Taxol Chemotherapy
Comments
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I hope all gets better for you claire, its no fun to feel like a pin cushion on top of everything else.
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I'm crashing really hard from the steroids this time..anyone else find that they cant stop crying during the steroid crash?? I cant wait for this crap to end!
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kelleysgroi - Me! I have four tx of Taxol to go with the last date on Feb 27 and then to finish Herceptin. I wasn't sure if it was the steroids, the Taxol, or just everything finally catching up to me and sinking in. I find that the day after I stop the steroids (Thursday), I would rather just stay in bed all day.......until Sunday when I start them again. Sunday night and Monday morning I feel pretty good until I go to chemo.
Has anyone had a ringling or more of a "tingling" sound in their ears from steroids? I haven't had any acne but I've had some swelling in my feet, this ear thing only on one side, lots of crying, and I'm just TIRED. I just keep counting down - five more weeks, four more weeks.....
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JulieLynn- it reallyis a roller coaster ride isnt it? My onc looks at me as if I am the only person she has ever seen cry their way through chemo..I guess I feel better knowing others are crying also. I've heard some others mention ringing in the ear..not sure if it is from the steroids or the chemo. I have not experienced this. keep counting down....
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Kellysgroi, I seem to crash a couple of days after pre-meds/chemo infusion. I find it very difficult to get myself together and am tearful and just plain miserable. My poor Mum gets the brunt of it.
I just noticed another side effect today - food tastes absolutely rubbish. I had a tuna melt sandwich with vegetables. I keep trying different combinations to see if I could make it taste better, ie. maybe without the cheese, or the tomato, or even the tuna. In the end I just ate the bread and it still tasted bad.
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Hi ladies - I have spent my morning reading all of your stories and I just want to say to those of you still going through chemo - there is light at the end of the tunnel. I finished my Taxol almost 6 months ago and am finally feeling better. I did go through radiation post chemo which can cause lingering fatigue but that is now much less. I had the dose dense Taxol which started after my first tx. and I still have some neuropathy in my hands and feet and a bit more joint pain than I did prior to all the treatments, but I am 53 so part of it could be just that too. To those of you suffering through the joint and muscle pain, definitely take some pain meds for this, there is no reason to suffer if you can treat it. (I am an RN too). In terms of hair loss, my eyebrows & eyelashes we're the first to come back but it took several weeks before I could actually wear mascara again. My skin and nails are still very dry, my heels have cracks in them most of the time. I try to use Aquaphor on them twice a day and this has helped some and I use hand creams several times a day. This being said - 6 months after finishing tx. I am beginning to feel much more Iike myself again so hang in there and soon it will all be behind you and just a bad memory! I keep you all in my prayers!
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Roller coaster today. Tearful and tired not so much physical as emotional. I have to drive to Phx for an unrelated eye evaluation (I might have a blocked duct that might require surgery or it might be chemo-related but I have to get it looked at) and then see the surgeons at MD Anderson too. I'm so over being poked and prodded and "felt up" if you know what I mean, every week.
I"m trying to teach part time and I just can't seem to focus. I'm not really interested in anything. I have 6 more Taxols to go--6 more weeks--and today I wonder if I'll make it. I'm feeling some weird on and off pain in my head and of course I wonder if it's some new, bad thing...I'm hoping it's from the neupogen shots I got Th/Fri but of course we are always afraid it's something worse.
No signs of hair regrowth yet. I kind of feel like my body has abandoned me.
Claire
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Claire, I hope you have a better week ahead! I get what you mean about your body abandoning you, I feel the same. Sometimes I look in the mirror and can't believe what I look like. I take comfort in knowing it's only temporary, but still can't wait to look like myself again. Thanks for the encouraging words Nancinurse. It helps to be reminded that there IS a light at the end of the tunnel!
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I didn't have problems sleeping when I took steroids with the 4 A/C treatments. I have a bag of decadron with my Taxol treatment. I had my 2nd treatment yesterday. I went to sleep at 10:30 p.m. and woke up at 1:30 a.m. I absolutely could not go back to sleep until 6:30 this morning and slept for only 2 hours. Does anyone else have problems staying asleep with Taxol? I come home and can barely stand but cannot stay asleep.
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Beth- I have trouble sleeping also..try taking a benadryl before you go to bed..I found that it helps. I didnt have any trouble sleeping during A/C either but he taxol seems different.
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Beth & Kelley,
I also have a horrible time sleeping while on Taxol! at first I thought it was the hot flashes awakening me and keeping me up (darn chemopause!) but now that I hear your complaints of it also, it must be taxol related. I also thought about it being from the steroids, but mine lasts the whole 2 weeks wil it's time for the next treatment! Hang in there ladies!
I go tomorrow for Taxol number 3! On,y one more to go after that! Then I can breathe again......at least until rads start -
Yes to sleeping issues. I stay up late (not like me at all) wake up at 330, when its too early and I shouldn't. Steroids jack me up artificially and I think they keep up that way till the next infusion.
I take a whole regime of stuff to help me sleep: motrin PM, trazadone, melatonin, magnesium and sometimes a Xanax.Hate taking all the meds, I feel like a druggie--but need sleep more than I need to worry about how I get it.
T #7 down today. And it was the fastest one yet--in and out in less than 3 hours! Woo-hoo!
Claire
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Kim- good to see you! Was the bone pain better this round? I am 6 days away from finishing this crap..yay!
Claire- I have never taken so many different pills in my life! I have Rx bottles everywhere!
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Yes to sleeping issues. It is definately worse closer to the date of treatment. So excited for this almost to be over. For those of you just starting, it seems long and miserable. I started my first weekly taxol the Monday after Thanksgivng and in less than 5 days I get my last taxol!!! I move onto another set of chemo issues but its almost there! Keep chugging, you will make it.
My onc says that with taxol he has never found any predictive factors to indicate what might make the SE worse. He says its been completely random from woman to woman. Age, race, whatever hasn't made a difference, especially with the pain and neuropathy. Its pretty much a crap shoot. I know some of you are new to this thread, and some have already moved on but keep the thread going its really nice to talk to ladies gong through the same things. I even have a BCO PM pal now!
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Kelley, the bone pain was still quite substantial but it was improved from the first round. My Oncologist thinks its completely Taxol related and since the pain always starts Saturday after treatment she instructed me to start taking pain meds either Friday night or first thing Saturday before the pain sets in. It seemed to help. Instead of excruciating pain, it was only unbearable. Lol!
I've been an emotional wreck this afternoon and now this evening. I guess it's because I know I'll be spending all day in that darn Chemo chair tomorrow! I just want it to be done and over! I cried my eyes out over my hair, and my lack of breasts and my 25 lb weight gain......then I cried some more for crying over such vanity.....then I cried for not allowing myself time to cry before.....y'all get the picture.......I'm on an emotional roller coaster and can't seem to get off
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Hey Kim - I've been following this thread (in case I end up getting Taxol), and just wanted to say I can completely relate to the crying rollercoaster. You described it perfectly. Add some angry outbursts and few cuss words before breaking into tears, and you've described me to a "T" lately. LOL. Hugs to you!
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Going for treatment #2 today. I hope that it goes better than #1.
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I had my port replaced yesterday. It sprung a leak!! I am feeling pain today and very mad at my surgeon for placement of first port!! #4 taxol next tuesday.
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Hi everyone, I finished #12 taxol/herceptin last week. I had pretty minimal SE those 12 weeks. But WOW, did the herceptin I got yesterday throw me for a loop. It was herceptin #13 and the first of the every 3 week herceptin treatments I will get. I guess I didn't realize I had been getting a weekly dose & now its a 3 week dose. Maybe that's why I feel so bad? Everything aches. I start tamoxifen tomorrow too - guess I should at least give the 3 page SE list a once over. Hope everyones getting thru taxol ok & that those of you doing herceptin too have an easier time than I have started off with a once you get to the every 3 weeks part!
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Shore, congrats on finishing Taxol, that's one thing done! Hoping for minimal SE's for you on th Herceptin.
Sandlake, wth? I've never heard of such a thing... I'd be mad too!
Gator, does this mean you're half way done now?
dancetrancer, welcome if you end up here. You and I have the same dx date. That's my birthday too!
Kim, I'm so sorry you're having a hard time. Sending gentle hugs your way. I think we all have our moments and it's perfectly natural. I sometimes look at myself and can't believe what I've been thru and how I look. I will never complain of having a bad hair day again in my life!
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Hi everyone
Just wanted to let you know I'm on the same roller coaster with you, my emotions are much worse with taxol, my kids are feeling it. I have to take activan around dinner so I don't yell at them then I'm crying off and on all day while they are at school. To top that off my onc wants to cut my meds because new Florida laws.. I'm just about over this. For the icing on the cake my eyebrows and eyelashes are almost gone, worse than losing the hair, as I was hanging on to those, now I have perfected the cancer look. One more month.....my liver enzymes are high also, so that's a new mystery, hopefully they come down -
I've been having the crying issues too with the Taxol - Thought it was maybe from the steroids but now I'm not too sure. Only three more tx to go and then to finish the Herceptin! I just want off this rollercoaster! FLislander - My liver enzymes were up last week but not this week. My MO said the liver is just working harder to flush out all the toxins. She even skipped giving me iron last week because of it but was able to resume it this week. We'll see what next week brings.
A friend took me to Merle Norman this past weekend for a makeover - They taught me how to do my eyebrows (with a powder). I can't believe what a difference it made! I knew they were mostly gone but WOW having some back on, even temporarily, made such a huge difference looking in the mirror! Still hanging on to half my eyelashes but don't think I'm talented enough to try the fake ones. I think the eyebrows and lashes have been harder to lose than the hair too.
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Yes I've heard merle Norman has good eyebrow powder, I may make my way over ther tomorrow. I think some of the emotions come from steroids, I'm asking for less next week. Sounds good on the liver enzymes, I'm drinking water with lemon to try to help out,we will see.
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Im on weekly taxol and i am down to 6 mg or whatever iv units they use. Plus benedryl and no oral steroids. It can be reduced or even dropped if u have had no sign of rxn to the taxol. Dont let ur mo blow u off.
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I found that I was crazy emotional right after my first taxol treatment. I never felt that way during the A/C. I cried constantly throughout the first 3 treatments. I am having a really good week ..not sure if that is because I know that next wednesday I finish this crap.
Hang in there everyone! My eyebrows are just about gone also. Went to MAC yesterday and got a pencil and it looks pretty good but I dont think I will draw them in if they fall out completely. Eyelashes are very thin and I am just plain sick of having a bald head. Plus- these tissue expanders suck..breast cancer is a bitch!!
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I'll second that, it sucks. I have 2 more then surg, then rads..
I am definitely getting steroids reduced, thanks -
Hang in there FLislander- we are doing this..and almost done!
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I'm hanging sorry can't get a positive post out today
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The TEs especially suck - Who knew it was going to be this hard to get new boobs?!!! I can't decide if I'm more excited to finish the reconstruction hopefully in March or April or for my hair to grow back! Then to think about nipples and tattoos....one step at a time! It seems at this point it wouldn't be so overwhelming any more. Happy thoughts, happy thoughts, happy thoughts....
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I think my expanders have expanded. I ran into the door the other day and it hurt so bad. I didn't realize 50ccs would make me that much bigger. My husband and I went to the grocery store and I innocently said I wanted chicken breasts. I started laughing so hard. He was laughing because it had been so long since he has heard my laughter!
Ladies, try the Look Good Feel Better programs. Hopefully, one is available in your area. They teach you to draw your eyebrows. My brows were so stupid looking--long hairs, no hairs--that I plucked most of them last night. I draw on the brows and line my eyes because I have so few lashes. My biggest decision of the day is which hat or scarf do I wear today?
My joint pain is starting but it will be over on Sunday or Monday. I have pain meds to take. I did get 9 hours of sleep last night. Feeling better today.
One more Taxol to go then I go into the "What now?" mode. I am doing chemo because of my Onco score. It is preventative. I really do wonder what I will do next.
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