August 2011 rads
Comments
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Thanks again everyone. I appreciate the support.
My tattoos are very small also. So small in fact that I have a sharpie mark and tape near 2 of them so the girls can find them. I have 5 because I am having rads in the prone position. All 5 are on my back, nothing on the front. My RO refused to treat me without them. I tried very hard not to get them.
I asked to see the skin nurse today. I have a small rash in an area that has had years of sun exposure near my collar bone . My nurse and I discussed possible problems that could develop this week during our appt last week. She said if I started with a itch, I should see her. She gave me a prescription for SYNALAR 0.025%. It works great. I won't have to worry about scratching while asleep tonight. I had #12 of 25 treatments today. Today/tomorrow are the half way marks for me. Good energy today.
Good luck at the RO tomorrow luckygmrabb. You are starting your final phase.
IRW333 now that you have started rads, you will be getting some of the best sleep of your life! Enjoy the sleep like I am.
Sweetcorn-I am very sorry about your dog. How much more can we handle?
Pat- Things get so much easier once you have a few treatments. You might actually start to enjoy activities in your life that have been on hold do to breast cancer. Just hang in there.
I also agree with everyone that exercise can help with the fatigue but over doing it will set you back. Walking the dogs (1 dog now) does help.
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Had day 2 of 32 today. Interesting, the doctor wanted a couple areas tested for the dosage I'm getting so they attached wires in 2 places. I guess tomorrow they will check two more areas. At least I know he is checking everything carefully! Feeling good. I've got to get the eating healthy and exercise back on track. Thinking of yoga tomorrow, I miss it so much so I'm hoping I can make 2 days a week and then something else on the other days.
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Hello ladies, I have been distracted in the best possible way for the last couple of days. To answer your question Sweetcorn I am in California gold country, renting a house on Lake Tulloch for a few nights with my family and dogs.
To BB26, and I guess Sweetcorn too, I'm so sorry to check in and see your posts about your dogs. They sound like very lucky dogs to have such loving companions.
Well, you've all zoomed ahead of me...I'm mapping on Friday morning. My only concern is that I seem to still have redness and lumpiness from the surgery. I have been alternating hot and cold to try to reduce it as much as possible this week. Does anyone have any tips?
As for the tattoos, I will pass along what a dear doctor said to me some years ago. These marks and scars are your badge of honor for bravery on the battlefield.
Good luck everyone, I wish you all easy rides!
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Welcome Pat H and others!
BBC and Jane so sorry to hear about your dogs, I'm sending heart healing prayers your way.
My start is pushed out to next week, so 0 of 30. The RO returned from vacation today and agrees we can wait for the BRCA results although she also believes it is likely to come back negative - 90%.
Our weekend away was great, I almost forgot about everything here. We kayaked across Scott's Flatt Resevoir, it was so beautiful and my boobie didn't hurt, yeah! The luau Sat night was corny and fun. The boys played flip the kayak until they were exhausted on Sunday. Only boo boo was I must have been in the sun in my vneck t shirt and got sun on my chest - yikes! I thought I had SPF 70 on all the time. Hopefully that will be all better by Monday. Any suggestions?
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SAB - Gold Country, you're a stone's throw from here, I'm just east of Sacramento. Are you local or did you travel far to get here? Enjoy your time at the lake. Cheers!
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Hi Sharon_W, I live in Santa Cruz so we travelled about 2 1/2 hours. First time here, and I just love the lake. I'll wave to you on my way home
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Going for #11 this morning at 7:20
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Had my dry run today. They lined me up with lasers, then did some xrays, then drew the outline of where the radiation field would go on my chest with markers, then took pictures. She said the markers were just a visual reference, as the actual mapping was done on a computer. It was a really quick appt., and so I start tomorrow with the real thing.
I'm pretty tired today, didn't sleep well the last couple of nights because of worry. But I wasn't as anxious at the appt. as I thought I would be. The good news was I qualify for the Canadian protocol, so I will have 16 regular zaps, then some boosts, how many as yet undetermined.
Do you start putting cream on right away, or wait for pink skin? They didn't mention anything about it yet, and I will need to go buy something.
Pat
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Actually, my RO this morning, after five treatments, said not to put anything on the affected skin until you need it. He said that when you rub the lotion, cream or ointment, it gets rid of skin cells that can help protect the skin. This after I followed the advice of a friend/survivor, who said slather the stuff on! Now I will wait until I see any changes.
Jane
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My RO also said to wait to use creams until they tell me I need to. I expect to start next week (pending BRCA test results being negative
Merilee, I LOVE the image!
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A little pink starting here on #11
Sharon, I would not have gotten through chemo without imagery
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Hey all! I had my consult with my RO today. Looks like I will be starting rads in a couple of weeks. I am scheduled for 25 full breast rads and 8 boosters. I am still not excited about this 5 day a week thing, but at least I now have a plan.
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neece, pat, any others - I am sure you'll be feeling much better now that you're beginning (will be beginning) your treatment. I know that I felt much better once I got started so that I could quite worrying about it.
This must be the week for equipment issues. Apparently there was a power surge or outage last night that shut the whole system down and they were having problems getting it to reboot. No computer equals no treatment. So, I was there for about 2 hours this morning while they tried to get it going but to no avail. Came back this afternoon and was able to get treatment #3. All is well though because I got to spend some time talking with my RO about details of my treatment and more questions from me. I learned that I'll be having 35 treatments rather than the 32 the other RO told me. Reason being...since I had DCIS and am in the middle of reconstruction with TE he has modified my treatment plan from what might otherwise be done with someone who had a different type of BC. For one...they have no idea where those narrow margins might be now that the surgery was done but they do know they can't be way over on my outer right side but should be somewhere in my inner right quadrant. So.....first, I am getting a lower dosage of radiation over a longer time to help minimize any scaring or complications that might happen to my reconstruction. Second, I am getting less radiation to my outer right side but more to my inner right quadrant. Makes sense when he explains it. Only thing I'm a bit bummed about is no matter what, some lymph nodes do get some radiation BUT luckily they are not the ones that drain into my arm. Going to keep positive on that one. Overall I am feeling very good about everything.
Thanks Merilee for the image. Does help so much when I'm lying there with my hands over my head....keeps a million other thoughts from creeping in.
Blessings to all and hope you had a great day.
Juls
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Hi everyone.
I am doing the happy dance...13 down and 12 to go. Over half done. We went out to dinner to celebrate. Had energy again today. Basically only had that 1 day of extreme exhaustion in the last 5 days. The area is pink and swollen, but no pain. The prescribed cream is working well with the itching. I am using my lotion 4X a day and leaving a heavy layer on that absorbs into the skin. I think my skin doesn't look too bad (yet). I also noticed that my hair in the area is falling out. I won't have to shave this weekend. That is a plus. I hope the following 2 plus weeks don't bring too many surprises.
My husband is coming to my appts tomorrow. The rad tech told me he can come in during set up and treatment. He really wants to go to my appt with the RO. I am not sure why but I will enjoy having company. Afterwards we are going out to lunch since it is my day off.
I opted out of the boosts because my margins are so good and my DCIS was very small. My RO said she would support that decision. I looked at the benefits and risks and made my decision. Research does not necessarily support boosts with DCIS with good margins. I have noticed that everyone this month is having boosts.
Good luck everyone!
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Chemobrain here, I just posted to April chemo site cuz I thought I was here...did ctscan and sim today, went just like you described, pat,took about an hour total. But I don't start until 6sept, since they want me to wait a month after chemo, and then I asked for an additional week so I can get my classes started. Once rads start, I plan to work the day, get rad'd after, and go home to rest. DH had to wait in recep room, first time he hasn't sat thru an appt with me.
Thanks for the imagery, merilee, and the rest of y'all, for being here. -
#12 today for me
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Met with the doc today. Said my skin looks great. He did a little art work for my boost template. Onward light warrior Goddesses!
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I had a lumpectomy, needed re-excision to get clean margins, no chemo, and will be starting rads August 15. Not looking forward to six weeks of this, but resigned.
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I met with the RO yesterday. He went over the procedure, side effects, potential complications, etc. Just routine stuff. I go back on Monday (8/15) for the SIM and then on the next Monday for the "dry run" and start treatment on the 22nd. I will get 33 treatments total......25 to the whole chest wall and 8 to the mastectomy scar line. Does this sound typical? I am ready to get it over with!
Sarah
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Merilee beautiful image today! #11 for me today.
Welcome newbies! We are all in this together! -
Had my first zap today. Very quick, and I wasn't very nervous at all. Rest of the day so far I've been in pretty good spirits. Yesterday I felt like I needed a good cry - instead I had a good drink
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#14 done, 11 to go. I am on the downward swing! (Happy dance.) I can't believe I am still working full time. I was told by my doc and nurse that by this point I would have to cut back or go on short term disability. Ha! I am proving them wrong. I have a very physical, demanding job and somedays with no break or lunch because we are short. I will cut hours if I get to the point of not being able to cope with the fatigue. But now it is a challenge to keep going. Hope my body can keep up.
Pat enjoy the wonderful sleep now.
Sarabob- Yes that sounds about right. Your are getting the boost that adds days. 25-28 days is the typical amount for the standard whole breast radiation with 1.8-2.0 Grays per treatment for a total treatment dose of 50 Grays. The boost adds another 1.8-2.0 Grays per day of boost treatment. So you will wind up in the 60's. The Canadian version is shorter because it delivers a high amount of Grays per day over 16 days with 3-5 days of a boost. (You would get the same amount of total Grays per total treatment or very similar.) But with that there might be some more short and long term side effects. My doctor stated she would do the shorten version but I had to understand the added risks and sign a waiver.
MamaV are you 1/3 of the way done??
Toni hey you start in a few days! Six weeks sounds like a very long time at the beginning but it goes fast because you live for the weekends. I don't look at the individual days but kinda look at the weekends. So really it is only 6 weekends. I know that is so illogical but it is a mind game and works for me.
jackifp you are also starting very soon.
Anyone planning on tamoxifen after rads. A new study just came out about the benefit lasting now 15 years after starting the drug instead of 10 years. That drug is looking better all the time. If you are interested in reading a summary of the article it is in the risk section of breastcancer.org under research. I read the article in the medical journal earlier this week.
The weekend is just around the corner.
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bb - I am almost 1/3. Gonna have 28 reg Plus 8 boosts. Feeling great!
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#8 today. I am also working and less tired today.
BB226 I am planning on taking tomaxifin. I am trying to learn what foods and stuff I can have with it. So far, no tumeric, benadryl or grapefruit. I wish there ws a solid list of how this drug iteracts with herbs, spices, foods and drugs.
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#4 down, 31 to go. All is going smoothly. Can't say I am feeling fatigued but I'm sure feeling tired at the end of my work day. Wait...maybe I've always been tired at the end of my workday.
bb - you sound so knowlegable about all of this rads business. And, you're so right about the more SEs short and long with the shorter terms. Guess this is why I'm doing a full 35 and I don't think any of them are boosts but I do know the RO is directing more treatment overall at the site of my DCIS but less in other areas.
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Merilee, I love the image and really needed the pick me up. bb, great info! I'm not starting rads next week. I'm not sure rads will be in my new wellness plan. The test came back positive for BRCA2, wah, I don't like the odds of a do nothing plan or stay on the same treatment plan so I see the breast surgeon tomorrow, then the gyn onc. I have a lot to learn before agreeing to the new wellness plan. I'm grateful my friend is also a genetic counselor... better to know now. Deep cleansing breath. Peace and healing prayers to you all!
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Lucky #13 for me this morning
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Hi all. I begin radiation on Tuesday next week. I agreed to be part of a trial on whole breast vs. partial accelerated radiation and I was randomized into the control group, so it's 36 whole breast treatments for me. I have to admit I was really disappointed but my family seems relieved that I'm getting the standard of care.
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jaykayjo - best to you as you start radiation next week. I'm on day 5 today and so far so good. It's been pretty easy.
My 2 cents worth on whole breast vs. partial accelerated.....after having spoken with my doctor and how he explained that less radiation over a longer period of time resultss in less short term and long term SE...I think that you got the best deal. I may be wrong but I'm all for less damage to my skin (think scarring and firmness to your breast).
Take care, do something fun and have laughter this weekend. Keep your mind on now and don't worry about Tuesday until Tuesday.
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Julianna - I loved your comment about being tired after work - thats me!
Had number 2 this morning, been edgy all week, last couple of days just plain sad and teary, and I'm not sleeping at night. Woman in waiting room was on her last one today, and she was as excited as if she were getting married, couldn't stop telling everyone it was her last one. I sat there all grumpy and envious, was glad when they finally called me in. Had a little cry in the waiting room. I hate feeling this way, it is just not me.
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