August 2010 Rads

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  • againmine41
    againmine41 Member Posts: 81
    edited September 2010

    Today was my last day for rads! Yippie! The tape comes off! No more being marked up like a connect the dot! 

    I got a certificate too!

    Ok, now a nap. 

  • janabananna
    janabananna Member Posts: 19
    edited September 2010

    I'm 10 days out from my last boost and am feeling much better physically.  My energy level is much improved, although not back to normal yet.  The boost area is still pretty pink and my nipple is sensitive and starting to peel.  It has been just the last few days that I don't feel uncomfortable on that side, and last night I was able to sleep on my tummy again!  The nonboost areas are pretty much healed - yippee!!!  For me, the boosts caused a lot more burning than the other ... maybe because it was so close to my skin and was a visible and bright blast (more like the sun) as opposed to the invisible beams from the full breast treatments?

    Emotionally, I'm still on the edge.  If I start thinking too much I can feel it all start to well up, but I just don't have the time or energy (okay, desire) to "deal" with it right now so I stuff it back down.  I know once I start crying it will be awhile before I stop ... I've got groceries to get, school open houses to attend, new TV shows to watch, friends to have coffee with, etc., all before I start work again on 10/1 and I don't want to "waste" the time crying.  Not very smart of me, is it?  I will probably break down at the worst possible moment ... I suppose I should try to "schedule" it soon?  Wink

  • sharonraew
    sharonraew Member Posts: 24
    edited September 2010

    Hi

     I'm 10 days out too.  Boost area is pretty burnt but the rest is good.  I have a very sore shoulder. I went and got a massage and it felt wonderful.

    The crying comes and goes.  I just let it.  I played super - person for so long and now I retired from that position.  I spent decades taking care of everyone else and now it's my turn.

    My rad-onc put me off work until Dec 13th.  She said I wouldn't be emotionally or physically healed.  I thought she was nuts.  Now I see her point of view.

    BTW, I've been on Arimidex for 3 months now and all the SE have subsided.

     I can't believe some of you ladies worked through all of this.  You amaze me.

     Good luck

  • Resting
    Resting Member Posts: 215
    edited September 2010

      So happy for you againmine ---  finished!!!! Maybe now you can relax and do something nice for yourself. Maybe go out and frame that certificate.  Laughing  I finish next Tuesday, it's three more boosts to go.

       I'm thinking of you Janabananna as you start work. Maybe the distraction will be good - I'll be out looking for a job sometime in the near future and I'm trying to get a jump start by walking and working more around the house. I want to see how fast my energy level will return. I'm a bit anxious about how I'll hold up. It's been nearly four years since I worked. The three years before I received my dx of BC I was taking care of my Mom - she was a full time job. You know I wonder if this emotional up and down business is part of chemo-pause or if it has to do with the whole crazy ride we've been on and we're finally winding down long enough to catch our breath. And with that we just go WOW, I really didn't want to do this. Everything comes at you so fast at dx, before you know it we're in the middle of tx. It's enough to make anyone cry.

       I too am amazed at the women who worked thru all this tx process, I think it would have been to much for me. But then we women tend to do what we gotta do, right? Somehow we just keep putting one foot in front of the other.

    Ladym and phxsun  and everyone else who it making progress with the completion of tx - so glad your doing well and that you improving with each passing day.

                          Blessings

  • AnnieBear
    AnnieBear Member Posts: 96
    edited September 2010

    Hi all...  I only have two more regular treatments and then I'll start eight boosts.  They did the CAT scan on Tuesday for that and yesterday they did a 'block' on the regular machine.  Not sure what that means but I think they make the block in the shape of the scar area and shoot the beam through that.  I am still not feeling fatigue.  I wanted to call off work today just because I need a day off, but I thought I'd wait a while and see how the boosts affect me.  Jana, I laughed when in addition to all of the things you need to do you added watching new tv shows.  I feel the same way - all of my favorites are back for another season and I can't miss any of them.  House, Castle, Glee, Bones, Fringe . . . . . . .

  • phxsunshine
    phxsunshine Member Posts: 242
    edited September 2010
    Lady Madonna, I am almost 2 weeks into Tamox and I am surprised at how well it is going.  I was dreading it in a way as I have 2 friends who were on it in the past, 1 of them developed the endometrial cancer we have all read about.  My stomach was a little queasy for a couple of mornings, I have had a maximum of 1 hot flash a day and sometimes none.  I was irritable for 2 days.  On the good side, my sinuses don't hurt for the first time in my adult life and I'm 54 tomorrow, and my pimples are all drying up and flaking off.  I keep waiting for the other shoe to drop, but I can live with this.  I'm keeping you in my prayers that you are done with the H in the blink of an eye, you get the port out and come on over to Tamox Towne with me!  Remember how life was the day before you got the diagnosis??  That's how I want to live again, spending my brain power on LIFE!!
  • againmine41
    againmine41 Member Posts: 81
    edited September 2010

    Felt so weird going to the doctor and walking past the Cancer Center. I know I should feel relieved but just don't have that feeling internalized yet.

    I decided not to have the hysterectomy right now and just have the D&C and look-see. I want to be ok to be with my brother here in a few weeks when he has his cancer surgery. Gyn said I would no way be up to driving/flying etc in 3 weeks and so I decided that this best for now. At least I will know what my path report from it will be and then know more what to do. He said the endrimetrium(sp?) wall is thickening and the smallest fibroid is 2cm so it isn't too far off to have it removed...just now with just having rads, my brother, etc...not good time. 

    My doctor upped my Effexor dose so I hope I will be less 'emotional' soon. I hear all of you on the crying...it doesn't take much to get the tears flowing! My dealing with frustration is almost zip! My 12 year old son has been a real 'stinker' (for lack of words) these last months. When I whenced the other day from my skin hurting when I bumped it..he said "Mom there are a lot more worse off then you." I know there are but it still hurt. My skin is broken open and blistered. His words hurt too. I just went into my sewing room and escaped. 

    Looking forward to healed skin and good smelling soap again!  

    Prayers still going up for all of us daily! 

  • lizinmontreal
    lizinmontreal Member Posts: 46
    edited September 2010

    Well, I finished my boosts on Wednesday! Yeah! It feels sooo good not to have to make that daily trek into town. I tolerated the treatments very well..very few SE......a little redness or should I say pinkness and a little fatigue. No depression but as I stood outside the hospital waiting for DH to pick me up after my last boost, I had this feeling of abandonment. It was as if I was left suddenly on my own to deal with cancer.

    OK, so I thought  I could start to relax. Not so! While talking with my onc, I found out that the oncotype dx test that my previous onc said she'd have done, was never done. Also, my new onc told me that my cancer grade was a 2 and not a 1. Now he wants to present my case to the tumour board meaning that I may have to have chemo. Ladies, I think I will turn into a basket case. (Some of you may remember that my pathology report first stated that my lymph nodes were positive and then retested and turned out negative.) My onc said that he'll phone me and let me know. So the waiting is starting all over again.

    I did have a surprise though after my last rad tx, My son came over and presented me with a wonderful bouquet of flowers. After dinner with DH,son, daughter & her boyfriend, there suddenly appeared on the dinner table a yummy ice cream cake with a huge, orange smiley face on it. I had put tiny smiley face stickers on my calendar after each treatment. It was a celebration cake and we all ate with delight and gusto! 

  • phxsunshine
    phxsunshine Member Posts: 242
    edited September 2010

    lizinmontreal: I'm not sure how Canada health care works, but have the Oncotype test performed.  My diagnosis was exactly like yours.  The biopsy said grade 1, but the pathology report after surgery said grade 2 and the chemo Doc said that with my age, etc, that TC chemo would be a possibility for me.  My Onco score was an 8, chemo would do me more harm than good.  The waiting drove me nuts, literally.  Keeping you in my prayers and glad you are surrounded by such a loving family.

  • sharonraew
    sharonraew Member Posts: 24
    edited September 2010

    Congrats on finishing.  A cake - how lovely.

    Good luck with the test.  Who is your new oncologist - at MGH?

    You are not alone in your feeling of abandonment.  And for a few days after I almost got dressed and ready to leave for radiation.  You are supposed to get on with your life but it just doesn't work like that.  I read the article on after the treatment ends someone here mentioned.  It is dead on.

    I had to go back today as my husband had his planning session.  It was familiar.  It was strangely comfortable.  Very very scary!!!!

    Take care and let us know how you are doing.

  • ladym13
    ladym13 Member Posts: 251
    edited September 2010

    ECT, I think I read that you are finishing rads on Tues, so am I....last day FINALLY!!! and I am also starting on the tamoxifen after radiation.

    Just wanted to say enjoy your weekend and congrats on you last day of radiation Tues.

    I also wish my hair would grow faster...lol

     Mo :)

  • chabba
    chabba Member Posts: 5,065
    edited September 2010

    One more boost to go.  Please God, give me some energy back soon.  For the last couple of weeks I've been sleeping 14 to 16 hours of every 24.  The skin on my breast and my side around to the back is red and has thickened and developed bumps and ridges.  The split in the fold under the breast has healed nicely but the black skin there and under my arm is peeling.  My normal bra size is DD but the radiated one has got to be at least a G.  Now the itch is so bad the normal breast itches in sympathy.  The hair follicles around the nipple turned into dark brown pits.

    I have an appointment with my ONC Thursday to discuss the next stage of my treatment.  When I first talked with him he said that at 68 and 12 years post menopause, I will probably be on an aromatase inhibitor.

    Tonight I've been going through some wild emotional swings.  I think until now I've still been a bit numb from the diagnosis and I do tend to keep negative emotions under tight control so it is real scary when they get loose.  I do not want to start feeling sorry for my self when there are so very many here, in fact most of those here at BCO, that are in far worse situations than mine.  So please forgive my complaints and I will continue to pray for us all.

    Thank you for listening.

  • cpjuly10
    cpjuly10 Member Posts: 29
    edited September 2010

    Hello everyone!! This is my weekend off and I'm so glad! Don't have much planned - just being at home with no work or treatments is great!! I only have two more boosts left - I also will be done Tues. Strange as it seems I'm anxious to be done but I also think I will miss the team there. I think there is a certain amount of security in knowing that even though its kind of like torture at least every day those techs, nurses and the rad doc are there if anything is going on. I'm like someone else mentioned earlier worried I've made all the correct treatment choices and the fear of it coming back somewhere else. I've never felt so vulnerable in my life. It is no wonder we are all so emotional. I always tend to hold my emotions in check, never show them but now it just doesn't seem possible. I'm weepy or angry alternately. Wondering if the tamoxifen will escalate that? Could be ugly!! It has been a priceless out let here to say what I'm really thinking and to listen to what you all have to say and think wow I'm not the only one feeling that way. I used to be a part of the critical stress team at a hospital where I worked as a paramedic and I know from all that training that we are all dealing with post traumatic stress on top of our medical issues. It all will take lots of time to work out and heal. The most important thing is to take good care of ourselves and remember that this is all a normal reaction to the stress we are under. We aren't nuts no matter what anyone thinks or says or what our self critical voice tells us. It may take months or years before the full extent of this hits us and we really grieve for what we have lost. One thing I fear losing right now is contact with all of you. Anyone else having that fear? Hopefully some of you will hang around here and comment once in a while so I know how its going for you and I'll do the same. Take care and have a great weekend all!!

                                                                   Carole

  • chabba
    chabba Member Posts: 5,065
    edited September 2010

    Carole,

    I, too, hope others will keep in touch here as we all move on to the next stage of our treatment.  I also have joined a thread you might find helpful if you haven't found it yet.  Calling All Stage 1 Sisters has women at all stages of treatment and beyond.  It offers great support and a lot of insight into what can lie ahead.

    Have a relaxing and healing weekend.

  • againmine41
    againmine41 Member Posts: 81
    edited September 2010

    Yes, I too don't want to stop this communication just because rads are done. I would like to continue here. Wonderful support !

  • lizinmontreal
    lizinmontreal Member Posts: 46
    edited September 2010

    I went to see my GP today.........yes, on a Saturday. I brought him up to date and I left with a prescription for a colonoscopy. So, what's one more "crappy" test! I was supposed to have had this test a couple years ago but had difficulties with the prep. I got sick.....vomited, dizziness, had heart palpitations & broke out in a sweat. Now there is an easier prep and I'm willing to give it one more shot. But, I'm not in a rush to have it done. I'll wait to see if I have to have any further cancer treatments.

    sharonraew........My new rad onc is Dr. Hijal, young, very nice & listens to concerns. Your husband is also at the MGH......I guess you know the routine. Wishing him and all our rad sisters the best!

  • Drim
    Drim Member Posts: 302
    edited September 2010

    Good evening ladies - it's been a long time since I last posted. I have been working around the clock so I'm very thankful that I did not have much fatigue. Maybe I didn't have fatigue because I had no choice but to work these hours. My project will be done on Monday so hopefully I can rest a bit then. 

    Friday was my last day of rads. I had 26+7! Overall it went pretty well. My skin held up great until today. There is an area inside the boost region that is very red. It feels more like a rug burn than a sunburn. They explained that the boosts are more of a cutaneous treatment which is why it causes more skin pain than the regular treatments. I too hated having that black sharpie circle around my scar and am happy to be done. I also will be continuing on with the H and in about two weeks I will start tamox - so on to more adventures.

    Congratulations to all who are done and almost done! You ladies have been a wonderful inspiration to me and I do plan on coming back even though rads are done. Babbalu, I hope they can find the solution to your problem!

  • cpjuly10
    cpjuly10 Member Posts: 29
    edited September 2010

    Hi everyone! How are you all today? Just got back from my 4th boost and tomorrow is the last one. Kind of a bittersweet feeling. Ready to be done with this but moving on has its share of questions about things too. My armpit burn is much better but still some sting in the one under the breast. My breast itself hurts now with the boosts though. Working 5 hours a day is definitely working out better for me. Still tired but not totally overwhelmed like I was. Ready to have my own skin back lol. Can't wait to use my deodorant and body wash and real lotion instead of aquaphor. Its the little things you miss. I'm afraid to start wearing a bra again. Don't know that I'll find one to fit or wear without pain. Guess I'll try going to sports bras when my skin allows. You are all in my thoughts and prayers!!

  • chabba
    chabba Member Posts: 5,065
    edited September 2010
    Today is a BIG disappointment!!!!!!!!!!  I went in for my last boost and the machine was down, needs a technition. I have to go back tomorrow.  Yell
  • Drim
    Drim Member Posts: 302
    edited September 2010

    chabba - OH NO!!! That really stinks. I just hate it when you're all geared up for something - especially something as special as this, and it gets cancelled!! Hopefully all systems are go for tomorrow. Congratulations in advance for being done. Congratulations to you too Carole!!!

  • chabba
    chabba Member Posts: 5,065
    edited September 2010
    Thanks Drim.  And I had brought donuts for the last day.  Told them they wouldn't get reruns tomorrow.  Wink
  • againmine41
    againmine41 Member Posts: 81
    edited September 2010

    It's so great to see each one of us come near to or  'graduate' from these treatments! It is a milestone, even if some people just don't understand...this was not easy for any of us..the skin troubles, emotional ups and downs, driving...driving...and more driving, dealing with issues we never dreamed of, and so much more.

    My skin is slowly healing and doing so much better! I have one circle that is still blistered, but it's getting there. (a place that was under a sticker). I wore a 'normal' bra for the first time Monday! YIPPIE!!! No more uno-boob! Those sport ones always made me look like I had only one breast and it was dead center!! (2 DD's make one really weird boob!) lol

    The fatigue continues, but now I am actually sleeping. Took a 5 hour nap on Sunday! Even slept through my phone text alert!. My husband came upstairs to make sure I was alive...I never sleep through my phone calls/texts. I do notice though...that by 1:00 I am very drained and have to sit or lay down. I just keep telling myself its the good cells making a comeback and that is why I am tired. I want so bad to get back to 'normal' but remind myself often...it will take time. The dust bunnies still have a home for a little while longer.

    My prayers are still going upward for all of us!

  • cpjuly10
    cpjuly10 Member Posts: 29
    edited September 2010

    Had my final treatment today!! Woo hoo!! I am so glad to be done. Glad for all my sisters who are finishing up too.  Hoping chabba got to get her last treatment in today!! My brother took me out to Red Lobster for a celebration lunch.- my husband is still at work. I got my certificate of completion and saw my doctor. He reminded me that just as the side effects don't come on all at once they don't go away all at once either but that things should get better over the next few weeks. My armpit burn is better already just from not being part of the treatment field this past week and that is a relief. Get to start tamoxifen tomorrow. Ready to get rid of my black circle - gonna stand in the shower for about an hour. Againmine its great that you are getting some sleep! Drim congratulations on finishing!  Praying for you all!

                                                                     Carole

  • ladym13
    ladym13 Member Posts: 251
    edited September 2010

    finished my last radiation treatment today....whoo hoo!!!

    Now on to tamoxefin

  • mofend
    mofend Member Posts: 140
    edited September 2010

    It's so great to hear from everyone who is finishing up - congratulations to all of you!!! Such a joy, I know.  Just took my first Tamoxifen about an hour ago.  Kind of nervous, I have to admit.  I've had such weird stuff during chemo/herceptin that I'm just waiting to see what the Tamoxifen brings - just hope it's nothing and that I can officially move on. 

    Anyone going to the breastcancer.org benefit at the end of October in Philly with Harry Connick?  Should be fun - got my tix.  Would love to catch up with any of you who do attend.  Just let me know - take care everyone - peaceful night to everyone...Mo 

  • chabba
    chabba Member Posts: 5,065
    edited September 2010

    Last treatment was to be Monday, machine down.  Reschedualed for today, Machine still down, rescheduled for tomorrow. Anyone want to take bets?

  • Drim
    Drim Member Posts: 302
    edited September 2010

    chabba - I can't believe it. Machine down again - booo!Yell Congrats on being done LadyM1

    mofend - I will be starting tamox soon. Probably next week. I almost picked up my first bottle today but I got to CVS just after it closed. Oh well.

    Question for all of you - I went to see my breast surgeon today and she said - "Oh, I see it's been 6 months since surgery. You're do for a mammo!" I was like - on this poor tender, sore, burnt breast? She said yes - 6 months, you have to get one. I thought I read that you should wait 6 months after rads to get a mammo. Can't they see what's going on in there from all the x-rays they've been taking every week??? What have your doctors told you about the time between rads and your next mammo?

  • rcca
    rcca Member Posts: 59
    edited September 2010

    I was told mamo six months afters rads.

    rcca

  • cpjuly10
    cpjuly10 Member Posts: 29
    edited September 2010

    Hi everyone! I'm siitting here enjoying the fact I don't have to go to radiation today. So nice. I even slept well last night. What a luxury! Chabba I can't believe you didnt get treatment again yesterday! How disappointing! Hopefully today will be the day! My rad onc said he just believes you should keep up with your yearly mammograms on schedule. He also said my regular oncologist might not agree with that and want one sooner. I guess there are different schools of thought on that too. I go back to see the regular oncologist on Oct. 20th I believe so we'll see what he says then. My yearly mammogram would be due next June. At any rate didn't start my tamoxifen today - going to start it the 1st. Have a great day everyone!

                                                                             Carole

  • mofend
    mofend Member Posts: 140
    edited September 2010

    Seems like things are different all over for when to get our first post-chemo mammo.  I am set for one in November, which would be the first since chemo began in February.  First gynecologist appointment today for pap, etc., and I have to say for the first time in a very long time, I'm really nervous about going - don't want to hear any more bad news - not that there's reason to believe there's something wrong, but when I found out about the bc I didn't think there was anything wrong either.  Hate how all this stuff has modified my former attitude of not worrying about things until there's a reason to - have to keep trying to get that back.... Mo

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