Starting Chemo June 2013!?!?!

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  • annika12
    annika12 Member Posts: 433
    edited July 2013

    Day after round 2 A/C and Im so much better then last time.Im getting IV fluids and my meds with it and so far so good. Im eating and drinking oh and sleeping a lot and it sure beats puking every half hour fir 5 days. Eating cereal, mashed potatoes with peeled sauteed zuccini and apple sauce. And the best news....my lymph node tumor has shrunk from 3 cm to 1 cm in one treatment made it easier to get that yucky stuff back in my body!

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Annika, that's great news! I start round 1 DD AC tomorrow. Nervous and ready to get rolling.

    Anyone have words of advice before I get rolling?

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited July 2013

    Dyvgrl,

    Good luck tomorrow. I did not do your chemo type, so i can't speak directly to that.



    I do recommend lots of liquid, before, during and after to flush your system.

    Bring something to entertain yourself, book, iPad, magazines.

    Bring food if your center doesn't provide it.

    I brought a light weight jacket (sweater) because my room was cold...and trust me, I'm usually "hot", so it must have been really cold to the "normal people".



    Wishing you all the best on your first go around, it's "not as bad as you think".

    Pat

  • OceanWarrior
    OceanWarrior Member Posts: 96
    edited July 2013

    Hi all, 

    I've not been posting much but I'm around.  Gearing up for my final AC on Thursday.  Yes, I do find emotions can swing to the depressed side leading up to it.  We JUST start to feel better and then boom back on the train.  I try to remind myself that it is short term - even though it feels like a very long journey.  So, this Thurs will be 1/2 way thru chemo for me and we are doing same thing as last time so that mean nausea beast has been beaten to submission and I am in control.  Next is 4 rounds of Paxitaxcil (sp?).  

    We can do this.  I try to only take on as much info as I need at one time.  Today I talked to the Onc about side effects for next round.  Just wasn't ready to hear it or think about it too much prior to now.  

    Annika - great news, nice to hear.

    Dyvgrl - best of luck tomorrow.  I wish you an easy time with few and manageable side effects.  Just go with the day, the nurses will be great and before you know it you will be back home.

    Making a bunch of individual pizza's for dinner.  A few will go in the freezer for hubs for next week.  Must get myself into the kitchen.  

    Best to all of you.

  • rachel22
    rachel22 Member Posts: 54
    edited July 2013

    Dyvgrl - best of luck tomorrow. I also am doing DD A/C and so far the side effects are very manageable. I agree with the others about drinking lots of water and bring stuff to keep you busy during the infusion. And stay on top of your anti-nausea meds. You'll do great!

  • annika12
    annika12 Member Posts: 433
    edited July 2013

    I would suggest very very freak went smaller meals. Im not sure it controls the chemo nausea but sure is helping me tolerate the nausea meds much better.

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    sitting in the chair, almost done but the Cytoxan was giving me a major sinus type headache and making me dizzy so she stopped it for a few mins then will slow it down so I can get it finished. Other than that, easy peasy. Waiting for the storm to come...

  • annika12
    annika12 Member Posts: 433
    edited July 2013

    Praying for no storms for you Dyvgrl. Had major nausea puke day today....oh well cancer feels worse!!!

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Annika. Thanks! Feeling ok except for a pretty good headache. I get one EVERYTIME they use Heparin. Has anyone else had sensitivity to the Heparin? I asked the nurse if they could use something else, and she didn't know of anything other than saline. She was concerned about clotting issues at my port, so I let her do it. Now I'm paying the price. Pain killers don't help either. Just have to sleep it off. Ugh!

  • Netter
    Netter Member Posts: 107
    edited July 2013

    I just got home from my 3rd infusion.  I have been falling for no reason, dizzy, low blood pressure and onco was worried.  Said she would cut infusion way down.  Right after infusion started I got throat tightening, hot, red face, low back pain and blood pressure 80/50.  Nurse asked if I was okay and I said, "not sure".  She shut it off and went to talk to onco, while another nurse stayed with me.  Nurse came back in and said, "you are finished with chemo!!!"  No more!!!!!!!!!  I will see her in 3 weeks and later will be starting radiation.  Nurse said I could have been in serious trouble if they hadn't caught it immediately.

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Netter - was that an allergy? I started with a bad headache, then fell asleep or passed out - I woke up and the nurse said, I tried to wake you but you wouldn't wake up so I just finished your infusion. My hubby had tried calling twice but I didn't answer. I felt all groggy and dizzy after and she just sent me on my way. This shit can't be good...

  • annika12
    annika12 Member Posts: 433
    edited July 2013

    Scary Netter Glad they saw it and stopped!!! Feel better, will keep you in my thoughts and prayers!!

  • OceanWarrior
    OceanWarrior Member Posts: 96
    edited July 2013

    Netter - that sounds so scary.  Very glad they were on top of it and stopped it.  Hope your body settles down and you are feeling good.  

    Dyvgrl - passing out not sounding good.  This stuff is strong and potent, and kinda scary.  

    Me - last of the red devil today.  Went ok but took 4 pokes to find a vein to co-operate.  There is this one nurse that I've seen the seems to have more challenges than the others.  I got her today and then they switched off to a different one.  Personally I just think my veins were shy today.  Still happy not to have a port or a pic line so its all good.  Everything worked out well in the end and as always, treated so great by all the team there.  Nausea at bay, just feeling tired and fuzzy head stuff.  

    Sending good wishes and caring thoughts to all of you.  

  • KatiAK
    KatiAK Member Posts: 138
    edited July 2013

    Did Round 3 of AC on Tuesday, then came home and collapsed.  Went back in on Wednesday for a liter of fluids and some zolfran.  Felt pretty good til about 2:00 this morning.  Have been exhausted ALL day today.  Finally made it my little boys championship baseball game tonight (and they won!).  But I'm headed for bed now cuz I still have to try to work tomorrow.  Ugh!  One more AC and I pray the Taxol is easier! 

    Netter - that is so scarey!  My blood pressure has a tendency to tank too but usually a couple days after tx. 

    Dyvgrl - strange that you passed out.  Hope things get better.  Eat a lot of protein, drink a lot of water!

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Better, hope you are ok! To me that is a sign that this chemo business is not all its cracked up to be. Still have fuzzy head, slight nausea, and now insomnia. Waiting for my Ativan to kick in. Ugh! Have work tomorrow. Today I managed, but just barely. I was so so tired. Can't wait to meet with my naturopathic onc to see if I have any other options. This truly sucks! Wishing the best for everyone here. Hugs!

  • dlm425
    dlm425 Member Posts: 209
    edited July 2013

    Chemo sucks so does radiation. Well as of this week we don't have to buy the Emend because they now put it in the iv instead. Also the dexadron pills but have to say round 3 has been very hard for me from day 1 feel so nauseous and tired. I keep saying I don't want to do this anyomore. My nails are turning dark at the cuticles. When the tuck can they come up with something that kills cancer and not kill everything. Else in our bodies everyone says you cant quit you only have 5 left well I'm just so sick of feeling sick for a person who never was sick in my life. Now I'm truly ill. Feel well to all have to go her neulasta shot now. Netter hope you feel week. Dvygrl Emend.

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Feeling nauseous this morning and the added gift of starting my period. Really thought I'd avoid it but guess not so lucky. Feeling so yucky today. Please tell me this gets better!

  • Alibeths
    Alibeths Member Posts: 656
    edited July 2013

    It does get better. Xo

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Anyone having issues with hiccups? It's sooo annoying. As if being nauseous and crampy isn't enough, lets add hiccups to the mix. I never get hiccups!

  • dlm425
    dlm425 Member Posts: 209
    edited July 2013

    Hey katiak that's exactly how I feel im trying.so hard to keep.from vomiting. I took Emend decadron and smoked a little the burning king my chest and throat and stomach is so intense have any ideas I keep crying for no reason too. I don't want to do this anymore feels like forever.

  • annika12
    annika12 Member Posts: 433
    edited July 2013

    Feeling fed up too!!! Day 5 on 2 round. Heat doesn't help...... but we can do it!! It sucks but the chemo sucks even more for the cancer. I keep thinking if all the brave women before us who beat it who are healthy and back to there normal lifes. It will happen for us too. Hugs and good thoughts to all junebugs.....

  • aaoaao
    aaoaao Member Posts: 593
    edited July 2013

    Just keep reminding yourself that this temporary regimen of chemo is necessary to prevent the cancer from spreading.  Once cancer has spread chemo becomes, more or less, a permanent way of life.  I'm in that boat now and have to accept chemo as a way to stay alive.  I hope that everyone here gets through their treatments and never have to fight this demon again.  Hang in there! 

  • Netter
    Netter Member Posts: 107
    edited July 2013

    I am a little concerned that not getting my last 2 treatments may affect whether my cancer comes back or not?  Since I am triple negative there are not a lot of treatments for me.  Guess I will be in the Lord's hands.  Will see my onco in 3 weeks and we will go from there..........

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Netter, will you be doing hormone therapy? I think that will cover you just as well. It will starve out the cancer instead of destroying everything.

    Anyone have any tips for the bone pain? I'm taking Claritin but its not helping. My hips and my legs are killin me!

  • aaoaao
    aaoaao Member Posts: 593
    edited July 2013

    I believe that if you're triple negatiive hormonal therapy isn't really used.  I believe there is a triple neg. thread at this site.  Netter you might get more info from those who have been there.

    I hope all works out for you and your OC has something up their sleeve.

  • KatiAK
    KatiAK Member Posts: 138
    edited July 2013

    It seems like each AC tx is a little bit worse, but I'm definitely feeling better today.  I can only take 1/2 dose of the decadron or I spin in place.  By evening I'm taking .25 mg xanax to hold still anyway.  Tonight I may take .25 mg more with Compazine.  I'm trying to eat good and exercise when I can but the oncs are inducing so much misery that by damn I'm going to make it as easy on myself as possible.  We'll deal with the repercussions to that when I'm healthy again.  Ice cream is my friend - but I do throw it in a milkshake with fruits and vegies and ground flax seed to ease my guilt.  I'm dreading the final AC and looking forward to it being the last one.  I've read that Taxol is easier and I've read that Taxol is worse.  I've read that taking B6, B12 and alpha lipoic acid helps with the neuropathy.  Can't hurt right?  Vitamin B is water soluble.  I am pretty nervous about a new set of SE's.

    dim425 - I've thought about how easy it would be to quit now.  Don't do it.  You have to know you did everything you could do kick this cancer in the ass.  I think about that C&W song "in my next 30 years".  Haha!  I also think about the moldy oldy "Go Ask Alice" cuz some pills make you tall and some pills make you small.  (Sorry - I love music and can relate so well!)  Anyway. . . I want to know I've done my best.  I still have three kids to raise.  I don't want them to grow up without their Momma.

    dyvgrl - Hang on girl!  You sound like a strong woman so find your nitch and get in it.  Do what you have to do to survive for now, then back on track when it's more feasible.  I should take my own advice.  :) 

    I swear it feels like they're trying to kill me - but so far I've come back so . . . good luck with that!  Alaskan summer's are fleeting and this has been a rare nice one so I'm feeling a little cheated.  And I never look forward to Thanksgiving in July but this year I am cuz then I'm done with chemo and rads.  I'm hoping for hair (peach fuzz?) by Christmas.

    Chins up everybody!  Hope you have a good weekend and minimal SE's.  Prayers for everybody!

  • KatiAK
    KatiAK Member Posts: 138
    edited July 2013

    It seems like each AC tx is a little bit worse, but I'm definitely feeling better today.  I can only take 1/2 dose of the decadron or I spin in place.  By evening I'm taking .25 mg xanax to hold still anyway.  Tonight I may take .25 mg more with Compazine.  I'm trying to eat good and exercise when I can but the oncs are inducing so much misery that by damn I'm going to make it as easy on myself as possible.  We'll deal with the repercussions to that when I'm healthy again.  Ice cream is my friend - but I do throw it in a milkshake with fruits and vegies and ground flax seed to ease my guilt.  I'm dreading the final AC and looking forward to it being the last one.  I've read that Taxol is easier and I've read that Taxol is worse.  I've read that taking B6, B12 and alpha lipoic acid helps with the neuropathy.  Can't hurt right?  Vitamin B is water soluble.  I am pretty nervous about a new set of SE's.

    dim425 - I've thought about how easy it would be to quit now.  Don't do it.  You have to know you did everything you could do kick this cancer in the ass.  I think about that C&W song "in my next 30 years".  Haha!  I also think about the moldy oldy "Go Ask Alice" cuz some pills make you tall and some pills make you small.  (Sorry - I love music and can relate so well!)  Anyway. . . I want to know I've done my best.  I still have three kids to raise.  I don't want them to grow up without their Momma.

    dyvgrl - Hang on girl!  You sound like a strong woman so find your nitch and get in it.  Do what you have to do to survive for now, then back on track when it's more feasible.  I should take my own advice.  :) 

    I swear it feels like they're trying to kill me - but so far I've come back so . . . good luck with that!  Alaskan summer's are fleeting and this has been a rare nice one so I'm feeling a little cheated.  And I never look forward to Thanksgiving in July but this year I am cuz then I'm done with chemo and rads.  I'm hoping for hair (peach fuzz?) by Christmas.

    Chins up everybody!  Hope you have a good weekend and minimal SE's.  Prayers for everybody!

  • dlm425
    dlm425 Member Posts: 209
    edited July 2013

    Good morning ladies I still feel so wiped out I slept all day. So nauseous dry heaving. Ativan makes me shaky decadron too. So miserable but I really do appreciate all your advice " aaoaao your.my hero". And I too cannot wait for thanksgiving and Christmas And mostly to get rid of 2013. 2014 will be better. 13 is not a good number for.me my husband died on April 13. I keep sing the Kelly clarkson song "what doesn't kill you.makes you stronger. And Netter maybe its time you try western medicine get the book knockout and see if that helps there are no other eastern meds except radation. I have the book and its very impowering. Does compazine make you loopy

  • aaoaao
    aaoaao Member Posts: 593
    edited July 2013

    Thanks dlm425 for the complement but truly you're a hero.  I'm so sorry about the loss of your husband.  Yep seems like 13 just isn't good for you.  You should really celebrate the end of your chemo and the Holidays this year.  You definitely deserve it.  I also love Kelly Clarkson, her songs are real unlike some singers these days.  Keep your head up and full of inspiring songs. 

  • Dyvgrl
    Dyvgrl Member Posts: 471
    edited July 2013

    Day four, round 1. Feeling ok except for the bone pain. Moving seems to help. The more I lay around the more it hurts. Need to get moving and get some housework done. Gonna shave my head tomorrow. Let the kids have their way with it. Any ideas on how to make this fun? Really wish a few bottles of wine were on the agenda!

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