Starting Chemo in July 2009

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  • gillyone
    gillyone Member Posts: 1,727
    edited November 2009

    Hi ladies

    I have numbness in my fingers and surprisingly in my cheeks!! My onc says I'm only the second person he has had this happen to. But it gets better as time goes on. As I am done with taxol I am looking forward to the end of the SEs, just not sure how long I will have to wait.(4 weeks like Josybee perhaps) I am VERY tired now, probably the cumulative effects of all the chemo, and not sure if having it all dose dense makes me more tired. I feel like I've done pretty well over the chemo time despite having a sinus infection, broken bones in my foot and shingles.

    I THINK I have been getting thrush too. Is it the white tongue thing? That would account for things not tasting great. But by the time it's my next appointment it has always gone.

    Those of you who have already started rads, how long between your last chemo and first rads? I have the consult on Tuesday and am worroed about starting quickly when I am so tired and still have shingles etc. But of course if it affects tx I want to get going!!!

    Hope you are all having a good weekend.

  • chrisct
    chrisct Member Posts: 2,662
    edited November 2009

    Gillyone - I started rads 4 weeks after last chemo tx (T/Cx4).   Hope the cumulative effects of chemo wear off quickly for you and that your shingles go away soon. 

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited November 2009

    Gilly, I had 20 days between last chemo & 1st rad (Sept 10-Sept 30)  I took naps almost every day for the 1st 3 weeks of rads-either came home at lunchtime for a power 20 min nap or took a half hour or so one right after work, but this last week, I didn't nap at all. My rad onc said that sometimes with chemo after it's out of your system, the energy level is increased even while undergoing rads--seems to be that way with me (so far!)

    Joni2

  • eliz46
    eliz46 Member Posts: 71
    edited November 2009

    Hi everyone just thought i would come say hello its been awhile i have finished chemo and now taking tamoxafen all is well just some hot flashes once in a while....

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited November 2009

    Eliz-how long have you been on Tamoxafen?  Did you chose that over Femara, Arimidex or Aromasin? Or did your onc just chose that for your treatment?

  • gillyone
    gillyone Member Posts: 1,727
    edited November 2009

    thanks Joni2 and chrisct

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2009

    Hi to all,

     So far taxol #5 has gone smoothly do not know whats different but I am doing much better. I even felt like going out day after chemo and had more engergy than normal. I am sure by Fri. or Sat. Fatigue will set in. At least I can eat and function more normally. Thank goodness!! 7more weeks of Taxol girls and I will be finished with chemo YEAH!!

    Take care,

    Edie

    I

  • jacee
    jacee Member Posts: 1,384
    edited November 2009

      

    Just checking in...just finished Taxol #3 on Monday. 9 to go. Feeling good, no side effects to speak of. Eyebrows and lashes gone, but hair returning on head...YAY!!  Some unpleasant taste sensations, but nothing like A/C. Hoping this continues to be tolerable.

    Hope all is well...July seems like ages ago in some ways.  We've gone through so much since then it seems.

    Enjoy the fall,

    Joni1

  • stef58
    stef58 Member Posts: 288
    edited November 2009

    Glad to hear the treatments are going well for all. I am finally starting to feel better. Met with PS  and surgrey is after the first of the year. Can't wait for the exchange. Ready to live life again. The hair is coming also.   Have a great day Dianne

  • LovingLifeToday
    LovingLifeToday Member Posts: 39
    edited November 2009

    Hi everyone... it's been a while since I last posted...  I had my Taxol #4 (weekly) on Monday... although Taxol is sooo much better than Ac was... the neuropathy is getting worse. I too have it in my face... my cheeks, lips and tongue... I feel it down my back and in my ears! I would say I have flashes... but I can't tell if they are hot or cold.... kind of like icy hot. My feet are kind of numb and tingling and on my right side I have it half up my leg and all of my right arm and into my shoulder. I was put on Neurontin and was told if this does not help I will start on Taxotere on Monday instead of the Taxol.   

    My hair is fuzzy... my fiancé says it feels like a tennis ball...  he is right!!  lol   but when I step outside... I can feel the wind blowing in my hair... makes people laugh when I tell them that Wink... lol

    Prayers for all!

    Elizabeth~LovingLifeToday

  • eliz46
    eliz46 Member Posts: 71
    edited November 2009

    Eph 3   i have done alot of research with some help from my onco.  i also went to some support groups to find out about all the different drugs out there for bc   i choose tomoxefen for my ++ hormones. i havent had any side affects other than once in a while i feel tight in my hands but i do have some arthrites anyway also hot flashes but everything is very managable.  i did also research vitamins and the projestrone cream but i am not going to fool around with my body .....I have been considered a health nuts since i was young and also brought up with homeopathic medicine all my life .this is very much a change in my life.  haveing cancer has change my life. if things change than i will check into other options ferema is to new on the market its still in the testing stage .....i do have a health doc i go to also and yes i still take homeopathic meds

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2009

    Lovinlife

     I  also have white fuzz and some hair coming back. Looks like a newborn babys head LOL. I guess time will tell if Taxol will make it fall out..

  • josybee
    josybee Member Posts: 86
    edited November 2009

    HI ladies, Started rads yestrday, today is only my 2nd day(can't wait to be finifhed) They wouldn't give me my Herceptin last week due to the fact that my mugascan showed ejection fraction at 50%. Now I have to see a Cardiologist on Thursday. I know I will probably have to have an echocardiogran but I don't know what else they do. Anyone have any info on that?? Any info would be helpful. Thanks,Joanne 

  • PauldingMom
    PauldingMom Member Posts: 927
    edited November 2009

    Popping in to check on ya'all. Sending prayers to those of you having yucky SE and rejoicing in all that have finished Chemo. Hard to believe we all started this in July and here it is almost halfway through November! 

    Stay strong ladies!!! Lisa 

  • stef58
    stef58 Member Posts: 288
    edited November 2009

    Hello triple j's. LovinLife, I just got done with taxotere and very little SE's. The only thing that I got was from the steriods. Little sleep the first night and thrush and fungus on the arm. they can be handled. The taxotere makes the bones ache but that might be the neulasta shot. Sleep when you need it and take tylenol or advil for the pain. it usuually popped up for me on days 4-6. Otherwise not bad. The hair is getting where you can see it. Going to ditch the hat if the hair on top thicker. It is coming. Had to shave the armpits and going to shave the legs tonight. Have a great day Dianne

  • LovingLifeToday
    LovingLifeToday Member Posts: 39
    edited November 2009

    Yes, Quarter405... baby fine!!  I have my hand on top of my head every time they are not busy doing anything else.. hehe  As soon as I don't see scalp anymore, I'm going out in 'my' new hair :-)  

    Thanks Dianne!  I do feel much better on the new meds, but he did say they only mask the systems not fix them. I did decide to stay on Taxol for a couple more weeks and then make a decision. With the meds, I do feel much better... I just don't want long term effects from it.  I'm glad to know that the se's are minimum with the Taxotere and you are doing well :-)  I'll be ditching the wig too when I no longer see scalp!!! And I may treat myself to some new earrings as well... I've tried on some that I already have... but they looked sooo much better with the much longer hair... lol

    I can't wait to get my eyebrows and eyelashes back again!! I have some... but you have to look really hard for them and my eyesight is not the best anymore!! lol

    I hope everyone has a beautiful day as we are all beautiful women!!! Kiss

    LovingLifeToday~ Elizabeth

  • LindaSueH
    LindaSueH Member Posts: 70
    edited November 2009

    ok....I have a new question.  My last chemo was Sept 9 and I have been on tamox for 1 month.  I now have fine, fuzzy hair all over my face!  Will this go away, or what can I do to get rid of it?????  Exchange surgery next Thursday....cannot wait!!!!!!!!!!!

    Hugs,

    Linda

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2009

     I also have fuzz on the side of my face so I would like to know if it will go away?

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited November 2009

    I've always had fine, light hairs on my cheeks, even before all this.  Maybe with your head hair gone you are just noticing it now or is extremely noticable? Mine's not.Joni 2

  • PauldingMom
    PauldingMom Member Posts: 927
    edited November 2009

    My fuzzy face fell off with Chemo. and hasn't come back. Small favors to be thankful for. I think Eph3-12 is right. I know I have seen freckles I never noticed before but I think it's from lack of hair on my head. 

  • josybee
    josybee Member Posts: 86
    edited November 2009

    I can't have my Herceptin treatments, ejection fraction was 50% and had to see a Cardiologist today. Have to start taking 2 pills for the heart and have echocardiogram and stress test in the next 2 weeks, so I don't know if and when I will be getting the herceptin again. Anyone else have this problem??? Still doing rads though, #5 tomorrow.

  • josybee
    josybee Member Posts: 86
    edited November 2009

    I can't have my Herceptin treatments, ejection fraction was 50% and had to see a Cardiologist today. Have to start taking 2 pills for the heart and have echocardiogram and stress test in the next 2 weeks, so I don't know if and when I will be getting the herceptin again. Anyone else have this problem??? Still doing rads though, #5 tomorrow.

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited November 2009

    Hey Triple Js-Just thought I'd report in.  Finished radiation yesterday!!!!!!  Start Femara on Monday-seems never ending!

    Joni2

  • o2bhealthy
    o2bhealthy Member Posts: 2,101
    edited November 2009

    Joni2 - Congratulations on finishing RADS!!!!!   

  • Jayne_in_UK
    Jayne_in_UK Member Posts: 517
    edited November 2009

    Hello Triple J's. I hope you are all having a good weekend.

    Congratulations Joni2 on finishing Rads.

    Josybee  I hope you get your heart issues sorted out. I cannot really comment on Herceptin as I am HER2- and cannot take it.

    I haven't started Rads yet, I'm going to be marked up on Tuesday, not sure yet when they will start. Can't say I am looking forward to it, but it is the next stage and I should be finished by Christmas.

    My hair has started to grow back a little, I have the fuzzy baby hair on my head and not much in the way of eyebrows or lashes. I am ready for my nasal hair to come back too, I'm fed up with the constantly running nose!

    Sending a wish for minimal SE's to all still going through treatment.

  • gillyone
    gillyone Member Posts: 1,727
    edited November 2009

    Hi Jayne

    I start rads today. Got my tattoos and dry run last week. I am beginning to post on the November rads thread. So many of the Js are on the October thread.

    Congrats on your hair!! I have not noticed the return of any hair yet, but I am only three weeks out from DD taxol so I probably need to be patient. Like you, I would love for nose hairs to return - I am sick of constantly wiping my nose. On the positive side, I am definitely less tired now than when on chemo.

    Have a good day everyone.

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited November 2009

    Good luck with the rads gilly!  How many? Joni2

  • gillyone
    gillyone Member Posts: 1,727
    edited November 2009

    Joni2 - you get done and I get started!! 33 is the total.

  • Jayne_in_UK
    Jayne_in_UK Member Posts: 517
    edited November 2009

    Gill good luck with your rads.

    I'll have to start reading the November rads thread to see what to expect. Today I went for my marking up, had a CT scan and 3 very small tattoos. My dry run will be 26th November and my first real session is 30th November. I am only having 15 though, so will be finished before Christmas.

  • PauldingMom
    PauldingMom Member Posts: 927
    edited November 2009

    Jayne- great news. I am looking into my crystal boob and I for see that everyone is going to do great in Rads.!!! 

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