Chemo June 2010
Comments
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I am scheduled for my first mammo plus ultrasound since diagnosis soon. Just like Jackie and so many other women (30% according to my BS) I was "mammo occult". Who ever heard of that term! I thought mammos were fairly reliable. My left breast has been scrutinized within an inch of its life, but now I am worried.....what if my right breast is "mammo occult"? I guess this BC journey will never end. I sure hope the fears start to fade someday.
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Hi Ladies I am actually using my new Kindle to send this out. Tomorrow is our 13th wedding anniversary. I have to say that I have a wonderful sweet loving hubby and I thank God for him everyday. Next week is my first onc f/u since finishing treatments. I am not sure what he will do. I do not think he will do much testing but I could be wrong. I will let you know after the appt. Hope all have agreat weekend and stay well.
Chey so glad to hear you doing so well. Jackie you are inspirational and we appreciate you. Joan please take care and I hope you get stronger soon. Hello to DMom Tmarina Latte toni daniel Sherry and all of you on this forum. I really love all of you. May 2011be abetter year for us all. -
gin2ca - congrats on your anniversary!!! I am so glad you have a wonderful hubby!!!
I hope you all have a great week!
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Does anyone else feel aches and pains everywhere after chemo? I feel achey all over, but especially in my legs. I'm wondering if this is from the rads or chemo. Hmmm....
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kitty- Count me in for the aches an pains. For me they seem to be mostly in my knees and feet. Having said that, my right shoulder was killing me yesterday! The worst part is always wondering if it "is something". Dear God, I hope these cancer mets fears subside someday. No telling if it's rads or chemo. My MO made a good point (which for some reason never occurred to me) that it could very well be chemopause related. Even non BC women, when going through menopause, get joint issues.
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Kittycat, I had bad leg pains for weeks after chemo and they eventually went away. I would also get terrible foot cramps at night. It's hard to tell what causes all this, the chemo, the inactivity, the femara, or the fatigue.
Dmom, I have given myself a 5 day rule. When any new disturbing ache or pain starts up, I give it 5 days to go away before I start worrying. So far it has worked.
I had a mammogram 2 years previous that did not show anything. The rads Dr. said from first cancer cell to seeing it on a mammogram takes 2 years. Yet here I was with locally advanced cancer. I no longer trust mammos and ultrasounds.....
Love and Hugs, Mimi
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kittycat, Dmom and mimi, I suffer from the aches and pains also but was having a slight problem before BC with joints but it has definitely gotten worse. I have started taking fish oil, calcium with D, and glucosamine chondroitin in the last 2 months and I think it is helping. I am taking Femara and it has a major side effect as joint pain so I am trying to counteract that with some of these supplements. Being a 55 yo woman with BC really does a number on everything I think.
Mimi, I had advanced BC also that did not show up on my mammo but mine was ILC that tends to be hard to see on mammograms. Mine did show up on u/s but not until I had already found it on my self exam. We are definitely our own best clinician in finding this stuff. I will tell you that the Breast Center where I work finds small cancers all the time just on the mammo but really dense breast are hard to see through and a lot of times the cancer hides in the dense tissue. I think one day they will have better imaging but we are not there yet even with digital. There is nothing that is 100% accurate and that is a shame. I pray they will find a cure and we can all breathe a sigh of relief.
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Also, On the anniversary yesterday. Wouldn't you know that I would wake up with a stomach bug and could not enjoy our day because I was in and out of the bathroom all day. Oh well, we decided we will plan a nice little trip in the spring when maybe I have a little more strength back. Ginny
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gin2ca--Happy Anniversary--sorry you couldn't enjoy it
Feel better soon!
Kitty--yes, many of us have complained of aches and pains after chemo. It hit me esp. hard a year ago after chemo for colon cancer. My onc also says it might have to do with the chemo pause.
mimi--I like your 5 day rule! My prev. mammos didn't show anything either, and when something did show up it was just some calcifications. I was told no hurry, but should have them biopsied eventually. Rad doc said if it was cancer it would only be DCIS. The MRI didn't show much else either, and biopsy only showed DCIS with a microinvasion. Well, lumpectomy found a 3.5 cm IDC tumor, and mx found DCIS all throughout the breast! I wish I would have had the other breast removed too, and still might. The cancer managed to get to my nodes with hardly anything showing up--so of course I worry about what might be in the other one!
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All done! Today was my last radiation tx. I, like so many others, thought this day would never come! Today was my second day back at work and it feels good! I, too, have experienced joint pain along the way. Mine must be from chemo because it started back in the fall when I was still going through chemo. It has worsened over time. I'm still sleeping in a recliner because I can't sleep laying down in my bed because of the joint pain. Some days are not so bad, some are very bad. Today is one of those bad days. I had to have the rads tech help me take my hoodie off today because my shoulders hurt so bad. I guess tonight will be a pain pill night!
Gin - congrats on your anniversary, but what a bummer to be sick. Hope you're better soon.
Bon - I'm so sorry you are having insurance issues. You have enough on your plate to deal with without having to mess with your insurance. What a mess! I don't understand why they have to be so difficult during one of the most stressful times of your life. Praying for strength for you and for a successful resolution to your problem.
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yay Sherry!! Congrats on finishing rads! Glad you are enjoying being back at work! Be gentle with yourself the next week or so, sometimes the rads fatigue gets worse after it's done--and the skin continues to get worse too, so keep moisturizing!
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Sherry, I am doing the Dance of Joy for you right now. Congrats on finishing rads!!!!Take care and don't overdo. I am better today after my stomach bug yesterday. Thanks for asking. Ginny
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sherry- Oh WAHOOOO! Can you hear me? I'm shouting with my happy dance all the way from NYC! You get the biggest, craziest happy dance of all!
mimi- I like your 5 day rule. Now if I can just remember to count the days....
gin- So sorry about the stomach bug. Be sure to take some good acidophilus when you can to balance things out again. Happy Anniversary! My DH takes glucosamine and chondroitin and swears by it. He said it took about 2 months to start working. He could hardly walk down subway stairs before (used to be a runner). Now his knees feel fine.
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SHERRY!!!!! I am soooo excited for you! Congrats on finishing rads and this whole chemo/rads journey. It wasn't easy on any of us, but you really had some obstacles! Congrats on overcoming those obstacles and completing treatment! You deserve to do something special to celebrate - we all do!!!!
Thanks everyone on the feedback on the aches and pains. My right knee has been bugging me for a little while. I had bad knees pre-chemo. I think chemo brings out the worst things in our bodies.
By the way, how does everyone's hair look? Mine is about 1.5 inches long and is super curly. I haven't been brave enough to go wigless yet!
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Oh wait.... I forgot to mention my work drama today. So I decided today that after all the months I spent doing chemo and still working, that I am going to take care of myself more. I got a mediocre to okay review today, even though I work really hard, taking care of customers and traveling on business... YES TRAVELING... DURING CHEMO and RADS! I modified a business trip I was taking tomorrow to leave in the afternoon. And I'm only going to work on my own projects and put myself first. Sounds selfish, but I've given more than necessary. You guys all got to hear about my work dramas during the summer. When I have my hysterectomy, I'm taking time off and not doing the work thing along with it. My friend Melanie told me that with my wig and makeup, I look good/healthy and act like I'm okay. That could work against me.
I stopped by a really cool place today that helps cancer patients, called the Caring Place. They have all kinds of things to help cancer patients... massage and reflex therapy, reiki, support groups, art & jewelry classes, etc...
This cancer jouney doesn't end when treatment ends. We still need to heal physically and emotionally.
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Sherry, WooHoo! for finnishing treatment. It has been a long haul for all of us and we are glad you finally caught up.
Kitty cat, my hair is only 1\4 to1\2 inch long even tho I finnished last chemo Sept. 17th. Still mostly bald at the top with just stubble coming in. I am so disappointed with this. Is anyone having bad chemo brain? I still do things like put the dogs outside in -30 C temps and forget about them for 30 minutes. My memory and concentration are just trashed and I really worry about going back to work in a high stress situation and trying to multitask. It just doesn't happen and I will look stupid.
Love and Hugs, Mimi
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Sherry ~ Congrats on finishing up the rads!!! Wow, what a long journey you've had!!! Now onto the next chapter!
Kittycat ~ I've been following your work related drama and can honestly say I know how you feel!!! It is so frustrating when you are trying to work through chemo and rads, and feel you're doing pretty darned good, and they hit you with the @$#%@$.....The very week after I finished my radiation, I got pulled into HR and was written up for some really 'bogus' stuff and asked what happened to me, that I wasn't the nurse I used to be!!! I was sobbing and asked "are you kidding me???" They said I needed to 'get over it', and move on with my life.....HELLO!!!!! The chemo is still affecting my body, and the radiation is zapping the energy out of me and I'm supposed to snap out of it!!!!!! They also told me that I needed to get some mental health, because obviously (I was crying) I couldn't handle it. The thing is, I was getting excellent feedback from all of my co-workers, but my boss was angry that it took so long to get through. Sorry, this had to be dealt with, not gonna die for my job...literally.
Sorry, I needed to vent. If I were you Kitty, I would definitely take care of YOU first when you have your hysterectomy! If (God forbid), I go through this again, I am going to choose not to work. The working was really good for me, but the stress of dealing with bosses who lack compassion is not healthy.
On the hair front, I have about 1/2" of dark, curly hair! I've been going topless, although I still wear my wig occasionally...
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kitty and janny- You have both given more than you should have to your jobs (while going through cancer treatment!!!). It is unimaginable that your supervisors wouldn't understand that you were extending yourselves. I say if you have the legal right or sick time available, take the time off. You need to reduce the stress in order to heal. I have often been in situations where I have gone out of my way to accomodate or help customers and it actually back-fired....wasn't appreciated in the least. I have a saying "No good deed goes unpunished!"
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Kittycat,
Try drinking tonic water to stave off the foot cramps. I really hate those, one minute I'm fast asleep, the next I'm hopping round the bedroom with rigid toes! Anyway tonic water stops cramping.
Julia
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Kitty--I just don't get people sometimes. They just have NO IDEA what we go through! I remember telling you to take of yourself last summer, and I'm glad to hear you will be doing that with your next surgery. You've earned the time girl--take it!
Janny--sorry for you having to go through that also! Grrrrr! I wish I could have a talk with that supervisor of yours!
As for the hair, mine is about 1/2 an inch. It looks like it might be trying to curl a bit. I've always had straight hair, so we will see what happens. It's not filling in evenly (the top is longer than the hair around my face), so I'm still wearing my scarves for now. And it's too cold here to go without something on my head! The weird thing is the hair on my legs is much darker than it used to be. I hope that goes away by summer so I don't have to shave every day! It's alway been really light and hard to see.
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Sherry - I'm also doing the happy dance for you. It feels great to be finished.
Kitty - I have had lots of aches and pains with the chemo and they continue, even though I am done with the heavy stuff. I still get herceptin every 3 weeks so that may also contribute to that. My toes are still numb until I get into bed at night and then they start to hurt.
I'm going to be starting tamoxifan soon - can't wait to see what SE's I have with that...
My hair came in all grey and is about 1/2 to 1 inch long...some are sticking straight out. I may go to my husbands barber and get it evened out a bit. I don't like my wig, so I just wear hats outside for the sun protection (now that I am in warm sunny AZ) and go without inside. Up until a few days ago (in CT) I was totally covered while outside, but again just using hats.
Sorry for those of you who are dealing with ridiculous bosses and co-workers. I am retired, so it was easy for me.
Bon Did you try contacting Susan G Komen or The Avon Foundation for help with the med bills? Isn't that one of the reasons that we walk and do all that fund raising. It might be worth a call to them.
Meeting with my new AZ Onc for a treatment (herceptin) on Thursday. Hope all goes well.
Hugs
Liz
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Bon--are you able to get your Herceptin this week?
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Janny and Kitty- I think that we ladies on the boards should all show up at your jobs with our weird, short, post chemo hair and tell your bosses exactly how they should treat you ! Yeesh ! How can these people be so self centered and short sighted. Take care of yourselves ladies.
A big WOOOOTTTTT !!!!! To Sherry. You've been through the wringer I am so glad you are done.
Gin sorry you got the stomach bug on your anniversary. If you are no longer contagious give your hubby a kiss from all of us for being good to you.
My hair doesn't seem to want to get much longer than it is. It seems like it has been a half inch for two months. Oh well. Like the snow, there isn't a thing I can do about it. But, like the snow it frustrates me.
Today I forgot to put on makeup before I went to work and someone asked me if I was feeling all right. Thank goodness for maybelline!
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Janny - I'm sorry you got written up! That is ridiculous, esp since your coworkers have given you high remarks!!! Hmmm...
JFV - I had to laugh at your last comment. I almost forgot to pack my makeup tonight. I'm on a business trip and it would have been funny to be all plain faced tomorrow! It could be part of my new objective to scare people! LOL!!!
Gin - sorry you got the stomach flu. That is awful. I hate getting sick like that.
Bon- did you get your herceptin? I agree that you should contact the local Susan G Komen or Avon affiliate.
I'm so glad I left later today for work than early this morning. No more pushing myself with this travel crap. And I'm not working on other people's accounts! NO MORE!!!
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kittycat - well done - stick up for yourself and put yourself first for a change!!
bon - any news about the insurance and herceptin?
i had to miss a day of rads this week - had a virus with 39 degree temperature, cough, and feeling awful. still have the cough and am not great, but am on antibiotics and the temp has gone at least.
i'm now looking into a surgeon for my ooph - the surgeon i wanted is not availble until april and i really want to get it done late feb/early march so i can get my life back!
i'm so jealous of all you with curly chemo hair - i always wanted curls - mine is dead straight and already 4-5 cm longso i don't think it's going to curl (and it has lots of gray - i bought an ammonia-free color rinse to see if it will help, but haven't tried it yet)
it's cold and rainign out so i think i will curl up with a book in bed soon!
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Latte - I'm waiting until April (or so) to get my oopherectomy. Good luck on yours!
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Hi girls! How's everyone doing? I got my review situation straightened out at work. Thank goodness! I'm still getting aches and pains in my legs. Ughhh... I thought I would start feeling better after chemo and rads was over! Maybe I'll try the glucosamine. Just add it to the rest of the supplements I'm taking! I had a bad week last week. I lost my friend to colon cancer. I've been having a hard time emotionally lately. I just want to be somewhat normal again.
I'm doing another speech for Susan G Komen this weekend at a women's college basketball game. I have a couple friends going with me, including my friend Melanie that I met from BCO. My DH has to work and he's so bummed. The game should be fun!
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Kitty--Sorry about your friend! Cancer takes far too many lives.
Sounds like you have a fun weekend planned--hope you and your friend have a great time!
I saw my gyno today--she hasn't seen me since before I was first dx with colon cancer, so we had lots to talk about! I have some problems in "that" area from the colon radiation, so I have to have an ultrasound next week. Then, depending on how everything looks, we might discuss having the ovaries removed. I'm not sure this is necessary though, because I am not er+. She did mention that she might refer me to a gyn-onc, depending on how everything looks. We talked about testing for menopause. She said that isn't a very reliable test, but we might do it anyway because while it can't always tell if you are in permanent menopause, it can show if you aren't. I've been menopausal since I had chemo and radiation a year and a half ago. Anyway, the ultrasound will tell us more of what's going on with the uterus lining and ovaries (I had a cyst there a few years ago). So, add another test to my list of many upcoming tests! Also I heard the dreaded line today "because of your history..." meaning we have to do every test possible to make sure you don't have any more cancer!
Thoughts? Comments?
We aren't posting as much here these days, but any of you that are still going through rads, or whatever--we are still here for you! And those that are finished--it's nice to hear what you are up to these days and how you are feeling too.
One more thing--did any of you gals have one of the "flap" recons? I've seen some pics and it made me more confused than ever. They just don't look real(sorry--not trying to offend anyone!)--I don't know what I was expecting! on the other hand, it would be nice to wear swimsuits, and not have to worry about whether my shirt is too low cut all the time. The scars from the mx are so visible if I even slightly bend over. I just am having a REALLY hard time deciding about recon! Any thoughts are appreciated!
Thanks for listening!
Tina
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Kitty, Latte and TMarina- Interesting to hear you are all planning oophrectomies. Maybe you have already mentioned this. I was wondering why your doctors reccomended you have one.
Kitty- Sorry you lost your friend to the beast. It seems cancer is everywhere.
TMarrina- I keep "forgetting" to make an appointment for a general physical because I don't want to face all that extra testing either. I don't like the special treatment.
On a very frivilous note I have been looking at the spring/summer dresses that are online and on sale. I have lost alot of weight and will need some new clothes for the warm weather. But, with the lumps and scars from my port, as well as the discoloration from rads and tatoos all on my chest, I am wondering what style of dress to get that is modest on top without looking too frumpy ? Anyone know a good style or shopping venue that would fill the bill ?
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HELP!!! hello my sweet sisters, ok i have been asked to speak this saturday night at a very formal fundraiser for cancer, 400 people EEEEKKKK, lol i said yes, EEEEKKKK again, what was i thinking? its tux and gown, silent auction, very very formal, 100.00 a plate, last year they raised over 200.000.00 in that one night.... omgosh, im not a public speaker, i think they want to hear how chemo effect us and how we feel going thru it, how its not over just caused we r done... im so scared ill make a fool of myself, i have never spoke in public before, even in college i managed to get out of it....hahaha... what do i say? what do i do? but i get to buy a formal pretty gown,hehe, i just have no new boob yet, i still lean to the left..... im going wigless, i have about 7 inches of thick hair so i figure its time... im so scared, what was i thinking? i remember how i thought i could let people know about all my family on this site and how wonderful we all are to each other, so i said yes, now i scared..... what do u think? its too late im in the program as guest speaker
i have to do this, i cant let them down...
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