Chemo starting in December 2010
Comments
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Hi All, I'm going for my second weekly Taxol this afternoon. Although I had side effects during the first week out, they seemed so much less than the two months of E and C. Just not having to take Ativan round the clock gave me the glimmer back in my eyes. I did have bouts of pretty bad nausea all through the week, but took Ativan for it on a bout by bout basis. I've feeling more like myself than in the last two months and have had more energy.
Fingernails were really sore on day 2 and 3. No sign at all of neuropathy. Lots and lots of nightly hot flashes.
What do we do? We soldier on.
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Had chemo on Wednesday and wbc was normal again. Yay! Kinda rough over the weekend. I was going to take my granddaughter Aubrey but my stomach was to upset to deal with a 6 month old too. Just enjoy my time with her. She is my cure.
LisaMomOfFour: When I had Taxol my nails hurt and became darken. Then they started to crack in the middle across the fingernail. I superglued them when they started cracking. What happened was the new nail started to grow underneath it. I was afriad of it breaking off at the middle of my fingernail that is why I superglued it. I wish you the best in it cause it is painful. Maybe yours will just stay discolored until the new growth comes through. I hope you do not loose them. Wish you the best!
My granddaughter Aubrey
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Awww Ebann Aubrey is just precious! What a wonderful cure!
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going in for 2nd weekly taxol tomorrow! i keep thinking, "after tomorrow, i will be 1/4 the way done with taxol!" it seems easier to think about it that way!
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Angel, Good luck with today!! I'm so jealous over the sleep you are getting!! I'm fighting to get 3 4 hours and I'm on 2 mg of ativan at night. just not working!! YOur getting to the finish line, yeah!
Going to get marked next wed for radiation, then start 1st week of march. hope its ok to hang out here too, can't imagine not catching up, being here with all of you. I have peeked in on feb rads to help me to understand what's next. Another journey, and so lucky to have everyone here help with it.
Wishing all peaceful, comfortable, s/e free day.
JoAnn
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JoAnn -- I never congratulated you for finishing chemo ! Yeah... a big milestone. I am jealous, I won't be finished until early April, so I have quite a ways to go.....
Of course you can hang out here....
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Aubry is such a sweetie pie! Congrats on chemo. I had #2 of lxempra yesterday. My counts were good. Hoping I get through the next few days with little SE. Onc said if I get bad hand foot she'll have to pull me off. (xeloda causes that). Got no sleep at all night, which I think was from the steroid and benedryl dose. The stress doesn't help either.
Speeking of stress, does anyone here meditate? any good guided meditation CDs out there?
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msjag, i found something that works for the sleep. it's my own little cocktail. i take 1 mg of ativan a couple hours before bed... that gets me relaxed... then i take another 1mg or ativan and a 3 mg of melatonin with theanine in it before bed... works like a charm! the theanine in the melatonin is supposed to help "turn off the noise' (what i call it) in your head so you can sleep.
hope this helps!
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I had my second round of Taxol today. I am eternally thankful that it is easier than AC.
One problem I always have is the strange taste I get in my mouth while the nurses are flushing the IV with heparin. To me it tastes like skunk and its getting worse and worse. So today the nurse suggested I put a really strong mint (an Altoid or something similar) in my mouth first. I tried it and it really worked!
So if anyone else has that problem, I think we've discovered a solution!
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nolaa, i had my second taxol today too. i can sympathize with the nasty taste when they are flushing with the saline and heparin. i found sour/tart candies help too.
ick, it is nasty though. bleh!
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Can't sleep
Had my second taxol today and slept thru it plus 4 hours because of the benadryl and now im wide awake at 4:30 in the am. So far so good on the SE's. none to speak of atm.
Hope everyone is doing well.
Hugs!
Lisa
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Hi All,
I'm 3 days out from my second weekly Taxol treatment. The side effects are so much less than the first round of Chemo that I feel like I've gotten a fair measure of quality of life back. Previously, I had to take Ativan round the clock for 10 days after treatment or I would hit the brick wall of nausea. Ativan took the glimmer out of my eyes, and it's good to have that back. I still have nausea but it isn't omnipresent. It just visits on occasion and so I take an Ativan on a bout by bout basis.
I had neck pains and a headache last evening that lasted into this morning. Not my usual migraine and it didn't respond to any medication.
No fingernail pain this week. I'm happy about that. Last week it was like someone slammed the piano cover down on all my fingers!
I've gone to work for a couple of days this week. Just 3 or 4 hours per day. I've learned to leave before I get really tired so I don't spend the rest of the day recovering. Tiredness also brings on nausea for me.
Wishing everyone smooth sailing this week and on.
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Hi my sweet December sisters -
I've been recovering from my 3rd TC - and was supposed to take my 4th and final TC treatment on Tuesday. It got cancelled. I have some sort of viral infection. I feel pretty crappy. The 3rd TC knocked me on my butt and I just never recovered my strength - now I'm sick. The doctor is running blood cultures, which I should get the results of by Monday. They've tentatively rescheduled my final TC for next Tuesday.
I just wanted to cry when they told me I couldn't get my treatment. I'm so ready to have this behind me and I'm scared of putting it off because I know there's a reason they do it in the succession that they do.
I've been home-bound for a while now - not feeling good and running out of energy so quickly. The neuropathy has taken over my fingers. There's no strength in my fingers and my nails hurt so bad. My toenails are starting the process, too. Also, my hands turn red and swollen at times and the skin on my hands is shedding. My onc said he could give me steriods for the neuropathy. I turned it down. I'd rather deal with the SE of the neuropathy than the SE's of the steriods.
I'm taking Theraflu and Musinex since I have a viral infection. I don't like being sick while being on chemo - I think it feels worse than if I was just sick. But then again, I could just be a wuss.
Sending you all love & hugs!
Shelle
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Wow Shel, sorry you are going through this. Are you taking L-glutamine powder? your hand SE's are the same as what I am to expect from being on xeloda. For xeloda, it is lathering on a good 'udderly smooth' or similar cow udder type cream several times a day on hands and feet. I take B6 and the glutamine (in a little juice, otherwise it all sinks to bottom). Take 15-30 grams. I would consider the steroids again too. they can low dose you. When I was on taxol, I took them for 3 days after treatment, but you can take them for just one or 2 days. I was also taking 2 pills (don't remember the mg), so when SE from steroids started to get to me, I just took one. Is the hand peeling from the taxol? Again, it can happen like that with xeloda, but I didn't know it would do that for taxol.
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my hands have started peeling a little since i started taxol. skin on my feet feel real tight too. when i did my manicure (on myself) yesterday, i noticed my thumbnails, and my big toenails are starting to turn black! they don't really hurt just look awful! i haven't been taking anything other than a multivitamin, and rubbing lots of lotion on my hands, any tips?
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I just came home a couple of hours ago from my final A/C. I know I'm probably close to the last one to cross that milestone, but I'm finally there!
Hoping that Taxol doesn't present with too many new SE surprises for me, I guess I'll find out in two weeks.
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Hi everyone:
Haven't posted for awhile... but I still read the posts regularly. I am going to have my second taxol treatment on Monday, Feb 14th and then will have two left!!! Taxol was so much easier than AC but I had bone pain on days 4-7 with lots of pain in my feet and knee and also in my one finger and ankle which I had previously broken. You can see the blood pulse in both my pointer fingers and the nails are slowly turning yellow and it looks like I am a die hard smoker using both hands. My two fingers and thumb feel like they got pinched in the doorway. My hands are a peeling mess from a reaction I had to one of the anti-nausea meds that started week 2 during AC. They are now starting to itch and the tips of the fingers now have little pinprick looking dots on them that are oozing water. Weird. I can now drink water again and food tastes better. I am not sleeping as well, though. I am trying to go to the gym everyday and walk as well.
The weather is starting to get warmer here so hopefully my hands will be well enough to get out and do some gardening next week.
Take care
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Good evening December gals...I have not posted for a while but read every day religiously and am so glad for the info and the reassurance that what is happening is "normal". Had my 2nd Taxol today and feel good tonight (probably the steroids kicking in) The first round made me more and more tired each day but it could be since they pulled me of steroids after treatments. I am also a bit more anemic than last week. My onc said she;s not worried enoungh to order a transfusion yet but retains the right to change her mind. Was pretty sick yesterday and day before and think I got behind on my meds thinking I would not need them since the nausea is supposed to be less of an issue so didnt take anything until around late aftrenoon when i felt horrible. Good news is that I worked everyday this time full time except today day of treatment when I worked a half day. It feel so good to be caught up and contributing to my team at work again.
I keep reading about the dry hands (which mine are starting to dry out) any soloutions other than finding a good lotion?
Good luck to all...my thoughts are with all of you everyday and I speak of you often to my medical staff who thinks this is an awesome avenue.
Leigh
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Just had my last A/C yesterday... on to Taxol in two weeks. Apprehensive of course, but hopefully the SEs will be tolerable. So far so good on this last A/C treatment... big family weekend planned, so I need to be up for it! Basketball game, and a music recital, with not one but two sets of extended family coming in from out of town to stay with us! Fortunately, it's family, and my family is not very high maintenance, so no one is expecting me to trot out any fancy hostessing thank goodness, I certainly wouldn't be up for that.
I finally went to our local Wellness House. So hard to walk through that door, but I'm so glad I did. I will be starting a yoga class on Monday, some one on one counseling, as well, as registering for a mindfulness class starting in March. All free, which is unbelievably generous.
Hope everyone is doing well today.
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YEAH LISAMOMOF FOUR!!! Yeah for being done with AC. I wish we had a wellness house close by. I could really use it. I will start looking for a gym after rads.
I don't know if this will help, but when I had T/C, one onc told me to use tea tree oil if nails were a problem with the taxotere, I put clear nail polish on toe/finger nails and every infustion I brought a zip lock of ice for my finger nails and toe nails. Onc nurses also said don't scratch itches just rub and use lotion as much as possible.
THird T/C was the worse for me, and I finally figured out one week after the chemo, the tears flow like a river and I can't stop them for a couple of days. gotta be the chemo, wbc being down the first week.
I hope I will be with some of you on the radiation thread, I will still stay here too and I will start rads end of Feb, begining of march. can't imagine not staying in touch with all of you.
Just saw the article on this page about parp not working for triple neg like they thought...great..just great...some news I prefer not to have.
Happy Valentines day weekend to all, hope you are able to do something special.
JoAnn
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lisamomoffour! your over the hump! hooray!!
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Re: Tea tree oil for nails.
I asked my onc re: tea tree oil and the reply was yes, please do, as it helps. I had crazy itchy hands for the first time today when my husband and I were out for coffee, and it was unbearable. This itch is a drive yourself crazy in record time kind of itch. I took an antihistamine and used some cortate cream but it's coming back again. First crazy SE that I could do without.
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Hi Everyone... kind of a boring Sunday here for me, but I don't feel that great anyways. Thursday the port was put in and Friday I had my treatment, which went really easy. No 20 minute or more search for veins! The port is itching me like crazy though-healing I suppose?
Not trying to be an alarmist or anything, but yesterday I saw an old friend who went through chemo too. She showed me the skin on her leg and it looked awful. She is dark skinned, and her leg is all discolored and scarred. She said she showed it to the nurse and the nurse said oh well use this medicine-but she demanded to see the doctor to have her look at her leg- she ended up in the hospital for a week! Just thinking about any of us if we get any really bad skin problems!
Lisamomof4-I still have yet to go to the wellness center. I plan on getting there though! I just had such a hard time at the end of the AC I have been recupping.
Not sure about the Taxotere yet. Just a little nauseas and achy. No fingernail pain this week either. Just worried that I am starting to gain weight! It doesn't help that I ate 1 and a half of those monster muffins from the grocery store! It tasted so good!
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the steroids from the taxol make me eat like crazy for 2 days too!!!
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Hd. Not good!!! I start taxol on Thurs!! I am terrified of the steriods!!
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karebear76, i will give you a little rundown on how i have been handling the steroid rollercoaster:
tues: taxol, then i eat everything in sight, feel ok, actually sleep ok
wed: still on the eating train, still feeling ok, sleeping ok (ativan ativan ATIVAN!)
thurs: the feeding frenzy stops, by thurs night, i can feel myself start "coming down' from the steroids
fri: totally completely useless, can barely do anything, just no energy whatsoever
sat: start feeling a little better, but an emotional wreck
sun-mon: feeling better, not sleeping, still kinda emotional, but the eating thing is back to normal
TUES:START ALL OVER AGAIN!!
all in all, though, i like taxol better, i am on 8 weekly. my onc divided my "dose dense" schedule into weekly doses. I have had no nausea, thank god, and i haven't had to take any meds beside the painkiller once in a while (i have ovarian suppression shots, they give me killer headaches). my nail beds have started turning black, so i keep polish on them constantly, which is kinda fun, change it up weekly.
i think i am getting a damn yeast infection, down below, though, gotta talk to doc about that. i think it's cause i have been trying to keep up my normal sex life (uh, not really working the way i planned!), and i have been having a beer or two the nights i feel well.
that's the other good thing, when i feel well, beer actually tastes good! and i never liked it before, and it relaxes me a little which is nice. i feel more "normal-ish" on taxol, like i can go out and socialize more.
i have started having tinglies in my hands and feet, but they go away as quick as they come on, for now, i still have 6 more treatments to go, so we will see!!!
hope this helps, remember, everyone is different and everyone reacts differently!!
(((HUGS))) HAPPY VALENTINE'S DAY!-ANGEL
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Hi All- I had my third weekly Taxol yesterday morning. I slept a dark deep black sleep all afternoon but woke up feeling tired and my husband said I was really pale. My blood work came back that I was anemic so I've been researching foods that will boost your iron and this afternoon I'll go out and buy some greens and beans. (I am a vegetarian). I'd rather stick a pen in my then get a transfusion.
With treatments on Monday, Sat. and Sun. are my best days. Last weekend my husband and I went on a cabin-fever drive out on the North Fork of Long Island to Greenport--an old fishing village on the Peconic Bay which has a great old downtown and not too commercialized with tourist shops. Walk around, stopped for some coffee and scones, had a great time.
Then next day, we walked to Setauket Harbor in the afternoon which is a 3.5 mile walk. And I wasn't too tired afterwards which is surprising considering my Hemogloblin numbers.
I am so happy not to have to take Ativan round the clock as I did on A and C. Because I had to take if for 10 days afterward, I was a constant zombie. Now I just take it when I need it.
Lisamomoffour--Hoorah for having your last A/C. I know you are probably still feeling it. When I celebrated mine I forgot that I had another 10 days of side effects. Still it's a great accomplishment! Will you be on weekly or bi-weekly treatments?
Smooth Sailing to everyone.
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Hdangel- your post makes me feel so normal today! You pretty much described how I am feeling on the taxotere. It is so strange how 3-4 days out you can feel so exhausted!
The last few days I have felt very anxious. My port feels itchy and achy-will this last long? Some of the anxiety stems from people wondering when I will go back to work. I am off until I am through with chemo. I am unsure how it will work if I have daily radiation for 6 wks.
Otherwise things are good. I hope everyone else is doing well!
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Hdangel: Thanks for that post! I have taxol every other week. I haven't even started it and I am exhausted all the time. I went to the store and out to eat and I was so sick and drained for a whole day. It seems that I am more tired now than I ever was and I haven't even had the taxol yet!!!
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Exhaustion seems to be ever-present for me now too. With AC I'd have one bad week (completely incapacitated) and then one week where I actually felt mostly normal. But now I go to be at 8 or 9, sleep until 7, up for a few hours, nap for a few hours, up for a few hours, nap for a few hours, do dinner and get kids in bed, then off to to bed for me. It's so hard to get anything accomplished since I always feel like taking a nap. On days I don't nap my eye just twitches with that annoying exhaustion twitch.
I had my 3rd of 12 taxol treatments today. My counts were low but just high enough to get the chemo. The nurse also said I was starting to get anemic. I asked her if that meant I should get some iron supplements and she said that wouldn't really help much - the problem is our bodies just aren't producing the red blood cells. (be careful -- too much iron can make you constipated). I don't think I can fathom another 2.5 months of being this tired all of the time. Anyone have any solutions?
Maybe I'll start taking sub-lingual B-12 tomorrow and see how that works. In mega doses B-12 is supposed to give you tons of energy. I just remembered that. I'll do an experiment with it for a few days and let you all know what happens.
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