Any February 2012 radiation gals out there?
Comments
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Sherrybaby, vent all you want!!!! It definitely helped me! That really does suck about the possible delay in your treatment. I hope that doesn't happen. I laughed out loud about the strong comment - I feel exactly the same way! I read this somewhere (surely on this board or someone's blog): I'm not really strong or brave. It's not like I ran into a building that's on fire to save others. I'm running out of it screaming my head off. LOL Sometimes I tell people that when they make comments about me being so strong - it usually results in a laugh and a nice conversation about how we all do whatever we have to do to survive. We just don't know what that is until we are put in the situation.
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Sounds like an ordeal you shouldnt have had to experience.
My experience with breath holding has been quite positive, though uncomfortable. I start my boosts tomorrow and will not be breath holding for these last 8 sessions. I am very burnt now. Dark areas in the arm pits, dark patches on the breast and very painful dark areas in the breast crease and on the chest wall under the breast. I am using aquaphor with lidocaine. I expect the skin to break soon...its close now. I cant wear a bra, which is a big deal for me. -
sherrybaby, my kids gave me a pin at christmas time that has a picture of a woman with a "50s hairdo saying "It's been lovely, but I have to scream now" Want to borrow it?
They also gave me one that says "I have reached the age where happy hour is nap time" They are both very appropriate.
so after complaining about the cheesy videos they were showing in the tx room, today they showed one of a hot air balloon ride over wine country. It reminded me of the ride my dd and I took in Nov and almost made me cry.
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Hi, Beebop and all.
I had a terrific experience w/emu oil during rads as did a number of others in the Class of 2010.
Also used pure aloe gel.
Still use emu oil for just about everything....Emu Gold.
Good luck!
God bless us all
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Howdy all!
I thought I would share this post:
http://community.breastcancer.org/forum/70/topic/783321?page=1#idx_17
I hope the link works. It was written by a RO. It really helped me understand what Radiation does to your skin. Well...the link doesn't work, so please copy and paste into your address bar.
El-Jaye: When did you finish chemo? Are you bald or in the mutant peach fuzz stage? It will come back. I felt just like you when I was Kojak. My hair is about an inch, inch and half long now. I finished chemo 10/06/11. I "style" it into a faux hawk. Although I really don't have much of a choice! I like it though.
Had #21 today. My rash is a little better with the Lotrimin. The RO said it would take a couple of days so it better be all better tomorrow...hee! I am quite tan now, especially at my axillary incision. My foob also has major freckles! I get the bolus everyday. Yippee. -
Geegster - thanks for sharing that post. Good info!!!!
I finished chemo Dec 30,2011 - I am just very impatient. I have a very sparse peach fuzz. I am getting really tired of scarves and hats. Cant wait until I have some hair to style again.
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Hello! My name is Geraldine and I have had two mamo's and two biopsies 2 weeks ago and am having surgery this FRIDAY. On this day I first go to the Breast Center EARLY in the AM for a Radioactive Seed Localization. Then after 3 hours I go to the hospital and have my Lumpectomy, I think. After getting in and taking a look will determine weather they just do the lumpectomy, or take the whole breast, so I won't know until I awake, what was done. I was told then I am to start on radiation treatements right away. They said it will be either 5x a week for 7 weeks (if lucky) or else 5X a week for 17 weeks or so! I wasn't really too worried about anything until I started to read these posts! Now I am really scared! The Biopsies were very unpleasant (had them both done the same day) and it really wore me out. I've been sleeping so much (not like me at all normally) and I am liking it and would rather rest or sleep. Sounds like radiation will make me tired also so looks like I'll be in bed a lot. Here I was thinking about 2 weeks after surgery I'd be up and around. Want to be because my new grandson is due March 14th by C-Section and I'll be caring for the others. They live with us. One 8 year old and a one year old (just turned). My hands will be full so I am hoping I won't be too sore, etc. I am a no frills, down to earth kind of person who just wants to do what I am supposed to do and get it all over with and get on with my life ASAP, but it doesn't sound from reading here that that will be the case. I still can't believe that I have cancer! I will stop now and go to bed. I have only tomorrow to get all my ducks in a row and get done what HAS to be done yet. I will come back to check this place after a few days after surgery and let you know what they did and what they expect of me next. You all sound so brave and up to date on all your treatements. No one mentioned any of those things to me....yet! I hope I can be as knowledgeable on the subject as you all are and able to map out a plan for my recovery. Thanks!
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To gjsquuezebox...
My surgery was not bad... but I was oow for 2 weeks and then was still tired and nursing that side. I was unable to pick up my niece for several weeks. My cs told me not to lift more than 10 lbs for the first 4 weeks. So the 8 year old may be ok.. but you will need someone else to care for the 1 year old. At one time (3 weeks in), while sitting I tried to pick her up with my non-surgery side and I could feel the pull and pain on the other side.
I did start doing even small arm movements the day after surgery (exercise from dr)... I wanted to keep mobility in my arm.. after about 1 week, I would hold 2 lbs weights and do simple arm exercises... this helped but still no lifting of 10 lbs for many weeks. Prepare yourself and your family.
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Geegster - thanks so much for thank link - fascinating!
gjsquuezebox - welcome to the group. Although I'm sorry you need to be here, you will find tremendous support on this forum. Right now you are in the "overwhelming" stage - first couple weeks are the worst. Hang in there and know that it does get easier to handle, although none of this is ever "easy". We are all here to help each other through.
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Anne - you need to get some moisturizer on your skin. Aloe Vera is great for burns but it is NOT a moisturizer. I moisturize heavily right after treatment, before bed, in the morning after my shower - ALL OVER my armpit, boob, chest area. You just are not supposed to do it within 2 hours of treatment (I have read). Moisturizer is like mashed potatoes, prayers and hugs - you can't have too many, just not enough. (I am almost done and my skin is great, just a tiny bit of rash on my chest area that looks like sun poisoning - I am putting cortisone cream on that and it is clearing up.) ALL THAT APPROVED BY MY RO!
Sherry - You are allowed to flip out here. This is the place, we have sympathetic ears. Somewhere on the BCO boards there is a "You might have cancer if you ..." in the vein of a Jeff Foxworthy redneck jokes. Go there when you need a laugh. One of them was a translation of "Oh you look great/are so strong!" which translates to "Your life sucks and I am so glad it is not me." So just keep that in the bubble and laugh to yourself when somebody says it (as opposed to poking their eyes out, LOL!)
I start boosts today.
Chicago - I LOVE the baseball analogy, I am going to start using that one.
On a sad note, I saw my sister last night (the 32 year survivor, who lost her middle daughter to BC 4 years ago). Her oldest daughter (age 46) was just diagnosed with ovarian cancer and also has a malignant tumor on her stomach lining. Surgery next week and the roller coaster ride begins. I am devastated, and also a little (no, a LOT) pissed off at her. She has not had a pelvic exam or mammogram for 4 YEARS! What did she have, a fricking death wish? Family history to include mother, sister, aunt - and your bury your head in the sand? I feel so sad and helpless. I am afraid she will not be a warrior. She is clearly a very private person - has been in pain for weeks - WEEKS! The has two beautiful, talented teenage daughters, a great job ... bleh.
Go forth ... be a queen ... be a WARRIOR.
Love, Debbie
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Hi All, checking in before the weekend. I had number 12 today out of 33. I'm starting to get pink. I'm using the bath recipe once a day and the caledula. So far so good. The funny thing today... I'm driving into the hospital parking lot and the security bar came down on my car...really?!!!!! I now have yellow paint on my black car... never a dull moment
Have a good day and fight hard!
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Redsoxfan - glad to hear the Emu oil worked well for you. The nurse told me today that everyone she has seen that has used it has had great results. Here's hoping!
El-jay - I finished chemo on November 4th and am just now able to go without a wig or scarf. Still very short, about 1/2 inch but I couldn't stand the wigs anymore! I figure it will be a few more months before I am really comfortable with it.
Debbie - I was told no moisturizer for 4 hours before rads. So sorry to hear about your family members -
Debbie, so sorry to hear about your family.
I wanted to add that the moisture bath recipe I posted a few days ago, can't prove that it helps the skin, but it sure helps with stress.
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Debbie - so sorry to hear of your neice's troubles!
Beebop - thanks for the info about your hair - there is hope that I will get mine back!!
I had treatment 18 of 30 today. I found a small freckled area on my boob that has lost it's skin. Crap! I have kept it covered in aloe all day so hopefully it wont get worse. I guess I will have to have the tech or nurse look at it tomorrow morning.
only 12 more to go, only 12 more to go, only 12 more to go!!! that is my mantra today!
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Good Friday Morning,
For all of you already doing radiation, I am guessing Fridays are a relief for you to have the weekend off. After 7 months of knowing I will need radiation, I finally have my schedule and will be starting March 12th. Two days ago I went for the mapping and simulation, which took only about 30 minutes. Prior to that I had an exam and consultatin with my radiation oncologist. My tattoos are only small little pinhead black spots that are actually hard to find. I asked if that was all there was to it and they said yes. My oncologist was reassuring about avoiding heart and lungs but said there is a slight chance that it can happen. He said in his 30 years of practice he has not seen it.
I was also told not to use any lotions and if I start to become sore or burned, they will recommend what to use. They were quite stern about that. They recommended Dove soap only for washing with.
So here we go. gjsqueezebox - we all know how you are feeling right now as it is all beginning for you. People keep telling me how strong and courageous I am and it gets to the point where I don't want to hear those words. They do not know what is going on inside my brain and body and I feel I am only doing what has to be done. I don't feel strong. I still feel pissed off and guilty for what is happening to my body. I wonder if any of you felt vulnerable between chemo and radiation when it seems we are not doing anything to fight this disease. I have been feeling that way. Like it is getting a chance to take hold again. My social worker who came to chat with me while in the "chair" says that is very normal for patients to feel vulnerable when they are all done treatments and there are support groups for those people. I live so remotely I would not go to a support group but find comfort right here on this forum.
Sorry we all have to be here but so grateful at the same time for the support. Ten more days and we have to move out of our comfortable home (boo hoo). This too shall pass. Enjoy your radiation-free weekend. Allagashmaggie
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gjsqueezebox, praying your surgery goes well today and that it is minimal!.
debbie, so sorry to hear about your family and praying for a good outcome!
I also wanted to thank all of you for making me laugh reading all your comments and that relieved some of the stress. macatacmv, I DO want that button!!
I wanted to share this as well. After tx yesterday I stopped at Sam's to get a few things. I happened to wear my VERY pink survivor shirt (which I rarely do) so I stood out. I was loading my car when this stranger comes up to me from across the parking lot and said that she survived breast cancer twice and I was going to be just fine. She then gave me a quick hug and walked off. I was so stunned I had to yell 'thank you' to her because she was already that far away. Between all of you and her I am in a better place so, even though it may change again tomorrow, thank you for today!!
Sherry
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TGIF, Certainly takes on a whole new meaning. I'm about to get on the boat, but am happy that I get two days off. And my son is coming home for spring break on Sat. So he will bring some cheer (and two friends) but it will be distracting and bring energy into the house. This afternoon I am having a chest xray. Never ending doc appts.
sherry, where do I send the button lol, we could have a lending library. I too have lots of encouragment from people I don't know, most of all from the drivers of the Road to Recovery program that pick me up from the boat and drive me to the center and back.
gjsqueezebox, also in your pocket for your long day. I have been so tired ever since dx (actually before) I got through the surgery and now my job is to take care of myself. It is real hard for me to accept help and just rest. So let yourself heal.
hello to everyone else, have to run now, boats have schedules and so do rads.
love to you all
Nancy
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Hello, Rads sisters, I will have number 20 out of 33 today! I have a tan under my arm now, and slight swelling-no blisters or broken skin. My RO swears by Miaderm cream, which I use all the time.
I have been losing a few pounds since I don't feel as bad as I did on chemo, so I am eating less "comfort food." It is a lot easier now to say, "I can't eat that anymore," because I don't feel so sick. I still get tired and sleep more than I used to, like many of you. I think that is okay. My body is going through a lot.
I had my fuzz trimmed on my head so it will grow out more nicely, and have about 3/4 inch. My stylist said to stick with the wig for now! Then in a couple months she will use an ammonia-free color to brighten/cover the gray. She said with a bit more hair I can sport a cute pixie cut, but not yet. I agree that waiting for hair is frustrating.
I enjoy going to my support group of women getting cancer treatment. It helps my perspective, and also is validating, when the rest of the world sometimes is not.
Time to get ready for Rads!
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Sherry - I loved the "kindness of stranger/sister warrior" hug. I had a man greet me in the grocery store parking lot a while back, when I had a hat on instead of a wig. He waved to me and said something to the effect of "hang in there my dear" ... maybe his wife, or mom, was a survivor and he knew what he was looking at. It made me smile, but also made me cry, if that makes any sense.
And all ... I am constantly amazed by the varying instructions about how to treat the skin during radiation. I read a comment on one of the boards from a lady in Germany who said in that area they tell them nothing but baby powder ... someone here today said no moisturizer at all ... my doc is cool with about anything. Everybody's skin reacts differently, just like people can have different SE from the same chemo cocktail. There are no cut & dried, hard & fast rules with this awful journey. You just get through it the best you can.
I had my 2nd boost this morning at 8, and will have the 3rd at 4 today.
Swim up bar ... swim up bar ... swim up bar ... Yeah.
Debbie
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Sherrybaby - love the random hug story.. this is a tough disease but there is sisterhood that is amazing! Allagashmaggie - I totally understand your fear between treatment types.... After my surgery I didn't see my ONC for a month before Rads started. He said I didn't need to see him for 6 weeks and I cried... totally out of the blue.. I even asked if it could come back and he assurmed me not in 4 weeks.... I was too told this was totally normal. Even with a good prognosis and clean PET i was terrified. I guess it's one more thing we will need to live with. My Friend is 5 years out from her breast cancer ...she says it does get easier and becomes less of your everyday thoughts.
13 done 20 to go!! Have a great weekend all!!!!
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gjsqueezebox- Speedy Recovery and best wishes for an easy surgery!
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TGIF all! Had my 19th visit today - only 9 to go - in the single digits baby!!!
Now getting some mild redness under my armpit, even though I am not getting nodal radiation. Techs said it is still in part of the radiation field. Overall, though, my skin is looking good so far - just mild redness and minimal to no discomfort. Had my 2nd bolus today.
So DH and I went to see Wicked last night...had to climb all the way to the balcony seating. I became sooooooooo winded...fatigued...slight chest discomfort...we had to slow down...so scary since I'm normally so fit. I could do intense dance cardio for almost 2 hours prior to all of this. When we slowed down, everyone started passing us by. Usually we are faster than everyone else when we walk. It was the first time I've felt the real fatigue effects of radiation and felt "sick". Glad I don't have much longer to go!
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Here is another "random act of kindness" story:
Last night in the grocery store parking lot, my husband and I were "gifting" all the empty bottles in our car to a homeless gentleman. We see him in the parking lot about once a week and every week we give him the bottles and he lets me know how his sobriety is going. (we have been doing this for about 5 years now). What made last night different, was while I was helping him load up his cart, another homeless gentleman (whom I had bought coffee for earlier) came up to me and asked me if I had cancer. The head scarf kinda gives me away. I told him I was almost finished my treatment and he asked me if I would be ok if he prayed for me. Told me he was a cancer survivor himself and wanted me to know that people cared. What a blessing! Here he is in a tough financial place, probably battling some sort of addiction or mental illness and he cared enough to care about me! Brought tears to my eyes!
Hope you all have a restful weekend full of healing! Here's hoping my skin heals up before monday!
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That's a great story el-jaye.
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dancetrancer - Hope you enjoyed Wicked! I saw it with my daughter a year ago and it was awesome!
Sorry that the fatigue is so bad. The good news is after this is all over and our bodies have a chance to heal, the energy will come back!
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El-jaye - it was awesome!
What's really weird about the fatigue is I haven't noticed it otherwise. I guess I have to push myself pretty hard before I'll feel it, so that's a good sign!
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The fatigue was my biggest complaint during chemo. That, and the digestive tract disruption. I never thought you could feel THAT tired ... you cannot explain it to an outsider.
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I was just checking on the fatigue factor. I have completed 22 of 25. I am so tired I can almost not function. It is actually scary, sick tired. I saw the Dr. after treatment 20 and he said all seemed normal and that some people react this way. The radation keeps working for two weeks after the last treatment and then it will take 4-6 more weeks to gradually get the energy back. I thought chemo was bad but this ranks right up there.
Has anyone heard how soon after rads they make you start taking the anti-hormonal drugs? I was hoping to have some time off as I usually have reactions to all kinds of meds and can't deal with that right now.
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Jean, I think how soon you start anti-hormonals is variable based upon your doc. I was reading about this as well. Some start it even while you are on rads, but it seems most start it afterwards - pretty soon (seemed like most posts said within a week or so). I'm so sorry you are feeling so tired...I can see how it could progress. :-( Hang in there, you are almost there!
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Jean - only 3 more! I am at 19 out of 30 and the fatigue is not too bad. I seem to run out of steam mid afternoon and need to take an extended coffee break. Today my boss has made me coffee and I am resting at my desk thinking about napping!
I hope I can make it to the end of radiation and working full time. So lucky I can take it easy at the office!
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