Winter 2015-16 RADS

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  • kbutler
    kbutler Member Posts: 66
    edited March 2016

    Katja23, yay glad you are halfway there and no SE. I'll be right behind you and hope I do as well as you have. I just got home from a screening colonoscopy that my onc likes all her patients to get. Guess she thought I was close enough to 50and results were grea

  • Moondust
    Moondust Member Posts: 510
    edited March 2016

    Great news on the colonoscopy, kbutler!

    katja, I'm impressed with your daily walk. I walk a lot too. I think it has helped get through these rads.

    Tessio, great to hear about healing skin!

    I'm doing the countdown now. Today was 10, tomorrow will be 9.

  • MaggieMae123
    MaggieMae123 Member Posts: 38
    edited March 2016

    Hello all, Well I finish tomorrow!! Am so excited. Wanted to tell those just starting out that it is doable. Not fun but not that bad either. I have some redness, but have been using Aquafor since the beginning. Also wanted to share with everyone a "hair growing back weird" story. So I used to have auburn hair. It started growing back salt and pepper with a weird hairline in the front. The middle had hair but the sides were receding. Well now the receding part is growing back and it is the auburn color. The lower back is a white blonde color and it is starting to curl:) Just had to share. I have 3 different colors and different textures too:) I feel so pretty:) Take care all and good luck to everyone!

  • Kkubsky
    Kkubsky Member Posts: 231
    edited March 2016

    Day 2 was a lot shorter! I am using cream that the dr gave me. He said it won't prevent any skin SE but will keep it in the best possible condition. So I slather it on 2x a day. I am having a hard time figuring out what kind of a bra to wear. I ordered several different ones, but none seem to be working out. I usually have an underwire but was told to forego those for now. Going braless is ok in the house but my girls are a bit too large to be swaying in the breeze in public! Not sure what to do.....

    Also...how do I add my treatments to the bottom? I have tried to edit several times but it doesn't change. I am having 16 treatments with 2 boosts.

  • biscuits
    biscuits Member Posts: 3,304
    edited March 2016

    MaggieMae123... Tomorrow is my last day, too! I am excited to finish up. Actually, it has been a fast 6 1/2 weeks. The techs asked me if I was planning a party and I told them that I want to just catch up on some sleep. I have worked full time through the chem and rads, only taking the day off for each infusion. I feel old and tired and my skin finally decided to " open up" so now I have Silvadene cream to add to the mix. With all that being said, I am tickled to finally see the light at the end of the tunnel. I gave each of the rad techs an angel pin to thank them for being "angels" through all of this.

  • Moondust
    Moondust Member Posts: 510
    edited March 2016

    Kkubsky, I think you might have to put the 16 treatments and 2 boosts in your signature instead of the treatment area. You create a signature by clicking Settings on the Discussion Board menu (left side of the page). I am a 36 D or DD and got some soft bras at Walmart for less than $20.

  • Musosgirl
    Musosgirl Member Posts: 387
    edited March 2016
    Kkubsky, I too am fairly well-endowed, but I did find a front zip-up sportsbra at Kohl's that has been a lifesaver. (Although if I forget to do the hook at the top, the bra will unzip on me. That can be a bit embarrassing when you just pop open at an unfortunate time and flop loosy-goosy, and in my case rather unevenly.) But the front closure makes getting in and out SO much easier.

    Yesterday I saw my RO and asked about my radiation area. I feel the box on my chest is too low. We were radiating a good 3 inches below my breast--I have mentioned how those ribs hurt--and the top of my breast is not red at all. She argued with me and I dropped it. I am just counting down the days to being done with rads and going back upstairs to my MO. BUT today I went in and the techs said we were going to do more films. She really listened to me! Now, I spent 45 minutes with my arms above my head and literally could not feel them by the time they were done filming, marking, resetting, and treating, but they readjusted my settings up by more than an inch! I feel better about the placement, although still feel it is a bit low, and even if it is only for 10 days. 9 now.
  • SeekingSerenity16
    SeekingSerenity16 Member Posts: 13
    edited March 2016

    Good morning everyone! Today is my last day too! Up way too early from the excitement. Have candy and Dunkin Donut gift cards ready for the technicians, going out to dinner with DH tonight. When I look back to that first day it seems so long ago; but, time has flown by. Over the past week, since starting boosts, my skin has stopped itching and the redness has turned to a normal tan. The boosts have added more redness to my stretch marks around the surgical site; but, I do not feel any discomfort or itching. The boosts actually take twice as long because the radiation head moves to 4 different positions instead of the 2 when I was in the prone position during whole breast rads.

    For those who are starting and asked, I used Aquaphor from day 1 immediately after treatment in the early morning. Before bed I showered and put on Miaderm, mostly because it is water soluble and in the morning my treatment area was soft and clean and I didn't have to shower again. As time passed I simply added pure aloe to help with mild itching a couple of times a day on top of the aquaphor or Miaderm. I haven't worn a bra since December; but, for work I wear several layers and loose clothing and no one would know!

  • MissV123
    MissV123 Member Posts: 79
    edited March 2016

    Welcome Kkubsky and CountryFrenchRose....this is a great place for information.....and Kkubsky, I am a larger woman, and I found a bra by Bali.....no metal or plastic strap adjusters, almost like a sports bra with a light padding for modesty in the front...the sides (underarms) were high enough to cover scar and keep the miaderm from getting all over my clothes....they come in small,med large and xlarge....I found them in Macys and in Kohls.....good luck....

    Sunnyone22 I used the Auqaphor at night and Miaderm during the day, now 2 weeks post rads I'm just using the miaderm 2 x a day.....I am healing very quickly.......

    Barbe1958, I feel your pain, my husband was Fired the night before I started rads...just adds to the stress. took 6 weeks for unemployment to kick in.....all I can say is there is some truth to the saying "things happen for a reason" He was here to drive me to work ,pick me up from rads, take care of the house,walk the dog,and feed me.....I guess I had to look at the positive side or murder him.....hahaha.

    Musogirl, Im sorry you are having such a hard time and Didel too.... I still feel fatigue....but I come home from work put on the pjs and rest when Im like that....otherwise ....I go for a walk with the dog...and if the sun is shining....I smile ...for the first time in months I smile......

    And Mdoc524, I cant thank you enough for starting this forum...it has helped me in so many ways....I am now (today ) heading to my MO to see if its tamoxifen vs armidex....Im so nervous....my friend is driving me cause my mind is all over the place......I will report back later to let you know which med I will be on

    Have a good day Ladies and Warrior On.......

  • KateB79
    KateB79 Member Posts: 747
    edited March 2016

    My tan is fading.

    Some things just never seem to change, in spite of it all! I'm very fair-skinned and tend to burn-then-tan-then-fade, and that's exactly what's happening now.

    Three weeks out.

    To all those still in the throes: you've got this. And congrats to those of you who are finishing!


  • edwsmom
    edwsmom Member Posts: 346
    edited March 2016

    HI everyone,

    Today was my second radiation day. So far things are going ok. I don't feel anything and don't notice any changes in my skin...yet. How long did it take for you to have any kind of skin reaction to the radiation? Or maybe you never did?

    A friend of my Mom's in NYC had treatment for breast cancer. She sent me a box of creams apparently made especially for radiation. Apparently she used it during her radiation treatment and had great results. I showed it to my Dr and he approved me to use it. It's called radiaderm. (http://radiaderm.com/) Has anyone here heard of it or used it before? It's a 2-step cream process. Right after treatment I put the first one on (it's a "cooling" gel) and wait 10 minutes. Then I wipe off any excess and apply the second cream. At night I apply a tube of the second cream again. They are packaged in little single use packets so I can just keep the packets in my purse. I guess we will see how well they work.

    Anyway, giddy-up...this is only the very beginning of this process for me. And, I have an appointment tomorrow for follow-up with my MO and I know she's going to get me started on tamoxifen - which I'm DREADING.

    PS - did your doctors ever tell you anything about how much doing radiation reduces the risk of recurrence? Like a percentage or something? Thanks!

  • Katja23
    Katja23 Member Posts: 46
    edited March 2016

    kbutler, that's brave of you to do a colonoscopy during radiation therapy. I am 50, but I postponed scheduling my first colonoscopy until at least a month after radiation therapy ends. I want to continue to eat, sleep, and exercise regularly and sufficiently to fend off any fatigue.

    At my annual PCP checkup in November I was reminded to get a mammogram, get a colonoscopy, and get moles checked by the dermatologist. In February I got a call from the PCP's office asking if I had made the appointment for the colonoscopy yet (but they didn't ask about the other two). I said not yet, since I was still dealing with the ramifications for the mammogram. I did go to the dermatologist in February, though, and it turned out one of those moles was skin cancer! (squamous cell carcinoma). I'm still doing the treatment for that: applying a chemotherapy cream to it twice a day for 6 weeks. It's getting more sore as time goes on.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited March 2016

    I've been suffering horribly with a bladder infection, probably brought on by Arimidex and am on my second round of antibiotics as the culture showed the first batch was resistant. Like I really needed this right now??????

    Thanks MissV123 for sharing your story about your DH's job, I don't feel I can take much more.

    I'm nauseous yet again today to the point I just took Gravol. Did anyone else get nausea?

    I do notice right after my zaps that my skin is pink but it settles down. I do see where I will eventually have problems. I've only done 3 and have to do 22 more. They keep warning me I'll blister. I'm getting what I think is a pretty large area done - from under left arm, across chest wall to sternum and up to lower neck! It's like a quarter of my torso! Thank goodness I don't wear a bra (flat from BMX) but have been wearing a cami under everything to keep creams off my clothing. I feel bad for those of you who have to wear bras as I'm sure underwire isn't allowed. Would sports bras work?

    Hanging in there....barely. At least we have this Friday off both work and rads for Easter. Will be driving 3 hours to visit half of our kids and 3 out of 5 grands. Should be good. We get at least one sleepover....love seeing the grands in the morning!

  • biscuits
    biscuits Member Posts: 3,304
    edited March 2016

    barbe1958...I, too, suffered a lot of nausea after I started rads. I talked to my RO about it and he believed that with my field of radiation, that some rays were coming across the top of my liver. He said that would create the nausea. It finally has settled down (took over 5 weeks) and I used my nausea meds left over from chemo to help with it.

  • KarenR0618
    KarenR0618 Member Posts: 78
    edited March 2016

    Kkubsky I understand the bra trouble. I ordered sports bra's that zipped up in the front. I didn't like them, Next I ordered from Geni and my first shipment I didn't like so I sent them back. I got some $7 specials from them after that. They are ok. The best were clearance ones form Walmart. They were $3.00. I am not to big so they are working fine. I have to wear something because I am continuing to work so I have to have something on.

  • KarenR0618
    KarenR0618 Member Posts: 78
    edited March 2016

    Today when I got in for my treatment one of the techs came up to me and said I have another appointment for sim. She said they will start doing the radiation closer to the spot where they did the surgery. More tattoos. Is that normal?

  • biscuits
    biscuits Member Posts: 3,304
    edited March 2016

    KarenR0618...yes, this is normal if you are having "boosts". If you have already been receiving rads, then the boosts are given at the end of your treatment. The reason for the boost is to target the actual tumor bed (where the tumor was located) and give it more direct beams.

  • KarenR0618
    KarenR0618 Member Posts: 78
    edited March 2016

    Thanks biscuits they never said anything about boosts just 21 treatments.

  • biscuits
    biscuits Member Posts: 3,304
    edited March 2016

    Karen...that's what they did to me. Told me 33 treatments. They just didn't elaborate that the last five would be boosts, until it was time for the new sim.

  • KarenR0618
    KarenR0618 Member Posts: 78
    edited March 2016

    They just gave me the appointment. They didn't ask if it worked with me. I came into work after and told them I now have 3 appointments on Friday. I meet with my RO on Fridays also. So my boss said it sounds like you will be worn out from it all so to take the day off.

  • MimiT49
    MimiT49 Member Posts: 2
    edited March 2016

    Hello, I'm a newbie to the discussion boards. I started radiation on 2/24/16. I have to have 33 treatments and I'm almost done (have 2 1/2 weeks left!). I have already been through 6 rounds of chemo, surgery and now doing radiation. I am so tired!!!!!

    Anyway, wanted to join this group because I'm having extreme fatigue and my underarm is starting to turn black and hurt, so thought I'd see if anyone else was experiencing the same. I also have numbness/tingling/pain in my hands and feet from chemo that are worse with the radiation.

  • Brimton
    Brimton Member Posts: 87
    edited March 2016
    Hi everyone CONGRATULATIONS TO ALL THOSE FINISHING! WE GOT THIS TO ALL THOSE STILL UNDER THE KITCHEN AIDE. I am one week out. Still peeling and under my arm is a tan color.Someone said your underarm hair won't grow back and so far that is true. It looks like Frankenstein under there part way hair part no hair. LOL Still slightly pink over all. But much better. My boost area is still pretty red. I can tell it looks bad by the look on my husbands face. I USED AQUARFOR THE WHOLE TIME. I would and still am putting it on 3x per day. i think overall I did pretty well and my RO thought so too. The last week my underboob was so bad I stopped wearing a sports bra. It was a blister which peeled under there. The RO said anywhere you sweat it will be bad. I can relate to not wanting to go braless I'm a D cup. But I did it anyway. I also lay for a while under the fan to let myself air dry after my shower. NOT A IU GRAD BUT BOTH MY CHILDREN WENT THERE. GO IU!!!
  • VickiRides
    VickiRides Member Posts: 211
    edited March 2016

    Congratulations to everyone finishing!

    I am getting quite red and sore, especially my underarm. Boosts start next week. SeekingSerenity, you have given me hope that my skin will start feeling better soon. My RO gave me a prescription for Silvadene this week. I find myself getting more tired and cranky. We had to move all of the furniture out of our bedrooms last night because we are having carpet installed today. I was pretty much useless and that frustrated me.

    barbe1958, I am sorry you've had to much to deal with. I hope you have a wonderful weekend!


  • barbe1958
    barbe1958 Member Posts: 19,757
    edited March 2016

    Thanks ladies, the one thing I didn't expect was nausea so it's annoying me desperately!

  • mdoc524
    mdoc524 Member Posts: 336
    edited March 2016

    WooHoo Big High 5's and Happy Dances for MaggieMae, biscuits & SeekingSerenity – Congrats on finishing! MaggieMae –thanks for sharing about your hair – mine came in all white and still is mostly 3 months post chemo – I am so ready to dye it!

    Welcome Welcome MimiT49 – so sorry you are here but so glad you found this awesome group! Hope your 2 ½ weeks go quick and easy and yes I have the same fatigue, black underarm that hurts .. I am one week post rads – it does get better! Hang in there! The tingling and numbness could be from Neuropathy from chemo.. I take Gabapentin for chemo-neuropathy and has helped!

    WooHoo Katja on hitting halfway mark – hope 2nd half goes quick and smooth! And wow – glad you went to the Dermatologist – hope it does not get too bad and heals quick for you! Hugs to you

    Barbe1958 – my radiation red area is the same as yours and my worst area was collarbone – it opened no blisters – my armpit started peeling but does not hurt at all .. hope your skins holds out! UGH on the Bladder Infection – does Arimidex cause them ?? Hope it gets better fast and last really hope your Nausea goes away .. I had what felt like lump in my throat indigestion the first week but it went away!

    Twnkltoz – so glad you enjoyed your party – well deserved!

    So Sunnyone and Tessio – I might have mis-spoke – I am not an IU alum .. I went to St Joe's University – a hawk forever! But I did pick IU to beat KY in my bracket. Sunnyone – hope your 1st Champagne was yummy! And I never used Aquafor. Initially I used Calendula 3-4 times per day and the RO presecibed Betaval Cortisone cream to use 2x per day and Calendula in between and then at the end she had me using only the Betaval ointment 4 times per day – it really did calm the heat and itch..

    Kkubsky – some women here wore cotton t-shirts under the bra to prevent rubbing/chaffing – just a tip! Good Luck

    Musosgirl – hope the break helps your skin and it holds thru boosts! Hugs and Great for you on speaking up and very interesting they adjusted! My Red Rectangular Box area went about 2 inches below my boob and not all areas above got red – my RO explained that skin in different areas will react differently

    Kbutler – glad you got your colonoscopy and that it went well! I am 46 and have had 2 (Mom is a colon cancer survivor 25 years!)

    Moondust, Marijen & VickiRides – the end is in sight – hope it goes quick and easy!

    MissV – Good Luck at MO – I head to mine on Monday for post chemo follow up and expect to have the Arimidex vs Tamoxifen discussion too! I am expecting to start Arimidex since full chemopause since September and having ovaries out in June ..let us know how it goes!

    KateB – same here – my Irish skin goes from Red to Tan to Fade and then more freckles! Glad you are healing well!

    Edwsmom – I was Red by the end of my 1st week and stayed that way whole time.. As far as rate of recurrence I had asked my MO's nurse and she said my MO would go over that with me at my follow up on Monday so curious about that discussion as I know there are no guarantees!

    KarenR – just to chime in – Yes it is normal if you are getting Boosts and they should have told you. I have 4 additional tattoos from Boosts but they are teeny tiny. The SIM for boosts was not as long as the in initial sim! Very nice your Boss is being supportive! Good Luck

    Brimton – my Boost area is pretty red still too. Glad you are doing well

    All I am a week post Rads and skin healing well - my collarbone area finally closed and scabbed up - underarm peeling but does not hurt! Mastectomy scar from Boosts still pretty red but hanging in there! This week so so tired (nightly Hot flashes are just crushing me) and really frustrated with my weak chemo legs .. I was wrapping presents on the floor and could not get up .. started PT this week for neck & shoulder issues from rads and the therapist threw in a few things to help my legs - very nice! Thanks for listening - patience is not my strong suit! Hugs to all and Happy Easter - hoping my 9 1/2 year old boys still believe in the Easter Bunny!!

    Mary

  • MissV123
    MissV123 Member Posts: 79
    edited March 2016

    OK, so here it goes....My MO is not in my new insurance plan...he was wonderful ,and said I could still see him, but he couldnt order any tests or labs for me, I would have to have someone else order them like my PCP.......and so now I will have to find a new MO ....and my Surgeon, with whom I have a follow up in May ..also not in the plan.....they broke away from the Insurance and New hospital that just took over the hospital where I work......YIKES.....also.....my BRCA test was never done, and this was the reason for the appt today....and it was because bcbs denied it....would have been nice to know......so I am having it done again under my new ins Qualcare and they will pay in full... this will let me know if my ovaries need to go.......but for now my sentence is ARMIDEX for 10 years......started tonight.....and will have to find new docs....to follow up with.....whew....time for a nice hot bath.....couple a xanax , and bed........night night Ladies.......

  • Brimton
    Brimton Member Posts: 87
    edited March 2016
    Vickie rides Watch the silvadene it can dry you out and make your skin crack my RN told me. I only used it a few days. watch your skin for dryness even if using it in combo with something else. Used it under my arm and it helped in a couple of days and then started to feel scratchy. Just an fyi.
  • DiDel
    DiDel Member Posts: 1,329
    edited March 2016

    whoop whoop seekingserenity Maggiemae & biscuits!!!!!!

    Feels so good to be done and sleep in!! I hope you do something special for yourselves . .you all deserve it!

    Missv sorry about your mo..that stinks..I hope you find someone you like or work something else out.

    Off to bed still so tired but slowly heeling skin. Good luck to everyone this week

    Hugs to all

    Diane


  • Sunnyone22
    Sunnyone22 Member Posts: 191
    edited March 2016

    First - congrats to everyone who just finished rads. You're an inspiration to the rest of us.

    Today I finished #7 of 28 treatments. Earlier I posted a photo of the way I'm marking progress - 4 champagne flutes, each containing 7 pink gumballs. Today, I finished the gumballs in my first champagne flute and am ready to fill the flute with champagne. Cheers to you all!!

    Sunnyone

    image

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited March 2016

    Hope you enjoyed the glass, Sunnyone!

    Yep, feels like a lump in my throat, too! Not a happy camper here. It is making my recurrence all too real.

    I was also told that 100% Aloe (without alcohol) will STILL dry your skin as well! It's only a "soother" for the burn feeling and not curative. Interesting about the Silvadene, too.

    Oh, and just an FYI, I was diagnosed Stage IV 2 DAYS after I started my new sales job and I'm still in second place in sales! Still beating almost everyone else since January. Woo hoo for me! I can only imagine what the general manager says to the guys when I'm not around....."she's beating you and she's the one with cancer and treatment - are you kidding me?" Goes to show that we gals keep going when the going gets tough!

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