Too early for April 2012 mastectomy?
Comments
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@lisamarie - i'm not having exchange surgery until October because i have too much going on in my life! Doc said i am "eligible" for it starting in end of July/August-- but i'm going away end of August and Doc doesn't want to do before then. and September is hard with school starting for kids. So...October it is. I don't mind the look of my TEs in clothing. And while not beautiful naked, i've gotten used to them. i think this whole journey is about "new normals."
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Lisamarie- I don't get my exchange until next April or May. I just don't think about it anymore. I finished round one of chemo and now on a 13 day break and then I start the cycle all over again. My blood work looked pretty good. White count still in the normal range, red were a little low. I will have to eat spinach to bring it up. The nurse suggested beef liver, I think not. I know I couldn't choke that down. Planting some flowers and yard work today. It makes me feel normal.
Longislandmom- You are so right about new normals. I don't mind how I look in clothes either. I actually fill them out better now than before surgery.
I hope everyone is doing great. Be positive and live life.
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Lisamarie, So sorry your still having such pain with the TEs! Hopefully you won't have many more fills and then once that is done, you won't have the pain. The PS told me Friday that I only have 3 more fills. I think he put extra in on Friday because I had a bit more pain but I'm trying to ignore it! I did modified push-ups today so tomorrow I might have to take a tylenol. Doing some exercise does seem to loosen thing up in there.
My exchange will be in September. Another drain is assured according to the PS. This means a whole week off of work for me because I can't go in with a drain attached. I just keep in mind the perky boobs and tummy tuck and that keeps me moving forward.
Anyone else getting ready to take tamoxifen or already on it? I'm getting my perscription filled on Monday. Another stage entered!
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I've been on Tamoxifen since late February - My SE's haven't seemed too bad so far. I have had some warm flashes, emotionality (especially at PMS time), and maybe some minor crampy feeling (but I'm not sure it's that or something else). On the up side, my last few periods have only lasted 3 days.
I see the gynecological oncologist on the 27th, hopefully everything will look fine to him too.
People's SE's seem to vary, hopefully they'll be mild for you too.
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Hello to all my April ladies. Hope everyone is doing well! Question for those who had mx/diep. I just about 8 weeks out from surgery 4/23 and still not feelng fantastic. I have aliens in my body (nerve ending) moving all the time and so so uncomfortable. Additionally from just under the breast all the way to the abdomin my skin is sensetive and hurts when touched or even if clothing are on or rubs against it. Just wondering if this is normal. going back to doc next tuesday but I thought I would see what other say. Let me know and keep cool (NYC 100 today, or close to it)
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Hi rtnyc, I didn't have a diep but my skin on my arm (on the side where I had 26 nodes taken out) is giving me similar feelings. I can't stand my shirt or anything for that matter, touching my skin. The doc said that there is a lot of collateral damage to nerves in these types of surgeries (BMX included) and that pain is the nerves trying to regenerate. I swear mine feels like shingles so my doc put me on Gabapentin. You may want to check with your doc to get some type of "nerve numbing" meds like Gabapentin or Lyrica (I prefer Lyrica but the VA goes the cheaper way first). Hopefully it is only temporary but if you go to the pain threads you will see that some have that kind of pain long term. I hope it just temporary for both of us. Stay cool up there and I'll try to stay dry down here.
Kristi
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I miss everyo ne , hope all are well
it's very hot here on Long Island .. bought some air conditioners yesterday , just got off working my 12 hour night shift .. a little tired . I have 2 more fills and I am done with filling my TE's .. doc says I am at the point i should be .. so these next ones are overfills , then I will rest my month and go for the exchange .. hoping its over soon .. other than that just working thank god .. and paying bills and routing for my Yankees .. hugs to all
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I have overly sensitive skin on the cleavage side of my chest. Feels too much, touch and cold especially. I think it is normal and diminishes over time.
I have adapted to my TEs, how about everyone else who has them? Thinking of postponing exchange until I loose some weight, so I may always have them in I suppose!
Hope everyone is well, I miss our group!
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I miss all you surgery sisters also! I guess it's a good sign that everyone is getting on in life (either that or they have moved on to another thread). I will always have fond memories of the April 2012 gals.
I meet with the radiologist on Monday to determine if radiation is needed for the tumor that was within 1mm of the margin. We are also doing the BRCA test and getting my oncotype to have a better picture of what to do next. For now, I am recovering nicely from the ALND (other than the horrible shingles like pain on my arm).
Hope happier days are upon each of you!
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keonghi: I have that "shingles" like pain;I call it aliens in my body, in my breast, upper torso and behind the arms. OMG just don't come near me. I should hang a sign from my neck "DO NOT TOUCH"!!!!! I just called the doctor to ask for nerve numbing med's; waiting for her to call me back. I was taking stuff to sleep but it doesn't work because I'm feeling the nerves all night. Anyway, let's talk scars. Someone just told that the best thing to use on the scars to deminish the way it looks is Arnica cream. Anyone know anything about this? I'll ask my doc at next visit...Let's keep talking April 2012 girls, still have questions as I feel everyday is something new...as longisland mom said, new normal...mine changes daily! xoxo
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I am so bummed out. MO said my hair would not fall out with CMF chemo and guess what it is by the handfuls. I am going to get it cut short tonight. I can't deal with the long pieces coming out in my hands. I cried halfway to work. Chemo sucks.
Lisamarie- I am glad you are almost finished withe the whole expander thing. What size implants are you getting. I know you are small like me. My PS said the biggest I can have are 275's.
RTNYC and keonghi- I am sorry you are both having pain. I still have a lot of numbness. I was getting bit by a bug and didn't even feel it. I wonder how he liked chemo.
Plymouthpeople- I too am used to the expanders. They even looked great in a swimsuit. I am hoping the implants have the same projection.
Glad to hear from everyone. I don't come here as much due to chemo and work. We should all try to stay in touch. Have a great night and for those in this dreadful heat, stay cool.
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No TE's for me so I can't relate to that. I have 9 more radiation treatments and my skin is on fire! The worst is my armpit...ouch!
Bathing suit season...sigh. I can't even begin to explain how ugly mastectomy suits are. I did find one and ordered it. I hope it's decent.
Can't wait for my DIEP next year. By the summer I should have the boobs of a 20 yr old! Looking forward to that.
Diana - chemo does suck and losing hair sucks worse but it does grow back. I have full coverage now and plan on going topless by August.
Work and radiation is all I do these days....oh, and root for my beloved Red Sox -
Diana rose , hope u start to feel better . sorry about ur hair. I miss u . I am working like crazy , days and nights .. playing catch up .. as of right now I have 340cc in left and 370 in right .. and he says 2 more fills .. over fill i guess, I am supposed to be a full B when all is said and done . I look huge right now . but thats because I never had any to begin with , i was a negative A lol...
Hope everyone else is well gotta get ready for work .. hugs
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dianarose and mardibra, sorry for your continued pain. Work and treatment must be very hard.
dianarose, i have fake hair as well as fake boobs, due to a genetic conditon, and I have to say that, psychologically, the hair loss was worse than the boob loss. So I feel for you.
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Got my hair ( what's left of it) chopped last night. The saving grace of it all is I have curly hair so the cut is in a way that I don't think anyone can tell right now just how thin it really is. It was still falling out this morning when I showered.
Plymouth people- you are right. The hair loss is more devistating than the boob loss.
Lisamarie- I wish I could go as big as you, but can't due to radiation. I hope you are happy with the end results. It is the only prize out of the whole dam thing. I have been working as much as possible to just to play catch up. I have chemo brain a lot though. Used the wrong attachment twice while making bread at work and couldn't figure out what was wrong for a few minutes. I threw my knife in the trash the other day and kept the stuff I needed to throw away on my work table. By then I finish up and go home before I burn the place down.
Have a great weekend everyone.
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Hi all
I have been reading but just not posting.
With not having to do chemo or rads I have been trying to get back to normal. But it's been hard as I just haven't had any energy and just can't be bothered going out or doing anything. It's winter here so with the rain and cold I just feel like staying indoors.
I've had a few side effects with the tamoxifen, I find it hard to swallow tablets and am having to chew most doses, will have to ask if I can get liquid instead, have heard it's available.
I at the moment have a throat infection and flu, am taking antibiotics and flu medicine, I haven't been having the tamoxifen side effects like I used to, wonder if it's something in the medications?
I'm still interested to hear how everyone is going, so keep posting. Cancer isn't over just because our surgery and most treatments are over.
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Hello, ladies. I have been so so busy and have not been checking in much -- but i have been thinking about you all. RTNYC-- so so sorry you are in so much pain. Hopefully it will get better with time!! You had such a major surgery with the DIEP -- i think much bigger than TE. Maybe you just need more time. ugh!!! I wish you felt better. I was burning for the first month or so after surgery...but mine has mostly all gone away. Still uncomfortable if you touch certain areas of my breast, and still don't wear the shoulder part of my seatbelt when driving...but mostly pretty good.
Diana Rose-- so sorry about the hair loss. sucks! grrr...... can you get a beautiful wig that makes you feel good? my friend got one that looked absolutely natural.
Keonghi- glad you are recovering from the ALND! sorry about the pain and am hoping your ONC is sparing you from RADS!
Other than still feeling stiff (particularly when i get chilly), i feel good. I'm doing PT 2 times a week and my ROM is much improved. PT says I'm at about 75% ROM. I feel good. Am working like crazy. And am trying to ignore breast cancer until my next surgery in October. I haven't even been giving any thought to implants, which i suppose i'll need to do in the next couple of months. Busy with work, end of school, summer and life! Still hard to believe I have breast cancer. WTF! miss all you ladies. am keeping the chemo girls in my prayers always. xxo
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Longislandmom...glad you're doing well. I am better this week started to workout in the park which has been helping. Going back to work July 16 and going to the beach in nj Friday and can't wait. I am going to try to fall back to sleep now, take care...
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Hi Ladies , had my last fill on Tuesday and boy it was a lot , I dont even know how much ... but by the time I got home I couldnt sit, stand , lay ..by 5 pm I had to call Dr back was in so much pain..he had to call me in the dreadful Percocet .. UGH ! stayed in bed and throwing up all night and all day and night yesterday. he says they wil call me and schedule my exchange in about 3 weeks .. everything is moving so fast . I am glad to be getting it over with ...I hate these TE's I feel like I have big balls under my arms .. it is so huge ...Hope all of you are in good health and spirits .. Love and Hugs
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Hey all! Just checking in quickly! I feel for you Lisamarie and those darned TEs. I have three more fills. One on Friday and two more after that. I only have right side TE....had a lumpectomy on the left side and that poor old girll is really saggy now, poor thing. I think my TE pain has been minimal but right after the fill tends to be the worst. I actually did 10 push-ups the other day and didn't really suffer like I thought I would. I will finish my fills in July but have to wait until September for the exchange. I guess my doctor likes to think on things for a while, lol.
I started Tamoxifen last Monday. That is my only "chemo". I did have the genetic testing done but haven't heard on the results yet. So far Tamoxifen hasn't done much to me. I'm having some tummy cramping and my TOM started one day then stopped......I've been a little cranky but they laid off 4 people where I work and we are all trying to circle the wagons now and picking up extra tasks.....I think the cranky comes from that more than the tamoxifen. It is a little chalky going down but I take it with a lot of water and haven't had it stick in my throat yet.
DianaRose, My prayers to you as you go through chemo! This too shall pass!
Prayers for all of us as we move forward through this situation! I keep telling myself it is making me stronger.....I don't know that I quite believe that yet.
Everyone stay cool! We are having record breaking heat here in Chicago today! Sure doesn't feel like June! more like August.
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Lisamarie- sorry about your pain. Just think in 3 weeks you can get the dam things out and get your squishy girls.
I went wig shopping yesterday. I need one that is heat resistant because of all the commercial ovens at work. I about fell out of the chair when she told me the price. It is 950.00 and my insurance will only pay 350.00. It all sucks. I hope my mortgage company is sympathetic because my payment for July is going to be a tad late.
Work is crazy busy, but I have a hard time sometimes with I guess what is chemo brain. I go into the walk in and forget what the hell I went in there for. Picked up all my meds today to start regimen #2 on Tuesday. I wish It was the last one. I just want my life back. The hair too would be nice. Well I used to have to bleach my upper lip, but now there is nothing to bleach. One positive thing.
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Dianarose , I will keep u close to me in my prayers. I don't know if I would have been strong enough to make it through chemo too
I am hurting bbig time with this last fill , usually I am okay by day 2 but no , I am at work and I feel like im gonna die . I have taken 2 flexaril already today . I just wanna go home and take a percocet and go to bed .. Oh yes and the anti nausea meds too cauuse I puke pn percocet ... but if I am gonna get sleep I must take it ...dr says the muscles are spasm .. but its just pain to me and burning ... oh how I hate TE's and will be glad to get the exchange . but still fearful of recovery all over again .. doc also says recovery with exchange is much easier . he said oh its like changing a flat tire , ur in and out .. lol.. I sure hope so ...Valerie , hope all gets better with the tamoxifen..
Hugs Lisa
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Lisamarie- I have never had pain after a fill. I don't get much each time because I can't get the exchange until next yr so there is not point in rushing. I am only at 210 each side. It's more than I had to begin with so I not going to complain. Are you going with silicon or saline? I took Xanax for the spasms. It worked great, no puking, and it helped me sleep. I am not a fan of pain meds or puking. I haven't puked with chemo, just nausea where you think you are going to. Hope you get some sleep.
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Hi gang! Good to hear from you all! Even though it might not all be good, at least we are healthier and kicking the Big C's butt!
Dianarose, you are my hero cuz you are always so positive (no longer need to bleach upper lip - too funny).
Lisamarie, sorry you are having so much pain again. I still have only 60cc in so I am not looking forward to the fills but at least you are that much closer to being done with all this stuff.
Valerie, my MO is suggesting Tamoxifen but I am very reluctant to do it. I am studying to become and acupuncturist and now that I have "cleared" most of the cancer, I am going to utilized the Chinese Dr's that I know to do the rest. But, good luck to you. It sounds like you have the right attitude. If you do experience any side effects (especially hot flashes or insomnia) check into you local acupuncture clinics cuz they can do wonders to help relieve the SEs.
As for me, I am still healing from my ALND. The "shingles" pain is subsiding finally. I am on Gabapentin and I found a miracle cream called Neuragen. The cream is used to relieve neuropathy (numbness, tingling, burning) for diabetic patients but it works great for my SEs.
Anyway, hugs to all!
Kristi
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Dianarose , I look like a mini dolly parton .. omg im so big but its just overfill he says , I am having a B at exchange and I am doing silicone. I am still in so much pain the TE's are so full they are even under my armpits and it sucks because I cannot shave good due to them . besides the fact that my arms rub on them each time i move .. its just gross.. This is the most pain iv'e have since having any fills , I am thinking I am over 400cc in each as he did not tell me how much he placed this time . I am praying that the exchange is not bad . I have not gone to bathroom since tuesday .. and the laxativs dont work .. im just getting more and more miserable , and I work this weekend .. anyway I complain too much and feel like a big baby .. but it really hurts burns pulls .. its crazy ... Hugs to u all
Kristi glad u are healing
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Hi- I got my wig today. I really like it. It looks real. I was taken by surprize when she said my insurance wouldn't pay for any of it. I didn't have enough in my account so she is going to wait until next week to cash my check. Dam bs is expensive. I am so in the hole now. I am using my mortgage money. Borrowing from Peter to pay Paul. Well, I look good dam it. It makes me feel so much better to have hair. I don't have many eye brows left, but still have to shave my legs and arm pits, WTH. I am going to try to work a few extra hours a week. I start round 2 of chemo on Tuesday so I better do it before then.
It sure will feel weird to put my hair on a styrofoam head at night. What can we do, we are all on this cruise ship together. It it starts to sink like the titanic maybe our tissue expanders will keep us afloat. LOL
Lisamarie- sorry you are still in pain. Did you get your exchange date yet. I am envious of you getting your squishy girls.
I hope eveyone has a good night.
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dianarose...I am sure that wig looks beautiful on you; wear with your head up and a smile on your face!!! If you haven't already check out Look Good Feel Better; they hold workshops to help women going through chemo look good and feel better. The workshop will teach how to apply makeup the right way for your new skin affected by chemo, will show you how to use makeup to make eye brows, etc etc...all FREE!!!!!!!!!!!!!
keonghi where do you use your miracle cream neuragen on what part of your body. I have the numbness tingle etc on my arms, under arm and boobs. Well I have the flap diep procedure and it's totally numb and the nerve endings keep me up at night. is that cream good for all my problems?? I was thinking about going to acupuncture for insonmia, I haven't had a good night sleep before surgery, even with drugs of all kinds. Does it really work? Do I need to go to someone who specializes in insomnia.
Everyone, please feel better, xoxo
Oh my PS said I do not have to wear a bra but if I want to I can, underwire or not. I went to Wal-mart and got a size up because I'm still swollen/numb didn't want it to be tight but my god, $8.98 each! I will wear one tomorrow hoping it's comfortable since I go back to work in 2 weeks. the brand is Dream Fit in case anyone else is in need of a comfy cheap bra..
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I am keeping you in my thoughts Dianarose. Geeze. insurance couldn't pay for the wig? Crazy, it is a prosthesis after all.
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rtnyc - Neuragen definitely will help and it is homeopathic. Also, one of the things that Chinese medicine can help better than western MDs is treating insomnia.
I put the cream all around my upper arm and on my shoulder blade 4xday. It has worked wonders with stopping that extremely sensitive skin and the sharp tingling. It doesn't take it away 100% but probably about 80%. Any relief I can get is better than nothing. I also tried Aspercrem and that didn't do anything except make me nauseous (one on its side effects).
I bought the cream in the muscle cream section of Walgreens (I'm sure any drugstore would have it). You can find a .15 oz tube of Neuragen PN in the diabetic's section for $30 or you can look in the section where there is Bengay etc and find a 4 oz tube of Neurogen cream for the same price. I think they charge more for diabetics cuz their insurance will pay for it. here's the website for it http://www.originbiomed.com/neuragen
Dianarose - Sorry to hear about the cost of your wig. Just remember when you are putting it on the wig stand, that it is only temporary. Your hair will come back stronger than ever.
Hugs to all!
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I thought insurance had to cover a wig? I would check with your insurance company.
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