MARCH 2010 Rads Group
Comments
-
Denise, so sorry for your family's loss. I am sending prayers for peace to you.
Raili, i have 2 tattoos (not counting the ones I got for rads) and yes they hurt! The one I have on my ankle was the most painful. And no lidocaine, you just grit your teeth and bear it.
I finished #5 today. I haven't noticed any effects yet, but my tech said I probably won't notice anything until about week 3. I'm glad to get a little break from feeling sick and tired!
Peace,
Shelby
-
Just finished 2nd week of rads (too many to count the days, 33, so I count the weeks), and just some redness but it doesn't feel uncomfortable.
Raiii, rads have been easier than wire localization before lumpectomy, dye injections (mri and sentinel node), biopsies (stereo and mri-guided), and lumpectomy -- at least so far -- so nothing to fear.
Asked tech. when folks really start to "cook" (I know, not very pc but I wanted to make light of a sucky situation) and she candidly said that usually 3-1/2 weeks into it. So here's to looking forward to next week, which'll be week 3, and not so much to the remainder.
Good luck everyone and have a nice weekend!
-
Happy Friday everyone. So glad the weekend's here. I have finished with week 1 of RADS and am happy to cross it off my calendar. Only 5.5 weeks left now. I feel a real sense of relief knowing that the time will pass quickly. My mom flew in to visit me, and will help out as the fatigue starts in. I hate to say it, but I am feeling it already and I am at the end of week 1. Someone else described it perfectly.... it's a dull, slight fatigue starting around 7pm. I have been going to bed very early as well (for me-- around 9pm).
Hope you all have a wonderful weekend. Sending peace and good wishes to all of you!
-
I'm just a newbie to this. Have radiation appt in a week for set up, simulation and whatever else they do. Are estimating a 1.5 hr apt. What I'm wondering:
1. Are you cold being half naked during the radiation treatment?
Also, rad. onc at first discussion talked about the holding breath technnique to keep heart out of radiation field.
2. How long do you have to hold your breath? How many times do you do that in a treatment session? How long are the sessions?
I'm sure he will answer my questions when I go on the 29th, but meanwhile I'm searching for the answers.
-
Hi All!
Finished #15 out of 28 yesterday and still the skin is holding up. It looks like a tan on my chest so it's not too bad!
I don't have any lines like some of the later ladies described but my radiation field is quite large - from my neck (just under chin) to my ribs and from mid chest to shoulder blade.
As for holding breath - I asked my techs and rad onc about it and they said not to. So I am thinking of my happy place and breathing normally while I lay there.
Yes the room is cold but they put a sheet over me after they've marked me up and that helps.
Sugar I bought some undershirts at Cosco - Calvin Klein I think. They don't have any shelf bra but are more like "wife beaters". They are very comfortable to wear and when needed I wear my bra and prosthetic over the undershirt.
I have tried wearing the ones with the shelf bra but the elastic bugs me now.
Those of you that can still wear your bras are so lucky!
I'm going totally braless most days - I did try wearing my no underwire bra with prosthetic directly on my skin in the early days of radiation but the band of the bra was very irritating and I didn't want any blisters or breaks on the skin. So now I go braless or wear the understhirts.
I saw the rad onc before my radiation tx on Thursday and told him that my jaw clenching was easing off but I was still having trouble sleeping (now I'm waking up to see if I'm clenching or not!) and I'm still feeling stressed. He suggested that if I wanted I could speak to a counsellor. They have them at the place where I go and it's free. I told him that I am doing ok - have a great online support group and lots of friends to talk to. Besides adding another appt to my schedule would only increase my stress!!
So he gave me some Atavan to help me sleep better and help me relax before bedtime. When I went into the treatment room the techs read my report and asked me if I needed the atavan for the radiation treatments. I told them no that the time I spend laying on the table for radiation is the most relaxing of my day and I needed the atavan because I have teenagers!
My husband said that if we can get the kids to take the Atavan then I wouldn't need them!
Well I'm refilling my hot tub and doing other "spring" stuff around my house - better go check to make sure it hasn't overflowed!
Later...
Marie
-
Marie - I bought a three-pack of Calvin Klein tanks last week at Costco so I think these must be the same ones you got. You're right, they are very comfortable. I slept in one the other night, I used to clench and grind my teeth at night so I got a night guard custom made through my dentist a year or so ago and it really helps. I now can't sleep without it. I often take an Atavan to help relax me for sleep...it really helps! My rads onc says I can't go in the hot tub during treatment so I'll have to wait to use mine for a bit. Are you using your's during rads or just refilling it?
Sherri
-
Sherri - no tub for me during radiation either. I'm just doing the grunt work today!
-
The countdown to my Monday start date is getting close. Eeeck! I'm a wreck this weekend. I did go out and buy the sofest wireless bra, and a tight camisole without the shelf bra in it. Hope one of these works out. I've never been comfortable without a bra.
I also planted some seedlings - I'm no gardener, but I love to watch things grow and thought it might be a good mark of time. By the time I'm done, the seedlings should be outside and ready to thrive.
-
My first radiation day was horrible.
It wasn't EVEN radiation...it was the simulation, where they just take films. But 15 mins before my appointment, while I was eating lunch in the car, I cracked a tooth - for the 3rd time in less than a year and a half. I have already had 5 root canals (and I'm only 31), and the thought of having a 6th - in the middle of radiation treatments, no less - made me just start crying. I ended up crying all the way through rads, partly because of my tooth, and partly because I just hate being there, hate the machine, hate having to get burned on purpose. I'm feeling bitter because I never had any pain or symptoms from the cancerous tumor and had probably been living with it for years, so happy & healthy & oblivious. And now, it is only the cancer TREATMENTS that make me feel awful... and that makes me resentful. I know that's weird and illogical, because had I left the cancer untreated, it would have eventually caused pain and symptoms. But illogical or not, it's what I'm feeling right now...So after I cried my way through radiation, I got home to find my landlord waiting in the driveway so he could verbally attack me over things that are not at all my fault. I gave him 5 weeks' notice that I was moving out, in order to move closer to the hospital where I'd be having my daily radiation treatments for cancer, but he is so heartless he doesn't care - he's now trying to evict my roommate and blaming it all on me, threatening to not give me my security deposit back after I move out unless my roommate moves out, too, despite the fact that I've never done anything wrong and I have an email from him from last month saying "You have been a good tenant." So why he flew off the handle at me yesterday, I have no idea. I was already so beaten down from the cracked tooth and radiation that all I could do was run into my apartment and cry some more.
-
Hi,
I just joined the forum yesterday but thought I would share my experiences and hope they are of some use. I finish my RT treatment on Tuesday March 23rd, after 36 sessions (which includes 6 boosts). I was lucky that my skin turned lobster red (my skin NEVER tans) and had some slight peeling under my arms which has started to get uncomfortable in the last couple of days but luckily I didn't get blisters or open wounds.
I got a couple of yoga bras which are made from bamboo and they are really comfortable. I did try the vests with built in support but I was told they were too tight and may cause problems as the seams were leaving marks around the area where I would be treated and that could cause irritation.
Once my skin started to go red I used Biafine which was recommended as being excellent and I believe it has helped a great deal.
As for fatigue I never really experienced it, I have got more tired during the last week but up until then I was fine. I do however start work an hour later but I still make sure I exercise for an hour every evening after work and that helps with the tiredness.
Julie
-
Raili et al.,
A nice walk and one day at a time attitude are excellent!
A couple of points that I hope will help:
1. Radiation is generally a bad thing to be exposed to, but ... it really can be effective against cancer. It splits DNA bonds and kills cells. Normal cells are quite good at repairing themselves but cancer cells cannot get their act together. Even if they try to mount a repair effort they cannot sustain it over the whole course of treatment, so the radiation kills off all kinds of cells but the normal cells can regroup and repair.
2. If that does not help, go for escape. While you are lying on the table try meditation, visualization, or prayer, whatever works for you. Music is good, too, on an ipod or your own CD on their system. Just make sure it does not have a beat that makes you want to move your body. Think Bach, debussy, Mozart, or New Age. During the simulation (which is much longer and more difficult than daily treatments), I visually travelled to many of my favorite places and along my favorite bicycling route. When the rad onc and therapist came back into the room to start marking I felt like I was travelling back from far away.
-
Redsox - great advice! I start rads tomorrow at 10:00 a.m. and am nervous, too. I will try the escape methods you mention. Do they allow iPods? If so, I'll be sure to take mine.
Good luck tomorrow everyone!
Sherri
-
Hi all
Railli- I totally relate to your tooth pain, feeling plagued by the fact that you were happily living your life while a breast cancer is growing inside, to only have side effects through the treatment. It's really like a big kick in the teeth to be told (after you've been living a clean, healthy life for many years) that you have breast cancer. I eat "clean", buy organic as much as possible, breast fed 3 babies, exercise like a nut, and generally embrace good living. So, yes, it's a big letdown to find out that the treatments will cause undue stress. I consider this time my sacrifice for a healthier future. I do freak out about it coming back, but have to try to keep myself in check. They found it early, the docs will treat me, and I will be back on my feet. As for the landlord, he can shove it. That's the least of your worries right now, and hoping you don't let it get you down.
Redsox- like your visualization idea. Whenever I get blood drawn, I think of my eldest son when he was 2 years old. I must have taken him to the park one day, and he ran around, giggling, looking back at me. For some reason, that image sticks with me, and it's my "happy place."
AndreaS- good idea on the seedlings. Best way to mark the time while it passes. Hopefully it's something organic you can consume when it's all over.
Sugar77- Are we not supposed to wear underwires? I forgot to ask that of my team at my hospital, but I've been wearing mine. For the first time, my left breast really didn't feel good on Saturday night. I've had 5 rad treatments, and I wore a shirt to sleep in-- it was chafing me, and it was really uncomfortable. I might have to get an undershirt that's really soft and clingy to help with that. And, potentially bras that don't have underwire!
I joined an organic co-op and got my first shipment of organic,locally grown produce yesterday. Mind you, I am so tired today that cooking it isn't the first thing on my mind, but I am going to enjoy finding recipes and eating all the veggies. Eating even more clean is one of the only ways I've been able to feel "in control" during this voyage.
Whew, okay, so need to lie down and rest a bit before my kids come home from a bday party..... so I can cook up some of my vegetables!
MaryAnn
-
Good luck to all you ladies starting rads tomorrow, I will be thinking about you and waiting to hear how it went......we are all in this together I am only 2 treatments ahead of you gals! Friday I was in and out of there within 10 minutes......
-
Sugar,
I don't know if they all allow ipods but they do need you to relax. Just tell them you are nervous and need the music to help you relax. That should be enough.
-
I'm not sure about the ipods either - I think I read somewhere not to take your electronics into the treatment room with you. Sorry I can't remember where I read it...
I've been taking my cell phone in my purse but one day last week after treatment I noticed that it was having trouble and was showing a clock on a black screen. I pulled out the battery for a few minutes and it eventually reset itself. Now I leave it in the car or make sure it is turned off when I take it into the room with me.
Not sure if the radiation would affect your ipod. Maybe take it with you just in case you can use it and ask one of the techs first.
-
I think I'll pass on taking my iPod tomorrow. I know my Blackberry didn't work in the waiting room right outside where they did the simulation so I'm assuming it's the same deal in the radiation room with electronics.
-
I think I'll pass on taking my iPod tomorrow. I know my Blackberry didn't work in the waiting room right outside where they did the simulation so I'm assuming it's the same deal in the radiation room with electronics.
-
Thanks for the info and advice, Julie and redsox.
MaryAnn, thanks for all of your support/words of encouragement! I'm like that, too - I was vegetarian for 9 years, eat lots of organic/local veggies, do yoga and exercise regularly, never smoke/drink/do drugs, maintain a healthy weight, get plenty of sleep, laugh a lot, have a great social network, use natural bodycare and cleaning products, ETC... STILL got cancer. I try not to go the "WHY MEEE?!" route, because it's pointless... can only move forward...one day at a time.
I love your "happy place" idea...
As for comfy undershirts/bras, I recommend WinterSilks - I just got two silk camisoles for about $16 each, which I think is a great price for silk.
I'm tempted to try bringing my iPod tomorrow, but I don't want it to break for anything...yikes.
Sugar, I'll be thinking about you in the morning, too...we can do this!
-
HI ALL
Well i had it today , my first time getting zapped and MARY I'm on my back i was on my back when they tattooed me with my hands over my head which for me is comfy thats the way i sleep ,Does any one else feel little zappy tingles in the area where they are zapping or is it just in my head and for about 2 hrs after thati have strange feelings in my boob .
When i was finished and getting ready to leave i just wanted to cry and when i got into my car i bursted into tears and had to ring D/H ,its in the same building as chemo was in so that bought in some anxiety feelings, i think that didn't help ,and the fact that ive had 6 weeks of since last chemo, and i was going along not even thinking cancer thoughts then hello I'm back in that same building, buggar . .Also when do you start putting on the cream do i start now, or, when I'm starting to go red all they gave me was sorbolene cream ,what about corn starch ,and alovera gel ,i just had Thia for lunch and a chockie yum that cheered me up .
JOJO
-
Hi girls - Good luck to everyone who is starting and for those who have started I hope the week goes by fast. I have had 8 treatments so far. The center I go to has a no-cell/no electronic policy sign in the waiting area. My breast has a "sunburn" so far. My oldest daughter was home for spring break and said Mom your getting so mauch color while your walking - as soon as she said that she realized what she said. I ended up going on Cipro for a breast infection. The doctor said its not a radiation side effect but the radiation probably brought the infection to the surface, it was probably there already. Who knows. Have a great week to everyone.
Kathy
-
JOJO sorry to hear about your tearful first time - once you get going you'll see it really is much easier than chemo.
As for putting on the lotion - I was told to start right away.
For those that haven't started yet - put on your cream before you start! Not the medicated cream but something over the counter like lubriderm (that's what I use), Keri Lotion or Glaxal Base.
Happy Zapping to All!
-
Hi, I was on the Jan thread but then couldn't do rads because my incision didn't close. It has taken 2 months for it to heal up so I could do rads Now I am 8 down and 25 to go, last three being boosts. So far no trouble at all. Yes I do feel the tingling during and after the treatment. My breast is definatly warmer than the other side but cooled off over the week end. I had blood drawn last monday for cell count and will again half way through and again at the end. Also will see onc and nuse each monday. Radiation still scares the heck out of me but I also don't want a reaccurence. I worry about lymphademia and the fact that they cannot miss you lung completly Hello to every one on this thread and I will be keeping up with you all through this phase we find ourselves in
Flo
-
Welcome Flo and sorry to hear about your delay in starting, that must have been really frustrating! Welcome Kathy and Raili as well.......Raili I am so sorry to hear all that you have been through hopefully this will be pretty easy for us after the initial shock of it all.......and as for the landlord (tell him to go to hell)!
I too felt the warmth on my breast and the sharp pains after the 1st treatment for many hours after. But on the 2nd treatment I felt nothing and the breast wasn't hot to the touch wither......very strange how that does that and to me that is when this really sank in how awful this whole thing is......I have been fearful of this from the get go, but after the 1st treatment and to feel that way so soon, how FRIED! I started to get a headache that lasted all day after the first 2 treatments and I was headache free on Sunday so lets pray this was not rads related as I cannot go through that everyday as the head never got better at all!
Good luck to all the ladies today and let us know how you are feeling!
-
Hello Everyone.
One more to go for me then done. Long weeks for sure but still standing!
Keep the faith everyone and soon enough you will be where I am and I wish you the very best.
hugs
-
Fan - so close to finishing - great news!
I start boosts tomorrow. I will miss the technicians that I had for the last three weeks, but I'll be sure to have a 'proper' goodbye with them next week. They made it a lot easier.
-
Had my first treatment today. It went suprisingly fast. I was in and out of there in 15 minutes. I did feel some slight warmth after the treatment, but not real bad and it subsided in a few hours. The oncology nurse told me to use Vitamin E oil and Jeans Cream which I dutifully put on in the changing room right after my treatment. I will use this, and the 100% aloe gel, 3 or 4 times a day and HOPEFULLY won't get too fried. We shall see. Only 29 more treatments to go! Good luck to everyone :-)
-
Thanks C2will. Yes the RAD "team" I have had are amazing and the other patients courageous in so many ways. I am involved in a clinical trial also here in Ontario that is Canada wide so will have lots of followup for a good time to come. I was pleased to meet the criteria for this trial to pass on just a little of this experience to future RAD treatment/ breast cancer women.My 25 year old daughter is now high risk so that in itself motivated me to take part also. Have a good day ladies.
hugs
-
Hi everyone - I had my first treatment today. It went well. I was a bit nervous at first but the technicans were terrific. I was on my back with my right arm above my head. I was told to put Glaxol based cream on two to three times a day. I'm going to put some on now.
Fan - are you doing the short twice daily for five days treatment? Or are you in the long arm for the standard length? I was offered the trial but in the end decided just to go ahead with the whole breast radiation.
I think I have 15 more regular treatments and then 5 boosts. The countdown is on.
Have a nice day ladies!
Sherri
-
HI Sherri,
I got the long arm after the computer randomization ~I was hoping for the short though.:)
So 25x and had no chemo though as negative for ER,PR and HER2. Did a resection and then had to have a re-excision but that produced a great path report so worth the second surgery.
Compared to some here and those I have met in various waiting rooms not so tough for me.
Bad burns though this week and quite a bit of pain but tolerable. Iching like crazy!
You are getting there Sherri.............I was so happy when I hit the single digits~little mind games to keep us going help! In less than 24 hours I am done with treatment.

Stay positive as much as you can everyone!
Karen
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team