August 2012 Radiation

Options
1235

Comments

  • rachel11
    rachel11 Member Posts: 99
    edited August 2012

    Hi everyone!

    It's been awhile since I've had a chance to come on the site. My daughters are in the midst of their hockey tryouts and I have been living in the rinks for over a week now.

    Rads are doing well, hardly any SEs so far, my right breast is a bit red with some little red bumps but that's about it. Today I go for treatment #14 and then I have 7 left!

    Welcome to all the new ladies! Looks like almost everyone is having minimal SEs.

  • Kay-in-NH
    Kay-in-NH Member Posts: 26
    edited August 2012

    Welcome aboard Diane ("Summer51" - that's a cool pseudonym !)

    You and I are on a similar radiation time frame - I think I started a day before you.  I just had #11 this morning, of a total of 28 plus 5 boosts, so I'm 1/3rd done with 2/3rds to go.  I've had some swelling & tenderness, and some initial jolts the first 2 weeks, but my skin is holding up OK.  I'm also using 100% aloe, and alternate between Acquaphor and Cure Intense Moisturizing Cream...  My only issue is the products take so long to dry, and when I re-dress to go to work, my clothes stick all over me for about the first half hour.  It's tough to wear a bra, so I try to wear clothes that I can go bra-less.  For my tiny boobs (with one tinier now), that's never been much of an issue.   Has anyone felt fatigue at this stage yet?  I'm feeling a bit washed out towards the end of the day, but not bad.

    Kay

  • ro-berta
    ro-berta Member Posts: 134
    edited August 2012

    Hi Kay, I also had fatigue  actually but i usually perked up on sundays (go figure) I also am not and did not wear a bra as it felt so tight and constricted and my skin was breaking down a bit. Now I am in a bra quandry hahaha mind you I don,t go back to work till middle of oct, so i still have time to figure that one out hahaha. What i did after creaming myself up to protect my clothes and not have the glob seep through was put a non-stick telfa pad over my boob it was soft and kept a barrier between my cloths rubbing on my skin and also kept the goop at bayI just left them on for an hour or two  after the cream was applied.

     So girl get some rest when you can and keep your fluids up!

       roberta

  • Joan1112
    Joan1112 Member Posts: 12
    edited August 2012

    Hi all,   I was diagnosed in early June and will be starting rads in the next week or so.  I'll only have 16 sessions, but it still makes me nervous. No chemo, but I had to have two lumpectomy surgeries to ensure clean margins....so that took up most of the summer. 

    I'm still working full time and hope to be able to take a break, go get radiation, and then head back to work.   Am I being too optimistic?

    Like the idea of non-stick telfa pad ro-berta.  Were you able to find them at a regular pharmacy store the right size?

  • ro-berta
    ro-berta Member Posts: 134
    edited August 2012

    Hi hon, I got the Johnson &johnson non-stick pads at w-mart although you can get them anywhere they are 3by 4 inches. no stick no owweeeees! I found the aloe made my t-shirts stick to my little old boob. I also had 2 lumpx actualy the second was a partial mast. I could not work but I do heavy lifting and stretching. As for working with rads it effects everyone differently You do need to have some rest as fatigue is very common ( again depends) but remember your body has gone through alot. The rads will go by fast and the proceedure is painless, you will feel more comfortable when you meet the rad techs they are excellent and will make you comfortable. I just finished up yesterday so during your treatments drink lots! and cream up lots! hahaha and rest when you need to. Nerves are are normal girl but it honestly wasn,t that bad you will be O.KCool

     roberta

  • Kay-in-NH
    Kay-in-NH Member Posts: 26
    edited August 2012

    Hi Roberta,  Congrat's for finishing up!  I'm sure that's a relief.  I'll look for those telfa pads.  Joan - welcome aboard.  Your radiation schedule sounds light (16 treatments total).  I'm getting 33 treatments, including 5 boosters, which they say is normal, but not conservative.  I'll be working full-time all the way through, which from what I hear is not unrealistic.  I'm a commercial banker, but have cut back on my travel with my boss's total understanding.  Everyone has been so supportive, and I feel if I need to schedule some rest time off towards the end, that wouldn't be a problem.  Best of luck - hope to hear how you do during your treatments. 

  • ali68
    ali68 Member Posts: 1,383
    edited August 2012

    One week today I finished and my throat is much better but now I have a itchy rash front and back. I am using steroid cream as well as my antihistamine tablets. Silly me thinking I would get away with no hives.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2012

    Hi, Today is Day 20 of 30!  Also sharp pain began yesterday along with significant darkening and redness both.  Suggestiosnf or pain relief and bra options for large breasts?  I need to return to work on Tuesday.

    VVH 

  • ro-berta
    ro-berta Member Posts: 134
    edited August 2012

    Hi girls it feels good to be done with the rads and especially the travel, I think that tired me out more. Still have some glitches to iron out but I guess that goes with the territory.   Kay-in-NH its great that the company is supportive and understanding.

    Ali hon I hope things improve and get easier for you hon! You definatley have been through it all.

    WH The quadry of what to put on the girls I am still stuggling with that one hahaha! My breasts were C-cups But my sick one is now much much smaller. I have been going braless and wearing cami,s, mind you I have a lot of healing to do yet from rads. Good luck with returning to work.

  • crazyride43
    crazyride43 Member Posts: 154
    edited August 2012

    VVH, when I met with the RO nurse today she gave me some "radiadress gel sheets" that I can cut up and put over any sensitive areas.  It's like a flexible piece of plastic with hydrogel that gradually absorbs into the skin and is really cool and soothing.  My main trouble area is my nipple (super sensitive) which makes it tough to wear a bra or have anything touching it at all!  Today was 18/22 whole breast treatments, which will be followed by 8 boosts, so I think we are at around the same place with treatment.  I am not getting too much pain, but when I do I take some advil and that seems to help.  My RO said Advil also helps with the inflammation.

    I am a D cup and wear a Warner's "Friday bra" that's really soft but gives excellent support too, and then underneath I put a rectangle of soft cotton t-shirt (I cut up some old ones) that covers my nipple and my underarm area so nothing will rub.  This also stops lotions from staining my clothes.  I know a lot of people seem to wear a cotton tank under their bra.  I tried this, but it added too much bulk and made my shirts look funny, so I stick with the cotton rectangles.

    Wishing everyone a smooth ride through rads and beyond!

  • Joan1112
    Joan1112 Member Posts: 12
    edited August 2012

    Wow....Lots of good ideas on how to handle wearing a bra after treatment.  I'll have to ask my Dr office about the radiadress gel sheets.  those sound like they'd help. 

     My Dr also suggested that I get a shingles vaccine shot before the radiation because the rads effect the immune system.  Has anyone else gotten this shot shortly before, or during rads? 

    I hate to take more drugs than I need and don't like things overlapping so it's hard to tell what's causing what.....but I'm also not excited about maybe getting shingles! 

    Anyone have any input? 

  • Alice72
    Alice72 Member Posts: 38
    edited August 2012

    So interesting that the subject of rashes has come up. I have developed a bumpy, itchy, burning rash these past few days. I showed it to the techs and my RO. He said to get some OTC cortisone cream. I'm not sure it's working yet. I am prone to eczema and hives, so hope that isn't going to crop up.


    Joan, I intended to get a shingles shot a few years ago, but never followed through. When I started chemo, I prayed I wouldn't get shingles. There was a time after an early chemo treatment when I thought I might have them. Thank goodness I didn't, but it goes to show that it's not a bad idea to take precautions when you're healthy.


    Also, Joan, are you in Canada, or are you in the radiation trial that is based on the Canadian treatment of fewer days of treatments with increased dosage and boost given on same day as regular treatment? I'm thinking that would explain your shorter schedule.


    VVH your symptoms are a bit concerning--pain, redness, and darkening. Did you have a chance to ask about it today or perhaps tomorrow? Your description gave me a flashback to when I had mastitis while I was trying to breast feed my new baby many years ago. Do you have any fever? That is the other symptom I had at that time.


    As for bras, I did some googling and found one bra made of cotton that was a sleep/leisure bra. I decided not to buy any b/c I am retired. When I get home, off come the wig, the shoes and THE BRA. So, I don't spend too much time in a bra most days. I might still get one depending on how things are when rads are finished.

  • ro-berta
    ro-berta Member Posts: 134
    edited August 2012

    Good morning ladies 1 week out of rads and talk about rashes hahaha. went to B.S she gave me some cream seemed concerned if it got worse i am to come back right away if it still there in a week to also come back (YUK) She also told me she would do reconstruction after 6 mths to a year if I wanted which I thought was nice if her. Next after this is trying to find a bra or camisol that I can wear to work even though I do love going braless( to bad it doesn,t look as good as it feels hahaha. 

       roberta

  • Joan1112
    Joan1112 Member Posts: 12
    edited September 2012

    Alice72.   No one mentioned my being in a trial, particularly based on a Canadian treatment system, but RO did mention that it would be a higher dosage.  I'll ask him about it.  Could be he's just following that treatment plan without actually participating in the trial? 

     Makes me nervous with everyone talking about rashes and comfortable bras.  i hope to work through the 4 week rads...  I guess I'll just wait and see and do what I can do Undecided

    ro-berta...hopefully your rash clears up quickly and you don't need to go back to the Doc.  Everyone have a nice Labor Day weekend!

  • docziggy
    docziggy Member Posts: 17
    edited September 2012

    3 of 33 done today and nothing much to report yet. Stocked up on calendula lotion and have been slicing and dicing our enormous aloe plant (glad we have it - it was a house-warming gift from my mother-in-law and has not only taken over one corner of our sunroom, but has regularly spawned numerous baby aloes).

    Onwards ... 

  • ro-berta
    ro-berta Member Posts: 134
    edited September 2012

    HI Girls, I hope everyone is as comfortable as possible!

    Joan how are the treatments going??? Believe it or not they do go by fast. Not everyone gets rashes, must be my skin type it is probebly just one of those things. My energy has picked up which is a good thing, I mean there is only so much of laying around eating bon bons one can take hahaha.

    Docziggy Glad you have a aloe plant I have heard they are great hoping your treatments are going well. The wknd is here! I loved the wknd just to have a break from going to the hospital

    Well evryone take care It,s Friday!!!

        roberts

  • Kay-in-NH
    Kay-in-NH Member Posts: 26
    edited September 2012

    Happy Friday, Rad-girls !

    Today was 19 of 33 treatments, and so far, things are not that bad.  I have some redness along the thin skin of my upper chest, with slight darkening everwhere else.  I'm using 100% clear Aloe whenever I can, followed up with lotion (various).  Still running about 3 miles every 3 or 4 days, but feeling a bit dragged down.  Hopefully, I can push through the next three weeks and be done with this!  "Talk" to you all next week!

    Kay

  • Belinda977
    Belinda977 Member Posts: 381
    edited September 2012

    Kay, I have been running too and it's just been the last few days where it has become VERY difficult.  I still do the 3 miles but it's a struggle.  One more rad for me and then I am done.

  • naan1004
    naan1004 Member Posts: 520
    edited September 2012

    Mon will b rad 20/36, only 16 more to go, no real bad skin breakdown yet, crossing my fingers. Just have an awesome tan in my right pit area woohoo!

  • Belinda977
    Belinda977 Member Posts: 381
    edited September 2012
    DONE DONE DONE. ...and I did cry. I guess we just get on with business while it's happening. It was a mix of relief, joy and stress relief.

    Boost area is doing the yucky, moist yellow peeling. Doctor prescribed silvadene and I have to debrid with a mix of perioxide and water. A little bit of an owie with my open incision but I will deal with with it.

    Cross posting this so forgive me if you read this more than once. Who's next to finish?

  • ro-berta
    ro-berta Member Posts: 134
    edited September 2012

    Belinda, CONGRATS!!!!!! I,m so happy for you.( Hope your healing goes  quickly)

    Julie and Kay, you are nearly there the big countdown begins!

    Take care everyone and may the rest of the week go by smooth

      roberta

  • Junif
    Junif Member Posts: 100
    edited September 2012

    Hi Everyone...this is my first post here.  Had a lumpectomy 3 weeks ago and just met with the RO. My big concern is that radiation can cause premature hardening of the arteries and since heart disease is the number one klller of all the women on my maternal side, this was no small issue for me. The RO indicated that he used a block to minimize this, but I asked about prone radiation and he told me if that made me feel better he would do it.  I go for the simulation next week.  Has anyone had prone position radiation?

  • Aruba
    Aruba Member Posts: 543
    edited September 2012

    Congrats to all you August gals!  I have been following this thread for all your ideas and tips.  You are almost done and for that I applaud you!!  Junif, I got a call from my RO today that my heart is located close to chest wall so they going to do rads with a breathing device.  Sounds like a snorkling tube and I'll hold my breath?  August girls if you know about this fill me in!  Anyway, I asked also about prone position from my RO who is head of dept at the cancer center of this large ranked hospital.  She said she would direct me to mayo or another few hospitals in the country but she won't do it because she does not think the technicians can get the good breast (which is squished on the table) in exactly the same spot everytime and she wants to make sure everything is where it must be.  She was happy to send me where they do this all the time since they are more experienced..but i felt very much at ease with her and now even more so since she saw cat scan and wants to avoid my heart with this technique as added protection.  Again August gals...I applaud you! 

  • Junif
    Junif Member Posts: 100
    edited September 2012

    Hi Aruba-glad your RO is doing something to protect your heart! I read the blog of someone using the breathing apparatus:

    In an effort to curb the potential heart/lung damage, I will be using a scuba breathing apparatus, of sorts, during each of the treatments.  It's a really interesting thing, and the tech and I spent well over an hour refining the way it would work.  In short - I take a deep breath and, using the mouthpiece, am forced to hold the breath at a very specific point in the exhalation, for 25 seconds.  Filling my lungs with air creates a space between my heart/lungs and the tumor site; holding my breath at that very specific point creates optimal space, decreasing the likelihood that radiation will cause damage (or, if it does hit my heart/lungs, will hit the smallest area possible).

    My RO did his residency at Sloan Kettering where the prone position was pioneered.  He was very surprised that I asked about it (I did a lot of research before I went in because I was willing to travel anywhere to get something that would protect my heart and lungs).  He asked me if I would feel safer using the prone position--I said yes--he said that's what we'll do.  There is still a question on whether they can successfully get the area using this method and I'll find that out next week.  I'm a C cup so I think that is large enough.  My cancer was in the 12 o'clock position close to my chest wall.  I understand the boosts will be given in the supine position using a block.

    I guess when your finish RADS, Aruba you'll be ready to take up scuba diving....wishing you all the success....

  • Medwick711
    Medwick711 Member Posts: 14
    edited September 2012

    Well I have had 20 rads treatment with 14 more to go. Skin is holding pretty well, but my armpit has been sore for a few days. I had my surgery on 6/21/12 so my nerves have not healed yet and the rads are not helping, though I now it could be a lot worse. My completion date is 10/01/12 then will start arimidex. Has anyone taken arimidex? If so could you let me know how you are doing



    Thanks

    Patricia

  • Mbradshaw
    Mbradshaw Member Posts: 1
    edited September 2012

    Hello Ladies, I have been under going tx since August 13th. So far I have had somedays where I had fatigue and just felt like I couldn't walk to the parking lot. Other days I was able to walk around in the mall and do some window shopping. My concern is the care of the skin on my breast, and armpit. I have been using bio-oil and cortizone cream. Any other suggestions as what might be effective? I feel very lucky so far I haven't blistered. I have 11 more days of tx. My arm pit feels like a real bad sun burn!

  • ro-berta
    ro-berta Member Posts: 134
    edited September 2012

    Mbradshaw Hi, the ceame I used was Glaxol Base and Aloe vera pure, I alternated them through the day and then slathered the glaxol on at night before going to bed. I still burned but it would have been much worsr without it. I know the underarm got to me also and the crease under my breast. Just think you and Medwick are about half way through if not more the countdown begins!Just focus on been done shortly girls, YEAH!!! Then you can truely start healing.

        roberta

  • Kay-in-NH
    Kay-in-NH Member Posts: 26
    edited September 2012

    Hi Belinda,  I just had #24 of 33, but started hitting the wall last weekend.  It has just drained my energy, so I took the week off from running.  I can't believe you were able to run all the way through your treatments, which by the way, CONGRATULATIONS on completing your radiation treatments ! ! ! Are you now onto Tamoxifen or Arimadex?   I understand that starts within a week of completion, for five very long years ....

    My best to you,  

  • Kay-in-NH
    Kay-in-NH Member Posts: 26
    edited September 2012

    Hi Aruba,  I too had similar concerns as my tumor was high on the chest wall on my left breast (roughly 11 O'Clock, looking straight on).  After my CT Scan and simulation, I asked the radiation oncologiest (an excellent doctor from Harvard Medical with Mass General Hospital) to see how the beams were modeled on my 3-D computer scan.  Most major hospitals with the newer radiation machines have very precise internal blocks so that they can cover as much of the breast tissue as possible.  This was true with my scan, as it shows the beams from both directions, which just brush over the top part of the lung but entirely miss the heart.  As a runner, I was very concerned that the lungs were not affected.  I'm still running through my radiation treatments and have not had any breathing issues whatsoever (although now, the fatigue is settling in "big time"!).  Best of luck to you in whatever method you pursue.  Ask lots of questions and insist on getting as much information as you need until you are comfortable.  It's all part of the "informed consent"! 

  • Belinda977
    Belinda977 Member Posts: 381
    edited September 2012

    Yes I go to MO on Monday to start Tamoxifen. My speed has slowed down but because my RO told me it would help with the fatigue I just keep going.

Categories