Starting Chemo October 2014

Options
191012141531

Comments

  • nottoday
    nottoday Member Posts: 162
    edited October 2014

    Dear speedcat88,

    Can you explain more about this: Well, the sponges stayed frozen and were a lot less messy than just straight ice.

    I tried to keep my finger and toes in bags of ice during the taxotere portion of my first infusion on Wednesday. Felt like I was auditioning for a survival reality show. If there's an easier way to keep my fingernails and toenails intact, I'd love to hear more!

    Thanks, as always, for everyone's tips.

  • ml143333
    ml143333 Member Posts: 658
    edited October 2014

    Had my first blood draw after my chemo last week and my white count is low which was expected, but the MO said that the blood is making the white blood cells, they are just not being pushed out yet.  He said to stay away from sick people and to call them if I have a temperature, cough, chills, anything of that nature.

    I guess the white blood cells being made is why my pelvic bones, sternum and lower back are hurting.  (I walk like an old woman) I thought it would hurt closer to the shot but the MO said that sometimes it doesn't hit until day 5 or 6 but everyone is different.

    I go back next Friday (Halloween) for another blood draw and then treatment #2 on 11/7.

  • Nomatterwhat
    Nomatterwhat Member Posts: 587
    edited October 2014

    image

    My last visit to the chemo palace!!!!! Love those ladies!!!!!! Not a bad look for a fat old broad after a BMX and chemo.  WOO HOO TO ALL OF US SURVIVORS and those almost done.  It has been a journey.
  • Tobycc
    Tobycc Member Posts: 789
    edited October 2014

    now THAT made my day a LOT brighter!  You look FABULOUS 

  • BookLady1
    BookLady1 Member Posts: 253
    edited October 2014

    Good Morning Sunshines! I'm on the other side of Chemo/Nuerlasta round 2 and doing much better than Round One in SE management thank in large part to your good and wise suggestions in being proactive about our care. 

    Kerensa75 - thanks for your advice in caring for my "new" baby scalp. How are you doing?

    Ilovecoasters - no regrets, I hope! You have earned the time off and the good will you have built on your career. No help on the weight. I lost some pounds from anxiety before this all started, small bonus?  Walking daily with my sweet Abby Airedale - we are more into ambling - and adding healthy where I can. Be kind to yourself.

    Nancy6540 - what a horrible thing for you to go though with the port! I have never been happy about how this port was sprung on me. Really just glossed over and I was NOT prepared. I'm ok with it now, but boy will I remain vigilant thanks to you. Enough, already!

    Becca - I'm with you on the water. Yuck! I can handle some of the flavored no-cal no sodium sugar free  sparkling waters -generic, even. Good luck my sister in hydration.

    Nomatterwhat - what a great way to begin today with that photo of yours!😘 Hooray!

    I'm glad to know we are moving through the chemo countdown together and that we don't get all the SE's at he same time.

  • Leto
    Leto Member Posts: 42
    edited October 2014

    Congratulations, nomatterwhat! I look
    forward to "Ringing of the Bell" myself. I'm not sure if they have one at my chemo center, but it does give me hope that I can get through
    this. WOO HOO TO YOU!

  • cbooklvr
    cbooklvr Member Posts: 66
    edited October 2014

    Congrats Nomatterwhat, you look great, so happy you are on the other side of chemo. Smile

    I am day 3 after my first Chemo infusion, had my neulesta shot yesterday. So far just some tummy rumbling and strange taste in my mouth. I have been drinking lots of water and taking anti-nausea meds as instructed. Was able to work as usual yesterday and planning on relaxing this weekend.  Wishing a good day to all.

    Cherice

  • nottoday
    nottoday Member Posts: 162
    edited October 2014

    Congratulations, nomatterwhat! Wishing you nothing but health and happiness from here on!

    I am 3 days post 1st infusion and 2 days post neulasta. Had a nose bleed the day after neulasta and was recommended to keep a humidifier running. The chemo dries out membranes, and now that it's getting colder, and we are turning on heat, that also is drying out our homes. I'm also rinsing my mouth with biotene 5 times a day and keeping my eyes moist with artificial tears (I wear contacts). Seems to be working. 

  • kerensa75
    kerensa75 Member Posts: 83
    edited October 2014

    congrats nomatterwhat!!! You did it! So inspiring.

    Booklady you are welcome :)

    Nottoday, I Just bought some aquaphor to put inside my nose. I'm hoping it helps with my bloody nose and dry nose. My only bleeds when I blow it so far. 

    I managed to catch a cold and got put on antibiotics. My voice comes and goes and my fever got up to 100.4 :( I hope to catch a break soon. 

    Hop you are all having a good weekend

  • Sjacobs146
    Sjacobs146 Member Posts: 770
    edited October 2014

    i picked up my wig today, and stopped by the hospital for my Neulasta shot on the way home.  The wig is a little darker than my hair (I'm blonde), but the style is cute.  I may do my hair that way when it grows back in.  I'll go back for hair cut and final adjustments when my hair starts to fall out.  

    So far feeling fine except for a little heartburn.  Might be the steroids.  I did have a little vaginal bleeding right after the infusion, I thought my period might have been triggered a week early, but since then, nothing.  Anyone else experience that?

  • wendeeB
    wendeeB Member Posts: 40
    edited October 2014

    Had infusion#2 this past Thursday, and Neulasta on Friday.  

    Been rinsing with baking soda and salt water whenever my mouth feels sore, and so far so good.  I drink 2oz of coffee every Saturday and my mouth seemed worse directly after.  As soon as I drink my green juice, all better. 

    My neulasta pain last time had already started by now.  Here's hoping the 5 days of claritin did the trick.  

    About 2/3 of my hair is gone.  Just enough whispy pieces so that when I wear my knitted hat, I look ok.

    Been reading about efficacy of fasting pre and post infusion.   Interesting. 

    Still keeping up with training.   6x week.  Pulled a PR on rack pulls this past Friday of 315# for 2, while weighing 125.  But, stadiums were difficult today.  Finished them all, but slower. Couldn't do abs because the pressure made me nauseous.    Tomorrow is walking. Haven't missed any work either.

    Blessings to all!  2 down, 2 to go!  I'm happy,  I'm healthy, and I'm 100% cured! (One of my affirmations)

  • Ilovecoasters
    Ilovecoasters Member Posts: 199
    edited October 2014

    For those of you taking Zofran, how often do you take it? My insurance will only permit 12 pills every 30 days.  It has me super worried.  

  • ml143333
    ml143333 Member Posts: 658
    edited October 2014

    Ilovecoasters - my Zofran says every 10 hours and my Compazine says every 6 hours.  If your meds aren't really helping, call your doctor.  They can help you, at least that's what my MO says!

  • ml143333
    ml143333 Member Posts: 658
    edited October 2014

    I have a question about the thing in my neck that was inserted when I had the port placed.  I was able to take all the sticky stuff off today and it feels like a stitch is sticking out but the NP that took my stitches out from the port said I didn't have any stitches.  Should I call the doctor?  Its 10:30 at night.  It isn't hurting or anything, just something I noticed today.  Husband is out of town hunting so it's just me, the kids and my mother-in-law plus the dogs, chickens, lizards, turtle and fish.

  • BookLady1
    BookLady1 Member Posts: 253
    edited October 2014

    Mandy - never feel shy about calling after hours. The glue had really hardened on my site and parts hung on, poking me, for a while. Don't know if that's the same as you - call the dr. if you want! I felt the port issues were not explained and really rushed over. It's my best friend now, but in the beginning, much worse than the lumpectomy. Be well, linda

  • BookLady1
    BookLady1 Member Posts: 253
    edited October 2014

    Ilovecoasters - my MO has allowed me to double up on Zofran if needed. We cut out Compazine because my gut couldn't handle it, so I agree with Mandy. They really don't want us suffering with SE's so talk with your dr. Have a restful night, Linda

  • Sjacobs146
    Sjacobs146 Member Posts: 770
    edited October 2014

    Ilovecoasters, compare prices for the Zofran, my understanding is that they can vary greatly.  Try Walmart if your insurance won't cover.  

    Had my Neulasta injection yesterday afternoon, I took Tylenol right away, but no bone pain yet.  When might that kick in?  I am taking so many pills, I don't even want to take Tylenol if I don't have to.  So far feeling good.  Having some heartburn, glass of milk seems to help.  Don't know if the heartburn is from the steroids or the compazine.  Any thoughts?  I will call tomorrow to ask about it anyway.  

  • Ilovecoasters
    Ilovecoasters Member Posts: 199
    edited October 2014

    My insurance will cover, they just won't allow more than 12 pills a month.  I offered to full self pay for the remainder but the pharmacy said no.   I see the MO Wednesday so I will definitely bring it up.  I am so anxious about starting chemo.  My infusion starts at 1:00. Is it ok to eat a light lunch prior?

  • BookLady1
    BookLady1 Member Posts: 253
    edited October 2014

    sjacobs - I did okay with Neurlasta - maybe you'll squeak by, too! Round 2 is behind me, and I had some hip pain round one that may have been from over walking the dog! Ibuprofen and a warm bath was all I needed. This time, nothing! I did substitute generic Claritin for my OTC generic Zyrtek for seasonal allergies throughout chemo. Also, I was already prescribed generic Prilosec from my GP to give my eshopagus a break. Compazine and steroids caused gut problems with me  - kept steroids lost Compazine per my MO.

    Ilovecoasters- I've heard its a good idea to have something light in your tummy but I know I was too nervous beforehand to eat. I took some light snacks along with splurging on a Starbucks tea and cookie as a treat. Be kind to yourself and get through this 1st round. We are all with you. Linda

  • Nomatterwhat
    Nomatterwhat Member Posts: 587
    edited October 2014

    Ilovecoasters, - You will do fine on your infusion.  Ask your nurses what they think you should have in your stomach.  I ate a high protein breakfast and made sure I had crackers, Ginger Ale and even ate a small ice cream during the Cytoxan.  Just take good care of yourself before, during and after.  Will be thinking of you. 

  • Sjacobs146
    Sjacobs146 Member Posts: 770
    edited October 2014

    Ilovecoasters, I'd eat if you want to.  I ate breakfast befor and had lunch during the infusion.  The steroids make you hungry.

  • Ilovecoasters
    Ilovecoasters Member Posts: 199
    edited October 2014

    Thank you! So I test drove my wig today. It's super comfortable and light.  I figured I might as well get used to it. Have to be honest, it was nice to not spend 45 minutes flat ironing my hair.  My husband is amazed. You really can't tell it's a wig since it's so close to my own hair.  I am feeling better about Wednesday too. 

  • nottoday
    nottoday Member Posts: 162
    edited October 2014

    Good evening, ladies,

    I'm planning to go back to work tomorrow for the 1st time after first infusion last Wednesday, and Neulasta on Thursday. I'm a little nervous about feeling sick, but today I feel quite good, and I'll take a Zofran in the morning, I guess, to stave off any nausea. All in all, looking forward to being at work. I'll just need to get up and move a lot - my job is very chair-bound!

    I wanted to let you know about a couple of cookbooks I've used and distributed to friends who've expressed an interest in cooking for me during chemo. They are both by Rebecca Katz: The Cancer-Fighting Kitchen, and One Bite at a Time. Both have yummy, healthy recipes. I've identified recipes that my family and I would enjoy, and it has been a nice way to work with friends and family who want to support us. 

    Llovecoasters, I took in a bag of dried fruit and nuts and munched on it during chemo, along with chocolate, cause everybody knows I love that. My nurse said a light meal before was OK. I hope everything goes well tomorrow. I think the infusions have gone well for most of us. We'll be waiting for you on the other side!

    sjacobs 146, I've been told that heartburn is part for the chemo course. I've been taking 1 CVS-brand omprazole every day - so far so good. I've had minor bone pain since my injection on Thursday, and I guess the claritin 24 and ibuprofen are helping, but I find that brief yoga and walking sessions (10 min each) are really helpful. 

    wendeeB, you are amazing and inspiring! All I can say is, "wow!" 

    cbooklvr, I spent a lot of years in Berkeley and still miss it. Hope you are doing well.

    Wishing you all a good week. 

  • Mulligan
    Mulligan Member Posts: 205
    edited October 2014

    Congrats nomatterwhat! How awesome.

    Speedcat, yes I recommended the frozen sponges. Also a cool tip, one of my nurses recommended if my frozen sponges aren't frozen anymore to put on 2 layers of the latex gloves they have at the infusion center and then soak your hands in the ice. The cold is a lot easier to deal with.

  • Becca9800
    Becca9800 Member Posts: 79
    edited October 2014

    My hair.... I knew it would happen. Still such a shock. 

  • Leto
    Leto Member Posts: 42
    edited October 2014

    Hair, I knew it was coming too so I went ahead and cut mine before it started falling out.  It was important to me that the grand-kids were part of the hair-cutting so I had a family get together. My daughter did the clipping and she also found a place to donate colored hair.  

    image

  • Sjacobs146
    Sjacobs146 Member Posts: 770
    edited October 2014

    Oh Becca, (((hugs)))!  Now that I have had my first infusion, I am wondering how I will feel that day.

  • kerensa75
    kerensa75 Member Posts: 83
    edited October 2014

    Hugs Becca! Mine started falling out Saturday, so I understand. I will be shaving it in the next few days as I cannot handle running my hands through and getting so much hair...yuck

    Leto...You look fabulous sweety!

  • wendeeB
    wendeeB Member Posts: 40
    edited October 2014

    @nottoday , thank you for your kind words. I know that getting up and getting moving seems really difficult, but its the only thing that honestly makes me feel better.

    @becca, hugs sweetie!  it is still kind of bizarre. Even though you know it's coming. I chose not to shave my head. And I still have about 1/8 of my hair left. I read one person describing it as a thin veil of hair. If you're going to go the beanie or knitted cap route, it leaves a little bit of hair to hang out at the bottom so its not so noticeable.

    only five patients to see today! I'm glad. I'm feeling somewhat fatigued today.everything taste like, well, nothing. All except for my hot cinnamon green tea. But that doesn't matter, because I know I have to keep the good food to get a good results. So I'm going to persevere

    blessing to everyone! Remember, we are happy, we are healthy, and we are 100% cured!

  • ml143333
    ml143333 Member Posts: 658
    edited October 2014

    Leto - You look amazing!  Thanks for sharing the picture.

    Sjacobs - Good luck today.  One down is the best way to look at it.  Manage your nausea before it manages you.  Take your meds.  Get plenty of rest.

    Becca - sorry about your hair.  Have you tried wigs or scarves?  I personally like the scarves.

    Nottoday - Congrats on getting back to work.  I hope it will go well for you.  I went back to work on Tuesday after my chemo on Friday.  It wasn't too bad and I made it all week without going home early when I did go back.  Now I'm gearing up for round #2 the first Friday of November.

    Ilovecoasters - That's awesome that you liked the wig and so did your husband.  We're in your pocket on Wednesday.

     

Categories