May 2011 Radiation
Comments
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TonLee- It's oral. I take 4 500mg pills 3 times a day. It's called Curcumin C3 Complex. The University of Rodchester is putting on the study. Here is a link: http://clinicaltrials.gov/ct2/show/NCT01042938
I take it during treatment and for 1 week post treatment. We'll see how it works...can't hurt to try it, it's natural : )
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I just finished my 2nd treatment of 35. I'm getting the bolus treatment too, as well as clavicle area. I feel super tired right now, but it's hard to know if it's an effect from the treatments or not. I've been seeing a lymphedema therapist as a precaution. She does lymph massage and has shown me some exercises to keep things moving.
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Finished 3 out of 21. Not bad but then I went to see my oncologist for the first time. Now I'm ready to cry. Turns out I will be doing chemotherapy after radiation.
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Sorry to hear that ew-swimmer. Hang in there. One day at a time.
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so' i'm not crazy....
I've had 3 out of 33 treatments. i have them at 11 then i'm wiped and napping around 3-4 pm. i thought i was nuts being tired already, but after reading these posts, it makes me feel better knowing it's not just me getting tired so early!
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cb451 - love those directions. What is it made of?
Kaseymomto2boys - Thank you for posting that information on the trial. I was really interested about it when I saw your earlier posting about it to help with your skin during radiation. I started drinking Turmeric tea several times a week when I first got dx with bc and continued drinking it on my off weeks during chemo. I noticed that it really helped my skin alot. So I thought I would try it during rads too. I think I might go out and buy some Curcumin pills to take on days when I don't have the Turmeric tea.
Does anyone know if rads would be delayed if a patient is anemic? I got my blood drawn today, although I don't know the results yet, and I think I might still be anemic from my exchange surgery.
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ProudMom: "Allantoin, Dimethicone, Lanolin Oil and Propylene Glycol in an Emollient Base." It feels greasy going on but it's absorbed pretty quickly and hasn't stained anything.
Ewa-Swimmer: That's really rough; I'm sorry.
Hdangelbaby: It's the same for me. I'm irradiated at 9 and napping by 3.
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Hdangelbaby and cb451 - I've got you beat. I've been counting my zaps during treatment. The last two days, I've made it to four...and then the tech wake me up after treatment is done!! Maybe because I'm sleeping on the table I don't need to sleep when I get home!
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Hey everyone...I had my 6th of 16 radiation treatments today...so far, still so good...
I did have an interesting experience yesterday...I had an appointment to see a doctor who has been treating me for vericose veins...he injects a saline solution into the vein and then it disintegrates or something (sorry, I should know the details...but you get the idea). Anyway, when I told him that I was a currently having radiation treatments, he said that he wouldn't be able to do the vein treatment as I would be at an extreemly elevated risk of developing a blood clot. Now I already knew that blood clots were a possible side effect of the treatment...although rare...but he said no, people who have cancer are much more likely to develop clots. He said to come back and see him after I have been on Tamoxifen for 6 months. I guess that if I don't have a clot in the first 6 months of taking the drug, that I'm probably not likely to. Interesting anyway I thought...not that we needed anything else to worry about. He told me to wear knee high compression stockings to try to prevent clots from forming. He also told me to lose 50 lbs...doh..he said I need to get to a 25 BMI...I haven't had a 25 BMI since I got pregnant with my first child.
I'm really looking forward to going home for the weekend. 10 days living in someone else's space without a break is enough for me...but, the people I'm staying with have been outstanding!
I have been feeling a bit tired too...I think the second day was when it started lol...I thought the same as everyone else...the literature says you don't get tired until the second or so week...strange. I'm still using the Glaxal Base..it works really well! No burning yet at all.
I also like the idea of a lotto ticket a day...I'm going to go buy 16 tomorrow and I'll have a bonus scratching day to catch up to my treatments...Great idea ladies! Thanks!
Ha ha...I have been counting during the treatment too...I am getting to about 250 each time. I find it keeps me calm. I don't know what it is, but I feel quite anxious during the treatment even though it doesn't hurt or anything...I think it is because my preconception is that radiation is bad in most cases...except this one.
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Hi ladies
Thank you all so much for posting your side effects and fatigue issues. I start on Monday the 23rd so I will brace myself for what's to come!
On Radiation Brain:
My DH just laughs. Said, "first it was 'pregnancy' brain, then it was 'chemo brain' and now you think you'll develop 'radiation brain'...have you ever considered the fact that you're just forgetful?"I just cracked up. He's so right

I'm off to the spa tonight (massage, facial, mani-pedi) and although I'm anxious to see how they will deal with my lack of hair, i'm excited to be able to go (figured i wouldn't want to go after rads started for me...)
Wish I had some hair though! -
cb451 thats so funny that your doc ecommended that. We own a feed supply store and carry that product, my husband uses it in the winter on his hands!
Kasey... I am taking tumeric oral supplement, dont think probably same as your trial? Just got at vitamin store because i read somewheres here it has cancer fighting abilities. Someone posted a website on the studies of curcumin (tumeric) for ca. Dont know what the c3 complex is?
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Thanks Kaysey,
I'm getting some Curcumin this weekend and will start taking it asap. Maybe it will work...I like to believe if researchers are convinced enough about something to invest precious research dollars in it, then somewhere down the line they see evidence of effectiveness...even if they are wrong....like you said, won't hurt.
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Moooooooooooo Mooooooooooooo to you cb451, I'm still laughing..........well think I'll go in and milk and massage my utters...............hysterical............gotta get me some of that good stuff.............thanks for the laugh, .........hugs
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HI Ladies - Started my rads on the 10th, Tuesday. Still haven't had a chance to buy the scratch offs but plan on it tonight. Hopefully I will win - need some pick me up.
So far so good with any SE. Just a little discomfort and tingles. Although everytime I have left the office after rads - I cry all the way to work. I feel like I am in a good place but there is this terrible feeling I get when they leave the room and shut the door and leave me all alone with the damn green beam.
In my head I say positive things and ask the green light to get my "crumbles" and make me better. But I leave so emotional everytime. I guess I need a good cry - I don't know. Anyone else feel this way after?
Nic
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Nic.....the only reason I don't is because one of my grown kids takes me everyday, so usually we are deep in conversation, but this week I have to say was a little different..............when I came home I felt like "Debbie Downer"..............not sure why, but I did..........If I was alone coming home, I would not be surprised I would do the same.............
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nic42 -
I was very emotional the first couple weeks of radiation also. Everyone at the center where I go is extremely nice and caring and there isn't any pain during the procedure, so why the tears?
Is it possible the crying on the way to work is due to the stark realization that while you're trying to carry on a normal life, radiation treatments aren't business as usual and certainly not anything you ever thought you would/should be doing? That's a hard transition to make.
I just retired in September, then was diagnosed in December, so I don't speak from first-hand experience. That said, the whole work world is still fresh in my mind.
I think it's good that you're talking to the machine. My nurse friend said that actually helps with treatment success (not so sure how anyone could measure that, but don't care). I do that too.
I've started to do things to make going to/from the treatments a little special. I have a couple routes to take to/from the radiation and I reward myself with the scenic route. Sometimes I stop at a little spot on my way back to my car that has lots of colorful flowers and just enjoy for a few minutes.
I hope things get better for you. Know that you're not alone in finding this part of the treatment very emotionally challenging.
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So.... four down, twenty four left. I'm a little different from many of you... I am having radiation despite having a bilateral mastectomy. I had one node positive and that node had some cancer outside the node, so they are radiating to the chest wall, superclavicle and underarm. My left breast (the non-cancer one) was getting in the way, so they have been taping it out of the way. However, my radiation oncologist wanted me to have some of the saline removed from the expander to be on the safe side so we wouldn't irradiate it unnecessarily.
So all this background for my cute story, entitled "when will my teenager realize I have a sense of humor?" I was lamenting the fact that I had to see the PS to have saline removed, and would be lopsided for a month. So I asked my daughter -- hey, you are in middle school, that's a popular age for girls to be stuffing their bras. I'm going to need to even myself out -- can you help me? What's the latest thing -- still tissues? Her reaction... "Oh god mom, please don't use tissues, they always fall out and you'll just be embarrassed!".
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Ducky, you might try putting that hand goop stuff that mechanics use on your gown to get the aquaphor stain out.
My mom used aquaphor on her burns 20 years ago. It is tried and true. I always thought it was odd that it was sold as hand cream when it is so good for burns.
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LisaMom - I have almost the same experience as you - bilateral, one positive node, radiation in the same places (28) and lopsided due to 50% of volume taken out of TE. Only difference is my right breast is the non-cancer side.
Regarding stuffing - go to the fabric store. I found some forms that are used when sewing swimsuits, lingerie, etc. I just bought a package of those and pin them inside my bra. I DO use two-sided tape so they won't shift around (even thought they're pinned). Seems to work okay for the duration. I AM, however, making an appointment for an expansion immediately following the last radiation!
Your daughter sounds like a hoot!

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Gmafoley~ my first meeting with the RO was him trying to "sell" me radiation, I told him he had me at "hello cancer"! After he stopped trying to convince me, then he explained how it works, what's it's supposed to do etc. and he did an exam. During radiation treatments I see him every Tuesday, I told him the other day I'd like him to atleast throw me some beads every once in a while!
cb451~ I was tired from the first treatment too and forward. Somedays are a little better than others. I can function and work all day, but getting out of bed is the most exhausting part of the day. Love the udder cream story! Mine sounds like something out of sci fi movie for robots "Radiogel"
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duckyb1 - My friends have offered to come along for the 45 min ride so tomorrow I am taking a dear friend with me - your right I do feel like "debbie downer". But after reading what you wrote GabbyCal - I realized it is daily reminder that I have breast cancer AND I DON'T LIKE IT!! I feel marked or tagged - like defective mdse. I'll get over it. There is no way cancer is taking over MY LIFE!!
Thanks ladies for your insights. Sadly I know I am not alone but very thankful!
sincerely, nic
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Hi JulieH and proud mom. Need to go back and read all the posts and catch up with everyone.
I am not quite a May Rads girl but I hope I can travel with you.
I finished Chemo today, my simulation is may 31 (that is just under the wire for May:))
Rehearsal is June 8 and Rads start June 9. I am scheduled for 25 rads and 5 boosts.
So glad to have buddies on the next part of our journey.
Jean -
Sorry forgot to say I had my lumpectomy and sentinel node biopsy on December 1.
Worried about fitting in the rads with working, somehow this is more stressing to me than Chemo because it is every day, basically with drive there and back and the time at center it is close to 2 hours every day and the center is only open until 4....oh well it is only 6weeks. I can deal.
Jean -
Just lost my last post.
Reading through I see lots of the January Chemo Ladoes, so glad to travel with you again on our journey.
I was also recommended toms of Maine for deorderant and given a booklet from the nurses with creams to use including eucerin which I used fro dry skin during chemo.
Derm that saw me at Sloan for my chemo rash wants me back before radiation to give me a rx for another cream to use proactively tom prevent rashes. I see him on the 15th I think....
Have a great weekend everyone
Jean -
Update: Went to see the surgeon for a recheck and Radiology Oncologist.. Surgeon said I'm good to go back to work in another week... then RO says that he is thinking 16 rad treatments and I will be good BUT we are still waiting to see if I need chemo... That appointment is Monday if the oncotype test results are back.. They weren't back when I saw the RO. I will probably start radiation in June. So I guess I'm not a May Rad person like I thought....
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Hi everyone!
I went today to get my form made and marked, next week I go for the dry run, and start rads on May 23rd. I am jumping on a little late, but just stopping in to visit!
Hi Angel, Lisa! and others from Dec chemo!
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Missed yesterday for a Shave to Save event back in KC but number 14 done today! YEAH!!!! I am ready to be DONE!!!!
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I had my seventh rad yesterday...number 8 today, and then home for the weekend...whooopeeee!!! I can hardly wait to sleep in my own bed!
I saw my radialogical Oncologist yesterday for my once a week checkup with him...he asked if I was having any trouble breathing...man I sure hope this doesn't happen...does anyone know anything about this? I am having radiation on the left side.
Invasive Tubular Carcinoma
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isee the RO told me that sometimes they catch the top portion ( a very small sliver) of the lung with the radiation, but says it usually doesnt cause any problems because so small. He told me this when I questioned him about rads effecting or getting my heart.
I went today for the films prior to starting rads and I thought cause I got tatoos last week that I was all done being marked but no, they put a large X on top of my boob witha sticker...lovely! i think my bathing will cover this..I hope. He very calmly said leave this on for the duration....wanted to put an X on his forehead, or elsewhere ha ha
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Carberry, lol X does mark the spot!!!! I have a big T on me!
Isee~ yes my RO told me the rads will get a small part of my lung. He checks my lungs every week at the appointment. I'm 15/33 and haven't noticed any breathing issues - not like with my first round of chemo!!! Fatigue is my worst SE so far.
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