Fall 2013 Rads
Comments
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MsP - thank you for your kind words. I see you are almost done! Good luck with your first boost. My mom will be doing the same very soon. Hope it goes very well. Best wishes. -
Good luck Annie11595. Yesterday was my first day and it was very overwhelming. I dint cry when i was diagnosed I was strong for my kids n my husband and not thru surgery either but yesterday I couldnt help myself. I just had a good cry though my husband,my sister and my brother in law came with me to give me moral support. It was too overwhelming all those machines moving around you I had my eyes closed and just kept chanting my prayers to distract myself and it ended before I knew it. I was shivering alot due to the cold and d fear I guess but I was able to calm down I just kept thinking of what someone here told me that to keep thinkinv Im beating this cancer thru radiation. Yes Bluebird thats 1 down for us and I hope it continues this way! Dint feel the fatigue on d contrary had a very sleepless night with active dreams that kept waking me up. All i can say is stress I feel is what did this to me always worrying about others doing for my family loosing my younger brother 2 years ago. He was only 34. My dad being diagnosed with chronic heart disease. Not operable. Son going off to college. Ive always taken care and gone out of my way to take care of others be it my family or friends,taking their problems to heart and stressing over it. But if we are going to stress over this we will just end up not letting the treatments work. So Karibari dont stress over anything. Im reading a book that says positive thoughts send positive vibrations to our body. Just think of positive thoughts and this too shall pass. Ive had a very supportive family. Especially my 16 year old daughter, whos tried to go with me for my doc appnts my first scan n radiation as well but the biggest support and encouragement Ive gotten is from this forum. I do feel itchy alrdy Bluebird n my onc. Says only aquafor for now. MsPharaoh I joined d gym even if its just to use their treadmill d do a bit of weights as u suggested. I felt a bit more out of breath than usual but I felt great! I just hope I can continue this way thruout my radiation. Thank you all of you for being here for me. -
Lav- my mom, who is 82, was really worried about the rads. Her skin reacts to everything. Well, she wound up doing really well I think. She is doing all her normal stuff and she is almost done with her treatment. The only real problem that just cropped up is a rash and the doctor thinks it might be shingles, of all the things to get. It is painful. But she would be the first to say the rads weren't as bad as she first thought. I bet your time will go quickly as did my mom's. We cross off each day of treatment on the calendar and it helps a bit to visualize the countdown. Hang in there and pamper yourself while you go through this. Your daughter is a good girl at 16 to go with you. Think positive thoughts - I will send you mine as well. -
Dear Lav, my heart goes out to you. Your family has been through a lot, and it is OK to cry, be sad, be angry, whatever. But.... when you are on the radiation table, you are a cancer-killer! And when you are on the treadmill, think about all the cancer that you have already killed! Get mean!
Hugs, MsP -
thanks Dobby. Wow hats off to your mom at that age and she sounds so strong. Give her a hug from me. Yes my daughters 16 but very matured. Instead of getting grossed out after surgery at the sight of my breast she would help me clean up since Im left handed and could barely use my left hand. Shes been a strong pillar for me at this time encouraging me and pointing out it could have been alot worst like a friend of mine thats in stage 3. When Im down she always senses it immediately and she wouldnt leave me alone and woyld give me company to cheer me up or distract me. Im trully blessed to be her mother. At 16 she sits and notes down what the oncologist would tell me and check on the internet and read on it and explain certain terms to me. Im sure your mother is as lucky to have a daughter like you looking out for her. Hugs to u too:)) -
thanks MsPharoah thats exactly what Im trying to do! Ive been strong thruout all that Ive been thru in life and Im not going to let this get to me. All of you inspire me and give me even more courage that I can beat this! -
Lav, you must be very proud to have raised such a daughter and to be a beloved mother. Congratulations.
Love, MsP -
StacieRae - I am having rads with a seroma. It was drained midway through my regular rads (due to pain) with the possibility of being drained during my boosts. Fortunately for me it has only returned slightly and didn't need to be drained again. I have my last boost tomorrow and I am done with this phase of my treatment. On to Femara.
Ladies with sore nipples, please ask your RO about Mepilex to cover your sore and peeling nips. It has been a godsend for me.
Take care,
Cakes -
Karibari, I too have a new technician! And it's a guy. They asked me if I would mind a male technician to "observe" but he's been doing a lot of the work. It makes me a bit nervous because the other techs are telling him what to do all the time. But he's very caring and I can tell he'll make a great tech.
Good luck to you anne!
Stacierae, I am also just plain worn out by all the chem and surgeries. I totally don't feel ready to go into six weeks of treatment! But we will and we will kick butt!
Cakes, thanks for the tip for the nip! ;- ) -
2 down 28 more to go. Im so e hausted today. It takes 5 hours just to go for my rads to the city and get back. Thank God they scheduled me for an early time when getting out of d city isnt as congested nor at a peak hour. Dint get to sleep well last night hope to sleep well tonight. Thanks for the tip Cakes I can see my skin turning slightly pink alrdy. Keeping my fingers crossed! Goodluck for tom bluebird. -
Thank you Ms Pharoah & Bluebird - I appreciate the kind words. I agree, it would be nice if the new technicians would at least act like they know - but I guess that comes with experience. I'm just super aware of how efficiently the gals who were doing it last week handled everything and how different this gal is (it's all women techs for me so far). I was very honest with my doc today about how I'm feeling and he was very supportive. I know in my heart it's going to get better and I'll be one third done tomorrow.
Thank you Cakes for the tip about mepilex - I will ask about that tomorrow!
Blessings to all and hope we all sleep well tonight!!! -
I have one set technician and the others may or may not be there - anyone of them is a guy. He's nice, but... I can easily bare my chest to male drs, but there's something about being in that vulnerable position that makes it a little uncomfortable. Not enough to say anything though. Not a huge problem compared to dealing with cancer
I'm tired. Tired of starting the day, rushing to try to get some homeschooling in, then rushing off on the long drive to rads and whatever additional appt i have, rushing home for supper and then work. My house is a mess, we're behind in school, and now the toilet is running, the kitchen faucet is dripping, and the washing machine broke. Oh, and somehow I have to cook and clean the house by Saturday because we have some overnight company coming. I feel like I can't keep up with my life anymore!
Anyway, I've finished day 9 today- fighting a slight pink tinge and some sore spots, but nothing too bad yet. The deep needle zings disappear for almost a week after an acupuncture treatment - yay! And there has been a wonderful lady I met in the rad waiting room. She's been so pleasant - brought a bit of normalcy to the craziness. -
SophiaMarie I totally understand how you feel. Its like your carrying all d load on your shoulders and thats stress. You need to ask for help and at this point I feel that its ok to say no or to have everything down perfectly. This is about you and you should at this time only concentrate on yourself and getting yourself better. I can never say NO to anyone and thats why I am where I am. You have to leave someone maybe your partner or if you kids or some family help out. If you dont hve family around then just say no. I lm sure your guests would understand of the house werent in perfect condition or if they had to help out or stay elsewhere. Your not going thru something easy if d fatigue i felt last night was only day 2 I can imagine how u must be feeling. Please give priority to yourself. Positive thoughts positive mind gives a positive result. Your first and foremost priority right now should be YOU. A big hug from me to you. -
Hello Ladies -
I am new to the Fall Rads group. I just had my second treatment and was looking for information about what to expect. I'm not sure if it is my imagination, but my armpit already feels a bit sore. Everywhere else feels fine so far. Is it my imagination? Did anyone else start getting sore early on? When does the discomfort usually begin? And the redness? So far I have no sign of any redness.
I am getting 4 different radiation fields - one from each side of my breast, one to the clavical/supraclavicular area, and a fourth one that comes from the back and targets my axilla. -
Hi KirklandGal and welcome.
Everyone is different. I would say that the discomfort you are getting after 2 treatments could be coming from the postiion you are in for the treatment and not the radiation itself. As an example, I am doing rads in the prone position and I started feeling a "burning skin" feeling under my boob pretty early on. I realized that it was from the ledge of the radiation table pressing on that area while I was prone.
I am having 28 treatments and 6 boosts. I started getting an itchy rash at about treatment 14. By treatment 21, my skin was pink especially under the boob and in the cleavage. If you get radiation in the supine position, you will probably notice the pink starting in the armpit and under boob area and not so much in the cleavage. From 21-28, my skin got progressively pinker and more all over the boob where you could see the line of demarcation for the rad field. After treatment 27, I went on a weekend trip to see my family in Chicago and I did fine. I had my 2nd boost today and I am doing fine, just 4 more boosts to go. Little bit itchy and definitely don't want anyone massaging my boobs (LOL). I'm very tired and have been going to bed pretty early each evening, but making it through OK. My RO said my skin was doing "better than average", so take that into consideration. I have very large breasts AND I am very fair and thin-skinned so I thought I was going to get fried....that did not happen.
As far as care and feeding of the breast, I am using Aquaphor really thick after each treatment and covering it with gauze pads to protect my clothing. Also making sure there is no skin on skin by placing gauze in the creases/folds before I dress. I use Fruit of the Earth Aloe Gel at bedtime...so cool and soothing. There is no way to predict how your skin will hold up during this treatment but many people do great. You had chemo...this will be easy for you!
Be radiated and radiant every day and kick cancer's a$$!
MsP -
sophiamarie - I agree with Lav. Focus on you and the essential elements of family life right now. No house guests should expect you to cook and clean....if they do, say no...they should be offering to come in and do those chores for you! As moms and care givers - we are so used to being the givers...for a while (it won't be forever) pls accept offers of help and support, and as necessary say no - not now. Best wishes! You will make it through this treatment !
All - I had my CT planning Monday. I saw a few posts about breathing for left side radiation. I will have that. Working for me in practice. If it seems foreign, get a snorkel (seriously) and just get comfortable, when you are not under the stress of an appointment. Can avoid 15% heart exposure - worth it. If that's not gonna happen for you - my RO says there are other options...ask! Dry run next Monday, treatments start Tuesday.
To all in the middle/end - you are my inspiration. Keep going! Best wishes to all! (PS - teased my girls that with new tats, I should be considering a Harley!).
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Happy Dance......I AM DONE with rads! Those of you going through rads be it the beginning, middle or rounding the corner to the end you are in my thoughts and prayers. You can do it! I will continue to monitor Falls Rads to support you any way I can. Please take care of yourselves and remember, you are no good to anyone else if you don't take care of yourself first.
Cheers!
Cakes -
Cakes. Woo hoo! So happy for you, oh radiant, fully-radiated one. Thanks for cheering us on!
MsP -
Hooray Cakes!!
I am also a member of the too tired for housework club. I've just not recovered from chemo and multiple surgeries and now rads. At night my bones and joints are hurting too. In the morning I'm like a little old lady tottering out of bed. But after i get moving I'm okay and nothing bothers me the rest of the day. It's really weird.
I will try to approach each day radiantly! Love that. -
Congrats, Cakes! Time for you to recover, then celebrate!
Lorrie
19/33.... im getting there....
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Cakes- Happy Dancing with you!! Hope the Femora goes well too. Just keep on saying and believing - I BEAT CANCER!!!! Hugs, Marilyn
Lav - You are doing great brave warrior! Hope you have someone driving with you to rads. What a long way you have to go. Just keep slathering on the moisturizersI Gentle hugs, M
Karibari & bluebird144 - I too have a young, cute male tech doing his training and he is great. The gal who is just before me for rads cracked us up. She told the male tech she had to park really far from the building and she wasn't looking forward to the long walk to get her car. He told her he would be happy to get her car and bring it to the front door for her. She said "wow if you do that for me I'll let you see my boobs" and she flashed him. All the rad techs were hysterical as were we when she told us. It's good to keep your sense of humor since we have lost so much. LOL.
SophieMarie - I'm at day 11 yea. Lav said it well. Take a deep breath - you are not supposed to be "superwoman" right now so don't put that stress on yourself. Do what you can, when you can and order pizza. I am sure your company will understand. Nobody cares if the house isn't spotless and I'm sure the kids will catch up on school work. We all have those days where everything goes wrong - remember tomorrow is a new day and all will be right again! Sending healing thoughts your way, M -
Cakes, congrats on being done! Time to rest and get back to normal....Enjoy! -
congrats, cakes!
I reached my halfway mark today. 22/44 done! The last 10 will be boosts. And today was the first day no bolus. Or was that yesterday?
PT starts tomorrow. My PA told me to take extra pain meds (Aleve) because the. PT is really going to work on my cording. I will get work on my LE and range of motion.
I had a great visit with my kids and parents this weekend. They came down for a visit. I think it really boosted my spirits. I asked hubs if he enjoyed being home alone for 5-6 days. Not as much as he hoped because the house is in need of some TLC: fix a sink stopper, fix a towel rack, replace carpet, touch up paint, etc, etc, etc. lots has gone by the wayside due to priorities and my fatigue from treatments. It's temporary but can weigh us down. I've worked through letting some things go but I think hubs is going through that now since I've been away for a few weeks. -
Hello Kirklandgirl..
I see that you are from Kirkland, Wa. I live in Everett. I am also about to start my radiation. I was supposed to have the dry run yesterday, but it didn't happen. Since my tumor was close to the heart area, I will need approval from my insrance for a procedure that moves the heart lower when I get zapped. That costs extra. I have been very weepy today. Wait, wait wait!! I am at the end of my stress tolerance. We will be able to compare notes if I ever get going. -
thanks everyone! Thankfully the overnight company are good friends. Three kids, but it's always lots of fun - makes my son happy too. When I got home from my appts today, my dh had already done a lot of straightening for me and had supper ready. He's been a great help! I just feel like I'm running so fast that I'm gonna fall on my face. I will do a simple meal though - my friends weren't going to even come for my sake, but I insisted. Even though its stressful to prepare, it's also a tonic to be with them.
Well, after I finished my first third of treatments today, I went to get a prosthetic. The surgery left me so lopsided that I could no longer wear any clingy tops in public. It was kind of emotional - I don't want to have to wear a piece of silicone - I just want my breast back! But it did feel good to look normal again - even if it was only through fabric. At least I will be able to wear my t-shirts again. I highly recommend asking your dr for a prescription if you feel self conscious!
Feeling some sore spots and slight redness, but nothing too bad.
(And dh also got the washer to work again and he fixed the toilet!
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stacie- I'm radiating the same fields as you! I started feeling sore in the first week- not in my underarm but right above it. I'm not really red though, just sore.
Lav, I also usually have a five hour door to door trip for rads, and it can get really tiring. Do you have anyone that can go with you sometimes? After my first week my friends volunteered to come with me on rotation two or three times a week, so I'm only going myself the rest of the time. It's so nice to have company and have someone else drive since I'm usually exhausted on the drive home.
Congrats to Cakes! I feel like finishing might be harder than going through treatment. Everyone around expects that everything will go back to normal as soon as treatment is done, but I've heard that you are tired for months after. I think by then I won't be getting special treatment, even though you really still need it!
I'm 15/28... Halfway through! -
Ladies - lets brainstorm and come up with some ideas.
Lets think of something we can do, or wear, or something, that reminds those around us, during and after rads, that we are pooped out and need help without us having to go all whiny or even simply ask. And I don't mean pink.
I am going to have to walk the fine line between getting the help I need and not using too many guilt trips (which no one enjoys taking!) or complaints.
I think I am going to get a T-shirt printed saying:
Superwoman - NOT
or
FOR GOD'S
SAKE
TAKE PITY
ON ME
AND HELP
or maybe a picture of a green lady with 3 arms resting sweetly in a bed!
Any other ideas so we don't appear to be fishing for sympathy (which we should be getting heaps of by the way)?
Kika 2013 - how are you doing? -
Bounce: I just had my first meeting with my RO this week. She mentioned it, but said she preferred to stick with the traditional six-week program. I did some googling, though, and found some studies that suggest fewer sessions with higher dosage each session (with a lower total dose) are at least as effective, with fewer side effects -- for patients with a specific set of criteria. (Small, low-grade tumor, no node involvement, age over 50 were the main ones.)
I want to talk her into it, since I do fit all or most of the criteria, plus I have non-refundable plane tickets for both Thanksgiving weekend and over Christmas. (Obviously I wouldn't go for the shorter program just for convenience if it didn't appear to be equally effective.)
Here's an article right on breastcancer.org: http://www.breastcancer.org/research-news/20131014, which includes a link to a study done in the UK.
And this one from the New England Journal of Medicine: http://www.nejm.org/doi/full/10.1056/nejmoa010874
Googling "hypofractionated radiotherapy breast cancer" should get you a bunch more.
Hope that's helpful. -
Hi I'm new here though I have been popping in and out. I'm finally done chemo and rads are coming on the 28th.
Question for those who did chemo first. Did you feel as though you had recovered somewhat from chemo SEs before the rads SEs began to happen? One thing that worries me a bit is that I'm pretty fatigued already from chemo. I hope there is time to get over a least some of that before rads-related fatigue sets in. Sigh.
Bounce: Great idea for a t-shirt! A poster would be good too saying something like: "Recovering Cancer Warrior Rules: 1) Give Me A Break, I've Just Run A Marathon, 2)If Its Dirty, You Clean It, 2) If Its Broken, You Fix It, 3) If You're Hungry, Order Out, 4) If You Don't Like It, Zip Your Lip."
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Hi LisaSp - Aah - that poster would never work in my house - I would be accused of having "attitude" and ignored. I have to soften things with humor or just go for all out pity (which I try to save for emergencies).
My kids are pretty bright and actually remember everything I told them when they were younger (when I thought they weren't listening at all) and now use my own words against me - in the nicest way - not badly.
So "attitude" has to be kept at bay.
I do like the ideas expressed in your poster though.
Its so funny - a long time ago my daughter used to complain about the laundry not being soft enough or not being folded just right etc. so one day I told her very calmly, with absolutely no aggression that she should take over doing her laundry as I had tried and just couldn't do it any better. I haven't heard her complain about it ever again. And you know what - now if she points out something else isn't quite right - she adds - "but I am not complaining" and smiles sweetly.
Come on ladies - keep the ideas coming How do we tell people when we need help so they can hear it and respond lovingly?
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