Winter 2013-2014 Rads

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  • bondsy
    bondsy Member Posts: 94
    edited February 2014

    Lilyluv - my nipple also turned yellow when cold! But that's all in the past now that I'm doing radiation because my nipple is so swollen and dark. It's very sensitive. My RO recommended I cut up an old cotton t-shirt (a soft one) into squares and put it under my tank top to protect my nipple (either that or a gauze pad, but I tried the t-shirt and it's a lot softer than gauze.) I'm also putting the cut up cotton squares under my armpit now because it's very painful when skin touches skin. My skin has taken a turn for the worst. But today is my last radiation day, so let the healing begin!

  • Holeinone
    Holeinone Member Posts: 2,478
    edited February 2014

    Bondsy...Congrats ! 

    Tomorrow is my last day, sore, itchy & once again fighting the fatigue. I have been taking Beneydral,  for   the itching so that is wiping me out.

    Skin is the worst on my back. Where the rads exited. 

    Good luck to all

    Someone else is done tomorrow, Candi ?

  • Hydavis42
    Hydavis42 Member Posts: 52
    edited February 2014

    Hello Ladies I haven't posted in a couple of weeks but have been checking in from time to time. I have just finished 21 of 33 and skin according to my RO and nurse is looking real good. I am more fatigued than usual which I guess is part of Rads but so ready to be done with this. My RO told me today that the last 5 treatments will be just boosts to the scar line where my mastectomy was performed. Did any else have this if so how did your scar hold up to that? I think he said it will be a minimal amount of radiation. I hope everyone continues to do well as we continue on this journey together.

  • Holeinone
    Holeinone Member Posts: 2,478
    edited February 2014

    Hydavis, 

    I have had 4 boost, last one tomorrow. So, the rest of the area is in healing mode. The boost are different, protons instead of radiation.   Uh,  not really sure, cause I have glazed over the radiation stuff. I burnt out after reading, everything I could about all the chemo. 

    The boost are about 1/4 the time as the radiation. So very quick. My scar is red, I have a large area of rash on chest & back but confident it will heal in a week or two. 

  • RedReading
    RedReading Member Posts: 2,143
    edited February 2014

    Hi all you lovely ladies. I'm almost to the countdown. Monday is my planning appointment and with your help, boy do I have a list of questions. I also have my initial appointment for Wellfit next week on Thursday and my old lady doc wants to see me on Wednesday. (he's an oby/gyn who specializes in peri menopausal and post menopausal women) Boy just full of appointments. The people who run the Living Well program will also call me next week, that's a program for women taking  tamoxifen. My dietician girl called today as well and has booked me for the 17th. And since I also have to quit smoking, Kelly is calling again next Tuesday. Dear Lord, I am so glad I have a cell phone that allows me to record all these appointments. If I ever lost it, I'd be doomed.

    To the new girls, Michele and O'Connor, welcome. Sorry you're here. Glad you found us. Read TeamKim's post about questions to ask your radiologist. It's super. Thanks again Kim. O and my doc is a no creams at all doc - not even Aloe.

    OK so off I go for a tub. Have a lovely evening. 

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited February 2014

    RedReading - Feel free to join us on the quitting smoking thread.  We're a bunch of nuts but support each other in all stages of quitting - just starting, trying again, made it xx months, made it xx years!!, not ready to try yet.

    Boy - when things start moving they JUMP. Met w/the RO today.  They had an opening so simulation/mapping tomorrow morning.  Rads will start towards the end of next week.  More details over the weekend.  Right now I have 30 pages of homework to read & new questions to get ready for morning.

  • LizzieK
    LizzieK Member Posts: 67
    edited February 2014

    Kim, glad to see my questions making the rounds.  I let the RO go through his assessment of my case checking off the questions he covered and then asked the remaining questions afterward.  If you have an IPhone I suggest you get the app AudioMemos (<$10).  You can use it to record everything the doctor says and play it back later.  I used it for all my second opinions and my post op appointments.  It's surprising what you don't remember.  

  • TeamKim
    TeamKim Member Posts: 568
    edited February 2014

    Welcome TB90 -- glad to have you on board the winter rads train!

    Tomorrow will be halfway for me (15/30), so I have two more weeks of whole breast rads, then a week of boosts.  So far the girl is decidedly pink, and I am getting scattered red bumps that pop up and last a day or so, then go away. I have a nice golden tan under my armpit.  The bumps higher up on my breastbone itch a bit, but Cortisone cream manages it.  Fatigue is minimal so far, and skin holding up.  So far, so good!

  • lonnie713
    lonnie713 Member Posts: 236
    edited February 2014

    Hi,

    I'm new to the group. Can someone explain boosts? I am getting 5 weeks of daily rads after taxol (5 down/7 to go) the radiologist never mentioned boosts.

  • Oncearunneralwaysarunner
    Oncearunneralwaysarunner Member Posts: 252
    edited February 2014

     lonnie713 - As far as I understand it, boost target the surgical site specifically and tends to be used when someone has a lumpectomy. When I first met with my RO before any treatment started we discussed doing 5 weeks of radiation if I had a mastectomy and 5 weeks plus a week of boosts if I had a lumpectomy. That being said, everyone's case is different. Some of the other ladies may have more information.

    As of today I have 6 treatments left! My skin is looking sunburnt but no blisters or any other issues other than being itchy. I have the cortisone cream but I find that it doesn't do much. According to the resident, the best way to stop the itching is to finish with treatment. I think I'll ask the techs this morning if there is anything else they would recommend, it's so hard not to scratch.

    I know that a fair bit of you have kept working during treatment but I was wondering if there is anyone else who is planning their return to work. I'm ready to start that plan and was wondering what others are doing. I'd love if anyone is willing to share :)

  • checkers
    checkers Member Posts: 95
    edited February 2014

    Didn't sleep well last night, lots of itching even though I used cortisone cream before I went to bed. I'm going to try some Benadryl tonight.  I discovered if I use the cortisone cream first and let it absorb into the skin and then the Remedy cream my RO gave me, I don't get the mottled skin I was concerned was an allergic reaction. I'm also finding I need to let my skin breathe. So I bought 600 thread cotton sheets (so soft!) and am sleeping "au naturale". Even with the itching, in the morning my breast looks so much better than it does after being covered up all day.

  • lonnie713
    lonnie713 Member Posts: 236
    edited February 2014

    Oceanrunner,

    Thanks so much for that information. I had a mastectomy so that would mean no boosts for me.  

    Regarding work, I am not physically or mentally ready to return.  I have been out on disability since I had the surgery in September.  My plan is to not return until after I've completed rads, hysterectomy/ooph, and exchange.  I am waiting to get the final confirm on Long Term Disability.  I don't want to go back to work and have to take time off again for those procedures - 4 weeks here or 2 weeks there.  I just want to be done with everything and transition back in smoothly. 

  • peaches12
    peaches12 Member Posts: 67
    edited February 2014

    Lonnie- Just to add a ditto re boosts.  I had never heard of boosts until I found this forum after having started rads.  So I asked my RO.  She laughed and said if I felt "left out" she would order me some boosts, but they are given to lumpectomy patients to give extra treatment to the site around where the lump had been and not done for mastectomy patients since the breast had been removed.   I said, "No thanks, 28 rads will be enough for me".  We both had a good laugh.  Welcome to the group!

  • lonnie713
    lonnie713 Member Posts: 236
    edited February 2014
  • alfranco
    alfranco Member Posts: 200
    edited February 2014

    I had a double masectomy and my RO has me for 5 boost. New question to ask when I see him.

  • jpteacher1
    jpteacher1 Member Posts: 52
    edited February 2014

    I've just completed nine radiation treatments out of 22.  Next week I am scheduled to have two boosts.  I am doing the prone position for my current treatments, but they said I may need to do the boosts on my back.  I have to have a simulation before the boosts.  What should I expect from the boosts that I am not already experiencing?

  • peaches12
    peaches12 Member Posts: 67
    edited February 2014

    That's really interesting, alfranco.  Please post his answer when you ask him why.  It may be like using creams; some ROs say start using immediately, some say no.  

  • aeryno
    aeryno Member Posts: 59
    edited February 2014

    Today is my last rad appointment!  It will be 25/25 - no boosts for me since I had a pathologic complete response.  The area under my arm and under my boob is really red and irritated, the top of my breast has that rash and my RO said keep using the Miaderm as much as I want. After rads are done he said I can use whatever I want, they are only nitpicky about what I use during the treatment.  He and the techs said the area will get worse for a few days after and then it will go back to normal.

    It feels like I'm stretching the skin if I don't keep it lubed up so I use the cream multiple times throughout the day. I was wearing super soft tank tops under shirts but as of last night I can't even do that. Just wearing big, baggy shirts now.

    I baked some brownies to take to the techs and nurses today. So happy it's almost over!  

    Best wishes to all of you!

    P.S. I ran a 5K on Sunday (very slow but I did it) and ran with Wonder Woman socks with capes and put the below message on my shirt. I got lots of thumbs up, way to gos, congrats throughout and let me tell you, it made this the easiest run of my life :)

    image

  • Holeinone
    Holeinone Member Posts: 2,478
    edited February 2014

    jpteacher, 

    The boosts, are very fast, and the machine gets close to your skin. Actually easier than rads, cause it is quick. Some ladies with a mx still get boosts. Every case is different.

    I am DONE ! 8 dose dense of toxic, scary chemo....33 rads...wish it felt better, but it's all takes time. I need to have a ultra sound in 2 months, I have a inflamed node, looked somewhat suspicious on my PET scan after lumpie..RO says he " thinks" it's benign. Start Arimidex next week.

    Thank-you Kim, and all. I know I was a whiner in the beginning, the chemo put me in PTSD...that's my excuse & I'm stickin' with it....Good Luck to all....

  • TB90
    TB90 Member Posts: 992
    edited February 2014

    I too asked about boosts as I have heard some women with mx receiving them to the scar tissue and where the drain exited their skin.  My RO also said no boosts for mx.  Interesting how things differ in regions and with RO's. 

  • Holeinone
    Holeinone Member Posts: 2,478
    edited February 2014

    TB90, maybe because your cancer was DCIS, and not invasive

  • desalonde
    desalonde Member Posts: 41
    edited February 2014

    Rosecal, I can relate to what you posted. My RO as well as my surgeon before that readily dismisses the side effects I report before they even give themselves time to think and consider it!

    I do believe that radiation scatter must impact the face, eyes, neck, etc but if nothing is studied and published ( time,money, interest) then it's like it doesn't exist ....

    Regarding tamoxifen.... are you post or premenopausal? if post , then aromatase inhibitors is another option for you maybe. Myself, I prefer to do the 3 yrs tamoxifen then 2 yrs AI because both have benefits ( and risks). I have very very bad nearsigtedness as well as astigmatism and early cataract. I need to have rt cataract surgery anyway but postponed when I got this BC dx in October. The tamoxifen may worsen but the tamoxifen-I was told- reduces recurrence risk of almost half!!!

    Hope that helps you shape some questions for your MO. Best to you.

    Desalonde

  • DawnCT
    DawnCT Member Posts: 143
    edited February 2014

    Congrats Holeinone!!!  Yay!!  You should start to heal very quickly.

    Rosecal - Let us know how your onco appt goes.  I saw my MO this week and came home with the Tamoxifen prescription this week.  I do think(like Desalonde said) that it is supposed to lower your risk by half so your risk may be 26% without the Tami.  How common are the eye side effects?  

    I finished rads two weeks ago and have healed up very nicely.  I had fatigue the last week of rads and for about 10 days afterward but am really feeling better now.  In retrospect, I really got  myself all stressed about rads and it wasn't nearly as bad as I feared.  

    You all will get to the other side and try not to worry like I did! 

  • bondsy
    bondsy Member Posts: 94
    edited February 2014

    lonnie, I went back to work part-time a month after chemo and worked three days a week during radiation. Now that I'm finished with rads (yesterday!!) I will start back to full time next week. My radiation appointments were at 4:30 pm every day, so I left work at 4:00 and went to radiation on my way home. It was totally doable.

    Dawn, it's good to hear that your skin and fatigue were better by two weeks after rads. My skin is so bad right now, and I'm so looking forward to the healing!

    My boosts were built in to my total 25 radiation treatments. I had whole breast and "boosts" each time.

    I start on Arimidex on Sunday.

  • rosecal954
    rosecal954 Member Posts: 79
    edited February 2014

    Congrats to all who have completed rads this week!  Celebrate!

    Two weeks post rads:  I've developed a rash all over my breast, doesn't itch, just looked pimply or acne- like, applying cream.  Saw my surgeon yesterday for post rads/lumpectomy and he says the incisions looks good. I don't have to come back to him unless I develop a problem. I have one spot of numbness and some slight swelling under my arm from the lumpectomy, just annoying while shaving. He said if it's not tingling it might go away in time.  Just waiting for my appt. on the 12th with my MO. I'm quite nervous.  As far as fatigue, it's about the same as last week.  Pretty tired in the evening, feeling done for the day at 8:00 p.m.  I am looking forward to getting my full energy back.

    desalonde and DawnCT:  Thanks for the posts, info and concern.  I am post-menopausal (age 59).  I have moderate osteopenia.  The plan was to take Tamox for 2 1/2 years, then switch to an AL for another 2 1/2 years but with my bone loss she would have to put me on another drug (along with it's own SE's) with the AL. She doesn't want to do that, so it looks like Tamoxifen is my only option. I believe the bad SE's for eyes are a small percentage, but not sure if I'm willing to take that chance. I know I could try Tamox to see how it goes.  I have an appt. with my eye doctor next month to see what he knows about eye problems and Tamoxifen.  26% is a pretty big number for distant recurrence.

    My face is still tingling after I wash it and my hands redden up in warm to hot water just a little.  I imagine this will disappear all in time.  So strange because I had minor redness on my breast.  Of course this was due to scatter; I was just one of those people who reacted in this way and you are right Desalonde, no one has published anything or have done a study on it. 

  • smrlvr
    smrlvr Member Posts: 422
    edited February 2014

    Holeinone, congratulations on being finished with treatment!  Enjoy!

  • RedReading
    RedReading Member Posts: 2,143
    edited February 2014

    Hi there. I haven't heard of scatter. Is it common? Can we do anything to protect ourselves from it? Should I be asking my RO about it on Monday at my planning appointment? 

  • LanaM
    LanaM Member Posts: 142
    edited February 2014

    I too had MX and my RO had me do 28 rads and 5 boosts - my boosts were targeting my MX scar/incision. Although, I was having some skin breakdown in the armpit and RO said if I wanted to I could take a break or even skip the boosts. I decided just to do them & get finished - also wanted to make sure I had done everything possible to improve my recurrence odds, especially since I'm TN. RO called the boosts "bonus rounds".

  • Jmfrankel
    Jmfrankel Member Posts: 86
    edited February 2014

    Holeinone...congratulations on finishing.

    Regarding the discussion about boosts...I think I am getting 3 after I finish my 25 and I had a BMX.   My RO didn't call it a boost but he said it wasn't going to target as much.  I am confused though because I asked if it was along the scar line and he said no the whole breast.  That doesn't seem like much less than what they are doing now.  Maybe no lymph nodes at my armpit and collar bone?  I will need to ask him next week.    Maybe I am getting the whole breast because I had two tumors that were huge and grew very close to the skin.  

  • mouse9587
    mouse9587 Member Posts: 53
    edited February 2014

    Today I finished #23 of 28 whole breast rads; followed by 7 "boosters". I'm ready to be done.

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