Chemo May 2013

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  • ReddHeddMomma
    ReddHeddMomma Member Posts: 38
    edited June 2013

    Hi ladies. Feeling a little better this morning. My onc called in antibiotics for me yesterday, and after going to bed early and getting 10 hours of sleep, I am starting to feel human again. Am hoping we can keep my chemo on track for tomorrow - no idea what they will do if my blood counts are wonky.



    Kate, am so sorry you are having such a tough time with this. I tried holding off on taking an Imodium and learned the hard way that waiting just made things worse for me. But I only take 1 so I don't end up making more trouble. I have been faithfully taking a probiotic supplement - no idea if it is helping, but I am honestly afraid to stop taking it to find out.



    Sorry everyone else is having such a tough week, too. My daughter has her dance recital this week, and with chemo on Wednesday, I am worried about making it through rehearsal and two performances with her. Let's just say that daddy sucks at doing hair, and you'll feel my fear. LOL. We'll get through it with help from the older dancers and other moms, but I am feeling awfully guilty about her having to go through all of this with me at the age of 10. But it is what it is, right?



    Am thinking about taking a slurpee with me for chemo tomorrow to try to keep the mouth sores at bay. Have any of you tried that successfully? Would like to avoid the painful mouth and throat, but I also don't want to block treatment if there is anything in my system there. Guess I am just getting so tired of over thinking every little detail and worrying about all of this - am really struggling this week to find any inner balance. Deep breath, it will all be okay, as my hubby says, I suppose.

  • ReddHeddMomma
    ReddHeddMomma Member Posts: 38
    edited June 2013

    Kate and everyone having diarrhea issues - meant to mention that the charmin wet wipes that are flushable are really, really helpful when you are sore. I used them for several days after my last chemo infusion to make certain I got every bit of liquid off for the first few days to help prevent soreness down there from chemo traces that were coming out. One of the nurses recommended this to me, and it worked really well. The wet wipes are much less painful and far more gentle when you get sore in your tender bits, let me tell you. Hope that helps!

  • Teresa_G
    Teresa_G Member Posts: 259
    edited June 2013

    My daughters dance recitals are next week.  She looked at me sad and said you'll be able to be there won't you Mom.  I've never missed one and don't plan to now.  She is 25 and doesn't NEED me there, but I am always in the audience supporting her.  She has been dancing since she was 2 1/2.  She is on what they call the college team.  Basically those out of high school that don't want to give up dance.  They get married and even have kids and just keep on dancing.  I think it is great.  They do some extremely hard routines and I won't miss it for anything. 

    Redhedd I am sure you will have tons of help from the other mothers at your daughters recital if it is anything like my daughters dance studio, it is more like a family. 

  • carla53
    carla53 Member Posts: 264
    edited June 2013

    Lorrie-thanks for the comfort re the pic. Good luck on round four on Thursday.

    Ukkate- Hope that Imodium works for you.

    LJaegar-Good luck with your treatment today. Thanks for the update on the stuck throat feeling. I too get that. Was actually getting it for several months before chemo. With chemo more prevalent.

    Okiecountrygal-My fingers are crossed for your results on your mammogram. That bone pain can sure be debilitating. I decided on the next go around not to do the neulasta. Instead, a few days after the treatment my white cell count will checked everyday for a few days. On any day the count is down I will be given a shot. Don't know the name of it, but it isn't supposed to give bone pain as an s.e. Will see how it works. Glad, all in all, it worked out better for you this go around.

    A blessed day to all -Carla

  • carla53
    carla53 Member Posts: 264
    edited June 2013

    Oh I missed a couple. Darn.

    ReddHeddMomma-Enjoy your darling daughter's residal in any compassity you can. Sounds like you will have plenty of willing, capable and caring people around that can take care of the physical aspect. It's got to be emotionally and physically tough having a 10 year old child and going through this. I bet she will always remember how brave mom was during the big C time and will always admire you for it. In re to the icy and mouth sores. During my last (and only so far) treatment, I sucked on ice for the entire 2 hours the chemicals were being administered. The next couple of days the checks on the inside of my mouth had a slight fuzzy feeling, but absolutely no sores.



    Carla

  • carla53
    carla53 Member Posts: 264
    edited June 2013

    Did it again. One more

    Teresa-How great that your daughter has kept uo with her dancing. That's beautiful. And so sweet and touching that she still wants her momma in the audience.



    O.k. I think that's it.



    A good day to all - Carla

  • MichelleRN78
    MichelleRN78 Member Posts: 64
    edited June 2013

    Regarding PICC vs IV  I have been doing some research about Lymphedema one of the risk factors is "the number of cycles of chemotherapy administered through the arm on the same side as the breast surgery".    I would take this into consideration when you have IV placement.  Sometimes there are only so many veins in one arm that could take an IV.

    Also I have seen many PICCs placed and none of the patients ever seemed to be uncomfortable and when it came time to remove it the PICC nurse would just remove it at the bedside.  The patient would leave soon after.  I have never had a patient complain about a PICC they are just happy they don't have to be stuck over and over again.  Again I have a port so no knowledge of a PICC being placed in me, everyone is different I guess.

  • Ukkate
    Ukkate Member Posts: 292
    edited June 2013

    Shelly, so so glad this round was better for you. Sorry for the bone pain tho. I too would swap that for the sickies and diharea.

    Redhedd, was it you that asked about ice? My onco made me ice my mouth this time and I avoided a sore but ended up with a "burnt throat" instead. I'm not sure which was worse. I hope you can make it to your daughters recital. I managed to watch my 6 year olds last soccer game on Sunday having missed most of the season. I felt like hell though and I couldn't yell at all due to my throat. It's really tough to miss our kids stuff. My daughter had her 7th grade awards yesterday and I watched her take top academic honors, 3 hours before being back at the clinic for IV fluids!!!

    Anyway I think the half Imodium has helped. My lunch has stayed in so far. Trying to down vitamin water too and determined to go to work tomorrow

  • MomofSam
    MomofSam Member Posts: 74
    edited June 2013

    Haven't posted in a while - just been busy with work and stuff.  Find myself wearing my wig to work, but can't wait to take it off - hot and itchy!  Have worn a scarf a couple of time but that gets hot too.  Anyone have any better suggestions for keeping your head cool?  I have to wear a business suit to work with pantyhose and it's hot outside so wearing a wig/scarf is just making me hotter.

    Have chemo treatment number 3/8 tomorrow...keep counting them down.  Just 2 of AC left and then I'll be on Taxol for 4 treatments.  Shaved my head, but still have a little stubble on it - find that to be uncomfortable...anyone else find that is the case?

  • ReddHeddMomma
    ReddHeddMomma Member Posts: 38
    edited June 2013

    Momofsam - my hubby and I have nicknamed me "the molting porcupine" for just that reason. I have barely any stubble left, but it feels like prickles or acupuncture needles in my scalp. I did find a soft cotton turban at a local wig store that is light enough to not make me instantly sweaty, and comfy enough to wer for more than 5 minutes before I throw it off in disgust. They had similar ones in the TLC catalog from American cancer society. You might try there or on amazon? Also, if I tie my scarf a little looser, I find having an air pocket helps a bit...but everything still gets hot if I am outside for very long. Hope something there is helpful.

  • MomofSam
    MomofSam Member Posts: 74
    edited June 2013

    ReddHeddMom-thanks.  That is actually helpful.

  • ItIsWhatItIs2013
    ItIsWhatItIs2013 Member Posts: 541
    edited June 2013

    ReddHedd...

    Glad you're feeling better & thanks for the laugh with the "molting porcupine" it's exactly how I feel right now! Haha



    Okay... So after my initial reaction, I did more research (thank you ladies for bringing me back to reality!)



    I did resolve to try an IV next Thursday and see how it goes... With what I have been reading about a picc, it's ideal for treatments from 3-6 weeks but is "possible" for it to start to adhere (stick a little) to the vein, so when they go to take it out, it may be uncomfortable too. My last treatment is Aug 22.... 9-10 weeks away... I want to give a normal IV another try & if it goes terrible, then I will reconsider a picc... Meaning I would only have to have it in for just over 6-7 weeks..



    Ipc... How long did your DH have his in? .. Any complications? Pain with insertion/removal?... Its okay if he doesn't want to share.



    I hope everyone is having a good day & sorry for my "less than positive" posts lately!



    I'm very grateful to have a group to share and gain insight from! Thank you all!



    Happy thoughts

    Lorrie

  • Teresa_G
    Teresa_G Member Posts: 259
    edited June 2013

    Here is my picture with my short hair.  I am holding a breast cancer quilt my Mom just finished for me.  I love it!

  • ItIsWhatItIs2013
    ItIsWhatItIs2013 Member Posts: 541
    edited June 2013

    Teresa... You look smokin hot! Not all of us look so good with a buzz! Good job!

  • carla53
    carla53 Member Posts: 264
    edited June 2013

    Teresa you do look great with a buzz. Lucky girl. And the quilt your mom made you is really pretty. Very cool. :)

    Most every day I pull on my hair to see if I'm beginning to shed. Well today, day 12, I pulled my hair in one spot and there it was. Hair gone bad..or at least gone. Repeated it in a few spots with the same outcome.Was hoping somehow I would escape this part. But I am looking forward to two of our girls coming over tomorrow and having a buzz party.

    Lorrie - Hope all goes well with your iv next Thursday.



    Good evening to all and a really great tomorrow -Carla





  • elkatho
    elkatho Member Posts: 159
    edited June 2013

    Teresa ...You look good!! Keep smiling. Thanks for sharing.

  • lpc
    lpc Member Posts: 303
    edited June 2013

    Lorrie



    Dh had it in for 2 months. Radiologist put it in with no pain. Nurse took it out in our living room with no pain.



    Hope this helps.



    Lisa

  • kobrien
    kobrien Member Posts: 82
    edited June 2013

    Hi all...Today is day 12 post chemo #1 for me....Woke up with my scalp feeling funny...The shedding is starting..

    I am NOT ready for this..Hope you all have a good day.

    Kerri

  • elkatho
    elkatho Member Posts: 159
    edited June 2013

    So, regarding periods, If all falls a normal, I should get mine today or tomorrow..we shall see. One thing I can tell you for sure...I am surely PMSing....I feel like ripping someone's head off. Should be a good day at work:)



    Keri...12 days is about the same time my scalp started hurting. For me it felt like my scalp was sunburn. The scalp would hurt a little when I moved my hair. It stopped hurting and felt good after I shaved my head and left a little stubble. It is a difficult process but you can get through it. I have always worn hats on weekends so I treated myself to some hat shopping while I still had hair.



    Itiswhatitis...good luck with the IV placement.



    I am happy I had the port placed. There was pain after the procedure but I took pain meds and relaxed that afternoon. Had chemo the next day. It was sore for about a week ...more like stiff. I would keep it forever...if I could...well maybe not but it sure is convenient. Do not even feel the pick when they access it.



    So glad we have this site to vent.

  • Goldie1431
    Goldie1431 Member Posts: 29
    edited June 2013

    I had treatment #3 of 6 monday and was also worried about my veins. I go and get hydration as well the 2 days after each infusion. I asked the nurse yesterday if she thought I would make it vein wise. She said that they will find a vein and make it work. They use the veins on my hand for the hydration since there is nothing toxic in it.



    Also regarding the hair stubble I still have a lot of my buzzed hair intact in my head. It is itchy and I wish it would fall out. I also have white hairs growing over parts of my scalp as well. They are very thin. Then I noticed a very furry covering on my lower neck going all the way around from side to side as well as the same fuzz on my forehead in about a 2 inch patch that grown from my eye area out to where my normal hair line would be. These I never had before. What in the world?????



    I hope you all have a SE free day today!

  • Teresa_G
    Teresa_G Member Posts: 259
    edited June 2013

    My scalp started tingling at about day 10, hairs started coming out at day 13 and continue coming out now.  You can see more and more of my scalp each day.  My scalp started hurting at day 16.  I have been using an all in one shampoo and conditioner so I didn't have to do be rubbing on my scalp more than needed.  Wondering if maybe a baby shampoo would be better.  Any thoughts?

  • carla53
    carla53 Member Posts: 264
    edited June 2013

    Kobrien-Yesterday was day 12 for me and that is exactly when the shedding started for me too.



    At what # or length is the best to buzz it at?If I remember correctly, shearing the hair completely to the scalp can cause ingrown hairs?! Suggestions please. Greatly appreciate it.



    A good day to all - Carla

  • Teresa_G
    Teresa_G Member Posts: 259
    edited June 2013

    I did mine at 3/4" I wanted a little hair there while I still had it.  Personally I don't think I would go shorter than 1/2" but that is just me....

  • Debwarrior
    Debwarrior Member Posts: 72
    edited June 2013

    Finally feeling better but tomorrow is my next treatment: 5 out of 12. Boy, it's going slowly.  Each time it seems a little harder to bounce back.  Feeling a little sorry for myself and my family.  My mother-in-law died from endometrial cancer right before I started chemo, we're all still reeling from that--it was so quick.  We were lucky to have a visit with her shortly before she went into the hospital. We were close and I wish I could still call her and tell her what's going on. My brother was just last week, completely out of the blue, diagnosed with prostate cancer and now we're both in the "cancer survivor" category.  My parents, neither one has had cancer at 81.  That at least is a blessing. 

    I went to the bookstore and bought a new book about someone walking the pacific trail called Wild to get my mind off things and what do you know, but the first chapter is about the author dealing with her mother's diagnosis with stage 4 lung cancer.  Hard to get away from it.  Maybe it's better to go into it though since we are in the eye of the storm, so to speak.   I have a 9 year old too and a 15 year old and my nine year old son asks me every day how I'm feeling.  It's sweet.

    I hope those who are feeling crappy, start to feel better today and good luck to those with treatment still this week.  I hope side effects are manageable for all of us.  I'm planning a weekend trip to the coast for next weekend with a college friend who is visiting.  I hope that I feel well enough to enjoy it. 

  • elkatho
    elkatho Member Posts: 159
    edited June 2013

    Teresa I was using baby shampoo. I told my beautician and he told me to stop immediately. He says it is the worse shampoo on the market. Something to do with whatever they add or delete so baby's don't cry. I cannot remember the details but the panicked look on his face made me stop immediately. He told me to use it to take ring around the collar out of shirts....what!

  • ReddHeddMomma
    ReddHeddMomma Member Posts: 38
    edited June 2013

    Elkatho - I have been using either aveeno sensitive skin body wash or dove sensitive skin body wash on my scalp. I figure I have so little hair left up there as it is, so I am not worrying about how well I am conditioning. But my scalp has gotten dry and really, really itchy, and using something with gentle skin moisture in it is helping a lot. Maybe it would work well with some of you who are also having issues. I think the aveeno is the one made for people with eczema? Both are really gentle and working well for me.

  • ReddHeddMomma
    ReddHeddMomma Member Posts: 38
    edited June 2013

    Happy to report that I was well enough for chemo this morning. My bloodwork all looked good, which was a nice surprise, given that I had to ask for antibiotics just a few days ago for an infection and fever. Had a reaction to the taxotere today - felt like an elephant sat down on my chest with a horrible burning sensation all the way up my throat, and I stopped being able to take a decent breath just out of the blue. My face turned bright red, and the staff came running over. They said this was not unusual, gave me extra steroids and benedryl and something else, and then we waited until everything had completely subsided, and restarted - no hiccups after that. They told me they will have to up the benedryl and steroids at the start next time to try to prevent a stronger reaction, but I am just so glad that we were able to finish this one that I don't care. ( although I may never sleep again...LOL)



    So, infusion 2 is done. Two more to go if all keeps going well. Even with the crazy reaction today, it feels really good to be halfway done.

  • Worrywart9390
    Worrywart9390 Member Posts: 101
    edited June 2013

    half way done, thats what i keep saying.....glad you were able to get thru the infusion today.

  • Gully
    Gully Member Posts: 268
    edited June 2013

    Redheadmom: so glad you made it through your transfusion reaction today. It is very nice you are half way done! I go for round 3 at 10 tomorrow, assuming I pass the blood test of course. I have had an intermittant rash after round 2 so I am a bit freaked out about having a reaction to the taxotere tomorrow myself. My brain is telling me I have to go though another two rounds but my body wants to run away. Maybe they should put seat belts on the chemo chairs...LOL I will defenitly need a pep talk from someboday tomorrow.

  • MomofSam
    MomofSam Member Posts: 74
    edited June 2013

    Teresa - you do look very pretty!

    I shaved my hair all the way down - not sure if that was the best decision, but that's what I did.  Can't go back now.  Had #3 treatment of AC today.  Overall went well.  Had trouble with my port though.  They had to flush it with heperin 3 time and when that didn't work, gave me TPA through my port (basically draino for the port as they called it).  That seemed to get thing going which made me happy.  So, a long day today, but it's over now and I feel okay - we'll see how the next few days go.

    Redheadmom- glad your treatment went well this time!

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