Winter 2015-16 RADS
Comments
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Jrowe - mine uses a wedge also and they allow me to get comfortable then they pull the sheet under me to move me left of right. If you let them know you have problems they will work with you I am sure. My techs are so nice I am sure you will do fine... Time does fly...
Helen
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Brimton - Coping suggestions - for me every zap of radiation I think of it as added insurance against recurrence .. if that helps!! I also try to find levity anywhere - even if it is me making the techs laugh or something ..
Duzy - thanks for the chemo well-wishes .. Taxol just crushed me! Yes positive thoughts on minimal se's for all!! I bought a cooling towel from Amazon have not opened yet - I have been using Calendula cream 2-3 times a day since a week before started at RO's recommendation..
Dorothy26 - Yes the waiting is the worst - Good Luck on the 8th and keep us posted - can add you anytime!
1957-2057 (Helen) Wow - I started Monday and every time the machine starts bussing I start praying - first thanking God my cancer was found at Stage 2 and then thanking him for Modern medicine Chemo & these Rad Machines and lastly I pray for all to be cured! Funny - Great Minds - Huh...
Marijen - I have pain in shoulder and armpit .. nurse checked my arms today and saw no lymphedema so I am writing it off to it being 1st week and arms in the air everyday!
KateB - so hope your 1st day went well!!
Welcome Welcome SeekingSerenity16 - so sorry you have to be here but glad you found us - great group here! Good Luck on the 8th and keep us posted on your treatment details and how you are doing!
And .. Welcome Welcome JRowe - also so sorry you have to be here but glad you found us - great group here! Good Luck on Friday and keep us posted on your treatment details... I have a compromised Spine and was almost paralyzed in an accident 5 years ago - not fun! I can do most things expect lay flat.. This was my 1st week and I shared that with the techs and they are great - they remember everyday and put 2 wedges under my knees and it is perfect - they always make sure I am as comfortable as possible. I would just share with them and I am sure they will help you be as comfortable as possible. I did not find lying on the table even for the sim nearly as bad as I thought it would be. Good Luck!
sos1125 - Great to hear from you - did you start yet? I can update your info at the top if you want - just let me know!
Fearless - HaHa about nose or something itching while on the table - that has happened to me everyday this week - nose or eye! I too am trying to find something comical about that - gotta be psychological or something - as soon as you can't move your nose itches!! Today there was good dance music playing and I started tapping my foot without even realizing it and the tech luckily was still in the room nicely reminding me no foot-tapping LOL!
Have a great night and Friday tomorrow!!
Mary
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First day went fine. I feel so much better now that I know what to expect! And I picked my favorite dish out of the saltwater aquarium--a fast little red guy.
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Tomorrow is my first rads...so ready to get started on this phase of the journey. I have kept up with this thread since I joined and appreciate all of the tips that have been shared. Thank you so much
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Remember that you might want to try cabbage leaves to deal with heat, inflammation and itching, ALL.
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I've now been done for a week, and I have to say, the peeling is incredible. It's only a little bit itchy, and otherwise feels fine, but it's like the sunburn from the beyond for peeling.
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Fearless: congrats on finishing
Yeah, I think I know who it is too, so I make sure I tell her how much pain I'm in when I'm there and have ALOE and Ice cube pack with me.
Etnas and octo:
Boss mentioned work at home policy to me as far as going along with the rules and being proactive in case of an audit. I looked at it and there is nothing about being sick, it's one-day projects to focus. I have no 1-day projects.
He said it looks like he's showing me favorites behavior. Hello, I'm recovering from radiation burns. I'm no longer asking for more than 1-day while my skin is sore. In fact, he's letting me work at home tomorrow. I'm so grateful. As far as the other people, he's doing what's best, but I know one woman mentioned something to me, and her job is different and she's not able to work at home. She has to deliver paperwork to team members. I told her our jobs were different and why didn't she mind her own business when this first started.
But, I feel that I have no "friends" in my dept. and it's not a great feeling, but today I'm oversensitive. I wouldn't want anyone else with breast cancer to go through what I'm going through. Or without it either ... you know what I mean. So, I'm just going to do the best job I can with G-d's help and your prayers.
KateB - I wasn't for rads either, but the numbers decreasing reoccurence spoke to me. Reduces risk from 30% to 5% and that meant something to me.
I'm glad to be done, but the fatigue is huge! I'm resting and not getting house cleaning, taxes or making jewelry done. Instead, I'm snuggling with our kitties.
I'll post pics when I copy them from my phone.
Hugs to all,
Linda
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Does radiation therapy improve survival for women with ductal carcinoma in situ?
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JRowe I too have a back that gives me fits. How did it go? I didn't have much trouble...harder to lay still that long for the sim and the first day where they take x rays. I'm a mover and a shaker :-) I'm sure they will work with you.
What has really helped me is bringing in tunes to play with headphones. I put on my selection for the day and visualize something positive.
Thanks Mdoc524
That will be my new thing. Focus on healing and laughter. -
Thanks everyone for the info. I will post how things go I just see my dr today I am sure they will set up the sim for next week if I have healed. My surgery was on Jan 5.
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Hi everyone! I've been lurking a lot and reading everyone's posts in anticipation of my own rads starting on February 15. I went yesterday for my CT and will have my simulation and possibly the first treatment on February 15. The techs yesterday were lovely and helpful--I'm at Duke, and so far, through surgery and chemo, every interaction with every staff person (techs, nurses, doctors, appointment schedulers, volunteers) at Duke has been positive, so I feel very grateful to have that.
I'm collecting skin care products--Eucerin, pure aloe vera, Aquaphor, Miaderm, Cicalfate (something my dermatologist highly recommends) to start using right away. My acupuncturist recommended drinking goji berry juice every morning--it's just a capful and not so tasty but not terrible. He believes it helps tissue health.
I have VERY sensitive skin and allergies to all adhesives, so I'm a bit worried about how my skin will handle 6 weeks of radiation, but here goes...
Thank you to everyone for your helpful posts. I hope everyone has a wonderful weekend!
:-)
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How does your skin hold up during boosts? Have anyone of you noticed any changes in your skin as compared to the regular radiation?
I'll be starting my boosts next week and so I'm curious. -
I did the 16 fractions with 5 boost at the end, the Canadian protocol. I'm very small breasted. Everything went very well. My skin didn't turn color until the end and then very freckled about a week after. I had no peeling or pain during the process. I had a few shooting pains last week, but started massaging and doing stretching exercises and everything has been great this week!
Enstagrl, I didn't notice any difference when I started boosts. Actually, my nipple stopped being irritated even though it was in the boost field. The boost field turned slightly more tan about a week or so after I finished. I finished everything on January 13. I'm still a little tan in some areas, but more than half of my skin looks normal color again.
I've read that the pectoral muscle gets a bit stiff and sore at three months when it begins to heal. Has anyone else heard of this?
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DurhamGirl, I'm with you on the sensitive skin. Today was my second day and, although I didn't expect anything to happen this soon, I'm still pleasantly surprised that nothing HAS happened. You might want to double-check with your RO about the goji berry juice--it's a pretty potent antioxidant, and a lot of ROs are opposed to antioxidants, thinking that they can protect cancer cells as well as healthy cells. My RO nixed my vitamin C and CoQ10. . . .
I have the following in my medicine cabinet or fridge: pure aloe, Miaderm (I layer those two during the day), Aquaphor (at night), and cabbage leaves (thanks for the reminder, HappyHammer!).
I saw my little fish in the aquarium this morning, and it made me ridiculously happy. It's the little things!
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KateB79...you're right about the goji. I was just looking at the bottle this morning and wondering if my RO would approve. I haven't actually started the radiation yet, so I have time to ask. In general, I haven't been taking any supplements and have even been avoiding green tea (my favorite!), at least in significant amounts, because of antioxidants. I sometimes feel that if I avoided everything that I hear I should avoid, I'd be subsisting on lettuce and bananas! Sigh... But thanks for the suggestion!
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DurhamGirl, during chemo I ate whatever I wanted; I thought of it as baiting the trap, so to speak. Now I'm back on low-glycemic carbs, quality protein, quality fat. It makes a big difference in how I feel.
For all: I've read some compelling studies on American Ginseng as a possible preventative for fatigue. I couldn't stomach it during chemo (literally), but my RO and I agree that I should try it during rads. Starting it today!
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Hi there - oh wow - how fabulous to know we're not alone in this! Please add me to this group.
I started rads on Jan 18 and have 33 treatments planned (eek!) - good to see there are a few of you on this list in the same boat. Had trouble with the positioning (I have back issues that make laying on that hard table a real struggle), but we seem to have sorted that out (I take Ativan for the port film days). I also am struggling a bit with nerve pain in my arm (left over from my surgery), which the arm holders exacerbate - have been prescribed gabapentin to help with this if I want, but so far I am just toughing it out as I'm trying to keep the meds to a minimum. No significant skin effects as of yet, but I'm at tx 13, which is still reasonably early in the process.
MY TIP: Make sure you take whatever time you need in your mapping session to get into as comfortable a position as possible for you, before they do the CT scan (i.e., wedges under knees, towels under head, different angles / heights for the arm holders, etc.). I didn't really understand until afterwards that I would not be able to alter / adjust ANYTHING about the position during the treatments, even by a smidge, and now I'm stuck.
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Happy Hammer -- Thanks for the reminder about the cabbage leaves. I hadn't thought about that for the itching and will definitely try it this evening before I go to bed. KateB79 -- Glad your first day is behind you. One more step on the journey. Your posts always sound like you are upbeat and I enjoy reading them. Biscuits -- How did your first day go? Lindab142 -- I'm sorry to hear you are having such difficulties at work. I started in a new position last July before my diagnosis and the people in my department have been super supportive and understanding since the very day I was diagnosed. My boss let me set my own flexible schedule around rads treatments so I didn't miss any paid time from work. Will say a prayer that your work environment improves. Marijen -- Thanks for sharing the article. Very good and very encouraging to read.
Hope everyone has a great weekend away from rads and finds time to do something special for yourself!
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etnasgrl - I had my first of 8 boosts today and the rad tech told me that the skin under my arm should begin clearing up so that's a good thing.
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I had my x-ray positioning session today in preparation for beginning rads on Monday the 8th. Got to "meet" the machine; looks like a giant, blocky version of RoboCop. Fun stuff. I'm having rads in the prone position; I kept my eyes closed and tried not to focus on the fact that my forearms and hands were going numb and that my neck was killing me. At least they provided warmed blankets!
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Welcome Morelandks! We're so glad you found us! Such an incredible group for support and sharing experiences. Thanks for posting and we look forward to hearing more from you soon.
--The Mods
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I join "Fearless" and who ever else finished radiation this week. Whoo Hoo!!! Done... Now the oral medicine can begin in a couple weeks. I was surprised that the emotions didn't take me over. I am feeling better now and hope it stays that way... I did have a Reiki treatment so not sure if my energy fields are in alignment now... ???!!! Keeping the rest in prayer as you continue with treatment.
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congrats grammy4 on being done. So exciting. Not sure how I will respond when I am done
Congrats on everyone completing the week and hope you can rest up over the weekend
I am saying 29 more to go instead of 6 weeks. It sounds much easier and 5 of them will be boosts
Have a great weekend everyon
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My mantra on the rads table, especially since I'm doing breath-gating and have to focus on my breathing anyway, is "I am well" on the inhale and "in every cell" on the exhale.
I'm already tired, but I think I'm fighting a cold, and I'm adjusting to getting up really early again (I'm on the table at 7:45, so I have to be up by 6:20, when I usually sleep until 7:45 or so). I figure two days of rads can't kick me into full-on fatigue, not this fast. Fingers crossed, per usual. I never, ever want to be as tired as I was during chemo, and I'm half-terrified that rads will make me feel that way again. Someone, quick! Jump in and tell me that won't happen!
I've joked before about writing a punk-rock song called "Gown Open in the Front." But it's ruined now, since the rads people want it open in the BACK. Maybe I need two songs. . . . The new one can be called "Sorry, My Hands Might be a Little Cold." There will be an entire verse about how freezing cold the bolus is around my chest, and how the techs (whom I already adore) call it my "armor."
Two down. Twenty-something to go.
Happy weekend to all. Enjoy yourselves!
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Linda, Congratulations on being done! My skin was a mess when I finished, but began healing pretty quickly. I used prescription that RO gave me, aloe and Radiagel that a friend gave me. The week after I finished I was very sore, but not so much from the burn; more like a heaviness in my breast. Also, I was much more tired the week after I stopped. This has been my second week without rads and I feel much better this week and skin is healing nicely. My RO said to keep using aloe, creams, lotions, etc for about a month after, so I have been doing that. I hope you will feel better soon, and shame on your co-worker! Karma' said bitch! Hugs, Patty
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Congrats to everyone who is done with their Rads ! Good Work !...and to everyone else....another week down....you can do this....Today was my 12th I have 23 more to go and I found out from my new RO the last 7 will be boosts....I was tired this week, and very emotional....I find myself so jumpy....but now a nice lazy weekend to rest and heal....breast only slightly pink and so far so good...wishing everyone a good weekend.....
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I, too, had my x-ray positioning session today. I thought I was scheduled for my first rads ( that's what the scheduler wrote down) but it is actually going to be Monday the 8th. I am having them done at the hospital that I work at, so it will be convenient to just walk down the hall at the end of my work day! It's a no frills room...nothing on the ceiling to look at and no piped in music. The techs seem pleasant enough and that's the important part and it will all be over in 6 1/2 weeks. I hope everyone has a restful and enjoyable weekend
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I'm on the same schedule as missv--i had number 12 today. I am definitely pink and freckled. My lack-of-boob is tight, and it's hard to get comfortable at night to sleep. I feel like I've been fighting off some bug all week... My throat gets sore but only at night, my head feels cloudy, and I'm so, so tired. Blech.
Kate, I was fatigued from the first day.
21 to go.
Congrats to all who finished this week, and wishing everyone a restful, healing weekend!
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I made it through 32 treatments (twice a day 16 days) and am surviving. Fatigue is settling in along with red itchy skin. I am so glad it is Friday and thankful for a two day break!
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I am so thankful this group exists. Thanks for the welcome. I will be prone for 33 treatments, 7 of which are boosts. done in time for Easter. I keep thinking rads during lent, how appropriate. By Good Friday I should be celebrating!
adarkadaptedi and Biscuits: We are on the same schedule. I start 7:15 Monday morning.
Anyone have experience with prone position and side effects? I wonder if over time it will be painful for my breast to hang during treatments. Also, I sleep on my stomach due to back injury and wonder if I'll be too uncomfortable to sleep.
Congratulations to all who are now through this!
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