MARCH 2010 Rads Group
Comments
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MzJ: I have nine treatments to go too, last full breast treatment tomorrow and then eight boosts. We can countdown together.
I didn't realize the markup for the boost would be so "in-your-face." The tattoos for the other treatments were the discreet little tattoos. Last week they put a huge X just above my nipple. I thought that was only temporary, but they refreshed that today and added a large box around it, all in bright orange marker.
Fatigue is finally setting in for me. I went to lie down for half an hour after treatment and fell asleep for almost two hours. The overcast rainy weather doesn't help. In my case I like to walk and if necessary, I break my daily walk into two shorter walks.
3monstmama: I agree with you about the exercise. It does seem to help.
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Day 6 over with...
My breast is definitely swollen, and my nipple feels sunburned/achey although the intensity of that comes and goes. Last night there was a sharp pain in my breast for maybe 30 seconds - while I was just sitting here on the computer. It was weird. And my breast hurt in the shower a bit. I'm frustrated that I'm experiencing such symptoms after only a week...makes me wonder what the next 5 weeks are gonna be like, if the effects are cummulative.

I've realized that when the techs have trouble positioning me just right, it's partly because of ME - I have this habit of keeping my body so tense/rigid that it messes it up. Today one of the techs reminded me "relax down into the table," and I didn't even realize that I'd subconsciously been arching my back a bit...and when I forced myself to relax, it made such a big difference and the techs were so much happier with my positioning. It's so HARD to relax under a linear accelerator... it's about the least relaxing place I can think of, except maybe the dentist's chair!!
Exercise is helping, I agree. I have done 30 mins of Wii Fit for 5 days in a row now, and it's great. I've also been sleeping 9 or 9.5 hrs each night.
Today was my SHORTEST rads appt yet - I was in and out of the building in 15 minutes! This is so much better than the 30-45 min appts I had all last week. Slam dunked my gown and thought of all of you.
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Raili, I'm so glad it went quickly for you.
I think once everyone knows what they are supposed to do, it does go quicker. One thing to be prepared for, if it hasn't already happened, is the days where they take xrays to see how you are doing. I had that today and the appointment with the nurse which made it last longer.I manage the relax thing pretty well but I did have trouble in the begining keeping myself from trying to help them move me into position. Also today I was jumping the gun on breathing---before the tech told me to do it.
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5th treatment done and it was very quick. In and out in 13 minutes! A new record. I am starting to feel a little tingle but nothing major yet.
There were a lot of posts about Vitamin D. Does Rads have an effect on this?
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Hello Marie,
I am commenting in reference to you asking if anybody gets headaches with their radiation treatments? Yes I do and I feel it nearly immediately afterwards and it remains with me until the weekend starts... Charmaine
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Had my setup appointment today with first treatment in 9 days. I thought I had been handling this whole thing pretty well, but today it just seemed to be in my face, especially when I saw the 6 x6 card I get to place on my car dash for parking next to the door in the special lot for radiation patients that says "Temporary Radiation Patient". Way too stressful/emotional of a day. This can't mean me. There is no history of breast cancer in my family, so why am I even here? The techs, nurses, and doctors are wonderful and they to really make you feel comfortable and at ease, but the rooms, the equipment, the routine preparation and testing they do on so many patients day after day, somehow just feel like a robot and not a person. I'm sure it's just me and dealing with the stress, but I found today particularly difficult.
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Well ladies tomorrow being Tuesday March 30th is the last day of my BOOST RAD and I am completely finished with radiation therapy. I actually started burning after the end of one week, and have pretty bad SE from radiation therapy now. The doctor into the beginning second week prescribed me a cortisone cream but it was only irritating me, so I saw him this morning after my treatment and he gave me a prescription for another cream to start after tomorrow treatment called "Silver Sulfadiazine Topical Antibacterial" . Have any of you ladies heard of this cream? I am to use this cream for 2 weeks. I so hope it takes the burn away, as it is really burning at sometimes and itching badly at other times and I feel a pain sometimes and a pulling of the breast skin too...
So cannot wait to get on the road to wellness again, as have been feeling really tired for the longest time. I am nearly 8 weeks post chemo as of April 2nd. Will post pictures maybe this coming week (am tempted to get this bit of hair shaved off). Seem to be getting some dark hair under the white hair the past week and half to two weeks...
Charmaine
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Charmaine: good luck tomorrow. I've been wondering what kind of followup there will be for me once I have my last rad treatment next week. Will you have followup visits with the radiation oncologist?
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Hi All,
Just came home last night from our family vacation.It was really nice getting away and not thinking (well - tried not to too much) of rads coming up. Boy, the thread has been really busy.
A BIG congrats to everyone that has finished their treatments! YEAH! Can't wait till I am there too!
Sherri - glad to hear that your rads are going so smoothly. . It's such a relief to get started - soon you'll be finished and it will all be a memory. Is your hair coming back much? Mine is starting to come in, but I can't tell what color it will be yet. Do you think the Bioten is helping?
I started my treatment today and other than having a last minute appointment time change(which really irritated me) everything went smoothly. As it was my first appt. it took a lot longer than normal appts The techs took quite a few x-rays and had a conference with my onc and then took more x-rays before the actual treatment. I'm so glad to finally started my rads, I have just been dreading it so much. Hopefully, it will be a smooth six weeks with no problems.
I did a mini slam dunk with my gown - a little to self-conscience for a full out slam dunk....maybe tomorrow.
A big thanks to who posted about the Fruit of the Earth aloe (can't remember
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OOPS! HOW DID THAT HAPPEN?

who posted about the aloe) I had been searching everywhere for pure aloe with no luck and I saw your post and was able to buy it at Walmart.
Hope everyone has a good night!
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Mary - I had my last treatment today. I have a follow up visit in six weeks, there will be another in six months, then one year.
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I went to get my rads today, and got marked up again for my "boost" treatments, which don't happen for another 3 weeks. Hmm. OK, then why did we put the marks on so early?
Another bad thing, my team at worked noticed that I was the absent minded professional and one of the VPs in our group complained about my work performance to my boss. My boss knows my situation. Even though I really am focused on getting well, it made me very upset today. I normally do a good job but I know my work has suffered, mainly because breast cancer is on my mind at almost every moment of every day.
So, aside from being blue for being labeled an insignificant contributor by our group VP, I had an okay day.
Cheers to you all
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anybody having radiation done to an implant? I'm starting on wednesday and am quite nervous about how this is gonna effect my boob and am also worried about getting lymphedema because i had 22 nodes removed.
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MaryNY thank you so much for wishing me luck on my last radiation BOOST treatment tomorrow. As for followup with the radiation oncologist, mine is scheduled for May 12 and I was given this appt 2 weeks ago.
Have a good rest of the week Mary. Charmaine
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Charmaine - I think that I have resolved the headache problem. I have increased my fluids throughout the day and am wearing my OTC reading glasses whenever I need to read anything. This has cut down on the eye strain/focus headaches and the fluids have helped with the dehydration headaches.
Also, I'm taking the Ativan every night and sleeping much better.
Today I had #21 (of 28). I've got a "spotty" kind of rash along my collar bone and under my arm. It looks like the pores are getting sunburned. It looks more painful than it is.
Tonight I applied the saline compress and it really helped. I'm also using the cortisone cream on the most imflamed areas.
The rad tech told me to use the cortisone first, let it dry, wash my hands and then apply the lubriderm everywhere else.
She also told me that up to 2 weeks after treatment I will continue to see redness and imflamation worsening so I should continue with the skin care treatment even after I finish rads.
I've developed a bit of a cough - of course I thought I had radiation neumonitis - but I really believe now that it is just a cold since my DD and DH have come down with colds!
It's amazing how our minds jump to "worst case scenario" when we're already going through all this!
Hugs to all!
Marie -
This is my first post, I have been reading all the way through for the past couple of days and feel SOOOO MUUCH BETTER having read your threads. I can not tell you how alone I had felt going through this.I am on my 6th RAD today. No side effects to speak of yet except just a very little bit of soreness under my mastectomy scar.I think of you all with a little smile whenplace my gown in the bin. I'll get the nerve to slam dunk it soon

Klawless9- Your post made me finally speak up. I had 24 nodes removed and 6 were positive. My surgery was Oct 14 and they warned me of my high risk for lymphedema. I was good until I went for emergency gall bladder surgery. While I was out, my left arm puffed up and now I officially have it. IT SUCKS!!! You are at high risk, especially now undergoing RADS. Just watch your arms AND CHEST. Some swelling with RADS is normal, just have your RAD ONC take a look if swelling occurs. I just graduated today from the decompression (arm wrapping) stage to the compression sleeve stage, and will have to wear that for the rest of my life. I am worried that RADS will aggravate it, but there is nothing I can do to prevent it. Unfortunately BC changes our lives completely and we need to remain strong. Some days that is easier said than done.
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MariannaHB
BIG HUGS!!!!! That stinks about work. I had something similiar-- I got diagnoised in the middle of a big project but was able to defer surgery until after the project was in. From Nov until about late January, pretty much no one except my immediate supervisors knew I had breast cancer. I told my partner on my project because my schedule was erratic and I was <big surprise!> sort of distracted at times. So the project goes off and Everyone is thrilled, thrilled, thrilled. Time for midyear: reviewing goes fine [though honestly at that point I didn't really care] until lower level supervisor makes some comment about my knitting in meetings and how some people are bothered though he and supervisor know that I am not ignoring the meetings because I am always making on point valuable comments. The knitting is nothing complicated, no looking at patterns or counting-- just kkkkkkkkkkkkkkk. It is my stress release, has been for a number of years. I sat there for a minute and thought about it and got more and more ticked. I looked him in the eye and said "I knit because I am stressed. I am stressed BECAUSE I HAVE BREAST CANCER and yet I am still here at work. You tell whoever made the comment that I am more than happy to stop knitting in meetings if they will take over having breast cancer for me, okay?"
He backed off FAST. Point being, while it is hard to share our circumstances, sometimes when we are working with people, we have to---the guy I had to talk to about my breast cancer was someone I had met ONCE in another office on the other side of the country. But telling him helped my stress because he understood that I was not simply a flake, that there was a lot going on. And reminding my boss was also good because 1] he's been great but 2] had he not been great, I'd be protected because he was aware I was undergoing a particularly stressful time. So say he gave me a crappy review, it would also be in the record that I had breast cancer and that would distinguish this review from a general bad performance, if that makes sense.
MARIE K and others with headaches I think increasing fluids REALLY helps. I think also many of us have probably decreased our caffine consumption ---at least I know I have--and boy can that whack you with a headache! I've tried to limit myself to 1-2 cups in the morning and then lots and lots of non-caffinated stuff all day long. Where I get rads they have tea and the like. I make a cup of herbal no caffine tea before I get treated and by the time I'm out its just the right temp for gulping down. 12 oz in! I think its really helping with the rads AND for those with germy monsters at home, its helping my body fight off all the cold germs my kids have been bringing home. Between that and the extra sleep [about 9 hours a night] I am the only family member out of five [knock wood!] NOT to get the miserable hacking respiratory thing going around our area.
Day six over and done...........
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Welcome Magooand Bear - sorry to hear about your arm. You'll get wonderful support from the lovely ladies on this thread!
3monstermoma and MarianaHB - sometimes people in the workplace can be so insensitive and I was sorry to read your posts. I'm on leave from work so I'm kind of removed from these sorts of things right now. Having said that, I had a laugh a couple of weeks ago when my boss called to tell me about my pay increase and that I got a bonus (all based on last year). I joked with her saying I probably got the increase because I wasn't there to screw up! lol I'm sending you good vibes that things will improve for you.
Mommaof2 - glad to see your post. I was wondering where you'd been then I remembered you were taking a trip. I hope you had fun. During March break, my family managed to get to Niagara Falls for a couple of days.
Today was day 7...14 more to go (9 regular and 5 boosts). I did the slam dunk with my gowns and thought of all of you.
Sherri
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Sugar77, don't get me wrong---in general, my prim ary boss has been awesome!!! But sometimes people just don't think. The person who made the comment was the underboss, for lack of a better term, and he's new at the job and trying to prove himself. I don't think he was heartless, I don't think most people are heartless. But I do think that everyone is capable of opening their mouth without engaging their brain. Most people, if you tell them you are dealing with breast cancer, are going to take that into consideration in their dealings with you. The exceptions are the cancer-phobes who can't even deal with the thought of cancer and so become more difficult instead of empathetic. Unfortunately, in my experience, you can't predict who will be a cancer phobe. Sometimes its even someone who has dealt with breast cancer themselves.
Hugs to all!
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Hi ladies,
3monstmamma- and Sugar Thanks for sharing your stories. I feel better knowing that there other ladies out there who've had their worklives touched by BC. I was hoping my place of work wouldn't notice that I am a distraught woman with health problems, and to be honest, I have been very distracted. I am feeling very much like a failture today.

Today's my 10th session, and I look forward to a short, shallow bath tonight so I can scrub the dirt off but not relax! LOL Oh well, I look forward to my first bath/shower post rads, when I can really go for a long soak. I am thinking of booking a massage for later this week. I think I am entirely too stressed about very non-important (in the grand scheme of things) topics. Has anyone had a massage yet? I guess I can just tell the masseuse to watch out for my tapemarks under my arm.
Hope all is well for you, ladies. GImme some feel good stories today! I need 'em!
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MariannaHB - I would love a massage too but the thought of laying on my front side for a deep back massage is just too painful. I'll wait a little longer until I can fully enjoy a massage again!
I wonder if a shoulder massage sitting up would do the trick? Just have to be careful of my burnt collar bone!
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Marie - have you tried Reiki? It's not like massage but it is very relaxing.
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Well I just finished my last radiation (BOOST) today... so that is it for me now. It is now time for healing and recovery (particularly of this bad burn). Not going to put all of the 'Silver Salfa' creame doctor prescribed all over my breast tonight, Nurse suggested putting it on a small part of my breast overnight and seeing if I take a reaction from it first. (bit nervous of using this 'silver cream'). So looking forward to being on the road to wellness again, and not feeling so tired...
When I went in for my last treatment today, it was a bit of emotional experience. The radiation therapists all came out and said to me ' your graduating today ' . I got up on the table, lied down and started to cry - it really hit me in a big way... and cried thru my whole treatment. Once done with the treatment the radiation therapists all gave me a big hug.
For the compassion I got from the ladies in radiation unit, and excellent care I got them a basket that consisted of allot of fruit, cheese and crackers and a tin can of danish cookies and they were so surprised and appreciative of it
and a nice card.Charmaine
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Oh WHAT A DAY. I almost didn't make it to rads! It's my moving day, and our U-Haul truck got a flat tire that delayed us for 3 hours, in the cold rain. Every time my stepdad called the U-Haul people who said they were sending a repair guy, they kept saying he was "on his way"... finally my stepdad called back and said, "My daughter needs to get to her radiation appointment!!", and whaddya know, the repair guy was there in 15 minutes. But then we were under such a time crunch to get all of my stuff moved to the storage unit and my entire pick-up truck bed full of junk to the dump, all in the rain, that we finished just 10 mins before I had to leave for radiation - and this was even after I had called to change my appointment to 2 hrs later than usual! I showed up at radiation totally water-logged and filthy. At the end, I joked to one of the techs that I was off in search of more chocolate, and then when I came out of the changing room, I was surprised to find her standing there with an open box of truffles.
The other techs were so surprised that she was sharing her chocolate, and it was so sweet. I would have felt like a jerk saying, "No thanks, I stopped eating refined sugar 2 months ago and only eat chocolate with a cocoa content of 70% or greater," so I took a truffle and ate it and enjoyed it!!!Marie, I'm glad your headaches are better!
Magoo, welcome to the thread! I'm sorry about your arm! Sending you healing energy! And slam dunk that gown!

3monstmama, I'm sorry that co-worker was so insensitive, but wow, I'm so impressed by your honesty and assertiveness and by how well you handled the situation. That's inspiring. KNIT AWAY, indeed!!
Marianna and Marie, what about at least a chair massage, of your shoulders and neck? I've been thinking of trying that. My back and shoulders are tighter than ever. I got a great chiropractic adjustment right before rads, but now I don't think I could lie on my stomach and have the chiro press down on my back like that...ouch.
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Marie- Thanks for the suggestion- I will try Vitamin D before bed and see what happens!
Marianna- My Vitamin D score was in the mid 20's(not necessarily abnormal for the normal non ca population) but my Onc. wants it in the 50's. Despite my age and heavy activity level I meet all of the qualifications to be an osteoporosis candidate. I think the Onc is being a little proactive since I have also started Femara. I don't mind the added protection- my horse(not intentionally) head butted me in the ribs over the weekend- fortunately no fractures.
So far - no other se's
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Has anyone found their tape/sharpie/tattoos to be a wardrobe challenge?
I have been trying to hide behind sweaters but its getting too warm here (although not today-its snowing). The husband says I should just tell people I got a new tattoo and go with it. My marks are not a work of art- but at least the big black box around my breast has worn off.
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tic that too bad about your tats--mine are so small I can hardly find them. And my techs have used kid markers that wash off when they do have to right on me. That said, to deal with all the creme an the like, I am wearing Hanes mens t-shirts under everything. It limits me to higher necklines but at this time of year, where I am, its not a problem. And it would give added coverage if they ever have to hit me with a sharpie.
Raili, sorry to hear about the stress but nice to hear they tried to help you with candy. And I think you get a sugar dispensation given all you have gone through today.
Our waiting room had sugar cookies today--someone was graduating, its spring, its easter, its passover, whatever. I told myself NO Cookie! while I waited my turn for zapping, I told myself NO Cookie! while I laid on the table, I told myself NO Cookie! while I got dressed after and even while I did my stomach crunches in the dressing room, I told myself NO Cookie.
And then I walked out the door of the dressing room, stuffed my gown in the bin and said "oooo, cookie!!!!" At least I took one shaped and decorated just like a carrot. . . thats virtually healthier, right ladies?
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3monstama - yes, carrot is definately virtually healthier. lol The way I see it, the are also no calories either....just like the samples at Costco!
tic - I have four permanent tatoos but some of the techs put a big "x" over them each day with a marker. It stains by new non underwire bra that I bought for the occasion. There is one tech, though, who doesn't use the marker.
Raili - you've had quite a day and you deserved that truffle. That's funny what you were thinking about with the 70% or greater cocoa level. I'm not really much of a chocolate eater but have been making an effort to eat two squares a day of high cocoa content dark chocolate. Dr. Oz says to eat two squares a day for the antioxidants and he suggested doing so with a cup of green tea. That has become my special relaxing night time snack after exercising. At first I found the taste bitter but I'm now really getting to like it. I think dark chocolate is an acquired taste.
Charmaine - congratulations on finishing rads!
Sherri
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3monstama - yes, carrot is definately virtually healthier. lol The way I see it, the are also no calories either....just like the samples at Costco!
tic - I have four permanent tatoos but some of the techs put a big "x" over them each day with a marker. It stains by new non underwire bra that I bought for the occasion. There is one tech, though, who doesn't use the marker.
Raili - you've had quite a day and you deserved that truffle. That's funny what you were thinking about with the 70% or greater cocoa level. I'm not really much of a chocolate eater but have been making an effort to eat two squares a day of high cocoa content dark chocolate. Dr. Oz says to eat two squares a day for the antioxidants and he suggested doing so with a cup of green tea. That has become my special relaxing night time snack after exercising. At first I found the taste bitter but I'm now really getting to like it. I think dark chocolate is an acquired taste.
Charmaine - congratulations on finishing rads!
Sherri
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Sugar77- Unfortunately I have all three- Sharpie "x," minute tattoo - all covered with a clear tape tab.
May I recommend Lindt Extra Dark Bittersweet or the Lindt Extreme w/ Peppers. Of course a glass of red wine tops it off!
Congrats Charmaine!
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