Summer 2015 Rads
Comments
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LBF - "....in the immortal words of Fall Out Boy, let's light'em up!" Cracked me up! Good thing I wasn't hydrating as I read that.
I think we'll put you in charge of the s'mores this weekend. And yes, we do start our weeks with a group bullet biting exercise.
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I just finished week 4 and have 7 treatments left. My skin has been doing great so far esp since I have a bolus every day but this week my lower armpit started getting red and tonight it is very pink and peeling in spots. Any advice? Does this actually heal up? I'm a little worried because it's right by my surgery scar / area for reconstruction.
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MotherofFour, you are a week ahead of me. I just finished my third week and have 18 more treatments to go. I hope the time off this weekend will help.
Peace and healing,
Nancy
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Hopeful: LOL ya all sound like my kind of campers! Making a radiation Playlist now...
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LBF - Starting with "Come On Baby Light My Fire"?
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LBF- Radioactive by the Imagine Dragons. I started listening to that during chemo. It perfectly captured my post apocalyptic sensibilities at the time.
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Fire,water,burn by the bloodhound gang?Good stuff ladies! Looooove the post apocalyptic sensability. What about Blitzkrieg Bop by the Ramones?
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Blondie, "Atomic"
X-Ray Spex (?), "Radiation"
The Firm, "Radioactive"
Johnny Cash, "Ring of Fire"
Bruce Springstein, '"I'm on Fire"
Surely Gaga has something relevant?
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burn baby burn, Disco Inferno!
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Hi ladies. Back from brachytherapy in AZ on Thursday. Still waiting for holes to close up or scab over so I can take a real shower.
Besides a pretty terrifying procedure where they put the 20 tubes in, it wasn't bad. A little fatigue, a darkened underarm, and my chemical sensitivities ramped up. My face started to peel, and I had red raw patches along my nasolabial fold. The doctor said, of course, "not from radiation". Doctors do know that things that happen in one part of the body can affect other parts, right?
In catching up on this thread, thought I would share a few sleep techniques that work for me. I'm a professional insomniac, once going for two weeks with no sleep!
No. 1, and the biggest to me, is the bed. As said, I'm chemically sensitive, but once you've been through chemo and rads, you are too. Perfect combination is a natural latex bed, with a bamboo mattress pad, cotton or lyocell sheets washed in fragrance free detergent, latex or feather pillow. It's very cozy. If you are close to an Ikea, they have most of this, but the bamboo cover is online.
No. 2, quiet, cool, and dark room. I don't like sleeping with a mask, so I make sure there are no lights, especially blue ones. And no electronics close to your body! I hate to say it, but husband woke me constantly and we now have separate beds. We both sleep better.
No. 3 no blue screens an hour before lights out. iPads, computers, phones, etc. Read a book, it works great. My Kindle paperwhite seems fine. I also have a special bulb in my lamp, it's called a Good Night bulb (not cheap, but lasts a long time). I would think listening to books would work too, sure puts my husband out.
Odds and ends: try to make lights out and rising the same time every day. Try to get some exercise and natural sunshine during the day. Take melatonin an hour before you want to go to sleep. Don't eat or drink alcohol close to bedtime.
I hope that helps someone. I managed to sleep well even at the hotel, even with tubes in my breast, though I had to go buy a cotton mattress pad. Such a prima donna, kept waking up in a full body sweat from the poly mattress pad the hotel was using.
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hi everyone. Checking in. I have 20 rads down. Doing well. Have slight red area under arm pit and a little tightness so far. Otherwise cant see any indicators of rad area yet. Have 8 regular and 5 boost left. Doing better than I thought since I am swimming and very active in this heat. I sweat all the time. I Keep using the gold bond and have moved to applying it 4 times a day now. Overall energy is OK still. when i get over heated it tires me out and sometimes I put an ice pack on my breast area to cool the area down. I am wearing the Cami during the day and a t shirt at night. I know things can change the more rad exposure so I'm cautious this could change at any point.
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Sounds like you are doing really well LiveDeliciously. I know exercise is supposed to help with the fatigue. I am at the gym on the elliptical three to four times a week and trying to get enough water which I know I important as well. But, I am exhausted. The fatigue has really hit me hard. My RO mentioned getting a blood count and I said well let's see how I feel on the next visit. I will see her Tuesday and I think it might be good to get that count. I am much more tired than I thought I would be. My skin is holding up ok so far.
Peace and healing,
Nancy
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Hope everyone is having a good weekend! 14/33 down - 19 more to go. Stepped on the scale today and lost 4 pounds this past week. (Not that I am complaining lol!) Anyone else starting to lose weight? (I am walking 3 miles per day, but I have always done that.) Started to notice I am sleeping more hours at night. Not fatigued during the day luckily, but have to turn in earlier at night.
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Fastwalker, it sounds like you are doing great. How many more treatments do you have?
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InStitches: Thanks! Sorry the fatigue is hitting you hard.
I find that getting a lot of sleep at night helps. (I slept nearly 10 hours last night, which I never do.
) . . . I think we started the same day -- July 13th.
I would've had 18 more to go, but the machine was down one day so now I have 19 more. . . Hope everything goes well for you this week.
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Welcome back to another fun-filled, exciting week at Camp Idonwannaburn, fellow campers.
I hope everyone had a good weekend, drank lots of water, stayed out of the sun and used lots of aloe!
This week we're focusing on learning new coping skills. If anyone has any, feel free to share
I'm off for my last WBI - number 28! After that it's 7 (not 8 as mentioned before) boosts, for which we'll do the simulation today. There's always something new to learn at Camp I.
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hopeful. Thanks for all your entertainment. Summer camp idea was great.
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I like the rowing machine because it gives me some pectoral exercise and doesn't make my arms rub against my armpits or sides.
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Midgiemoon, congratulations on Bailey, she is adorable, plus Beagles are my favorite! I'm sure that she is grateful to have a new home and will be spoiled in no time! I have six dogs (4 German Shepherd mixes, a Jack Russell and a Beagle) as my username states and wouldn't trade them for anything! They make me laugh every day!
Have any of you had problems with your hips, tail bone and shoulders while on the radiation table? They rubber band my feet together so that my legs stay straight and the table kills my tailbone, there have been two days that I have been like that for 25 - 30 minutes, I think that is why my shoulders hurt as well.
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6doggies: thank you for bringing this up...I haven't started my rads yet, but my back's still a bit drama queenish after fusion etc. surgery last year. Lying flat, prone or supine, still causes flares for me.
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Live Deliciously - I'm glad you're enjoying the silliness. Think someone else started it, way back when and I've had fun playing with it.
I'm glad you're doing so well and I envy you the opportunities to swim. That would really feel good... Enjoy a lap or two for me when you have time
I hope your skin and energy continue to hold up!
6doggies - do they place a bolster under your knees? If not, that could help. let them know you're uncomfortable, please! (On the other hand, have you ever heard of a sleep away camp with decent beds? Remember, we're paying a lot for the privilege of roughing it this summer.) -
6doggies - they rubberband your feet? That sounds terribly uncomfortable! They but some sort of form thingie under my knees, so I had that and the body cast, and then the would position me. For the boosts, no body cast but they still put something under my knees - way more comfortable. Wondering if you can request something like that.
I graduated today! I'd jump up and down, if I could jump. Or do much else. The fatigue hit me hard, and I'm developing a few little blisters in areas that didn't not receive the boosts, but mostly my skin has held up pretty well. This is such a weird treatment and surreal experience. Now I start on the road of recovering from treatment. It didn't seem like this day would ever get here, but here it is. I hope you all reach the end treatment with the fewst possible SE., and eventually find a way to celebrate. Not sure when I'll have the energy to do that, but it will happen.
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Congratulations, Dragonista! Now you get to start healing for good. We'll do the jumping up and down for you.
You're right about it being a surreal experience. It's hard to explain to people who haven't been through it just how strange and disconcerting it can be.
Enjoy your day without RT, continue to nourish your skin and let us know how it's going. -
Dragonista, YAY for finishing your rads! I am with you on the fatigue. It hit me hard after treatment number 13 and I am still really tired. It is hard to work and do rads. I am trying to do everything that is supposed to help. I am drinking lots of water and going to the gym three to four times a week. In the last few days I have started paying a lot of attention to my protein intake. It is hard to get 60 grams of protein a day, even harder when you don't eat meat.
I hope you plan something wonderful to celebrate.
Peace and healing,
Nancy
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was just at rads and tech reminded me diet and exercise and hydration just as important right now as taking care of our skin.
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Good point, LD. I do think exercise helps fend on (or work through) fatigue.
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Hopeful82014, yes they do put a bolster under my knees and I have told them a few times that the table kills my tailbone and today was the day for me to see the doctor today and he scolded me, apparently they can't line me up the same each day because I move, breathe or whatever, heck I thought that I stayed still the entire time. LOL I told him about my tailbone issue, so he is going to have them put a thin towel under me tomorrow, I hope that helps!
dragonista17, Congratulations, that is awesome!! I'm so happy for you, that has to be an amazing feeling and one that I am definitely looking forward to myself! Yes, they do rubber band my feet, which I thought was odd but I guess it works, it is amazing how each treatment center does things differently.
Fastwalker, congratulations on the weight loss! I gained about 15 lbs from Chemo and am just now getting back into my pre chemo clothes. I'm into my second week of rads and find myself tired at the end of the day, does it get worse from here?
Institches, are you a vegan or vegetarian? I'm a vegetarian and I drink a protein shake everyday at lunch and then eat a teaspoon of natural peanut butter everyday but with that it is still hard to get 60 grams of protein a day!
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6doggies - Sorry you got lectured! Our center uses a pad (covered by a sheet) under the body, as well as the body mold. It's not at all uncomfortable, although sometimes I need 2 heated blankets rather than just one as it is SO chilly in there. At any rate, I hope the little bit of padding helps you get through this.
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Congrats Dragonista! Please let us know how you do post rads.
I finished 22/25 today. The fatigue is really hitting me, but I'm trying my best to exercise everyday, I think it helps the fatigue from being worse, and think it's helping me sleep better at night. My skin is starting to get pretty red, hoping it can hang on for last few treatments.
PB
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Costco sells a whey-based drink, low carb, 30 g protein in 11 oz.
I've also been using a rice bran protein powder in my smoothie--also high protein, low carb (and vegan).
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