April 2015 Chemo Crew... Starting in April? Please join us!

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  • swissrn2002
    swissrn2002 Member Posts: 27
    edited May 2015

    Kbee, after my AC infusions, I drink tons of water/ lemon waterto flush my bladder, kidneys etc. seems too work.

  • swissrn2002
    swissrn2002 Member Posts: 27
    edited May 2015

    Lovlilynne, I only feel queasy most the time for a few days. I am too, on neupogen, I start mineon day 3(today) until the 9th day post infusion. I don't like the shots either, with Tylenol at the hint of bone pain, I can seem to get past it easy. At least my WBC count has been excellent, so no mouth sores at all. I do notice some shortness of breath when climbing stairs.

  • Positive_spirit
    Positive_spirit Member Posts: 218
    edited May 2015

    fought off anxiety and attended kids event at crowded school with lots of sneezing people. :( but managed to do it! My hair continues to fall out, it began fast and now I use a lint remover to roll out the bald cap.

    Lynne - love the bummer pun! I cracked up, too. Ok..too many puns!

    ksusan - you said something so important about SE not determining whether treatment is working or not. Thank you.

    Kbeee - your exercise routine on AC is motivating me to walk more.

    My MO told me about Live Strong programs at the YMCA which are free 12 week fitness programs for cancer patients. I am going to look into it. If anyone else has experience with these, let me know

  • Stephmoen
    Stephmoen Member Posts: 563
    edited May 2015

    so I will have to possibly be hospitalized for my last 3 treatments depending in how #4 goes they don't want to take me off this regimen because it has been proven to cure my type of cancer ugh annnnd I was exposed to cdiff at my mother in laws while she took care of her sister who recently had surgery so I have to watch for that it just keeps getting better

  • StacyMc329
    StacyMc329 Member Posts: 48
    edited May 2015

    wow this taxol sure does make your nails sore. Phew. Feels like they are about to fall off.

  • Positive_spirit
    Positive_spirit Member Posts: 218
    edited May 2015

    Stephmoen - I wish I had the right words. We'll get you through the treatments, one step at a time. Just one baby step forward each time...it's okay to slide back and then keep moving forward as chemo is tough on the body. Wishing the best care for you

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited May 2015

    Stacy, bummer about the nails, but please do keep posting on your side effects! it helps those of us about to start so much to know what to expect...even if it's yucky sore nails...

    Hugs,Steph! Big hugs. You can do this.

    Positive spirit, crossing all my fingers and toes that the school cooties keep away!

    Anyone drinking kombucha? It's fermented tea..kind of tangy and full of probiotics. I think I'm swapping that for Braggs vinigar.

  • Scarlett152
    Scarlett152 Member Posts: 175
    edited May 2015

    I've wondered about kumbucha. I love it, but is has raw cultures and I'm not sure that ok. Has anyone asked a doctor/nutritionist

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited May 2015

    I haven't asked...didn't even think to. Do you think raw cultures might be bad???? I've been downing yogurt and diluted vinigar with active cultures and taking probiotic pills as well....not all at the same time, just whatever seems most tolerable depending on side effects.

  • Karen30
    Karen30 Member Posts: 135
    edited May 2015

    AC#4 done - felt ok I asked my MO to reduce my decadron which he did from 10mg to 6mg - I'm convinced that's what's been making me feel so weird on days 3 and 4 we will see if it helps- SO glad to be done with AC - my friend brought in martinellis apple cider to celebrate which was fun- I know I have at least a week probably more of feeling crappy ahead but yay- no more red devil !!! On to taxol starting 12th my MO wants me starting the glutamine powder starting now - does snyine have a recommendation on which is next one to get- he is insistent it's the powder not tablets .

    KBeee you are truly an inspiration - enjoy your run - you go girl!!!!

  • Beachbum1023
    Beachbum1023 Member Posts: 1,417
    edited May 2015

    LiveStrong at the YMCA - Positive_Spirit - I applied for the program, and I have just finished the first three weeks, and I love it!!! We go twice a week for the program, and the other 3 days I go on my own. I take Spin on Mondays, LiveStrong on Tuesday and Thursday, Aerobics on Sunday, and Yoga on Tuesday evening at my local cancer center. It is FREE for us, and the class here is 12 people, we are the first class. The 3 month membership is free so we can use all of the classes, pools, track, and machines any time. If it is available, I would highly recommend it. And I am losing weight, a bonus! I also walk 6000 to 9500 steps per day.


    I do feel really good right now, 6 months out from Taxol. I just wish the exercise and Yoga had started sooner so I wouldn't have to lose the weight and get back in shape. Thankfully I was pretty fit when the shit bus hit me. All that exercise is really cutting the fatigue as well. After chemo, surgery, and rads it is nice to be tired from something other surviving treatment!



  • gkodad
    gkodad Member Posts: 188
    edited May 2015

    littleblueflowers, I was told to avoid anthing  "raw" -  drinks and veggies, sushi, etc while my WBCs are down, as there is no way to control for the potentially "bad" bacteria.  But most commercial drinks are not truly raw - they are either heat pasteurized or pressure pasteurized.   Unless you're drinking it or anything else at a juice bar, it's probably fine.  But you may want to read up on it.

    On a related note, I watched the grocery store "fish man" stop scrubbing a sink full of discarded fish parts with his bare hands to come over to help me.  He didn't wash his hands, just put on a pair of gloves and smoothed each on with his bare hands as he put them on.  When I said "you didn't wash your hands", he said he didn't need to because he put on gloves.  I pointed out he had just rubbed his contaminated hands on the outside of the gloves, and he just looked at me like I was crazy.  Since the WBC drop, maybe I am.  Since I planned to cook the fish, it wasn't that big a deal, but it made me take the "raw" food part  a little more seriously.   It's easy to assume food in the deli, etc is safe when you really don't know what happened you didn't see. 

  • Addie29
    Addie29 Member Posts: 307
    edited May 2015

    Stephmoen hang in there. I will be thinking of you

  • allicat1214
    allicat1214 Member Posts: 84
    edited May 2015

    Yes, Stephmoen: We are all thinking and praying for you! One day at a time...

    And to our Kbee: I'm sure you're on the course already but YAY for your half marathon today!

    Hope we can all enjoy the weekend with few SEs and lots of energy!

  • Alibeths
    Alibeths Member Posts: 656
    edited May 2015

    STEPH, hand in there girl. Halfway!!!! ❤️😘❤️😘

    Momma, that pic of your daughter kissing your head is beautiful. How old is she?? My LO is 5!!!!


    Positive spirit, you look great. XO.

    Hang in there ladies!!! This too, shall pass. ❤️

  • AndreaC
    AndreaC Member Posts: 220
    edited May 2015

    Good morning!

    This group has so much to say...I missed one day and there were so many posts to get through. It is wonderful though, reading about people's experiences.

    Hugs to you, stephmoen, I'm thinking of you and sending positive energy your way. You will get through this! We all will.

    littleblue, I toast you with a mouth-soothing smoothie! You are funny.

    Kbeee, how did the race go? You are amazing!

    Momma, sweet picture of your daughter!

    positive spirit, love your photos!

    Re working during treatments...it is, of course, a personal decision...but for me I can't imagine working. My job right now is to look after myself and get better. Mind you, as a nurse my job involves 12 hour shifts and can be mentally as well as physically demanding. I have been told by my MO not to expect to return to work until at least Feb. of next year. I will have been off work a year.

    I have been reading about people's experiences with PA's - I live in Canada and we don't have them (at least, not where I live). But I was in Phoenix earlier this year and had to take my mom to ER and she was seen by a PA there. Not once was she assessed by a doctor. The PA kept leaving the room to go ask the doctor questions or run things by him. The doctor wrote my mom a prescription without ever seeing her. And this hospital is supposed to be one of the top hospitals in the country. It seems like a really backwards system to me.

    I am feeling pretty much 100% now, nine days after TC#2. It's a good thing too, because my husband has planned a big backyard BBQ today for my birthday! (My birthday is actually Tuesday). The weather is gorgeous and I am so glad to be alive! Can't wait to see the grandchildren today!

    Andrea

  • KBeee
    KBeee Member Posts: 5,109
    edited May 2015

    Steph, so sorry you will have to be hospitalized for the last treatments. uuugh. One. day. at. a. time.

    Karen, Congrats on last AC!!!

    I did it!!!!! My goals were: 1. to finish, 2. to finish in. the alloted time of 3:15, and 3. to finish in under 3 hours. I will see my final time once posted tonight, butit is somewhere between 2:40 and 2:50... probaly in the2:45 range. I will post a picture of my hashtag shirt I made to wear. There are 2 hashtags shoutouts to my April 2015 chemo gals on there. It was my of taking you all with me on the run. Here it is.image

  • kbta032803
    kbta032803 Member Posts: 10
    edited May 2015

    Kbee thats awesome! Congrats on finishing

  • allicat1214
    allicat1214 Member Posts: 84
    edited May 2015

    Oh KBee: So so very proud of you! We were all there cheering you on in spirit!

    You are my hero!


    I did mow my backyard today .... that was my accomplishment for the day!

  • SueH58
    SueH58 Member Posts: 632
    edited May 2015

    Kbee, that is truly unbeilievable!!! Congratulations. We need to put you and Theresa (Italychick from March board) in a match - she'll bike and you can run!

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited May 2015

    Nice work kbeee! I'm 3 down 10 to go! You are a beast!!!😁

  • gkodad
    gkodad Member Posts: 188
    edited May 2015

    Kbee, you are amazing!  I can barely walk around the block right now, so I do not know how you do it.  I guess I should look forward to Taxol!


     

  • gkodad
    gkodad Member Posts: 188
    edited May 2015

    Karen30 - glad you're through with A/C.  I'm bringing up the rear and will be joining the A/C finishers in just 11 more days. 

  • KBeee
    KBeee Member Posts: 5,109
    edited May 2015

    Littleblue, The weekend after my 3rd and 4th AC, I was lucky to get a cew miles in. A week makes a huge difference!!!!!

    Thanks gals. Just thankful to have had the energy to do it today

  • SueH58
    SueH58 Member Posts: 632
    edited May 2015

    Are you totally (but happily) exhausted, Kbee?

  • Stephmoen
    Stephmoen Member Posts: 563
    edited May 2015

    awesome kbee you go girl!! I have a question for the girls who had a mastectomy how long is it to complete the whole procedure from mastectomy to implants I'm guessing I will need tissue expanders so far I am not going to get radiation because they don't believe lymphs are involved unless the SNB proves other wise which they don't think will happen

  • Addie29
    Addie29 Member Posts: 307
    edited May 2015

    Stephmoen I had bilateral mastectomy on 4/1 and I think my ps is waiting until chemo is done to do the swap with the implants. So it will be a total of 5-6 months.UNLESS my MO gives the approval and my counts stay good. But I am in no rush for them. I feel like my body would do better after chemo is done but that's just me

  • GingerChi
    GingerChi Member Posts: 252
    edited May 2015

    Congrats Kbee!! Thats awesome!! I still think you're wonder woman! :)

    AC#4 has hit me pretty hard. This is day 3, starting to feel better, but have mega chemo brain. I had a long post typed up but lost it. Arg! I'm thinking of all of you...wishing few SE and a nice weekend to everyone!

  • KBeee
    KBeee Member Posts: 5,109
    edited May 2015

    I had BMX in late August of 2013. I finished chemo at the end of November 2013. My exchange surgery was 1/22/2014. I had my fills during chemo, so I took my time. If it were not for the delay during chemo, I could have had the fills more often and the exchange sooner.

    Gingerchi, I hope you feel better soon. AC 4 hit me the hardest too, but after days 3-4 which were the hardest, I turned the corner and felt better and better each day.

    SueH, I am happy. I am tired, but not as exhausted as I thought I would be. Alternating walking and running, walking the uphills and running the downhills, and just doing it for fun made it really enjoyable. The cool teperatures and winds from the north helped too (the run goes north to south, so the wind was pushing me along the whole way!!!). Final time was 2:39.45. That said, I have been up since 4:10 am, so I should sleep well tonight, and will be heading to bed early

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited May 2015

    6 miles down..7 to go...😁

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