Spring 2016 Rads
Comments
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I started RADS on 4/4 for 6weeks .. Today will be # 11 and so far so good, no changes in the skin or fatigue. The only issue I have had is that my Lymphedema in the left arm has gotten worse... They tell me this can happen in the beginning and won't be swollen for the remaining 4 weeks.. I sure hope they are right!!!!
Summer is coming and I am ready for RADS to be over and hair to grow back...
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So I went for treatment #4 today and they were sending everyone home because the machine was down. Has anyone ever heard of such a thing happening? I'm a little freaked out to have skipped a day of treatment. Hopefully it will be back up and running tomorrow.
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When I started the machine was down day 2 and 3. Then further along it was down for 4 days because of the hack of Medstar computers. It was all added to the end.
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I think the machines go down a lot. At the end of my treatment, I congratulated the RO that his machine never went down. He told me that it went down right after my treatment at 11 am one day and was down for the rest of the day.
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Thank you Karen and Moondust! I feel better knowing that this is a somewhat common occurrence! I was worried my facility had shoddy equipment! Hopefully I can get in today.
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Had my first boost today. Wow, what a difference. I was in and out of there in no time! Yay for five more boosts, then we are through!
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Had rad #6 today and so far so good! No fatigue, no redness, no sore breast...nothing! I get to work around 6:30 am, leave around 9:30 to go do my radiation, then go back to work until 5:00. I'm grateful I haven't had any fatigue. I'm not using the lotion that was prescribed. My RO said that I could also use non-alcoholic aloe vera gel, so that's what I'm using.
The only downside is I did find out that I'm not eligible for the shorter rad time and then the boosts. Since I had chemo, my RO won't do boosts. She says that boosts don't react well with people who've had chemo, that chemo patients need to be given low dosage radiation. So that means I have to do the full 6 weeks! Oh well, better safe than sorry!
My hair is looking pretty hilarious! It's coming in white (which I was brunette before), and the sides are all laying down, but my crown is standing straight up! I look like I have a mohawk on top!
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Hi all! I finished lucky #13 of 33 today. So far, I experienced days of fatigue beginning since treatment #6. I have good days and some I feel like my face is dragging on the ground. My skin is an odd red/purple color. My scar from the SNB is sensitive and so is my nipple. I've been using Aquafor on my nipple and Aveeno lotion on my boob. I do work until 1:30 with the treatment facility about a 10 minutes away from work. Then I head home for the day. Usually, I can take a 30 minute power nap and be good to go for the rest of the day.
I hope everyone's RADS fly by quickly!
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My RO is recommending Miaderm Radiology Relief cream. It's quite pricey, 4 oz for $36 on amazon. Anyone using it? It has great reviews on amazon. Wondering if it's worth the price?
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Nope. My RO had me putting aloe vera gel on starting a week before I started rads. For about the first 2-3 weeks of treatment I just used that. Then I started using Aquafor at night and aloe vera in the morning for the next 2 weeks. Yesterday was treatment 27 of 33. I just picked up the prescription silver sulfadiazine cream, which was $10, to use twice a day. My skin is pink, not bright red, except for a patch on my neck which looks and feels like a small sunburn.
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igay1ord- Sounds like your rockin' some super stylish hair!! And, for what it's worth, I haven't had to go through chemo but I can't have the boosts, either. Because of the amount of tissue that they had to remove I had a breast reduction. My RO said that it was too difficult to find the exact site of the tumors so boosts won't work for me. Here's to easy does it....
My RO recommends Aquaphor or Calandula cream, much less expensive.
Good Luck, all!
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Start tomorrow on my 21 rad tx's, the last 5 boosts. hoping my skin holds up, nice seeing everyones tips on skin care. Cancer sucks. My employer has been awesome thru all this. Good luck to everyone out there living with their breast cancer and treatments.
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I have an appointment tomorrow for mapping. My radiologist said that I will have four weeks of treatments, three days a week. A total of twelve, yet I will have the same dosage of radiation as if I had the six week/5 days per week regimen. He said it is less fatiguing, easier for the patient, and that it's a new method. I haven't heard anyone else getting this. Has anyone heard of this type of treatment?
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Hi Ivegotthis -- the shorter radiation has been done in the UK/Canada for a while now -- US is just starting to catch on. Here's a link that you might find informative https://newsatjama.jama.com/2013/09/20/study-confi...
I'm starting radiation soon myself -- I believe I will be doing 16 fractions (treatments) plus four boosts, so in total four weeks.
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Yesterday was treatment 11 of 21. Yay for being on the downhill side of this thing!
Here's a tip in case it might help someone: I am doing the breath hold machine. About treatment 6 I started having anxiety and difficulty getting to the breath level. This past Monday I had a different tech and she noticed I was breathing in really fast and hard. She offered to let me practice the next day and said to take a slow and steady breath. On Tuesday we practiced before my actual treatment and it has made a tremendous difference. So if you are having difficulty don't be afraid to ask if you can do some practice breathing and try to breath in slow and steady. My anxiety level is so much less now.
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August I did 21 treatments with 5 being boost. My skin held up pretty good. The last couple days I got sore right next to my underarm where the sports bra touched. I had a itchy rash also. I just put on lots of the aquafor and went without the bra when I could. I am about 1 1/2 out of radiation and the sore spot is almost gone. Good luck with your treatment.
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Thank you, Grazy. As it turns out, my radiologist moved to their other office 30 miles east. I have a new radiologist. The difference between the two is that Doctor #1 is in his thirties, and Doctor #2 is in his sixties. Doctor #2 is not quite on board with the shorter span of treatments. I told him I was hesitant and not comfortable with the four week plan. I don't want to have to go through breast cancer ever again. So I'm have the six week/33 treatment plan.
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Arista-I'm using miaderm per dr recommendation. 3x day. Have had 9 tx no problems yet.
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Arista, I know the Miaderm is more expensive than some, but I used it all through 30 rads and I think it is good stuff. For the entire course of treatment I used two tubes. Among other ingredients, it contains Aloe and Calendula. It is non-greasy and always feels nice going on. My skin has never liked vaseline based products such as Aquaphor, which is why I didn't try that one.
Hang in there everyone!
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Hello all Spring Rads ladies!! I'm a Winter graduate and just wanted to drop in and say hello and wish you all the best with treatment.
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Hi All;
I just finished 6 months of chemo and radiation is next; I will likely start in the next 2 weeks. I have my first appt wit the RO on 5/2 for meet and greet and plan. I have been a loyal poster in the TAXOL group but since I have finished I wanted to find a radiation group. so here I am
I had 4 surgeries in the fall then AC followed by TAXOL and graduated chemo and rang the bell on 4/7! My diagnosis was invasive ductal.
I am going to go back and read all your posts so I can see what folks are doing to deal with radiation. I am going to try to work and go to treatments in the afternoons; I see on here someone is doing that and its working well.
2 weeks out from chemo I am no longer feeling "sick" ; but I am still tired, bloody noses, and sore muscles. I am having a bone scan Monday as the MO wants to make sure the pain in my hips is nothing more than post chemo muscle soreness. I understand radiation can be exhausting after chemo but I am happy to no longer feel "sick".
I look forward to following this thread
Sawyer
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Hello. I just got marked up today. I have 2 more weekly Taxol then I will start rads. Ready to get this over with!
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Week 2 of 6 down! So far all is good! No pinkness, redness, nothing! I have a question....has anyone else had a problem with itchy and really dry skin? My skin is driving me crazy! I actually broke down this morning and used straight baby oil all over my back, arms and legs. And it's still itchy! I'm meeting with my RO on Monday, so I'll ask her if radiation could be causing it.
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Went to rad teach today. I start 5/2. The biggest thing tooted is Miaderm. My RO and his pts swear by it and I started a thread and several in there toot it too. She was kind to give me a full 4 oz tube since I'm on fixed income and told me for my 6.5 weeks of applying 3 x a day, I should be ok with 2 total tubes. Seems the first 2 weeks most are fine. So she told me ok to just use aloe vera 3 x a day and on #3 before bed put aquafore on. After week 2 then it's Miaderm 3 x day with aquafore before bed on top. She said don't bother buying aquafore as she has a zillion samples. As for Miaderm, she's going to try and stock me beyond the 1 tube so maybe I won't have to buy another tube. Very nice of her as I about fainted hearing $36 for a 4 oz tube of Miaderm! :O
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Two more boosts and I am outta here! Good thing 'cause I am a crispy critter! Under my arm, breast and chest above breast are the worst. Healing can't come fast enough!
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igay1ord, I have been itchy all over for a couple of months now. I think it is still side effects from the chemo. I finished chemo on March 10th. I have little tiny flakes of skin flying everywhere! They collect in my car seat even. I have just been using Aveeno lotion.
I finished 14 of 33 rads yesterday. So far only some redness under my breast. No fatigue. The further I get from chemo, the better I feel. So far rads are a piece of cake compared to chemotherapy!
Best of luck to you all!
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Anyone getting their neck on the affected side done as well?
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For the initial CT scan did they use contrast? forget what my RO said. I just finished chemo and I'm ridiculously tired of IV s and stuff being dumped into my veins.
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Hi All!
For those of you who have started rads, did your RO tell you whether the cream or aloe you were using was helping you heal, or just making the area feel better? I have a list from the doctor, but am wondering if any of them helps in the healing as well as making you more comfortable.
I see the RO again on Tuesday and can ask her then, just thought some of you might know!!
Thanks!!
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No contrast used for the CT scan.
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