Any May 2009 Chemo Starters?

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  • Hemen
    Hemen Member Posts: 33
    edited July 2009

    Dear May Marvels

    I go in for my last T/C this morning!  I cannot believe itSealed.  I've been up all night due to aniexty and steroids and now hot flashes! I feel the hot flashes on my bald head like crazy:)  The sun is actually out for my final infusion-- a major miracle:)

    I'm hoping they don't make me get the darn neupogen shots this time--I've had 5 shots following each infusion and the bone pain has been REALLY bad.I think I am getting some neuropathy in my hands--they tingle and they actually fell asleep on the steering wheel when I was driving the other day which was a little scary...

    Glad to see that everyone is surviving this chemo nightmare!  You guys are so inspiring-- I get such comfort from all of your posts--

    Big hugs to everyone

    Helen

  • jaelsne
    jaelsne Member Posts: 82
    edited July 2009

    Debbie,

      Sorry that you had such difficult SE's.  The Neulasta hasn't given me bone pain, just a stiff neck.  I've tolerated the t/c that I've been on pretty well.

      The other night my husband told me that I look better now than I did before my diagnosis.  I said "You're telling that to a bald, browless woman with one boob.  I looked better before?"  Pretty funny.  

      The truth is that I'm probably happier on my "good days" than I was pre-cancer.  I appreciate the ability to get out and do ordinary things--even grocery shopping is a treat.  Maybe that's what he picked up on.

      Hope everyone has a good week,

    Jo Anne 

  • glostagirl
    glostagirl Member Posts: 388
    edited July 2009

    Another MIA checking in.  I have been reading, but very little posting.  

    I got a bad infection after my first infusion.  2nd infusion was delayed several weeks. I'm back on track and go for the 3rd inf. this Wednesday (22nd).  

    I have open sores from the infection, they are healing, although it will be a slow process while still on chemo.

    I want to report good results from using generic Claritin (Loratadine) and Aleve for bone pain from Neulasta.  I seem to get the pain where I already have age related degeneration, which for me is lower back and hips.  

    Thrush has been a problem each time for about a week, also a sore throat with accompanying sinus headache that doesn't respond to pain relievers, any thoughts? 

  • jabl1252
    jabl1252 Member Posts: 40
    edited July 2009

    Hi May Marvels, I have been missing in action also. Had number 4 last Monday and it was the worst so far. I was extremely tired and had to work more hours then I usually do on chemo week.Still pretty tired but hanging in there. Think I had chemo brain last week cause I was not thinking very straight.Hope everyone is doing ok .Has any of you started rads yet? I have two more chemo treatments ,ending the last week of August.My son will be coming home sometime in Aug.for three weeks.He is a Military Police Officer and will be going overseas when he goes back.Its been pretty stressful knowing that he will be going over there,but I am so proud of him . Hope you all are getting through se and feeling well. Take care Julie

  • gmp300
    gmp300 Member Posts: 351
    edited July 2009

    Hello May Marvels present and all who are MIA!

    I too have been gone camping all week but it is close to the house and I do pop in and keep up on everyone.  Iam still camping and probably will keep the camper there 1 more week.  Why not!  My dd is having fun and Iam trying to take it easy.  Summer is short might as well try to enjoy what you can of it. 

    I find that I get fatigued alot easier now.  Not that Iam not doing anything, Iam just tired alot.  That's ok if that's the worst of it.  I have one more tx to go on the 29th.  I hope that doesn't get a whole lot worse than this one. I can't wait to be done.  Iam almost done with the expansion of my TE's.  That's a whole other story.  Ps goes so slow,  I probably have 4 more fills till he's done filling (maybe less?)

    Well I hope everyone is doing fine.  You's are in my thought's and prayers-always.  For anyone who is feeling bad- here's a (((HUG))).  And Debbie 6122-one for you too (even though your feeling better!  YEAH!!  Everyone hang in there  Geri

  • debbie6122
    debbie6122 Member Posts: 5,161
    edited July 2009

    Hemen- So glad to hear from you and all the MIA's  Horray on your last infusion i will be praying for you to have minimal SE today. Hope you dont have to have the shots maybe your counts will be in the normal range and you wont need them, i too have the terrible bone pain with the shots and the only thing that helped was pain pill, hugs to you!!

    Jaeslne- LOL it cracked me up what DH said sounds similar to what mine said to,insert foot in mouth lol!!

    Glostagirl- Sorry you been having a bad time with the infection, im surprized they did chemo with open sores, when i had my mx i had an open wound in my chest that didnt close for a couple months they had me on high antibiotics and wouldnt do the chemo till it closed, glad you are one of the ones that DIDNT have bone pain! The only thing i can tell you about thrush is i have asthma and use a inhaler i get thrush the dr. told me to rinse with warm salt water, a few times a day, but with mouth sores from the chemo i use prevention it helps alot, there are all kinds of washes out there but i like this one

    Julie- You should be very prould of your son, i will say some prayers for him to be safe(hugss)) I heard that the 4th one is a lot harder, especially for you and all the ladies who are working while going thru tx, hope you are able to rest and feel better soon

    Hey there gmp-hope your not working your a $$ off while camping!  Have fun

    debbie

  • deb6563
    deb6563 Member Posts: 179
    edited July 2009

    Good evening May Marvels.  Welcome back to all you MIA's.  We were beginning to worry about you. 

    I am on day 4 after my first taxol and still feel pretty good.  I worked 9 hours today and it was HARD.  Told hubby that I can't do that again.  Even though I thought I was able, my body just didn't co-operate. I came home and collapsed.  Thank goodness for church family that is bringing us supper at least once a week.  There is no way I could have cooked tonight.

    Take care and don't overdo it.

  • TexasRose
    TexasRose Member Posts: 740
    edited July 2009
    • Hey May Marvels! I am home from my weekend away. Missing the beachy sunsets and the sand. I have my first of 12 Taxols tomorrow. It almost got postponed as my hemoglobin is low. Onc said he would go ahead with treatment though. It's only slightly low. They think my iron is probably low. I am going in early tomorrow for more lab work to see if I need an iron supplement. I'm nervous about the Taxol. Everyone keeps saying it is easier. I hope so. I had my AC routine down though. I'm nervous not knowing what to expect from the Taxol. Sounds like the first one will be a long day. Especially since I have to go early for more labs. They took four vials today. You would think they could use some of that!

    Everybody might remember that I was having some issues with painful bowel movements. Onc prescribed something called proctofoam and it was a godsend. Really has helped with the pain. I know a few others had the same problem so thought I would pass that on.

    Thinking of all of you. Nice to see some of the missing and catch up with you. Hope everybody is well.

    Hugs, Mary

  • debbie6122
    debbie6122 Member Posts: 5,161
    edited July 2009

    Deb- You are somthing else, you just keep going and going, i dont know how you do it, and then work a 9 hour day, makes me tired just reading it lol!  Hope you get plenty of rest

    Mary- Good luck tomorrow with your first taxol, hope it is easier for you, im sending positive thoughts your way

    hope  evey one is having minimal Se and feeling good

    sweet dreams debbie

  • lassie11
    lassie11 Member Posts: 1,500
    edited July 2009
    Mary - I think Taxol and Taxotere are somewhat different drugs -  yet have similarities. I have found after one run of Taxotere (3 doses will be 21 days apart) that the side effects really are much less than the previous drugs (FEC in my case). You may be pleased to know that it brought diareah instead of constipation! No nausea and a whole lot of tired. Also some joint pain but only for a couple of days and, for me, solved with a Tylenol.
  • jaelsne
    jaelsne Member Posts: 82
    edited July 2009

    Hi everyone,

      Just checking in to say hello.  I'm enjoying my last week before #3 t/c out of six.  My infusion is scheduled for next Tuesday.

    Mary:  My hemoglobin has been low each time I get an infusion--sometimes very significantly low.  I've avoided a transfusion thus far--the iron pills have saved me.  I sure get tired when my count is low!

    Jo Anne 

       

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Marvels

    Just dropping in to say Hi and have a wonderful Wednesday. I am okay, had stomach pains yesterday and getting mouth sores. I thought I had got off lightly. Still working but have cut hours back as I get too tired. Doing about 5 hours a day at the office. Hoping to go to golf today if it is fine weahter. We had rain all weekend and it has been very windy down here.

    Pink Hugs to all Susie

  • benisse
    benisse Member Posts: 81
    edited July 2009

    Mary - thinking of you and hoping all went well.  Hello to all.  I'm enjoying a good week.

  • TexasRose
    TexasRose Member Posts: 740
    edited July 2009

    Hi all,

    First Taxol went pretty well. I was at the hospital forever though. They asked me to come in early so they could run more lab work and check my iron levels. Onc added an iron supplement even though my lab work came back that my iron is fine. I had to wait on lab results, wait on appt with onc, wait on orders to come through and wait on drugs to come. Waiting is not something I am good with! And this was my first chemo I did without Xanax. For all of my AC, I took a Xanax the day of chemo to keep my blood pressure down. Today, we decided I better not take one because of the Benadryl. I would be a zombie!!

    Anyway, I feel pretty good. Tired, but I feel like the steroids and the Benadryl are fighting it out. I'm tired, but I can't sleep. LOL  Onc did warn me there might be bone pain and asked if I still had any Vicodin left from my surgery. I do, but I will only use it if it's really, really bad or at night if I can't sleep. Glad to have one down, 11 more to go!! Ugh...that sounds like forever but it will go fast.

    Forgot to mention I think that I went to the boob store yesterday. A very interesting experience. I am a 34 to 36 band. A or B cup, mostly B. The fitter started out with a 40 bra with a cup that Dolly Parton couldn't have filled. My mom and I just busted out laughing. We went down from there but never really found a bra that fit well. She tried one on that was a pretty good fit but was an A cup and still a little large. She is going to order one in a AA and we think that will fit well. Should take two weeks to come in and she doesn't want to fit the foob until we fit the bra, so I am still the unaboober. I have no idea why the fit is so different from my old regular bras. She said it had something to do with the fact that I have a lot of muscle there and also because my boob hangs low. Well. of course it does. I'm 47 freakin' years old!!!   

    Hope everybody is doing well! Love and hugs!

    Mary

  • TexasRose
    TexasRose Member Posts: 740
    edited July 2009

    Benisse- Glad you are doing well!

  • debbie6122
    debbie6122 Member Posts: 5,161
    edited July 2009

    Mary- LOLOLOL!! you crack me up, thnaks i needed that!!  sorry you had to wait so dang long at he hospital, some places are different i guess, when i go in for lab work they run it thru right there in front of me and give me a copy within minutes, who knows! anyway, hang in there i hope the nest 11 go by fast

    hugs to all

  • luvtheocean
    luvtheocean Member Posts: 87
    edited July 2009

    Mary-  Sorry that it was such a long day for you today...hopefully the next 11 will be easier/quicker.  I'm not quite sure about the whole bra thing, since I only had a lumpectomy.  I do know that I can't find a bra that fits because I have 2/3 of a boob on the right and a full one on the left, so a D and a DD..........seriously they don't make bras like that.  Thinking it is a great business to start!  Has anyone found a place to buy a bra with 2 different cup sizes?

    So if Mary is a unaboober what am i lopsy?

    I hope everyone has a great night!  I am still having a terrible time finding energy and I am 14 days out from my final chemo....starting to worry about my counts but I don't see the onc until next week!

    Good night all and good night of sleep without s/e's is my prayer and wish for you all!

    Becky

  • luv4my5girls
    luv4my5girls Member Posts: 34
    edited July 2009

    Laughingmy theme song

    Hi everyone,

    I just wanted to share this with all of you...I heard it a few days after I was diagnosed and it has kept me positive! Hope it works for you!

                                            I JUST WANT TO CELEBRATE- BY RARE EARTH

    I just want to celebrate another day of livin' 

    I just want to celebrate another day of life

    I put my faith in the people

    But the people let me down

    So I turned the other way

    And I carry on, anyhow

    That's why I'm telling you

    I just want to celebrate, yeah, yeah

    Another day of living, yeah

    I just want to celebrate another day of life

    Had my head on the dollar bill

    But the dollar bill flew away

    But the sun is shining down on me

    And it's here to stay

    That's why I'm telling you

    I just want to celebrate, yeah, yeah

    Another day of living, yeah

    I just want to celebrate another day of livin'

    I just want to celebrate another day of life

    Don't let it all get you down, no, no

    Don't let it turn you around and around and around and around and around

    Well, I can't be bothered with sorrow

    And I can't be bothered with hate, no, no

    I'm using up the time but feeling fine, every day

    That's why I'm telling you I just want to celebrate

    Oh, yeah

    I just want to celebrate another day

    Oh, I just want to celebrate another day of livin'

    I just want to celebrate another day of life

    Don't let it all get you down, no, no

    Don't let it turn you around and around, etc.

    Round, round, round, etc.

    Don't go round

    I just want to celebrate

    I just want to celebrate

    Well, I just want to celebrate

    Said I just want to celebrate (celebrate)

    I just want to celebrate (I want to celebrate)

    I just want to celebrate (I got to celebrate)

    I just want to celebrate!

    I know it's an old song but it seems to make me feel good when I hear it and we all have to CELEBRATE OUR LIFE!

    My love and prayers to all of you...Good night! Wink

    VikiInnocent

  • Gekko
    Gekko Member Posts: 11
    edited July 2009

    luv4my5girls

    I was just checking in before I go for my 3rd Taxol and read your post.  What a great way to start the day.  Thanks for sharing it with us.

    Mary

    Sorry to hear about your long day.  At least you know the next Taxol won't take as long.

     The taxol han't been too bad for me except it has made my lymphedema  worse.  I think it is the steroids.  I was just getting it under control and now nothing seems to be helping it.

    Well got to go.  Hope everyone has a bright and beautiful day with minimal se's.

  • Hemen
    Hemen Member Posts: 33
    edited July 2009

    Hi ladies

    I made it through my last infusion!  Onc gave me 25% less taxotere as I do have grade one neuropathy-- tingling and pins and needles in hands.  It was either cut back on dose or postpone chemo 2 weeks... as I have to go back to work week of Aug 17 it was a no brainer to take 25% less.  Have to take multi vit and B6 for neuropthy and report back if it gets worse... bummer. Have to do 4 neupogen shots (at least it's not 5) -- it was kind of funny as my DH was trying so hard to negociate no neupogen for me:)  Too sweet, but onc won out!  Actually feeling worse after this treatment-- I think the multivitamin is making me nauseaous and I've had no nausea until now--blah. Fatigue is awful as I cannot sleep at all between hotflashes and bone pain-- might be time to ask for sleeping pills.  Now waiting for rads schedule... fun fun!

    Jo Anne: I know what you mean about appreciating the good days now-- this process really gives  us a unique perspective on life and appreciating it.  Take those iron pills!!!  I hope they work well for you and keep you on schedule.

    Julie-- hand in there and enjoy every minute of your son's visit.  I pay he will be safe on his tour.

    Geri-- fatigue is definitely so much worse now I agree-- I am wondering if the rads is just going to do me in--hope not:)

    debbie6122: Time to endure bone pain again-- but you are right--just keep ahead of the pain with the aleve /advil claritin and I sometimes do vicadin at night if it's really bad...  I cannot wait for the day when i don't walk around like an 80 year old woman....

    Deb6563 and Mary: Hang in there through the taxol-- you are amazing.  I hope it is easier than the A/C which sounds so nasty. Mary-- I will say a prayer that your iron counts are good....  I imagine iron pills must give you some kind of nausea, no?

    Mary and Becky-- AKA unaboober and lopsy-- you are killing me!!!!  I too only had a lumpectomy so am not having to deal with the foob and reconstruction. 

    Viki-- abeautiful song for a bunch of beautiful women.

    Sorry if I missed anyone--( I am such a bad typer that writing these posts is a challenge as it takes forever -- and I've lost a couple of posts as a result!).  I wish you all a beautiful day and I send hugs to everyone!

    XOXOXO

    helen

  • deb6563
    deb6563 Member Posts: 179
    edited July 2009

    Good evening ladies,

    Sorry I'm not addresses each one of you but I know all of you understand.  Chemo brain and fatique make it hard to remember from post to post.  I am reading everything and laugh and cry with each of you.

    Today at work we somehow got to talking about Activia and constipation.  I told everyone just be glad they are not on chemo because nothing short of a pipe bomb works on this kind of constipation.

    Hope all of you have a good night.

    {{{HUGS}}}

  • Janet22664
    Janet22664 Member Posts: 155
    edited July 2009

    Deb, you are just too funny!  But I know exactly what you mean about the constipation! 

    Has anyone heard that with Taxol you feel your worst right before your next treatment (unlike the A/C where you felt your worst right after treatment).  Just wondering...read it in a book tonight.  I just had one Taxol treatment last Monday, so I was wondering when the "good days" would be. 

    Janet

  • luvtheocean
    luvtheocean Member Posts: 87
    edited July 2009

    Well Marvels, I go for my appointment with the Rad-Onc tomorrow to do my prep session.  I'm not really nervous, but I am not really looking forward to it either.  Still feeling kind of tired but I think it is the mix of drugs I am taking for depression, anxiety, and sleeplessness.  I'm kinda in the down mode right now.  I don't get it though.  I am done with Chemo, shouldn't I be on top of the world!?  Anywho, I hope all are doing well tonight and have big hugs for each of you and have been thinking about all of us today and our laughter, struggle, tears, prayers, and hugs we offer each other on a daily basis...........we really are a strong group of women!!

  • LRM216
    LRM216 Member Posts: 2,115
    edited July 2009

    This is just my situation, everyone seems to react differently.  I had my first Taxol on a Thursday, 2 weeks ago and began to feel my side effects kick in on Saturday.  By Saturday night I had tremendous bone and body aches which continued into Sunday.  Sunday I began the neuropathy of bottoms of feet and all my fingertips.  I normally would go to work on Monday after the AC's, but I still could not muster the strength to go in until Tuesday.  I began to feel better daily; however, I have not lost any of the neuropathy.  About 6 days before my next Taxol (which is tomorrow) I began to feel just fine other than the neuropathy.  Needless to say, I am hoping tomorrows (the 2nd taxol) chemo will not be any worse than the last one.  So far, if you could omit the Neulasta shot, I would take the AC over the Taxol any day.  Again, we are all different, why it's effecting me the way it did, onc can't say, but she has seen that before, so at least I know I'm not alone.  I am sending wishes for you that your Taxol goes "like a walk in the park" which I was told mine would!

    Linda 

  • deb6563
    deb6563 Member Posts: 179
    edited July 2009

    Linda - sorry you are having so many SE's from the taxol. 

    Janet - I go for my 2nd taxol tomorrow and I have had no SE's so far other than fatique.

    I think it is like Linda said, we all react differently and it depends on whether we go weekly or every day for 4 days and then skip 2-3 weeks.  I go weekly and I have been fine.  I am working 9 hours a day this week and I could never have done that after A/C.  I always had to take a week off after A/C.  I come home every day extremely tired and usually take an hour nap, I had a little rib pain one day and a little shoulder pain one day, but Aleve helped both.  I think taxol is a piece of cake compared to A/C.

    I hope everyone has a blessed day.  Just keep in mind, no matter what we are going through, it is saving our lives.  All the SE's will go away and it is better than the alternative if we don't go through chemo.

    {{{hugs}}}

  • TexasRose
    TexasRose Member Posts: 740
    edited July 2009

    Morning all.

    Just a quick check-in. I'm on day 3 of Taxol #1 and I feel fine. A little tired, but that is it. So far, this has been so much easier for me than AC was. Like Deb, I go weekly also. No bone pain yet. A slight little neuropathy but that started with AC for me.

    I hope everybody is doing fine. You are all always in my thoughts and prayers.

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Marvels

    It is 3 am and I am wide awake, my dogs woke me up barking at the wind!! Yeah tomorrow is  Friday and the weekend is here. Am going to be busy, golf, lunch & dinner invitations and new boyfriend meeting friends and family. Next Thursday is last chemo, I can't wait and am so excited that it is nearly here. Already planning my ITS ALL OVER party for Oct 10th.

    Thinking of all of you.

    Big pink hugs to you all

    Susie

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Whoops just realised today is Friday, is that dumb blonde or chemo brain? Haha

  • LRM216
    LRM216 Member Posts: 2,115
    edited July 2009

    Hi to all -

    Thanks to all that wished me well with Taxol #2 - It didn't happen!  They refused to give it to me today due to the neuropathy in all of my fingertips, since the first round.  Feet are better, just a little numbness in toes.  They plan to switch me to Taxotere from now on.  Even though it too can cause neuropathy (so does Abraxane), they said it wasn't as bad re neuropathy as Taxol.  We will see, I guess.  All I know is I have numb fingertips, can't button things and have now just added another week to my treatment. 

     Hope it's going well for all of you fine ladies.

    Linda 

  • LoriR
    LoriR Member Posts: 131
    edited July 2009

    Hey to all May Marvels - haven't checked-in in the last couple of days.  Yesterday was my last chemo (YEAH!)  It was a close call tho - almost didn't happen as my WBC count was below the cut off of what they will usually allow but onc gave the ok since it was close.  I would have been so dissappointed if I wasn't able to get my last one.  I feel good now but I am worried that this one will cause a crash since I was low to begin with.  I have been getting Neulasta with every tx so I don't really have that to rely on if I would "crash" .  I don't know - do they give another one if need be?  Also got set up to start rads on Aug. 17th so I am anxious to see what that is all about!  my PFC party is scheduled for Aug 15th I am calling it Boobapalooza!

    Hope you are all doing well - take care and hugs to all!

    Lori

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