January 2012 rads
Comments
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I'm past the halfway point now. 16 out of 30 done. I'm not feeling much fatigue, but I'm taking a day off every week so that I only have to work 4 days in a row. I start feeling tired around 3. A cup of coffee perks me up. My skin is starting to look really sunburned, but it isn't unbearable. It will help having the weekend to recover. I'm trying to keep it exposed while I'm home. Good luck everyone. We can get through this.
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Hawk, we have to assess whether to take the uterus as well. My breast surgeon would like to let me keep it, but only if it is deemed prudent. It has some fibroids, and that makes me uneasy.
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Have been recomended Glaxal Base by several people... Was told NO oils of any kind... Costco has large tubs of Glaxal .. Going for my muga on monday.....Have a great weekend everyone
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Hello all,
Anyone know if cooling the skin down with ice packs is worth while? I know that when you get burns in a kitchen its the first step to stopping the burning.
I have ice packs with casings that are soft. Makes sense to me????????????????????
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chef127 - I would check with RO nurse or tech. Literature I was given said specifically no ice packs or other temperature extremes. I know it sounds like it makes sense, but maybe it has to do with the vulnerability of the tissues.
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bgirl
thanx for the info. I'll put away those ice packs...............................I did not get that literature.
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Hello ladies. See everyone is continuing on their pace. Sorry for those of you that the machine broke down. That's a bummer. I sure hope they call me welllll in advance since I have to leave almost an hour before my appointment if that ever happens to me.
I have managed to get 2 weeks (10 treatments) under my belt and now my breast is sore and I feel achy all over. Really get stiff if I sit a long time and kinda hard to get going again. I'm going to blame it on the rads. LOL! I don't know what else it could be. I do feel much better as far as SE's go. Taste buds are returning and I find myself eating a lot right now. Guess I'll be gaining back that 12 pounds I lost. Oh, well! Still have some swelling in my feet and legs. I wonder when that will go away. Maybe never huh?
Hope everyone has a wonderful weekend.
HUGS!
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Had a nice lunch with two BC sisters today.. One who finished rads. in Oct, one starting friday.. The one who is done told us to keep using Glaxal cream and Aloe long past rads. are done.. No one told her that the skin will keep deteriorating after rads are done.. She got red during rad. but 10 days after she was done her skin started to blister.. So keep slapping on the cream ladies..
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Ossa, thanks for that info. Had no idea that after radiation I would need to keep using cream. Hope you gals have a good weekend.
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Rjbaby, did you have taxotere chemo? If so, that may be responsible for the swelling in the feet/legs. I had the same problem and because it is inflamation related, I have been taking an anti-inflammatory on the weekends, when I am "off" from the rads.
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Rjbaby, Momine is right. I had horrible swelling of my ankles after TCH. It only lasted a few weeks, and now I am fine.
Ossa, good to know that we need to keep the lotion going.
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Rjbaby,
I also had lots of swelling of arms and legs. lasted a few weeks.. Lost 15 lbs of fluids..When measured by PT pre op and then again 4 week post op there was a 3 cm difference in the circumference of my arm..all good now
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I just had my 12th treatment on Friday. I was catching up this weekend on all the posts as I have so little time during the week. One of the things I learned this week is that I didn't ask the right questions. Of course it's hard to ask the right questions if you don't know what to ask. So I learned to ask where the entire treatment area is. I have faithfully applied cream to my breast after each treatment and all throughout the day but no one told me how high up on my chest this was going to go and now I have a rash all over my upper chest. I'm trying to really cover the area heavily in cream now but there really is no catching up what was lost. My breast on the other hand is holding up well so far though it has become somewhat swollen, heavy and stiff (I'm big breasted). It aches most of the time with some twinges of stabbing pain.
My experiences with fatigue have been kind of strange. I get my treatment at 8 in the morning and faithfully hit a wall at 2 each afternoon. I'm wondering if I had afternoon rads if I would be asleep when the fatigue hits and I wouldn't notice it as much. Anyway, I started getting some fatigue the first week. I don't care if that's too early. It was a fact. But then the second week it wasn't quite as bad. I have good days and I have bad days. But so far, it hasn't just gotten progressively worse each day. It varies. And mine is a strange kind of fatigue. It hits suddenly and I feel shaky and empty, like I just can't move another inch. But I have found if I have tea with caffeine in the afternoon around the time I usually fall apart it isn't as bad.
My RO tells me that the SE should start around the 3rd or 4th week (so I guess I just had to do it early) and that the worst of all will be the week after the rads are done. I may either take that entire week off work or work from home. I have an hour commute both to and from work and I get my treatments in the same city as I work. Because of this I think I might start taking Wed. afternoon off so I can get some extra rest. There just aren't enough hours in the day for me to get everything done and still sleep!
One of the hardest things for me is the moments of depression. I'm so tired of doing all this. I've been in "cancer" mode since September and it feels like it will never end. And at times the dark seems so dark. And then for no particular reason it will lift and I'll feel just great. Who knows why. Anyway, thanks ladies for being here so there is a place we can share and whine and have people around who get how we feel.
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Hello ladies. Hope you are all doing well this evening.
Momine, Anafoefana, Ossa: Yes I had the terrible Taxotere. My nails have pulled away from their beds and look horrible but appear to maybe be getting better. Hands peeled like a snake skin and hurt really bad but they have healed up nicely and now my skin is just dry, but not peeling anymore. So I hope this swelling goes away soon. I sleep with my feet on a pillow at night and that helps alot.
Other than that, I am bracing for SE's to set in this week. My Rad Onc told me that they normally start seeing SE's around the 3rd week and I am beginning my 3rd week tomorrow. But CARTI, which is where I go, is really good about taking care of their patients. I see a nurse once a week and the Dr. on Mondays. Both check for any unusual appearance or swelling of my breast or arm. They did tell me that they have creams for me to use if I need them. So far, I have not used anything. But I am prepared to ask in case I do.
Hope you all have a wonderful evening. We have had tornadoes all around us tonight but things seem to be quieting down now. I am glad! I hate to have severe weather at night. Can't see nothing!
HUGS!
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Christy
I know exactly how you feel. It's like suddenly I am fine and then on the way home from rads I just start crying. I am on 18 tomorrow and I also have a rash. I use the cream faithfully but still have a red,sore boob. I go at 11:00 and sometimes around 5 or so the fatigue begins. Caffeine does help a little.
It is nice to talk to ladies that understand.
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Christy, I hear you. I have been on this cancercoaster since June 1. It is close to 8 months of being a fulltime patient, and it is getting OLD! At this point I don't even feel all that horrible, physically, so maybe that is why I have the energy to be getting grumpy about it all.
I try to focus on having some fun, eating well and other pleasant things to take my mind off, but there are days when it doesn't work all that well.
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Momine, I hear you loud and clear. This all started with me at the beginning of June too and I'm SICK OF IT! I had a really good attitude for so long and kept getting compliments on how I was handling everything. I had so much positive energy up until December and then all my upbeat thoughts, etc. crashed. Now, I just want to get to a place where there is no more treatment, doctors, etc. I want my body and mind back so much. Sometimes it feels like cancer, SEs and treatment is all I think about. My favorite time of the day is late at night when I watch a TV show for an hour and then drift off the sleep.
Well I'm off to lucky #13 this morning. No call from the RO so machine must be up and running again. Sorry about the vent, but just want to let you guys know that no part of cancer is easy and we all have good reason to cry and be grumpy from time to time.
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Rocky, yeah looks like we are in almost perfect sync here. I am trying hard to start thinking about other stuff, but it is slow going.
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I can relate to the depression we experience during cancer treatment. I think it is worse during rads because nothing screams "cancer" like that radiation machine and the otherworldly vault we must be inside alone while the machine is on. Since we have it five days a week there is no escaping the screaming "cancer." At least during chemo there was time between treatments to regroup. Also, by the time we reach rads, we are all tired of treatments and "down to our last nerve." Sending hugs to everyone. Please know you are not alone in your feelings.
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Morning ladies.
I can so relate to everything you all have said. I am so sick and tired of being sick and tired. I am tired of feeling like crap most days. I'm tired of swelling. I'm tired of driving back and forth to the big city every day. I just want my life back. I want to be okay and well and living wild and free like I was. I am so tired of "being the one with cancer." This all just sucks and I will be so glad when the day comes that active treatment is done. Maybe then my dr appointments will slow down and I can get on with living again without being reminded every day of what I have been through.
Take care ladies and thanks for letting me vent! Felt so good!
HUGS!
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1 of 25... My "foob" has felt hot all day... Am I a hypochondriac?
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RJ you said it, I am so tired of "being the one with cancer!". You said it perfectly!
I guess we can't go back, but then I still think, how can it be me? No answer but no end either.
Plus, what the heck with hormones or lack there of, hard to know what is going on inside our bodies, but I can't say I like it at all!!!
Sara ♥♥♥
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Ralston, I sincerely doubt that any of us could be classified as hypochondriacs at this stage of our lives. I had #3 today (of 33) and like you I feel that I am already noticing a difference. I'm tired, but attributing that to a whirlwind trip over the weekend to Colorado for my grandson's birthday. I refused to let this damn cancer rule my life, but it has altered it some since I had to be back for treatments. I am feeling some pain in the breast, more than before. I think one of my biggest issues is that I keep hearing how fortunate I am that I "only" need radiation. I guess since I only had a lumpectomy and no chemo then I really do not have cancer. Funny how the divit in my breast says otherwise. Can't wait to see what rads do to it.
On another thought, my RO gave me lotion (Medline Skin Repair) at the intial consult and told me to apply 3x/day beginning on day one. I don't find the actual treatments so unpleasant, but I am having a harder time staying upbeat even though I am generally a glass half full type. I keep trying to visualize the radiation killing any stray cells, but my thoughts always return to the fact that is is also destroying the good cells. I do find that it is good prayer time and that is what I am going to take with me from the treatments.
Hugs to all, we're gonna get to the end and we're going to have some stories to tell. Each of you are in my thoughts. We can do this!
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I went today for my CT scan to set me up for rads. I wasn't prepared that I would go into a tunnel and I'm claustrophobic, so it took all my strength not to freak out and make a fool of myself. I thought I did pretty well, but on the way home, my eyes started burning and I felt like I had a fever. My boyfriend said it was stress...I hope the machine didn't malfunction. Anyway, I took a nap, but still don't feel 100%. All this and I haven't even started rads yet! I'm supposed to have my first treatment next Wednesday...unless I chicken out. I still have my study in hand that says 70 year old plus women don't benefit all that much from radiation, but my RO says that study is not meant for women like me who are healthy and will live another 25 plus years...hope she's right!
I've also been living with this challenge since September and it is very draining. I've held myself together for the sake of the family and my boyfriend who hates to see me stressed out. I've been without my BHRT for the first time in 20 years and that is taking a toll on me as well. For the first time ever, I'm starting to feel old...well....I am 71, but I didn't feel 71, I felt more like 40. I'm sure hoping this funk will pass soon and I'll be back to my old self.
Sorry ladies...I really have no right to complain. So many of you are going through so much more, and I should be comforting you instead of feeling sorry for myself. I send you all prayers and positive healing energy!
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Newksmom100 - I hear you loud & clear! While grateful to not have to go through chemo right now, not having chemo doesn't make you have cancer any less. Cancer isn't a competition of diagnosis or treatment, even small tumours can met. People think since I didn't have chemo that it is not that bad and I will be better as soon as rads are done, which makes them feel better. In reality had onco test that said I would only benefit 2% from chemo, so actually slightly higher chance of recurrence than if I had done chemo. Not to mention MRI repeat on opposite breast in couple of months to look at something suspicious that showed up while doing pre-op MRI. Thought of starting over makes me crazy and very annoyed at people who think the cancer will be over soon. Once there, always there. Like grief you figure out how to go on with your life, but you don't get over it.
For now trying to concentrate on where I am an not what others think. Off to rads and weekly apt with RO today.
As for thinking symptoms are in your head - I think you feel what you feel. Other people just have to accept that.
Kaara - Hating cancer and how it changes our lives isn't defined by age. Yes some of us now have a goal of reaching your age, but if it comes back in 25 years I would still be mad too! It is crappy all round - rant all you want. Doing rads & hormone therapy and yes I am tired! I am in my 40's but felt 70 some days - planning on bouncing back and hope you will too.
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I did not have any of the fatigue that so many suffer from. I had 33 treatments and my breast got kind of peely and sore towards the end. But I felt fine the entire time. Now that I look back, I could have milked this for a lot more sympathy at the time.
Keep a positive attitude - it goes quicker than you think.
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I have been catching up on everyone. I just started with my first radiation today. It was fine. They have a very nice huge picture on the ceiling with light filtering through the leaves of a tree. I wanted to close my eyes though and say a prayer or two or just be still and think healing thoughts. It was done fast. rjbaby- I never had swelling through my TCH routine but yesterday I took off my socks and woa- a lot of swelling- three weeks out of chemo. I guess it is normal from reading all the other posts so I am not going to worry about it. Are your nails black or just the same color but lifting? I can't tell if mine are going to fall off or not.
Christy- I get radiation near my work also and work 45 minutes away. I will have to see if I take off later on or not. I think a bit of depression is normal for all of us. I try to be patient with myself and not anticipate how I should feel. If depression is what I feel and it moves me to lay around a bit more, than I do. From my past experience, I always feel better in a few days. This cancer thing has made me feel a bit down for longer as I go through this but who knows, I am receiving blessings also through all the support and am looking at life differently, gaining in wisdom, patience and possibly changing a few things in my life because of this. If I have to be sharpened by the sword, so be it. If I am to suffer, well, who's to say I shouldn't? Though I try to avoid it. Funny thing- I was at the appointment and I was laying on the radiation treatment bed and the techs were adjusting the lighting and angle of the machine and I looked to the left of me and there was a huge shadow reflecting on the machine and it was my breast! As if I didn't have to be bare breasted, now I have a big shadow of my breast reflecting in the room! Anyway, I am very small breasted and when I lay down, it seems they just flop to the side but this shadow was of a very nice looking breast, all kind of perky. I am sure it was the angle of the light and how they were adjusting the machine but it was funny to me to see this big breast shadow of my little breast. And so ends my first radiation treatment. God Bless!
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HI
I am seeing my oncologist for the 1st time tomorrow and I gotta admit I'm a little afraid. I have been debating on whether I'm even going to have radiation. I had a lumpectomy and one lymp node was removed, which was clean. However I have read some things and I'm not sure I want to go through with all the "after"surgery preventive care. Does radiation really help that much in the long run? Can someone please tell me if I'm being too paranoid?
Thank you
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amf099
Only you can choose what treatment is right for you.. I have chosen to take whatever they will throw at me. Want to do whatever I can to prevent a recurrence.. Have had chemo, mastectomy and now starting radiation.. Want to make sure all the potential microscopic cells left behind will be blasted and gone.. Good luck with your decision.
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Amfo99: Based on what I have learned, the only people who do not get the total benefit from radiation are women who are over 70, and then only if their life expentancy is less than ten years..meaning they are weak and frail already and have other health issues that could shorten their life span.
I'm over 70 and didn't really want to have radiation, but after careful consideration and talks with several RO's I have decided to go with a shorter version. I have the same situation...early stage, small tumor, clear margins and nodes. I don't want to deal with this again in ten or twelve years when I might not be healthy enough to withstand more treatments.
I have changed my diet and lifestyle and am taking supplements to further prevent the recurrence of bc. I feel I'm doing all I can do, so now I am just going to live my life.
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