Chemo June 2010

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  • cheyenna
    cheyenna Member Posts: 379
    edited August 2010
    JFVdid the wellbutrin help you, does it work fast. its been one day
  • workmother
    workmother Member Posts: 78
    edited August 2010

    Some side effects have settled in from the Taxol. A bit of pain in my hips. Some pains in my right thigh. And an odd sensation in my knees - kind of tingly, kind of a tightness, followed by them just feeling weak. Strange. I slept really well last night but i'm definitely very tired today. I was getting frustrated that I had no energy to do anything and told my husband I didn't understand why I was so tired. He said "because you're on chemo! Don't worry about it. Just take a nap." So I did. Sometimes I need to be reminded that its OK to be totally wiped out.

    mittymuffin - I had stopped eating red meat when I was diagnosed in April. After my AC treatment wiped me out really badly I had a steak. Felt a million times better. Whenever I get that weak feeling again I eat some red meat. Helps me. I was trying Ginseng for energy too but someone posted that Sloan's website says it may be bad for breast cancer. Haven't had the mental capacity to research that yet but now I stopped taking it. My onc. is from Sloan and he suggested it for energy so I don't know!

  • JFV
    JFV Member Posts: 795
    edited August 2010

    Chey It may take a couple of weeks... I'm sorry about that.  If you have the energy can you exercise.  Even if it's marching around the inside of your house.  Any type of exercise will have an antidepressent effect and you can do it in your pajamas.

    workmother-  I am totally with you on the fatigue thing. 

  • brat352
    brat352 Member Posts: 41
    edited August 2010

    kittycat:  The half moon things are called "Beau Ridges" and they are from chemo.  I have them too!  You can actually see where each treatment began and ended.  But someone else very early on in this thread mentioned to use Revlon "Post Trauma Nail Treatment"  This stuff is FANTASTIC.  It's very pale pink and it is expensive ($7.00/bottle), but this stuff really works!  My nails have always been less than desirable as they would grow so long and then either break or start peeling.  I have two full hands of long, growing nails!  And they are very hard and durable.  Love this stuff!  I'm going to continue to use it even though I'm through with chemo.

    Bon:  I always have to take 2 OTC Prevacid/Priolosec instead of 1 to get relief.  And after taking Rx Prevacid for over a year, I only have to take OTC Prevacid/Prilosec when needed.  I guess by surpressing the acid reflux, my esophagus has had time to heal, now I only take one when I have eaten something that has upset my tummy/intestines(?) 

    And I went and did it again!  Had a new couch delivered yesterday and opened the door to the delivery guy bald-headed!  Then I put on my little hat - he just smiled.  Oh well, won't be seeing him again!

    Now I have to see the dentist tomorrow as a chipped tooth has finally broken!  I'm assuming that chemo has ruined my teeth.  The dentist is going to take one look at my mouth and see dollar signs!  I will have to tell him to just fix the broken tooth and one molar that has a big cavity in it.  I'll have him fix everything else after rads are finished.  Just can't afford anymore bills!

    I go for simulation for rads on Wednesday and am hoping that they can do the rads while my boob is hanging down through a hole.  I have heard that this type of treatment allows them to more precisely aim for my breast tissue and keep it away from my heart/lungs.

    Well, off to the pharmacy to see if I can find some dental putty to put on my broken tooth until I see the dentist!

    Have a great day ladies!

  • mimi9186
    mimi9186 Member Posts: 127
    edited August 2010

    Brat, please let us know how the simulation for rads goes.  I will not be doing that until mid September but am always worried about lung damage from the rads.  I would love to hear how it goes.

    Blessings to all,  Mimi

  • Latte
    Latte Member Posts: 1,072
    edited August 2010

    brat - i also broke a tooth and it's because of chemo. a girl who i sit next to during tx also told me that she broke a tooth because of chemo. where I live, dental tx is paid for by health insurance during and one yr after chemo. I also saw a posting by someone in the USA that their insurance paid for dental tx because they agreed it was caused by chemo - don't know if this is maybe somehting you could look into.

    anyone know how low your counts can go before they postpone a chemo session? mine are pretty low and i'm waiting for the call to tell me not to come in tomorrow because they are too low, but maybe they are still ok?(I phoned the onc office but they said it would take them a couple of hours before they could check them and let me know)

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited August 2010

    brat-  I'm glad the Revlon "Post Nail trauma" polish is working for you too.  Isn't it fantastic?  I swear my nails have never looked better!  And it doesn't even chip.  Who knew?  Sorry about the tooth. Don't get me started on dental bills!  I have had 2 root canals, one crown, 1/2 a dental implant (waiting for the crown till after chemo) in the past year.  I'm a great brusher and flosser and have always had great teeth. I can only imagine what is in store for me after chemo!  Thankfully my family dentist is the most caring, supportive talented man and let's me pay as I can.  He never even sends me a bill.  There are good doctors in the world.

    latte- I hope your counts hold up. I know you know all the things to support your body.  Remember to sleep and rest as much as possible, even catnaps help.  Stay in the AC if it's hot. Try to avoid anything that takes extra energy to allow your body to re-build and re-charge.  BREATHE to get that oxygen into your cells.  I actually find that I forget to breathe deeply and almost feel short of breath.  When I take a deep breath it is almost like I'm coming up from being under water.  I can feel it!

    For all you ladies beginning rads (I'm headed there soon), there is a very informative thread called "Radiation treatment in a prone (face down) position".  I know that is the "new" method, but some people actually think the supine (on your back) is safer for the heart as the heart falls back and out of the way of the radiation.  I have this same concern as my BC is left side and almost where the breast attaches to the ribs.  I am meeting with my Rads Onc again soon and will let you guys know what I find out. 

  • JFV
    JFV Member Posts: 795
    edited August 2010

    My sister got something called GC MI paste plus from her dentist for me to use.  I  smear it on once a day to cover the parts of my teeth that are being exposed as my gums recede (thanks chemo!)  I put it on at bedtime.  I've only used it a couple of times. I am hoping it will prevent further problems.  Maybe you ladies can ask your dentists about it.

  • cheyenna
    cheyenna Member Posts: 379
    edited August 2010

    im so scared to start taxol tomorrow,

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited August 2010

    cheyenna- Remember, "you don't have to be brave, you just have to show up".  We'll be right here for you! 

    I just saw this posted by a newly-diagnosed sister.  Her little daughter told her "I do not have to tell God how big my problem is, I have to tell my problem how big my God is."  I think kids are smarter than we are many times.

  • cheyenna
    cheyenna Member Posts: 379
    edited August 2010

     Designer mom, wow how very true, thank you. ill show up and remember how big my god is.

    Tmarina, goodluck tomorrow, its me and you, ill be thinking of you the whole time!!! sending you love and hugs

  • grneyd5600
    grneyd5600 Member Posts: 420
    edited August 2010

    Chey - you are going to get through tomorrow.  Hang in there and just keep telling yourself every tx puts you closer to the end.  We will be there in spirit - cheering you on!!!!!!

    Question for you guys getting ready for rads - have you finished your chemo?  I was wondering if anyone ever does the radiation stage before they finish up the chemo?  Not that I really want to combine themn but I am just so ready to be done that it crossed my mind I wonder if I can do that last 4 weeks of Taxol along with rads........

  • TMarina
    TMarina Member Posts: 692
    edited August 2010

    Chey--. Yep, you and me! Wish we could really go through it together, but I'll be thinking of you and praying for you  (until the benedryl puts me to sleep, that is!  lol!)

    Jackie-->  I was told by my rad onc that I can't do rads while on Taxol.  The chemo makes your body more sensitive to the rads and therefore the se's are worse.

  • workmother
    workmother Member Posts: 78
    edited August 2010

    Chey and TMarina - good luck tomorrow with the Taxol. You'll do great!  I am such a big baby, so if I can do it, anyone can!!!

    I'm doing OK. Just tired a lot but very different from AC. No chemo fog to speak of. I can function with a nap. I do have some joint pains: hips and knees mostly. Everyone talks about their toes, guess it hasn't worked that far down my body yet! So far it seems like Taxol is easier than AC. Keeping my fingers crossed it stays that way!!

  • TMarina
    TMarina Member Posts: 692
    edited August 2010

    Thanks workmother!!  I'm REALLY hoping this is easier for me too, as it seems to be for most.  AC really kicked my butt!

    I've had a 4 week break, and I'm feeling great, but I think I am ready to get on with this, so I can get it DONE!

    Smile

  • JFV
    JFV Member Posts: 795
    edited August 2010

    Chey and Tmarina Thinking of you both. 

  • Trusting
    Trusting Member Posts: 43
    edited August 2010

    Hey SKD,

    Sorry to hear that you had the flu, it is bad enough to have chemo but to have the flu with it would be not fun Frown. I start my first dose of Docetaxol on Tuesday.I am a little worried about changing drugs but I hope I do well. Most people say they find Docetaxol easier. I hope I am one of them.

    Take care,

    Trusting

  • julia2
    julia2 Member Posts: 183
    edited August 2010

    Last chemo tomorrow.  Just finished my huge doses of steroids to keep me from reacting.  Not too keen on that, lots of potential nasty SEs, but what're you gonna do, my last infusion went great so I guess I just hope for the best.  This time tomorrow hopefully it will all be over.

    Julia

  • kittycat
    kittycat Member Posts: 2,144
    edited August 2010

    Chey - do you have a local Susan G Komen office or some place where they have breast cancer survivors?  Have you met anyone at the onco's office that seems nice?  I met up with a couple girls here from BCO that live near me, plus another gal that goes to the same onco (we all see the same onco).  We get together and have dinner or lunch together.  It has made a world of difference to me.  This board is also very helpful!  Once I realized I had BC again, I opened myself up to the people around me that really support me. 

    I won't lie - I break down and cry.  I think it's normal.  Plus, I was pre-menopausal so I'm now going through chemopause and it doesn't help with the emotions.  Between chemo brain and chemo pause, I couldn't grasp how to do something at work the other day.  I called my manager and had to keep from crying on the phone (he heard me cry right after my 2nd dx, so he's becoming used to it).  I think he sensed something was wrong and gave me a quick fix to my problem and told me turn off my computer and enjoy my weekend! 

    AND.... what's with your onco telling you that IF BC came back, it would be stage 4???  I had it come back and I'm stage 1.  She doesn't know this.  Sure, chemo is to prevent any possible floating cancer cells from going anywhere else.  BUT IT DOESN'T MEAN THAT IF YOU HAD A RECURRENCE IT WOULD BE STAGE 4!!!  I wish I lived closer to you, so I could slap your onco upside her head for saying this!

    I hope you feel better!  I want to give you a BIG HUG!!!!  :)

  • kittycat
    kittycat Member Posts: 2,144
    edited August 2010

    brat - thanks for the info on the nail polish.  I will have to try that.  I've been using Tree Tea oil on my nails, since starting Taxol.  My husband is getting pretty used to stopping at Walgreen's and picking up some crazy thing I need for chemo!  First it was the Sea Bands, then the Tree Oil, now it will be the nail polish.  I have really strong nails, but I'm going to use this stuff anyway! 

    Julia2 - congrats on your last day of chemo tomorrow!!  WooHoo!!!!!!!

  • kittycat
    kittycat Member Posts: 2,144
    edited August 2010

    Chey & Tina - good luck on the Taxol.  I was a nervous wreck for it and it was so much easier than the AC!  I'm keeping good thoughts for you both!!!  :)

  • PearlGirl
    PearlGirl Member Posts: 549
    edited August 2010

    Up and pacing in the middle of the night...still suffering from GI issues. Taking Prilosec 2X/day, Pepcid AC, Tums and Gas-Ex. Thought it might be working but apparently not well enough or I'd be sleeping now instead of clutching my stomach. 

    Reading all your posts and hoping the Taxol goes well for all who are about to start or just started on it. I hope this regimen is virtually SE free.

    Which is what I wish for all on this board...some time in the NO SE zone.  Wishing it for myself, too.  Have 4th and final Cytaxan/Taxotere coming up on Wednesday. Will be glad when it's over and I can concentrate on gettting a GI consult to get this gut thing under control before moving onto radiation.

  • jenweg
    jenweg Member Posts: 195
    edited August 2010

    Chey and TMarina good luck today!  You will be fine, positive thoughts.  Julia congrats today on being the last one!  Must be a wonderful feeling.  Had my fourth taxol Wednesday, still doing good, no bad se's, nails still good, etc.!  Have a great Monday all.

  • julia2
    julia2 Member Posts: 183
    edited August 2010

    Thanks ladies!  BTW, I went to Harry and David and bought a box of individually wrapped truffles for my Onco nurses thank you gift.  That way they can share with patients if they choose without worrying about germs from other's hands.  Had I been more organized this week I would've ordered the gift pack of Montana Monster Cookies http://www.mtmonstermunchies.com/product/1/1

    they are totally fantastic and wrapped in packs of 2 for 24 cookies total, but I ran out of time to order :-(  Just a couple ideas if anyone else is looking to do something similar.

     Julia 

  • VickyThomas
    VickyThomas Member Posts: 54
    edited August 2010

    Okay.. four days after taxol, my fingers and toes feel funny, my body aches so bad.. and I skipped the Neulasta shot. Two more treatments to go.. Uggghhhh..Now I am afraid that when I go back I won't be able to have treatments because my counts won't be up..

    for those having trouble drinking I found that vitamin water helps..appetitie has improved although I can't taste anything..

    JUST TIRED...

  • PearlGirl
    PearlGirl Member Posts: 549
    edited August 2010

    My soon to be 89 year old Mom was diagnosed yesterday with Salmonella after nearly 3 weeks of uncontrollable diarrhea.  It was most probably sunny-side-up eggs she ate at a local restaurant.

    I have an app on my iPhone from the FDA regarding recalls. Not only have they recalled eggs in the past couple of weeks for Salmonella contamination but also some pistachios, alfalfa sprouts, and frozen mamey pulp (a tropical fruit often added to smoothies and other things).  All for Salmonella.  It's getting scarier by the minute.

  • JFV
    JFV Member Posts: 795
    edited August 2010

    Dear Bon-  I am so sorry about your mom and your gut.  I pray that you and she improve quickly!!!  

    Congrats to Julia2 and Bon for seeing the light at the end of the tunnel. 

    Vicky I am in a similar boat although I do feel better each day.  Made myself ride the stationery bike for 10 minutes it was alot of work but I feel like it at least pumps some stuff out of my body.

    My daughter went to an outside venue to see the Jonas Brothers last night and then had a sleep over.  She saw them in the pouring rain.  I am wondering how she is!  Son is downstairs watching something about King David on TV.  My dog is snoring up a storm  We are experiencing the first rainy days we have had in weeks.  My husband is off at work.  There, I knew there was life outside chemo!

  • toni30
    toni30 Member Posts: 252
    edited August 2010

    Vicky- I'm with you. This second Taxol has made me so tired - I almost couldn't move all weekend. Thanks goodness I took today off from  work but I am wondering if I can put in a full day tomorrow. I don't remember the first one wiping me out as much.  Congrats to Julia for being done! Toni

  • grneyd5600
    grneyd5600 Member Posts: 420
    edited August 2010
    Ok so I did the elliptical today.  Managed to do 30 minutes but I was pushing it.  I couldn't believe how high my heart rate was either.  It amazes how fast you get out of shape!  Tomorrow is my second Taxol.  Hoping I make out ok because it is in the AM and I am hoping to still be able to work the afternoon.  The good news is two of my 3 sisters are coming out to stay with me for a few days.  We will have a fun time in the Ya Ya Sisterhood tonight!  Wink
  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited August 2010

    Oh congratulations to all you ladies who are finishing up this crazy chemo dance!

    Bon- Dang! I am with you about worrying about eating everything.  Just eating is like avoiding toxic waste!  I'm so very sorry about your mom, that is so scary, especially in the elderly.  When this recent egg recall hit the news, I researched the codes on my egg carton to make sure.  For anyone who wants to know, the first four digit number is the plant (you can go to FDA and find out location).  The second set of numbers is the day it was packed (0-365 one for each day of the year).  My carton date is 203, which means it was packed on the 203 day of the year, July, 24, 2010.  I think the site said they can be sold for 45 days after packing.  Now that just can't be good!  Gosh!  I'm avoiding dairy and chicken (hormones), gave up beef years ago, now eggs.  You would think I would be a twig! I'm actually a size 8, I just keep it well padded so it doesn't get scratched!  Hoping all your stomach problems go away soon!

    kitty- I'm with you.  I think we should both pay cheyenna's Onc a visit.  Maybe we should bring grannydukes!

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