruising.
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Well I wonder is this a tick bite then? I showed it to the surgeon this past visit..telling him "I know this is not your specialty but I want you to look at this..and NO YOU CAN'T AMPUTATE MY LEG..which he got a big kick out of..I asked him before last surgery was he trying to meet some kind of quota..He looked at it and said.."Oh something bit you"..I assume is spider, but maybe tick? Well, I will try the peroxide.
I know i have thing of off and they said to make sure I wore that as they didn't want any insect bites on "affected arm" because of lymph removal..but, I keep forgetting and its sticky. They also said I needed ..when I could do it..to garden with long sleeve and gloves..I do gloves..but Jeez! the humidity and heat here is awful! Not sure about long sleeves.
Catey-Was it you that worked for postal service? Are you back at work walking your area? Picking up pkgs? I just thought about that last night and wondered.
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Yes I work for USPS but am not scheduled to go back until 7/15, my BS wrote down 6 weeks minimum for FMLA, I go back to see him 7/8 and depending if I still have tightness in right shoulder underarm may ask for PT referral and another week off. Regardless of surgery Im really enjoying having this time off work
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Hello lovely ladies,
Sorry I haven't posted in a while. Been busy managing household matters and my 3 kids. I'm a single parent so a lot falls on me. My ex isn't consistent so I'm the center of their universe. One was packing to leave for her summer job, one was getting in from a lacrosse tournament in VA late Sunday night and I needed to drive her to a lacrosse camp early Monday morning and 2 out of our 3 used cars broke down! Also need yo provide a lot of support to my son , who frequently gets jacked around by my ex. And then there's work....
But, I'm handling things as best I can.
Had my second fill on Wednesday and now I've gone from concave to an 11yr old pre-pubescent girl sporting some little breast buds. Whoopie!
I am 6 weeks post op and I am feeling much less discomfort from my bear traps, AKA TEs. My PA said as they continue to fill, that will balance things out in there and that would help continue the discomfort. I can actually lay on my side now a little so I may try sleeping in my own bed tonight. I'm only averaging about 4 hours of tossing and turning sleep and that needs to change.
Chemo #2 was yesterday. My blood count just barely squeezed by the minimum due to last weeks infection but it did so I was very grateful. I am TURBO-hydrating which is so key to flushing it out of your system and reducing side effects.
Honeybunny, same thing happened to me. Was hoping to escape chemo and rads but that sneaky cancer got into one if my 2 lymph nodes. They also opted not to surgically remove any more lymph nodes and will radiate instead. In fact, I read an article on this site that suggested a trend to radiate versus removing more post surgery. If you scroll back a week or do, I posted a bunch of insights I took away from my first chemo treatment.
Ckmoss: honey, you just hang in there, girl, and keep your eyes on the future outcome if a healthy, active you. That arm will be raising up to the sky soon enough.
To the rest of you, keep it flowing forward. We will all get each other over that finish line!
AnnBR: love the sleepover idea!
Best to all. Gentle hugs and warm thoughts. -
Oops. Typo in my last post. Continued fills of the TEs helps to reduce the discomfort. Not increase it. Sorry, chemo brain.
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Ambnh, its good to hear from you. Sorry your ex isnt any help. Bet thats why he is your ex lol.
Hope you continue on path of healing. -
AMBNxyztbs..... Sorry I can never remember all the letters, so I thought I would just add a few extra ;-) I'm sorry your ex is not helpful...but you sound like a strong woman...good for you!!!
Ann...Was your second fill painful when you had it? My first wasn't painful but I do have a bruise where she injected me on my left foob....I go in a week for another fill and hope it was like the first time...uneventful!!
Woke up in the middle of the night with heartburn...ugh...time to make a trip to the store for some meds. ckmoss I should have emailed you early this morning I was awake too!!
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AMBNH-1st-I think you are going to have to break down and give us a name..as some of us are having letter diff..lol..I've actually got it down..which is MAJOR for my brain (meds plus perimenopause.lol). 2nd-I think I want to be like you when I grow up! WOW! You must be something else!! You are handling your busy life..single..and going through chemo and TE fills..my hat goes off to you and I will never complain again. You give us all hope that this is doable! May God grant you continued strength!
Run4-LOl..anytime from 4am forward..Im up and staring at tv..would love conversation!
Catey-I would make sure your arms were ready. You've got a demanding job! I've enjoyed the time off right before I think Im about to go back to work (feeling my best)..then they slam me down for another surgery...at which point, I'm whining about missing my job and normal. IF ALL STAYS ON COURSE..I will be going back Sunday after next.
Ok good day today. I haven't had my hair cut in FOREVER because kept thinking I was going to have it buzzed or shaved for chemo 2 or 3 days after my first treatment...well ya'll know how that's went..and my hair has been looking horrible! So I called and got in at noon today. My mother was out with errands and was only appt she had until next week..so drove myself to her (luckily haven't took meds today). First time I have driven in over 2 weeks...OH MY GOD IT FELT GOOD!!..and she gives these new modern shampoos there ..they last about 20 minutes..she massages your head and puts aromatherapy stuff all in it..your head is all cool and tingly..HEAVEN..then got great cut..then drove myself to the Cookout (fast food burgers. taste charcoal cooked out) got me chili cheeseburger..and came home...I am sooo happy right now..very weak and tired but that all felt so wonderful!!!! One thing about the big crappy C...it makes you grateful as hell for the things I have never given any thought to.
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I have no hair to wash but the head message sounds wonderful! :-)
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Sweetpickle-It is. She said that she would not charge once I started chemo and wanted to just come by for that..stimulates growth and all that..all I know..it takes care of any headache at all..plus kills my arm to do it myself. She runs her thumbs up your neck and whole 9 yards...I try to get my husband to rub my head when I have headache from meds..(theres no icon in here for eye rolling).
How are you today? Is the pain better?
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Hi Ladies. Ok, just call me Annie. The A stands for Anne. The M stands for Marie and the B is my last name. NH is where I live.
Ckmoss, glad you got to drive.
BTW, second fill was fine. Little sting when the needle goes in then it's fine. Some discomfort for the rest of the day but Advil helped. Feels much better 2 days later. I'm also not wearing the surgical bra unless I have to because it puts too much pressure on the area.
Glad to know some of you are awake at 4AM. I'll have to check it out when I'm lying awake then! -
Annie-Love your name! Mine is Cyndie. Are you doing inplants or Diep? The drive was great..and I think when I got home and posted about it I was on pure adrenalin..I have crashed now..extremely tired..but still smiling!
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Cyndie- Im doing much better today thanks! I think the silverdene is helping me to be more bendable. lol
Annie- I think we need to form a group called the "Its 4am and we're awake club"
I added my name to my sig, its Heather -
Well,ref to names..looks like we are all "coming out of the closet!"..LOL
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well, okay. I'm Janet!
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Wow. You guys are PROLIFIC writers! I've been keeping busy the last couple of days, and when I finally sit down at night, I read a post or two, then crash. My biggest problem with not catching up regularly? It's hard to keep track of who's doing what, and how each of you are doing. Anyway, know that even if you don't hear from me, I'm trying to follow all your activities!
Ann: if I remember correctly, you are having the DIEP done in October? I was lucky enough to be able to do immediate reconstruction. I was sooooo relieved to wake up and find boobs, even if they were swollen, bruised and deformed looking. I knew right away that having boobs meant that the cancer hadn't spread to my nodes. RELIEF. I cose the TRAM flap, mostly because I was told insurance wouldn't cover DIEP. Given my ability to heal quickly, I am confident that I will not regret the TRAM v. DIEP. For what it's worth, my PS said that the DIEP is the "Cadillac" of reconstruction.
Sweetpickle, I have cleavage, too!
Cyndie, my doc ok'd me to drive on Tuesday, so i know how liberated you feel! Of course, I went out Wednesday and Thursday, managed to overdo a bit, am and still chillin in my pjs today at 4:30. Oh, well, it's all good! He also ok'd my return to work next week, but only 10 hours a week. I plan to go in for a few hours on Sunday, then split what's left between Wednesday and Friday.
Annie, you truly are a remarkable woman. Your situation with your ex makes me extra grateful that I have a supportive dh! If you'll like, I can call or text him to let him know that your kids need a little extra from him while you are fighting your battle!
Cyndie, I understand about the hair cut. I haven't colored my hair in weeks. What's the point until I find out if I need chemo? I have a good inch of silvery roots to add to my unfavorable self-image. -
If we do get together, it'll be someplace sunny and warm, preferably with a beach, right?? In other words, not northern Michigan. We have a saying here:"if you don't like the weather, just wait five minutes." Even when it's hot outside, the water (great lakes) are cold.
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Ok, one more post, and I'll stop rambling for a while. I have this CRAZY idea that I couldn't share with anyone except you guys: there is a part of me that WANTS to do chemo. I think I am afraid of not doing everything I can to prevent recurrence. I know it's crazy, and I'll do whatever my onc. suggests, but still I have this feeling that I need to do chemo. How do I resolve this?
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steph, how confident are you in your doctors? If you are confident, mention how you feel and see what they say. I know I tried to back out of radiation and they gave me a laundry list of reasons I needed to do it. So I do what they say. On the other hand, my BS told me I could do lumpectomy, but I gave him my reasons for wanting to do BMX and I won out. He couldn't convince me otherwise.
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Steph01: You need to do what you feel in your gut is the thing to do. Listen to your onco and do your research and pray. I'm sure you will do what is right for you.
My onco has recommended chemo for me even though my nodes were clear. My onco score was borderline high. After much research and reading about all the side effects and other cancers Chemo can cause, I chose not to do it. I also had two relatives that had breast cancer and had the MX and did not have chemo or rads and lived many years and died from something totally different. Hopefully I take after them. Chemo would only give me a 7% improvment in my recurrence so it wasn't worth the side effects for me. And even with that 7% there is no guarantee it won't recur. Had my nodes been involved I would have jumped on it.
My onco said I was technically cancer free so I don't want to destroy my immune system and use up my resources now in case I may need it later. I'm just leaving it in God's hands and moving on.
By the way, since we are sharing names, mine is Cyndy. -
Ladies, several of you asked about my delayed DIEP and TEs, so here's my story... I was diagnosed in Dec. 2012 with IDC in my left breast. I had an MRI which did not show anything usual in my right breast, so I opted for a UNX. When I went for a consultation with my PS in Feb. of this year, I was required to send all my records including the MRI to their breast center prior to my visit. This was at the Mayo Clinic in Rochester. (My first MX, was done locally, but we don't have a PS in the immediate area). Their radiologist noticed two suspicious areas on my right breast and scheduled me for a biopsy. I decided I did not want to go through anymore testing, so I chose to have my breast removed which was done in May. I'm glad I had it done because they found DCIS and LCIS, which put me at a higher risk of developing IDC. At the same time as my BX, the PS inserted TEs under my skin because he said the skin on my left side needed to be stretched and he wouldn't have to do any grafting. I guess the results will be better in the long run.
Of course, now I wish I would have had both breasts removed at the same time and at Mayo, so I could have reconstructed immediately, but I'm not going to beat myself up about it. I believe things happen the way they're supposed to. -
Steph-I understand wanting the chemo..I had 2 positive nodes anyway..so no choice..but I want all this out of me. I think though if they had of all been clear..like Cyndy..I probaly wouldn't because, like she said, it is hard on heart, lungs and other organs. But I do understand..I'm calling it my chemo cleanse!
I, also, just got my sleep caps from that lady on Ebay..they are simple, soft and cute (plus cheap!)..I ordered 4 because you have to handwash. Lisa did you get yours? I'm very pleased with mine.
Janet are you doing ok today? What is the radiation like? Does it take a long time? Does it hurt?
Heather...I've known your name because I could, of course, see your signature..but I swear you will always be Sweetpickle to me! That user name fits the personality that comes through your post!
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Cool, looks like we have two Cyndie's! I agree with someplace warm for a get together. :-)
Steph- I echo what othes have said, talk with your Onc. About how you are feeling. I really like my doctor and trust his judgement so that is why I did chemo and surgery with no rads. Im sure you will make the rigt choice for you.
Who has fun plans for tonight? Let me live vicariously through you since Im still stuck at home :-) -
I'm good with warm as long as there is a blue ocean involved! Its hot and muggy here
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Hi ladies. My situation is similar to Ann's. my right breast had to go as the cancer took up too much real estate. My left breast in a follow up MRI showed 2 suspicious areas. One was atypical ductal cells and one had atypical lobular cells. I had 2 choices. Right mastectomy and robust follow up on the left breast in an ongoing basis. Second choice was a double mastectomy. I felt that the lobular cancer on the right breast started out as an atypical cell and morphed into an invasive cancer. I wasn't willing to wake up every morning wondering if the atypical cells on the left changed into cancer so I opted for the double mastectomy.
My breast surgeon advised me to have the TEs put in but hold off on the diep reconstruction until it was determined if I would need rads or chemo. PS won't do a recon until 6 months after the last rad.
So, I anticipate an April or May 2014 diep reconstruction surgery.
Bottom line: every woman has to make the decision with her surgeon that is best for her. -
Annie im so sorry I wanted to post first that we should all take a guess at what the letters mean. My guess is " America's Most Beautiful kNowlegeable Hostess" ...... Whatcha think lol.
Steph, I totally get what you are saying. I didnt want chemo because I heard that it didnt have much effect on ILC but they said that because I had the 8 positive nodes with extracapsular invasion is why I had to have it. However, I have done everything. Bmx, axillary dissection, chemo and radiation and I still get that gripping fear that its metastisized. I believe that all that we have been thru gives us some form of ptsd and it just takes time to emotionally heal and put it all behind us. It iswhaf it is and we have to find a way to except it. Oh and I have some bad bone pain and neuropathy from the chemo. They will have a hard time convincing me to do it again. But I wanted you to know those feelings could be there even if you do chemo. Always worrying. Tell your mo that you want to know if chemo could benefit you andtrust his response.
Healing hugs to all
Melanie -
Cyndie,
Radition doesn't hurt. If not for the beeps and buzzes, you wouldn't even know it was happening. The position isn't the most comfortable, but on most days it's okay. Yesterday they did about 15 minutes of xrays before my treatment, so by 25 minutes or so, I needed to take my arm down for a minute to rest it.
Getting a light to medium shade of pink in the area. A couple of spots hurt some, but just taking pain meds and dealing with it (along with slathering myself with lotion as much as I can)
Another vote for the beach. We can sit in the sand and giggle all day.
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Gowith, how many more treatments do you have
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Janet close your eyes and don't read this...
I'm still not convinced about radiation. I don't get the purpose for me. From what I can tell, it gives you a 8% chance (of an already very low) chance of recurrence in that that one spot they radiate and the % of mortality is the exact same percentage for..once again..that one spot they radiate. Also, you have an increased risk of lymphadema..something I am very scared of. To me, if I've done the MX and had chemo (which I was told at this point chemo is merely a precaution..and one I understand as cell could have broke loose they can't see). I debated this heavily with my oncologist and he couldn't tell me any reason that would make a difference..kinda more that well that's "whats done". To me, I would understand if they were going to radiate my remaining breast..as that's probably ..if it comes back where it will be. I don't know...My surgeon said he didn't see any point as I was cleared and even skin I had saved was tested to be clear..and won't chemo knock out..I keep going around and around with this.
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