July 2011 rads

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  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    Cora - Personally, I wouldn't need a driver if I took Xanax.  I take 0.5mg and I'm fine - just a little more relaxed.  I took it regularly after I was diagnosed because I cried so much.  My DH commented that he liked me a lot more on Xanax.  lol

    Lena - I was frustrated about losing the rest of my summer, too.  My kids are at the pool and my DH is teaching my twins to ride their bikes - and I seek shelter form the heat (it just drains my energy) and sun.  I cannot imagine how you're feeling though.  <hug>

  • PSU222
    PSU222 Member Posts: 127
    edited July 2011

    Here we go again, another week of rads.  I have a strange rash in my arm pit and my stickers have all slid into new positions.  It will be a long morning on the table.

    pejkug-  Twins are so much fun!!

  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    PSU - I'm dreading this week.  I an ever so slightly pink and I think that could intensify by the end of this week.  But, on Friday I will have passed the 1/2 way point.  That is a GOOD thing!  And  my freakin' ribs are so tender.  Ouch.

    Twins are so fun!  They're 7 year old boys and so wild and crazy.  They learned how to ride their two wheeler bikes this weekend.  YAY!  They head to 1st grade the week after I finish rads.  That just really ticks me off.  I mised the whole summer!  But next year?  Next year will be different!  (Oh, please Lord....let next year be different...)

  • Elizabeth37
    Elizabeth37 Member Posts: 84
    edited July 2011

    Hi all I started  June 20  but will finish July 29 do you mind if I join this group. I will have 30 treatments i have done 19 I'm starting to get red and it itches.I was very tired and down on Saturday but Sunday was better and now I'm sitting here just not wanting to go to treatment today but know i have to.I know others have had it worse as I only had to have a lumpectomy and Rads and I thank god for that but it is still hard and I cant wait till it is all over.I hope everyone has a wonderful week and that your treatments all go great.

  • GmaFoley
    GmaFoley Member Posts: 7,091
    edited July 2011

    Momoftwo11 and all the ladies here - You CAN do this!!!  hydrocortizone 10% cream is good for the itches and keep using your other creams (aloe, miaderm, xclair, aquaphor, emu oil etc.) you will make it... Just because you are red now doesn't mean you will get worse... I stayed the same shade of red/pink until my last week.. the creams really helped me get through it.. I am going to my 2 week check post-rads thursday... most of my breast is fine just open blisters under the breast - everything else is healing nicely... Doc gave me meds to help with any pain...

    This weekend I got to play with all my grandkids... exhausted and have to drive home this morning (3.5 hour drive)...but they are such good medicine for me :-)  Remember, God is walking at your side and is there for you..

  • Maybe484
    Maybe484 Member Posts: 170
    edited July 2011

    Good luck to everyone this week. 

    Lena, yes, my RO said that the ribs on the rad side are slightly more vulnerable to fracture, but only with a significant injury.

    I too was bummed that my summer got sucked up by rads.  I was supposed to be spending the summer out of the country.  Instead, I've been out of the sun and out of circulation.

    My armpit is the pits right now.  

    Thanks, Gma Foley, for being our cheerleader.  It's great to hear from those of you who've made it to the other side!

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited July 2011

    I feel bad for everyone who is missing the summer due to rads.  My treatments go from July 11 through August 24.  My first thought when I looked at the schedule was "good-bye summer."  Thank goodness we have each other on this forum.  I don't think anyone else truly understands.  Here's hoping for a lovely and warm autumn.

  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    Autumn is my FAVORITE of all the seasons.  I keep reminding myself how much I love autumn to get myself out of the funk I fall into over losing summer. 

    14/28 WBR - completed as of today.  Plus I'll have 5 boosts.  But I'm done with 1/2 of the WBR!  Woot!

  • Lena
    Lena Member Posts: 1,036
    edited July 2011

    One down, 32 to go. Coraeliz, no Xanax is necessary for rads; I'm the biggest sissy going and I didn't need my Ativan at least! LOL

    I've put on the Jeans cream twice already today -- once immediately after treatment, then again at home a few hours later.

  • badboob68
    badboob68 Member Posts: 2
    edited July 2011

    I will finish my rad next week. At first it was very uneventful. They were rad three spots including my armpit where the lymph nodes were removed. Well the surgeon left a little cup like arera under my arm that does not allow air to penetrate the pit. You can imagine what kind of issues this is causing. My arm pit has become extremely irritated and changes odors from dead shrimp to a dirty trash can to God knows what's next...but no regular body odor.....just gross. I can not wait til this is over. Had that area not been put back together that way, I doubt I would have had one issue.

  • Merilee
    Merilee Member Posts: 3,047
    edited July 2011

    Badboob

    Maybe it can be corrected?

  • janinnj
    janinnj Member Posts: 89
    edited July 2011
    Lena- Looks like we're on almost the same schedule.  I had my first of 28 treatments today.  Pretty uneventful.  They did draw all over me with magic maker but cleaned it off when they wre done.  Said this was the only time they will be doing that.  I have 2 little tattoo dots that are so small I can hardly find them.  Hope the techs can.
  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    I have one tattoo that is so tiny they have to mark it every few days.  No big deal though.  I have 5 tattoos in all.  They actually get a flashlight out to hunt for the tiny one.  lol

  • Lena
    Lena Member Posts: 1,036
    edited July 2011

    They did more drawing on me too Jan, only they told me they'd probably be doing some drawing on me at EACH treatment. Maybe that's because I said I didn't want tattoos? But the magic marker-appearing marks they made and stickered over (instead of tattooing) at the sim are still with me -- they just drew on me MORE today and said I could expect a little bit of it every session. Supposedly though, putting on cream (and taking showers) would make these "new" marks go away....haven't noticed yet, but I've only applied cream twice so far and haven't taken my shower yet. So who knows.

  • Elizabeth37
    Elizabeth37 Member Posts: 84
    edited July 2011

    21/30 treatments. well had to see the RO today I am very red and have a rash all over and my arm pit is swollen. So had to get new kind of cream. And thank you GmaFoley for telling me about the Hydocortizone 10, I got some and it helped alot.

  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    Lena - I do get some drawings on my skin everyday.  One tech draws a heavy black line across the top of my breast.  The other three draw a light dashed line in the same place.  I have said over and over how much I appreciate the light dashed line.  And I've done it in front of the woman who draws the dark black line.  She hasn't gotten the hint yet...but I think she's on vacation or something.  I haven't seen her in a few days.

    Momof two - when did you start getting red?  I'm constantly checking to see if I'm red.  (14/33)

  • coraleliz
    coraleliz Member Posts: 1,523
    edited July 2011

    1 down......the tech was very efficient today. He put larger dots on my tattoos with a sharpie. The whole treatment lasted less than 10minutes, so it wasn't so bad. I can't see any skin changes so I'm not really sure where to put the creams. Clavicles, armpits, mastectomy areas....

  • mamaoftwo
    mamaoftwo Member Posts: 267
    edited July 2011

    Hi everyone, 

    I start radiation tomorrow with my dry run, then every morning after that for 28 visits.  Several of you wrote that your summer is ruined from radiation and I was wondering what you meant?  I haven't been given any instructions yet and wasn't planning on doing anything different than I am now, and I spend a lot of time swimming in lakes and pools and running outside.  I was assuming that as long as the skin is covered, being outdoors will not be a problem - but then again, I have no idea what to expect.  I was just not expecting anything too terrible.

    Laura

  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    For me, rads means I'm teather to home for the summer.  My DH works every weekend, so if we don't go during the week, we don't go.  And now I can't go.

    Fatigue is just starting to hit me but when I'm done, I'm DONE.  I just flat run out of gas.  That's making it difficult for me to keep up with my four kids and run around like we normally do during the summer.

    I was told to stay out of the sun and no swimming on chlorinated pools (too drying).  My RO said to avoid sun exposure because the skin is and organ even though most people don't treat it as such.  And since it's being assaulted during rads, go easy on additional sun exposure.

    So far (14/33), rads hasn't been horrible to me.

  • LovesChristmas-Barb
    LovesChristmas-Barb Member Posts: 706
    edited July 2011

    I was told to stay out of the sun and no swimming. Also, it means no family summer vacation this year because I won't be finished until it's time for our son to start college. I am more tired than normal also so I end up taking naps and am not getting much accomplished, but it hasn't been terrible yet. I almost halfway finished.

  • Lena
    Lena Member Posts: 1,036
    edited July 2011

    OK, I've had my shower. I'm still Graffiti Girl. Oh well. Since the rads nurse had told me that if I put cream on after showering but before bed, my chest would still be considered "clean" for the next day's treatment, I put on some more Jean's cream. Not as much as earlier (I cannot stand any kind of gooey "stuff" on my body after I shower) but some because I hope to forestall any more opportunities to feel REALLY lousy. Guess you figured it out by now that I don't shower in the morning. I take just about all my showers at night (a few in the late afternoon if plans get different) -- anywhere from 8-9 PM usually). Most folks say a morning shower wakes them up and energizes them -- not me. Evening showers are sooo relaxing and make me feel like I'm washing the day off me. I like to spend the evening/go to bed clean and in clean jammies. Morning showers make me homicidal (at least the two I took in the past did). All I wanna know about in the morning is sleeping as late as I can and then my COFFEE! And sitting there slowly drinking it reading on the computer while it dispels my morning coma. To hell with that get up earlier so there's TIME for a shower crap too! LOL

    Coraeliz, you should put the cream on all your radiation fields. Yes, clavicles, armpits, mastectomy area sounds right for you. I do halfway up my neck though. My other fields are both mastectomy areas (I had a BMX) plus a bit below where my right breast used to be, on the skin over my right ribcage. No armpits for me though. I wouldn't let them near my nodes.

    Pejkug...OK "good" I guess, I'm not the only Graffiti Girl here. LOL. But yeah, some medical staffers are pretty dense, huh? Most were at my former facility, but after I moved and had to get all new, I found that the new place and new doctors/nurses/technicians are MUCH better and more cognizant of patient preferences. 

    Hmmmm, I was also told not to swim in chlorinated pools (fat chance of that happening anyway -- who is dumb enough to think I'd be wearing a bathing suit in public anyway?) and be careful about excess sun exposure. Since I don't swim and other than (weather and my energy level permitting) my daily or almost daily walks, I'm mostly a creature of the Great Indoors anyway. I became a sun avoider back in my 20s because I have fair skin which burns quickly and badly, so no swimming or sunbathing isn't a problem for me. It does kind of bother me that I have to wear "high collar" T-shirts though -- no blouses or tank tops which show the clavicle area since I'm being irradiated there too. Even though I'm only outside when I "have to" be, I do realize that even what minimal sun exposure I get might be "too much" for the radiation areas. This hit me this morning when I was getting dressed to go out for treatment. I was going to wear one of my black tank tops, but it showed off too much clavicle! LOL. I'm trying to get in the habit quickly.

  • coraleliz
    coraleliz Member Posts: 1,523
    edited July 2011

    I was told it was alright to swim. Swim laps anyway. I do this 2-3x/week. I'm going to try to swim in the morning or evening when the sun is low or down. If my skin becomes an issue I'll stop. Swimming has really help me get my mobility back following BMX.

  • Maybe484
    Maybe484 Member Posts: 170
    edited July 2011

    I have no tattoos or tape/stickers (the former due to choice, the latter due to sensitive skin).  I get remarkings with each rad, and as the weeks have gone by, the markings have changed slightly.  Yesterday, I got preliminary markings for the boosts, beginning on Fri.  I look like a 2nd grade class' art project gone awry.

    My axilla is swollen and red--that's where my tumor was and where my boosts will be.  My upper arm and my breast have also been swelling slightly after rads, beginning around week 3.  Anyone else experiencing this?   I'm very concerned about developing LE.  I'm already seeing a LANA-certified therapist. 

    Today is #15 for me and also my weekly check-up with my RO. 

    Good luck, all.

  • Elizabeth37
    Elizabeth37 Member Posts: 84
    edited July 2011

    Pejkug3 I started to get red about 16 or 17 treatments .They also remark my tattoo with a marker every time I come in. We also had to change our vacation do to this but that means next year will even be better.

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited July 2011

    Today, I saw the RO for the first time since I started rads.  I was hoping to feel better about things after finally seeing him, but I ended up feeling more upset.  The visit lasted less than five minutes.  I told him I was having a difficult time emotionally and all he said was that he understood and everyone was doing all they could to make things easier for me.  Then, I told him I was concerned about the swelling in my left arm.  All he said was to elevate it and not let anyone do BP's or needle sticks in that arm.  I knew that months ago after my first surgery.  The visit was a total waste of time.  I am happy for those of you who have a more attentive RO.

  • jbadge
    jbadge Member Posts: 2
    edited July 2011

    I just want to throw my two cents in and let you all know that you can do it. I just finished rads on Friday, 26 WB/7Boosts. I am very fair, blond hair, blue eyes and burn if I even look at the sun, so I was very worried about rads. I was pink the first week, which slowly moved to red on my chest, SN scar, and under my boob, but my skin held up nicely and I never got any blisters. My boosts were right over my nipple which wasn't happy and is still quite sore, but everything is already starting to heal quite nicely and is moving more towards a tan with a little peeling. I started using creams from day one and was very diligent. My treatments were in the morning which I loved because there was never a wait. I got bumped to the afternoon a couple times and the wait could be an hour or so. I showered before every treatment, lubed up with Miaderm immediately after and throughout the day, used a thick layer of aquaphor at night and put on an old tank top that I didn't care about cuz it stains. I really didn't like the greasy/sticky feel of the aquaphor, but my skin would actually look so much better in the morning, so it was worth the effort. I had some itchy spots and my RO told me to use 1% Cortizone cream, wrote me a script for 2.5% when it got worse, but the creams really helped keep the discomfort down. I am large breasted and was able to wear an underwire bra throughout my treatments. The fatigue came and went, and I just napped when I could. I had a hysteroscopy to remove 5 uterine fibroids in the middle of my treatment, and in hind sight I probably should have waited. My RO said it was fine to go ahead, but the fatigue really hit me hard right after and I got slammed with a horrible cold and still can't shake the cough. I am experiencing some pain in my sternum and having heart burn this week which I never have had before, but all in all, rads were very doable. I made an effort to walk every day, and I think it really helped my fatigue. Some days my husband had to push me to go, but I was always felt so much better afterwards both physically and mentally. My heart goes out to those of you that are really suffering from the SE's of radiation, but I wanted to throw it out there that that is not the case for everyone. I certainly would not like to repeat the last 7 weeks, but it wasn't as bad as I thought it was going to be. My biggest complaint is that because of my rads, we weren't able to go see my daughter who is working in Italy this summer. We had never been and were so excited when she got an internship there. I guess I now have to look at it from the perspective that because I did the rads, I will have a lot more summers to go travel and do the things I want to, so this is just a bump in the road so to speak. Hang in there everyone, you can do it! Hugs.

  • Damaris51270
    Damaris51270 Member Posts: 16
    edited July 2011

    HI LADIES,

    STARTED RADIATION TODAY THOSE OF YOU WHO HAVE ALREADY HAD A COUPLE OF WEEKS OR COMPLETED YOUR RADS CAN YOU PLEASE TELL ME WHAT CREAM I SHOULD BE USING AND WHAT I SHOULD BE EXPECTING/

    THANKS A MILLION!

    DAMARIS

  • pejkug3
    pejkug3 Member Posts: 902
    edited July 2011

    JUDY - Thanks for posting your positive and encouraging story.

    So far, rads has been easier than I expected.  I kept getting warnings about how terribel it would be because I'm large breasted.  I think I'm doing pretty well compared to some who really suffer through rads.

    DAMARIS -

    I'm following another BCO member's (OMAZ) skin regime...

    100% pure aloe by Fruit of the Earth right after treatment

    Miaderm (2-4 hours later)

    Faulding Essentials Vitamin E cream (4-6 hours later) --I'm using Fruit of the Earth Brand Vitamin E cream because I couldn't find Omaz's recommended cream

    Progressive Emu Oil (2-4 hours later)

    Aquaphor (before bed)

    Be liberal with your creams and use them regularly.  I'm through nearly 1/2 of my treatments - 15/33 -  and this regime is working for me so far.  I'm just a tiny bit pink, no pain and no itching or peeling so far.

    Good Luck!

  • janinnj
    janinnj Member Posts: 89
    edited July 2011

    Lena= Did you try Baby Oil to remove the grafitti?  I agree evening baths or showers are the best way to end a day.

  • DenimBlue
    DenimBlue Member Posts: 23
    edited July 2011

    Today was treatment #10 of 33.  Nothing bad is happening, but I have to smile because just last night at a get-together I was answering everyone's questions and saying "well, I don't have any side effects at all yet."  I don't believe in jinxes, but it cracks me up that I woke up this morning to pinkness, random stabbing pains, and feeling like I needed someone to light a fire behind me to get me to go anywhere. Those were the 3 things I was told to expect, and it's funny they all started at once. I am using my aloe vera gel and drinking my protein drinks.

    The pattern is getting familiar - Tuesdays they weigh me (ick) and I check in with the RO who seems relieved when I don't have any questions and he can go on to the next person. Wednesdays they X-ray me (on the same table, so I can take a nap while they're waiting for the RO to look at the X-rays) and they peel off the stickers, re-draw all their artwork, and put on new stickers.  Today a dietician popped in, told me to eat my 5 servings of fruits and vegetables and be sure to exercise, and popped out. I really do like all the techs and the nurse. They make me feel as comfortable as it is possible to feel in there.

    This is also cute - the techs are so careful to put a "modesty blanket" to cover my other side while they're doing the treatment - like I'll be twice as embarrassed if they're both visible?  I do really appreciate their efforts though. They are very nice people.

    Time to hit the pool - they have said I can swim as long as I'm comfortable (and wear a white T-shirt before the sun goes down). I am guessing maybe later into treatment if my skin is uncomfortable then I might not swim, but I will do it now while I can. (High of at least 101 today so the water will be quite warm.)

    Hope everyone had a good day.

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