anyone starting radiation in September
Comments
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Today I went for the CAT scan and tattoos. Everything went well. I like the clinic I am going to and the people were nice. The only hard part was holding still for 15 minutes (or however long it was) for the CAT scan. Also dealing with the emotions like 'this is going to make you sick for life' and garbage like that.
My next appointment is Monday the 24th and I officailly begin on the 25th.
~ Helen
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I had my tattoos this week I go in for dry run tomorrow and start rad treat on Monday, 9/24. I'm surprised how depressed this makes me...
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I have been in my second week of radiation. I already did chemo and my Surgery in July so this was the next logical step. I did fine at the Pre CT set up for the radiation but I must admit I had a bit of a mental meltdown on the first day of the real thing. It just seems counter-intuitive to lay calmly on a table while people shoot high dose radiation at your body. They had to stop for a few minutes to wait for me to collect myself so I wouldn't be moving but they were very nice about it. I suggest you bring an IPod if you can because the Sting music (the Fields of Barley) in the background made me cry even harder! That being said, the other 7 treatments have been fine and they get quicker as they get to know you because they can set you up faster and get in a routine. My skin is only mildly red at this point. I guess the 3rd week it gets pretty angry. Good luck to all of you...just one more step to get through.
Amy
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Joanne Elizabeth, I had a left mast. with no positive nodes (13 removed) and am doing a session of 25 rads. As the surgeon said when I asked him about having them "When you finally get the guy down, give him 1 more big kick to keep him down "
I loved that one.I finished treatment #10 today and so far so good. I am using Lubriderm as suggested by the techs and it seems to be working well.
Have a great weekend everyone.
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Are you worried about lymphedema? That is a major concern for me I think the risk is something like 30% if you have had axillary dissection + radiation.
Joanne
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Yes I am but I am more woried about cancer. For me I will do whatever it takes to get the risk of reoccurance as low as possible..
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((Amy)) I'm sorry you had a hard time. It does seem counterintuitive to have radiation beams aimed at your body. I take comfort in knowing that this is a highly researched and technical proceedure, so most likely it will be OK.
My husband has been going to many of my appointments with me. He asked me if I wanted him there for the first one. I said I don't think so. We'll see if I change my mind. I go for the trial run this Monday (24th).
Great idea about the ipod. Music always helps me.
Pam, sorry you are feeling depressed. I hope it passes soon.
Weet, they said to use Lubriderm, eh? Mine said to use 100% Aloe Vera, which I happen to have, though it might be getting old, so I will buy a fresh bottle. They also said Sween (?) lotion could be used. But it has a fragrance, which gives me a headache. So I'll stick with the Aloe Vera.
Whew, I hope I can remember all the things they told me to do, and to not do. I'll have to read all those papers over again.
~ Helen
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Hi all,
I started rads on Thursday, am scheduled for 33 total. I didn't have to do chemo so I'm hoping to have a pretty easy time of it. The most difficult time for me will be the 50 min drive each way through rush hour traffic. My breast seemed a little sore today after 2 treatments - has anyone else had this happen? I guess it could be from having to hold my arm over my head but my shoulder isn't really stiff. My rad onc also told me to only use 100% aloe gel. Hope the next 6 1/2 weeks goes by quickly!
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Helen and Jayhawk. I was told to use Lubriderm to keep the area moist. If I burn they said to use 100% aloe but to keep using the Lubriderm as the aloe will take the burn out but is very drying so the moisturizer is a must. I also was given a "recipe" for a treatment if it burns. think it is just salt and water but I will put it up tomorrow for anyone who would like it.
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Jay, you have to drive 50 minutes each way in traffic? Yikes. I have a 15 minute drive each way, fortunately. I start on Tuesday.
Weet, I'd like to see the 'recipe' when you have time to post it.
Have a good weekend.
~ Helen
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Hello Ladies,
The "recipe " from the hosp. is for a Saline Soak.
Mix 4 cups of water and a level teaspoon of salt and boil for 10 minutes. When it is cool place a clean soft cloth in a bowl and pour the solution over it.Put the cloth on the reddened, cracked or open area for 10 to 15 minutes but be sure to remove the cloth before the cloth dries.Leave the exposed area to the air for another 10 to 15 minutes.It can be done 3 or 4 times a day if needed. Very simple but supposedly very good.
I had a wonderful surprise last night. We were going out with friends and when they arrived at our place my friend presented me with a hand done quilt she has been working on for me for the last few months.On one corner it has a breast cancer tag on it saying " Quilted for my courageous friend and then my name, hers and the date." Of course I cried, it is so beautiful but the work and thought she put in is even more special.We are now off to my son's for my DH and my 3 year old grandaughter's birthdays.
Can life get any better !!!
Pam and Helen good luck tomorrow, the build up to it is much scarier than the actual thing, you will be in and out.
Hugs to all
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Hi all, Well I just finished my first week, only 6 more to go, went pretty good, just a little tried, skin still looks good. My computer has been down for a week, just got it back up yesterday.
Hang it there everyone
Darleen
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i started august 27th, so i've done 4 weeks so far. my left breast is a bit pink, but that's it. i've been using sween cream when i remember, and not wearing underwire bras. i only have 4 non-underwire bras, so i supplement with camisoles, and just wear DH's shirts so no one can tell the girls aren't being supported.
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my last chemo was 7/11, and my hair is about 1/4" long all over my head, nice and soft, like a stuffed animal. i'm using nioxin cleanser, scalp treatment and therapy and follicle booster.
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((Weet)) That is SO sweet!! I'm getting tears in my eyes, too. What a total blessing for you. God has given you a dear friend!
Ahh you are a grandmother, how wonderful. I look forward to being a grandmother one day. It will be awhile, my oldest is 15! I'm feeling pretty peaceful about tomorrow. My dh reminded me that there is radiation everywhere. I turned on the light and he said - you just were exposed to radiation. That helped me to think that it isn't so bad to be irradiated. I looked up the word irradiate and it said "illuminate and enlighten." Hmm there must be a lesson in that. Perhaps this trial is an opportunity for me to be enlightened into a higher purpose for my life.
Weet, thanks for the recipe.
Darleen, congrats on finishing one week!
Playwriter, I'm glad your hair is growing back in and hope it comes back in a wonderful way for you.
Blessings,
Helen
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Hi all. I just finished typing up a pretty lengthy post and poof it was gone. I hate it when that happens.
Anyway, I still have not started rads. Had another set back. Rad onc said that the only thing that could be done is for my plastic to stick a need in my left breast and extract the fluid that has built up because he told me to get the expander deflated. Either that or have plastic remove the expander. If not, I am going to receive radiation to 2/3 of the left breast (right one is where the cancer was). If I have plastic do what he asks, he says he is still going to have to radiate 'some' of the left breast. Well, faced with those options, I did the only thing I could do...............
I got a second opinion! Now I have a new rad onc who is listening to my concerns and is willing to work around them. (Biggest thing, I have a spot about the size of a dime on the left breast that has very thin muscle coverage and a cherry red bruise. I don't want it radiated and run the risk of more damage to the area) I go in for a new setup on Tuesday and new onc is going to try and use the rads tats I already have. I am praying it will go better than it has up to this point. I am sure it will since it is a new doc who seems to be listening!!!!
Patti
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I got a chance to speak in front of the congregation of my church this morning. I prayed and I read verses in the bible dealing with God's grace. But what I found that really shaped the direction of what I wanted to say was the dictionary. I looked up the word grace and read the definition:
a. The freely given, unmerited favor and love of God.
b. The influence or spirit of God operating in humans to regenerate or strengthen them.That was the definition in the dictionary but I got to thinking about how many different definitions there truly are. I came up with a few definitions that God has put in my own personal dictionary.
Receiving treatment for a life threatening disease despite the fact that I had no insurance and no money
My surgeon telling me that she is honored to help me and I would never have to worry about getting a bill from her
The surgery that removed the entire cancerous tumor in my breast
Waking up from surgery - 4 different times
My children
Being able to humble myself enough to let a friend help me shower after surgery when I was unable to do it myself
Friends taking care of all of the carpool duties to all of the girls' activities
My boyfriend
The chemotherapy that ensures that there are no cancer cells lurking in my body
Participating in the Race for the Cure and experiencing the overwhelming support of other survivors and co-survivors
My parents
A garage sale to raise money for the girls and me because my treatment left me too sick to work
Friends scrubbing my bathrooms, vacuuming my house, doing my laundry, cleaning my kitchen and mowing my lawn
Phone calls of encouragement when I wasn't sure I could hold the phone because I was so tired and ill from chemo treatments
Standing here breathing
Having someone come to my front door and say, "I don't know you but God wanted me to give this to you." And then hand me an envelope with money
Prayers, lots and lots of prayers
When I was looking really bad from chemo and standing in front of the mirror crying and saying how bad I looked only to have daughter tell me, "you just look like my mom"
The nurse who gave me chemo calling me just to see how I am doing even though I am not her patient anymore
Everyone in this church
A benign ovarian tumor
My youngest daughter choosing to follow Jesus and her baptism
While sitting in a waiting room to receive yet another treatment, the wife of another patient walking away from me to cry because she didn't want to upset me - having the strength to pray with her when she returned - her thanking me and telling me that I was her angel that day
Two dogs lying at my feet
Being able to minister to others while being completely taken care of by others
Being alive
The list could be much longer but I'm giving a testimony, not a sermon. All these things just reinforce the fact that God's grace is all around us and that He uses His earthly angels to help us. We should experience His grace in a manner that sustains us and carries us through this life into the next one. When I was first diagnosed with cancer, I would have wished for something different but now that I am on this walk, I wouldn't trade it for anything. If it weren't for cancer, I wouldn't have been able to see so much of God's love and grace in others or in myself. I am undeserving, as we all are, but God has chosen to love us all unconditionally and I am appreciative of that now more than ever before. I can't say thank you enough to God and His angels here on earth.
I found a scripture verse that I think sums it all up for me.
Acts 20:24 However, I consider my life worth nothing to me, if only I may finish the race and complete the task the Lord Jesus has given me-the task of testifying to the gospel of God's grace.
Patti
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lol, and then I get a duplicate. Does anyone know how to delete a post nowadays?
Patti
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Hello gals;
Patti, sounds like you have a very positive attitude despite set-backs..good on you!!
Weet, the quilt sounds like it is filled with love. I think we are courageous ladies!! In fact, that is what I want my tattoo to be (can't believe that I actually want one!!)
Jayhawk, my breast was not sore but just below...the rib area feels strange?? that's the best way to describe it... and I, too, have only had 2 tx's!! Holy!!
Playwriter, my hair HAD grown bigtime the wk. I was away and now, it fell out...WTH??? Also, a chunk of my eyebrow disappeared...ok, who took it?? Fess up ladies!! So now I am baldER and look like shit.. I was at church this morn. and a sweet gal that I haven't seen for a few months sees me and starts crying! Ok, I did NOT look good today and the missing brows don't help...LOL
Pam, I had 2 meltdowns just prior to starting this 2nd journey...thought to myself "Is chemo not enough? When does this end?" but then I pulled up my panties and life goes on... right?? So it goes with the territory!!
Amy, when I had my tx, I asked if they had any ACDC and they said that I could bring my own music in...SO tomorrow I will then Beaches by Bette...followed by the Beatles! Hopefully I won't cry...or jiggle to the music! HEEE HEEE
Take care
Cath
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cath, my brows and lashes held in there during chemo, but since chemo is over, they kinda gave up the ghost. i have about 4 lashes left on the right side, and both brows are fuzzy. my chin hairs are coming in fast and furious, however.
my left nipple is sore (that's the side that gets the rads).
patti, what a great testimony. i remember u telling us on the chemo cruise about some of that. how awesome. i'm so glad u can see the love of God thruout all this.
i have an ultrasound scheduled for my right breast tmrw. a surgical biopsy was recommended back in March due to some radial scarring, but i never knew about the recommendation, so it was never performed. plz pray that it turns out to be nothing.
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Patti, what a beautiful testimony. I too have grown so much in my faith since this all started.
Cath I have losted all my eyelashes and brows--I miss them!! My hair is coming back like an old man all around the sides but not on top, bless tell me it will start growing. My last taxol was the 15 of August! i am still on herceptin until May. they say that slows growth.
Playwrite my prayers are with you that your ultrasound comes back fine. let us know.
Debi
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Patti, that is awesome! What a great testimony you have. My verse for the time of my surgery was the one that says 'God is able to make all grace abound to you.' That really blessed me. Now my verse is 'Let not the wise boast of their wisdom...' (Jer. 9:23)
Playwrite, I pray everything goes ok for you.
I went in today and had my 'dry run.' They spent a lot of time inching me this way and that. First Rx starts tomorrow at 3:30. I'm feeling ok about it.
You are all very courageous. Keep it up!
~ Helen
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Hi all, I start rads on Friday (7 weeks post chemo). It was a hard decision to make as I only had 1 positive node and so rads isn't mandatory, but decided better safe than sorry. Had the sim. today, and got the three little dot tattos. Kind of odd to have blue freckles, lol, but considering that I have no breast on half my chest, not such a big deal. Anyways, will be reading up on what you all are going through, and if you have any advice pls let me know.
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i get done october 11th, by my calculations. i'm pink on that side, but no blistering or weeping or anything, knock on wood.
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You're comin' down the home stretch, Playwriter. I'm glad to hear you are only pink so far. How did the ultrasound go? Any news there?
I had my 2nd Rx today. No biggie at this point, eh? A friend will come with me tomorrow. I will enjoy the company. I want my family to see the radiation machine, whatever you call it. That thing is an amazing piece of technology. Though I have to say it scared the heck out of me with the beeeeeeeeeep the first time. Was praying and remembering someone calling it R2D2, that helped.

How are others doing?
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Hi All , Playwriter I will be just behind you, my calculations say I will be finished on the 17th.I am good, seems almost like a bit of a tan more than a burn and I am not sore or dry at all.
We are hoping to go to Aruba for a week in Nov.,about a month after finishing so will ask the Dr. about a good cream in case I am a bit sun sensitive. I am being radiated to the neck on the one side and hard to keep all that covered.Gosh it will be nice to get away and know that the tx are all behind us.
Debi, my hair is coming back like yours, male patterned baldness, my eyelashes are good now and my eyebrows are finally coming in. I finished chemo in May.I need to get a hair cut to get rid of the frizzies,( very tight curls,) and to get rid of the puffiness on the sides and back. My DH said to let it grow so I could do a "comb over " LOL.
Have a good day everyone.
Hugs
Weet
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Weet, they told me to get a compression sleeve if I fly (some forgot to tell me so I thought I'd mention it). The rad doctor gave me a prescription to see the lymphedema clinic to get measured for it. Did someone mean a filtered mask like you get to paint, while flying? What about the smack of vitamins you get with "Airborne" made by the schoolteacher for germ attack?
Cynthia, I had rumblings of a period yesterday, 9/26, i started rads more than a week ago on Tuesday (32 changed to 33). Also, the doctor called after last week's pap, I HATE when they leave a message and don't say what's wrong! She never calls me!!!!
I had had an abnormal pap earlier and thought it might be because chemo gave me a yeast infection. Apparently I have something else to worry about (is that premature?!!, maybe she just wanted to chat, ha!)......during chemo I had anti fungal pills and then was advised to take Monistat 3 because it seemed it still itched (and I forgot the pills for 3 days while i had cousin company).
I too planned on getting my ovaries out as soon as it can be scheduled after rads, and before the end of the year.
I have discussed it with a lot of people on the forums and groups, doctors, the oncologist said no because my Mom is brca negative (but he is the only one), but I'm going to try to get tested myself and will go ahead regardless, due to my Mom having been dx'd with ovarian cancer June 1998. She has had 2 recurrences, 2001 and 2003.
Kate
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Hi all
Hope everyone is well. I am done 10 tx and have 25 to go. So far so good. No redness or skin breakdown. I am using the 100% aloe vera and it's fine. The only thing is at times, I have pain in my chest muscle. The radiologist said this is normal as they do radiate part of the lung and the muscle. I am a little tired but nothing like chemo. I was speaking to a lady who is having rads but had no chemo and she was really complaining of fatigue. She was done almost 3 weeks. I should be done the week of the 22 of October. Going back to work in November. I can't wait. I am going to Toronto to be with my family. It is the Canadian Thanksgiving. I haven't traveled yet since this all started in April so I am a little apprehensive. I'm sure we will all have fun!!
take care out there
Kim
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I looked at Walgreens and could not find 100% aloe, and the Internet was confusing...someone said 100% gel isn't same...?
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Hi Sweetie, How have you been doing? Did you start your radiation? If you did I am sure your doing okay. Remember take one day at a time and you will get there. Let me know what your doing now.
God Bless,
Kaloni

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