Spring 2014 Rads
Comments
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hi , just started reading these posts as I am finishing chemo phase soon and starting rads. I am sorry to hear about some of you having problems ...even about where you get marked, but thanks for sharing as it gives me an idea what to expect.
I have a question to ask , I finish chemo April 11, and I am booked for my consultation for rads. On April 22... Is that too soon , should I have more time to recover or just go in wanting to get her done ???
Thanks for any info , and sending hugs to all !
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gardengirl, welcome!
My MO told me 4-5 wks after last chemo. But, by the time you have your consult and they do the planning, etc, it may take them that long before you start. My last chemo was Feb 11th. I had a consult/planning on the 14th and have not heard back from them as to when I will start rads. I had a 3 wk post chemo consult with my MO in order for her to release me to my RO and the RO would not start until my MO released me... I hope that made sense. It's a process!
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keepthefaith, thanks for the info, every bit helps...will ask more next time I see my oncologist. Just know researching rads more now, since I decided I will do it ...throw everything I can at bc.
Thanks, I appreciate the info !
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AnneB - I hope you get to start soon. It's too bad they didn't tell you it would be awhile so you could have travelled.
Girlstrong - sorry to hear about your cancellations. I've been given odd times because of machine maintenance but not cancelled.
LDN - Good luck to your Mom on Monday!
Dogsneverlie - I don't envy you at all, I think I would have trouble holding my breath that long.
Welcome FightBC, Beenheresince1957, and GardenGirl66!
I had to cancel my treatment on Friday due to a snowstorm. Earlier in the week I stayed over in a hotel due to storm but the amount of snow on Friday took me off guard (8 inches). More snow predicted this week, I think I will stay again. It's time for winter to be over!
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Hi everyone: going to go for my MRI and CT scan tomorrow. I had my first infusion on March 18/14. 1/18 seventeen to go. I go every three weeks. I start my radiation on April 1st, staying till Friday. I'm coming back on weekends. I stay at Cancer Lodge Monday to Friday for five weeks
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Just finished 25/33 tx this morning. The fatigue is starting to catch up with me. Also, my nipple is very sensitive and my skin is showing more redness. The nurse gave me Aquaphor to use one my nipple and said I should start using 1% hydro cortisone cream on the really red spots. I was told to wait at least an hour after I apply the radiagel before I put on either the Aquaphor of the hydro cortisone cream. I was also told I shouldn't use anything on the radiated area with in 3 hours of treatment and that all traces of the aquaphor need to be gone. Otherwise, my skin will absorb a higher dose of the radiation. That sounds like it would be a really bad thing, so I am going to be very careful. I was also warned that the aquaphor will stain my clothes. As long as it makes my nipple less sensitive to clothing, it can stain whatever it wants
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done the markings around my breast area. Everything is ready to go, thanks for all the tips. I hate needles but they explain everything as they go along which is good
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Hi there --
I got the word last week that I do not need chemotherapy so I am heading into rads. I met with the RO last Friday. I was under the assumption that it was simply the six-week, whole breast regimen. He threw me for a loop by offering an acccelerated partial breast option. Mind you, I live walking distance from the hosptial so travel, etc. is not an issue. I researched like a madwoman all weekend and never got comfortable with the shorter partial regimen; also consulted with my MO who felt it was not the best path for me. So, I am going for the mapping for the tried-and-true six-week plan on 3/26 and hope to start next week.
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Went for my first treatment today. They remarked with black marker and said it was no problem they will just touch up as needed. Not doing tats like I thought. Glad to hear stillrunnn... that you are doin well in the 25 out of 33 tx, good to hear. Sounds like we are all just trudging along smoothly. Hugs to all-
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I had my first rad today. I wasn't expecting to feel the " heat" of it so soon. I was expecting more the non feeling of an x-Ray. I had that done too. But I am glad an earlier poster mentioned that. My right breast was zapped & still feels warm to the touch. To Beat BC, I tried to get an early morning appt, but there were none available. So I go for mine at the end of the day. I'm lucky that I don't have a ton of running around to do most days, but it may be easier to go home and rest if you need it instead of starting your day out. I think I'm glad the scheduling worked out that way.
Thank you all for sharing your experiences.
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one week in - looking for anyone doing rads post reconstruction! i'm finding it painful already - everything is tightening up...
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I'm a week in and suddenly very tired and the chemo-type muscle aches and pains are back. My surgery was back in August so post-op pain doesn't appear to be a problem. Hope you all feel better soon!
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Hi everyone! So my "fitting and tattoo" session did not include the body mold!
I laid down on the CT table and my radiation onc came in and drew all over me, then I was scanned (was a little hard for me to keep my left arm above my head, I am still sore). After going thru the machine, they then taped this electronic box on my chest and gave me these glasses to wear and asked me to take a breath deep enough so that the red bar lined up and then I had to hold my breath for 30 seconds. HA! Doesn't seem like a long time until someone tells you to do it, don't move and run you thru the machine again!!!!! Looks like I am going to be required to hold my breath while getting treatment......
Then I got the three tattoos! So the one on my left breast smarted, the one on my right was fine but the one in the middle of my chest - owie!!!! I have to admit.....the day before I went and the day after I was a wreck. So teary. I don't like feeling this way at all - helpless and having to do this. And such a pain - every day for thirty treatments..........I selected first thing in the morning because I have a 30 minute drive to the center, then it will be a 45 minute drive from there back to work so I'm looking at losing about 3 hours/day............
I was also a little surprised at the size of the treatment area. I asked the tech why the three tattoos and he said they have to treat my entire breast area and then the nurse I met with said when the burns appear it will go up to almost my collar bone. I did not expect that..........
Also.....man....my back muscle kept tightening up on the table! How embarrassing.
So my dry run is Friday afternoon and then my first treatment is Monday March 31 at 9:15am. Then on my tenth treatment they were able to get me in the 8:15am time slot.
OK, I'm going to go read some threads and reply to people now that I am done my cry baby note!
Donna
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Donna - I can sympathize! For some reason that part of treatment really freaked me out. More than the chemo infusions. I'm on day five, it is much more old hat though sometimes I find I still get anxious for no particular reason. Hoping that will go away in time. You can do this!
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Dogsneverlie..
Don't fret things will get better. The zap time is like fifteen seconds twice. It takes longer to put the gown on than getting treatment. Take a deep breath everything will be fine. Moisturize, moisturize. Had my second treatment today on the left breast. feels warm afterward and stays that way for a while. I put aquafore on it right away when I get home and the use again before bed. Use an old tshirt so it won't ruin clothes. My breathing seems short and harder to take a deep breath for a few hours afterwards. Should I be concerned about this or it's normal?
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Welcome Lidzy, DisneyGirl and Notbuyingit !!!
Flagirl - your "zap time" 15 seconds twice sounds quick. For me the machine moves to three different positions and there are 3-4 "zaps" in each position.
10/33 finished so far....after tomorrow I'll be 1/3 of the way done!
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maybe my zap time is different. Typing from cell phone. Breathing is definitely affected for a couple of hours. Dr said to pick up ocean potion aloe lotion to calm down skin contains lidacane to relieve pain. Walmart carries it picking it up this morning. Looks like I am going to get the spider veins already starting. It seems like I am going to be sensitive 31 more tx and I will be getting five boosts the last week. Good luck BC sisters.
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Hi Donna - Looks like we'll be going thru this together - I start two days after you, I hope your tattoos aren't smarting anymore.
I just got back from the CT scan and it was a piece of cake. Put me on the table in a firm brace - place for my head, bolster under the knees, both arms up over my head in kind of stirrups - honestly, the table looks like a backwards gyne room table. Then, the RO taped some metal strips in a square around my left boob (which he later removed) to delineate the treatment area. The actual CT scan took under five minutes.
When, the metal strips were removed by the tech, I declined tattoos and was told that was fine so she gave me three big x's - one on each side of my boobs and one in the middle of the chest. Covered those with clear tape of the kind that is used to hold in an IV.
She took me over to show me the actual treatment room and went through that protocol with me - no deo w/ aluminum, etc. She told me that the RO will see me each Friday, as will a nurse.
I have the simulation next Tuesday and begin the zaps on Wednesday, April 2
The only thing that surprised me is that the RO once again brought up an accelerated treatment plan after I firmly told him I'm an old-fashioned gal and that my schedule permits me to do the longer, conventional six-week plan. He told me, again, as I lay slayed on the CT table, that this is done in the UK and Canada. Seems like he has an agenda and I don't really appreciate that - but, big deal - I'm moving forward with the plan that suits my psyche best and he and the staff all seems more than competent.
Hope the rest of you are progressing well!
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Oh - and the staff recommended Alra non-metalic deodorant, which contains aloe vera. It is sold in the pharmacy of the cancer wing so I picked up a stick - not bad smelling . . . but expensive.
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Hi Ladies, Although I'm done with Rads as of 2/10/14 I can tell you it is doable with going back to work. I was suprise how well I did, after hearing so many stories of other women. I wasn't tired much, I had maybe one of two days out of that whole time that made me tired. I was able to still wear my regular bras (wire ones too). My breast held up very well. I used aquaphor for my skin. was no peeling, soreness, nothing. Just want to let you ladies know not all treatments are horrible, painful, tiresome, but can also turn out well. Good Luck to you all!!
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Hi Ladies,
I've mostly been hanging out in the winter rads thread, as I began in February, but as I'm almost done, I thought it would be good to hear from someone who's made it almost all the way with little to no SE's. I had a MX with no recon, so the rads are to my chest, and nodes, including supraclavicular. I've done 25/28 as of today, and the supraclavs are now done. Collar bone is a little pink, but doesn't hurt. My chest and armpit are a weird tannish, pinkish, purpleish color, but the skin is still intact. The area below my collar bone, at the upper part of the IM nodes is pink and itchy, but not painful. The only pain I've really had is under my arm, about 3 inches below the SNB scar. It occasionally hurts a bit (4 out of 10) and feels like the skin is being pulled too tight, but it's inconsistent and hasn't been a big issue so far. Last night was the first time I took anything more than Advil or Aspirin. (took half a percoset). The RO said she didn't think my skin would blister (fingers crossed).
I've been working the whole time, although telecommuting mostly. I've had a few meetings I've had to go to, but other than the hole put in my day by the appointments, it's been doable.
My recommendations are to keep light exercise as long as possible as I think it helps counter the fatigue, and to eat well.
You'll get there soon
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Have not posted in a while but I have been here reading everyone's posts. Thank you for all the posts, support, kind words, encouragement and information. I KNOW how hard it is on some days to sit down, organize thoughts and post.
I feel very cared for and less alone every time I read and re-read the posts from you wonderful women on this website. Feel so grateful for all of you. Thank you everyone! I also appreciate all the informative posts. I am getting a clearer idea about what radiation will bring, so I'm feeling a bit more prepared with each passing day.
Mentally, people are noticing that I am slow. Chemo-brain is a real thing despite the controversy that surrounds it. I am still feeling awful side effects from my last chemotherapy but I am anxious for my simulation & tattooing (April 10th), which is also the day of my first post-breast cancer mammogram.
I will keep everyone posted about my progress. And I WILL contribute and "give back" because that is important for me to do. I feel selfish just lurking and reading...it took some time but I posted lots under the "November 2013 Chemotherapy" Thread.
Thanks again, everyone and feel well!
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Good to read all these posts. I finished No. 8 today out of 21 (16 whole breast, 5 boosts) and so far I am good. Have been working the whole time, coming into the office at 9:30 and working straight through to 5:30 p.m. I have not felt any fatigue yet and my skin is holding up well with the RadiaGel I am using. I also purchased some Aquaphor on my own but have not used it yet. It is good to hear that some people get through this with minimal SE's. I agree, get a little walk in every day if you can, even just 15 mins is good. Eat well, lots of protein. I drink a lot of water and I get to bed at 9:00 every night. I will keep you all posted as I continue. I have a wonderful team of people and we laugh every day.
When I woke up this morning and turned on my radio, first song I head was an old 80's number that Eddie Murphy sang in 1985 "Party All the Time." I think "my girl likes to party all the time" as well. Made me laugh. Been singing that tune in my head all day and smiling.
Oh those were the days! Have a good one everyone and find something to smile about today and everyday!http://www.youtube.com/watch?v=bDbpzjbXUZI
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good to hear encouraging results! major meltdown over last weekend - wanted to quit Rads badly! guess I was expecting it to be easier
only in my second week & have some pain & tightness - Doc says there can be some swelling in the beginning & that it should pass. Also have read that increased tightness around the armpit - if you've had lymphnode removal - is normal - but youch!
just hoping my new "breast" survives - hate to think of all that expander time for naught. Still looking for advice from someone else doing rads with implant in.
thanks, Ladies!
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hi all, thank you all for the support. My zap time is more like Pam's - the 3 - 4 times. It is strange. I guess I've been in denial the whole time but the rads is the first time that I've felt like cancer has affected me. I've downplayed it, that's for sure. But that is mainly because I am a weenie. If I can do this, all of you can! It's really getting easier on day 3.
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I am scheduled for appt with surgeon friday. Was just reading your new group posts and have a question. What is radiation simulation? thanks in advance.
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hi Renee, It is when they customize your radiation treatment to your specific needs - where your tumor and margins are,etc. For mine they took a ct scan of my breast and my radiation onc mapped out the lasers (for lack of a better word to describe it) that were going to focus in on the site of the tumor. That is also when I got my tattoos - more guides for the treatment. That is the basic simulation experience. There seem to be variations - like some women are placed into a form like thing that molds them. I didn't have anything like that. It wasn't horrible for me, but you do need to be still for some time. I hope this helps. My simulation was done almost 2 weeks after surgery.
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Pam, you and I are on the same schedule, and it seems treatment plan. I finished 10/33 today also. I also get zapped in three different locations, so the machine moves around. I get a bolus every other day. So far no skin irritation. I am using aquaphor as per RO instructions. It works but it makes my skin oily and I always feel like I need a shower!
Best of luck and hoping no SEs for all you ladies.
Missed you, Tonilee.
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Lojo: Our experiences are very similar. I finished 24/25 today and my underarm area is the only tender and tight area. Am very red though and itchy, itchy, itchy! Glad to be almost done. Skin can worsen for a week to ten days, so hope that nothing breaks down. I worked out each day and definitely could have worked throughout except for my huge daily commute that took up 5 hours daily. I got used to the trip and started to actually enjoy my music, shopping trips, lunches with friends, etc. But back to work on Friday.
Good luck everyone.
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Hi Renee -
This website does a good job of describing the simulation:
http://www.breastcancer.org/treatment/radiation/types/ext/expect/simulation
I think I mispoke when I called the session next Tuesday the simulation - I guess today, with the CT scan and the marking was the simulation. Next week, I go for a "verification" session and, if all is correct, begin the radiation treatment the next day.
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