Fall Rads 2014

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  • Gilesmt
    Gilesmt Member Posts: 65
    edited November 2014

    blown away, since I have to research everything, because my docs do not give me any info in a format I can read. I researched, and rads will fry your thyroid. It usually takes longer, but I had problems to begin with so mine wnet faster. But it is known to be the most overlooked, and most under estimated side effect of breast radiation, because usually it is 8 or 9 years out when you get it, and they just blame old age

  • Gilesmt
    Gilesmt Member Posts: 65
    edited November 2014

    blown away, from everything I read it says the boost do much more for you than the whole breast so it is good you are getting more of them, I asked many times to have more boost and less whole breast but they refused.

    Also I can't figure out why, the part of my breast that had Cancer shows no signs of being radiated at all. It is white and perfect, like a moon shape there. Everywhere else on the beast is red, raw, burnt, purple, black, cracked, blistered, or something during this treatment but where I had Cancer, is white, healthy and fine. I think they missed big time. All seems to be healing nicely now, one week out

  • Jaimieh
    Jaimieh Member Posts: 2,373
    edited November 2014

    Post rads follow up was today and I am going to be starting on a drug that helps vascular issues to try and prevent fibrosis in the breast. I sure as heck hope it helps.

  • Blownaway
    Blownaway Member Posts: 760
    edited November 2014


    Gilesmt - I already take Armour for hypothyroidism which is why I wanted to 'protect' my thyroid but the doctor and nurse acted like I had grown a flower pot out of my head. They didn't break out and laugh but 'scoff' would be a good term for their reaction.

    I'm glad you are healing fast. It sounds like you really had some reactivity going on there. Mine is really angry looking. Hubby gets scared just looking at it.  Men are such wimps.....

  • clarrn
    clarrn Member Posts: 557
    edited November 2014

    Giles- yes they did talk. I was sent to the hematologist who ran a bunch of blood tests and determined it was safe for me. When the 3rd arm of the SOFT/TEXT trials come out (the tamoxifen alone arm) I will reassess what I want to do. He did give me the option to stay on Tinzaparin ... ha! As if I want to give my self that stinging shot everyday for the next 10 years!

  • jeanelle
    jeanelle Member Posts: 179
    edited November 2014

    Blownaway - They say the same thing to me, telling me that even though I think this looks horrible that it is nothing. The skin under my arm by my SNB scar is peeling now but it doesn't hurt like the area under my breast. Oh and i forgot to mention that every pore on my breast is now visible so it looks like a freshly plucked chicken. LOL I can't wait to see what it is going to look like when all this is over.

    I'm also surprised you have so many treatments. I have just 30...25 whole and 5 boosts. I'm not sure I could handle 36.

    Today is my last whole breast treatment! Hopefully, the sore spots will be able to heal quicker now that they won't be blasted every day.

  • Gilesmt
    Gilesmt Member Posts: 65
    edited November 2014

    I think they are so numb to it, they all say you are doing good, or you look great, or whatever. I would have loved my RO to have gone thru this and have her look at black, dead skin, like I was in a fire, skin raw, blisters, red, cracked, purple, brown, itchy and say oh you look great.

    I will say it gave me one perspective. My dd has CP I had to put night cast on her and day braces, she use to scream and swear at me, but I was doing it for her own good, since she now walks and runs like normal. I felt the same way she must have with the nurses, I hated them thinking this wash lol great, when I was in pain. More respect for my dd

  • skbrown
    skbrown Member Posts: 40
    edited November 2014

    Hey ladies. I had my first radiation yesterday.  I am scheduled for 23 with 7 boosts.  Does the 23 include the boosts or is it 23 plus 7 boosts?  Also, are the boosts always at the end or are they done here and there?  Is anyway dealing with anxiety issues.  If so, how are you working through them?  I was on depression meds a while back and quit cause I did not need them, but this is getting me feeling the same way I used to.

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited November 2014

    SKBrown, it means a total of 30 trips for radiation :) Boosts are usually done at the end. I didn't have any anxiety issues - just very happy to be doing something else to kill the cancer cells. Someone else here will be able to talk to you about your possible depression and anxiety. Try to think positive!

  • skbrown
    skbrown Member Posts: 40
    edited November 2014

    my schedule has 22 on it so far.  I guess I will get another one for the others.

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited November 2014

    Probably you will, SKBrown. Most of us get between 25-35 and radiation treatments. I had 33, 27 and 6.

  • Jaimieh
    Jaimieh Member Posts: 2,373
    edited November 2014

    skbrown ask because some places will do 16 with some boost. I did 25 on my super clavicle, 26 at the other two fields and 7 boost.

  • labelle
    labelle Member Posts: 721
    edited November 2014

    I guess I'm signing up for radiation in the near future too. Was actually thinking about skipping it but because they found a few cancer cells in one of my nodes, it's off to radiation I go and I'm not looking forward to it, but there are lots of really good tips on this thread. Thanks to everyone for sharing. I'll soon be shopping for those all cotton sports bras-the ones I bought for my lumpectomy are mostly spandex and nylon, and so apparently no good. Geez. I'm buying more damned bras this year than I have in the last 5 years combined. LOL.

    I don't know if I read it here or somewhere else, but someone wrote they were going to buy scratch off lottery tickets, one for each day of scheduled radiation treatment (40 if you have 40 days of rads/30 if you have 30 days, etc.) Sounds like a fun idea to me. I think I'll do $1 tickets for regular radiation and $5 ones for each boost. The way I see it, with a breast cancer diagnosis we're all overdue to have a bit of good luck coming our way.

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited November 2014

    LaBelle, if you are comfortable, go bra-less. I suspect if you are well-endowed that wouldn't work but if you're small like me it was a good option and saves the bra $$$ :)

    I didn't do the scratch off tickets but I think it is a great idea. Go for it! We all need a big dose of luck and joy!

  • labelle
    labelle Member Posts: 721
    edited November 2014

    Going bra-less is an option at home (I'm medium sized) but not so good for work and I'm hoping to work at least part-time thru at least a portion of radiation therapy. I'm lucky I have the option of taking time off pretty much as I need it, but don't want to miss too much for too long. Eventually I'll run out of paid time off (accumulated sick and vacation days over the years) and I don't want that, but at least my job is safe.

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited November 2014

    LaBelle, I think most women work through radiation. I am retired and had other issues with DH to contend with so I couldn't have worked if I'd wanted to. That said, you may find you tire more easily.

    You're still "fresh" from your lumpy so don't rush things. Follow the instructions your surgeon gave you and don't overdo things.

    Very glad that your job is safe. I'd take the time off now if I were doing it but you know how you feel and how your post-surgery limitations work with your job.

    Heal well and HUGS!!!

  • MarieBernice6234
    MarieBernice6234 Member Posts: 202
    edited November 2014

    Hi All -

    May I introduce a new topic here in this forum? Has anyone had an a rash from radiation that kinds looks like a prickly heat rash. It is only on the right side of my body - which makes sense as that is the side that is being radiated Pretty sure it is not related to any changes in medications. I am using simple soaps - the Aveeno line - either the regular bar of soap, or the baby body wash. Tomorrow I have to see the PCP to see what they think it could be or not be in any case.


    Any thoughts?

    MarieBernice6234

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited November 2014

    MarieBernice, it could be punctation - irritation of the hair follicles. Just slather on Aquaphor. I had that. No itch, just looked "different." See if that helps.

  • jeanelle
    jeanelle Member Posts: 179
    edited November 2014

    MarieBernice, I did have a rash over my chest (not really on the breast) and between my breasts, basically where I probably had been sunburned in the past if that makes sense. It was red and prickly and a bit like a heat rash. They told me to put hydrocortisone cream or benadryl cream on it to help the itching. It did help with the itchiness.

    labelle, good luck on the radiation. I worked full time through it all. There were maybe 2-3 days when I left after about 4-5 hours because the fatigue really got to me but overall it hasn't been too bad. However, I do work a desk job most of the time so have no heavy lifting or strenuous activity. I also love the idea of the lottery tickets! What a great way to count it down and maybe win a little extra money too. :)

    I have 25 done and just have the 5 boosts to go. My skin is healing. It looks worse in some spots than it actually feels. Even the really bad spot under my breast is healing well though it still hurts like the devil. It felt so good yesterday to finish the last full breast treatment.

  • KKay5525
    KKay5525 Member Posts: 65
    edited November 2014

    Hello All,

    I am starting Rads Dec. 1st for 22 tx with 5 boost. Feeling a bit anxious, but I keep hearing that it will be OK. They certainly sugar coat it at the doctors office (compared to some of the issues I read here). I realize everyone is different, but I would rather be prepared than blindsided.

    Any suggestions on what to do to get ready. I saw where someone put creams on week in advance to help hydrate breast area - sounds like a great idea to me. My sister made some 100% aloe cream from her gigantic plant - so I have this and the aquaphor the Doc suggested to use during tx. Also have goat milk soap and some sensitive skin Dove (suggested by Dr.).

    Hope everyone has a great day!

  • yikes1
    yikes1 Member Posts: 120
    edited November 2014

    Hi,

    I had my simulation on wed, Nov. 19 and received 4 tattoos. One of them is very high near my neck, just under the collar bone, so will be very visible with most clothing.

    Does anyone else have a tattoo so visible?

    I had my 1st radiation tx yesterday, Nov. 20. I did not know I would start this quickly. I wrote before with questions about what to put on my skin and other questions.

    I know there were some responses, but when I go back I cannot find them! I am not sure what forum they are in. I tried the Aquaphor ointment sample and found it very difficult to spread around on my skin. I am not sure what area to put it because they had outlined an area way bigger than just the breast.

    Where do others apply it? How far out from the breast? Apply it on the nipple itself?

    I had asked yesterday for another suggestion of what to use, and the radiation place told me to find Fruit of the Earth Aloe Vera 100% Gel because it does not contain alcohol. I did go out and buy it, and did apply it. It was easier to apply because it is a gel, and did dry quickly. Has anyone used this product?

    This same product type is also sold by Trader Joes (their product) so I am going to try and compare.

    I am going to try and find the other responses later but just wanted to check in for now and ask some more questions.



  • lilyrose53
    lilyrose53 Member Posts: 216
    edited November 2014

    yikes1, I finished rads about 10 days ago and I have very little pink skin left. Mainly a spot about 2x3 inches long near my nipple where I had my boosts. I only used emu oil and then also a little Benadryl cream towards the end because of itching. I never blistered and haven't even had peeling of the skin-yet. So far it is just fading quickly. Maybe I was just lucky. But I had 26 rads plus 8 boosts. Also I am pretty fair-skinned. I think we all react a bit differently to the rads. I think my biggest issue was fatigue. I needed a nap everyday. My RO recommended starting the oil a few days before I started rads to moisten the skin. He also said drink as much water as I could stand. I drink a lot, about 64 oz per day. Good luck with rads!

  • lilyrose53
    lilyrose53 Member Posts: 216
    edited November 2014

    yikes, also I have five tattoos. Only one is visible if I wear a v-neck shirt

  • Puffin2014
    Puffin2014 Member Posts: 961
    edited November 2014

    yikes, I asked my rad techs where all I should be putting the creams, and it was a very extensive area, they made a point of showing me that I should apply way down to where my side met the table, across and over to the other breast, yes, nipple too. Guess I pretty much did my whole left side from clavicle to waist and from right breast across the left and down to where my body laid on the table.

  • jeanelle
    jeanelle Member Posts: 179
    edited November 2014

    Yikes, I did my entire breast including on the nipple area, under my arm and down my side, over my cleavage area and a little on the other breast, and up to my clavicle. My thoughts were the more the better. My center recommended a Skin Repair cream made by Medline. It worked really well except under my breast. I don't think anything would have helped that. I am down to 5 boosts now. Under my breast got really bad with blisters and raw red skin. I received a 3 day break from rads because of it. It has been about a week 1/2 since I had the break and it is healing really well. Just one small spot that is still red and weeping. Under my arm is peeling but never was wet and doesn't hurt at all.


  • Blownaway
    Blownaway Member Posts: 760
    edited November 2014


    skbrown - if you can avoid adding another pill to the regimen, I'm all for toughing it out. At this point, for what you and we all are going through, we have a right to feel some depression and have a few mood swings. I am taking things one day at a time and not dwelling on the whole cancer patient routine. I'm enjoying my 'penpal' relationships on this website and family and friends and staying positive. A glass of wine with dinner every night when I get home from work really helps, though.

  • Blownaway
    Blownaway Member Posts: 760
    edited November 2014

    Labelle - I'm still wearing my regular bras but using so much aquaphor they have become greasy so I will have to replace them all once healed. Regular clothes detergent hasn't degreased them so I'm thinking of try dish detergent. So far, I'm not very uncomfortable and haven't felt a need to by cotton bras.

  • Blownaway
    Blownaway Member Posts: 760
    edited November 2014

    KKay - sounds like you have it covered. Be sure to wear an old t-shirt or undershirt beneath nice blouses to keep the ink and greasy Aquaphor off your nice tops.

  • Blownaway
    Blownaway Member Posts: 760
    edited November 2014

    yikes - I'm only using hydrocortizone cream and aquaphore every night.  At this stage (I'm almost finished) I have to gently pat it on - no rubbing.

  • KKay5525
    KKay5525 Member Posts: 65
    edited November 2014

    Thanks Blownaway. That aquaphore is really thick and sticky - don't love it, but my husband does! HaHa..he has started using it on his hands and says they are "baby soft" :-)


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