I don't want to go to my planning rads tomorrow
I don't want to have radiation.
It's just too much validation of breast cancer
I hate it
I am afraid of blisters. I am afraid of burns.I am afraid of fibrosis showing up in 6 or so months.
I don't want to go
I am not as nice as you ladies.
I know the options, and know I "have to" which makes me even more upset I hate to even have people touch me to have my hair or nails done
I want to be left alone.
Comments
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((((bedo))))
Yep, it sucks to have to have radiation. I can't tell you that you won't have any problems from the radiation. That said, I went through this a little over a year ago (finished right around this time last year), and it has faded to a bad memory. 6 weeks seems like a long time, but it passes and then you go on with your life. Hang in there!
Karen
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Don't worry about radiation! I've had 2 surgeries and chemo. I was very scared before radiation too. Cancelled my first radiation mapping appts because I was stressed out! I did get burnt but I applied saline solution and cream and that really helped. It is not a cakewalk but it is over before you know it. If you want to PM me feel free!
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Bedo - I am in the identical situation as you.
I too want to be left alone. I do not want to go for radiation so much so that I am going for a second opinion this Wednesday. I already know what they are going to say - rads or mastectomy. Two equally unappealing alternatives.
I am afraid of blistering, peeling, cording, fibrosis, left side etc. I just do not want to go and it has given me extreme anxiety. I am not sleeping at night and I feel forced into something I do not want to do.
I was supposed to get going on this within the next week or so, but I am getting my second opinion, then going away for a week. I need a break from all of this. Then I will decide what to do. I do not want my breast removed either. I hate this decision!
I empathize, I really do. If you want to pm to commiserate feel free.
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I just went for mine on Friday. I totally hear what you're saying and get it.
Hope tomorrow goes ok for you. Hugs. -
I felt the same way. I didn't want to do it but I did & I got through it.
You can do it! NJ
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Dear bedo, I get what you are feeling. It's scary and I don't like people telling me what to do, it's annoying and feel out of control. I went to the planning session and thought, let's hear what he has to say, still my choice. Once I saw the place, and the people, I was okay with going forward. It wasn't easy by any means but you can do this, I just thought of it like labor (2 kids natural child birth) the only way out of it, is through it. It will be over in 6 weeks and you get the prize, a long, happy healthy life. Please keep us posted how you are doing. Put me in your pocket when you go to the session, I'll be with you all the way...let me know how you did.
((((((((((((((cyber hugs))))))))))))))))))
Maureen
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I did not find radiation bad at all, but even if it had been bad; I wanted to do everything possible the first time around because I never want to play this game again!!!!!! Hang in there. It is just a little tiny bit of time in compared with the rest of your life. Ruth
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I started RADS with an attitude. They were treating me like a cancer patient & making me meet with the social worker & giving me all this information about how to eat. They measured my arms, to take measurements(baseline). Even though the LE risk is low........Where I go, they don't use the terms mapping or dry run. But during those 1st 2 days when they were figuring things out, I found myself losing patience. I had a BMX & they expected me to hold both my arms over my head for what seemed like eternity. Since I was going to have both sides zapped, I was going to demand they treat me like 2 patients & give me a break in between sides. But the social worker was nice & not pushy. The treatment time was much faster when everything was figured out. Some of the staff I like better than others. My favorite tech hasn't missed a day with me in the last 5 weeks. I have 2 more treatments to go. The skin thing is the hardest for me. The lotions & potions didn't work & seemed to make matters worse. After 2 days of no improvement or worsening symptoms on each one, I asked for something else. Finally came to a gelsheet dressiing. I'm actually trying to thinking of some unique way to say thanks
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I felt the same way, and felt like I was the only person to ever react that way. I got through chemo and surgery, but radiation is the one that seems to be freaking me out the most. The fear and anger has been overwhelming. I rescheduled my "simulation" twice. Finally I asked to see another rad onc, but they really didn't like that idea and made that process super difficult. I knew the second would also say I had to do it, but I still had so many questions that my rad onc wasn't answering. My fear hasn't been so much about the short-term side effects, but the long-term risks, but no one seemed to hear me saying that over and over. The idea that I could go through all of this and then have the treatment cause more problems has been one that has been literally keeping me up nights. Lung damage, heart damage, secondary cancers, lymphedema. I don't sleep at all these days unless I take Ativan. Trying to sort out what to do and how it might affect the rest of my life has been anything but a simple equation. I am more than this breast cancer. Getting rid of this breast cancer is only one of many things to weigh out here. None of the doctors seem to get that, neither do most of my friends or family. I did finally go. I had my third treatment today. We get through this the way we get through it all, we show up. One foot in front of the other. Breathe. Hope for the best, deal with whatever comes. I've started walking an hour a day. At least it makes me feel like I'm actively doing something to battle the inevitable fatigue that's coming in a few weeks.
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I opted for a left mx with the thinking that I didn't have to have rads. Turned out with 4 nodes positive that I still had to have it:( Rads weren't pleasant but got through it okay. You will do great too.
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Do you know about brachytherapy? This is internal radiation and is over in 5 days. Best place to get it done is in Arizona. Google it. They treated me like a spa patron not a patient. Plus it spared my heart, which was directly under the tumor, and lungs. External beam has a bit of "overspray". They can't totally prevent it. It is covered by insurance. This was the best decision I made.
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I had minimal burning, and rads were, on the whole, extremely uneventful.
I used a combination of Aloe gel and Bag Balm (for bovine udders, but worked perfectly on my own personal udder). I had minor peeling, but less than a sunburn from a few years ago.
I did get some fatigue, but nothing that a nap or 2 here and there wouldn't cure. And not until the last week, then for about three weeks afterwards.
The biggest challenge was staying perfectly still. But I did that too.
A year later, I am glad I did this. I got to keep my breast. Yes, it isn't quite like the other, but overall very normal.
Suspect I would have needed rads anyway. BTW - you can't tell which side is which and I wear mostly what I want. Not the worst outcome by any means. - Claire
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bedo: My heart goes out to you. I hated rads all the way through and I now have only two more boosts until I am done. Can't wait to be finished, but I knew I needed to do rads to have the best chance of living a long and happy life. I showed up begrudgingly and sometimes grumpily everyday, but at least I showed up. Looking back on it, I still would have done rads, but I wish I had gone to a different center. Oh well, hindsight is always 20/20. If you have a choice of centers, check them out before choosing the best place for you. I knew I needed more help than the rads staff could give me so I got an ativan prescription from my PCP and I started seeing a therapist. Both have been a huge help. We are always here for you and you can vent here all you like. Sending hugs to you.
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I cried, I was grumpy and I felt like I was speaking Martian. No one answered the questions I was asking.
Now my landlord wants me out because he does not feel that I can afford this place where I've been for 4 years and my daughter convinced him the stairs were "dangerous" I'm middle aged for the Love of God! He sees it as a liability with "cancer"
Now, I have no job, breast cancer and at the end of the month no apt. I have no money for deposit and no one wants two black cats. ( or 2 cats)
5 weeks ago I was happy. Oh and my sis's promised financial help never showed up.
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thank you all for "getting it".
With your thoughts I will do it and Maureen I will keep you in my pocket. I start tomorrow.
I'm not Suzy Sunshine these days. I used to be. Maybe when the hurricane ends..
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Hi Bedo, you don't have to be Suzy Sunshine, it is not required. You need to go to the meeting with your head held high, when it's over, take me out of your pocket and scream, swear and cry. It will be over soon enough and you can get on with your life, a happy healty life. If you have se, deal with them as they come not one moment sooner. You can do this, I know you can and yes I really do understand. Give the techs a chance, they can be really helpful. Then go and get yourself a treat. You seem like a very strong woman with many years to live a great life. Please let me know how it turns out. Good luck
Love,
Maureen
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Best of luck!
I used visualization to help me through. I pretended I was sunbathing on the dock of a camp I worked at when I was young & thought about what our schedule for the day would be, what skit our cabin would do for the talent show etc. When the machine came overhead, I pretended it was a cloud blocking out the sun. Also bring whatever ointment you are going to use with you and slatter it on in the dressing room as soon as you are done (but never beforehand could as that could intensify the burn).
Really, truely, it will go fast and then you will be DONE!!!
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Hi Bedo, I am right there with you. I don't want to do this. I did go for my simulation and am scheduled for a "dry run" on 9/7. I am so sick of dr's. and people treating me like I am dying, which I am NOT. I have always been a care giver, dealing withthis disease for 20 + years with various family members, so being a patient really Sucks for me. I don't want to be touched anymore, I feel like my life belongs to my dr's not me. I will go because I know its the best thing and I will keep positive thoughts. Hang in there and if you want to PM me I am here.
Good luck.
Clelia
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Ah, Bedo - I felt the same way!
I was hostile all through rads and I never did like any of my techs. My doc is a gem though.
I'm 2 weeks post rads and althought I had three areas open up on my skin, everything is healed now and I wore a bra on Wednesday.
It sucks though. I know what you mean. But better than the alternative...
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Good Luck tomorrow Bedo!
During my rad appointments I started to memorize my settings. I would say them out loud along with the tech. It was fun!
Don't be mad at the techs or the RO. They didn't give you cancer. They are here to make sure you never have to deal with this again.
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I found radiation to be by far the most annoying, but easiest, part of my treatment. My poor techs probably though I was the biggest b&$@! in the whole world. Not everyone has the horrible skin reactions that you read about. In fact, I had nothing ....zip...nada...other than a light "tan" which is now gone at less than 6 weeks out. I had EVERYTHING possible ( whole breast, clavicle, axilla and boosts) radiated so plz try not to worry about SEs. You'll sail through and it's OK to be grumpy about it!!!
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hello ladies,this is msphil, it is a common feeling to just be left alone, we can all identify with you sweetie, but take it from a long time survivor(17 yrs) and I believe in my heart that is a important part of my surviving to help others like you to "get through" and you CAN and you WILL. God Bless you and I pray for you also. idc,stage 2,0/3 nodes, L mast, chemo, rads, and 5 yrs tamoxifen.
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I'm not a visualizer, so I just counted. During the actual treatments, I never counted much past 50 for any of my 4 fields that got zapped. Sometimes I'd watch the green & red lights. Not much of a show for my 1/2 hour drive.
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Thank you all. Here I go and I'll be really really nice.
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bedo - Hope all goes well for you today. I think getting through the first day is the hardest. I'm hoping everyone will be great to you and they'll get you in and out of there fast. I finished right before Easter and felt such a huge relief when it was over. But it was a necessary step in this long journey that none of us asked for. Just keep soldiering on . . . you can do it. One day at a time!
Take care,
Kathy
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bedo: Wishing you good luck today. It is not easy, but each day brings you closer to the end of rads.
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Good luck Bedo. Count 'em down and you'll be done before you know it. It became a part of my daiy routine and I didn't mind it at all. The techs were wonderful. They had a big bell you could ring on your last day. I cried when I rang it - didn't expect to. But in some way, I think I was holding my breath the whole time.
Never had much skin reaction other than a bit of tan. Used Calendula gel which I liked.
Good luck.
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Bedo, just thinking about you and hope you had an okay day.
((((((((((hugs)))))))))))
Maureen
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Bedo and everyone,
I go for ct tomorrow and I feel the same way. To say Im scared shitless is the biggest understatement of the year! I am always a positive and happy person but this is f@#%!@g me up mentally so bad. The people at work know everything as I am an open book and share all, however they seem a little pissy with me I think because Im not joking and laughing as usual. I dont know how I want them to act but I feel like they just dont get it. When I tell them what the next step is they just say well your almost done. WTH... Im just starting! I just want to scream!!! -
Here's a John Wayne quote I like; and I think fits our situation well: Courage is being scared to death - but saddling up anyway.
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