Spring 2013 Rads
Comments
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Hi y'all & TGIF!
Today I wore a sticker that said...I'd like the left chick breast all white meat easy on the rads!
Rad team:))) received a call early this morning that my rad machine was having computer issues and gave me two options...take a day off and continue Monday or go to their facility in neighboring town with my rad team. Hummm more waiting or continue the countdown???
Got in car drove across the valley (drive usually is only 6minutes...yes/no on feeling guilty) and had rads! Daaa so drumroll 22/33 yippee! 6 more reg then 5 boosts:). Skin, girl, mind hang in there! Oh how I wanna go home.
Glove - Welcome & Congrats only 2 more to go! Yippee. How are boosts...what should we expect? Luv hubby is team carrier & good score giver. Rest up this weekend...he can fan your breast like cleopatra
)
I'm with Lemon ... Y'all are awesome so (((hugs))) loving safe comfort place to share this horror of a disease. Thanks for being here...the journey is better shared.
Cindy -
Hey i finally got my cyberknife appt the 17th then i'll start rads on Monday what questions should i ask my ro? i think i'm more anxious about starting this then any of the chemo or cybeknifes i've had also its the lefty what was that about special breathing to protect the heart and lungs? i do Kundalini 3x a week will this help? any other suggestions would be appreciated. thank you all so much i feel the love and support here!
love and blessings to u all
chris
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Sallyann,
I loved your post and wouldn't it be wonderful if our doctors would actually speak with each other?
Sheryl
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braids, your doctor will tell you to hold your breath because it pushes the heart out of the field when they are radiating your lefty. In my case, they will only radiate the lumpectomy field but since it is near the heart, I may have to do the breath holding too.
Some RO's do rads in the "prone" position, lying on the belly with your boob hanging through a hole so that they don't nick the heart and lungs as well. You can also ask about that. Your boob has to be large enough to hang down far enough. The way I am being treated, I can't do that type since mine are all boosts in essence. So, I will likely be breath holding to push my heart out of the way. I will talk to her when I see her on the 19th for my final check before I start on the 22nd. My heart may not even be in the field for all I know since it is partial breast rads.
So, ask about this when you see them since it is your left. Hugs and know it will go fine!
Cindy, you are in the homestretch! Seems like yesterday you were starting!! Of course, it probably does not seem like that to you though..lol
Hugs to all the brave warriors. Soon I will join you, albeit briefly for my tx's. One week from this Monday! Twice a day! I am going to work in our New Haven office that week since it is like 5 mins away. I will go there in between the tx's and then go home after the second one. That way, I will only use about 3 sick hours a day instead of the whole day! I need to save those just in case. Short term disability is only 2/3 of your pay and I can't afford to do that.
I have taken enough time off for doctor appts etc. I have never used this much sick time in my working life. I have used like 76 hours since January! That is more than I used in three or four normal years.
Hugs to all!
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Good morning sisters! Rads going great for me, 3 weeks down, 4 to go, no SEs yet. Mine is on the left so I do the breath holding thing too. It's not hard, they just have you take a deep breath and hold still while they zap you. It isn't long enough to be unpleasant, no worries. They did the original CT simulation both ways, with the breath holding and with normal breathing. I guess it's not always needed, but in my case they decided it gave a better angle or whatever. It pushes the heart out of the way a little more.
Hope everyone is having a great weekend, resting and healing. -
Jennie93, we started rads the same day! At first I was told 33 days, but now they're saying 30, not sure why it changed. April485, your explanation puts to rest my little envy about the prone position. My breasts are anything but large, so I would not have been a candidate. I do "deep inspiration breath hold" like several others here. I count in my head. The first beam is about 28 seconds and the second is 25. In truth think I'm counting a little fast, because I asked them to tell me when it hits 15 seconds and my count is usually at 16-19, so maybe in real life the zaps are a bit shorter. Braids3, yours may vary. What is a cyberknife?
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RunFree16- Congrats on not needing to do the chemo, I am sorry I missed that post. What great news!!
Cindy- You will be done in no time. I know the techs are going to miss you!
briads3- I am sorry I also dont know what a cyberknife is?
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I started last week. I have done 3/33 (possibly 28 depending on how skin looks at day 28). I am just 4 weeks out of my bi-lateral mastecotomy. My skin feels irritated and I have been using the aloe from the leaf. I drink tons of water and I am drinking a Nutri-Bullet in the morning with coconut water, berries, banana and kale.
I thank you for the info about the Aquaphor. I have used it on my daughter who is 4, but I will ask my RO if it is ok for me to use as well. My skin is EXTREMELY sensitive so I had a feeling this would happen. So far energy level is great. I am helping coach my daughter's T-Ball team and threw a baseball for the first time since my surgery today. It felt GREAT!
Good luck ladies on your journey! We can do it!!!:-)</p>
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Cyberknife is for brain mets. It is a type of rads for the brain I think to shrink the tumors. Chris (braids) is stage IV and is a very brave sister. She is going through a lot and in comparison, I feel like a whiney little brat at times. Hugs to you Chris as we start rads together my friend! xo
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Thanks April. I have a friend who recently had brain surgery to remove a tumor, thank God it was not attached to anything, it had metastized from her lungs. She didnt know she had lung cancer never had a symptom. She had a numb lip and got concerned she was having a stroke, CT showed the C in both brain and lungs. She just finished her rads on the brain and is beginning her chemo in 2 weeks. She is a Warrior like so many here and has no plans on letting this beast win. I hadnt heard of this cyberknife before and went and looked it up, interesting. Imagine 10 years ago we wouldnt be getting the tx we are today. I only hope in another 10 years these boards wont be needed.
God bless all of you here. xo
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Lemon68.yes i am so gratful forthis treatment i was dx stage lV from get go.this will be my 7th cyberknife trearment and ya know this breast rad thig as me more anixous then allthe othe stuff onc told me i'd be getting 6.5- 8 weeks i guess i'll find out more thurs going to do a little get away till wed so good lick this week to all.lots of love and blessings to u and thanks April so glad i have u in my pocket!
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Good Morning y'all!
Oh my, so much activity. Been working on taxes ugh ... poor accountant never been so last minute but its done..meet joe black - death and taxes
Welcome to those new on thread & congrats to those who finished & yippee for those of us counting down tx. Healing thoughts to all!
Wish deep inspiration breath hold was offered at my rad center...wonder about my heart too.
Debb- ask your RO if you may use emu oil...or my girls...have been my salvation
Lemon- got a blister under girl driving me crazy...despite all efforts for no contact...wonder if cornstarch and cami rub and irritated free boobing big time today! Hope your seeing improvement in your skin.
Jennie&RunFree- congrats on 3 wks behind and 1/2 way done this week:). There's something about having more days behind then ahead that is up lifting.
Braids3- in your pocket Thursday warrior!
April- your clinical is soon:)) take good care of yourself this week so your body&head are ready:)
Ok warriors lets get some more R&R! (((Hugs)))
Cindy -
April, thanks for the explanation about the cyberknife. Chris/Braids, you're a hero to be keeping your spirits up with all you're facing! Good luck with the cyberknife on Thursday, and I hope your getaway before that is just what you need. I hope you can feel better about rads too. Some people breeze right through it. I always feel sheepish saying how well it has gone for me so far, but my hope is that it could dispel fears for people who are scared. I don't know how the next 3 weeks, plus recovery after that, will go, of course. But at least I've had 3 pretty darn easy weeks.
Cindy, my center did not initially offer breath hold. I met with an RO at my surgical hospital who would have used breath hold for me, but she knew I was going to look into the closer hospital for rads, so she said to ask about breath hold there. They got it going just for me and even fashioned a doorbell for me to ring if I had to breathe out mid-beam. I say this for anybody that is told their center doesn't offer it. There were some initial bumps in the road, like an extra planning session when I had to lie in position for an hour while they did x-rays with my breath held over and over, because they weren't sure how much variation in my chest inflation was acceptable. That really bothered my treatment arm, ouch. But I considered it an investment, for me and perhaps for people later on. They wouldn't have to put someone else through that, I don't think. It was the techs' learning curve.
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I'm new here but have been reading the posts from all of you nice ladies. I finished chemo on APril 1st. (Yippee!!!) And although I have lingering side effects from that (and will for a long time, I suspect), I am feeling hopeful and optimistic for the first time in a LONG time. My sweet hubby and I are even taking a long weekend and spending it at the beach this week to celebrate the end of chemo. (Hooray and Yippee!!!)
I'll be seeing my RO next Monday to do my mapping and simulation. I do my first Herceptin only infusion early that morning at my MO's office and then go straight to the RO from there.
Does anyone happen to know if having a seroma from a lumpectomy makes radiation treatment any worse? Does it get in the way of effective treatment or anything? It's not that large, and my breast surgeon said they could drain it if it really bothers me. And it really hadn't until I recently had my first mammogram on that side. Ever since then, it has been more tender and felt more hard and knotty. I'll ask my RO about it when I go for simulation next week. But I was just curious if any of you had any insight. My breast surgeon didn't seem too worried about it, and generally I am a "let nature take its course" kind of girl myself. But after reading about all the side effects of radiation, I am second guessing my decision to let it be. Any advice?
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duckiedee- welcome to the forum - you will learn lots from the ladies here!! I cannot speak about the seroma - never experienced that - but hopefully someone will come along who can help you. Congrats on finishing chemo - it is truly a milestone and an achievement - well done! Now relax and enjoy the break in between chemo and radiation. Good that you are taking time away at the beach to rest.
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Just got back from rad#14 - only six treatments left - two of the whole breast and then four boosts - not sure what to expect from the boosts!! I was gardening over the weekend which meant using my arms a lot - and I noticed the friction of skin on skin in the armpit was getting quite irritated so I made a "roll" to put under my armpit. I filled an ankle sock with cornstarch, tied it tight at the top (I actually used an elastic wrapped several times around until tight), then I put the sock inside the leg of pantyhose, I put the roll under my arm, and tied the pantyhose around my shoulder - it worked wonders at creating a space between the upper arm and the armpit. Today I wakened up and it isn't even red - yeah!!
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Duckiedee - Welcome we are so happy that you are joining ...wow, you've come so far on your journey already! Congrats on completing chemo and yea for a well deserved beach trip...ah the ocean waves and mist.
Make your list of questions for your RO and then cross them off as they are answered to your satisfaction...ask...ask! Is your hubby your appointment buddy, hope so:)
Rads for me reduced my risk of recurrence significantly it was not an option it was life!
Take time to hydrate, moisturize, rest, and just know that rads are doable and like all things time is a great healer. Sending calming confident thoughts your way & laugh!(((hugs)))
Cindy -
Adagio - you need to file for copy rights...you are clever girl:)
Drumroll 2 full 4 boosts you have rocked rads. Heard boosts are aimed at tumor site and much shorter in duration yea! What color dancing shoes would you like...got some serious noise makers too!
(((Hugs)))
Cindy -
Welcome Duckiedee! Congrats on completing chemo! Enjoy every moment of your holiday. Live it to the fullest!
Adagio, yay for only six more rads! That is awesome!
I have two more full breast and then 7 boosts. Can't wait! April 26 can't come fast enough. I'm meeting with the genetics counselor this Thursday and will probably do the testing same day. I didn't want to put off rads until after the genetics results came back because chances are I won't have any positive results. Why delay the inevitable (rads)?! My RO agreed. I meet with my MO on May 10 for my tamoxifen rx.
Happy evening everyone! Hugs! -
You do get the clever award, Adagio!! My arm pit, as well, is one of the few spots that is peeling and feels cracked, irritated...
My full breast Rad (19/33) has gotten an interruption with some boosts, finished 21/33 today. Feels good to give the full breast a break, pain/swelling was getting pretty bad. Didn't think of this kind of flexibility (RO changed my tx plan) so if others are struggling with symptoms you may want to ask to have some boosts throw in before the final countdown.
The boosts are the same dose but for some reason the positioning takes a bit longer and they break the treatment up into 5 parts at 5 different angles. I imagine everyone is different depending on the size and placement of the surgery.
Almost there Amy!!!
Cindy, you're on the home stretch, too!!
Welcome DuckieDee!!
Comfort and Healing to Everyone!!! xo Lisa
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I've been reading here, but I don't think I've posted. I get chemo on Fridays. I have 5 more weekly Taxols. Then I start rads sometime in June.
What are the best lotions to use? Before & after?
What are boosts?
Blessings
Paula -
Hi Paula! Welcome! June will be here before you know it. 😊 I've only been using aloe and occasionally Aveeno. I used Aquaphor for awhile but found it to be too sticky. Great for a baby's butt, not my boob! I will be starting my boosts (7 of them) on Thursday and from what I am told they are directed only to the tumor site. I will be having the same gray for my boosts that I'm having for the full breast, which is 2 per day for a grand total of 60. I hope this helps a bit. Hugs!
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I have finished 28 rads and was supposed to start my boost yesterday, but I had intense pain for 3 days. Skin and internal pain and intense tightness...(I had immediate reconstruction...so I have implants) I am still in pain today and it was my choice to take the time off....I am considering to take 2 more days off....
well..anyhow...has anyone done this before? I had very little problems with chemo...
Thanks....this site has helped me so much thru this.....
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Duckiedee, I don't know if a seroma makes any difference in terms of radiation sensitivity. I think the incision site itself may possibly be a more sensitive spot, at least mine was. I did have a seroma at the lymph node incision site. Mine actually burst and drained spontaneously. When I called my BS office, they said to just let it keep draining and close naturally. I did this, but I had an open wound for about 3-4 weeks. If I had a do-over, I think I would have gone in to have them drain it so that it wouldn't have burst. Again, I don't know that the seroma itself made any difference in radiation sensitivity because it was healed completely by the time I had rads. But, the cosmetic appearance is likely worse than it might have been if the wound hadn't reopened and taken so long to heal. My BS office did say that it was better to have the fluid come out (either drained or spontaneously, as mine did) as compared to waiting for the body to reabsorb it because it lowered the chance of infection.
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Paula,
My RO recommended a cream called "My Girls", it has calendula 10% in it as well as a bunch of other oils and creams. It is really pure. It cose a bit $25 but spreads really easy and absorbs well. I also have pure aloe and aquaphor. I am only 6/30 so my skin is ok but I use the cream to have my skin in the best condition. Also drink tons of water.
Hugs, Sheryl
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Hi y'all
Welcome Paula and congrats on approaching the end of chemo land:)
There's a long list of skin care products, but most important ask your RO. They usually have samples of what they prefer. Ok here it goes: 100% pure aloe, miaderm, jeans cream, my girls, aquaphor. Emu oil, and more.
I think free boobing is good airing out the girl. Soft cotton cami without shelf, soft cotton boob sock to keep girl off chest, soft pillow for underarm.
Moisturize your front and back. Hydrate, eat well, rest, and take your sense of humor with you...each day. Be. Kind to yourself set priorities and live with grace. This is just a few weeks of your life...it will pass...so breathe.
Always ask your rad team if questions and take a few pics to document this part of your journey and celebrate a wonderful life!
(((Hugs)))
Cindy -
Cindy~~Thanks for all the great tips. I was thinking Aloe, and I have Aquaphor, but I will ask the RO.
Blessings
Paula -
Hi All
I am so pleased so see some done or almost there and doing fine. I was back in RO Office yesterday, 1 week since final zap. I thought I might be going crazy as I could feel the heat and burn moving, he said I am not crazy it is now in the tail of the breast tissue under my arm and its exiting out my back. Has anyone heard this before? I cannot raise my arm as the burn now extends to my back and is raw. He said I am having a severe reaction and hopes within the next few days I feel some relief. They did wound treatment and it felt good. One thing is certain I will be scarred from this. My SNB scar and surrounding area is black and charred and it looks like I have other incision scars where the skin is ripping. I did have a seromona that was drained before I began rads. I am very swollen in that area, almost like rolls of baby fat. I am not going to get graphic about the actual breast but I dont recognize it as mine right now.Mentally I feel better today, I think I am getting used to hurting.
I just wanted to say that days 1-14 I was pretty good. It wasnt until after #14 I almost overnight got bad, #15 was horrible and #16 put me right over the edge. I didnt want to do 15 or 16 but I felt forced to finish. Keep a close eye on things because for me during the TX was not bad, its after that I am suffering. I am sick of seeing myself post whining here, this is it for me on this thread. I only post today in hopes I can help someone else. I am a regular poster on Team ILC Warriors, stop by its a great group with wonderful women and information.
Thanks all of you and good luck to you with the rads. xo
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lemon - nice to hear from you. Don't worry about thinking that you are whining - I am so interested to hear how each of us react so differently to this radiation treatment. I have never heard about the radiation exiting the back - that is scary! I pray that your skin will heal very soon!! I just did treatment #15 today and my breast is itchy and red, but no broken skin yet. After #16 I start getting boosts to the incision area - don't know what to expect there - hoping it is not painful! Maybe I asked you this before, but do you know the amount of Gray that you got during your treatment? I am wondering if it is the dose that causes the different reactions? Thoughs are with you in the days ahead - hope all the pain is worth it in that your cancer NEVER comes back!!!
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Sweet Lemon - don't go we need you...you're a brave warrior!
This is a safe play to share the truth of our journey...don't hold back. We need to hear and know that we are here something's just to hear. Sit close share your heart...(((squeeze)))
Today I ask RO about my escape...but without sharing I would not have known that the accumulative effects of rads would present after zaps were over. Now I'm aware that I can't just get out of dodge...I must wait and see...RO said the 1st 2 weeks would be the tell.
Oh Lemon I need your feedback ... The truth .... We are each so very unique, but there's a bond in tx that extends beyond our dx&tx.
Sending healing thoughts to you and to all on this journey!
(((Hugs)))
Cindy
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