October 2011 Chemo group

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  • WIMusicMaker
    WIMusicMaker Member Posts: 78
    edited October 2011

    Welcome to all the new members! I am so sorry you are members of our club. For those who just starting chemo I hope your next few days are very uneventful.

    My scalp is extemely itchy. I know the end is near for my hair. I did go out and look for some hats today. Target had some really cute winter ones! I have not purchased a wig and am not sure I would be comfortable in it. I think once the hair all falls out, I will set up an appointment and see how one feels.  

    Tappy I drank vitamin water and that actually tasted pretty good when water alone was terrible. Flavored selzer water worked well too. Don't forget popsicles count as fluid also.

    Timbuktu I agree. The anticipation of each event is always worse than the actual event! 

    Dia123 The Claritin for is bone pain if you get a shot to help with blood cell counts. I am not sure you have to worry about this on AC. I think it is for those of us on TC. 

    If you want to have a good laugh, google text messages gone wrong. Ellen reads these on her show and they are hilarious! I was laughing so hard I was crying.

    Take care all! Wishing everyone few side effects! 

  • TAPPY
    TAPPY Member Posts: 283
    edited October 2011

    Lori - so glad all your tests came backpositive:)

  • sue_from_wi
    sue_from_wi Member Posts: 40
    edited October 2011
    Tappy - I'm not a big juice drinker but for awhile there all I could tolerate was pineapple juice - 100% juice. Pretty sweet but I diluted it down.
  • wildrumara
    wildrumara Member Posts: 450
    edited October 2011

    The first week after chemotherapy, every drink tasted bad to me.  Obviously, I drank as much water as I could, but nothing tasted better than a big ol' cherry Slurpee from Target!!! 

  • stjude10
    stjude10 Member Posts: 390
    edited October 2011

    Thanks for all of the best wishes on my test results!

    thanks for the slurpee heads up wildrumara! will def. keep that in mind.

    start my steroid dex tomorrow, and get my shot. think I'll see how it goes, I have Claritin on hand in case. waiting for my meds to kick in and hope I can sleep!

    Big relief, my DD had good blood counts at her clinic visit today, so she'll keep on keepin' on!

  • barbyjean
    barbyjean Member Posts: 108
    edited October 2011

    Am I the only one who will be painting myself blue and going as blue man group?  Loved all the ideas, but I might just go "as is" and scare the hell out of the little kids ringing the doorbell.

    Little tufts of my hair coming out (I'm on day 14) but my pubes think they are on the Titanic and jumping ship like crazy! Here in SD every cancer patient gets a free wig, I'm sure glad I didn't have to pay for one because I don't know if I will be able to stand the feel of it. Especially during hot flashes. I have been practicing with scarves.

    When I couldn't stomach another swallow of water, I tried Sobe water - all natural, slightly sweet and slightly flavored. I love it. Or Sprite Zero goes down ok if I want carbonation.

    For the neulasta shot - my serious pain came on days 6 and 7. I was taking Claritin but it didn't seem to work very well, but I have pain issues already. I may try heat this next time, and will give Claritin another try.

    I'm  so sorry to hear of the husbands who aren't able to step up and take care of you. The ones who do should definitely give lessons. But don't be afraid to ask for what you need, even great husbands can't read minds! I am divorced, by the way, from someone who was awful when I got sick a few years ago. (He wasn't great before I got sick either, it was just the last straw.) I have great friends and I have learned to ask for help, and have been overwhelmed by how supportive everyone is. 

    I hope all of you who just got first chemo are feeling ok with few side effects.

    Take care!     Barb 

  • Terry71
    Terry71 Member Posts: 293
    edited October 2011

    TAPPY: i drink alot of grape juice and it helps, also sounds kinda strange but cream soda Crush, or grape soda crush I can tolerate and taste, dont kow why its just those 2 but LOL....  Ive never heard of Claratin for th joint pain Im gonna call my primary care nurse and ask,  Im telling you I was down for 8 days with massive joint pain so bad I could hardly walk..... I just dont understand how Claratin would work????  Also TAPPY I take malox fruit chewables for heartburn they work good.... 

    Lori- Happy to hear all your tests and scans came back clear, Mine did also including my recent liver ultrasound.....

    A warm welcome to the new people, this is a great site and a warm, friendly place to be.....  

  • kathyrnn
    kathyrnn Member Posts: 393
    edited October 2011

    Hi Ladies,



    I hope that you won't mind me popping in, just hopefully to give you some encouragement.



    I have just finished my chemo. ( 12 weeks of Taxol, 4 DD A/C)



    I just want to let you know that while of course there are SE's, everyone is different and won't neccessrily get all the ones you hear about. I sailed through with almost no SE. ( the only major SE I got was neuropathy from the Taxol, which I would be prone to due to a serious back injury right before chemo). That being said, no vomiting, no strange tastes, no mouth sores, minimal fatigue. I just wanted you to know that I got a bit scared when I first came on here and read all the info, but found in reality. that the experience was much better than I expected.



    The tip I took on the Neulasta, was a Claritan and Zantac

    combo, one day before the shot and then for 3 more days. I had no pain whatsoever, but that doesn't mean it works for everyone.



    Wishing you all an easy journey.

  • TAPPY
    TAPPY Member Posts: 283
    edited October 2011

    Lori - glad to hear about DD tests - one less thing for you to worry about:What is the steriod dex you are talking about ?  (I think they gave my that in my port yesterday)

     I woke up with a wicked headache and nausea at 1 am so I started on the Z, I have to take it every six hours or I have break thru, but it kicks in 20 minutes later...but I do feel tired on it.

    How long will have I have take this after treatment, nurse said about 3 days.

    My face and chest are bright red (I get this after surgery as well and it is miserbale as it makes my eyes swell shut/burn ...they tell me to take Benedryl - which I can eat like candy with no effect due to all the allergies.

     I just cant drink water...it gives me heartburn, so will try some of your suggestions...i really like a cola icee, but I am sure that is not what they have in mind LOL...but what ever works right ????  Right now stale ginger ale and yourgut/saltines and banannas seem to work just fine as far as food.  Nothing makes me hungry, poor hubby likes to cook

    so I told him to make home made mash potatoes for me tonight...and I am looking forward to it...tis the little things.

    Off to get the shot and hoping for no bone pain.

  • cfdr
    cfdr Member Posts: 549
    edited October 2011

    NancyJill,

     I also got rashes on my hands. Talked to my onc about it, and she said that taxotere makes your skin very sensitive to the sun. I had taken a few short walks in our neighborhood...mind you, it's mid-autumn, our streets are very shady, and they were short walks, but with no sunscreen on the backs of my hands they both broke out in painful, itchy rashes. I am normally a "tan, not burn" person, too. Now I won't step off the front steps without sunscreen on every exposed inch of skin, even in the late afternoon.

  • cfdr
    cfdr Member Posts: 549
    edited October 2011

    I've been lucky in that water has not tasted bad to me. What's also worked well, though, is to get an assortment of single-serving beverages, and always have one of each in the fridge. That way I can have a choice without clogging our fridge with a dozen big bottles. I have prune juice, cranberry juice, orange juice, V8 fusion (mix of fruit/veg), vanilla soy milk, vanilla almond milk, chocolate almond milk, chocolate milk, and ginger ale. The juices I usually mix with water so I'm not getting a huge amount of sugar at once. I also made a huge pot of vegetable broth (beets, carrots, sweet potatoes, kale, onion, garlic, ginger, scallions, celery) and have been trying to drink about a quart of that every day. We kept some fresh, froze some and my husband canned some (which I'll reboil when I open them just to be safe). I also have an assortment of herbal, green and decaf teas. With all those choices it's been easy to stay hydrated and always have something that is helpful no matter what my symptoms du jour.

  • TAPPY
    TAPPY Member Posts: 283
    edited October 2011

    Lunch today was a micro packet of Brown Rice (Uncle Bens)

    It tatsted good, settled in good.  And gave me that little boost I needed.

     Nurse told me that the rash on face and neck was from the steriods they gave me at chemo yesterday.  Why do they have to give those ?

  • Maya847
    Maya847 Member Posts: 41
    edited October 2011

    Went back to the surgeon who put my port in yesterday as my port site was very red and burning.  He is concerned the port leaked...put me on an antibiotic and will recheck Tues next week (I am scheduled for second infusion on Wed).  He said if it was not better they would have to remove the port "and that would not be good."  When I spoke with the nurse today they scheduled me to have a picc line put in next tues just in case the port has to come out.  Has anyone had one of these lines?  What are they....and why would they not have just put one of those in me the first time round?  Also concerned about what damage was or could be caused by the port leaking.....

  • Lady-di
    Lady-di Member Posts: 150
    edited October 2011

    Hi,

    Had my first treatment of DD A/C, acuual treatment only took 1 hour but was there for 4. Also very happy to say I made it to the LGFG class. Glad I did. Feeling a bit weird right now. Not sure if it's the medication or chemo.

    Kind of worn out now so I'll post more tomorrow.

    Night all!

  • stjude10
    stjude10 Member Posts: 390
    edited October 2011

    dia123= glad you made it thru the 1st tx. I had mine yesterday. The decadron wired me for sound last night and couldn't sleep. Got my shot today and refused to nap hoping to sleep soon. The chemo itself didn't take long at all, it was all the other stuff. I'm signed up for the LGFG class on Nov. 7th. I got to go to the bc center and they gave me 2 sacks of free stuff. I got a wig, halo, scarf and a bunch of hats. We have a huge fundraisers for our center because our area has a high percentage of bc. Don't drink our water! The center is very good to us.

    Will check in w/your post tomorrow

  • stjude10
    stjude10 Member Posts: 390
    edited October 2011

    cfdr= thanks for the tips on hydration. I like the idea of having so many choices. Am going to store tomorrow, so you gave me some good ideas.

    Maya=so sorry to hear about your port issues. I hope they can save it. I have seen pic lines in the arm, it's like an iv that they can block when not using that way you can go home. I think it stays in instead of placing a new iv every time. Not sure if that's what you'd get, you might find better info looking up online. Let's hope for the best. Keep us posted. Will be sending good thoughts your way!

  • NancyJill
    NancyJill Member Posts: 218
    edited October 2011

    cfdr-thanks for sharing about the sunscreen. I was on steroids 5 days before my rash got better. You have good ideas about drinks. I'm not up to making my own broth, though! Sorry, Maya. Leaking port? Does that mean you had a treatment in it and the meds leaked around the area? That stinks. I'm glad they have another way. But major bummer, getting the port in correctly hurts enough, I think.  Good luck! Dia123 glad you made it to class!

  • Lady-di
    Lady-di Member Posts: 150
    edited October 2011

    Morning everyone, I have been up since 4 and didnt go to sleep till after 1. But I'm thankful that I'm not feeling horrible. I know its the first morning and it wont last. On.friday i get my needle. The LGFG class was good. Alot of free products such as makeup, moisturizers, and face washes. I was also glad to learn how to pencil in eyebrows. Not sure I really trust myself to do that though. I'll have to practice.



    Lori- glad to hear about you DD and her good blood counts. I'm sure you will enjoy your class. Lots of laughs and smiles.



    Maya- hoping everything works out with you port. I'm keeping fingers crossed for you. My DH has a friend who had one put in and said it was very easy and painless. Of course everyone is different but I think it's an easier procedure it get done.



    Tappy- sorry to hear that you re having so many issues so far. One day at a time and i hope it passes quickly for you.



    cfdr- I love your idea of all the drinks and think I'm going shopping for some.



    Has anyone driven themself the day after first treatment? Or have you been told to avoid it till your off pills? There is always something I forget to ask about!!

    .

  • sue_from_wi
    sue_from_wi Member Posts: 40
    edited October 2011

    Maya - so very sorry to here about your port issues. Praying that the anitbiotics clear up the infection. There is an article on Wikipedia and other sites about picc lines. My port has been trouble free so far, I'm thankful to say.

    Dia123 - poor night of sleeping for me too. I'm glad you made it to class. I didn't drive until Saturday after my Tx on Thursday - just felt too disconnected and unfocused. Thankfully, my DH was available to drive me that time and my sisters are here this time.

    Gearing up for Tx #2 at 1:30 today. Curious to see how it goes. I had lunch with a work friend on Monday. She went through this 10 years ago and said she thought the first Tx was the hardest as far as side effects go. She felt her body handled the subsequent treatments better, because it knew what was coming and how to adjust. I can see how this might be the case and am hoping it applies to me and to all of you as well! 

  • Lady-di
    Lady-di Member Posts: 150
    edited October 2011

    Sue- "disconnected and unfocused". That describes me perfectly. Only words I could come up with last night was that I felt weird. Lol.

    Good luck to you today and I have read other peoples posts saying that the first was worst for them also. Hoping that I the case for you too. For all of us!!!,

    Diana

  • stjude10
    stjude10 Member Posts: 390
    edited October 2011

    dia123= I drove the day after my tx. I was so jacked up on that steroid, it was like a bag of nervous energy they gave me. Almost got on treadmill at 1am that night. Would've slept better last night, but this acid reflux is miserable. Ended up getting up and coughing and spitting up as much as I could. I ended up taking a doozey of xantac that my DD had left over from her chemo and after about an hr. slept like a baby.

    Sue= good luck w/#2. Will be thinking of you and wishing you the best!

  • stjude10
    stjude10 Member Posts: 390
    edited October 2011

    Oh, and I woke up day after tx w/red face and chest. Looks like I just got back from vacation. It's not blotchy, so I may go w/that. still have it today. Any tips?

  • sue_from_wi
    sue_from_wi Member Posts: 40
    edited October 2011

    Lori - my latest blog post shows one chemo cap option you may want to consider for days like these - it's called 'Paper Bag Over the Head'. Just for laughs, of course, but I think we all feel like that sometimes during our normal lives and I'm feeling it ever more now during my chemo phase when there is just so much going on with my face and hair.

    Sorry to say I don't have a more serious tip for you.

    I used Zegerid (now OTC) for heartburn and had good results (for those who may not like Zantac). The Pepto Bismol I usually use didn't touch the chemo hearburn. Anyway the Zegerid came packaged in 14 day doses but I stopped after 4 or 5 days. I would have started again if I needed to but I trying to keep the between chemo drugs to a minimum.

  • TAPPY
    TAPPY Member Posts: 283
    edited October 2011

    Feel better today (knock on wood)

    Rash is better

    I dont have the headache - I am still takeing the nas pill as I feel it creeping in - but not like yesterday.   Still sticking to the bland food.

    Gonna try to go back to work next week.

    So far no bone pain from the shot -not sure when that kicks in.

    Hope everyone has a better day with NO ISSUES !!!  I love a no issue day

  • bethu77
    bethu77 Member Posts: 320
    edited October 2011

    Hello everyone! I am joining a group I really don't want to join...chemo but then, who wants this? I had bilateral mastectomies on 9/19. I am doing the expanders with reconstruction. I got the results from my Oncotype testing and I need chemo. I don't have a start date yet. My oncologist wanted to start me on 10/24 but I have my first fill of the expanders that week and can handle only one thing at a time!

    How do each of you feel about your decision to have chemo? Did you have a choice to make? I don't want a recurrence because this is my second time. My first was bilateral DCIS with surgery and radiation in 9/08. I am so scared of the whole chemo thing!

  • Terry71
    Terry71 Member Posts: 293
    edited October 2011

    Maya: I hav a picc line in my right arm on the inside of it.. It really isnt bad at all just a glorified IV that stays IN for the duration of treatment, It doesnt bother me at all... they freeze your arm before it gets inserted and you dont feel it. It really is easy to have put it.... Im glad I got it :-)  I can send you pics of it if you would like to see what it is I dont mind..... and it doesnt hurt at all..... 

  • TAPPY
    TAPPY Member Posts: 283
    edited October 2011

    Welcome Beth...and I am sorry you had to join the group.  But you are in good hands here.... good advice and love and moral support.

    What type of chemo will you be having ?

     I just had my first round this week(AC and then T) ...and it was not horrible like I had it built up in my mind.

    Yes a few side effects, but very manageable.

    I am thinking of going back to work next week....have any of you Oct. ladies headed back yet ???

    Any tips ?

  • Normandy18
    Normandy18 Member Posts: 30
    edited October 2011

    I had my first chemo treatment (FEC) on Oct. 11th, so this is day 9 post chemo treatment.

    I had my hair cut on Tuesday. I had long hair and it has not been short in 40 years. I thought it would be traumatic, but I actually like my cut and may keep it short.

    I went to look at wigs today and found a couple--they weren't in my color--so I go back on Wednesday for another refit. I have not lost any hair yet and I am seeing in this group that it tends to be around 2 weeks, so a few more days to go (fingers crossed).

    I was wondering if I can expect to feel the same with my second round (Oct. 31st is next date) of chemo as I did with my first treatment? Or does it accumulate and build up with each session?

    I did not have it too bad--a sensation of fullness--like I just ate a big meal--so no appetite, things tasted odd, some headaches and just feeling a bit run down. I feel much better this week and have been feeling better each day. I have noticed that my nose has really started to drip--no cold--just a runny nose. I noticed someone else had posted this as well.

    Take care!

  • perts1
    perts1 Member Posts: 62
    edited October 2011

    I had my first chemo on Tuesday, Neulasta on Wed. morning and port in Wed. afternoon.  So far (knock on my wooden head) everything has been fine.  Pretty foggy headed but that's about it.  I found a drink that really tastes good - boil a quart of water and juice a lemon in it and drop in the lemon peels, grate some fresh ginger (about a tablespoon) and let it steep a few minutes.  Great hot or with ice. 

     I can't believe what a wimp I've become.  When my husband leaves for something I actually feel rather frightened.  Never had that happen before in my life.  Guess I'm turning into a complete chicken!  I'm wondering if I really will lose my hair.  If I will get sick. All kinds of stuff.  I guess we all have our own reaction but I sure like reading how everyone is handling this.  Best wishes to everyone!  Chin up, chest out (even if it's a little less than it was).  

  • perts1
    perts1 Member Posts: 62
    edited October 2011

    By the way - does anyone use prilosec (otc) for the heartburn?  I take it every day and it's great.  Also called omeprazole and available at WalMart.  Also, the lemon/ginger tea I mentioned before really calms heartburn down.

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