November 2009-Starting Chemo

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  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    SherriV: Thanks for that - I'll check into it. I did buy one so I can look at it's contents. I don'tcare if I stink I'm not going anywhere while I do it anyway.

    Sue

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    I checked out Crystal Stick Deodorant - it does not contain any aluminium chlorohydrate and has no perfume which was the main requirement. The rad oncs here recommend it.

  • mommy2two
    mommy2two Member Posts: 130
    edited March 2010

    Good morning all!  I have been out of it for the last few weeks as I've been very sick.  I feel a little better today, not great but good enough to come to work Cry

    Good luck Alicia

    I use Crystal deodorant per my radiologist and it contains no aluminum or at least it doesn't list it in the ingredients on the package.  I also use Purpose soap which you can get from Walgreens or CVS while I'm going through radiation.  

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited March 2010

    Surgery went well.  I am in quite a bit of pain...have a drain on each side.  But glad to be done !!  Thanks for thinking of me and praying.

    Toyah. Hope you are feeling better real soon.

    Hugs ~

    Alicia

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    Great news Alicia!!! (((HUGS)))

  • micheleboots
    micheleboots Member Posts: 1,993
    edited March 2010

    Glad to hear all went well today Alicia..

  • mommy2two
    mommy2two Member Posts: 130
    edited March 2010
    Alicia - SO glad everything went well today, that is the best news I've had all day!  Still praying for a speedy recovery!  
  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010

    Alicia:  Gentle hug and I am not just trying to cop of feel of squishy boobs!

    Chemo 5/12 today, moving closer to halfway point!

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited March 2010

    Alicia,

    so glad your done~~~Sorry you are in pain though. The road is winding down and that is AWESOME for so many of us now.

    Cathy,

    I am so sorry for all you are having to deal with. I hope your family will come to terms with all they are going through. I know you will be fine. Keep fighting warrior and know my heart and my prayers are with you.

    Going back and forth to rads each day with the 3 hour ride has kept me from being able to keep on board as I like. I will continue to read posts and keep up with smiles, etc as best as I can.

    Love to all "Warrior Sisters" ((((((((((((((Gentle Hugs))))))))))))))))

  • Sherri_V
    Sherri_V Member Posts: 159
    edited March 2010

    Dehydration: A Blessing & A Curse *Ü*

    WOW!!! I know I haven't been feeling "right" since my infusion last week but on top of chemo, I also have allergies/hayfever, and, on top of THAT, I also currently have THRUSH *Ü*

    I haven't been able to drink or eat much of anything due to taste & texture issues. Drinking water has been like drinking baby oil.

    Anyway, it's okay...it goes away after awhile so I'm not trying to complain, just telling you all a funny story. So, yesterday I was talking to my sister and told her how I keep biting the sides of my tongue. She told me that the tongue swells when one gets dehydrated. That still didn't motivate me to drink. But, this a.m. I got up (finally slept 5 straight hours!) and weighed. I have lost ELEVEN pounds since last Wednesday!!!  Of course, as soon as I start eating and drinking again, it'll all pop right back on but I'm feeling rather svelte this morning!

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited March 2010

    Brenda ~ so sorry about your long ride each day.  :(  Hang in there sister !!! 

    Sherri ~ get drinking some water, but hey 11 pounds sounds nice but a heck of a way to do it.  Hope you feel better!!!!!!

    Thank you everyone for your well wishes.  I am doing pretty good.  A bit of pain where they stitch the pocket shut at the bottom of the implant "internally"   Hard to get up when laying down, so I have resorted to an old recliner we had in a spare room propped in my bedroom. 

    :)
    Hugs and wishing everyone a good day!

    Alicia

  • SharaD
    SharaD Member Posts: 100
    edited March 2010

    WAY TO GO, ALICIA!   I'm glad you're doing well.  My lumpectomy is next Tuesday so I'm reading a lot about surgeries these days.  They sound like so much FUN Undecided.


    NO IVORY SOAP, girls!  Breastcancer.org calls it a "surprisingly harsh soap".  Sensitive-skin Dove or Aveeno is recommended.  It's in the "Do's and Dont's" section on this page:

     http://www.breastcancer.org/tips/lymphedema/avoid.jsp

    HAPPY SAINT PATRICK'S DAY WARRIORS!

  • RedheadPam
    RedheadPam Member Posts: 98
    edited March 2010
    Hello Ladies!  I have to share something with you, since I feel so brave and hardly anyone in the non-cancer world seems to think its a big deal.....I have started going hat-less! And scarf-less!  it's been not quite 3 months since my last chemo, and yesterday I just decided I would try going 'topless' at work.  Today I just left the house bareheaded....see what you think....byebye hats!
  • Sherri_V
    Sherri_V Member Posts: 159
    edited March 2010

    Love it, Pam! 

    I had to go to town to get some prescriptions and forgot any headcovering.  I went inside anyway and it was okay :)  I applaud your bravery!

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited March 2010

    Pam ~ love it.  I don't have quite as much hair and I went to my mailbox and was sitting on my porch topless as it is a beautiful day.  MY UPS MAN came ~ I said sorry to scare you with the bald head, he said no problem I did battle with cancer last year.  He left me with a smile and said stay strong !

    You look great Pam ~ soon as I have that much I am going TOPLESS too ~

    :)

  • micheleboots
    micheleboots Member Posts: 1,993
    edited March 2010

    Pam I love it...I feel more powerful without my hats...I look a little Golemish righ now....

  • littlebird75
    littlebird75 Member Posts: 120
    edited March 2010

    My head now looks like legs that haven't been shaved in a while - very thin and fuzzy in places. I'm still sporting hats and scarves and my head itches a lot. Had my second radiation today. I'll be glad when I adjust to the new recurring morning appointment. 

    I'm enjoying the new energy - almost like old times before chemo. My swollen leggs aren't AS bad as they had been - when that goes away that'll be the last of those icky side effects. 

     Sorry I couldn't make it yesterday - I hope those that went had a great time. Still have to catch up on my reading of the lastest posts.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    SharaD: Good luck with your lumpectomy!! Are you still in the motel?

    Pam: Wow, you look fine naked.

    I'm gradually recovering from the last chemo but taking it a day at a time. Looks like our week at the beach might be spoiled by a bloody tropical cyclone (hurricane) - rain is forecast for the whole week.

    ((((((Hugs)))))) to everyone still having chemo and feeling bad.

     Sue

  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010

    Pam, you look great! Is it growing back evenly? Do you have the top layer of duck fuzz?

    Maybe I am just a freak, I have so much less hair than any of you and I am pretty much "naked" 99% of the time. The only time I scarf up is when I am dressed up a bit and choose to accessorize (which isn't often).

    Out of curiousity the other day, I took mascara and colored all my duck fuzz. It really made the hair show up, but it also highlighted how much scalp is in between those hairs. Maybe I will buy some hot pink or orange mascara wand temporary color.

  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited March 2010

    Wow Pam! I'm jealous :) You look great. Melinda, don't worry, I look like I have white fuzz on my head. I've had grey since I was 17. And I can't color my hair for a year? Yell

    Alicia. Congrats on the squishy boobs! The pain, like clouds, will part and allow the sun to warm your body. You can finally breathe!! (((HUGS)))

    Cathy. I'm so sorry for your family's loss. You all are in my prayers.

    Toyah, are you feeling better?

    OK... my BIG news. My breast tumor is now 1.5 cm...not 11! My liver tumer went from 16 mm to 6 mm! Regression for a Stage IV girl is like winning the lottery! I meet with the surgeon on 3-30, Surgery will be followed by ablation to the liver met and meet/start with the Radiation Onc. The ball is rolling!

     Thank you for all of your hugs and prayers and well wishes! Thoughts of you all bring me great comfort! Love to my warrior sisters!

  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010

    Linda: Way to go on shrinking those SOB's !!!!

  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010

    hair 3/10/10

    This is the current state of my hair. Please ignore the bags under the eyes.

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited March 2010

    Nice 5 o'clock shadow Melinda ~ it is coming in nicely.  You are looking good girl !

    :)
    Hugs ~

    Alicia

  • micheleboots
    micheleboots Member Posts: 1,993
    edited March 2010

    Now I must get a new picture like you ladies...only this one will scare the crap out of you all....

    Linda  WWWWWOOOOOOHHHHHOOOOO...great news.

    Melinda, you crack me up, you and your mascara. LOL

  • doronet
    doronet Member Posts: 342
    edited March 2010

    SherriV:  I'm still dealing with the thrush, for 2 months now (not to be discouraging). I'm on my 4th round of medication:  2 of oral pill called Diflucan and 2 of dissolving tabs called Mycelex. I found that when it was at its worse, I could eat tomato-based foods and chicken noodle soup.  The only drink I could tolerate were the sparkling waters, some flavors were good, some horrible.  It was pretty much hit and miss.  Sorry you have to deal with it, too.

    Alicia:  keep resting up and thinking about how nice it will be when those new boobies heal!!!!

    My hair is now long enough to pinch between my fingers.  DH says it's coming in fast, though it doesn't seem fast to me.  Mine looks to be about 1/2 white and 1/2 brown.  Did someone say you can't color hair for a year?!  Gad zooks!  But guess that will be a small price to pay to at least have hair.  (I'd post a pic, but it took me a long time to figure out how to put the wigged one on here.)  I think my length is somewhere in between Pam's and Melinda's.  And last night, I lost the last of my eyelashes with the exception of one, and am still slowly losing eyebrows.  (And I'm 4 weeks past chem and in my 2nd week of rad.)  go figure.

    Linda:  great news on the tumor sizes!!!  Wonder if going from 11 to 1.5 is a record?!  That's incredible!

    My rad session yesterday was almost canceled due to machine problems.  Tech called to tell me and said I'd have to add a day on to the end of my rad treatments.  I was really upset but didn't tell her.  I just hung up the phone really quickly.  I was in tears then because not only did I not want to extend this crap, but it would actually have added 3 days, since my last day is on a Friday and that would add Monday. Well, she called back later and said they could work me in at the end of the day if I could come in.  DH volunteered to take my son to his bi-annual physical so I could go to the session.  Was very glad to get it that day after all.  Still can't seem to make a routine out of these trips there yet, though.  Still get very nervous before going and the only reason I can figure is that it's the whole hospital thing and the getting undressed and being exposed.  You'd think I would just compare it to the chemo and be grateful.  Oh well.

    Happy Thursday (if it's Thursday where you live. Smile)

  • doronet
    doronet Member Posts: 342
    edited March 2010

    Guess I need to post more often:  they are always so long when I do!

  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010
    Nette: I can completely understand about adding that weekend to the rad schedule, something like that would have set me off. If you were planning on being done on a Friday, you probably had a big mental party planned. I am glad they got you in.
  • Sherri_V
    Sherri_V Member Posts: 159
    edited March 2010

    Chemo last week was the toughest so far.  On top of the chemo, I also caught a cold and have that case of the dreaded thrush.  I haven't been able to sleep for days.  My dr. called in prescriptions earlier this week.  I am on antibiotics, etc.  The good news is that I finally had a full night's sleep last night.  The bad news is that my oncologist just called and said my weekly blood work results were in and not good.  My white blood count has dropped from 10.8 pre-chemo to 1.7.  My sister is picking me up in a bit to take me to get the neupogen shot.

    How bad is 1.7??

  • Melinda41
    Melinda41 Member Posts: 672
    edited March 2010

    Sherri: the lowest my WBC's got was 2.3 and I never got the shot. I stayed in the 3s during AC. Get some rest and let the meds do their job. Sorry you are in a rough spot, but this too shall pass.

  • RedheadPam
    RedheadPam Member Posts: 98
    edited March 2010

    Ladies - thanks for the kind words!  I feel like my hair has really taken off -- like I can almost watch it grow. I do have the "duck fuzz," but I don't want to cut it off, since it kind of fills in the spaces.  My onc told me as soon as I have enough hair to dye, to go for it.  Believe me, I will!

    Melinda - Looking good!  I have bags under my eyes big enough to pack for a trip, so no worries.  It seems like about 2 weeks after the end of rads, my hair really started to come in...you'll get there!

    Cafelovr - AWESOME NEWS!  Sending you thoughts for maybe even more shrinkage and easy surgery!

     Sending warm Springtime hugs to all...

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