March 2011 Rads
Comments
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Ms Jag I also had a lumpectomy. I wanted a shot at keeping the nip. my RO and oncologist both said the difference in mast and lump with rads is very small. If there is a recurrence I can go mx. Don t worry, you are in the home stretch. Libraylil
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doreyme: That's exactly what I've decided. I'm not going to obsess (though I can't help it if it pops into my mind from time to time). But it the BRCA comes back positive and I do have a recurrence, I will definitley do the BMX. What will be, will be, right?
lovemylife: I know I am one who said not to care what others think, but I am also concerned about going out with no hair this summer! So, there you go. Just thought I'd let you know that I understand where you are coming from.
You are SO lucky!! I love Charlie Daniels. Don't know how many times I've seen him, but it was always good. We used to take the kids to their concerts when they played at this little beach/picnic area in Massachussetts. Good times!! (Love 38 Special too, but have not seen them play.)
Happy Friday and a good weekend to all!
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doreyme: That's exactly what I've decided. I'm not going to obsess (though I can't help it if it pops into my mind from time to time). But it the BRCA comes back positive and I do have a recurrence, I will definitley do the BMX. What will be, will be, right?
lovemylife: I know I am one who said not to care what others think, but I am also concerned about going out with no hair this summer! So, there you go. Just thought I'd let you know that I understand where you are coming from.
You are SO lucky!! I love Charlie Daniels. Don't know how many times I've seen him, but it was always good. We used to take the kids to their concerts when they played at this little beach/picnic area in Massachussetts. Good times!! (Love 38 Special too, but have not seen them play.)
Happy Friday and a good weekend to all!
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Wow guys, my hips are crazy achey! And my right hand is swollen and very sore. I thought it may be arthritis didn't think about it being related to the rads.
Lovemylife- hee hee hee. Sammy Hagar. That made me laugh!
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I had the genetic testing done before I finished chemo and it was neg (I have 3 daughters...that was GREAT news!). I was told that if I had a lumpectomy, the chances of it coming back were 5%. If I had a BMX, the chances of it coming back were 3-5%. Not much of a difference, so I decided to keep 'em! I also think that most Dr.'s are afraid of the "if it was your wife..." question and don't like to give an answer. But since he did, I would say to take his word for it.
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My gut reaction to my diagnosis was "take 'em both off!!!" but my surgeon very calmly talked me down to only removing the one with the tumour, then went forward to explain all the pros and cons and percentages and by the end of the session, I was agreeing to a lumpectomy but if she didn't get clear margins the first go, it was to be a mastectomy the second time in. That was our "deal" lol.
It was my choice but all ready knowing that I was going into chemo and then rads(regardless of lumpectomy or mx) , I agreed with my surgeon that I shouldn't really weaken my system with a bigger surgery than was really needed. I have been comfortable with my choice.
Lovemylife - Don't ever be jealous of SNOW!! I love the heat and truly believe that I was born in the wrong hemisphere!
Saw my RO today, and he gave me a couple solutions for skin care for itchy, rashy, boobs....so far the Glaxal, Aloe and over the counter hydrocortisone cream are working. He also said to bathe in water and epson salts and then use a blow dryer on your breast - never a towel. The epson salts are especially soothing on peeling/blistering skin...that surprised me but so far he hasn't lead me astray! He also said that often, skin problems occur a few weeks after you finish treatment and he wanted me to be prepared.
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marjie: Are those kitties direct decendents of Bengal Tigers? They are incredible!
msjag: I have a low grade cancer but I understand the fear. I'm 37 and I wonder if this BC is just the begining of a life in and out of the surgery center. I've noticed a several women with my type of cancer have had persistent issues, and it nags at me. I've never been a really religious person, but I'm finding there is a spiritual nature to a BC dx. I just keep focusing on "handing the fear over" to the powers that be. What will be will be. It's become one of my many mantras.
BRCA testing: I know I've whined before about this, and I'm actually on the upside of the pit of despair thanks to the above mantra. I just met with a genetic counselor and a MO that specializes in the genetic aspects of BC. I gave them my entire family Hx of health, and there is NO cancer of anytype. They said there is a 12% chance that I may be BRCA+. I currently have a uterine fibroid that's 3cm, and a complex ovarian cyst that is 3x2x3cm. This was found 30 days ago, and was my original reason for going to the Dr's...I thought the previously dx uterine issues were acting up after 3 years of silence...then BC took center stage. So the genetic counselor and the MO, are trying to fit me into a PTEN mutation or Cowden's syndrome very rare 1/200,000. But it just doesn't fit, I don't have haratoma's, I don't have developmental disabilities, And I don't have macrocephaly, or an abnormally large head, (physically speaking
), and my uterine fibroid is really not concerning me, it's my ovary, but this syndrome is heaving on uterine issues not ovarian issues. no one in my family has any such issues. There is an inordinate amount of $$$ going to genetic research for BC...I think that this study that is available thru Cleveland Clinic is one that the Dr's want to be part of, so they are trying to fit me into it. For instance when she measured my head the tape was really loose. I would never measure anything like that...it's just not accurate. I know I sound like a conspiracy theorist, and most likely I am, but I have read articles about the $ in genetics and how this $ incentives are shaping the Tx plans for BC survivors.
Needless to say I have really mixed feelings about the genetic aspects of BC, and the $$$ behind the testing. I would encourage anyone who is consdering the tests to research thoroughly before you spend big money, and have mixed results.
25/33: I'm bright red and the rash is migrating...healing in the original part, and moving around my breast. I was told this is the hair follicles giving up and dying from the radiation. If that's true, why couldn't they nuke my arm pit? Then I wouldn't have to shave! I also found out that I am 28 reg, and 5 boosts,
Somehow I reversed the numbers. I think these last three whole boob sessions are going to be a beotch!
Happy Sunday!
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Sandymess: We got at least a foot of snow. Yesterday was a wonderfully refreshing snow shoveling day...It was heavy and wet and I sucked wind after the first 3 shovelfuls. I'm so lucky to be able to shovel snow in April! Don't you feel the same?
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Oh, yes, GirlFriday! And the contrast of the beautiful white snow with the mushy, muddy driveway is JUST beautiful. Lucky, indeed!!
I also have mixed feelings about having the genetic testing done. I am really not convinced of any benefit--to me or to my family. Perhaps the doctor can better explain why I should have the testing done. I guess I'll find out in May when I see her.
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GirlFriday & Sandymess - you make me laugh with your "love " of snow!!
This week I have the last two regular rad sessions and then on to my 8 boosts....so only 10 more days left! Just like chemo, in the beginning it seemed like it would be such a long time but it has really flown by and I can't believe I am looking at the end of this soon
Wednesday I have herceptin tx as well as rads - makes for a very sleepy day. Just counted forward on the calendar and my last herceptin is not until next Christmas....wow.....seems like such a long time
. Ah well - this is the drug that is saving my life!
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Wow, marje, seems like just yesterday that you started this thread. Good for you being so close to being done, I'm a bit behind due to weather, illness, hope all goes well with the Hercepttin, after rads, that's it for me, no pill or other drug, due to being triple negative. I gotta just have faith that the chemo and radiation blasted those cancer cells!
Snow is melting fast in MA, nice to feel spring in the air!
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How many of you ladies will be going on to Tamoxifan or something else after rads?
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I meet with my MO in early May. It remains to be seen whether I choose to take it or not. I know it's part of my survivorship plan, but I have mixed feelings.
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Marjie: I am exactly the same- 2 regular rads left and then 8 boosts. My skin really took a beating on Friday. It is bright red pretty much everywhere with a few preblisters on upper chest. I've got RX for those and that area only has Monday/Tuesday left. Then on to the boosts to my BMX scars. Sure hope these boosts are as easy as the techs say. Am now slathering stuff on 5x day. What did your RO say about boosts? Is it just as tough on the skin or less?? My Herceptin's next Monday. Yep, long day...
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3teacher - It is my understanding that the boosts are not as hard on the skin and they are a weaker or less intense "shot" of radiation. But that being said....my RO also told me that my skin would continue to be irritated for a few weeks after the last treatment. A friend of mine who had radiation told me to expect to "contiue to cook" for a bit afterwards too. I guess we'll find out.
Right now I have an itchy rash just above my breast, and the whole radiated area is darkly tanned. I'm not being as vigilant as I should with cream but at least once a day and then once at bedtime. It seems ok.
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Marjie - We're ending on the same day, but mine are all tx - no boosts because of the problem I had healing from surgery. I don't want to stress that area more than we have to and the RO agreed. They did do some type of boosts when I was so burnt last week, but they put a bolus on the scar.
Shooshoo - I have been on Tamoxifen since the beginning of January. It's not horrible. I do have the hot flashes and I itch when I get one. Other than that it's ok. The biggest problem was that I was on anti-depressant for anxiety and that had to be changed. That was the roughest part.
Hope everyone has a good Monday. Back to GroundHog Day.
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Marjie and GrandmaBubba, I too will be done with rads on the same day. I will be getting only 5 boosts so a couple more days of regular ones than Marjie. My RO techs said the boosts are really easy. I sure hope so, because under my arm is burnt to a crisp!
ShooShoo, I will be taking Arimidex for 5 years if i can tolerate it. If not some kind of AL for the next 5 years.
I hope everyone had a good weekend!!!
Pam
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Hope everyone had a good weekend and is ready for their week.
Shooshoo23- I'm meeting with my MO tomorrow about going on tamoxifen or other meds. Don't know if she'll start me on it tomorrow (I'll be 22/36 including 3 boosts) or just give me bone denisity and whatever other pre-tests need being done.
Marjie- No tan or burn but I've got an itchy red rash covering area where I'd been sunburned before and it's getting angrier looking by the day. The cortisone cream hasn't helped. Who prescribed your RX for yours? I'm wondering if my RO is just reluctant to write prescriptions or can't write them.
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Marjie: Now it makes sense. That's what happened this weekend...I "continued to cook". I thought after Friday's tx things would have the weekend to settle down. Friday night was fine and Saturday morning, but by Sunday morning- yikes, so really bad spots. I thought that was so odd, but your explanation makes sense.
Let's get these 2 regulars over. Yep, Ground Hog Day (GrandmaBubb, that is tooo funny, but so true!)
Ginger: My RX for these "preblisters" is called Triamcinolone Acetonide Creme USP, 0.5% Have no idea what the heck that is, but it has sure helped. My skin is major fair and these issues only started on like tx#20 (can't really remember- they gave me this RX way back when one area started to show signs, but RX stopped it) I think the next RX will be silvadine if these places open up, which I think they will after today's zaps. Hope not, though.
Here we go this Monday! Good luck to all you Warriors!
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I cooked this weekend too!! What a great way to describe how my chest feels. . definitely overcooked!! I love watching Top Chef and they always talk about taking meat out of the oven early to let it "rest" because it keeps on cooking. I guess as we rest, we keep on cooking. All I know, is that I am itchy and in pain more today than ever-with my last regular tx on Friday. Owww!! Even my tech commented on how raw my underarm is. If I could wander around my house shirtless, I would. I think I would scare the dog!!
But the good news was that my first boost was short and quick. I counted the red flashes on the wall, 35. And the odd thing is, my scar area is the least red of my whole chest. Is anyone else like that??
Here's to healing, and lots of lotion and a little chocolate in between!!!
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cmblastic
I have also cooked under my arm. had the last tx today and 5 boost to go. My skin was doing okay for 4 weeks and in the last week, I am literally burnt under my arm its dry extremely sore and now peeling. It the same under my breast but not as intense as the under arm area. the rest of my breast is red but the scar like you has not been affected. I find it difficult to sleep have to keep my right arm straight out to air our my underarm. The only good news for the day is I got to toss the cup they put around my breast for the last 5 weeks. It was very freeing. The nurse also recommended Mepilex Lite bandages to put under my arm and breast. very expensive at $32 for 5 but if anything can relieve the pain I'm all for it. Cant wait for the ridge to be over..
Good Luck to everyone and good health!!
Lisa
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Help! I had my last chemo 19 days ago and I woke up in the middle of the night with bad nausea and bone pain in my legs. I have surgery on Wednesday. Why am I feeling like I had chemo last week? Please help,
Nancy
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Woke up this a.m. with scratches on my breast, I guess it must have been bothering me when I was sleeping. Found the trick to feeling better is getting lots of sleep. Going to ask for a refill on Ambien and maybe wear a glove at night on one hand like Michael Jackson - LOL! 18/30, red under arm, and tired, but still keeping up with working, cleaning, and cooking. I think I deserve a vacation afterwards, just not someplace sunny! Blessings to all.
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IllinoisNancy: Sorry I didn't have chemo...maybe your question would be better answered on the chemo board? I can say that all of us have felt side effects and other issues outside of the expected routine of SE! Remember stress has a huge impact on all of our treatments too, so maybe you just maxed yourself out? I would encourage you to call your MO or maybe a nurse at your facility. They should be able to talk you down if you feel like you're on the edge of a cliff, or get you some assistance if your body is screaming for it! Call now! Don't delay!
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26/33: You all are totally correct about the delayed cooking thing. I was twice as red Sunday as I was on Friday! The RO said my skin looks great, but I'm having trouble not scratching at night too! He encourage me to put the hydrocortisone on first and than cover with Aquaphor. I didn't tell him that I haven't been using it at all...I think I am to a stage where my Baby Aveeno is just not up to task. I'm going to pick some Aquaphor up tomorrow!
And for those of you who have diligently not shaved...last night I was reading in bed with my arm up over my head, and my beau said..."There's a mouse in your arm pit!" I'm happy to say he's still breathing!
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Re: the armpit thing, my husband likes it which I find kinda disturbing. Didn't know he was a "George of the Jungle" kind of guy.
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My beau said that too, after I suffocated him in a hairy head lock. He said " I don't know why women shave there anyway...It doesn't matter to me." I almost felt bad for rendering him unconscious, but then I remembered that early when I asked him what he wanted for dinner he said "Something good"
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IllinoisNancy - it takes awhile to get all that chemo out of your system. What were you on? Could be some lingering SE's but I would check with your onc.
GirlFriday - my armpits are bare because of chemo, and my RO said that it is quite likely that I will never have hair under my rads arm....ok by me!
My tech today said it looked like my skin might "open up" - lovely
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marjie: You are so close! It's not going to happen! I refuse to believe it!
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Keeping my fingers crossed for you, marjie!
I just noticed this weekend that I have hair growing under my arm. It's very sparce but there just the same. I was hoping it would NOT grow back after chemo!
Finished 12/33 today. Didn't have to see the bobble-head nurse, so that was a plus. My skin is still fine--no red whatsoever. (I'm knocking on wood right now.)
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