Summer Rads 2014
Comments
-
You can add me to the list of those starting rads in July. I meet with my RO on July 8 and expect to start about a week later. Don't know much more than that. I worked throughout chemo, missed a couple of days following surgery and expect to work the entire time I do radiation. My plan is to get a first up appointment if possible or do them a lunch time. I am so ready to get this done!
-
Sunshine, Thanks for the info. Mine is already so, so sensitive. I can't even have the seat belt going over it. Looks like it was going to be hit with either set up, but the new one is going to be a little more invasive on that area. Working on courage.
Missing, yes I use aloe, aloe, and more aloe. And I use emu oil that also has aloe and calendula in it. My RO told me my last visit that whatever I was doing to keep it up. I just have a little sunburn under my arm and a little tanning but it really looks good. And only 1 whole breast tomorrow. Yeah!
Anyone have any stomach issues. For about the last week I have been feeling like I'm bloated, and a little upset. No change in diet. Fatigue it me hard yesterday, why is it always on Sunday . . . . LOL .. ... slept an hour in the afternoon. And stomach being a little upset went to lay down about 8:00 woke up about 11:30 turned off all the light that everyone leaves on, went back to bed and pretty much slept until my alarm went off.
-
You can add me to the list of those starting rads in July. I meet with my RO on July 8 and expect to start about a week later. Don't know much more than that. I worked throughout chemo, missed a couple of days following surgery and expect to work the entire time I do radiation. My plan is to get a first up appointment if possible or do them a lunch time. I am so ready to get this done!
-
Been off for several days as I had my wedding! Such a wonderful celebration AND I came away with a major beauty tip!
My white hair was still sparse on the top of my head, the girl who came to do my makeup brought an aerosol can of dry shampoo. She sprayed it in my hair and it remained as a white powder and filled in my hair!!! If you have white hair, this will work for you too! This shows a before and after.
I am now 3 weeks PFC and start Rads end of next week! This was a good break!
-
Good idea, I will try it. My hair is white and very thin but it might work.
Dee
-
jb, YOU LOOK FABULOUS!!!!! Love the white hair. Congratulations!!!!
-
I am seven week post surgery and reconstruction. I was supposed to get my set up done this afternoon followed by my first treatment. I waited over 90 minutes beyond my appointment time before I was taken to the room. My RO wants me to do the breath hold because they are radiating my left breast. The breath hold entails breathing through a tube in my mouth, a nose plug on my nose, and goggles to be able to view a computer screen. The set up x-rays took one whole hour during which time I was not supposed to move whatsoever. After an hour of agony, the techs claimed that I had moved, and therefore, the set-up had failed, and I will need to do the x-rays tomorrow again. Looking through the Discussion Boards, most folks find very little trouble with the RADs, but I feel that I am set up in a torture chamber, and I have not even begun treatment. It was such a dreadful experience today that I almost do not want to return tomorrow.
-
JB Congratulations!! You do look fabulous!!
I had a short vacation before starting rads last week. 5 down 28 to go. Got the OK to swim in a tee shirt and was told just to use only the elta lite the RO gave me for now. I actually like going (so far). It is very cheerful there. I was lying there today and Lucy in Disguise came on their sound system. I could only tap my toes but so wanted to MOVE!
Also found a new electrician maybe while chatting in the waiting room! I am sure I will feel quite different a month down the road when I am red and peeling.
That Toms of Maine deodorant is not so good but I guess there is a problem with aluminum with regular. My husband is in charge of laundry and I apologized for the huge volume. Everything except pants is only good for less than a day especially in the warm weather!
Have pretty much given up on a bra for now though so less of them in the wash..
Rettemich - The nurse suggested seatbelt pads. They have them on Amazon really cheap so that may help. I think I will try one.
-
M_Mah, you are not alone. My rads have not been pleasant. It takes a very long time for the techs to set me up. Simulations lasted more than an hour. I was spending countless hours waiting in the waiting room for my turn on the table. I was miserable. The ladies on here encouraged me to speak to a manager. I did, but after a week and half of torture. I don't have to do the breathing thing, but I have to have a bolus applied which is wet towels placed over most of my chest and wrapped around my side. It starts off nice and toasty warm, but quickly gets cold and by the time it is done, I'm wet, cold and shiverring. I spoke to a manager, had my appointment time switched ot the first one of the day. That eliminated the waiting around bit, but my set up still takes a great deal of time. It is painful for me to keep in the position for so long, but I keep thinking I would rather they get the machine lined up correctly than deal with dire consequences. I just wanted you to know you are not alone. Wishing you the best and hope it gets better!
-
curlyq and M_mah....you poor things!! I couldn't imagine having to go through that...maybe the techs are new at both places?? I hope it gets better for both of you! Rosie
-
curlyq and M_mah......wishing I could share my techs with you, my treatment only lasts about 10 minutes from when I walk into the room and then walking out. They use the rubber bolus and I hold my breath but nothing like you describe. Hoping this gets much better for you both.
Just finished #10 out of 30, the skin is starting to turn pink/darker, especially under my arm. I've only been using the aquaphor and aloe, what does emu oil do?
-
M_Mah, You are not alone. I also had a nightmare of a setup. I didn't have to hold my breath, but the techs were just so unprofessional. Another nightmare when they set me up for the boosts. I had only one tech but she was there at my original setup. She asked If I remembered I replied I remember it being a nightmare. She was MUCH more attentive this last time. An hour is too long to be laying there. Ask that the supervisor be in attendance. Keep us posted.
curlyq, wish I could just give you a big but gentle hug. I often think there has got to be a better way. Sending (((((((((Hugs))))))))) to you.
I am suppose to talk to the RO today about the boosts. Since she never even said a word to me when she was there in the treatment room for my 2nd setup for boosts. I don't quite understand how this is going to work. My clips are around the 7:00 position but they are going in from the 11:00. I know part of it is I was unable to tolerate the compression, but for a short beam seem a long ways away.
-
M-mah - that sounds awful! My breathing consists of taking a deep breath and holding it. No tube needed. My sim was much shorter, and I didn't have to lay still the entire time like you did. Who is able to be absolutely still for an hour? Probably no one! Can you maybe find another rads place? Yours does not sound very professional or caring.
-
Had #1 of full breast yesterday. The techs were great. It took some time since they did xrays and took pictures again. They said today should be much less time. I noticed lefty is pink this morning.
Which makes me concerned since this is only 1 of 16 full breast. I ordered a swim shirt last night, thank you everyone for the encouragement. It will be here before the 4th. I had visions of looking out the window all day at my family frolicking in the pool without me. At least this way I can join them for a short time, with a hat and in the shade. Hope everyone has a great day.
-
WOW!!!! I can't believe the rads experience that some of you have gone through! Compared to yours, mine was quite easy. The first sim was about an hour (didn't think to time it) without moving and holding my breath at certain times. They did the boost sim a day before scheduled do to someone cancelling their appointment and having the time then. No breath holding and it only took about 15 minutes. The RO was there, but I could only hear his voice. Mondays were x-ray days to check for positioning and Tuesdays were RO days. "How are you?" "I think I'm doing well." "Your skin looks fine. Keep doing what your are doing. See you next week." and that was it. The techs were personable yet professional. All in all, a good experience. Not what I had anticipated. Better. Wish others could have been treated at my facility.
Wishing everyone a good week and a great weekend. No Friday rads! (Why are treatments every day, but not weekends or holidays??)
-
I am so sorry that some of you are having such a bad experience. There is no excuse that everyone can't get the same standard of care. Some things like cancer are not fair and that sadly is just the way it is but unnecessary distress during treatment does not seem right in this day and age. Apart from the arm hurting a bit (lot) in the 20 minute set up I have been in and out in 5 minutes. I feel fortunate and very guilty that my insurance (nothing special) actually allowed me to go to Shields that also does MRIs (separate facility I think) for the New England Patriots football team not far from where I live. They have a signed shirt in the waiting room so its all a bit surreal. They keep saying they won't let me burn but we will see. Its only been 6 days plus simulation and they recon I may notice some "changes" after about 12 sessions.
There is a mole right next to my breast but apparently the kind of radiation we are getting does not cause melanoma. I told the RO that it would be a pity to be treated for breast cancer only to get that but he said that although there can be issues 20 or 30 years down the road, melanoma is not one of them.
-
Ohiofan I wish they could come to my facility too!
I'm very happy to say that my team at rads is spectacular. I have burned and it's something they could not avoid. I do think that perhaps my treatment there may institute change in wound care for all of their patients. We have an amazing wound care center in our town, I have taken my father there several times for wound care. I told my RO a couple of weeks ago that cancer treatment was just barbaric and that anything and everything should be done to minimize physical discomfort caused by radiation burns. I sometimes don't think they realize the physical pain we suffer. Today, was,"see the doctor day," and I was VERY happy to hear that they had consulted with the wound care doc about what else they could do for me. I have refused pain meds (which they use quite frequently to control pain) and told them we would need to heal the issue and not just mask my pain. I left there today, pain free. They used something called mepilex dressing over my burns. It literally stopped hurting immediately. So today, I'm thankful and I just hope it holds thought the night!
I only have 5 more boost. So yes, I'm getting excited!
-
Started rads today...scheduled 30 and 3 boost. If you are nervous, FORGET IT. it was nothing...Now it might get more exciting later, but the actual treatment was nothing. 6 minutes of nothing. Yeah
-
Iglodie, and all those just starting or about to start- rads starts out very easy. I got sudden fatigue at about the 20 th treatment. I suspect the new computer upgrade at my office and the mass confusion the 2 days that was started added to the sudden onset of fatigue. Really looking forward to a 3 day weekend. Just plan on extra rest by the halfway point.
Sunshine, count down those days. I have 10 left, 5 reg and 5 boosts (no compression). I a getting some mild redness (more then the pink before) on my clavicle area, but no pain. I will remember about the mepilex dressing if I get in any trouble.
JB fabulous look for your wedding. Bumble and Brown ( or something like that) makes colored powders that you can put on your scalp to cover thin areas. They have white also.
-
Sunshine, Oh I am soo happy that they followed up with a wound specialist. Funny you should say you thought radiation were barbaric. I've touted that ever my mom went though it. Granted it was several years ago but it gave me nightmares, seriously. Any kind of radiation or chemo is just barbaric. Where's Bones (Dr. McCoy of Star Trek) when you need him.
Igoldie, your right, usually the treatment itself is no big deal. It's all the junk that goes with it.
What is everyone's plan for when they stop rads. Detox, getting strength, energy back?
I have an appointment to see an Integrative Oncologist mid month. I was trying to get in after I started rads but it got screwed up. I'm excited, so I don't want to waste the chance. I'm trying to think of anything I can to talk to him about. I don't want to forget anything.
What would you ask if you had the chance?
-
Had my followup mamm today and all was good!!! Whew! One less stressor out of the way. I got my CT planning session scheduled for 7/8 and anxious to get it srarted and rads completed!
Sunshine- awesome they found something that worked for the wound pain. I'm noting that in my book of good treatments to remember!
lgoldie and crazywabbit-keeping my hopes up my sim goes well and rads as well!
-
Rett I'm not even sure what an integrative oncologist is! Cancer treatment is barbaric! It's necessary and we often just say yes.. yes.. yes... to our docs. I finally just had enough. It was probably a combination of tiredness, tamoxifen and pain and my old personality came out. lol. I have a serious, "no nonsense, let's fix it" personality. It had sorta of disappeared during the last 3 months. It felt refreshing to see a bit of the old me pop back up.
Barbara... you're getting close too! Hang in there. These last 10 have kicked my butt. Just take care of yourself.
Mripp I'm sooo glad your mammo was good!!
-
Subshine, glad to hear that your nearly done with rads and that they found something that works for your burns.
Crazywabbit, There is nothing like a computer "upgrade" to increase confusion and fatigue, the absolute last thing you need right now!! I am dreading the 2 weeks of computer on call that is scheduled for around weeks 3 and 5. My mind feels like mud, even with no chemo. Its like my brain and body have decided to slow down, and tasks that should take a day or 2 are taking a week or more. All I want to do is edit my photos for relaxation When I was diagnosed I did a piece of "artwork". Now I think its too pink and sugary and cancery (if thats a word) but I am taking it to the rads people as they are so nice. I secretly hope somebody will like it but of course I will tell them they can just put it in the closet or throw it out if they dont!
The photography is a great escape and distraction . I just ordered a home studio - lights and a backdrop. Goodness knows where I will put it all as our house is very small!
-
Mripp. great news on the Mammo!!
Sunshine, I think I know what you mean by your regular personality disappearing for 3 months. I am usually a high stress kind of person, but something is different at the moment. For me it is not necessarily a bad thing. I mentioned dreading the oncall. it usually terrifies me but now I am "worried" because I just don't care, just want to keep my job for the insurance until I get through this.
-
Iyzz I so understand what you mean. I've always been a high stress type too. "Anal" as my husband calls me! I never left the house without my hair and makeup done and the house had to be spotless. Today I went to rads without a bra and makeup. I also went to the store... and the bank lol nobody seemed to notice! The things that used to be so important just aren't anymore. it's like I'm just trying to muddle my way through. I agree, it's not all bad!
-
izzysmom, would love to see so e of your artwork and photos. I have just started color me your way coloring books recommended by Robink from another forum. They are detailed beautiful pictures to color using colored pencils or markers. It has actually been relaxing.
Sunshineink, I understand how the perspective changes, I feel the same way
17 down, 17 to go. Half way through, but still so many more.
-
Rett, what is an IO?? Enjoy your artsy side. It is nice to have a relaxing outlet.
I received a "Certificate" at the end of rads......just like kindergarten! Kind of silly, but I liked it.
Wishing everyone a great weekend! I get to see my 16 month old grandson!!!
-
Lisa, My late mother in law used to do something similar where she would color using paints to produce some lovely pictures. Art, whether it be drawing, painting, photography is so relaxing and theraputic. One lady I work with does wonderful quilts. I was never good enough at painting but always liked taking snapshots but only got a good camera a couple of years ago.This is the link to the thumbnails on my NatGeo Gallery. right click and open in new window should work. Not sure if it will work from here. I have not posted on there for a few months. I started a photography course so some of the photos are a bit weird. Originally I took birds and nature and sunsets mainly. I look at them now and most would not pass muster with my photo teacher but I don't care. I feel bad as things started getting overwhelming and I need to get back in touch with my photo friends. We had a nice community on weather.com but they messed with the website last year and some went to flicker and some to NatGeo. Some of us tried to do both and it all got too much. Then with the diagnosis and surgery and everything I have gotten out of touch apart from my course, and a few photos I have posted on this site. I am still taking lots of pictures though. The latest are farmers markets!
http://yourshot.nationalgeographic.com/profile/359...
This is the pink thing...
-
That was scary . I just got banned. The system threw out my post until a human checked it. I guess the thing to do is just to describe where to go, not to include an actual thing. Not mentioning the L word again for a bit LOL.
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