Starting chemo November 2012

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  • maryah930
    maryah930 Member Posts: 322
    edited January 2013

    When did the common cold not become the common cold? Starting coughing up bloody sputum, headache, chest burning and so painful. No fever. Was told to go to the ER. No CXR, but a CT scan instead. No standard blood tests, but all sorts of tests, including cultures. 4th round is supposed to be this Friday. Cross your fingers! Finally really hit home I have a new normal... Yes, I am crying because this is so not me, but now I have a new me I have to get to know and accept. :(

  • michellej1980
    michellej1980 Member Posts: 342
    edited January 2013

    Aw I'm so sorry. It's so unfair that we have to deal with this crap at all never mind all the nasty unexpected complications. I hope you recover soon and are okay for #4 on Friday. Keep us posted. 

    Hugs

  • michellej1980
    michellej1980 Member Posts: 342
    edited January 2013

    Ladies - I found something that tasted good!! Warm croissant with Nutella! Yummmm.

  • 5LuvBugs
    5LuvBugs Member Posts: 506
    edited January 2013

    Michelle I'll try the nutella, my grandkids have a jar here...

    Maryah - this sucks, now don't cry it will pass and NO, this is not your new normal - that will come back for all of us eventually.  Hope your tests come back ok.  I still have a cough (since Jan 1) but no chest pain.  Listen, if your on antibiotic they will postpone your treatment for a week and you get a recheck from your Onc - don't be upset, that just happened to me...Now I'm done!!! Keep us posted...

    Girls, I am wondering if we have colds at all - I'm thinking this is all part of our chemo - lots of us have been having "colds" coughing, runny noses - this has to be another side effect from chemo, what do you think?

  • Megan2
    Megan2 Member Posts: 70
    edited January 2013

    yes, i think some of it is the chemo, but then all of our bodies are also more prone to catching a cold, so colds can lead to infections more easily. marayah, i hope the antibiotics kick in quickly and you feel better. as much as putting off #4 would be awful, so would adding chemo on top of a chest infection which could then get worse... old normal will be back soon, for all of us.

    in case anyone needs a laugh, am i the only one who gets ferocious gas from the stool softener syrup? seriously, i work in a closed office and it is a very embarassing situation waiting to happen. kids can laugh about it, but will my coworkers? what do i tell them, chemo farts? sorry?

  • txjunebug
    txjunebug Member Posts: 212
    edited January 2013

    Maryah - I hope this passes quickly.  Was your WBC low before this cold?  Luvbugs is right this is only temporary.  We will kick cancer's butt and we will be a stronger better version of ourselves!!!  Sending you hugs.

    Megan - Miralax does the same thing to me.  Lots of fiber in diet too so double whammy.  I sit near several men who I swear pass gas at times.  Thankfully I'm working from home right now so I'm the only one hearing the chemo blast.  Might have to paint the walls if this keeps up because the fumes are going to peel the paint off them soon!!  Wink

  • 5LuvBugs
    5LuvBugs Member Posts: 506
    edited January 2013

    You girls are making me "piss my pants"  Now I on the other hand have passed the contstipation/gas stage and am in the gotta go,gotta go,gotta go right now stage - barely make it.....Peel the paint heck - my husband wants me to knock the walls out Surprised....Remember laughter still is the best medicineWink

  • Sickofpink
    Sickofpink Member Posts: 190
    edited January 2013

    Does it seem like anyone else alternates good days and bad?



    Today is day 12 but my face is horribly blotchy and hemmorhoids are like knives (too much of good day spent sitting at desk i guess) and achy breaky legs! Eyes and nose starting but not a cold....

    Hang in there everybody!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2013

    Sickofpink~This may sound crazy, but I've found that Vicks Vapo Rub is great for hemmroids. It feels warm when you first apply, but within about 15 seconds you will feel a cool soothing somewhat like a cough drop. It's hot when you put it in your mouth, but immediately gives that cool breath effect.



    I've used this for years and always had good results.



    I hope you get relief soon.



    Blessings

    Paula

  • politicomama
    politicomama Member Posts: 187
    edited January 2013

    Oh Sick, I have had the roid issues on and off...  praying that you get relief soon.  

  • txjunebug
    txjunebug Member Posts: 212
    edited January 2013

    Sickofpink - I hope you get some relief soon. Seems like I have a good day then a bad one. Everyone expects you to just have bad days for a week or so then switch to feeling better.  I thought I was the only one on this alternate cycle.  Good day then bad day then maybe a couple of good followed by some bad days. Just can't seem to have a full week of feeling normal in between round 3 and now 4.

     The only thing that helps with the achy legs for me is a long soak in my jetted tub BUT doctor said to stop them immediately.  Bad for neuropathy and the hand and foot syndrome.  Maybe it will help? 

  • Sickofpink
    Sickofpink Member Posts: 190
    edited January 2013

    Thanks megan and tx and soteria and all, vicks? Will try if not bleeding..yes we need to walk everyday! . hmmm baths help but hope it doesnt approvate the neuropathy tx, hmmm... Getting dressed only to see therapist today.. (Have appts/work the rest of the week) back to bed after ... 48 hours of sleep sounds amazing...scary to play the genetic numbers games... And shrinking boobs from rads - they dont tell us this stuff on purpose..,,



    Feel better everyone, fingers crossed for more good days ahead....

    Xo

  • Megan2
    Megan2 Member Posts: 70
    edited January 2013

    I am on the good bad cycle too. Yesterday I had energy, today I am falling asleep in my chair at work and feel like my head is empty. It's 2pm here, and I am not able to do a single other task. I keep forgetting what task I am working on and meanwhile, my teeth ache and my food is sitting at my solar plexus causing me annoyance. I just want to sleep. But you gals make me grateful I don't have hemorrhoids or that awful hand foot thing.

    Thankfully for me, in this country, Wed is Thursday, so tomorrow is it and then weekend. I promised my kids I would get off the couch soon, so I hope I can keep the promise... I am looking forward to leaving for Sinagpore for radiation  because I will alone and can sleep all day... in a hotel room this time (not my sister's busy house)... total bliss.

    Hope all you guys feel better soon. And that the editing is progressing despite the physical discomfort, Sickofpink.

    Hey - for those of you who were in school, are you back in coursework again? Is that going ok as the chemo makes you so tired?

  • 5LuvBugs
    5LuvBugs Member Posts: 506
    edited January 2013

    Megan, how long is your radiation schedule and will you have to be staying in a hotel room ?  I give you so much credit girl..Enjoy your peace and quiet..

  • keetmom
    keetmom Member Posts: 432
    edited January 2013

    5 days until my last chemo...I have actually been feeling ok the last few days...other then being tired...but that is ok because it is SO cold here so I am laying low...luckily my hives seem better....but I tell you I am really missing my hair with this cold...cant wait for it to start growing back...Just  a few weeks I keep telling myself!

  • txjunebug
    txjunebug Member Posts: 212
    edited January 2013

     I should be working but I don't have the patience or desire to deal with any of their issues today.  I have some SE going on .  Just don't seem to want to do anything lately.  Don't go anywhere because the flu is extremely bad here and I'm afraid of catching it.  I need to find something to pick up my mood but really feel like sitting on the couch and do nothing. 

    Is there such a thing as chemo blahs?

  • politicomama
    politicomama Member Posts: 187
    edited January 2013

    It sounds like we all have the mid week blues!  It is freezing here too, but I gearing up for the bi weekly girl scout meeting this afternoon.  The new semester starts for my students today so I am trying to keep them or get them motivated to start working (I work with at risk truancy kids).  I go for weekly taxol two tomorrow.  Hoping I don't have a reaction so the premeds can be dropped next week.  Anyone else have the stinging neither regions when the steroids are delivered through iv/port?  I may have to take and Ativan just to go tomorrow because of this.  If I wouldn't have been drugged up on Benadrly already I would have flown out of the bed! We also meet with genetics tomorrow. 

    I was so proud of my almost 10 year old daughter yesterday.  She understands that my mil is BRCA positive, which means daddy and she could be too, plus with myself ( I am neg.) and my mom....  I explained why we were meeting with them and that it was so she and her brother had all of the info they needed as adults to make educated health choices.  She looked right at me and said "mama when I turn 18 I want to be tested too because I do not want to go through this."  Made me cry how mature she has been all throughout this.  It then provoked a good discussion on the Miss America contestant. 

    Wishing everyone an easy side effect free day.  Stay warm!

  • Eleni
    Eleni Member Posts: 130
    edited January 2013

    I spent the whole evening yesterday at the hospital...as a visitor. For the first time. A friend broke her leg in a very ugly way and she called me. She's also a foreigner here, with no family, her partner is traveling. So I was there with her yesterday and today but now I'm so tired.

    I came home and went straight to bed. I'm still tired.

  • michellej1980
    michellej1980 Member Posts: 342
    edited January 2013

    I take oral dexamethasone but years ago when I was being treated for Hodgkins I used to get IV dexamethasone as an anti-nausea med. I didn't sting but it used to really itch down below! I was too embarrassed to say anything to the nurses and they didn't warn me, but I used to sit there wriggling around for 10 mins till it wore off! 

    when I was at the hospital for TC #3 last month I heard a nurse warn another lady about it so I only just realised that this was normal! How bizarre! 

  • Sneakychiquita
    Sneakychiquita Member Posts: 292
    edited January 2013

    Hi ladies,

    If you've got a few minutes and want to help a fellow BC gal, please visit the thread "Let's Help Ann Today! - author of But Doctor I Hate Pink blog".  There you will find instructions on how to vote for her blog via Facebook or Twitter.  She'd like to win the top prize and put the $$ towards her son's education.  I've been doing it daily and really hope she comes out on top.  You can still vote without anything showing up on your FB newsfeed.  

    I'm on Day 7 (round 4 of AC) and am finally feeling the chemo fog lift.  The fatigue hit me way harder this round and I was pretty much bedridden for 3 days.  Yesterday I tried jogging (at the walking pace of somebody 40 years older than me) and was completely overwhelmed by how little I had in me.  I'm heading out for a jog now and hope it goes better.  Although based on the fact that I keep laying down on the kitchen floor in between chores I'm not all that optimistic.

    We're almost there, right?

  • Loafer
    Loafer Member Posts: 121
    edited January 2013

    Hi ladies -



    Wishing you all well with minimal SEs. Sounds like many of you are struggling with flu, colds, low BCs and fatigue.



    I just got back from another business trip to Florida and I'm wiped out. It's now been 3 weeks since last treatment and I'm experiencing swelling in ankles and feet. My ankles look like elephant ankles - made me nervous to fly home!



    I also was randomly selected to participate in the accelerated rad trial. Rads will be over three weeks with boosts. Starting within a week or so. Will let you know how it goes.



    Sneaky - will help out Ann



    Hugs to all!

  • maryah930
    maryah930 Member Posts: 322
    edited January 2013

    Sneaky ~ I've been voting for her blog every day for the past couple of weeks.  Love her blog.  My husband reads and votes on it as well.  

    Was in the ER Monday night with blood-streaked sputum, loss of appetite, short of breath, fatigue, etc.  After many blood tests and a CT scan, the final diagnosis was severe bronchospasm (the cough cause broken blood vessels; hence the blood-streaked sputum) with acute bronchitis.  No antibiotics or fever, so called the onc today and was given the okay for my final round tomorrow if blood work comes out okay.  Cross your fingers, toes, and anything else you think will help, please!!!! Cancelled my business trip to Omaha and SLC and have just stayed in bed.

  • Sneakychiquita
    Sneakychiquita Member Posts: 292
    edited January 2013

    I've just crossed the few remaining hairs on my head for you, Maryah.  And so glad to hear you're voting.

    Please vote, people!  Ann's in the lead, but just barely.  You know how sometimes you just need that little something to boost your morale? I could see how winning this might be one of those things for Ann.

  • 5LuvBugs
    5LuvBugs Member Posts: 506
    edited January 2013

    sneaky I just watched Ann's video, I cried and then I voted...She is a winner either wayKiss

  • txjunebug
    txjunebug Member Posts: 212
    edited January 2013

    Sneaky - Just voted. 

    Maryah - hope your feeling better.  Got fingers and toes crossed for you!

    Chemo blahs continue here.  Frown

  • Eleni
    Eleni Member Posts: 130
    edited January 2013

    Q: how long does the SE of taxotere "to feel as if you have a cold" last?

    (I've to go through 2 more of these, I almost want to give up)

  • Eleni
    Eleni Member Posts: 130
    edited January 2013

    Yesterday I went to a gathering in honour of a good collegue of mine who's leaving with pension. I managed to get dressed, put make up on and my wig.

    Once there, someone told me: "You look healthy".

    Me: speechless....what can I say? The stupidity of people is immense.

  • Sneakychiquita
    Sneakychiquita Member Posts: 292
    edited January 2013

    Eleni - I try to look on the bright side with such comments.  Either (A) I've done a really good job with my make up, or (B) they're trying to be nice.  As long as their hearts are in the right place then I like to cut them some slack... mostly because I'm sure I said similar things when I was on the other end of the situation Embarassed

    5LuvBugs - Did you watch the Soul Pancake video?  I watched Ann's and everyone else's one night... heartbreaking and beautiful at the same time.  I have lots to learn.   

    So happy to hear you ladies are voting for Ann's blog.  Please try to do it every day if you can.  And spread the word if you're active on other threads!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2013

    Eleni~I think people are looking for ways to compliment us or make us feel better. They have NO idea what goes on behind the scenes...amputation, tests, tests, and more tests, chemo, SEs, hair loss ( not just the head, but the whole body ), rads, Bloodwork, fatigue, fear, knowing we will always be looking over our shoulder for BC to rear its ugly head again.



    Before dx I thought BC was BC. End of story. I had absolutely no idea what's involved.



    That person probably wanted to convey to you, "considering what you're going through, you still look good."



    My Pastor's wife came to me at church on Sunday and asked how I felt. I said, " I'm having chemo fog, but otherwise ok." It was only day 3. She replied, "You certainly look pretty."



    I'd rather people think I look good than think I look like I'm dying.



    Blessings

    Paula

  • michellej1980
    michellej1980 Member Posts: 342
    edited January 2013

    I think I've asked this before but does anyone else get sore, runny eyes? I think it's the Taxotere. I have had it in week 2 of my last two cycles.

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