April 2011 Rads

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  • MizChiz
    MizChiz Member Posts: 36
    edited May 2011

    Wow... All of you turning so red and peeling! My RO stopped me at 19 (last Monday) after he saw my armpit was getting red. Of course, I do live in the area of Ohio w/ the largest rate of medical lawsuits, so I guess they're just extra careful here? I go back tonight, see the other RO in the office (who I like MUCH better!) and he'll determine if I start RADS again tonight. I was using Silvadene and I think it healed up quickly.

    Lisa, congrats on your last one tomorrow!

  • duckyb1
    duckyb1 Member Posts: 13,369
    edited May 2011

    Hi Ladies..............did #11 today.......so far so good, but I'm not allowing myself to get too excited considering I have 22 more to go...........Way too early to start celebrating.

    I did scratch # 11 lottery ticket today, and I won $10.00.  So that makes me $36.00 winners...........I'm $3.00 ahead and still have 22 more tickets to scratch...........Gotta love this...........at least i'm winning......................I figure if I get my original cost back literally I played for free, and I'm watching the pile go down, each ticket means another Rad done................Happy winnings to the ladies who are scratching too,.

  • sagina
    sagina Member Posts: 1,219
    edited May 2011

    Hi Susan,

    I bumped into my MO's PA who does a hour and half of chemo education before you start treatment and we got to talking, I asked her how long chemo brain lasts and she said a good twelve weeks, I looked at her funny and she asked if I was in radiation.  I said yes and she said that radiation lowers your red blood cells too.  I didn't ask for any other explanation, but will ask my RO tomorrow, that is if I write it down now and don't forget I have questions for him!!! lol.

    Welcome Wally.

    Ducky I think I'm one treatment ahead of you, but I really can't remember.....I did get my $66 back already on the sratch offs.  Remember I got those stupid bingo ones that take 20 minutes to do ($2 each)?  Well I scratch the bar code off, take it to the machine to scan and call it a day.  The numbers are really way to small to see or scratch off!!!!

    MIzchiz, my MO said she would postpone the treatment herself if she felt the need....With large breasts I guess that is her concern.  This 90+ degree weather is not helping either.....

  • ReadingMama
    ReadingMama Member Posts: 573
    edited May 2011

    Sammolisa - congrats on your last day tomorrow and good luck!  Were any of your boosts or all whole breast? 

    I had my planning for my boosts today so they marked me all up.  I know some of you have markings instead of the tattoo's, how did you keep the marking from getting on your clothing??  I'll wear an old tee shirt when I work from home, but when I go in, I have to be dressy. 

    Both the RO and the Rad Tech commented on how good my skin was holding up, so I'm crossing my fingers for the last 10.  And actually only 3 more whole breast. So even though I don't like the Aquaphor, I guess it is doing very well.

  • BlueLily
    BlueLily Member Posts: 60
    edited May 2011

    Readingmama- I too got my boost markings today.... I have two more whole breast zaps. I had Sharpie markings all along.... but they had clear tape coverings. I picked up some cotton shelf camisoles that I will retire when this is over. I never had any clothes ruined over the camisoles. But honestly today's markings have a lot of ink...and its 90 degrees. Maybe a gauze pad? It's going to be a long two weeks.

  • sagina
    sagina Member Posts: 1,219
    edited May 2011

    Say it isn't so, we have to get re-marked for the boosts? Is it a long process?

    Is everyone else getting x-rays once a week? Just what do they see on them?

  • BlueLily
    BlueLily Member Posts: 60
    edited May 2011

    Gina- new markings took maybe 10 minutes with more xrays even though I had them on Friday. (Always on Fridays.) I asked why and they said checking bone structure on the form ... I don't understand but was too tired to ask.

  • MizChiz
    MizChiz Member Posts: 36
    edited May 2011

    Gina... Lord, you're in Texas? I bet you're a little warm! My sister lives in El Paso. Wanted to go see her on spring break but RADS kept me here. I just wanted to get them over with. Thank goodness I don't have big boobs... At 50 I can honestly say that gravity hasn't had its way with them yet? Esp. the one that is now half the size of the other. Perky little thing it is! About the 1x a week x-rays... My techs told me they're looking for a change in size of the breast. I guess there's not supposed to be any change.

    Hey everybody... I'm not getting any boosts? Is this unusual?

  • walley
    walley Member Posts: 231
    edited May 2011
    susan g     # 21 today.......   they are just going to set me up today for the boosts. I have 8 more regular and the 5 boosts..I have 33 altogether.My rash seems better.Been putting on the lotion and sleeping in a lite tank top.My armpit looks pretty angry put some aloe on it.Well one more down today.I am in Florida and it is in the 90's..I try to stay in and stay cool as much as possible.KissHave a good day Ladies
  • SusanHG
    SusanHG Member Posts: 655
    edited May 2011

    Congrats Lisa on your last day tomorrow.

    Gina-Maybe there is such a thing as radiation brain after all! ;)

    Walley-I keep slathering on the aloe after treatment to keep the redness down, then Aquaphor as soon as I get comfortable at home for the night.  I slept topless on Sunday night.  Can't stand to have anything on my nipple, not even the sheets!!! Good thing everyone and their brother has seen my breasts by now ;) I doesn't even phase my son... He keeps asking me if my booby still burns.  He is so sweet!

  • duckyb1
    duckyb1 Member Posts: 13,369
    edited May 2011

    Sagina..........My adorable tech with the gorgeous blue eyes, who calls me his "little lady" (trust me I am neither little or a lady, and 76)........ok let me continue....................

    He said last week............we're going to do an x-ray little lady, and of course no one ever does anything to me without me saying "why", and he smiled and said..........to make sure we're doing the radiation where we should...............Not so sure I'm buying that, but that was the answer I got...........

    So I said, "well considering we're on # 9 isn't that a little late if you find out your "not", he smiled and said .................nah, trust me, I know what I'm doing.............To which I said "you better", and at that point he laughed.....................So today I am going to follow-up and ask the RO when I see her, the same question..................

  • sagina
    sagina Member Posts: 1,219
    edited May 2011

    The techs told me the same thing, about positioning.  I have the x-rays on Thursdays, but last week they did another one on Friday and the techs said the RO wanted to make sure on something.  I'm guessing they line up the x-rays with some coordinates or something?  But I will ask today as well.

    Has anyone had any dental work during Rads?  I have a tooth ache popped up out of nowhere.

    Susan~ are you having to adjust your sleep positions too? I'm a stomach sleeper and that's already getting a little rough.  Maybe we should chalk up the chemo brain now, to just overwhelmed brain?

  • duckyb1
    duckyb1 Member Posts: 13,369
    edited May 2011

    Ok, I made more damn mistakes this morning before leaving for Rads I could not believe it......I had a form to go out of network to a LE board certified specialist (won't get into why), but Aetna gave me paperwork that had to be filled out......I put all my information in the space where my RO had to write............then had to "white out" all the info, ...........forgot to ask the RO a question about skipping one of my days, and then laid my parking ticket down somewhere and could not find it.......The who place was laughing, and got me another ticket......we park for free.........Now mind you this was all before 9:30am.........my son (who takes me) just shook his head..........

    I did ask about the radiation killing the red cells.......RO said.......yes it does, but very few with BC since they don't touch much bone while doing Rads..........Other types of Rads she said "yes", but usually breast cancer "no".......you will lose some, but not enough to make a big difference.

    Also asked again today about the x-ray........said it has to do with positioning...

  • SusanHG
    SusanHG Member Posts: 655
    edited May 2011

    Gina-I can't sleep on my stomach because of my back problems, but I couldn't  even if I had a healthy back.  Also, my left side (my left breast is the bad one) is now out.  Way too painful!  So now, i only have my back and my right side!  Sometimes, sleeping is hard, but not toward the end of the week.  Iam way too tired at that point to care!

  • ReadingMama
    ReadingMama Member Posts: 573
    edited May 2011

    I get xrays every 5 days as well and was also told it was to check the positioning.

    My boost markings did not take long either, maybe 20 minutes total, they did the markings then did a CT scan on me, same as the planning session for the whole breast (except I have tattoos, not the markings for the whole breast).

    Saw my RO today and he said the skin was holding up great, much better than most people at this stage, so still crossing my fingers for the rest.

    Ginger, not sure on boosts, most people I talked to have them, but I don't know how they determine if you need them or how many.  The boosts are done to a smaller area of the breast, just where the lumpectemy cavity is, i.e. where the tumor was.

  • sagina
    sagina Member Posts: 1,219
    edited May 2011

    HI everyone.  I saw the RO today and asked him about the x-rays.  He said he uses them to lay his "map" over and make sure the radiation is right where he wants it.  He showed me my x=ray (digital of course), then he showed me the next picture where the lines showed the map, then I saw an x-ray of me with the whole radiated area shaded in red.  My eyes got huge!  That's a mighty big chunk of body when you look at it in relation to the x-ray of the chest!!!!

    I also asked about the red and white cells since I have a cavity!!!! and ouch is it hurting all the sudden!  He said the same thing Ducky, that it does lower them but not like chemo.  He said if I was needing surgery with a lot of blood loss that would be a different story but dental work is ok.

    Good think I bring a bag with me, magazine etc, and put my clothes in them instead of using the lockers - the didn't have my size gown today!!!! Free show - thank goodness for the bag to cover up!!!!

  • ritaz
    ritaz Member Posts: 186
    edited May 2011

    Had #22 of 30 today - this is the first week that my whole breast is sensitive - the nipple is really, really brown (started out pink) and lots of brown spots all over.  The RO said that the brown spots were going to happen - apparently some people think they're getting skin cancer but it's just a reaction to the rads...She also said that it would take about 2 weeks after treatment for the reactions to calm down...

    Yeah, belly sleeping is challenging with a sore breast - I fall asleep on my back and wake myself up when I flip onto my belly while sleeping - ugh!!! 

    Didn't know about more markings for boosts...Hoping they aren't more tattoos - didn't like those tattoos one single bit.  Don't like to be permanently marked thank you...

    I have had x-rays once a week - I was told by RO that it's about positioning too... 

    Ducky:  Ended up buying an additional 10 more scratch tickets this weekend because I got sick of not winning on the original 30... (have won $6.00 on 3 of 22)  Won $25.00 on the first new one yesterday - Yippee!  

    I don't know if I have Radiation brain or Arimidex brain (didn't have chemo) But I find that I can't find a word I'm looking for and I forget to do things that I've said I'll do...I've always had a very good memory so it's annoying as all heck...

  • DLL66
    DLL66 Member Posts: 700
    edited May 2011

    I am having my boosts drawn tomorrow as well.

    I'm glad we don't have to wear gowns where I go (shudder), except on the 1 day a week we meet w/the nurse to check how our skin is holding up. I just wear a hoodie & they toss me a towel on the way in to the rads room.

  • lesleye
    lesleye Member Posts: 38
    edited May 2011

    I get xrays (they call them pictures) every 4 days.   Had them yesterday at #9/33.  Yee hah... #10 today, and better than the lottery tickets, I am going to Foxwoods for the night with 2 girlfriends.  Foxwoods is a very large casino in Connecticut.

    Wondering if anyone else here is tired?  I am trying to lose weight, and if I do not eat enough, I am wiped.  Really wiped.  Also I need to drink a ton of water.

     I anyone else having any nausea or heartburn?  Or is it just what I am eating?  

     Thanks all...and lots of hugs. 

  • ritaz
    ritaz Member Posts: 186
    edited May 2011

    Lesley:  I had nausea when I began - it went away after the 2nd week...

    I was cautioned by my RO that now is not the time to try to lose weight - to wait until the rads were over so that you are bringing in enough nutrition with what the rads put your body thru...

    So far, I'm in the 5th week and no fatigue...

  • Rachel2
    Rachel2 Member Posts: 32
    edited May 2011

    Finished 20/20 treatments yesterday, with the final 4 being boosts to the tumor bed.  Had a little pain in the tumor bed area, but otherwise no other complaints.  I did catch whatever my older daughter had:sore throat, sore chest and feel quite miserable and has knocked me for a loop energy wise.  I was just thinking on Tuesday how great I felt and was at the gym working out, running on the treadmill and now feel pretty tired and miserable.

    I get a mammogram in October and see my oncologist in September.  Then its a mammogram every year and a 6 month check up with the GP for the next 5 years I think. I asked my oncologist if I now look for symptoms of metasis and she said no just live your life.  Easy to say harder to do.  She said keep exercizing and eating a low fat diet and now I could start with more antioxidants.  Is anyone taking any supplements besides vitamins?  I take multi vitamin, vitamin D, complex B and a calcium.  I try to eat blueberries everyday, as well as broccoli kale et cetera. 

  • SusanHG
    SusanHG Member Posts: 655
    edited May 2011

    Ritaz:  I asked my RO about Radiation Brain and he said only those who are getting radiation on the brain get that.  AllI know is that I keep forgetting and losing everything!  One day, my shoe, which i finally found, then my keys and purse, then aloe vera gel, which i still haven't found.  I forgot to send money to school with my son for his Book Fair.  When he saw me, first thing he said was, "Mom, you forgot my book fair money!"  with this really pitiful look like he was about to cry.  I felt terrible!!!  Now, I am double and triple checking everything.

    lesleye:  My RO told me not to lose more than 10 pounds, or the measurements will all change.  I planned on still losing weight very, very slowly, but found I was much too tired.  I even started to eat a little meat again (I was only eating fish before).  I actually feel quite a bit better now and I'm in my fifth week!  Just a little sleepy, not too bad.  Plus, I was able to walk 2 miles today, which there is no way I could have done this earlier in rads.

    rachel:  You are triple neg like me.  My MO wants me down to the bottom of my weight range, diet less than 20% fat, plus I take lots of supplements (but have stopped them during rads-don't want any antioxidants to interfere with those rays).  I only eat fish normally and drink loads of green tea, which 1 cup contains 32 times the amount of antioxidants as one serving of blueberries.  I also plan to start exericisng vigorously as soon as my boob (and back) can handle it.  I have herniated discs in my back and neck that I have been in therapy for for two years.  My chiropractor kept telling me that there was something going on in my body that was preventing my back from healing.  A few months later, Voila!, breast cancer...

  • kalyson
    kalyson Member Posts: 15
    edited May 2011

    Hi SusanHG,

       Your rad onc lets you drink green tea?    I had to stop that and all the antioxidant supplements, too.    I found that lots of them tell their patients this because they are afraid it will interfere with the rads killing the cancer cells.

        I miss the green tea....

  • SusanHG
    SusanHG Member Posts: 655
    edited May 2011

    They never told me not to drink it or not to take anti-oxidants.  I had asked whether I needed to change my diet at all, and they said there are no conclusive studies about anything so no changes necessary.  Well, I've found that a little meat has been helpful, at least in my case.  I've stopped supplements all myself, but do still drink a little green tea, but nothing like I was.  Maybe a small glass of iced green tea everyday. 

  • walley
    walley Member Posts: 231
    edited May 2011

    Hi All:)

    Tomorrow is #23/33. Going okay .I am very pink, sunburn like.I asked about taking anything like vitamins...all they said no fish oil.I guess they are all different.My rash seems better ,so that's good.Only 2 more days this weekLaughingHave a great night.

  • MizChiz
    MizChiz Member Posts: 36
    edited May 2011

    May I vent? I don't know how everyone else is financially, but I'm single and have a son. During chemo I missed half my days of work and therefore got a little behind on some utility bills. Returned to work full time about the beginning of March and have been doing my best to catch up. Have already been turned over to collection for the surgical facility I had my 2 surgeries at and today, this is the kicker, the water department turned off my water because I missed paying for 1 month... $73.53! I zipped down to the water department to pay before 4 pm and it was about 3:55 and they were already locking the doors. I called the water dept. again and told the woman the security guards were locking the doors and she said that they were still there. I went into city hall when people were coming out and was met by a NASTY security guard... He yelled at me and wouldn't listen when I told him the woman told me they were still there. Then he just kept yelling "Good night!" "Good night!" at me because I wasn't moving. I think I was stunned. So, I asked him his name and he told me. I told him he wouldn't have a job tomorrow if I have anything to do with it. UGHHHHHH!!! I cried all the way home. I have never had a utility shut off. OK, I'm done venting, I guess.

  • sagina
    sagina Member Posts: 1,219
    edited May 2011

    Ginger, I was a single mom when my daughter was young...l didn't have cancer then, but I struggled everyday financially....I would leave the porch light on all the time, so when we got home I knew what I was walking into.  After a while of that, my little one (now 20) would exclaim when we pulled up to the house "Look mommy the lights are on!" Kids are sooo smart aren't they.

    Call the other people you are behind with and ask to set up payment plans.  If you have a home, make that first....the water, electric, and cable don't do you a bit of good without the house....learned that lesson too!

    So sorry for the added stress during this time.

    I asked my RO yesterday about food, vitamin, etc restrictions, he said there are none.  I read on this website about radiation and side effects etc. and this website talks about no supplements....I guess it's all about who's doing the talking?

    12/33 and I now have pain, can't tell from where, just hurts in general.

  • BlueLily
    BlueLily Member Posts: 60
    edited May 2011

    Ginger - hold on to your strength ... some days are just meant for venting...that's what we're here for. Sending positive thoughts that better days are ahead. I was fired the day I was dx'd ... I told a friend at work and a few hours later was shown the door...insurance risk that I was ... we just have to keep our eye on the goal ... "survivor" after each of our names. The rest can take a number.

    I had my first boost today ..not as bad as the whole chest ...RO said I should start seeing improvement on my nipple in a few days...7 more to go... then hopefully I'll find a job!

  • MizChiz
    MizChiz Member Posts: 36
    edited May 2011

    Thank you Gina! I don't whine too much but this really got to me. I hope I see the security guard again tomorrow... I probably won't say anything, but I will give him the "stink eye"...lol.

    And Debbie! Thank you too! It upsets me that you were fired. Even after I became a teacher (not teaching this year) I always wanted to become an attorney for just this type of shittery that you've experienced. Oh, how I wish I had the means to go back to school! Just think of all the people that get screwed over in this sort of way w/ no way to fight it. And the elderly who are ill and have no family and possible memory problems. I wish I could save everyone from injustice, you know?

    Thanks again for your support. (((((HUGS)))))

  • slg2130
    slg2130 Member Posts: 140
    edited May 2011

    Ginger - definitely talk to the billing departments that you're behind with (surgical center and any others).  Work out a plan with what YOU can afford  - not what they tell you they'll accept.  Also, find out if your state allows interest on medical bills.  When my mom was diagnosed 25 years ago, there was an interesting little regulation that didn't allow for interest on medical bills. 

    We set up payments on everything, sometimes as little as $15/month.  And we also kept track of payments on medical bills minus the interest being charged.  Once we paid off a medical bill, I wrote "paid in full minus all interest charges" across the final bill.  Every single medical facility accepted the final payment.

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