January 2011 Rads
Comments
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13 RADS done! I have been using deodorant because my radonc never said not to wear it. Today I asked the techs abour deodorant because so many people in the boards had said they were told not to use it, or were told to only use certain deodorants. My RADonc says it is OK to use the same deodorant I always used. That is good because I do not want to go an entire day at work without it!
Someone mentioned abou their machine going down. That happened to me last Mon. I think all machines break down once in awhile, I wouldn't worry about it unless it was a constant thing. My session was almost over so they just added the time to the next day.
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i always have nausea.way before i started doing the rads.now it did get worst.never thought it was a S/E..maybe so.the rad onc says no.not too sure about that one.
I did #15.tomorrow i reach the 1/2 way point.im doin good.just hoping it stays that way.Jan 30th is my granddaughters baby shower....please God dont let it hit me then.
It didnt start snowing in NJ yet....we are expecting 6-8 inches tomorrow.NOOOOOOOOO.
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Lots of info from all of you ladies! I have a heard time keeping up but I am trying! Some of you have answered my questions-I love your feedback!! I had 3 treatments and then we had snow in Atlanta which brings everything to halt. I will miss treatments-does this matter? I am worried. I am so relieved they told me not to try to make it when the roads are horrible but I worry!
All of you Texas ladies-I enjoy your posts. I know where Frisco is and you have an amazing Christmas light presentation. Very cool!
Hey Canada girls don't think the US has horrible healthcare-I am paying for this treatment but compared to the cost it is very small. I am thankful. I have choices and I do NOT want the government to be a part of my health care.
Debbie
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Wow, lots to catch up on! I'm very happy for the ladies that have the rads finish line almost in sight. I've had 6 sessions now and I'm already a bit pink and the outline of the treatment area is already visible. The nurse suggested I wear a bra as little as possible. My breast is a bit achey but not too bad. I don't have nausea but I do have headaches, they usually start not long after I come out of the treatment, not sure if it's tension or rads related but I don't normally get headaches. I'm using a crystal deodorant but I'm not sure if it's that effective. I've dedicated a storage box to the old tshirts and bras that I'm going to use during rads (and will probably get rid of when I'm done!), so that makes it easier to find my comfy clothes for the top half when I need them. Good luck to everyone this week!
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Hey Suepen - are you okay there in Australia? Please check in! Just reading about the horrific weather and small tsunami that battered a town.
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Hi Oakley,
Yes, we're fine - we live on a hill but our city (Brisbane) is due to flood in the next couple of days. We have a big river running through the city and low lying areas will be affected.
That "tsunami" was in a city 2 hours inland up on a range!!!! A creek that runs through the town just exploded with a torrent. The loss of life has been very sad. Towns down the range from the first city were also devastated by the water and lots of people are missing. Houses actually washed away.
The rain has stopped for the moment thank goodness, but there may be more on the way.
Sue
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Michcon - about my 4th treatment my skin was warm and red to the touch. The aloe helped with the redness and Miaderm helped with the heat. I get these bolus treatments everyother day and seems to make my skin more red as it radiatiates just under the skin. I am well prepared for those days now.
A close friend who finished her rads treatments in December saw RO yesterday and he said he did not need to see her any more. We have the same RO. She had a two month head start on this journey. Hope the same is with me not that I don't like him, but I am at a higher risk % of BC coming back than her, so I maybe different.
Paula - Where is Center Valley, KS? I grew up in Fowler, KS; SW corner near the OK border.
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victoria67--I used the crystal deo and did not find it very effective. Luckily for me about week three my glands quit working and no more underarm odor. Kinda hope it stays that way.
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Jo - Thanks for the artwork! I always know it's you!
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Omaz - Just trying to keep things on a positive note.
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Hey Ladies,
Sounds like everyone is doing well in the first weeks. I can say that I had nausea in the beginning. My Onc nurse called it "general malaise". It did go away by my appetite has been less since I started. I have been haing a Boost drink on my way to rads in the am. With extra protein which I think has helped. I think the fatigue just makes you not want to fix anything to eat - I would eat if someone put it in front of me but I don't really want to make anything (don't you wish chef/maid service was covered on insurance!)
Had my last boost yesterday and will finish my 4 make-up rads this week. Hopefully the snow won't be too much of a hassle here in New England. Hope everyone's week is going weel
jen
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Jen - wishing you no hassles over the next few days so you can get through the 4 make up rads. Hope everyone else's treatments are going well too.
Is anyone experiencing a warm arm as well as breast? It doesn't feel warm to the touch, more like it feels warm/hot on the inside if you know what I mean from my shoulder to my forearm. I've only had 6 tx's.
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Jen---Here's to finishing your rads ASAP! I also wish that I had a chef to fix meals--granted this wish was there even before cancer! I am just about to head to radiation #2 and although don't have any SE, can see how going to the hosp everyday will become a hassle.
Victoria--I went to my first radiation yesterday and was feeling like my breast was a little achey--I am guessing mine is mind tricks not real symptoms. I am so fair that I think that I am just on guard for any side effects! Hope that you are feeling OK.
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I think my radiation is planned to start for the first week in february, but I had my planning session today. I was excited about finishing up chemo last week and feeling that maybe I was going to survive this cancer thing afterall. It was odd...my radio-onc seemed totally doom and gloom. She even went as far as to say if the cancer had moved to the lymph nodes then it was probably already somewhere else in my body and that in the past they didn't really think radiation would do much to help with that...then she said "we're starting to find that radiation does increase the chances of survival for people in your situation." Um, starting to think?
I will admit I've been pretty depressed this last week, which tends to happen to me a couple of days after cvhemo, but she acted like I was already dead!! She went through the path report with me and explained that I had 3 positive lymph nodes (as if I didn't already know this information) and basically said we would need to wait until my cell counts are up. She acted like she was talking to a little kid who had very little chance of survival. I'm so frustrated and upset. I hope everyone else is having a better start to radiation than I am and a little more positive outlook from the onc. -
Heather--I'm so sorry that you had bad experience with the RO. My RO has very little personality but provided a lot of information when I first met with him a couple of months ago. He answered lots of questions. In my case, I had lumpectomy so rads are really important to ensure that any remaining cancer cells are killed (or that's the hope). I am very surprised at what the Doc said to you--crazy. Some Doc's should be in a lab not in front of a patient. If you really have a hard time with her, ask for another Doc if it is possible.Take care, Rachel
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#7 today, energy seems zapped this afternoon, I think it is my Tuesday blues. Happened last week for some reason. Saw my RO today, walked in and said "Hey Sweetness", I wonder if he says that to all his female patients or just me. Forgot to ask. I ask next week.
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Mjbmiller, sorry your energy is low today, I hope it picks up for you
Heather - I'm sorry to hear about your experience with your RO, bc is hard enough without having to deal with someone making you feel that way. Hopefully things will improve or you can tell her you feel, sometimes I wonder if they get caught up in their reports and numbers and forget there is a scared human being sitting in front of them. I agree with Rachel, some docs should be in a lab, not seeing patients.
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heather - Before I chose my current med onc I met another one. She was so negative. I also met with two breast surgeons and one was also negative. I thought it was important that my doctors be positive people since I 'catch' their 'vibe'. You may want to consider changing rad onc if at all possible. Hope you come out of the chemo ughs soon.
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Heathermcd: Nothing shocks me these days, so the disgraceful, downright unprofessional, behavior of your rad onc just confirms my feelings about many members of the medical profession. If at all possible, seek another rad onc even if it means delaying the treatment a bit. Warm wishes, Barbara
mjbmiller: I think my energy has been blown away by the wintery wind. Frankly, if my RO greeted me as "Sweetness" I would scream--which just might boost my spirits. One of my rad techs, a beefy bald man, annoys me by his repeated comments about the color of my pants; it's gotten to the point where I no longer want to wear my favorite purple velour. Silence has its merits.
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What happened to professional ethics in the medical community? Men can be such "pigs" and some women are just down right cold. I remember my rad onc as being a moron with the personally of a piss ant. Just pisses me off.
Sorry about the ranting - but I feel better now.
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Heathermcd - I am really sorry that you had such a negative experience with your RO today. That kind of negativity is not what you need when your worn down from chemo. I second what several others have said that you should seek a second opionion. I too have positive nodes and my RO has been very positive. She shares all the latest research with me, such as a study that was presented at the ASCO meeting in December that showed radiation decreased the risk of recurrance in women with 1-3 positive nodes. It's important to know how the radiation plan is set up. Will you be getting radiation to the breast, supraclavicular node area and/or axilla and why? You need a RO that you can have a meaningful discussion with. Don't let that @#*$& take your hope away. Sending you hugs.
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Hi Ladies - Just jumping in from Dec rads... ONE MORE TO GO -- woohoo!! I'm lubed up, peely, itchy and saggy but thrilled to almost be over this hurdle. My magic lube potion was - aloe vera gel (GNC sells purse sized tubes), hydrocortisone cream, topped w/zinc oxide - the tech recommended this combo when Aquaphor and Xclair didn't help when I had the severe burn last week (RO said it happens only 15% of the time) I'm rather large breasted (34H) and can't wear a bra - fun times at work! I wear cotton v-neck cami's w/spaghetti straps, one boob in/one out so they don't fight or rub, topped w/a cotton long sleeved shirt - the tightness around the arm & pit keep my skin from rubbing. I wear everything inside-out so the seams don't rub my skin. Old Navy has the tank's/cami's and I got the long sleeve shirts @ Target. To disguise the sagging nipples, I got a poncho/wrap thing @ Kohl's, pin it shut and walk very intentionally or hold something at chest level!
I'll stick around to see if I can offer any support to y'all. Hang in there - you can do it!
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Congrats marriedblis on your graduation
I am not looking forward to getting to a point when I am unable to wear a bra with these DD's.
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raincity and marriedblis - Congrats on finishing married! I can't imagine not wearing a bra to work. Oh dear. I have only done 2 tx but last night I was trying to figure out some kind of sling thing in case the part underneath the breast has trouble and I want to 'lift' it up. Felt like a Star Trek outfit from the original series!
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ANyone have some difficulty breathing or catching their breath after RADS? I've had 14 treatments and have noticed that I am having trouble breathing here and there. My RADS is direced at the 1:00 spot where my tumor was. I know that is close to my lungs. Does RADS damage the lungs?
Heather, so so sorry your radonc was so negative. Cancer is a big business and a big money maker for docs and hospitals and cancer centers. You and/or your insurance Co is paying for your treatment. Take your business elsewhere if your radonc makes you feel bad. There are many many radoncs and treatment centers. You have enough to deal with without having anyone add any negativity. Yes, you want to hear the latest statistics, but you certainly don't need her to make you feel like you should be planning your funeral instead of your recovery.
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heathermcd-so sorry about your RO's attitude. I can tell you that I have a very good friend who had a very agressive stage III ILC in both breast with node involvement. She had a double MX went through chemo and rads on both breast and is doing great. That was 4 years ago. You might want to consider another RO with a better attitude, it will not hurt to put rads off a little if that would make you feel better.
Jen wouldn't chef service be great to have. I know what you mean about sometimes I just don't feel like cooking and fast food just does not appeal to me. DH is great with takeout so I give in sometimes instead of going hungry.
marriedblis-I have to chuckled at the picture you give about your braless getup. I am lucky that I am small breast and ditched the bra 2 wks in. Silicone nipple shields have been my saving grace at work that no one knows I am going braless, pluss my nipples have been sore and that has helped protect them. My RO suggested that I get them and they have been great. Good luck on only one more to go.
CMF it is pretty rare but it can happen you should talk to your RO about it and ask how close they were to your lungs with the planning. I've read that you can have leasons but I don't think it causes any real problems.
I have 3 more regulars tx and 6 boost left to go. My RO said my skin looks really good (even though I am peeling like a snake) so if it still looks like this next week even though I finish on a Monday he will not make me come in for a skin ck on Tuesday. I can wait for my 3 month check up to see him. Also this cancer was my 2nd lumpectomy on my left breast and it is smaller than the right. I have been planning on having an implant to fix the lopsisdedness. WE talked today and he told me I should be OK to go forward with in July depended on what my PS says about it. Will wait on that appt until some of the swelling goes down. It feels good to finally be able to start planning the future.
Good Luck to everyone!
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cmf-you don't say if you are left or right rads. rads can hurt lungs but a good rad onc will plan your treatment as best he can to avoid that. at my meeting today, he was able to tell me that for the first 3 weeks, we have not done any lung damage. you say your rads is directed at 1:00 - the full breast radiation does not direct it to that spot, it does the full breast but your boosts will direct it there but those are done at the end. I also have had 14 treatments
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#7 today. I can feel something sort of "twingey" deep within the breast, unless my mind is playing tricks on me. Also, feel a little tug in the armpit area. I had many nodes removed and have a nasty scar there, so maybe just the constant having the arm up in that unique position is all.
Also, I still have my port. It is causing me a lot of grief. The actual port part moved and seems to be pulling the tubing with it. It is red and hot to touch, aches constantly and is driving me nuts. I have told everyone that will listen and finally they have decided they will remove it this Friday! I pray I can make it 'till then.
take good care and just breathe. . .
Teklya
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Tekla good luck with removing the port.
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