Spring 2014 Rads
Comments
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thank you so much. This has been a long weekend. My mom was diagnosed with heart disease at 59 without the risk of radiation so at 55, it is definitely on my mind. On Tuesday, I will definitely ask my RO what my choices are. It has been 7 weeks since my lumpectomy so I know I am running out of time. All I want to know is: if I don't do breath holding, will my lungs and heart be zapped?
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maryfox- I'm astonished you had no pain with chemo. I had serious pain and its lingering a bit even three months out. By comparison, rads really were a cakewalk. I guess it shows how truly different we all are. Hope you feel better soon!
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Vintagegal Hang in there. Your body will adjust. It will pass quickly. I just took it one week at a time, helped me stay focused. Five more days, four more days easier to handle. The weekends really help the skin catch up. Use the aquafore 3x day and liberally. Make sure to get underneath in fold area of breast and the upper chest. Good luck this week. Hugs
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does anybody have hot flashes during radiation ?
I thought I will get those only if I am pre menopausal . Not sure if it is happening due to rad or due to premenopausal.
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Thank you all for the great advice. I wasn't able to get out to the health food store yesterday and they are closed today. Part of me is thinking, I only have 3 more tx's, it will be fine with just the aquaphor and cornstarch. Then I totally flip to the other side and I am getting into the I don't wanna go back! meme.
It really is crazy how we all have such different tx's and reactions to it. With my family and Lyme, we all have the same infections but each of us have different symptoms and react to meds differently. You'd think I would expect that with cancer too, but I am still quite the newbie in this arena.
Hope that you all have a wonderful day today!
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mom2- great news on the PET and I hope all goes well when your onc meets with you.
Mirka-thinking of you and your mom, I hope she heals quickly
Donna- how is your fur-baby doing? he is a beauty!!! I don't know what I would do if any of mine got sick right now. My dogs have always been a huge source of comfort to me. In fact, my dog- now gone 3 1/2 years was my BFF in so many ways, and when I first got my cancer dx, all I wanted to do was bury my face in her fur. I miss her so much.
Mary, i hear you on the black undertones. I look like I am all dented in and bruised at my scar.
Joan -- rant away, you need to get that out. I go through major periods of that with my Lyme and I am sure that as I get "done" with BC treatments and it has more time to sink in, I'll have to deal with that too. I hope that you feel better today.
That makes me wonder-- how long after you all finish rads are you planning on doing the lotions? I have a feeling, knowing how I can be, once I am done, I am going to get "lazy" about that and I don't want skin issues to pop up afterwards.
Mom2- that "new normal" is exactly what my SW has been talking to em about. She feels that I have been minimizing/in denial about what I have gone through -- dx, surgery, rads, then will be doing hormone therapy, and then having the dx stay with you for life. How do you all cope with that? Guess that should be a thread, and probably are many of them here that I should look into at some point.
No hot flashes for me, just the constant heated up boob.
xo
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Thanks flagirl
I slather up 3-4x a day. It is easy to do that on a totally flat chest! (I can do it while in the car!)
The pings of pain were pretty annoying again last night. And the itch! LOL I scratch but it's numb, ya know how you can't feel/scratch your lip when it's been novacained?
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I hope you all are doing well this week-end! I am getting the IMRT rads and there is no breath holding or bolus involved. My tumor was close to my chest wall, but on the right side.
I am looking forward to getting rads over, but I think it will be challenging moving forward, also. Maybe we expect too much of ourselves sometimes...or are trying to meet others' expectations. One thing is for sure, it has changed us all. I hope I have the strength and courage to make the best of it. I'm sure it will be a long road, but one step at a time. Look what all we have accomplished so far!
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Good morning all
I get what you're saying Vintage girl - while I had a rough time with chemo, I could feel the cancer shrinking, so I knew it was worth it. With Rads, the cancer is gone. I know this is to prevent the reoccurrence, but by burning my whole upper right chest? I have a lot of trust in my doctors, so I am doing what they tell me, but I gotta admit, I am still a little unclear as to why I have to do so much of it. My SE's are not awful - just redness and a little swollen, but I just want my life back already. I have missed an entire school year with my granchildren - I used to be at everything possible- awards assemblies, holiday programs and parties, volunteering in their classrooms, etc. I want to be in control of my life, not BC.
Anne
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I think I will continue to use the lotion for at least a month or so afterwards. And I have never been one to use lotion much, except on my legs and my hands. My guess is the skin will continue to have dryness issues for quite some time. I feel like i've been baked from the inside out---like a microwaved muffin.
I am still irritated underneath the breast and using the lotimin, but it is so hard to keep the skin to skin contact from making it painful. My little toilet paper roll "prop" i made has collapsed-either from use or from the weight of my boob..HA. I got to thank every woman on these boards who told me the t-shirt with the bra on top trick. That has been the best advice.........
This week is NURSES WEEK, and I have some wonderful ones at the community cancer clinic.
My jack in the pulpits are up- and I mowed the lawn yesterday. Spring is here, spring is here---even if I am wearing a turtleneck sweater.
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Bigheartbeating----you need to let your RO know about these skin changes since you completed your rads/ Some skin changes will require a different regimen. At least call them.
I was told by the nurses when I started that if I peeled, I would be restricted to use of aquaphor. Did your RO not schedule a follow up appointment for this month?
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BigD, thanks for letting us know how it has been going for you immediately after rads ended. That's the part I'm most interested in because I know the skin can keep changing for a few weeks afterward.
MaryFox, I'm sorry you skin is so dark already. I think we are a day apart on rads.
Vintagegal, I got a lot a pings early on with rads too. I think it's from my nerve endings not being very well healed yet from the surgery and then getting irriated by the rads. I think of it as my "early warning system" for LE too because I get a lot of pings in my underarm area and my arm. When it's hurting, I cut back on activity with my arm. My RO (and I) are keeping a close watch on it for LE.
Today is day 25/33 for me and I'll get marked up for the 5 boosts at the end today. The boosts will start this friday. My skin is holding up surprisingly well. I'm just slightly pink all over with a "hotspot" at my collarbone. I'm thinking that spot will most likely open and weep at some point. My stickers have stayed on without falling off! Aren't they lovely?
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Finished 18 or 33 today. Then had CT to plan the boosts. I"m sort of pink from collarbone down and a bit tan under arm. Using aloe 2x day and cornstarch 4-6x day. I think of Rads as a healing beam that's been optimized just for me and the tats don't seem so bad.
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Feeling much better today, antibiotic kicking in. Trying to catch up on housework. Only three more full to go! See the RO for the last time tomorrow. Yey skin holding up good but I felt the burn. Hoping it holds up. Good luck with your treatments this week. Load up on the aquafore
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simple4life Does it itch or just burns? Don't let it get any worse if you can help it. I used Epsom salt soaked washcloths for the itching and real aloe plant. Then put aquafore on after aloe dries.
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1 week out & the skin is looking good - still not letting up on the lotion/airing tho - i want this skin tip top for my vacation - 2 more days! sooo sorry i let myself get freaked out by the "what if's" - but radiation definitely was a tough one - mentally & physically.Still worried about future consequences but for right now i am looking forward to nine days of no work - no treatments - and NO WORRIES!!
"only worry in the world, is the tide gonna reach my chair?"~~ Zac Brown Band
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Notbuyingit---Love yourworry quote----are you done now?I got the lymphedema class this a.m, so praying I don't have to deal with that. Said if we plan to fly we should probably get the sleeve to wear because of the change in cabin pressure, etc. She had them in every color of rainbow, including leopard print---now who would want one that wasn't flesh colored...
Just us old cougars, right/
Then had them look at that mess under my boob, and now I am doing "saline soaks" 5x aday for 20 minutes each and RO said she hopes we don't have to give me a break in my treatment. I hope not too, since I only have 10 more to do.
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why so frequent treatment of saline soaks, Redheaded1?
I am on my 5/30 treatment today. Over the week-end, the hotness cooled down little bit. Redness is still there. The pain comes and goes.
I got walmart 2 sizes up cotton bras, cotton, fruit loom, not sports. I was uncomfortable with sports cotton bras as they were feeling tight.
The new ones are almost like wearing small top just covering chest. Hopefully, it won't ruin my work clothes.
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Hello Ladies,
I'm joining you all. I had my first of 27 today. I hope my RO was correct when she said I would do "fine." I didn't bother to ask her to expand on what exactly she meant. It's funny- with my first diagnosis I was all over it- researching, questioning, wanting to know it all. This time I've been more "whatever." Of course last time it was during my summer break and this time not.
I'll start reading through the radiation threads and get back in the knowledge game.
Lisa
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Lisa, sorry you are going through this again, but welcome to our group here. Lots of good info in this thread on rads. My RO, MO, and surgeon all said about rads: "It's not that bad, you will be fine." I really was for the most part. Some fatigue here and there, but I worked full time through it all. I did have some pain towards the end and that still comes and goes. I am just over 3 weeks post-rads. I had no skin issues at all, but it was itchy towards the end and afterwards. But as you know, we all are so different. Hang in there, we will keep you in our pockets and be here for you when you need us.
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I joined today too. Had my first of 30 treatments. Living 3 1/2 hours away from home for treatment. So far that is the worst part of it but I am enjoying exploring Houston.
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Thanks for the welcome BigD. It's good to know you are all there. I am a little apprehensive as I have sensitive skin and burn easily (even though I know it's not an actual burn) and because of the bmx they are using a bolus. When the therapist explained what is was and how it worked I said, "Great. Sounds like it will lessen the redness," to which he responded "Actually it tends to make it worse."
Maybe best to stay in the "whatever" mode. Ha! :-)
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Hi Warrior50
I have a commute too but not as long. I drive 30 mins to work then 40 mins to treatment and an hour home. I will enjoy re familiarizing myself with parts of Los Angeles I don't see much.
We will help each other through.
Lisa
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Welcome Warrior and intothewoods. You will meet some great folks in these discussion boards. We don't know everything but we share what we tips we have to make sure you know you aren't alone. sometimes its easier to share with the strangers who are going thru this than it is the folks you've known all your life but haven't had the "C". This is the first Monday evening I have been home to see a show on TV called MOMS---the older woman was diagnosed with breast cancer and getting her first chemo---her two friends who were trying to "help" were hysterical, but yet factual to real life......
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Welcome Warrior and Intothewoods!
Into, I have a bolus as well every treatment today was 8/35 and so far so good, my soreness right now is along the chest wall. Dr's did tell me that there may be more issues under the bolus. I have bolus as I had very little tissue and it was all removed in that area.
I suffered fatigue issues before this due to vitamin deficiencies, and this is already hitting me. From the time I leave until around dinner time. I'm 46, not young, but not old. I guess still considered young for this. Today I was sitting in the "holding area" with 2 other ladies and one of the ladies daughters. Both are stage 4, as you see some of the same people you get to know them and they share a lot. I'm not real chatty, but who knows down the road, I tend to be more of a listener right now. And one of the volunteers has taken great interest in me. One is just there for radiation to get rid of her pain and onto hospice, the other has a horrible family situation and has to take taxi's to and from radiation everyday. It all makes you really enjoy each day as it is a gift, even as we go through this trial, or as I say chapter.
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Hi Lisa and Warrior! This group of amazing women will help you get through it all.
I am 21 days done and 2 more boosts to go. Yesterday, right before I was set to go in, the machine broke. They told us that they had a call in to get it fixed, but they didn't know how long it was going to take. Gave us the option to go home and they would call when it was up and running, or we could wait. All I could think was that Wed was my last day and no way was I going to push that back.
My nipple is still peeling and it looks like I have broken blood vessels under my skin, but other than that my skin has held up well. I am more upset about my weight, Getting weighed weekly causes me anxiety (have a long history of anorexia) and I gained 2 pounds, yuck. I hope that doesn't trigger me once I am done and have more time to focus on *that.*
Not-- woot on getting close to vacation time!
Red- sending healing thoughts to you and your poor skin
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Redheaded this old cougar is super jealous over that leopard print sleeve!! they said i have to have one for the plane & all they offered me was black ( to FL? i don't think so) & beige
didn't say how long to wear it before & after - anyone know? i will prob call today & ask...
hang in there, ladies!! so many different experiences but we all have the same goal - do what we can & get it over with!!!
i have about 4 more Herceptin treatments...i need a little more "touch up" surgery - maybe nipple reconstruct - July is my one year!!
the sun will rise, and it will be alright
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Truly great to have you all out there!
Momto3boys, I'll keep good thoughts for both of us bolus gals. Hearing others' stories- a taxi? does help us keep things in perspective. (Cue faerywings' signature.)
Faerywings: a broken machine so close to the end is the kind of thing that would previously set me into a tizzy but I'm getting better at the perspective thing. I absolutely love "No Day But Today" Never saw Rent but I did see Idina sing that song in concert and she was so cool- she invited people to come up and sing it with her. One more day for you! Whoo! Please use us for support with "that" other issue if you need to.
Redheaded1 it is easier to share with strangers because already you don't seem like strangers. That TV show sounds great- haven't heard of it.
Notbuyingit, I just love your name!!!
Thanks all,
Lisa
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I go today for rad #11. Today is bolus day, every other day & I know my chest will be a hot mess! I started with the burn & pangs #5. I am at the point now that I think I am getting a rash (allergic reaction) from the Eucerin & Aquaphor. (both recommended, by many & by RO & tech) Soon as I put it on the picky pain starts & I see the rash more pronounced. The main ingredient is a petroleum product. Not good! I think I see the RO after treatment today so will talk to him about this.
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Welcome Lisa and Warrior
I am exactly halfway thru, but they are going to try to increase my treatment just a bit each day, because my last 2 treatments are scheduled for the week after Memorial Day and my grandkids have special things going on in school in FL that I don't want to miss and I am being treated in Ga. I met with RO yesterday and she said they are going to back the bolus to once every three days instead of every other day, because I am very red. She asked if I was itching and I wasn't. Guess what- I am now. Power of suggestion or did she know by looking at it? When I mentioned to the ladies who do the ladies who give the treatments that I was at the halfway mark yesterday, she responded, " yup, it's all downhill from here" What?!? Then she realized what she said, and rephrased it to " I meant you are on a countdown now, not going downhill." We all had a good laugh.
Anne
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