Winter 2015-16 RADS

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  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited January 2016

    Etnasgirl- sorry you are sore- I ended up needing to wear a bra almost 24/7- the support seemed to really help. Just a softcup/no wire. Near the end- wore a cami under it sometimes. Hope the time goes by quickly!

    Twnk- You're on your way. Know it can be a very emotional time and am hoping the time goes by quickly for you w/ min or NO SE's!

  • phoebe58
    phoebe58 Member Posts: 193
    edited January 2016

    I am 13 of 28 down - almost half way :) -- swelling a bit more [so a bra is annoying unless its my super soft t-shirty kind], and achy tender [feels like a wearing a bowling ball, but I exaggerate!!]. I am also getting a bit pink over breast not used to seeing sun, yet more tan below and above that has had sun exposure from bathing suit over the years. I feel a tight banding effect across lower part of breast too, as if I am wearing a super tight sports bra that has ridden up. Day seems to be spent remembering to slather on creams, soak with saline compress, and cradled in cabbage -- boy that takes a chunk of time to schedule in -- I tried multitasking with cabbage leaf by walking around, and lost it somewhere in house -- later found in laundry! My physio says to keep doing a variety of stretches to maintain flexibility. I do crawling arm up wall till extended and lean in - front and side, arms out to side and up overhead, clasp hands behind and gently extend up, etc -- anything really that involves a stretchy pull but not pain in multiple directions, and a gentle short exercise routine.

    Duzy, they will support your arm in position. Mine was cold and achy by end of sim, but actual treatments very quick and no issues.

  • Duzy
    Duzy Member Posts: 134
    edited January 2016

    Twnkltoz and Phoebe58 thank you for the information. I am a little apprehensive but ready to get started so glad to hear they support my arm. I am surprised I did not receive any exercises to gain range of motion and I called them to ask and they said just gentle stretching.

    Good luck to everyone having treatment this week

  • LMN
    LMN Member Posts: 35
    edited January 2016

    I am getting twice a day radiation for 22 days and finished my 6th day Friday. Is there anyone going twice a day

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited January 2016

    LMN- have not heard of that protocol- but we have seen that different hospitals/docs/states/countries do things differently. Where are you? Hope it is going well for you!

  • LMN
    LMN Member Posts: 35
    edited January 2016

    I went to the IBC clinic at MD Anderson in Houston for a consult following chemo and also went back after trying a second type of chemo and had surgery in Houston. There is an MD Anderson radiation center here in Albuquerque where I live. I have the impression the twice a day is unusual here

  • LMN
    LMN Member Posts: 35
    edited January 2016

    happy hammer how is your radiation going? When will you be done

  • Twnkltoz
    Twnkltoz Member Posts: 215
    edited January 2016

    welcome, LMN! I hope it's going well for you.

  • etnasgrl
    etnasgrl Member Posts: 650
    edited January 2016

    LMN.....I've read in Dr. Susan Love's Breast Book that some women do receive Rads twice a day. I don't think it's all that common, but it is done. (If you don't already have that book, I highly suggest you pick it up. It's fantastic, full of SO much info on EVERYTHING breast cancer.)

  • theearthlaughsinflowers
    theearthlaughsinflowers Member Posts: 23
    edited January 2016

    Hello everybody~ I have received 24/25 regular treatments and then I have 5 boosts.

    I am concerned because my RO only wants to boost the areas in my breast where the surgery was- he does not plan to treat my area where I had positive lymph nodes (and all removed).

    Has this been the case for others that have had an axillary lymph node removal?

    Thank you,


    Pam

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited January 2016

    LMN- finished rads last Tuesday. Skin healing though am still a bit uncomfortable. Using the creams and Aquaphor and taking Ibuprofen.

    How is your skin holding up?

  • 1957-2057
    1957-2057 Member Posts: 35
    edited January 2016

    Morning all, Welcome to all those starting and CONGRATULATIONS to those finishing. Last week was my first full week of rads so finished with #9. Thought I was doing good but Thursday I hit the fatigue wall. Have been resting as much as possible to hopefully stay ahead of it but bamm. Last 3 days I have been going to bed way early and slept well but still feel as if I can nap at the drop of a hat. I sure hope the weekend sets me straight, I don't want this to be worse. I have been hydrating to the point where I am spending more time in the bathroom than any room in the house, lol.

    Does anyone have any good diet tips that help with fatigue? I am eating healthy but would welcome any advise to keep this at bay. I plan on working full time all the way through but if this gets much worse I don't know that I will make it.

    Next week will have me seeing 1/3 way through all treatments and also 1/2 through my 25 full breast. It does seem to be going pretty fast. Other SE are not bad, little tender in the breast and notice a little tenderness in the rib area. Skin is doing well so glad of that.

    Once again hats off to all the soldiers in this war, we will beat this enemy.

    Helen



  • etnasgrl
    etnasgrl Member Posts: 650
    edited January 2016

    You know, as strange as this is going to sound.....the reality that I have breast cancer is finally starting to hit me.
    Prior to this, I accepted the fact that I had cancer but was in attack mode. I wanted the surgery and treatments to begin so I could get this crap out of me and move on. That was my sole focus.
    Now that surgery is done and I'm going through Rads, attack mode is not as fierce and my focus has shifted to getting the cancer out to....wait, what?....I have cancer??!!!
    I'm 41 years old and I have breast cancer. I'm young so the chances of the cancer coming back is pretty good. How do I move forward while I'm constantly worrying that a recurrence is just around the corner?
    It did for my mother. She was 42 and went through the exact same treatments as me, (lumpectomy and radiation), then at 50, it came back. She passed away at 56. Am I doomed to the same fate?
    How do you look this monster in the eye and get on with life?

    Most days, I refuse to give in to the worry, but today it's just overwhelming.

  • DurhamGirl
    DurhamGirl Member Posts: 100
    edited January 2016

    Hi everyone! mdoc524, please add me to the group list above.

    I have my last round of chemo this Tuesday (January 26) and will start rads on February 15. It has been great being on the October 2015 chemo support with so many strong and supportive women. I'm sure it will be the same here!

    My plan is to do 5 weeks (25 treatments) in the superclass ulnar and heat area, and then possibly a one week boost in the scar area. I have gotten two opinions on my radiationplan from two oncologists and they are both in agreement, so I'm going to go with it. I am very grateful to live 5 minutes from my hospital.

    I have VERY sensitive skin, so I'm worried about the cumulative burn that I am going to get.

    Good luck everyone

    Jennifer

  • beryl
    beryl Member Posts: 4
    edited January 2016

    I near Ottawa and am awaiting phone call from Cancer Center with oncologist to discuss whether I need radiation only or also chemo. The invasive ductal carcinoma did not enter the lymph nodes. I'm weak and underweight (90 lb) from severe arthritis, so I'm particularly hopeful that I will not require chemo. Thank you for your supportive postings.

  • Jabe
    Jabe Member Posts: 185
    edited January 2016

    eartglaughsinflowers: I think boosts are generally only in the area where the tumor was. The lymph node is not a tumor but rather shows that cancer is in your lymphatic system (hence chemo which goes more systemically).

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited January 2016

    Beryl- hope you get a good plan in place that you are comfortable with!

    Welcome, DurhamGirl- you are almost done with chemo-YAY YOU! Hope last treatment goes well. Try not to worry to much about your skin. It seems that many people with sensitive skin do not have and SE's or as many from rads as those who do not have sensitive skin. Think it is just so individualizes. Expect no SE's- you are going to do great. If you do have some SE's you are in the right place for help! BTW: Did you get much snow your way? I'm below Charlotte and we got about 3 inches of sleet/snow. Beautiful!

    Etnasgirl- so sorry you are having a hard day. Sometimes it can just be overwhelming! Sending you HUGS!

  • KateB79
    KateB79 Member Posts: 747
    edited January 2016

    Has anyone tried American ginseng for fatigue prevention? I've read a few studies about how well it works in a lot of chemo patients. I would have taken it during chemo, but the smell of it was just too much. . . . My RO is fine with it, so I'm gonna give it a try.

    I start on 2/4. I'm already hydrating the crap out of my left side.

    In the shower the day after my sim, I kept trying to scrub the blue dot off of my sternum; I thought it was leftover adhesive from surgery. Um, nope, it was my rads tattoo!

  • Shopgal2
    Shopgal2 Member Posts: 649
    edited January 2016

    Etnasgirl take it one day at a time. That's the best advice my chemo nurse gave me. I also had a family history; my mom dx at 69 and had lumpectomy and rads. My grandmom also had bc at 69 but had a uni mx and no rads. I was 44 at dx and am triple neg, which has a high reoccurrence rate in the first 5 years. Do I worry about my cancer coming back and mets? Yes, but I am working on living for today and taking it one day at a time.

    Kate too funny story about your rad dots

  • theearthlaughsinflowers
    theearthlaughsinflowers Member Posts: 23
    edited January 2016

    Thanks Jabe. I want to feel I'm doing everything possible and being aggressive with all treatment but that does make sense to me

  • Natejordlee
    Natejordlee Member Posts: 61
    edited January 2016

    LMN - we have the same diagnosis and my doc is from the US but now works here in Canada. She did tell me since we get a higher dose For IBC in some states they split it to twice a day.

    Beryl - I too am in Ottawa they are a great group over there and I am sure you will do great !Dr chang is incredible and I highly recommend her. I am currently doing rads at the general so I can use the Tomo machine but most of my treatments were are the QCH.

    So I had 14 of so far and noticed a blister today, luckily on the numb part. Should I be putting anything on it to prevent infection ? My creams have been great and I can ask tomorrow but wondering if anyone had been given advice on if they come up.

    Lee Anne

  • PattyMeg
    PattyMeg Member Posts: 56
    edited January 2016

    Etnasgrl, we all have those days. Hang in there. Once that initial biopsy comes back, everything happens so fast, that I don't think it sinks in right away. I had to take three weeks off when I had my lumpectomy, because I did a reduction as well. I'm a teacher and wasn't sure what to tell the kids, as to why I would be out. My boss said she had a book written to help teachers tell their students they have cancer, and I was like, " cancer, who has cancer?" It was a little surreal. Going through rads, I felt empowered, as if I was killing off all those nasty cells, so I was not stressed or worried. Now that I just finished rads, I'm getting a little worried. If I feel a pain in my good breast, I think, what's going on there? I'm supposed to meet with oncologist tomorrow to start tamoxifen, but one tumor was hormone positive and the other was not, so I worry that it will come back. I'm sure all of the women here have the same worries. You are not alone! Try to do things to de-stress. Maybe yoga or meditation. I started back on my treadmill and that helps me deal with the stress, and I've been making juices every morning. I usually make one called "mean green detox machine". If the cancer comes back there's not much I can do about it, except deal with it, but by doing these little things, it helps me feel a little in control. Good luck to you. Feel better, and best of luck to all of you wonderful strong women. Patty

    P.S. A glass of wine never hurts either.

  • etnasgrl
    etnasgrl Member Posts: 650
    edited January 2016

    Thank you everyone!

    Hug

  • phoebe58
    phoebe58 Member Posts: 193
    edited January 2016

    hi Natejordlee -- I don't have a blister yet -- 13 of 28, but my rad nurse said if something happens, a tiny dab of polysporin helps -- use after not before your radiation time

    Etnasgirl -- I worry too at times about what the future holds, what this symptom means, etc, but at other times it is off my radar and I feel pretty normal and try to keep busy doing the things I enjoy and trying to do my bit to stay healthy -- I think it is a pretty normal feeling that happens to most of us at some time or another -- so you have company here that understands.

    Love the wine advice pattymeg and hope you [and other easterners] are coping with the big blizzard

  • DurhamGirl
    DurhamGirl Member Posts: 100
    edited January 2016

    Hi HappyHammer! Thanks for your encouraging words! We got about 3 inches of ice and snow. No school Friday or tomorrow, since the buses can't travel on the still icy side roads. So all the kids (I have three boys) are happy for a chill day tomorrow, and I'm happy to not have to be up at 6 getting everyone out the door!

    Hope everyone has a lovely evening

  • violethope
    violethope Member Posts: 32
    edited January 2016

    PattyMeg- can you post what you put in your "mean green detox machine" smoothie!? Thanks!

  • mdoc524
    mdoc524 Member Posts: 336
    edited January 2016

    Welcome Welcome luzeelu, Jclc83, JuniperCat, Duzy, LMN, DurhamGirl & beryl... So sorry you have to be here but glad you found us! Loads of great sharing & support here- keep us posted on how you are doing & any updates on your treatment details.

    Sorry Marijen - I misunderstood your post about pneumonia vaccine & Rads

    Fearless1956 - glad you & your Mom are doing well - 80 years old God Bless her! My husband's mom just diagnosed with Brain Cancer & will be 80 this year & wants to do treatment -...

    TallnTerrific - hope your throat & eye flashes subside - sounds annoying

    Duzy - I just had my sim & arms were up maybe 15-20 minutes - was not as bad as I thought it would be

    Etnasgrl - hope soreness from Week 1 subsides & does not get worse! Sorry about your Mom & I would feel the same - I think the anxiety is the worse part - hugs to you!!

    1957-2057 - hope fatigue gets better

    Natejordlee - hope blister heals quick

    Phoebe58 - thanks for sharing details on your arm stretches - very helpful!

    My RO advised to use Calendula cream 3x per day starting this coming week (week before starting rads) - she recommended Califirnia Baby which can be found at Target/Walmart ..

    Question - is everyone working thru rads? I am still dealing with chemo fatigue & curious going into Rads already fatigued how much worse will it get?? I am planning on going back to work in mid-February & afraid will be too tired ...thoughts?

    Hope those impacted by #Blizzard2016 are doing OK .. Got 2+ feet of snow here & now kids are off tomorrow from school because if the snow!!

    Have a great week everyone!

    Mary




  • PattyMeg
    PattyMeg Member Posts: 56
    edited January 2016

    Violethope, Here it is. I usually add more ice after it's blended, because it's not cold enough. The photo was a little hard to read, but says you can substitute mango for pineapple. It sounds like it would be terrible and the color is very very green LOL, but it tastes pretty good. You taste the apple first and then the cucumber. I leave out the celery, because I hate it! Haha if you blend one up in the morning, you start the day with 8 servings of fruit and veggies. Enjoy! Patty

    image

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited January 2016

    Patty- that actually loks good...not sure about getting the Hemp seeds but will look at EarthFare and/or Whole Foods. Would leave in the celery but what kind of pineapple? It has something beside it but cannot read it.

    Thanks so much for the recipe.

  • PattyMeg
    PattyMeg Member Posts: 56
    edited January 2016

    Happy Hammer, I use fresh pineapple. Next to it says you can substitute mango if you don't like or have pinapple. My daughter Jo loves it, so I usually have it in the house. I found the hemp seeds in the health food section of Stop and Shop, but I'm sure Whole Foods would have them. The cold pressed coconut oil can be found there too. Patty

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