Any April/May 2012 rad girls out there?
Comments
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I had a choice between first thing in the AM and 4 in the afternoon. I decided the afternoon appt would be better. I can lotion up after treatment and just wear a ratty coverup home. Hopefully I can pull together a work wardrobe out of sports bras and poncho type tops. I'm very fair skinned and big busted, so I'm as risk of burns too. I'm supposed to meet with the rads nurse before I get started for a skin care lesson...
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Cathy ~ The chemo you had (ACT) has been the norm for awhile. As you described, that is administered with A/C, every other week for 3 months, followed by Taxol, given the same way. What I got (TAC) was all three drugs at once, given every 3 weeks for 6 rounds. These three drugs have only recently (according to what I've been told) been administered together in this fashion. When I first found out what chemo regimen I was going to be on, I called a friend of mine who went through this 2 years ago. She assured me that I had it wrong because nobody could survive all three at once. Hahaha! My MO told me that it was a more difficult way to go (side effects wise), but it was shorter. The difference is that in my "cocktail" I had Taxotere which is a derivative of Taxol. Anyway, I'm glad I went that route. It was brutally hard, but I was done in 18 weeks instead of 24.
Cindy ~ You'll figure out what works for you clothing wise. I am using some fairly messy skin care products, so I have had to get creative with what looks decent and also keep everything from getting ruined. I've had a couple of gals tell me they bought men's t-shirts from Walmart and wore them under everything! I haven't gone there yet....but I'm not ruling anything out
SAN
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Hello ladies!
I recognize a few of you from the December 2011 TC Sisters board (hellow MomOf3Boys and Gayle!) - I had my consult with the RO last week and I'll be getting a whopping 36 treatments in all. 28 regular and 8 boosters at the end. I go for my sim on April 10th and then I think I'll start tx the following week (probably the 16th).
Really glad to see all the information regarding ointments/creams. The RO's office told me pure aloe vera is the best but to get the 'sterilized' kind (aka not directly from the plant). The concern with getting directly from the plant was the added potential for bacteria but otherwise would be ok.
I was hoping I'd be done with tx by my birthday (5/31) but no dice. Oh well, will hopefully be shortly thereafter assuming machines don't break down or I don't go sideways with SE's.
Just want to get it all behind me, ya know?
Chickenpants and She_Is_Virgo - love your senses of humor! Is THE best medicine hands down!!
Heather
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I had bought a radiation bra. But when wearing it under clothes because of the seems it makes it look like I have 2 new nipples, one lower and one higher. Not prety. I'm wearing a workout thing that is really soft.
I also found some higher neck tops this week.macys had tank tops for 10 each, that cover everything. I have those stickers with magic markers on my chest. Then I found some cute tops at kmart. Most expensive was 12$. -
Hey Heather, welcome aboard! I just finished 5 of 25 today. It goes by quick. I'm in and out of there in 10-12 minutes. They did have to replace my middle sticker today (no tattoos), but that only took a minutes.
I experienced fatigue and a tension headache over the weekend after only undergoing 4 rads tx, so, I'm not sure I can blame it completely on that. I don't usually get headaches, but, had a stressful day at work on Friday and my youngest son (7) has that congested cough back again, and it poured rain all weekend...
Hope everyone has a good, uneventful week!
Joyce -
Momof3boys,
I really didn't want to do the rads because of the reconstruction, but it was recommended by my breast surgeon, MO and 2 RO's, so I ultimately chose to do it. I decided to do everything possible up front to prevent a recurrence.
Unfortunately, it's not clear cut whether rad is indicated in early stage with negative nodes, but there is a study going on that will answer this question some time in the future. My breast surgeon gave me an article that identified several features associated with a higher risk of LRR: age <= 50, tumor size >= 2 cm, positive LVI, close or positive margins, and absence of adjuvant systemic treatment.
My RO has recommended 28 treatments. I see alot of variation in # of treatments in this discussion board. Did your RO say why 25? Just curious.
Best to you.
LovesDogs
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Sandyland:
Where do you get the Emu Oil? I've heard good things about that as well and would like to try it.
lovesdogs
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Lovesdogs ~ I got my Emu Oil from this website. I did tons of research and even called the owner of this company and spoke to him at length. I am very confident that this company is reputable and sells a superior product. Good luck!
www.emuoildepot.com
SAN
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I haveno idea why mine said just 25 zaps, maybe its cause they done beat me down with almost 6 months of chemo and the mastectomy. mine was easier yest. been doing lots of stretching of the arm/boob. 22 more and I am outa there!
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Hello ladies!
I had my consult with the RO last week and had the SIM as well. The hospital is going to call me for the therapy to begin possibly next week. I am supposed to have 16 treatments. The items the nurse recommended was Galaxal Base, Lubriderm, Aloe Vera and cornstarch. Would love to hear about your experiences as we all go through this together. -
hello again everyone, just checking in. I had my 2nd rad treatment today. If I didn't know any better, I would think nothing was being done to me - don't feel a thing (practically falling asleep on the table) - I didn't expect to feel anything though. But from all I have been told, I should expect to start seeing a burn in about 2 weeks and possibly fatigue setting in at about 3 weeks which is a bummer because I return to work right around that time!
Quick, funny story: On Saturday, I went out for a night for the first time since I was diagnosed to hang out with my brother and meet up with some friends at some local pubs - I'm not a big drinker, just needed to get out of my isolation and see some new faces, and in particular there was a fundraiser going on for St. Baldrick's - if you are not familiar with what happens at a St. Baldrick's event, the participants sign up to have their heads shaved at the event. So myself and my brother were hanging out for about two hours, and then started to get ready to leave. As we were saying our goodbyes, we heard the DJ announce that one of the bartenders was willing to donate $500 on behalf of the 1st woman to step up and shave her head. Jokingly I said to my brother, "if they up it to $1,000, I will do it!" (really didn't think I would actually do it). Well, the next announcement said the amount went up to $1,000! And I actually raised my hand and said I would do it. Sat down in front of everyone and had my head shaved - not bald, just a crew cut. Now, mind you, I was there hanging out with a head scarf on, so everyone there knew I was a cancer patient (I must tell you, it was quite interesting to walk into a bar in a head scarf on a Saturday night - the looks I got really made me laugh - mostly surprised looks, some smiled at me that gave me the impression they were saying "it is very cool to see you here with all that you are going through", some looks were like "wow, I am grateful and have nothing to complain about". And now that I think about it, it would have been REALLY funny if I had my wig on, and then sat down to get it cut and ripped it off! Of course, it wasn't that hard for me to do it as my hair has only recently begun to come back, so I would say they cut off 1/2 an inch maybe. But I must say that the response from the crowd was an overwhelming great feeling and I was actually shaking while the barber was shaving my head. The looks on the faces from the people in front of me made me feel both proud of myself as well as very loved (even though I barely knew anyone there). I think I had a big impact on the crowd for having done that. It was a great night for my first time out socially since getting diagnosed with BC (which was in August 2011).
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Cigi56, you're a better woman than me. I wouldn't allow my hair to be cut for any amount of money! A half-inch is a LOT on my head... Glad you had a great time!
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Lovesdogs: I don't remember why he said 25 tx...I've seen women getting 20, 25, 30 and 35. I have no idea why... I was node negative and negative for LVI and had a BMX, but the tumor was a little larger than 4 cm, and he (along with 3 other RO opinions) wanted me to o the excisional scar.
I had my sixth tx today and saw him afterwards. All good so far, no redness yet. I am definitely feeling tired though, but I'm going to work everyday right after tx. For chemo, I mostly stayed home and worked from there because I was afraid of catching something, but was able to get rest whenever I felt like it (I own a real estate company). He said the best thing for fatigue is forging right through it and not giving in to it??? Ha! But, starting tomorrow and each week thereafter, I will be getting bloodwork. He said it's standard, as radiation can cause anemia, so they check the levels each weeks.
Cigi56: good for you!!!! I'm impressed that you'd get your head shaved in front of everyone! I'm waiting for hair growth... Over the weekend I was complaining of a headache. My 7 yr old son heard me and said "Mommy, maybe it's your hair trying to push out" lol -
Oh... My RO made a point of asking my opinion about the facility, if the technicians were polite, kind, how was their timliness, professionalism, etc. So, that was good. Also forgot to mention that there is a certified assistance dog (I think that's what they call it) running around. Her name is Ruby... Cute little thing. Does not bark, just has the run of the place and makes everyone smile. She even has business cards up at the front window :-)
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Hi Sorry that we are all her but at least we have support. I am on day 2 of rads, was told today no deodorant on that side. Talk to a nurse who told me at get Crystal body deodorant stick. It is a made of salt. Got it at CVS and it is endorsed by the cancer treatment centers and it also has the pink ribbon on it. Just wanted to pass that on, hope it helps.
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Wow Cigi56 think of all great things that 1000 donation will do.!
Does anyone know, what to do if one ve of your stickers wants to come off? I just noticed one is all gunked up. I only have one little tiny tatoo. The. rest are clear stickers covering black markers. Oh well. I'm going to bed -
I will start rads at the end of April, beginning ot May for a second primary BC diagnosis. I just finished rads on December 14th for the first diagnosis of DCIS and am now being treated for multifocal IDC, ILC. I didn't experience the fatigue but did get burned very badly and had to take a week off work. The treatments themselves weren't bad at all but it was a pain trying to get out of work to get there on time. I hope things go a little better this time!
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Hi Claire,
I start my first treatment Monday, April 9 - nice to meet you and glad to join!
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Still waiting to find out when rads will start. Tatoos up front stickers on the back. Come on guys. Let's get rolling I want to be done before it gets too hot and before a new insuramce year starts! I also have stuff I need to schedule here at work...
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I will be starting on Monday .. want to get this done and on to summer..BEFORE it gets too hot- Also I got selected for Casting for Recovery and am praying for no lost time. It is 1 1/2 weeks after my completion..
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Hi Rads Sisters ~ I am 5 treatments in and I already have slight reddness and some pain under my arm in the "high friction area" as they called it. Also, I am already feeling the fatigue. I thought SE's didn't really get ramped up until a couple of weeks in?? I am REALLY hoping I'm not one of the blisters/open sores people
I'm using my Emu Oil and Aloe religiously and have just ordered Mia Derm (per Linda's suggetion) too. Chemo was such a nightmare....I'm ready to fall on the "easier" side of the SE scale for once!
Hope it is going smoothly for the rest of you!
SAN
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Rad Sisters- I will be starting radiation by mid April. I met with RO today and saw facility that I will be going to. They went through procedure and answered every question. I cant get anything started till swelling and bruising goes down from LX on 3/13. They said that they would not get an accurate measurement for scans. I am looking at 6.5 weeks and ready to get started. I have not decided if I will do b4 work or after. MY RO is really nice. He said that my Dcups are too large for the rad that you do 2 times a day to get done faster. I asked about cream to use and they said they provide it all. It seems like a nice place.
I look forward to sharing stories and getting questions answered..
Kristi
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I'm 8 down, and so far, so good. I'm taking care to lube up really well morning and night with the vitamin E and aloe cream that was recommended. I was a bit disappointed to learn that it won't actually prevent skin SEs, but keeping the skin hydrated and moisturized will ease the discomfort. I haven't felt particularly fatigued - just the usual tiredness at the end of the day.
My RO gave me a sample of Miaderm yesterday, with instructions to apply to my nipple (which is now retracted since surgery). She emphasized that I really need to keep the area clean and dry, as I am more likely to have a reaction there. She also gave me a small tube of Aquaphor to try.
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Ive got number 6 of 25 today.
So I've got the stickers with the marks under them. And one under my armpit came off the other night. She said not to worry about that one. It was right in crease. But I'm wondering about the skin under the stickers. She said to just be carefull putting on the lotion/I'm using miaderm or whatever its called. Said to not put it around the stickers so they don't fall off. Said that the skin under stickers would be fine. Since this area isn't getting lotion. How come they just don't cover the entire area with stickers? IDK was just thinking. I guess the big area for concern is the TE area. And I think my area does maybe have some redness starting. See my RO friday.
My brother in law got his liver last night. He found out about his liver failure last summer when I found my -
When I fouund my BC last summer. I've been so worried he would die. And I know he's not out of woods yet, but at least he has chance now. Surgery was 12 hrs long and he got 12 units blood.
Does anyone have this nagging pain its like under my left chin/my left port was removed few weeks ago. I kind of felt it before that. But now I think I feel it more. I can feel it hurting some when I swallow. But its up near my jaw. I've felt all around the bones and there is no pain there. Kind of like muscle pain. Sucks having every little thing freak us out now. -
Fredntan ~ So weird that you mentioned the chin thing. YES! I have that pain too! I had it even before my port was removed, but it got worse after. I kept thinking I was getting a sore throat, but it never materialized. I also felt around meticulously, but no lumps or anything. I think maybe it has something to do with the Jugular Vein being messed with. Could it have bruised and irritated the whole area? I didn't even think to mention it on here, but I'm so glad you did. If even one more person suffers from something I have, it makes me feel like, perhaps, it is a common thing. I am now 3 1/2 weeks out from my port removal and the feeling has subsided. Also, I am so happy for your family! What a blessing for your bro-in-law to get a new liver! Our whole little "community" rejoices with each other over good news
Wiskris ~ I don't know if this will impact your decision about when to schedule your appointments, but I am now 6 treatments in (of 33) and I am very surprised at how tired I am all the time. Particularly after my treatments, I feel not just fatigued, but sleepy! If I worked outside my house, I would definitely schedule rads for after work. In terms of skin care, everyone seems to favor different things. I know lots of RO's recommend Aquaphor, but I have to wonder if it is because the pharmaceutical company lobbies hard to get their business. I have noticed that many of the RO's carry lots of samples of that product. I am using Emu Oil, Aloe (straight from the plant), and I am planning to add Mia Derm to my regimen this week. Good luck and I hope you tolerate rads easily
SAN
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fredntan- I am so happy for you family! My husband had a kidney transplant over 22 years ago and is doing great. My brother in law just went on the kidney transplant list so I know what you went through. I am on my 4th treatment and see my RO today. Hopefully will get some cream since it looks like my breast is already turning alittle red. Doesn't hurt but makes me nervous because I have so many treatments left
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Finally got my rads schedule. Dry run tomorrow. Start the real thing next Monday. Last appt. (4:45) daily for 30 treatments. Looks like setup number 2 (slightly tilted, on back) is the winner.
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Cindy - good to here they finally figured something out for you. Very nice that you were able to bag that treatment time. I have to wait for someone else to finish and then they will move me to a later slot.
I have a sample of Aquaphor - it's way too greasy for my liking. I'm sticking with Colonial Dames vitamin E/aloe cream and miaderm for my nipple.
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Yeah I was tickeled to get 4:45. Originally they had only mid morning or mid afternoon... but having been dinking with this for several weeks and asking them to go as late as they could everytime anyone asks... and finally I'm in luck.
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