January 2013 chemo group

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  • martha323
    martha323 Member Posts: 79
    edited February 2013

    Sheryl,

    Good morning to you as well - We're in the same time zone and I often see your early posts. I hope that your day today is much better than yesterday. I'm glad that your Angie was by your side. My ancient black cat, Buddy, often senses when I'm down and out and he curls up right next to me. He likes to hang out in the same room, but he isn't ordinarily a lap cat.  Prayers and Hugs, Martha

  • shawkins64
    shawkins64 Member Posts: 8
    edited February 2013

    On Monday through Friday at 6:30 am (EST) I join my church Changing Lives Christian Center (Columbia, SC) on the prayer line and it gives me a little extra pep in my step every morning as I go through this journey.  The devil has meant my diagnosis of BC for bad but God has told me that he is going to use it for good.  I know that I will be a testament of how great God's power is, if you only allow him to hold your hand and walk by your side during this journey you will see that too.  If anyone would like to join us on the prayer line the phone number is 605-562-3000...Access code is 869575#...May God bless each and everyone of you!

  • MandyNJ
    MandyNJ Member Posts: 73
    edited February 2013

    Good morning ladies. I do hope you all are felling better and wishing those going today to have minimal side effects.



    I *think* I feel better today than yesterday in terms of wooziness but I cannot eat. I know I need to, but the thought is enough to make me want to hurl. I think I may call the doctor. I couldn't stomach my Fage yogurt. I was able to get a mixed fruit cup in but had to leave all the pears behind.



    I think my husband will get me something with an egg on it as he swings back from dropping the kids at school.



    I hope I'm not being too whiney. You have a lot more experience with this and I value your help/ideas.

  • honeybair
    honeybair Member Posts: 746
    edited February 2013

    Mandy, since I am on the same chemo drugs as you, hope I can help you.  I too had nausea and took Zofran and Compazine which did help with the nausea.  Constipation is a miserable side effect for me as well so I take Colace and Miraaox twice daily.The MOM I took the day of treatment did nothing, so I was advised to drink half a bottle of magnesium citrate and that finally opened the pipes.

    I was unprepared for the tiredness, sleepiness and misery that the AC and Neulasta caused.  Chemo week is just hell week.  At least we know what to expect.

    Hang in there with the rest of us.  We will all make it.

  • smethot
    smethot Member Posts: 161
    edited February 2013

    NO such thing as whiney, Sweetheart...it is what it is and every one of us deals with things differently.  You should never apologise for how you feel.  And i hope you feel really better, really soon...and the rest of my bad SE sisters, too.  May your tomorrows be better...and better...and better...but don't apologise for how you feel.  For example, i feel perfectly fine physically today (and yesterday) but i'm now starting to do the funky-chicken thinking about the loss of my hair...impending...t-minus 7 to 10 days at best and counting.  Like it makes sense to obsess about THAT through all of this???  Really?  Carly Simon is singing in my head again...I know most of you are past this stage and have debuted your scarves, hats, wigs and beautiful bald heads but now that its actually HERE, i'm feeling quite sad.  Appt is on Sat to cut my current hair into the Susan Powter spikey-do and get my wig fitted- its in and the colour match is great. 

    I think i'm gonna go back to work on Monday with WIG (i've been working from home for a week to avoid what appears to be tuberculosis running rampant through the office) and even that is giving me the screaming horrors.  Someone here said something (and my brain is not letting me remember who but THANK YOU!!!)- when people look at you they expect to see hair and they do...not the wig.  YOU feel self conscious about the wig but everyone else just sees hair.  But the vanity of the situation is killing me...i have thick, very blonde hair that was way down past my bum for 20 years and while its grown progressivly shorter in the last decade, it still defines me to a ridiculous degree.  And I know i'm not saying anything you ladies haven't already internalized but i feel pretty damned sad.

    That said, to quote Galaxy Quest, "never give up- never surrender!"  Its HAIR...i'll get over it and i refuse to cry over hair that will come back...i'm VERY OPTIMISTICALLY expecting to sport a headcover-free convict cut (1/4 inch???) for my b-day at the end of July.  Would it help anyone else to pick a "goal" date or time or event to focus on?  Or am I just being wildly optimistic again???  I also find it helpful to read the forums that are ahead of us...they've DONE IT and it is doable.  Soon, it will all be a bump in the rearview mirror...xoxoxoxo

  • Nicole503
    Nicole503 Member Posts: 295
    edited February 2013

    Happy Valentine's Day, to a group of the most beautiful women I know ~ inside and out!

  • Bryona
    Bryona Member Posts: 214
    edited February 2013

    shannon, is today's pug getting ready to fly or heading out for a glamorous drive with the top down? Just wondering. As for the hair thing, I think it's like everything else in this ridiculous journey: The waiting is the hardes part. (Did Tom Petty have bc?) Once my hair started to fall out, I buzzed it down to about 1/4 inch and stopped worrying about it. Up to that point, I was checking constantly. Of course, I had an advantage over many of the Bellas: I really don't like my hair to begin with! Even so, it was stressful. So cut yourself some slack, honey, and remember that Carly can't be singing to you because she's singing to ME! Shoot, I don't think you'd even been born yet...

    Mandy, yes to everything Shannon said about not being too whiney. My therapist once pointed out that if I apologize for talking about my bad feelings, I may unintentionally make other people feel that they shouldn't share theirs. So, for the sake of unburdening yourself AND of giving your sisters permission to vent, I say let it out! I hope you find some palatable food today, and do remember that many little snacks seem to work much better than a few meals. Hugs, honey.

    Well, I still don't like AC #3, but as honeybair said, chemo week is hell... but it's just a week, right?

  • Skigirl72
    Skigirl72 Member Posts: 478
    edited February 2013

    Mandy- I had to bump up the colace to two pills for a few days while I was taking compazine. Compazine was the one that worked flawlessly for me the last two rounds. I haven't bothered with the others. The MOM was the other thing that saved me. Don't take too much of all of this at the same time or you will be tied to the potty... There is a tea Smooth Move. Here is a link. I think you can get it at your local drug store.

    https://www.google.com/shopping/product/1753483616090536921?q=smooth move tea&hl=en&client=firefox-a&hs=SzM&rls=org.mozilla:en-US:official&bav=on.2,or.r_gc.r_pw.r_qf.&bvm=bv.42452523,d.dmQ&biw=1920&bih=894&sa=X&ei=zQUdUfTXH8i80QGvwoDQCw&ved=0CFQQ8wIwAA

    Martha323- Heading to the bar friday morning... today is my day of anxiety. I know exactly what going to happen... this will be round #3 and I still get a little anxious the day before... I need to learn how to breathe...

    Good luck to all of us! Hoping for minimal SEs for everyone!! Fight on warrior sisters!

  • smethot
    smethot Member Posts: 161
    edited February 2013

    Today's pug is the Grace Kelly of pugs, scarf on, shades on and ready to criuse with the top down.  Unfortunately, its overcast and teh weather-jerk is predicting snow today so the convertible isn't really an option.  Maybe Lee can cruise in So Cal for all of us snowed in today...

    Glad you're back, Bryona...hope you're feeling more alive...

  • Nicole503
    Nicole503 Member Posts: 295
    edited February 2013

    Bryona ~ AC #3 week is hell.  Wishing you all kinds of goodness and kindness.  You will emerge from it.  Any remaining pesky breast cancer cells won't.

  • jessica57
    jessica57 Member Posts: 11
    edited February 2013

    I'm new to this forum and feeling a little anxious.  Just completed my 2nd round of chemo last Thursday.  Now I feel like I have the flu with sinus headaches, runny nose, stuffy head, muscle ache etc.  Stomach is doing very well.  Does anyone know if this is an allergic reaction to the chemo or just the side effects, or is my immune system slow and I did catch something? I feel really stupid not understanding any of this. I can understand the loss of stamina and energy over time but does anyone know if I will react the same way next time?  (the big #3 is in 2 weeks)  Really scared but trying to be brave.  I only have 2 more treatments of the A/C then it's 12 weeks of Taxol.  Will that be any better.  They have me on Decadron which is making me crazy.  The PA told my I won't be on Decadron with the Taxol.  HELP!!!!

  • LeeA
    LeeA Member Posts: 1,660
    edited February 2013

    Shannon, I'll don my shades and ski cap and think of Pug Kelly when I hop in the trusty Prius and go for my Neulasta shot this afternoon.  Also, re: the hair - yes.  I obsessed.  And obsessed and obsessed and obsessed.  It bothered me more than losing my breasts.  There.  I said it.  And I didn't have great hair and never have.  It just always felt like my hiding place (yes, I'm weird - as has been previously established). Part of the post two chemo experience was all tied up with the hair.  My scalp felt like it had been pounded with a ball peen hammer and in whacked out Britney Spears fashion, I took my husband's beard clippers to my head and made it even worse but it did alleviate some of the scalp discomfort.  Fortunately, I didn't go so far as to brandish an umbrella at anyone (but hey, give me time).  All that said, I am with you all the way on the hair grieving process.  

    Bryona, hoping you feel better today!  Thought about you so much last night.  Also, I love what your therapist said about unburdening. 

    Mandy, re: getting things down - have you tried Jello?  shawkins mentioned it in one of her posts and I've kept it on hand since.  Last night I added a dollop (that word makes me think of an annoying commercial we used to have out here) of Fage to the top of the Jello and it was pretty good.  Also, an egg sandwich sounds good as well!  

    SherylB, thank goodness for Angie!  Hope you start feeling better asap!

    Nicole, I continue to love the gems you put forth in your posts; i.e. "You will emerge from it.  Any remaining pesky breast cancer cells won't."  Happy Valentine's Day back to you.

    Skigirl, your post is now in the screenshot gallery!  I hope things are going well at work this week.  Also hoping you're feeling better. 

    honeybair, perfect description:  "chemo is just hell week."  The Discovery Channel should do a special - we could put shark week to shame!

    Martha, so glad Buddy is a sentient cat and companion!

    Wishing everyone the best day possible given the circumstances. 


  • LeeA
    LeeA Member Posts: 1,660
    edited February 2013

    Welcome, Jessica.  I don't know anything about the Adriamycin combo but so many here do so I'm betting you'll get some insight from the others.  Congratulations on being halfway through AC!  Are you keeping a chemo diary/journal?  I've found it really helps me keep track of what's going on when I look back and try to remember how I felt on a particular day - however, I also know full well that my body is not completely my own these days and can pull all sorts of surprises.  My "diary" is very short - just a few sentences on how I felt that day - what tasted good - what didn't feel right, etc.  I have two ways of dating each entry - i.e. 

    February 13, 2013 - (Day One/43) 

    February 14, 2013 - (Day Two/44) 

    The "day one/two" part is the day of the actual cycle.  The numerical entry marks the number of days since starting chemo.  

    I have never been a calendar-keeper, journal-keeper, diary-writer, date "rememberer"but something about chemo has really put me on track.  

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

    Jessica~I had the sinus issues with AC 2 & 3, but I just had AC 4 on Friday and that has finally gone away. I don't know if its just a side effect or from losing the nasal hairs.

    I went to the dollar store and got a generic sneezing, runny nose, sinus pressure pill for under $3. It helped a lot.



    I'm glad to report, that so far on day 7 after final AC , the SEs don't come close to what I had with AC #3.



    Blessings

    Paula

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

    Shawkins~Thanks for sharing about the prayer. The ladies in my church meet in the prayer room on Thursday mornings for corporate prayer. I called Pastor's wife, Miriam this morning to ask for special prayer for my legs that are so swollen and painful. I can feel that pain leaving my body even as a I type this.



    When I was diagnosed I asked my Prayer Warriors to pray that through his journey, I'd be a blessing to someone else, and that Above All...I Glorify God!!!!



    I have complete peace over the cancer. After all, I was Healed on a Friday Over 2000 Years Ago!!!! By his wounds, I was healed. I peter2:24.



    Blessings

    Paula

  • smethot
    smethot Member Posts: 161
    edited February 2013

    Hey all!!!  Last of my tests (the abdominal/pelvic and the dreaded transvag) came back ALL CLEAR!!!  Woo hoo!  Headin' into a long weekend here in Canada (Family Day), have an awesome weekend menu planned of homemade pizza, glazed ham and fixings and gooey baked fiorelli pasta (sorry for those of you with food ills) and feeling good!  Here's to all of you...my best to everyone and all the love, hope and support you need.  xoxoxo

  • jessica57
    jessica57 Member Posts: 11
    edited February 2013

    That is a good idea.  I will start keeping a chemo journal. Thank you Paula

  • jessica57
    jessica57 Member Posts: 11
    edited February 2013

    Does anyone know how I display my diagnosis and treatment.  I went into my profile and clicked on treatment and set it to public but it still doesn't display.  Any advise?

  • jessica57
    jessica57 Member Posts: 11
    edited February 2013

    Never mind,,, I guess it is displaying

  • SherylB
    SherylB Member Posts: 450
    edited February 2013

    Shannon,

    I too am hoping for the boot camp buzz by my b-day July 21st.

    Sheryl

  • smethot
    smethot Member Posts: 161
    edited February 2013

    I'm July 26th, Sheryl.  When are you finished chemo?  With no issues (knock-on-wood and all that twaddle!!!) my last treatment should be May 16th...heading into our long weekend here in Canada, Victoria Day...the harbinger of summer.  Bring on beers and tank tops and warm weather and planting my flowers and garden and growing me some HAIR!!!

  • LeeA
    LeeA Member Posts: 1,660
    edited February 2013

    Hear, hear to hair!  

    My son may be coming out in August with a friend.  I would like to pick them up from the airport without a wig, 99 Cent ski cap (tuque) or Buff.  

    Today a man came to check on our heating/air conditioning and I let him in wearing one of my styling new 99 Cent store caps.  Unbeknownst to me, the little plastic hook tag was still perched on top.  Ha ha.  Why this strikes me so funny I don't know - well, maybe it's because he said "is everything okay?"  LOL!

  • LeeA
    LeeA Member Posts: 1,660
    edited February 2013

    Congratulations on all those clear scans/tests/vag explorations, etc., Shannon!

    Scanxiety be gone!

    Poutine is not on the celebratory menu??


    ETA:  I think poutine was discussed on another thread - I have a guy friend I've never met who lives in BC and loves that stuff.  And Tim Horton's coffee.

  • Bryona
    Bryona Member Posts: 214
    edited February 2013

    jessica, I'm also on AC (just had my 3rd round yesterday). I'm on a dose-dense schedule (every two weeks), which is a little different from you, but I also got sick after round 2. It was the worst cold I've had in 20 years (or maybe ever!), but it was just a cold in the end. It isn't surprising that you would catch something now, since you're at your nadir white cell count. Keep an eye on any fever; you know if it goes above 100.5 you should call your MO. And call them even without the fever if you're worried or looking for suggestions for treatment. They may want to see you; mine wanted to do a full exam and chest x-ray to rule out pneumonia or other bacterial infections. Hugs to you, honey. A cold in the midst of this seems like adding insult to injury, but this too shall pass.

    Nicole, you've said it exactly right. Die, insurgents!

    Lee, how's your crack monkey this morning? I'm posting the picture; we haven't seen him for a while.

  • Bryona
    Bryona Member Posts: 214
    edited February 2013

    Lee, mmm... poutine.... Boy, I hope that sounds good when I'm done. I'm heading across the border to drown in it!

    Shannon, woohoo for clean scans! Hooray for Warrior Nodes!

  • Italflamingo
    Italflamingo Member Posts: 9
    edited February 2013

    Hi everyone

    Haven't been on here in awhile. So I completed my first cycle of ac now on to taxol and herceptin. For some reason I'm nervous. I conquered the ac pretty well. Any tips?

  • smethot
    smethot Member Posts: 161
    edited February 2013

    Poutine is awesome...but honestly, you really have to go to Quebec for the real-deal.  It HAS to be cheese curds.  And the fries HAVE to be double fried (something my American friends understand in spades- you guys will deep fry anything...pickles?  Mars bars???  Bring on the chicken fried fat-bastard!!!)  And the poutine gravy has to be thick and dark and meaty...with no meat...its an art the Quebecois have PERFECTED.  Now i'm hungry...thanks.

    And don't even get me started on Tim Horton's coffee...here in Ontario, there's a Tim's on every corner...you are ALWAYS within walking dostance of at least 3 Timmy's.  They are in hospitals, grocery stores, hockey areas (yeah, we like hockey, too) but it is really THE BEST coffee...Starbucks be damned...and sorry Crispy Creme, the donuts are better, too!!! Now the complete shit thing is, i can't drink my Tim's since starting treatment.  I drank one small and thought my heart was gonna pound right outta my chest.  So i am in Tim Horton's coffee mourning every morning...until treatment is over...then i'm growing me some hair and getting me some COFFEE, damn it!

    p.s.  Love the Crack Monkey

  • Skigirl72
    Skigirl72 Member Posts: 478
    edited February 2013

    I went to work last night. I proudly wore Cousin It. Everyone loved what I did with my hair. LOL. I had a real hard time keeping my laughter at a minimum. A bunch of people obviously knew it was a wig. Some of the younger guys liked my 'stripper hair'. It was very amusing and just what I needed. I obviously was anxious about going back and they all made it ok. So, all in all it was a good night and we were very busy! I really did feel like the new girl. It took me a bit to get my groove on and then all of a sudden it was like... "she's back!!" It's nice to be working again and now I need to tame the germaphobe in me. I bought a gallon size purell to leave behind the bar. lol

  • LeeA
    LeeA Member Posts: 1,660
    edited February 2013

    Skigirl - I loved reading your post!  I've been wondering how it went and it sounds like it was a triumphant return for both you and your customers (and co-workers).  

    I hear you on the inner germaphobe.  They're talking about this stranded cruise ship on CNN and all the yuck stuff that goes along with a cruise ship that's been without power for five days.  Ultimately, Sanjay Gupta has downplayed the risk of infection so I figure - wow, if those people can traipse around in that day after day...and in those close quarters I guess I can be a little less paranoid (or something).  Anyway, it has kind of quelled my inner germaphobe (probably only for five minutes or so!). 

    =

    Bryona - I hope you're feeling better today!  I've been thinking about you since last night.  My inner-crack money has relaxed somewhat but I have managed to whip through today's list quite handily.  I still have to go walk the track and then get the Big N shot.  My brain feels pretty clear - which I like - but I know what's probably coming.  I've been trying to get in a lot of protein and have definitely been drinking more water than usual. 

    =

    Shannon - I'll take the fries but I'll take a nose-held pass on the curds and the gravy and even the coffee (I'm not a coffee drinker - unless it's all frou-frou'd up with white chocolate or salted caramel flavor or gingerbread, peppermint, etc.  In our little village/town (it's more like a village) there's a Coffee, Bean and Tea Leaf shop on one corner and now, a Starbucks across the street.  As soon as the Starbucks opened the Coffee, Bean and Tea Leaf added outdoor heaters around their outdoor seating areas.  It's the coffee shop wars!  And then there's a yogurt shop on the other corner and a very strange pajama type store (looks like a time warp from the fifties/sixties) on the other corner.  I've never been able to figure out how a pajama store can stay in business... I've never been in there because I'm not one for sleep sets.  

    p.s. Pajama sets, coffee and french fry gravy aside, it sounds like you're doing really well so far!!

    =

    Italflamingo - congratulations on making it through AC!  I had one dose of stand-alone Herceptin and it was a breeze.  I'm not doing Taxol so I can't speak to that although I am on Taxotere.  I don't know how or if they're related but apparently Taxotere is derived from a Yew tree native to the South Pacific.  From what little I have read here about women who go to Taxol, it sounds like it's easier on the system than AC.  I'm thinking I've even read that hair starts to (maybe) grow back on Taxol but really, I don't know.  I'm just the resident crack monkey :-) 

  • macyhen111
    macyhen111 Member Posts: 754
    edited February 2013

    Italflamingo, I have been on Taxol for 7 tx weekly and it's a breeze. The worst se is the taste buds and dry mouth. I still have all my hair, even some where there has never been any. It has started to shed a little bit. My worst days are days 3 and 4, I get really tired on those days. Hope you have a easy time with it too!

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