Winter RADS 2012 Club...Please come join the fun!
Comments
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Made it through the snow and back home.. so ONE MORE TO GO... hurray!
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Yes, made it through the snow also! My RO decided that she wants me to have a 5 day break today. So no rads for me until next Wednesday. My skin is so red and sore, I was like thank you, thank you, thank you. Picked up some emu oil last night. Hoping this will help as some of you have suggested it.
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I made it through the snow too!! My skin was fine until yesterday and had to peel my bra off as it stuck to my skin and I really felt like a prune (wearing a camisole until it gets better) I wasn't supposed to see my RO today but due to the weather the RO's were all in the hall waiting for patients. She happened to sit down and ask me how it was going. After examining me, she gave me 5 days off too. Jennsmc - wonder if they are managing patient schedules due to the holidays but I don't really care as I'm thrilled to have the time off to recover. Where did you find the emu oil?
My girls had to go with me today as they didn't have school. They were excited to watch me on the camera. They got to watch a celebration of the last day of treatment for a three year old. My kids were excited for her but not sure what to think as I don't think they realized that kids get cancer. -
I had treatment 7/28 today. I got a headache the first two treatments, that went away then I got nausea after the next 4 treatments. I didn't have any symptoms today, so I'm happy! My TE is still holding up pretty good, we'll see what happens in the next few weeks.
On another topic, I think I'm developing LE on my left arm. Radiation is on the right side and I had a double mastectomy in Sep. My arm hurts and it's getting a little swollen.
I hope everyone is enjoying the holidays as much as possible!
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Kittykoma05: ask your RO for physical therapy. I was having tingling in my fingers and forearm numb and couldn't wear my wedding ring. I went to pt this week to be evaluated and the exercises they gave me have really helped. I noticed a huge difference and it wasn't that bad. The therapist thought it was being caused by scar tissue around the nerves not being able to glide vs. lumpedema.
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Thanks for the reply Loving. I'll talk to the nurse tomorrow.
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Just wanted to share that my rads onc is doing a phase III clinical trial using Herbal Aloe Force versus other aloe ointments. They said they have seen excellent results with it. I am enrolled, but plan on buying a bottle to compare and make sure I am getting the "good stuff". So if anybody wants a good aloe, they swear by this stuff. Just wanted to pass it on.
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Had my second boost today. Five to go. I lay on my side for the boosts (on my stomach for tx) and that warm sheet feels so good..., though being on my stomach was more comfortable. I don't think I could have maintained this position for 23 treatment sessions. My skin has held up and the RO thinks it's as bad as it'll get. Boy do I hope she's right! I think fatigue is starting to creep up on me now - but at least it waited till week 5 and it's not too bad.
Kittykoma, you may want to ask your RO about being evaluated by a lymphedema specialist, if your facility has one. If you do have lymphedema, they will probably want to follow you even after you finish rads.
Shachar and everyone else who just started, I'm really glad your rads are starting out well. The time will pass quickly and hopefuly all you'll see from your spa treatments will be mild.
To all you girls in the mid-west, wow! This storm seems like a doozer. I hope you'll all be OK getting to and from your rads. Be safe.
Lifeonitside, how are you doing?
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Andrea, so glad to hear you are healing. I have three boosts to go, then done, done, done! Maybe "overdone" is a better term. The open area in my armpit is now big and nasty enough to require hydrocodone, which pisses me off because I hate the vacant and lethargic feelings it gives me and usually my pain tolerance is very high, so I am not used to needing anything. Either this is worse than I think, or I have just " had it" with the discomforts of treatment. Anyway, enough whining, this too will pass!
Heidismom, ALMOST THERE!
Shachar, I had the gelpad, which I am told is called a bolus, every other day for regular treatments and every day for the boosts ( not in the area where my skin opened, so don' t worry) My RO said it was to make sure the skin surface is treated as well as the underlying tissues. Most of my skin did really well- the open area that I have now had a hard time healing after surgery and then reopened several times during chemo. I think I am destined to look like a many times repaired old teddy bear!
Elimar, sorry about letting out the secret that radiation is boring! Must be the hydrocodone talking. Will try not to reveal any more fundamental truths:) -
Cowpower, thank you so much! Bolus, that was the word he used! I knew it was something like that but could not recall the word. He said they will use it for every single treatment, uhg. I am sorry for your open wound.
That must be very painful, and glad you are almost done!
On my way to round 3. I have never had a sunburn in my life (olive skin) so hoping my skin sails through this even with that gelpad. I am thankful to see someone else who has had it, though I would not wish it on anyone. -
Hi everyone, Just checking in from the fall rads board..sounds like you are all doing ok and getting through treatments with the holidays upon us. Has anyone heard from Luvofcritters? She was active at the start and should be done with treatments I would think. Anyway, wanted to wish you all well and to have a happy holiday season...and the start of a very different and better year ahead! Keep Loobin!
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Hi Aruba, thanks for checking on us. I have been wondering about Loveofcritters, also. I hope she is ok. I think she was scheduled to finish one day before me, which is next Monday. Anyone else been in touch with her?
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Thanks Aliahgirl, I will ask for a referral. I am curious to know if everybody gets the same beam potency when you get radiation for breast cancer. Every time I ask a medical professional they always tell me that the treatment is customized for every patient, bu that does not answer my question. Does anybody know? I asked the tech what frequency or energy level I get and she said I get Energy 6. What is everybody else getting?
Thanks!
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Hello Everyone... had my LAST boost today... another ride through drifting snow, but I was determined to make it! Got a nice certificate of achievement for being brave, which almost made me cry. Came home, put a hot water bottle on my freezing cold feet and took a 2 hour nap. Will start tamoxofen Jan 1... as a marker to a new year.
It's an odd feeling..being DONE.
have a very merry Christmas (that's the holiday our family celebrates) or a joyous holiday for whatever your families celebrate!
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Hi Girls...Just thought I'd jump in (kicking, screaming and still in denial) because I started my RADS 12/17/12. But I have a question--is it normal to burning and be sore this early in the treatment? My RO says its too soon, but I swear on day 1 it felt like someone had stuck a match to the inside of my skin, and then on day 3 I was so tired I couldn't hardly hold my eyes open at work and was in bed at around 8-9 that night.
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Hi Tedebarre I just finished 10 of 35 treatments. By the end of my first week I was so tired I took Friday off from work. By the end of this week I seemed to find a second wind. I also started going to bed at 9pm instead of 10pm. I am a bit red. I have been putting aloe on and it seems to help. I now have 4 days off for the holiday but I have to go in next Saturday to make up one of the days.
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Chickenlady, CONGRATULATIONS! I have two more to do next week, then I will join you. I have been on tamoxifen since Sept- achy legs at first,but gone now, same with hot flashes. The leg aches may have been taxol/taxotere leftovers. Hope it goes smoothly for you. I bet it will seem like we have tons of spare time without rads- I know we can all find hobbies that are more fun!
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Kitty, my rad onc said they like to give us a minimal of 3000 total (watts, jouls, gigawatts, I dont know, lol).
Tedde, I was wondering the same thing. During my first treatment I KNOW I felt warmth during treatment but not since. Today I had #3 and I am exhausted. Of course, I just got over the flu before rads began.
Chickenlady, a big congrats to being done!!!!! I am so jealous. Enjoy the holidays with your family. -
Chickenlady-congratulations and right before the holidays! How nice!
I just finished 12/33 and get 4 days off. So far no side effects except for a little pinkness. But I use Miaderm 3 times a day so I hope that's helping me. I was getting redness under my breast and one of my radiation techs recommended cutting strips of a man's heavy cotton t-shirt and placing it under my breast, which is large. Also, buying bra extenders so the bra didn't get too tight. It has really helped a lot so I thought I'd pass it on to others. I bought the extenders at Joanne Fabrics.
Have a wonderful holiday and stay warm if you are in the midwest like I am.
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Thanks Shachar. Merry Christmas!!
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Hello everyone, today is half way day 10/20...and the days only get lighter from here too!
Tedebarre- Try not to worry. I had the worst first two days. My boob got so red and angry. It really threw me- if this is what it's like on the first day then....?!?!?!?!! So i marched in to the lab on day three and said how unimoressed i was...They were so caring and interested and said they would check the notes and get the boss if it didnt get better in the next 24 hours. and it did. much better. Now I mostly forget about it. Lots and lots of aloe. On day three i staretd spritzing some magnesium oil on it- just on a whim...but it might be a coincidence...
I'm small chested so can afford to not wear a bra and the rad tech sad that was probably saving me a lot of grief. About the only time I've been grateful for my little b cups! 😉
I know it's not possible for a lot of ladies but maybe the first thing you take off when you get home?
Anyway just want to send some love out there in case anyone needs some tonight. Hope all is well with you all. -
Day 12 for me as well. I found I was more tired the first few days and then just a couple days ago. I've been fighting getting to be earlier. I went to bed earlier the past 2 nights and I feel worlds better! I'm going in on Monday. They are letting me and I want to get it over with ASAP. Skin is just getting more pink. I wear a stretchy tank, a stretchy cami, or no bra! I get a little creative with the layers. I'm loving infinity scarves.
I have no idea how much I am getting. I don't think I would understand anyway. I started counting seconds like you guys! I get a total of 4 machine positions. The first and second are left and right side angles, each around 16-17 seconds. The third is on top with a filter for the 16-17 seconds. The fourth position is from the back and is only about 5 seconds. -
Congrats, Chickenlady!
I had 15/28 today, so have passed the halfway mark. My skin is fine. I get four rounds, two are 15 seconds and two are 8 seconds. I think.
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13/16 today and I am beat. And I seem to be getting some soreness on the inside. Just made the saline for compresses and hoping that soothes the deep pink a bit. Other than that, it's all good. Two more days of work, shopping done, house sort of decorated. Just waiting for a bit of snow to really make it seem like Christmas.
Hope everyone has a great weekend and no skin issues! -
It is encouraging to hear those of you further along not having major issues.
I tried counting the seconds last time, but will try again Monday when I go for #4. I have two positions (left breast). The first is up on my right side for about 30 seconds, and then it goes to my left side for about 25 seconds. I am not wearing a bra at all and am thankful it is winter so I can wear big, baggie sweat shirts.
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Hi pals! I finished #13 of 30 on Friday. I go 4 days xmas week and 4 days New Year's week too. My skin is just starting to show a little pink with a visible defining line between the radiated skin and the non-radiated. I either go braless or wear a bra OVER a soft t-shirt or silk-undershirt (WinterSilks - it's a long underwear thing). I cannot have my usual bras against my skin. Luckily I have gone down a cup size so there's room in the bras for the shirt now too.
I hope everyone's been having lovely Holidays, whatever yours may be!
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Hello this is my first post I feel like I'm reaching out for anything I can find to help get thru all this! I'm 37 and on Halloween i had a mammogram because I found a lump in the shower. On nov 14th the surgeon told me it was cancer and I swear I just shut down! 5 days later had a lumpectomy and they said lymph nodes were clean and he got all the cancer out. Test results came in last week and I got lucky no chemo...so on Friday I got mapped out and on the 28th radiation starts. I'm trying to be strong and positive but with three kids and being a single parent (moved out nov 1st) lets just say I'm a mess right now! All of a sudden I woke back up and am feeling all the pain, loss, anger,fear, and anything else you can think of! I can't sleep at night I don't know what to do...
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Hello fellow rad warriors:
Wishing you love and peace this holiday season. I hope all if you going through radiation this winter and dealing with the side effects can get some rest this next week. Easier said that done, especially if you have kiddos.
I am going to be starting my internal radiation therapy in AZ right after the new year. I know most of you are doing the external rad, which was not recommended in my case due to the bilateral treatment needed, but if there is anyone who is or will be doing internal radiation (interstitial brachytherapy), more than happy to share my experiences with you. I will be going for the first treatment right after the new year and then returning for the second side, probably in February. I have a friend coming to help me for most of the time there. Makes it a bit less scary!
Wishing you all a blessed holiday and good health and energy to enjoy your time with family and friends. -
Cancersucks- what an awful time to have to go through this! (Not that there is really ever a good time.) I am so sorry that you had to have this on top of everything else. It's pretty crazy how fast the diagnosis/ surgery/ treatment decisions take place, isn't it? It's like you barely have time to process it, and everything changes. It's rough when you have kids at home, too- I have four little ones all at home and it gets pretty insane. (I mean, on top of the regularly scheduled insanity, LOL.) Lots of gentle hugs to you- and welcome!
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Cancersucks - welcome to a new "home" of wonderful, supportive, and wise women who are always here for you. From here you'll draw lots of strength and good tips as you go through rads.
While I'm almost finished (4 more boosts) my case is very similar to yours - no nodes, no chemo (thankfully), and lumpectomy straigt to rads. Except that I'm postmenop. and my kids are grown so I'm not going through this with small children. I'm so sorry that you have so much on your plate but as so many wonderful women who went through this told me, you get through this and go on with life.
The anticipation and mystery of rads is so much harder and worse than the treatment itself. While many women experience various severity of side effects, the majority of which pass shortly after rads are finished, there are many women who experiencee minimal and sometimes no side effects. So don't assume the worst. Just stay open and strong and be patient. Go day by day. And slather on whatever cream your RO or the women here tell you works.
Hoperfully, your RO will also be helpful with suggestions and tips of how to stay in shape so you maximize your health and minimize the severity (or risk) of side effects.
All the best and good wishes for a gentle journey through rads. The time will pass quickly. And good luck with all the other issues you're dealing with. Hope 2013 will bring you lots of joy and good health.
Jazzygirl - good luck. Hope all goes well for you!
Happy holidays everyone
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