October 2010 rads
Comments
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Hi gang,
I am now on boosts--was going to start yesterday, but doctor never showed, so had to leave. My skin is holding up fairly well, but I've got a very dark band under my breast which is weird and alarming. I saw a gal yesterday with a lot of peeling and burn. If you have chemo, the skin degrades much faster, and she had a lot more chemo than I.
The hair thing is an obsession. I am 8.5 weeks, and all I have is fuzz. I am nervous and distressed about it, and most of all, impatient. I keep being told it's normal, but it sure feels unfair after this long and difficult road.
I have about 1/2 of my eyebrows, no bottom eyelashes, and thin upper lashes. I wish all this stuff wouldn't happen.
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Here is an interesting article I found on getting your hair to grow after chemo:
http://www.ehow.com/how_4760650_make-grow-faster-after-chemo.html
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I'm with the Nov. rads group, but I had to thank MHP for mentioning the hair distress. I'm sorry for all of us dealing with the aftermath of chemo, but it made me feel not so alone. I wasn't prepared for finishing chemo and feeling absolutely depressed. It's like, now you're done ... and left with utter exhaustion and no hair! I know it's temporary, but sometimes the temporary feels like forever.
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I'm almost half-way through, and have a band of mildly red skin in an arc from under my arm up toward my clavicle. It's mildly tender, but doesn't hurt or itch. I'm going to go from twice a day to three times a day with the moisturizing.
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Hi All,
Update from seeing rad onc...
He didn't reply to my email re dirty sheets but he acknowledged that he spoke with the office administrator that the turning over the dirty sheet was not acceptable. It was just an isolated incident with the student (NOT), I too think that the student was telling the truth. Thank you all for the info and support. I will bring my own sheet from now on
The machine is down today and I have 12 zaps left. Chest is tight so breathing is on the shallow end. I do have this pain below L shoulder blade. Felt like someone punched me and there's an internal bruise. Rad Onc again said that there's no infection cuz he can't see it. No kidding. I wonder why he can't tell me that it's all the side effects from radiation that something is disrupted inside and causing this. He instead said that it's because I laid on the hard surface which I can't quite believe it is due to that. Sigh!
I'm pink, no blister or peeling. Pain under the arm and little bit of numbness on my Left arm.
I used Miaderm and not agreeing with Aquafor.
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So strange, Eileen, I also have started to get a little depressed. My darling radiation nurse said that she saw it in my face today. She must really understand our ups and downs. I think chemo is such a shock your body is in another mode. Now, somehow, the whole experience is sinking in. Things are making me emotional very easily. Time for some therapy, I think.
Riley, if you are developing symptoms now, I suggest you ask your doc now for a backup. I wish I'd started a few days earlier with the soothing packs they hand out to those who get burned, and I could have been putting some cortisone in, too. Under my breast is getting kind of raw. From what I understand, you have to balance burn care with the moisturizing, and in my obsessive reading, seems those who do Aloe or Calendula mixed with a moisturizer do very well.
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Thanks very much, MHP70!! I'll bring it up on Monday. I don't have a breast on that side, so I wasn't worried about skin folds and such. Thanks for reminding me to be careful.
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My rad appointment was delayed 3 hours today. Oh this is getting old! The one machine was apparently "down" for a while delaying all of us. Couldn't they call and tell us they were running late?? Two hours of waiting and I asked the nurse when the Margaritas were being served! Even the nursing supervisor must have felt guilty, he went into his office and brought us his box of Godiva chocolates! Finished #19 today. So far, only very pink and sensitive, like a sunburn. I'm using the Boiron Calendula cream and fresh Aloe. The Aquafor is just too sticky and gloppy.
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Well, I am DONE! Finished #28 today and just feel so relieved to have it over with. I had wonderful rad techs and will actually miss seeing them. Protocol has me back there in a month for a follow-up, then again in 6 months. My rad ONC says to expect my skin reaction to continue to develop through the weekend but should peak by Monday and then rapidly improve. I am quite pink, especially along my collar bone so plan to keep after it with that gooey Aquaphor, Hydrocortisone, and aloe. Of course, I will be seeing my reg ONC along the way also. So, not sure about any follow-up tests yet, still have my port and need to do my TE/Implant exchange.
Hair... wish I had alot more with this cooler weather moving in. Brrrr. I am 10 1/2 weeks PFC and seems that my fuzz is starting to look more like hair and getting thicker, but not getting any longer fast enough. Patience is wearing thin!
DesignerMom... that is an awful long delay today. So sorry that happened. This disease does present us with so many ways to test our patience. Everyone enjoy the weekend and take the time to kick back and relax with NO doctor appointments!
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Whoo hoo! Congratulations, Joan!
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I have eight treatments left, total 25...my crease(sp) under my breast and ( I have large ones..lol) are starting to get raw and peel a tiny bit. I too have run into the waiting game in regards to machines down....it makes the process even longer...but as a Canadian...I am thankful that all of this does not cost me money health system wise....my heart goes out to you all that have to pay insurance costs...etc...to have this disease to start with and than to deal with the aftermath...is unacceptable to on top of it.. to worry about finances....you must be an advocate for yourselves...always...thinking about you all...wishing you the best...wish I could do more...xx
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A big congrats Joan!!! Woohoo!!!
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Hi All- I am another Joan who is done. Right now I am feeling happy. But, I am told to not be suprised by times of depression. The possibility of recurrence or mestasis will always be in the back of my mind. As far as hair goes I am 6 weeks post chemo and have fuzz alover my head with the exception of the nape of my neck. I have a rash there. I will be seeing a dermatologist about the rash. If I receive any hair growing wisdom I'll let you all know.
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Congrats to both Joan's!!!
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DiamondGirl - I have found that the Radiation dept appears to be very defensive of their process. I have had nausea and they insisted it was not due to the radiation. I had an abdominal CT and an ultrasound to get checked out as a result. My primary MD told me that one could get radiation to one's foot and get nausea. Why the radiation dept gets so defensive is beyond me. I hope things get better for you! Hugz! MichelleC
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MichelleC, you are on point on that. My rad onc even said it to me point blank when I told him about my underarm being swollen and all. He said that he will blame it to the surgery and it was never the radiation that caused my inflamation. I told him point blank that I was already 95% healed. I never had any pain under my arm and it was in all my post surgery (recovery) reports, both in 2003 and 2010. And that I never took any pain medicine. I fine it amazing that I am having swollen armpits and pain now 2 weeks into my rads. I also told him that I am not looking to point a finger at anyone but the mere fact that I need to know if there will ever be a solution to this discomfort. Sorry to say that I've lost trust to my rad team
{{{hugs}}}
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Hi Ladies: Well, I'm done with rads tomorrow. It's been a loooong 6 1/2 weeks, but I made it! I can't even begin to describe the fatigue. I think working full time through all of this wasn't the best decision. I will start on Tamoxifen sometime within the next month. I just want to feel normal again for a bit before I start taking it!
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Hi there~been a while since I posted. Today will be Day 18 out of 30. Up 'til now, pretty smooth, altho I am now noticing that I am starting to get itchy. I upped my use of the Miaderm to 3x/day. I see this is fairly common from other posts. I will mention this to my onc tomorrow. Feel like I'm slowing down by the end of the day, but that seems reasonable given the fact that I leave the house at 7am, work all day, drive 45 min. each way for treatments, and get home at 5:30 to figure out something for dinner. I should be finished during the first week of Dec. and hope my energy returns for Christmas! My rad techs aren't that bad, not very communicative, but they do okay. I'll start with the generic Arimidex mid-December, and am slightly nervous about those side effects! It's a real journey, alright.
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Congrats to the other "Joan" who also finished up last week. And congrats to Linda who will be done tomorrow. It is so liberating. Today is my first Monday in a while without that daily trip to radiation. Lovin' it!
My rad ONC thought that my skin reaction would worsen a bit over the weekend, but I did not experience that and things do seem to be getting better today. Still going after it with Aquaphor and other lotions. I'm thinking that it will take a few weeks for my skin to totally recover.
I will say that I hardly noticed any fatigue at all through my radiation treatment, but I do work from home and that probably made things easier. I also got in my daily walks and played tennis a couple times a week. There were a couple nights during the last week that I went to bed pretty early to hopefully pre-empt the fatigue and maybe that helped also.
Thinking of all of you who are still going through rads. You will be done soon too!
Joan
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Congratulations to both Joans (!) and Linda, I know you can't wait till tomorrow! You're one day ahead of me and I will be done Wednesday.
Well, I made it as far as last Friday without any skin issues except redness, but now the peeling has begun and it's spreading. Not on the actual breast nor in the boost area, but mainly under the arm. I'm using aquaphor like mad and hope it stops. I can't imagine what it would be to have the whole breast like this. At least I'm almost done and hopefully things will start improving in a week or so.
May we all one day be back in our underwire bras!!
Kathy
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Finished 33rd treatment today....Yeah!!! Underarm has started sloughing off. See rads doc in 4 weeks. Doing Tamoxfin in December.
It's crazy or maybe because this is my second go around with cancer 2003 and 2010, my co-worker was trying to be excited for me...which believe I am glad i am done with chemo and rads....but i just can't seem to bring myself to be excited at all...I know still have to do tamoxfin, see the chemo (5years), surgeon (for life), and rads docs (5years) PLUS the fact that it is always in the back of your head that this may come back again.......people without cancer truely are not able to understand the feelings behind the cancer..but it's not their fault.
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One thing for newbies--I wish my rads team had mentioned UNDER the breast while I was slathering cream everywhere but. It's a real trouble spot, and my radiation onc just said I'm a 2.5 on a scale of 1 - 3 for skin damage. Thanks, boss. If you'd told me to watch it, I would have. Thing is, the skin goes from great to bad in the blink of an eye.
Roberta, it's true people who don't have cancer can't understand our situation. But as I go along, darnit, I realize I was a good friend to my friends with cancer. I read studies on their behalf, had their backs at work, visited hospitals. Trying to imagine what it is like for someone else is a basic human skill, one I wish more would hone. If I get one more "think positive" I might go postal.
I have six more to go (yay!) I had very mild fatigue one or two days, but like some others, I really did great. I think the walking to and from treatment helped a lot.
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YAY Roberta!! You did it!
I agree with you, too, and with you, MHP70. I've gotten a lot of the think positive crap, and heck, I thought positive after every mammogram I ever had, and then there was this last one! And there it was, a "suspicious area"---that eventually measured 2.5 cm. I don't think positive thoughts keep you from getting BC, nor do they prevent anything else. It's sort of like a card game in that you play the hand you're dealt. Sort of like getting the Queen of Spades, I guess. And all of us, right now, are taking what we're told is our best shot and just carrying on as best we can.
I'm just looking forward to the end of this hand and waiting for the next deal, which in my case will be arimidex, which I inagine will cause it's own set of problems. But like all of us, I'll take them as they come and I can cope with it at the time. (Said she, hopefully.)
Kathy
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I'm DONE!!! YEAH!!! I was happy crying this morning
I'm so glad to get this behind me! You will all have this day too! Now, it's on to Tamoxifen in a few weeks.
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Congratulations Linda! Another step in the process finished.
Colleen
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Congratulations Linda!! I start rad #1 of 33 today, yikes!
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Linda and Roberta... CONGRATS! Go celebrate! Heal the past, live the present and dream about the future... with no rad appointments!
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Congrats to all the October gals that have finished!!! Can't wait to get there myself!
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Well, I don't start rads today after all, maybe tomorrow...dr office says storm caused power outage...
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Roberta,
That is true about others not understanding. I do think they try. I also did not feel excited when chemo was done as I knew I had radiation. Now that I'm in radiation I can only wait till my hair grows back. I hope I can some day feel normal again.
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