Starting Rads in March 2017
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Good morning all,
Heading to my verification today and will begin treatments tomorrow. I'm ready to get this show on the road!
Thanks a bunch for the link to the video. I started yoga last week and will make every effort to get to the gym on a regular basis. Going to move from elliptical to tread mill which is better for my osteoporosis. At the very least my goal is to walk around the block .,, weather permitting. I'm reading a lot about the benefits of exercise so I hope it helps with possible fatigue. To be totally truthful I'm trying to get myself "ready" for beginning Arimidex and Prolia. Exercise is supposed to help!
Good wishes to all today. The trees are beginning to bloom and Spring is in the air.
Namaste
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Check-in day with RO team today. Nothing too exciting, although my slightly pink area got visibly darker over the weekend. I now have a defined reddish/tan area that lines up with all the stickers still stuck on me to guide the radiation treatment.
It doesn't hurt at this point, will see how it goes from here. This is definitely darker than any reaction I had when I had radiation the first time.
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javamama, I've also had pain deep inside... like my ribs hurt. My RO did think it was from rads. And that was in my second week. So I don't know!
I don't think I've changed my activity level at all. I had chemo, then surgery, 3 months off then started rads
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LynnieRich- I do think it could be from the rads. I woke up this morning and it's tight in there again like it was last week. It went away over the weekend, but is back after yesterday's blast.
butterfly- I hope you enjoy the yoga as much as I do. I love it more for my mental state after I do it than for the physical benefits. It just gets my mind calm and right, you know?
15 more to go.
I can do 15 of anything.
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javamama--I do like yoga and going to class this morning before my first treatment. I've got aches from the poses but it's good aches. I know what you mean about the mental state of mind. In so many ways it helps me connect with my body and to a greater power. I'm meeting nice women which is an added bonus. I'm thinking positive that I can stick with it during treatment. Namaste.
Gentle hugs to all!
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Hope you enjoy your classes, butterfly. I haven't gone since I started cancer treatments. After my hair comes back, I'm looking forward to it. Right now, I'm doing some light yoga every other day at home. It's kicking my butt. I haven't really engaged in any exercise other than walking my puppy for the last 6 months. Surgery and chemo really left me weak. But surprisingly I have tons of energy on rads. Now, I have zero reserve. So when I've shot my load, I'm done. But it is noticeable.
I'm gradually increasing the activity to meet left arm. I refuse to get lymphedema and have been babying my left arm since surgery. And since my rads are superclavicle and chest wall, not under arm, I might get away with no lymphedema. Got my fingers crossed.
I get new x-ray pictures and repositioned every Tuesday. To make sure that just my chest wall and not my lungs and heart are in the field. We do deep inspiration breathing as well. And since this past Tuesday, when we redid everything, the pain in my chest wall has gone away. So, is this a good thing? Like are they hitting my lungs and heart instead which is why my chest wall feels great or what. Ugh.
Half way done. 2.5 weeks down. 2.5 weeks to go.
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javmama - do what you can regarding exercise, even a slow walk will help. I haven't gone all that you've been through so please don't be too hard on yourself. I've exercised on and off for years but when I slack off it takes time to get back into it and not be sore and exhausted. The yoga is causing me aches and pains. Maybe when I start the Arimidex I won't notice the difference. A gal can hope.
I was really concerned about my heart but RO team reassured me several times that they've come a long way in protecting the heart and lungs. I don't have to do the breathing but they also said if I needed to do that to protect my heart I'd be doing the breathing treatment. They leave nothing to chance. I'm a worrier but I decided to have faith and let this concern fly away on butterfly 🦋 wings.
Gentle 🤗 hugs.
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javamama, I got lymphedema from my surgery. Very mildly though and I went to PT and it helped tons. I think it's not too big a deal as long as you don't let it go. I could feel my arm getting achy and my rings tight and so I mentioned it and thy sent me to the PT. I would have ignored it as no big deal but they asked specifically. So that's my biggest advice on that front. If you notice your arm feeling heavy that's a sign of lymphedema and don't hesitate to have a PT check it out!!
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Lynnie, that seems like a very rapid appearance of lymphodemia. I agree everyone needs to stay on top of it as there's only treating it and no cure for it. I'm glad you caught it in time.
My skin is healing pretty quickly now, it's just itchy but nothing I can't handle after everything I've been put through the past year. My MO released me yesterday. He told me to get out and stay out. I hope I don't have to go through all of this again. I'm not crazy enough to think I'm scott free and I'll keep a close eye out for any changes. I'm just not sure how to check for lumps and bumps when I have no breast tissue. Hhmmmm
My best wishes to everyone here and praying you all have smooth sailing for the rest of your treatments. I'll be still checking in every few days to offer my support in any way possible.
Good luck!
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Lynnie- I don't have lymphedema. Even though they took all my auxiliary nodes. My MO says that the skill of the surgeon and extracting the nodes makes a huge difference in whether ones gets it from surgery. Now, he says that radiation will give almost half of women wove had node dissection lymphedema. I am ever on guard for the beginnings of it. Having a heavy arm, however, doesn't work for me. I've had so much nerve damage that the upper part of my arm is mostly numb and feels weird to me all the time. I wouldn't be able to tell if it was heavy. I check my arm every day. Sometimes, more than once if I remember.
Chest wall pain is back, but slightly different. So... make what you will of that.
I got nausea again after rads this morning. I do think it's radiation related.
Even if doc doesn't think it's related, I will tell him again when I see him on Monday. I am also getting slightly fatigued. Nothing crazy. Just a little tired by late afternoon. I will tell him of this as well.
Skin is holding up well.
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I had finished my last radiation 2 weeks ago, skin was looking dark and burnt for the last 2 weeks and now it began to clear up and looked more like my own skin color. The weird thing is there is no p
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Oasis, my skin has started to return to its normal color too. All the skin under my arm that had peeled off is coming back nicely with no pain, thank goodness. The only thing I have at the moment is a tearing sensation across the center of my left DBMX scar. We've been keeping an eye open for any changes in the scar and the only thing we can see is a deepening in an area that took forever to heal after my DBMX. I wonder if it's opening up from the inside out? I'm being very careful not to move to fast and avoiding the position that increases the tearing sensation. I have a f/u with my RO on Wednesday and I'm hoping to get an appointment with my PS soon to discuss TE exchange date. I know I have 6 months before PS will even think about doing the exchange surgery. If my scar is tearing open then lets go ahead and do the exchange. Wishful thinking I know lo
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Three weeks down, two more to go. 15 treatments done. 10 more to go.
I can do this.
I can do 10 of anything.
Oasis- glad there's no pain.
WenchLori- a lady I know did her exchange too soon after rads and her skin tore open. I want to RUN to my PS to get some stuff done, but I'm waiting for a long bit before I do. She said she woke up to a pool of her own blood and goop as her skin had just ripped open. Now, I'm sure that was an exaggeration because her husband drove her to the hospital and I can't see that happening if it was substantial. But still. Think about how tender your skin is. How new. How damaged on the molecular level. And just maybe think about waiting a bit for the exchange even if it is tearing a bit. The visual she gave me is haunting me. Probably because I had planned on pushing it and going to get stuff done earlier rather than later. My PS is willing to so the work 6 weeks post rads instead of 6 months like most. So, it's an option and yet...
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javamama, Yay! Your almost done! You can do this! I think what I'm feeling is nerve endings?? I'm in no real hurry if my PS says 6 months I'll wait 6 months. Besides, he ruined my pool time last summer I WON'T let him do it 2 years in a row lol This Fall is soon enough for me 😊
Waving hello to everyone 👋
I have my balcony door open to enjoy the cool night air, I may need to close it. All I can hear is the coyotes howling! What a racket!!
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Lori, happy to hear that yours returning to normal color too. My skin is also clearing up and there is absolutely no peeling. I wonder where the "burnt" skin disappear to.
I can't wait for the exchange too, especially my TE has shifted towards my armpit and upwards, so uncomfortable. I did not allow my PS to inject more saline, so I will see him in 2 months time and discuss if fat grafting is an option.
Javamama, you can do it!
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I'm hoping my exchange goes well when the time comes as my PS doesn't do FGs. He says if it's done right the first time there's no reason to have to fix anything?? It'd be nice if I needed FG, I've got lots of fat that can go someplace else. My TEs have always been up under my chin and over into my armpits. I call them my hooker Fools. I've seen my PS's before and after photos of reconstructions and Ihave to admit they are amazing.
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Foobs not Fools lo
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Good Afternoon ladies,
I finished my last treatment on April 11th. Very happy that this is part is over! I had mixed emotions on my last day. But really cried when my husband gave me a beautiful crystal necklace to celebrate the end of my treatment. After 1 week, my skin is starting to clear up, but still very tender. My skin got very dark in some places, raw in some and developed a rash in the rest! I managed to keep working through treatment, but was pretty tired by the time I got home from treatment! Mostly used aquafor ointment for the skin but had to get the benadryl cream for the rash! Started taking the pain pills so that I could sleep at night! I wish you all the best and all I can say is keep a positive attitude and take it one day at a time!
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Congratulations, Fighting GMA. And that's good news for those of us waiting to start this leg of the adventure. I'm not holding out any hopes of getting a gift at the end of my treatment, but it sounds like you're got a real keeper there!
MJ
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FightingGMA - Congrats on your last treatment. Tomorrow is my half way mark. Heal quickly! Gentle hugs,
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Awesome FightinGMA. I've got a week and a half left.
So far the skin is tender and lightly red. Chest wall pain is steady.
Nausea has gone away. And a little fatigue is creeping in.
My hair is coming in like a boss. But I can't stand all these different lengths. So I set up an appt with my hairdresser and I'm cutting it all to one length and going Amber Rose hair for the summer. Buzzed and platinum blonde. Which should be interesting. Ha!
My DIEP foob isn't getting hard or anything like they tell you. I found a few studies indicating that radiation after immediate DIEP doesn't have flap failure rates any greater than delayed DIEP. In fact, my foob is getting a little softer and hanging more like a boob would. REALLY glad about that.
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It's 3 weeks since my last treatment and my skin is on the mend. I had a f/u with my RO today and he saw a lot of fresh new skin developing. I need to make an appointment with my PS as the muscle has contracted some and I may need to have a little saline removed. I can handle that. It was nice to see all the girls while I was there. They all came out to say hi.
FightingGMA, yay! Congratulations, what a beautiful thoughtful DH you have he's definitely a keeper. I'll keep mine also. We started to plan our trip to Australia, Greece, Italy, France or any other place I'd like to go as my treatment graduation gift. We have a year to figure out exactly where we're going as he wants me to be able to enjoy myself and not spend 4 hours a day sleeping. By then I'll have my exchange surgery over with too.
🦋, halfway there! Yay! It'll be over before you know it!
Hello to everyone 👋
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Wench Lori - thanks for the encouragement! Glad to hear your skin is on the mend.
To all: I asked this question on the April 2017 Rads thread. Is it ok to dye your hair during radiation treatments?
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Butterfly, I don't see why not. But do a test patch. Orange seems to be the result if chemo drugs are still in the system. Be careful. Maybe go check out the hair threads.
I have 7 more to go. 18 down.
Skin is starting to get really irritable. It's slightly red. But it's almost like a breeze brushing against it is just annoying. Chest wall pain is remaining steady.
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hey ladies!! I have four more to go!! Woohoo!!
I can't really believe it. Seems like it's happening so soon and like "that's it?"... but it certainly was more than enough. Just seems so anti climactic.
I got off pretty easy in the skin department, just pain/soreness near my clavicle. I have a palpable lymph node there now too which is disconcerting but the RO didn't seem worried about it.
I have definitely been tired the last 2 weeks when I wasn't really before and then I got s cold from my son so I'm down and out. So looking forward to feeling like myself again.
Glad to hear you are mending Wenchlori!! And what a fabulous trip! I bet you can't wait.
Javamama, we are so close!! Glad your nausea got better.
Fighting, what a sweet hubby!
Ly
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9 more to go for me out of 28 treatments. Darker redness in the area, and seems to be a little puffy but that's about it. Doesn't hurt, though I write that off at least in part to nerve degradation in the area after multiple surgeries.
One thing that is a little weird is that it's quite dark red for most of the area being treated, but part of the area inside the perimeter they marked doesn't look more than lightly pink if that. May try and remember to ask RO about that.
Best wishes to all.
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20 down
5 more to go. I can do 5 of anything.
Meet with the doc yesterday. Asked him some questions about being out in the sun. He says no problem just keep the radiated area well suncreened or covered. Also, traveling isn't a problem either. When you fly, you get hit with tons of radiation. I also asked about the weakness in the bones of the side radiated. He said that the seatbelt in an accident might break the radiated side easier than the nonradiated, but nothing to worry about there either.
Today is x-ray and positioning day. Can't wait. 5 more to go.
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Javamama, yay! You can do this! I'm in your pocket
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Thanks, WenchLori!
X-rays and positioning done. Today's blast done. 21 down.
4 more to go. 3 this week. 1 next week.
I started on a Monday and I will finish on a Monday. Which I really like because Mondays are seeing the doctor days. So I will get to blast my RO with one more round of questions before being handed back to my MO and getting started on the tamoxifen.
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Javamama, my RO scheduled another appointment to see him in 3 months then he'll release me permanently. So we hope! All ROs are different, hopyou'll be done on Monday 🤞
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