Starting chemo January 2009?
Comments
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You ladies are making me feel guilty that I have not really thought much about what I eat or don't eat. I have been one of those people who lose weight, gain weight, lose weight, gain weight all my life. I have been a person who exercises - sometimes more than at other times - depending what stage of life you are in has a lot to do with that I think. When my children were young I did not have as much time so I did not do as much, but as I have gotten older I have gotten more regular in the exercise thing. Food has always confused me. I can not keep up with what is GOOD for you and what is not. Seems the experts change their minds all the time. I have decided that moderation is the key. Don't overdo anything but don't deprive myself either because that sets up cravings. I have been spending all my time getting through treatments and keeping my job at the same time so haven't spent much time thinking about how I got BC and if I need to make some major life changes. Being in my 50s makes me feel like I really just need to enjoy the time I have left and not worry myself about every little thing I put in my mouth. I eat fairly well, I don't smoke, don't drink (excessively) was working out four times a week before dx - not so much now...hopefully will get back to that. DH wants to take me and the two kids left at home to Europe this summer and I worry about the costs. I hate fly...etc etc. but know what..I think I'll take a valuim and get on that plane and have some fun..Enough ranting from me. In the meantime, I am going to pick up some of the books mentioned here. Thanks for motivating me to think pass tx.
Patti
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I hope all are having a better day today. Afer the long chemo weekend I feel like I am back to "normal" today.....day 6 after treatment! I am looking forward to really making the most out of the next 2 full weeks until tx 3!!! My goal over the next 2 weeks is to do what ever necessary to get myself in tip top shape physically,mentally and with my diet so I can go into it 100%. I think I went into tx #2 in better condition than tx1 and it seemed to go a lot better. So now I'm committed....I'm putting all other trivial life stuff aside and focusing on "me" for two weeks!!!! I hope you all get a chance to do the same......
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ddlatt; My hgb dropped by 2 gms after TC #2. I felt short of breath and my heart raced with any exertion -- that is normal -- the body is compensating for having fewer oxygen carrying molecules. I had to slow down and pace myself and rest more. Your body will adjust and accomodate to this change... it takes awhile. This is not an iron deficiency anemia, so increasing iron isn't the answer. I am on day 6 after TC#3 - so my nadir is soon and I expect I might drop further. My onc talked about giving me erythropeitin (sp?) if that happens - apparently it boosts the RBCs like neulasta/neupogen jump starts the WBCs. I get my labs checked tomorrow...
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Symptom check -- anyone experiencing a problem with a dull headache in the temple area? I'm getting them almost daily, even during my "good" 2 weeks, and always starting in the afternoon. Not unbearable, but they do make it hard to help the kids w/ homework, do the "mommy taxi" thing, etc. They tried me on Emitrex, but that didn't do anything. Thought it might be dehydration, so I've been drinking tons of liquids, but no difference. The onc. nurse was very frank about being completely stumped & told me to ask the doc when I see him next week (had a clear head CT a few weeks ago, but it was clear). Anyone else having anything like this, and if so, has your med team told you what it is or how to treat?
Thanks!
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ddlatt - they told me I was borderline anemic just before they started the iv on my first treatment. Then when they did the blood draw right before my 2nd treatment they said everything looked good except my platelets doubled and were very high so they told me to take an iron pill everyday. This treatment I have alot more headaches and I'm wondering if things haven't gotten worse in that department but they don't check me between treatments so I guess I'll find out on the day of tx 3. Sorry you are feeling bad...you seemed to be doing so well until lately... ugh... I hope you stay on schedule... oh well, at least you're in Reno... if I were there, I'd be playing video poker and trying to escape this madness for awhile...
kt57 - I loved your story about the M&M's. Little moments like that will keep us going... finding the humor in all this madness... I like your husband and I haven't even met him..
spooky - I am so sorry you had to find us.. but I'm glad you did. This is my 2nd time around too and it sucks.
Bev56 - we have more in common than the schedule... I'm snapping like a turtle at people when I don't feel good too.... lol. As far as I know... I will get Taxotere again on tx 3... and we will all be nervously crossing our fingers when that damn bag is hung on that little pole... this time, I'll make sure the nurse doesn't leave the room....
Marymoir - geez this round I am having headaches galore.... in the middle of the night I wake up and I have one... I'm trying to fight thru hoping they go away... I was thinking maybe they were from a drastic drop in caffeine as coffee isn't my friend and all I do is drink water... maybe I'll try some Diet Coke...
Alo - I'm thinking the same thing.. use the "good times" to beef up and get strong for the next round.. it's like in a boxing ring... that week, 10 days before the next round we're sitting there in the little chair in the corner and someone is putting that squeege of water down our faces and we're resting for a minute to go back out in the ring and put our fists up again... then the ring girl walks around with the sign that says ROUND 3 and we jump back out there with renewed energy to kick some ass... LOL Ok, I know weird analogy.... just ignore me.
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jillyG - thank you! chemo-inducted anemia is very different from regular anemia, unfortunately. can't take iron pills. thank you for the good wishes!
berkeleykim a week ago i was 12.4 for hemoglobin, which is in the normal range. my RBC was 4.16, which is low. everything has dropped since then. i get 88mg of adriamycin but i know it's calculated according to weight, and i'm up to 113 now (was 102 at surgery in november!). i'm really glad you ate that roast! i've been a vegetarian for so many years, i felt horrible eating that steak, but i'd eat a whole cow raw right now to avoid a transfusion! i guess i have to cancel my subscription to PETA.haha stay well!
spooky - i was told to take claritin the morning of my neulasa shot, and evening of, also twice/day for one week afterwards. it has helped me tremendously. i have had soreness, but never any bone pain. i also had a double mastectomy in november and started chemo jan 14th. stay well!
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Alo---I LOVE THE BOXING ANALOGY!
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Hi Everyone!!
Well it seems I have a infected TOE???? they called me in auugmentin....what erve that is wil start it tonight, I have had a low temp 99.9 for days..............and I am in bed at 800!! I am on the countdown!!!!......................Sorry about the periods,...........you will hate me I never had one all of my life yes I did say all of my life cause I was always only 99 lbs...................hard for me to relate..but when I tryed to get pg it was very hard!! Wishing you all a great week!! Pamela
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ddlatt: how many years in between for yours?
LisaLisa: I lived at 761 35th street. Love Manhattan Beach and hope to go back there someday. Maybe when my daughter leaves for college. She's in 8th right now.
I bought the 24 hr. claritin, who knew there were tons of kinds these days, so I don't really know if to take it this morning before my shot this afternoon or right after the shot. Since it's the no drowsy I'm thinking tomorrow morning may be better for me. Thanks for the tip, I just heard about claritin yesterday.
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Holtbolt--Wish I had the energy to put my gloves on!! (I probably will a couple of days before my next tx!!)
Ddlatt--don't like eating cow much, and am going to load up on beans, cream of wheat, spinach, etc. Sounds like it won't make much difference. I hope my counts catch up during the 12 weekly Taxols I'll be getting, but from the posts I've read that also knocks down the RBC. Hang in there!
Pamela--take care of that toe. Is it from the new Taxol treatment? Feel better.
Headaches here too! Haven't had one in months, and woke up the last two mornings witth dull ache. I think it might be sinus or dedydration after sweating and not drinking all night.
Good wishes and hugs to all.
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HoltBolt: You are a hoot. Another good laugh for me this week. Thanks for that. Sorry about your reaction to the TC this time -- they will be prepared so it won't happen next time. Glad you were able to finish it. Four rounds will be plenty!
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Any chance the headaches could be from the anti nausea drugs? I get one after the infusion (I forget what they give me with chemo and I know taking the Zofran for a few days gives me a headache. Butt I can live with that and a few tylenols much more then the nausea if I don't take them. Just a thought.
Ellen
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REKoz -- the onc. nurse thought it could be the anti-nausea drugs at 1st, but then ruled it out b/c I'm still having them 2-3 weeks after my infusions. But I'll ask the onc. about it next week. Thanks!
Holtbolt: Your boxing analogy ROCKS!!
That is a perfect description of what I feel like during days 8-21! Mind if I steal your analogy for my CaringBridge site (I'll be sure to give you appropriate credit!!!)
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Holtbolt - love the boxing anology. I go in for AC #4 on Friday and I am really dreading it, but I'm trying so hard to be positive and get my body strong before I'm back in the chair. Somewhere inside of me I just know this one is going to kick my ass from here to San Juan.
This was my 3rd full day back to work. I just feel like I am trying too hard in very way. I'd like to be completely taken care of for a while and I'd really enjoy letting myself get good and crazy. That's not going to happen any time soon. Its something to daydream about.
My FML runs out on Monday. My place of work also has a leave bank. I sent my materials in for it today....you aren't supposed to apply for it until FML runs out. Don't ask me to explain that one. I was warned by our payroll expert of an unwritten rule that it is not granted for intermittant use. I know that an unwritten rule is not a rule at all, and I know I probably have nothing at all to worry about, but I will feel much better when I hear back about my request. I think I did a very nice job with the request letter and gathering all my docs. I know the Director of my division is strongly behind me.
I am mad at my man. That's a rant for another thread, but his gestures are seeming awfully superficial to me and he hasn't been willing to take time off to go to chemo with me. He says he can't but I know that really means won't. Plus I am pissed that he eats and buys so much crappy food and I am sick of his idiotic TV habit. Sorry, I am a book reader. Ah well. We are giving this a shot. The only thing to do is let him know how I feel. I'll save that for a rainy day. I don't want to deal with it right now.
After my mast I found myself swimming in a Banana Republic silk blouse. The boobs just don't fill it out anymore. I could have given it to Goodwill but I decided to sacrifice it to the wig liner Gods. The wig is much more comfortable now. I got two compliments on my hair today from people I hadn't seen in a while. Both were surprised that it was a wig.
My darling just turned on a dreadful TV show and I lost my train of thought. Gonna go read now.
I have to say, I was realizing today how much the support from this board really helps me get through. When I am able to be happy and brave, it's really because of you all.
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Holtbolt....you are funny!!! Glad we're on the same wave lenght!!! BAM!
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Year of the hat....I like the banana republic idea....turning lemons into lemonade.....
don't deal with your husband now.....let it go!!!!You'll probably end up feeling worse in the end...
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WIGS--Help! I bought a new wig, and it looks sorta like my old style without any grey (my dd said it doesn't exactly match my face-oh well!). I'm having trouble with the bags though. They need to be thinned I think because they keep falling in my face. I'm afraid to have my stylist cut it though and make a mistake. Has anyone had theirs cut? Did it come out ok?
I'm hoping to wear it when I go back to teach. I'm so comfortable in my beanies around the house and even out shopping. The wig is itchy, but when I see it on me I feel sort of like the old me.
Year of the Hat-maybe I'll try a liner. I've got a bunch of fabric around and bought some silk remnants to make a scarf which of course I haven't done. Reading has been my savior for keeping my mind out of the dark places. I've been so enjoying the time to do it, so it's a bit of a silver lining to the dark bc cloud. My FMLA is done on 2-26, but I know I won't be able to work full time.
Hugs to all. I was feeling so dizzy and crummy today but the rain cleared today and I went for 30 min walk with a friend and it really helped.
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BerkeleKim-- I took my wig to a cosmotologist that the wig store recommended. She was very good.....perhaps you could ask your shop for a name. My wig was to "poofy" on the sides and the bangs were to long so she cut it to fit my face. She did just a little at a time and had me watching to tell her what I wanted.
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I had a great experience with a wig stylist. She advertises herself locally as a wig specialist. I knew she did good work because a friend who had cancer a couple of years ago went to her and she looked so natural. I know someone else here had a bad experience with it, but maybe try a recommendation from your local American Cancer Society.
I wanted to comment also.....I have been thinking about the stage 3 and 4 people. I read an article that advocated for them. Even though it's depressing that that can happen to anyone, we also need to advocate for them to get the best life saving treatments possible and to be as comfortable as possible during treatment. Personally, I only go to the on-line boards for my support so I am not saying it's necessarily productive to go to support groups for the stage 3 and 4s, but the article I read said we stage 1 and 2 gals kind of steal their thunder in the medical world and in the outer world because our cure rates are so much higher. We are the darlings of the breast cancer experience. I just think we have to remember that just because they drew the short straws, their care and well being are no less important than ours. They are us really....one for all and all for one.
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spooky - you used to live very close to me! i'm in the tree section too! i love MB.
ddlatt - i'm anemic too. i posted on that last week. i'm trying to eat foods rich in iron but don't know if its helping or not. i was also anemic when pregnant....so i'm not shocked. ugh.
year of the hat - um, some of us here are stage 3. i'm one of them! and...i feel that my prognosis is good! i'm doing all i can. i generally feel good too!
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BerkelyKim--Are you getting lymphadema therapy? Suddenly, my arm hurts soooo much. My PS says to massage it, but that isn't even helping. Whom do I turn to for physical therapy? Kinda bummed I have to search this out and more bummed my "cancer team" isn't on board to help me. Sigh. I will get through this---JUST NEED TO VENT!
Lisalisa- I am so glad to see you write words of optimism and hope. This is so much a part of getting trhogu the tx.
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Good morning!
Is it twisted that I'm counting the minutes until I go to my 4th A/C tomorrow? It's such a huge milestone to me...halfway done! I can't wait to have it behind me..even if it kicks my butt.
Jess, sorry about your arm. Mine is still tight and slightly numb. I'm not sure about the PT, though. Can you go to just a regular PT, I wonder?
Re: Stage III and IV...it's disappointing to me that an article was written with that sort of slant to it. I am Stage III and have never felt that I was receiving any less care or treatment than anyone else, or that I have any less chance of surviving. My optimism doesn't come from just having a good attitude, it comes from the math presented to me by my oncologist...do everything we tell you to do and you will only have a 10% chance of recurrence...and with the clinical trial I'm going on it's even less than that. Year, I would love to know where you read that article! It's bad enough being viewed as a "poor Stage III" from folks outside the BC world but if that actually came from someone in the know...shame on them!
Ok, that was a little more of a rant than I meant it to be!
Everyone have a great day and feel good!
Diane
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Hi everyone.
shockedat39-I'm with you about some of us with stage111 and 4. There's hope for all of us. I happen to have IDC and IBC.
My doctor is very pleased with my treatments. My blood counts have been excellent. I feel good most of the time. I pray a lot and am keeping a postive attitude. I plan on being around a long time. My oldest daughter graduates from high school this year and I plan on seeing my other daughter graduate in 3yrs, plus I just got married last year and I would like to spend a lot of years with my husband. Everyone just need to stay focused and take care of themselves and we will all get through this. Tomorrow is #3 a/c for me. Hoping I don't feel crappy like the last one. Take care.
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Hello Jewels! Greetings from sunny Alberta. I am leaving my house for the 1st time since Friday (when I got back from ER with pneumonia). I am going for my bloodwork to see whether I am going to get chemo on Monday. Was supposed to get it this week but it got delayed a week. Wish me luck, I will be so upset if my counts haven't improved. My family doc said I should ask to see the oncologist and let him know what's been happening with my health and give him an update while I am there , so I will see if I can talk to him. I see him on Monday anyway, so not a huge deal. My family doc is married to my oncologist...total coincidence.
Plutz, good luck with AC #3 tomorrow, hopeully my AC #3 is Monday (fingers crossed).
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Enjoy the day JillyG, keeping finders crossed for you!!!
Postive wishes for everyone today!!!!!
As a rad/onc I met said to me one day......he loves his job....he gets to cure cancer every day.
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Hi Everyone,
it sounds like almost everyone is smiling today!!! Myt oc called in orgmenton for me never been on a medicien in my life, the pill is hugh!!!!!!! Hopefully it will fix my infection in my toe!! Does anyone here watch idol.......yes I am old and I watch, I love Adam Lamberdin from Phx Think he is going to win, anyone else?? Maybe we should start a bet....that would be fun and get our minds of of our problems.
Does anyone else have severe pain in their chest weeks later??? I am very please my under arm is starting to look normal, I thought it would look strange for ever.
I don't know how any of you did it with the recon, I just think the pain and strecking would kill me.
My port also was in pain for 5 days pass the treatment??? The sun is out and it is a beautiful day ENJOY!! Pamela
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Just got off the phone with my aunt who finished treatment for Stage III BC in 2001 -- she is doing great, no recurrence in 8 years! (My step-mother is also a Stage III BC survivor -- just past 7 years out w/ no recurrence). It was great talking to my aunt b/c I've been in that "dark place" the last few days, torturing myself with the "what if it comes back" line of thinking (I have a high Oncotype DX score, which is why I worry when my diagnosis is Stage I). I asked her how long it took for her to stop worrying about that on a daily basis, and she said she never really worried about it...she just assumed that her treatment was going to take care of it, and that was that, and that if it was going to come back, then that was that, but worrying about it was pointless since she was already doing everything she could do wipe it out. I'm going to try to think more like her, but I have a worry-prone personality, so it will take some work! Guess my faith could definitely use some improvement!
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Pam - I LOVE American Idol... my money is on Danny Gokey so far this year, I think he's great.... but haven't heard alot of them, except little pieces of auditions here and there... which one is Adam? Wow this week I was shocked at how horrible a few of them were... how did they even get through? lol
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Hi all--Just lost my post. Dang-here goes again.
Jess--I did get LE massage, which is VERY different from PT. It helped me alot, and they taught me how to do it because I got just 6 appts. I'm not as effective. Definitely ask for a referral. Anyone who has had lymphnodes removed is at risk. I just got fitted for a sleeve to fly with or to go to higher elevations. I've had sore shoulders and also sometimes pain under my arm running to my elbow. They said it's not "cording" but just tightness, which I try to stretch out gently. I was stretching in the shower today and unfortuantely pulled my back on the good side. Will it ever stop???
Year of the Hat and Bevr-thanks for the wig advice. I just don't want to ruin $200, but cutting slowly is a good idea. Do you use styling gel, and what do you wash with. I can't remember what my wig guy said, I think just gentle shampoo?
I think stage III is very good prognosis these days. I'm borderline with almost 4 lymphs and 3 separate tumors. When I told my onc mid AC that I hoped the tx worked, he said it will. Made me feel better but I know there's always the chance (especially since I've visited the rec/mets thread a few times). Makes you appreciate each day.
Marymoir, I love your aunt's attitude. I have never before worried about my health--always my kids' and DH's. I am definitely focused on myself now, not all for the good.
Pamela--you're right about getting out in the sun. We finally have a really nice day before the rains hit again. I'm gonna get out, although the antibiotic warns about sunlight and a million other things (levaquin). Don't watch Idol too much, but loving LOST!!!
Plutz and JillyG (and whoever else gets tx this week!!!-I just look up a few post before and loose track of all us fighters!)--GOOD LUCK, and YOU CAN DO IT!!!
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BerkeleyKim - I LOVE LOST!!! .... a little Sawyer will lift my day by a few notches!
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