Any May 2009 Chemo Starters?

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  • deb6563
    deb6563 Member Posts: 179
    edited July 2009
    I had my final A/C two weeks ago today and FINALLY  no constipation.  Thinks are looking up or should I say coming out! Wink Now just to get through Taxol.
  • Gekko
    Gekko Member Posts: 11
    edited July 2009

    Titch So sorry to hear about your scare with your son.  One of my sons is just 18 and every time he takes the car I get worried something might happen.  Thankfully in your son's case he wasn't hurt.

    I go for #2 of 12 Taxols tomorrow and I'm dreading it.  The first one wasn't too bad but the second one is where if you are going to have an allergic reaction to the stuff it happens this time. Also, I have been using cold packs on my hands and feet to help ward off neuropathy and ever since the 2nd AC my hands and feet have been very sensitive to the cold so it is hard to keep the packs on.  I am petrified of getting neuropathy especially in my hands because I depend on them for some very fine motor skills to be able to make the jewelry, quilts and papercrafts I love to make.  Take my ability to make things away and I would be lost.  I already have problems because of osteoarthritis so I don't need any additional problems.  Unfortunately the neuropathy SEs sometime don't show up until after treatment is finished.  So I won't know for a few months whether or not the cold packs did the trick.  Oh well.

    It' s fun to hear about everyones' getaways.  I wish I could get away from our house for a few days.  The only thing I get to look forward to this week is a fitting for a Lymphedema sleeve and bra on friday.  Hopefully they will help me keep it under control.  I need to get some handle on it now because rads can make it worse!

    Hope all you May Marvels have minimal SEs this week. Take care.

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

    Every one is probably in bed by now, but thougth i would say hello,

    GERi- Hope you are having a great time camping- i forgot you told me about DA Bomb! lol! i forgot the part about microwaving it, it still worked, wonder if it would of been sooner had i done that will try it next time and let ya know!

    Vicki, lol funny story on the foobies!

    Echo- Sounds like a fun trip, being from grants pass, oregon i have been to crater lake several times it is so gorgeous, im jelouse(sp?) Have fun!!

    Becky- i had to laugh when you mentioned that you were laying on your back with the lap top, we are twinsies!! i do the same thing lol!

    Deb- I hear ya on the consiptation thing it sucks, hope your doing better

    Gecko- Good luck with your taxol tomorrow, i will be thinking about you and hope your SE are sweet and minimal

    I was hoping i would remember every one on the previous page, but i totally blanked out on some of it and dont want to go back for fear of losing this post, but thinking of you all

    debbie

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Marvels

    Well another good day at work became another shiite day again . Oh not to work, I wish. Tania I hope you are still not doing 10 hour days and to anyone else working I hope are  you having better days than  me.!!! Crikey Swine flu has arrived in  Waihi , New  Zealand, popn 4000. and we have 4 cases a day. I am going to stay home for the next few days, stuff work , getting bolshy due to lack of sleep and ongoing problems with work,. Have decided it is now doing my head in!!!!so I quit for this week.

    Pink Hugs SusieKiss

  • lassie11
    lassie11 Member Posts: 1,500
    edited July 2009
    Way to go zuzeee !  You sure don't need work with the threat of swine flu thrown in at this point. Best to look after yourself. And I am guessing it is not a good thing to go "bolshy"?
  • debbie6122
    debbie6122 Member Posts: 5,161
    edited July 2009

    Susie- I give you kudos just for the fact that you even have been working going thru all of this,i just want to lay around and be lazy, maybe if i worked i wouldnt feel as bad who knows, just stay in bed and rest, rest,rest, and be careful around crowds too, with the swine flu lurking there, hope you get some sleepy time in today

    Well im off to get another shot in tummy, counts were low yesterday have to have shot all this week, i feel sick with a sore throat too so hope shots keep my numbers up, seems like its taking me longer to bounce back from # 3 infusion, jsut feel crappy all over,and did i mention I HATE NEEDLES!! sorry didnt mean to yell, but if someone is trying to get me to overcome my fear of them, its not working !! hugs to all

    debbie

  • luv4my5girls
    luv4my5girls Member Posts: 34
    edited July 2009

    Glad you all liked my foobie story! 

    LaughingI am going for my last chemo tomorrow and I am kind of nervous, happy, excited, all kinds of emotions are going on inside me...Oh, wait that is just my mood swings! LOL.  I finally got my"monthly visitor" it's much lighter, but the nausea is still there...I don't understand.  I never stopped my cycles throughout all this, but this one did come later than usual.

    I will ask my onc tomorrow.  

    my thoughts and prayers are with all of you!

    Innocentmay the angels wrap their wings around all of us and help us fly through this with faith, love, strength and courage!  

    happy hump day!

    Viki 

  • AbuelaBoricua
    AbuelaBoricua Member Posts: 62
    edited July 2009

    Viki good luck tomorrow! BTW I loved your story!

    I took a day trip with my sisters to Antietam National Park where the bloodiest battle (over 23,000 soldiers died) during the civil war happened. The scenery is beautiful.  I had a great time but I am tired.

    On Monday I have my 3rd treatment and I am not looking forward to the SE.

    Well, I hope everyone has a great night and you get lots of rest. To everyone else have a great day. To those who finish their treatments, CONGRATULATIONS!

    Lots of hugs, Innocent Diana.

  • LoriR
    LoriR Member Posts: 131
    edited July 2009

    Hey everyone- Hope you are all doing well - just a question - I was asked to participte in the clinical Trial for Zometa (I think the word is bisphosphates) and I think it is the SWOG study.  Has anyone else been asked to participate - there actually is a thread on here for it.  Also when I got the paperwork in the mail and I was reading thru it - it said I would or my insurance would have to pay for everything.  I can't believe that??? 

    take care - I get my last chemo on Wednesday and can't wait!

    Lori

  • Sukiann
    Sukiann Member Posts: 310
    edited July 2009

    Hi ladies,

    I haven't posted for awhile.  I've been enjoying feeling better after my last chemo 2 1/2 weeks ago.  You will feel great when you are finally done.  I can't wait for you all to get that point.  Now I'm onto rads.  I have a planning session at the end of the month then I will start the second week in August.  I thought I would be done by the end of August but things take time and now I'll be going into September.  This has been one very long year, hasn't it??? 

    Lori - I am meeting with the research nurse on the 31st about the biphosphonates study.  I don't konw if I want to participate yet.  I guess once I get the info I'll know for sure.

    I had my first lupron shot last week.  I am or was premenapausal but I can't take tamox because of a risk of blood clots (family history) so it is lupron and arimidex for me.  I haven't received the arimidex yet (mail order).  I'm interested to see how my body will react.  On the lupron I have some slight swelling of my ankles and knees.  Hurts to bend them.  Other than that, it's the darn hot flashes!  Chemo had those pretty much going all day for me now the lupron is going to continue them.  I wonder how hot I'm going to feel when my hair grows back!  I'm one hot mama! 

    Hope all of you are having minimal side effects today.  For those of you who have finished chemo, Congrats.  For those of you who are on your almost there, hang in there you will be done soon and will be in for better days.

    Love to all.

    sukiann

  • deb6563
    deb6563 Member Posts: 179
    edited July 2009

    Good Morning May Marvels.  I am headed out this morning for my first Taxol treatment. Hoping the SE's are not bad.

    Lori - I can't believe they are asking you to pay for a study.  I am on the Avastin trial and the company doing the research pays for it.  My insurance pays for the A/C, taxol, bloodwork, neulasta shot, and all test.  But not the Avastin.  I have never heard of having to pay for a study drug.

    Sukiann - Isn't it great that we feel good after A/C?  I finished almost 3 weeks ago and I feel great.  Just hope Taxol doesn't get me down.

    Hang in there ladies.  Some of you are going for rads now, some of us have 12 more weeks of chemo then rads, but just think.  We will all be done by Christmas.  Yes, it has been a long year and will get longer still.  But we will make it.

    {{{HUGS}}}

  • luvtheocean
    luvtheocean Member Posts: 87
    edited July 2009

    Good Morning Ladies..........I am 10 days out after last A/C.  I still feel tired??  I took like a 3 hour nap yesterday.  How much longer till I feel good??????  I am so ready!  I see the Rad-Onc next Thursday and have my test run rad.  I think I am going to be right there with you sukiann, I think she said I would start 2nd wk in Aug also.  Which is actually fine with me, I am looking forward to feeling better and would love a week where I feel good before I start the boob burn!  After this is done in Sept, the new hubby and I are going back to FL to St Pete Beach (our fav) to FINALLY have our honeymoon.  For those of you who don't know, or chemo brained it out Tongue out I got married on 4/4, saw a surgeon on 4/6 and had lump & sn on 4/8!  So we are soooooo due for some normal alone time!  I booked the flight yesterday to give me something to look forward to!  Hopefully the S/E's from the rads and then tamoxifin won't be too bad.  I went over to one of the radiation forums and read a bit, looks like the S/E's range from next to nothing to blisters, etc.  IM STAYING WITH MY MARVELS through the rest of this.  I see no reason to try and get to know a whole new group of ladies when most of us have been here since our 'day 1' and I feel like we know each other so well!

    That is probably it for me today, maybe for the weekend......I always read but don't always post.  Sorry girls, it has just been a draining last 1.5 wk!

    Hugs to all........

    Becky

  • gmp300
    gmp300 Member Posts: 351
    edited July 2009

    Hello May Marvels-Just wanted to say hello. 

     I just came home for a few hours to tend to the animals and house from the campground.  It is so relaxing there right on Lake Huron.  Trouble yesterday was that I was so fatigued I could hardly move (first time I felt that)  but it was ok because I could see the campfire fom my camper!  It is still more enjoyable than being home.  I hope I feel better today, if not I'll just sit all day!!

    Hope everyone has a nice weekend.  Glad some of you's are done with chemo.  And the other's we are almost there too!!  Take Care Everyone--Geri

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Marvels

    A shite week at work but a great night outlast night dancing to Abba . I feel as if I am back in the real world again. Great to read that some of you are out of chemo, my last is 30th July and then 1 month off and then rads. I am also staying with Marvels for rads. We are a great group of strong positive gals. Saturday morning here and it raining so no golf for me today.

    Have a wonderful weekend all.

    Pink hugs Susie

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

    Sukiann- So glad to hear that you are feeling better i had wondered since your last chemo how you were, hope the rads are easy on you and the time you have with it goes by really fast

    deb6563- Your right we will get thru this because we are fighters and never give up!! hang in there sweetie

    Geri- Hope your having a relaxing time at hte camp grounds sorry to hear you arent feelong good, get plenty of rest and try not to over do it

    lovetheocean- I hope you wake up tomorrwo morning feeling like a whole new person, and have your energy back, Im staying with the May Marvels too, we are a bunch of great gals if i say so myselfl LOL

    Diania- good luck monday with tx hope you sail right thru it!!!

    sVickii- glad you got your montly visitor lol! How did your chemo go? Hope you are doing good

    Susie- Dancing the night away, at abba too, you go girl!!

    I myself have been feeling bad, had to go get shots 3 days in arow this week and 3rd shot put me in so much pain since yesterday, have been taking pain pills every 4 hours to stay on top of it, hate the feeling on pain meds but i will do anything to keep this bone pain at bay, at times it is excruciating- ARGGGG!  On the way home from onc yesterday i pulled a Long blonde hair from my hat, dont know where it came from, but i pulled it out and said Hello Hair its been a long time since i seen you, i missed you, DH laughed at me and gave me the oh shes losing look LOL!! I think i kept this one long strand in my hand for at least an hour, then i finally rolled down the window and let it go,,, sooo sadUndecided

    Every one have a great weekend

    debboe

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Gals

    Have to tell you the rugby is on now New Zealand versus Australia, The world down here has stopped, This is like Superovl but cannot ring anyone now. Bloody ozzies winning  13 - 10.

  • AbuelaBoricua
    AbuelaBoricua Member Posts: 62
    edited July 2009

    Debbie6122- I hope you feel better soon. Keep up with the pills even at night.

    To everyone else have a great day,  good health and I hope you get lots of rest during the weekend!

    Lots of HUGS, Innocent Diana.

  • lassie11
    lassie11 Member Posts: 1,500
    edited July 2009

    Anyone else on FEC-T? I am Day 6 of the first round of the Taxotere (2 to go and that's it!!)  and am quite pleased to find that it comes without nauseau! I have been super tired and there is some joint pain but I think someone specially organized this so that the worst part was first. A friend sent me a card that said something about "the middle is the worst" and you are half way through and you can do this. Just in time. I was getting annoyed - want my hair back and my PICC line gone. Now. This too shall pass. Just not yet.

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Have to tell you New Zealand won, yeah. All will be well here tomorrow. Have a great night. I am awake again at 1.30 am . Not impressed and I am itching like mad with great big welts coming up. It hurts!!!

  • deb6563
    deb6563 Member Posts: 179
    edited July 2009

    Good morning May Marvels. 

    I had my first taxol yestereday.  I had 50mg of benadryl IV beforehand and when I got home, I slept for 3 hours.  Then dozed on and off the rest of the day.  Today I feel great.  No nausea so no zofran so no constipation so no hemorroids so no bleeding so no pain. WOW!!  I don't have any muscle or joint pain.  So far taxol is a piece of cake compared  to A/C.  My white blood count was good so I don't have to take neupogen (sp?) shots this round. I know that the muscle and joint pain as well as fatique will come later as I get more of the taxol in my system, but I am going to enjoy this week pain and fatique free.

    I'm headed to Wal-mart to spend some money on food that I can now eat because the yucky taste is finally going away then back home to clean house.  I could never have said that the day after A/C.

    Janet - where are you?  check in.  haven't heard from you in awhile.  How are you feeling now that you are finished with A/C?

    Take care everyone and have a great weekend.

  • taj72
    taj72 Member Posts: 50
    edited July 2009

    Hi ladies!  I've been out of the loop for awhile due to vacation travels.  I've missed too many posts to catch up with everyone, but just wanted to let you all know you've been in my prayers!  

    I'm sorry so many of you are feeling so crappy.  I am happy that many of you are almost done or have completed your chemo schedules.  For those of you starting Taxol, I don't think you should be too nervous, the taxol from what I can tell just makes you very fatigued, but no nausea.  My mom has another 5x of Taxol (she's completed 7 tx of Taxol already).  She is very tired and had to start neupogen due to low wbc count.  Mouth soreness and sensitivity and, of course, she's lost her taste and had some diarrhea.  Those were her SE from taxol.  She did experience some neuropathy but the doctor recommended glucasomine? and that seems to have helped with that. 

    I'm not looking forward to A/C because it sounds like the SEs from that are a little more severe? Anyway, hope you're all well and keeping your spirits up!

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

    Hi Taj- glad you back and hope you had a nice relaxing vacation, i pm you  take care

    angel hugs debbie

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

    Have you all noticed we have MIA"""S  there are a few ladies that have not been posting for awhile and wondering if anyone heard from them, like- Janet- jaelsne-mom2twins- if your not feeling good but come here just to read, your all in my thoughts and prayers and hope you are doing better;

    angel hugssssssssss debbie

  • Titch
    Titch Member Posts: 141
    edited July 2009

    Hi all

    I am sorry I have not been around.  I have had massive computer probs this week.  I purchased a new laptop and had dramas with it since.  Will be taking it back tomorrow to get it fixed. 

    I have had a couple of crap days, which is a change for me.  I finished chemo late on Thursday and missed the chemist, so had no steroids.  Then by the time I got to the chemist the next day, I had missed my time (have to take at 8 am), so didn;t have it till the next day.  Since then I have felt really yuk.  The steroids definitely have been what has kept me well.  I have been very irratible myself, which is not normal for me, but it is how I am just feeling.  So hoping tomoroow is a better day. 

    Take care gals, and no matter what life throws ya keep smiling.....

  • Sukiann
    Sukiann Member Posts: 310
    edited July 2009

    Yay!!!  I went to the radiation oncologist last monday and I now have a date for my "planning session" for radiation.  I guess I'm getting my first tatoo???  It must be a marker for the radiation to zoom in on?  Gee, I've always wanted a tatoo and now I'm getting one.  Do you think they could fashion it into a rose for me?  I'll ask Wink

    Also, I just took my first arimidex tablet this morning.  I can't possibly have any more hot flashes than I'm having now with the lupron shot, or can I?? I'll let you all know.  I'm scared!!

    Titch, hope you feel better soon and your darn computer cooperates!

    Debbie6112, you're right, there are some MIA ladies.  I hope they are ok.

    Love to all

    xoxo Sukiann

  • zuzeee
    zuzeee Member Posts: 171
    edited July 2009

    Hi Marvels

    Monday morning is here and I hope everyone has a better week this week. I have to start it by contacting my insurance company.  My tenant rang to tell me the ceiling in my kitchen has collapsed!!?? so have a laugh girls and enjoy.

    Hugs Susie

  • lassie11
    lassie11 Member Posts: 1,500
    edited July 2009

    Hey  Susie - it is still Sunday afternoon here in Ontario Canada - if my Monday is like yours I think it would be OK to put it off! Sorry to hear about your ceiling.

  • Janet22664
    Janet22664 Member Posts: 155
    edited July 2009

    Hi everyone,

      I just got back from vacation.  Had a nice time at the beach with the family, although, I was a little less active than in years past.  Before I left, I had a little scare...thought a new lump turned up in the healthy breast.  After having an ultrasound it was determined that it was just fatty tissue. (Hooray for fat!!!  Never thought I'd say that!) 

      I also met with a plastic surgeon before I left for vacation.  Now I'm deciding between implants or a DIEP procedure (where they use tissue from your belly but not the ab muscle) .  Unfortunately, the second plastic surgeon who I talked to about the DIEP (who just happens to be the Chief of Plastic Surgeon at University of Pennsylvania Hospital who specializes in reconstruction) totally contradicted what the first plastic surgeon I meant with said about implants.  

      Tomorrow I start Taxol.  Once again, the "unknown" has me a little nervous.  I understand that the nausea is less than with A/C, but since that wasn't an issue for me, I don't know if the taxol will prove to be more bothersome with bone pain and "tingling" fingers and toes!   What I do know I'll hate is being in that chair for five freaking hours!!!!   I told the onc nurses that they better give me something to do like filing or my ADHD is really going to get the better of me!  

      That's it for now. Hope everyone is doing well. 

    Janet

  • jaelsne
    jaelsne Member Posts: 82
    edited July 2009

    Debbie,

      Thanks for mentioning me as one of the MIA's--sorry that I haven't been posting.  I guess the reason is that I haven't had much to say.  I healed up just fine after having my implant removed, though it looks like I had a bomb go off in my chest.  I will need reconstruction (again) even if I decide not to put an implant in.  Part of my right side is concave, part is convex--not a pretty sight.  In any case, I decided against the surgery until I'm past chemo, rads, and start feeling "whole" again.  Probably will do it during the early part of next year, in order to avoid problems over the holiday season.

      I'm on t/c chemo day 13 and feeling very strong--had a very busy weekend, and the anemia that has plagued me seems to have lessened.  I went to the Getty Villa today with friends (the old, renovated Getty museum in Malibu, CA) and was able to keep up with them.  I know I'll be exhausted tomorrow!

      I do chemo number 4 out of 6 next week, but will take a break to go to a family camp at the University of California/Santa Barbara.  We have gone there every year for ten years, and we stay for two weeks.  SB is a beautiful place, and it should be a healing time for me before I face the dreaded chemos 5 and 6.  My onc said that if I'm going to have any trouble with neuropathy or need a transfusion, it would be after those...  Oh well, one day at a time.

      I've been reading and following everyone's posts.  Unfortunately, it's hard for me to track and respond to each person individually.  I guess that's why I've been accepted into UCLA's study about chemo brain!  lol...  Anyway, I hope that everyone has a good week ahead!

    Jo Anne 

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

    Susie- Sorry about your ceiling, when it rains it pours it seems

    Janet- good to see your back i mentioned that you were mia and wonderd how you were, good luck with the taxol tomorrow

    Jaeslne- I knew that your were having problems with the implants but i had no idea how bad it was, im sorry you had to go thru all that, thats one of the reasons why i have decided to wait at least a year before i decide what recon i will do if any, it to much to handle for me right now. I hope that your SE are minimal this time around, i too had really low white and red counts and my hemoglobin was on the low side to, i have had to get he shot every time, in fact this last 3 days has been really hard on me with the bone pain,stayed on pain meds the whole time,tonight i finally feel better, but not looking forward to next infusion, My heart goes out to you and all those that have more than 4 to do, i will do my last one at he end of this month.

    I have been to SB it has been about 25 years but it is really beautifvul kind of reminds me of hawaii.

    hope every one had a good weekend

    debbie

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