Taxotere/Cytoxan starting July 2011
Comments
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Hello, I am starting 4 rounds of T/C in two weeks. Feeling very nervous about it of course. I had a local recurrence after 2 years. I didn't have chemo or radiation back then, but I had double mastectomy. Took Tamoxifen for 2 years (no side effects whatsoever just few hot flashes.. )
I am not happy to be back on this site, but glad you ladies are here sharing your experience. Take care!
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Sorry, I just noticed this is a JULY group! Ups! Have to start my own group I suppose..
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Hello everyone I am still around. Had alot of trouble with number 3 of my adriamycin/cytoxin chemo treatment. I just was not bouncing back physically or mentally.My oncologist had no interest in my problems. I thought I was literally losing my mind. I switched oncologists to a wonderful man who could hear the terror in my voice that I just can't do any more chemo treatments. So sympathetic, he said I would not even dream of of making you go through anymore with your side effects! I just finished 33 rads, skin held up very well because I had to take about 5 days off for personal reasons. Made them up at the end. Getting a pet scan on Monday,had mammogram and ultrasound in november all good. Will be starting Arimidex this week. Hope everything goes well. Glad to see everyone is doing great, this truely was an amazing message board!
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Theatercat, good to hear that you are finally done with treatment and that you found a doctor that you liked. I've been on arimedex for a couple of months now without any bad side effects. Hoping for the same with you and a healthy 2012. I'm starting to make travel plans and hope that this tme, I'll actually be able to go!
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Hi TheaterCat - great to hear from you and glad you are done and feeling better. It is so important to have doctors and a whole team that you can trust. Be well!
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Hi all ladies, glad to hear alls well. I have been back to work for almost 2 months now and things are creeping back to normal. Busy busy busy. Let's toast to normalcy:)
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Hey, ladies! I'm back . . . I have hair. It is pixie style. All of you look so cute with yours. I hate mine. I still won't go out without the wig. I am feeling good - almost like I never had any treatments. Hubby and I are going snow skiing at Taos ski Valley, NM next week. So excited! And I may get brave and go wigless. I am glad to hear everyone is doing well. I started Tamoxifen on 12/13. Absolutely no side effects. I have started a good workout program and try eating better. First mammo and checkup in on 3/20/12.
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I want to share my newest health care tip - lemon water! I started putting lemon juice in my water during chemo because it helped the taste buds. Since then I have found multiple articles on how healthy lemon juice is for the body. Just google "lemon juice in water" and you will see what I mean. I now wake up every morning to a tablespoon of lemon juice in warm water. And I also put a tablespoon in the quart bottle I take to work. Have a good day, my friends.
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Ladyboss, glad to get your update and health tip. Have a great time skiing! It's an opportunity to go wig-less because nobody jnpknows what you used to look like.
Frances, nice to hear that you are doing well.
Have a nice weekend all. -
Hey ladies,
Guess everyone is super busy and not thinking about BC so much. I still have some pains in my fingers around the nail beds; mostly my left hand. Funny how the neuropathy bothers me more now than during active treatment. Got my hair colored and cut again. I like it really short and with lots of product to keep the curl down. I definitely have the "chemo curls" thing going if I let it grow. Not used to that. Gotta get serious about working out again, since calories seem to actually stay with me now and I am getting soft.
Been working hard, doing lots of social stuff, cooking, making pasta, and crocheting! Have a bunch of caps to wear over my real hair.
Enjoy the rest of the weekend.
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rossileo/phillybird: so good to hear from you. BC is in the back of my mind all the time, but I am not going to let it vapor-lock me. I went wig-less the entire time I was in in New Mexico. It was quite liberating. I am work today - without the wig. I am not having any residual effects from treatment - thank God. I have no chemo curls. My hair has always been fine and straight. I don't think that has changed. I did not gain any weight during treatment, but I started looking "puffy". Got to work on that. I still work out every day. I just need to watch my calories as well. Love you guys! - Diana
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OK. Here I am with my short hair. This picture was taken Sunday 2/19/12.
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Diana,
You look fab!! So glad you are doing well.
Robin -
Hi , both Diana and Robin, you gals look fantabulous. I have had 2 haircuts since dec. hair is growing out thick and fast and curly. Decided to keep it pixie cut as many of my friends and colleagues commented I look younger:). Anything to look younger right? Most days I don't think of BC but there are some horrible days when nightmare hits and fear creeps into me and no matter where I am I will feel my breast for lumps!!!! My breast hasn't fully healed from radiation and the recent infection. It is now hard and lumpy and really I wouldn't know if there is any new growth because the breast is now so lumpy... Well I have to keep telling myself -live for today for we don't known what tomorrow holds. Heading to Hong kong on Friday for a weekend of shopping and eating with my girlfriends and then off to shanghai for 2 days for work, back on 1 march. Have agood weekend you all....
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I have had two haircuts as well. My stylist says to keep trimming, and it will come back thick and gorgeous. So far she is right. It is THICK! I have been told I look younger as well. I like that! You are so right - live for today and enjoy life now. Frances - Have fun in Hong Kong! - Diana
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Diana, you look great! I haven't cut my hair yet and it definitely looks pretty straggly. It's just so hard to trim anything off when I've been measuring it weekly to see how long it is. Now that it's pushing a couple of inches I have noticed that it's a little curly. Well, I'll see how it turns out.
Glad everybody is getting on with life. I too occasionally worry about recurrence, but there's really not much we can do about it but take care of ourselves and be vigilent for any unusual symptons. Enjoy the weekend everybody!
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I just wanted to vent about my chemo curls. I cannot stand how curly my hair is!!!! I love having hair, but really was not ready for it to be so curly. Okay, I feel much better now.
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Vent away! So what happens with chemo curls? Does the hair stay curly, or does it just grow out and gets cut off eventually? Mine is just curly at the nape.
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I hear the curls eventually go away. I don't have any. I plan to keep my hair short, so I may never know if I would have some curls. - Diana
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I have my first post-treatment mammo tomorrow at 8a. A little nervous . . .
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All the best ladyboss! I am dancing as my tumor markers are all within range and my liver functions are good. Onco is happy to report I am doing well.
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Hope you have good news tomorrow Diana. Keep us posted.
Frances, glad to hear that you are also doing well. -
Keep dancing, Frances! Stay in touch. I think about you ladies all the time.
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http://www.nytimes.com/2012/03/08/fashion/postcancer-women-get-a-boost-from-coloring-their-hair.html
Saw this today and got kick out of it in view of our posts about hair. -
I think the mammo went OK. They made me stay until the radiologist looked at my pictures - in case she wanted additional tests. She didn't, so I guess that means they looked OK.
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Bravo, Diana! Thanks for the link to the article in the NYT, Rossileo.
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Oh - and Frances - congratulations to you as well!!
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HAS ANYONE STARTED ARIMIDEX FOR US POST MENOPAUSAL WOMEN?
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Diana, sorry for the late post but this is good news!
Theatercat-- yes I am on arimidex. Started right after I finished radiation so it's been just over three months. So far no really obvious side effects. -
Phillybird, just noticed your new pic. Looking good!
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