SEPTEMBER 2009 RADS
Comments
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I'm in and would love to get together.....however, as Betsy knows the meeting place will need to be clearly marked since I couldn't even find her this summer in Portland at the Race for the Cure! LOL!
I am on my way to a town about an hour south of Cancun on Monday. My husband who had prostate cancer surgery two months ago and I have officially closed "Camp Cancer" and this will be our celebratory get away! I figure if I plan this right and use a variety of sunscreen strengths I may be able to blend that big black rectangle on my chest into something that resembles a tan.

Betsy, eight years out you can still get fibrosis? Holy s#*t! Do they say there is any way to do things to avoid it? you know....one more watchful undertaking to add to the litany of activities we're already doing to keep cancer at bay. BTW, does anyone remember how they spent their time before BC came along. When I look back at this past year it has been all about managing side effects and keeping a list of what I should and should not be doing to stay safe.
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Just stopped by to check in and saw that Betsy has drawn the short straw again. That truly, truly stinks. Betsy - You know you are our inspiration; super strong in the face of adversity. Big Hugs !
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Echo..I'm so jealous but you and your DH certainly deserve it! You will have soo much fun...be sure to keep that boob covered though...the rest of your body can work on that tan! It feels so darn healthy soaking up that sun....will help your Vit D. levels too
Mtg..and Betsy...you are right,,Betsy has certainly been an inspiration (though she probably won't like us saying that)..but she and the rest of you too have always been there..for everyone..no matter what we have going on...Hang in there Betsy...if anything you could write a book and possibly make millions...
Did anyone read the article in the newspaper today about radiation? I read that and thought..I'm glad THAT is over....A couple of hospital's accidently fried 2 people and they died from it...not their cancer...The article did go on to say that radiation DOES benefit cancer patients and since we have all been there/done that with rads...we can just hope for the best...I remember laying there on the table.hoping to hell that everyone knew what they are doing! I also remember during chemo asking where the nurses went to college to get their nursing degrees..I felt it was my right...I also looked up where the doctors when to college too...!
Everyone..have a great week...Betsy...PLEASE GET BETTER! I will be thinking of you..Echo..don't even think of us at all...EAT, TAN and have some..well you know..fun with your DH...enjoy every minute!
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Hi all-- havent been posting much lately-- but I do checkin on everyone-- Betsy hope you are getting better-- a book deal sounds like a great idea!!! Vegas has definitely changed a lot since 1970 and even the past 10 years -- we were there before all my BC shit and it has already changed more-- a favorite place to kick back--it would be fun to see everyone for sure--and since it looks like Titan you are from Cleveland we might have some things to talk about--I am from Cleve. too-- anyway just thought i would post since i didnt want you guys to think I fell off the face of the earth-- I just seem to still be really tired -- The Arimidex is really making me achey and I am trying to ignore it--just cant get back to myself --they say a year --I dont know maybe i am just impatient--hope everyone has a good week-- see my onc . on friday for blood work --take care all Laura
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Laura - hope your WBC is back to normal on this round of blood work.
I'm feeling better as the swelling has gone down a bit and the pain has subsided with my most recent round of antibiotics. Now I'm just dealing with a pesky yeast infection. Some days I feel like I just can't win but just when I start feeling sorry for myself, I think how good I have it. At least I'm not having to deal with a stage 4 situation. My heart goes out to all those women and men.
Echo - I'm thinking about you in warm Cancun. You and your dh deserve it. I've never been there but is sounds wonderful. My dh & I are planning a trip this fall to Quebec, New Brunswick and Nova Scotia. It replaces the trip last year I had to cancel to France with my sister due to my bc dx. We might be going a little early for fall colors (end of Sept) but it's something to look forward too.
Amy - you don't get your port out until April? Wow...is it bugging you? Mine really got uncomfortable about the beginning of Sept. after I stopped using it but I had mine put in at the beginning of April 2009. I had a power port.
Titan - I think you should just pick a date and place and see if we can coordinate a get-together. If we go to L.V. maybe some time in May or if Chicago works better for everyone maybe June. Are dh's invited? If not, then the long weekend in May is out for me as that's when we celebrate our birthdays.
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I am not done Herceptin until some time in April so will keep my port until then. That will be a year of treatments it will have seen me through. Will be glad to say goodbye to it but it has been a good friend too.
Whether we bring spouses or not, i'm in. I guess I envisioned it to be just us girls but either way, I want to meet the ladies who got me through this ordeal!
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Hey, ladies. Does anyone out there know what could be going on. Woke up this morning severe body aches. Thought maybe it was due to all the rain. Went for my walk, couldn't make it the entire distance. As the day has progressed, my body really, really, hurts plus now I have a fever of 99.5. I had my flu shot, but not the h1n1. Is that still going around. Tell me no. Had to cancel appointment with onocologist today. Just as well, he's going to throw a fit cause I'm not taking my tamoxifen. Is that the only reason we see the oncologist is because of the drugs we take (or supposed to take)?
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Sounds like it could be h1n1. I hope not but perhaps it is. I got the regular flu shot but when i asked my GP about getting the h1n1, he said that most people who got the h1n1 flu didn't present with too many severe symptoms and not to worry about it. So i skipped it! I hope if you DO have it, it is mild and goes away FAST.
But on another topic, why are you not taking the Tamox? Did you make a choice not to take it, but haven't told your doctor yet? I am curiuos what he said. A woman that I know locally just told me she got an upset stomach the first few days so she quit. I didn't know you could do that. (I guess I'm a directions- follower at heart.)
Feel better soon!
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I don't know, It's a heavy duty drug. My brother-in-law had a minor heart attack, they put him on Plavix. One year later, after his brain bleed, he's shuffling his feet, can barely walk, is confused, yada, yada. I read about this drug and since my tumor was 1 mm and barely ER+PR+ (10%) I guess I just decided, not worth it. Both my rad onco and bs told me try it, if it bothers me, don't take it. Rad onco said he didn't really think it was necessary. Onco says differently.
What's a girl to do????? That's why I asked, is that why we see Onco. Only because we take drugs. If I decide not to (maybe I already have) do I need to see him at all?
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Kawee - I've been on tamox. since August and have had no SE's. I've gained weight but I think that's from a combination of things. I did have about two weeks of severe hot flashes but since then they just come and go occasionally, very manageable. I wasn't so worried about Tamox as I am about the next drug...I think its Armidex. It has bone pain as an SE and based off of how I did on chemo...I don't want to go there. I'll cross that bridge when I have to.
RE: the girls weekend. I'm fine with no dh's just thought they might enjoy a get away too. As they had to deal with us through this ordeal. In my case my dh deserves a medal! I was just throwing it out as an option. I do think we need to share some plain ole sistas time...so the boys could go off on their own during that time or share some war stories over some brewsi. Just an idea...I will drop it if no one else thinks it sounds good.
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I'm okay with husbands. Who's gonna carry the luggage?
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Betsy--I am on Arimidex since Oct.-- i am having some bone and joint achiness and some muscle tiredness but not all the time-- I keep exercising which does help-- but still dont feel like myself yet-- If I take 2 tylenol occassionaly it does the trick-- so trying to hang in there with it-- see my onc this week and will talk to him about it--just dont want to keep changing from one to another-- but I know some people cant take it at all--will let you know how it goes-- Laura thanks for remembering about my wbc's I am concerned about my cholesteral and vit. d level and etc etc etc--
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Hi Ladies,
I will start my rads in February. I need to decide whether to do them before or after work. Any advice?
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I did mine in the morning but it would have been fine to do after work as well.
Occasionally there was a little bit of a wait, so if your company is a stickler for punctuality, it might be better to do after work, so that if they run late, you won't be concerned.
Good luck to you as you go through rads. Did you have chemo? Rads was NOTHING compared to chemo, for me, anyway.
Amy
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I am so glad you say rads are easier than chemo. It seems there are soooo many ladies that have horrific burns. It is truly reassuring that there are some ladies that did not suffer. Thanks.
I am wondering about all the lotions that rad onc wants you to put on. Do you think my breast will be all gloppy when I go to work if I do the rads in the morning?
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I wondered about that, too. I used Calendula gel but only put it on at night. After rads, I just put my bra or camisole (which was softer and less irritating) and clothes and went about my day. I usually put the gel on after a shower at night. To be honest, I wasn't very diligent about it and never felt it made all that much difference. My radiology onc said that NOTHING you put on can prevent burning, it can just make it more comfortable. So since i didn't burn much, I didn't use much. Seemed to work fine. If you do burn, and if it is uncomfortable, you could put the gel on and tuck a cloth into your bra. I read that some women buy baby wash cloths (because they are very soft) and cut them into the right size. I was going to do that but never had to.
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Chinablue - I am VERY fair, but was one of those ladies who only turned slightly pink toward the end. I was totally freaked by the whole rad thing, but all turned out okay.
I used aquafor, that's what they gave me. Even after showering, it's still there. Amazing. They should grease cars with that stuff.
Let us know how it goes.
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Chinablue- I went to rads in the afternoon. Towards the end I got very swollen and needed to air out after, so I was thankful I got an afternoon appointment. I too did chemo...both were not pleasant experiences for me but doable..(but I seemed to be the bad side effect Queen). I also used aquaphor...I'm allergic to aloe. It is sort of greasy...and watch for stains on your clothes. Good luck and be sure to join a forum of ladies walking through it with you. They provide SO MUCH support and great ideas, sort of a collective mind, it's truly wonderful.
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chinablue - I did mine in the morning so I wouldn't have to miss much work. Was never a problem but I think it is all individual. I was albe to just use aloe until I started the boosts near the end. I would put it on right after rads and again at night. Would just fan myself a little before putting my bra back on. I am pretty fair skinned so was worried but no real problems. Good luck with yours whatever your decide.
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Ladies, thank you so much for all of your advice. I will meet with my rad onc over in a week that is when we will set up the plan. You gals are great!
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The Mirage just sent me a offer on the internet, stay 2 nights, get one free. Good til April 6. Rooms during some weekdays, $115 a night. Depends on when you go. Some weekends $185 to $295 a night, again, depending on when you go.
Also, if you don't mind not staying on the strip, there's a place called Southpoint (approximately 4 miles from the strip. New casino. Very nice rooms, tons of restaurants, movie theatre, wonderful beds, big plazma TVs on the wall. $75 a night weekdays, $125 weekends.
Anyway, we go there quite a bit and stay at both these places. Those are the only all the ones I know about.
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We could always take the bus to the strip or to the old town...Southpoint sounds good..and it does have a casino so that would be cool....$75.00 bucks on a weeknight would be sweet...and if we don't go with our dh's we could share rooms...I don't snore..at least I don't think so..but...I do really like to party..alot!
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Go to www.southpointcasino.com. You can see the rooms, etc. and look at the prices. In April, internet special $59 weekdays. In May, $70 weekdays.
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Oh, LV is a 8 hour drive for me, it's the best way to get there. Can only get a flight out of here on Wed and Fri and then have to go to LA and that's 4 hours right there. So we always drive. Therefore, I will take my husband. It's too long of a drive for me. He'll keep a low profile when necessary.
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You ladies going to Vegas...be sure to book you show tickets ASAP..That way you will get your best seats...any of the Cirque du Soliel show are amazing..I love Vegas...
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Hey Girls, I'm baaaaaaaack from the Yucatan. This sickly white pasty body has a tan! I'm looking less like a cancer patient, wooooohoooooo! So I see a meet and greet vacation is in the works. Did any of you see the link for the 2nd TaTa Sisterhood trip to Vegas? They are planning for Sept. or Oct. this year if you want to get in on that bandwagon.
I would love to go anytime/anywhere if you all decide to do a trip.
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The frustrations dont seem to end....
Went for my 1st post BC ultrasound today and the doc in charge REFUSED TO GIVE ME MY READING !
It's been 14 months since my last Mammogram and it's "his department's policy" that unless I have a Mammo every 12 months they wont give - or in my case, read - an Ultrasound. I explained that my BS (who also happens to be Chief of BS ) (i) has me on a 3 month schedule, (ii) that I'm supposed to have the Mammo in June and (iii) that because my cancer developped quickly, it was decided to space out my appointments rather than having both Mamo and ultra sound together and then nothing for 6 months). He flat out didn't care.
So, I'm left knowing from the Tech that both breasts have "cysts" (which is what my BC was originally diagnosed as), could get no reading from the doctor in charge and since my BS is out of town till next week just have to suck it up and wait. AARGH !!!
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MTG, that is the sign of a man with a very small penis that can only get satisfaction from thinking he can control things that are not going on in his life!
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And, don't you just hate people being in control of you, especially when you don't even know you. Yesterday I went to the oncologist and actually had a panic attack in his office. I covered it up, but nevetheless. Everytime I have to go I am really, really anxious. And that is just the reason why!!!!!
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