May 2010 Chemo

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  • Redbarb804
    Redbarb804 Member Posts: 299
    edited May 2010

    Summer38:  What a wonderful idea!  Isnt' amazing at how many people are out there willing to help when someone is in need.  You are really lucky to have so many supportive people in your life.  I'm a firm believer that without our support systems this would be almost unbearbable to deal with.

    Barb

  • packjen
    packjen Member Posts: 281
    edited May 2010

    Hello Strong Ladies,

    Summer - I love, love, love your co-workers.  The story brought tears to my eyes.

    Yesterday was TC#2.  Unfortunately I had to go alone because one of my twins woke up in the middle of the night with a fever and DH had to stay home with her.  I was feeling a little bummed until one of my friends showed up at my treatment unexpectedly.  Some of you may remember that my first treatment was on 5/5 and I dubbed it "Chemo de Mayo" and brought non-alcoholic margaritas for the staff.  Well yesterday I had planned to do a "Finding Chemo" (based on Finding Nemo) theme.  I just didn't have the energy to make cupcakes like I had planned.  So my dear friend Jenny showed up with a cake made of cupcakes with Nemo and Dori on it that said "Finding Chemo" and a giant stuffed Nemo and a bunch of little plastic fish and bubbles.  Basically a party in a bag.  The staff loved it.  Now I am on the hook to think of 2 more good themes for my next 2 treatments.  Any ideas?

    I did have a reaction to the Taxotere this time.  I leaned over to pick something up and suddenly got nauseous, face flushed, shortness of breath.  They immediately stopped the Taxotere, gave me more steriods IV and an Ativan by mouth.  The discomfort only lasted a couple of minutes and they were all on top of it.  The pharmacist even brought in a whole slew of vials of meds I might need and said "Every time I bring these magic meds in the room, patients get instantly better and don't need them."  It was true. So they waited a half an hour and restarted the Taxotere at a slower drip, increasing gradually.  All was fine.

    I did use my home made ice packs on my eyebrows before and during the Taxotere in the hopes of keeping my brows.  We'll see.

    Hair update -- I got my buzz cut last Friday and by Wednesday night I was so patchy with bald spots I could not stand it.  So last night I used my dog clippers and my razor and did the best I could.  There were still some hairs I could not get, so this morning I went to a local barber shop and had him give me the "mr. clean" look.  The sweet man did it free of charge.

    So now I am walking around totally bald and out there.  I have started applying a little eye make up and found a couple pairs of my grandmother's clip on earrings.  I wear a long scarf around my neck to warm me up.

    I did try to wear my wig last week.  I picked up the kids from school in the wig then took them to the library where I started having hot flashes.  I was so hot I took off the wig.  How odd it was to be carrying around a wig.  So I just stuck it under my jacket!

    Ah, how life changes.

    Jen

  • Redbarb804
    Redbarb804 Member Posts: 299
    edited May 2010

    Day: I feel so bad for you with everything you have been through.  I hope you have better luck with the new onoc.  This disease is hard enough to deal with without having idiots that are suppose to know whats going on! 

    Barb

  • patricia48
    patricia48 Member Posts: 121
    edited May 2010

    You all are so inspiring!   Pacjen, I love your chemo themed ideas and your new pic is amazing.   Summer, your underwear bearing (not bare all ) friends are so awesome.  Day,  really I am so sorry.  It takes a lot to be emotionally ready for a chemo session. In the best of circumstances, it is hard. I hope you are able to get better care soon. To all of you with children at home, and those who are working outside the home, I really am so impressed.  Nanaoftwo, I am Mimi to my 7 month old granddaughter.  Her name is Nadia Simone, she has a head full of black hair,( both my kids are redheads)! JennyB, I am so glad to learn more about you. Tell me about your kids when you can.  This disease makes no distinctions.  I am 62, and I can't imagine going thought this earlier in my life.  Heck, I can't imagine it now.  Before BC ( BBC I guess), I took no meds, did all the"right" stuff, and what can I say.  Last year my mammogram was clear, this year, Stage 3 Grade 3.  8/12 lymph nodes positive.  What a shock!   Anyway, everyday I think of all of us, and all of our collective wisdom, love, feminine energies, trials, tribulations. I think of all the people who love us, and those we love. In spite of it all, or because of it all, this group that none of us ever wanted to join, is really very, very beautiful.  

  • JennyB100104
    JennyB100104 Member Posts: 237
    edited May 2010

    Lovely words, Patricia!

    Jen, you look great, and you're so creative. Sometimes I feel like yanking off my wig too (especially when I start to sweat) but I haven't had the guts yet!

    So the latest on me, TC #2 follow-up appointment today--they didn't even draw my blood today--onc wants me to keep all the blood I can (I'm anemic and have had a never-ending period for the past 4 weeks). The bad news is she thinks I might be accumulating fluid in my lungs as a reaction to Taxotere, so I need to get a CT scan next week--if it comes back that my lungs look bad, that's a pretty serious long-term side effect, I  guess, and she's going to take me off chemo altogether. And I need to see an opthamologist for the crazy eye twitching I'm having. The fun never ends, does it? 

    It'll be my first CT scan ever. What should I expect? Any tips?

  • GolferGirl
    GolferGirl Member Posts: 121
    edited May 2010

    Hi All - Had TC#2 today and it went well.  Both my sisters came with me this time and it was nice to spend the day with them, notwithstanding the chemo. 

    Summer - your coworkers really are awesome!  I haven't really told too many people at work, not sure why.   I don't really mind people knowing, but just don't really want to talk about it, either.  Except here, of course!  Actually, I had a clean mammo 4 months before I found the lump myself, so I have been telling other women to feel themselves up, just not at work!

    Day - I can't believe all that you have been through.   I'm not sure how I would take a delay in chemo.  I hope things improve for you soon!

    packjen- I love reading your posts.  You have such a great attitude and handle all this with such good humor.  Sounds like you have some awesome friends, too! 

    Drim and others with treatments next week - Good luck, I'll be thinking of you and sending positive thoughts!

  • packjen
    packjen Member Posts: 281
    edited May 2010

    Oh, JennyB, I am so sorry about the uncertainty you are suffering right now.  I am a little surprised they didn't even take a chest xray, though.  It seems unthinkable to make you wait til next week to figure out what is going on.  As for your anemia, you should call and ask your doctor about the Slow-FE that Victoria mentioned.  My obstetrician put me on it when I was pregnant with my twins.  It is supposed to be very good and must be quite gentle or they would not have let me take it with my high-risk pregnancy.  And as Victoria says, a stool softener is a must with iron supplements.

     Hang in there.  I am sending you a big-ol', bald-headed, cancer-beating hug right now.

    Jen

  • sacphotomom
    sacphotomom Member Posts: 366
    edited May 2010
    packjen you look so good nice head shape!   love all you ideas about your Chemo trips...
  • njbhwgirl
    njbhwgirl Member Posts: 295
    edited May 2010

    Day:  My thoughts and prayers with you.. All of us are counting down our treatments and a slight setback is so devastating.  Hoping your new onc. and team make it all better for you!!

    JennyB: is CT with or without contrast? if with contrast you drink this kinda yucky stuff but good news is it is all non invasive... If not, it is just like an xray..no brainer. certaintly nothing like a biopsy...Hope it all works out and you feel better soon,,btw my eyes twitch when I am extremely nervous. Maybe this is all it is. With all you are going through, my whole head would be twitching.
    PackJen:  you crack me up..You are so darn funny!!!  Maybe for 4th of July you can dress up in red white and blue..bring some watermelon, and flag cake...just a thought
    Is anyone on treatment #3 yet....I am 4 days after my second infusion.. Starting that fuzzy feeling but so far so good.  I need my neigbor to buzz the rest of my hair. I have about 2 inches left. My onc. nurse said not to shave the head but just buzz it because she did not want me to get ingrown hairs...Will be interesting to watch us all see who gets the peachfuzz back first...For me, mine will be grey(lol)
    I so admire all you young ladies with small children.  I think you are all so fantastic.  I have my granddaughter who is 10 months old living with me but I have family and friends helping me out when my daughter is working at night.
    Kinda rainy dreary day here in NJ..Okay by me, I want no heat this summer..that darn wig is hot hot enough...thank god for air conditioning
    Have SE free day all
  • JennyB100104
    JennyB100104 Member Posts: 237
    edited May 2010

    Hi Everyone!

    Jen, I'm going to start the iron pills, definitely. Onc said they were okay to take the last week before chemo, so starting next week I can take them. Are the Slow-FE available in drugstores?

    njbhwgirl, Hm, she didn't say whether it would be w/ or without contrast. From what you're describing, it sounds a lot like an MRI...

    Have a great weekend, everyone. I'm off to my son's baseball tournament. Fun! I just hope my wig doesn't blow offf... :) 

  • packjen
    packjen Member Posts: 281
    edited May 2010

    JennyB - i got my SlowFE from our local health food store.  Not sure about the drug store.  Good luck.

    Jen

  • cleob
    cleob Member Posts: 20
    edited May 2010

    Hil adies. had my second weekly taxol chemo yesterday in addition to daily study group medication (neratinib). today is my 9TH day of treatment and I still have no side effects. COULD THIS IN ANY WAY SUGGEST THAT MY TREATMENT IS NOT WORKING? HAS ANYONE HAD A SIMILAR EXPERIENCE? PLEASE ADVISE.

    My blood work was ok except with the Doctor's concern about me being slightly anaemic(strange to me). I also need advise if you've had a similar experience and it was remedied.

    LOVE YOU ALL.

  • Summer38
    Summer38 Member Posts: 253
    edited May 2010

    Packjen - You shaved head looks great! I hope my head is shaped as nicely...should find out in about a week. Right now I'm just hoping it's not covered in freckles! Also I love how you're making your treatments like little chemo "parties". What a great way to make the best of a situation!

    JennyB - good luck with the CT scan, keep us posted. And don't worry, the scan itself is no biggie. 

    I hope everyone is feeling well enough to enjoy the beautiful holiday weekend! Laughing

  • Shrek4
    Shrek4 Member Posts: 1,822
    edited May 2010

    cleob - I dont' think it means that - it just means that your body is more resilient and can cope better with toxic substances. Remember cancer cells are not exactly your body's cells anymore (not sure if that makes sense). When are you scheduled to have your blood test? You will see then that it's nto really with no SE, your blood counts will be off.

  • nanaof2
    nanaof2 Member Posts: 112
    edited May 2010

    Leanna, love the websites, thanks!  I ordered a bunch of the bandanas for summer.

    Sacphotomom - I cannot believe how rude people are,  I remember when I broke my ankle a few years ago and had to use a wheelchair in the mall, people were amazing, just knocking into the chair - no one offering to help.  Opened my eyes - big time.  I vowed I would always help, although I like to think I would have anyway.

    Fotopet, truly hope you enjoy your weekend.  I love the mountains in the summer.

    Jennyb, Leanna, and all of you ladies with children hope, you are my heros.  My children are grown and I have two grandchildren, but I come home from work to a wonderful husband and don't really have much to do.  Seriously, you are remarkable!!!!!!!

    Packjen you are incredible with incredible friends.  When is your next treatment, maybe we can come up with an idea.

    Day, I am thinking about you and sending good thoughts your way.

    On a great note, I too found out how wonderful friends and coworkers are...yesterday almost the entire staff came to school wearing scarves.  I was so touched. We took pictures after the kids left.  I will never forget the feeling of love, support and concern.

    And my ‘buzz' went as well as can be expected.  My sons and husband were great.  My youngest son clipped it short and then my husband shaved my head.   Today woke up thinking - I'm really bald.  Not wearing anything around the house, went to the store wearing a hat.

    I hope you all have a fabulous few days off. Rest and stay healthy as you can....

  • patricia48
    patricia48 Member Posts: 121
    edited May 2010

    Hey everyone.  Hope your day has been SE free.  For me, it is the 8th day since my neulasta injection and I have had a lot of bone pain, including(anyone ever have this?) swelling over the rib cage on my mastectomy site.  My ankles, legs, hips, back and almost every bone I can think of hurts.  I have gotten some relief from tylonol, but mostly from watching 8 episodes of Jane Eyre.  Ha.  Nothing like the Bronte sisters to create a mini vacation for me.  Second only to Jane Austin's Sense and Sensibility.  Anyway, I bravely kept my yoga practice and walk, although it was difficult. I am on a two week A/C chemo schedule, so I am scheduled for #2 this coming Thursday.  That should be about the time I loose my hair.  I plan to buzz it very short.  I already have a wig, and some scarves.  I did not want to shop for these things when I was feeling  so emotional.  My yoga instructor left a surprise at my door, carbonated water  and  fresh mushrooms.  How nice are theses  little surprises we get from our friends and family! Nanaoftwo, how great that your coworkers wore scarves, and that you got some pictures  of this !  

  • Ca1Ripken
    Ca1Ripken Member Posts: 1,254
    edited May 2010

    JennyB - CT is quicker than the MRI.  The pre-contrast you have to drink is a little yucky, but nothing we can't handle!!  I will be praying for a clean scan (((HUGS))).

    Cleob - I remember you saying before you were not having an SE.  You and I (I believe) are the only 2 on the taxol now.  I just finished #3.  I have NO taste buds... water tastes like dirt, and I have to add loads of salt and dressing to stuff to taste it, which is fine because my serum sodium levels are low because I have been drinking so much water.  I also have frequent heartburn.  I'm also on herceptin so those maybe causing some SE.  My hair is not wanting to stay in my head when I pull on it, but it's not coming out on its own (if that makes sense).  My taste buds seem to return on Tuesday or Wednesday before Thursday infusion... maybe you'll feel something this week- or maybe not - no SE does not mean it isn't working (wow, that was a lot of negatives).  :)  And, as Day said - you should see changes in your blood work. 

    Summer - that's an awesome story!  It made me tear up too!!  You are lucky to have such wonderful people surrounding you! 

    Packjen - LOVE the shave - you have an awesome shape head... hope I am so lucky!!!

    Day - Ugh - good luck with the new onc... that is so frustrating - I'm so sorry!

    Patricia48.... me too - clean mammo last year... actually clean mammo this year too!  Ha!  Felt my BC, and it had to be picked up by biopsy.  And, Nadia Simone - that is a beautiful name!!  I'm sorry about all of the bone pain you are having, but yay for mushrooms!

    GolferGirl - Glad you got to spend the day with your sisters.  Even if it is chemo, it's still time together! 

    Nanaof2 - you are very welcome for the websites!  It was kind of hard to find larger bandanas... most are 22" which won't go far on a bald head - and those prices were just awesome!  I can't wait to get them!! 

    So, pluggin' along... waiting for taste buds... cramming down dirt-tasting water (yum) - switched to propel this week - kiwi-strawberry!  I'm working Sunday, Monday, Tuesday night this week, having chemo Thursday -then leaving for Disney right after treatment.  My husband has things set up for him and the boys if I don't feel well.  We're staying at the Nickelodean Resort in Orlando - so it's really an amusement park in and of itself.  And, the pool has covered cabanas we can rent... learned first-hand this weekend that we are sensitive to sun on chemo - got a little burned!  Oops.  One of my friends just called too - I had her look up my labs, and my blood work is good - similar to last week, but WBC still ok.  :) 

    Have a great night - hopefully SE free!  And, ((((((((((((((HUGS))))))))))))))) to all my sisters!!!!!!!!!!!

  • nanaof2
    nanaof2 Member Posts: 112
    edited May 2010

    patricia48, so sorry to hear about the pain from the neulasta.  I have not had the shot yet, but everyone seems to get the pain, so I am not looking forward to it. Feel better...I too love watching those type of movies.

    Day, I still cannot believe what you have had to go through.  Is the new Onc. from a bigger cancer center?

    Leanna, good luck working this week and have a great time at Disney.  Everything Disney does is first class and fun, so I know you will enjoy it. Glad to hear about your blood work! 

  • Shrek4
    Shrek4 Member Posts: 1,822
    edited May 2010

    nanaof2,

    Yes, it is the same center my BS is, OU Medical center, the Hematology Oncology department.

  • njbhwgirl
    njbhwgirl Member Posts: 295
    edited May 2010

    Leanna:  have so much fun in Disney...My favorite place on earth...That shall keep all SE's away form you.. Do try to avoid too much sun and stay cool.

    well my neighbor finished buzzing my hair. Now my wig is slightly bigger so I had to adjust the tabs. For anyone getting a wig, try doing so after you cut it, I think makes for a easier fit.

    5th day after treatment and I feel UGH..

    feel like novacaine head...hopefully better tmrw

  • nanaof2
    nanaof2 Member Posts: 112
    edited May 2010

    Anyone have a rash with little blisters?  It is on my hand between my fingers, don't know if I could have touched something or if it is another SE....

  • patricia48
    patricia48 Member Posts: 121
    edited May 2010
    Hey there everyone.    Still here with the neulasta back pain.  Nanaof2, I got a rash and itching from percocet, after my surgery.  Are you using any pain meds?  I am back on it for the pain today and last night.  As long as I do not take too much, I can take it without incident.  I called the on call oncology line today because my pain seems unrelenting. Yell The dr. seemed to think it is the neulasta, but said it might only last a few days.  Anyway. my oncologist   teaches at a medical school, so I can talk with the  on call oncology residents 24hr a day.     Wishing you all the best.
  • sacphotomom
    sacphotomom Member Posts: 366
    edited May 2010

    Made a Lemon pie today ..made it using my taste buds....it was very tart..to everyone else but me  but I could taste it and I liked it...

    Hair Update  OK so I have been loosing hair everywhere ...but today I noticed that haven't had to shave my underarms or legs since Friday..so day three without shaving....my head is almost completely bald...but I have a bunch of sporadic little hairs that are refusing to leave..even if I try to pull them... guess that will give the next chemo something to attack..Is anyones else head itchy...and what are you putting on it to stop the itch?

    OK so someone wondered out loud if they were getting enough chemo because they weren't having any SE...well now I'm wondering if they are giving me to much...come on its only my 2nd chemo with #3 coming up on Wednesday...at this rate I will have no hair on any part of my body  except my right arm! Tiredness is finally starting to go away.Had a wonderful walk around the park with my DH felt really good!!

    Wishing everyone a really Great day !

  • nanaof2
    nanaof2 Member Posts: 112
    edited May 2010

    Patricia, I haven't taken any pain pills recently, but will keep that in mind.  I have not been given the Neulasta shot yet. Hoping I never need it.  Everyone seems to suffer such pain from that, they sure don't put than in the commercials.

    Round 2 for me tomorrow afternoon, I will see the Dr. first, maybe he can tell me what to do for the rash.

    Sacphotomom, I love lemon pie and love that you made it so you like the taste~

    Have a great Memorial Day everyone.

  • MNLinda
    MNLinda Member Posts: 204
    edited May 2010

    nanaof2, I never had a problem with the Neulasta, except for a slightly bruised feeling around my jaw, lasting maybe a day or two.  I hardly noticed it.  Neulasta doesn't produce that intense pain in everyone, but I think the people who don't have a problem with it don't think to mention it in their posts very often.

  • GolferGirl
    GolferGirl Member Posts: 121
    edited May 2010

    Hi All,  I'm 3 days out post TC#2 and my period has started again! And it's heavy....again.   My ovaries are so confused and now I'm getting worried about becoming anemic again.  Hopefully not, but could really do without a heavy period every 2 weeks.  Ugh.  Otherwise, just the usual fatigue.   Nuelasta shot tomorrow because of the Holiday today, but I didn't really have any SE's from that last time, so hoping that will be the same this time.  Last time, day 4 was the wost fatigue and it got better from there, so thinking I'm about to hit the worst of it tomorrow.  I had a bit of a rash on my chest yesterday, but no blisters and it went away on its own.

    Leanna - Have fun at Disney!  that should be a great distraction!

    Sacphotomom - love the idea of leamon pie.  I bet that would be great...it's really hot here in MI this weekend and lemon pie sounds perfect!  But I don't have the energy to make it :(

    nanof2 - That was so great ofyour coworkers to do that!  I love hearing about such supportive friends!

    patricia48 - a little of the Colin Firth version of Pride and Prejudice always makes me feel better, too!

  • Drim
    Drim Member Posts: 302
    edited May 2010

    Hi all - haven't posted in a while. I have TC #2 tomorrow. I hope it goes as well as #1. Should be interesting tomorrow since all the Monday and Tuesday patients will be there due to the holiday today. Laying low this weekend trying to get all my water in and just here watching the French Open. I'm a big tennis fan although I have not played in a while.

    nanaof2 - sounds like you have a wonderful support system around you between your husband, sons and school staff. I'm sure that helps a lot.

    redbard - i'm so happy you doing so well be sorry that your son's team lost the baseball game in that fashion. Another one of my favorite sports - baseball. This is actually the first year in a very long time that I had to miss softball season. Frown

    njbhwgirl - been thinking about you. I hope your mom is doing better!

    summer38 - what an amazing story about your coworkers/friends. I just kept thinking I wonder what the men were thinking. It's so nice to feel the love!

    Day - I bet you can't wait to get the new Onc. Its terrible what this doc has put you through.

    PackJen - you are so creative. Definitely sounds like the pressure is on to top yourself but it sounds like you will have no problem doing that. I am so NOT creative. I really admire you.

    JennyB - good luck with your CT scan. I had one a few years ago with the contrast and its not that bad. The stuff you have to drink is a little yucky but with all the stuff we've been going through it will probably be no big deal to you.

    Leanna - have fun at Disney. It's one of my favoirte places to go on vacation but definitely keep re-applying that sun screen.

    GolferGirl - Yikes - your period again. I keep wondering what's going to happen with mine. We are the same age and I got my period one week after TC#1. It was a little heavier than usual but not terrible. Lets see if my ovaries make one last stand.

    To all - I hope you're having a great memorial day weekend! I'll check in soon to let you know how #2 went.

    (((((hugs))))

  • JennyB100104
    JennyB100104 Member Posts: 237
    edited May 2010

    GolferGirl and Drim, how old are you? My period is going nuts, too. After TC #1 it was heavy, but then it didn't stop. Spotting until...well, today. Haven't seen anything today yet! Anyway, I'm 39 and I don't know what's going on. I had an onc appt on Thursday and he said, "Do you want me to check you?" I said, "Uh...no, thanks." So he told me that if it didn't stop, email him to let him know. 

    I'm exhausted. Baseball tournament all weekend and I'm just beat! I hope everyone had a great weekend!

  • Drim
    Drim Member Posts: 302
    edited May 2010

    Hi Jenny,

    Sorry you're having this issue. Maybe it has finally stopped now. Let's hope!!! I'm going to be 44 in a couple of weeks. They told me there was a good chance my period would never come back. I wasn't suprised to get it a week after Tx #1 even though it was a few days earlier than normal.

    I hope you will be able to get a good night's sleep tonight after all that baseball and I hope your kids had fun!

  • Redbarb804
    Redbarb804 Member Posts: 299
    edited June 2010

    I love hearing the stories about the awesome coworkers.  I also have awesome co-workers.  They formed a relay for life team in my honor.  It's this weekend, June 5-6.  Pray for good weather, no rain.  They also came to my head shaving party to support me.  They have also offered to go with me to my chemo treatments. 

    I am so sorry to hear about those of you who are having problems with your  periods.  I was very irregular prior to my treatments and now I haven't had one at all.  My onoc said that if I was menopausal before chemo I will be for sure after.  He was right. 

    Leanna I hope you are having fun in Disney.

    Day:  When do you start with your new onoc?  I hope you have better luck with this one.

    Everyone getting a treatment this week will be in my prayers.  Good luck.

    I have my 2nd treatment on Thursday.  I'm a little anxious about it, but I did great the first time so I am hoping to do the same the second time.  Did most of you doing TC have the same experience the 2nd time as the first time? 

    HAve a great week everyone!

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