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

Options
17475777980204

Comments

  • Stephmoen
    Stephmoen Member Posts: 563
    edited June 2015

    sheshe I'm very interested that you have received 4 infusions and getting surgery then determining if you need more it makes so much sense! So if you have a pcr they are not going to do the last 2 infusions? I'm having a difficult time with the taxotere with allergic reactions so it would be nice to only do 1 more rather than 3 more! Really hoping for a pcr for you that would be awesome!!

    Littleblueflowers you have such amazing views from your house I'm so jealous we don't have views like that here in michigan although we do have the Great Lakes which is beautiful in the warmer months

  • sheshe3
    sheshe3 Member Posts: 70
    edited June 2015

    Steph, yes your correct. My MO told me they would withhold my last two tx if pcr. Not quite as sure about the rads, but they indicated considering skipping it. I know you've had a really tough road with taxotere. I hate that stuff and it hasn't been nearly as bad for me... bad enough though😨 It would be great if you could get your surgery after your fourth tx. Maybe run it passed your MO!

  • Rpayton
    Rpayton Member Posts: 235
    edited June 2015


    Happy Sunday Everyone!

    Have been reading posts all week but really having issues recovering after #3 and have to head back to the chair Friday for #4.  Definitely considering taking full disability now and getting me time to take care of me.  I'm getting now that the effects are cumulative and coming harder and longer to deal with now. Mostly fatigue as we are all experiencing.

    Karen30 know all about those fissure issues. Sorry you are going thru and hope healing comes fast.

    Allicat CONGRATS on finishing chemo! Looking forward to your share about radiation. I will be headed there too.

    Littleblueflowers that view is priceless! Just too much rain here in Northern IL but good for the crops.  Just wish it wouldn't be rain EVERY weekend. Errrgghhh

    So many others of you have posted and shared. Keep sharing. Everyone hang in there. We are doing this together.

  • raisemeup
    raisemeup Member Posts: 11
    edited June 2015

    i haven't posted since my 3rd A/C because I have been exhausted. I've had 4th A/C and first Taxol. 6 days after 4th A/C on May 27th I have had a low grade fever and it will not go away. I don't know if it's the chemo or fever making me so exhausted. I have had to take more time off work and I hate that. My MO has had me on round the clock Tylenol and Motrin since Friday but it doesn't seem to be helping. I go back Wednesday for taxol number 2. I hope if I still have this temp they do something to make it go away. My hemoglobin was 8.2 so I know it's getting close to transfusion time. Any one else have issues with temp? This is depressing.

  • lovlilynne
    lovlilynne Member Posts: 405
    edited June 2015

    Denise, no fevers here, although I've had some days when I checked frequently because I felt so sh*tty. Are you doing weekly Taxol?

    Lynne

  • lovlilynne
    lovlilynne Member Posts: 405
    edited June 2015

    Rene, I can totally relate. Sorry about #4 - it was, as predicted, the worst. But, it will be behind you soon.

    You may have read my update that I decided to take a full MLOA after talking to MO before 4th AC. I just felt like I couldn't give 100% to work anymore, and work was taking all I had for energy. No energy for self care, family, etc. Hope you come to terms with whatever you decide. It's hard!

    Lynne

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

    I just got off a 13 hour shift, which really was not too busy, thankfully. It was just busy enough though. It's nice to be the caregiver for a change, instead of the patient! I can't remember all posts, so sorry for those I miss!

    Little blue, Glad you called. Did he have suggestions? Speedy healing to that back. When I was on Taxotere, I had horrible bac spasms/back pain. It felt like back labor.

    Andrea, May e FH could compromise. Tell him you are glad he can go out a few nights, but that you would like to have a movie night at home with him too. Men are often not sure how to cope when the see us suffer, and avoidance is unfortunately a common coping strategy. Either that, or call a friend to come hang out with you. He may think he is tiving you time to rest. Be sure to clearly communicate that you could use him home more.

    Raisemeup, No fever this time (yet) but in 2013 on TC, I had fevers very ofter...usually when my counts were a bit low. I hope that hemoglobin comes up too. You must be exhausted.

    RPayton, This is what disability is for. Me time is important now.

    Who all hits the chair this week???


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

    rpayton! I go to the chair on Friday too....Good luck with #4..I'm going for taxol #2..

    Lynne, I hope you have time for radical self care now, as my therapist calls it. This is definitely the time to be good to ourselves..

    Kbee, your words about husband's really resonated for me too...thanks for saying it!

    My back popped back in! Fingers crossed it stays put now that I've lost so much muscle tone! MO said yes to muscle relaxers and chiropractic, no to ibuprophen. Feeling darn near normal today, but I noticed that the cord of muscle or something in my surgery side armpit has cranked even tighter. Probably time to set a PT appointment.

    My ankle hair has suddenly reappeared . Not the rest of my legs. Just my ankles. Maybe my eyebrows are migrating? Feeling pretty normal today..even a sore back is normal. Have had a phantom itch on my chest, but when I scratch there I can't feel myself scratching..weird. Feeling so much less agressive and angry on taxol...even my music choices are more bluegrass than rock. And I want to eat fruit and veggies now whereas on AC I forced myself to eat lots of protein..just another day down the rabbit hole inguess..

  • ksusan
    ksusan Member Posts: 4,505
    edited June 2015

    I am grateful for my mother, who is visiting.

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

    littleblue, I have been craving fruits and vegetables too!!!

    I have always been a throw hair in a ponytail and go type of girl. My hair could finally fit in a little ponytail when rediagnosed. I so have missed my pony. I was reading a breast cancer blog this morning... one I have followed since 2013. she posted somethong called pollysponytails. They use hair extensions attached to headbands...so you wear just a headband with a ponytail on it...much cooler than a wig. That sounds so very me...and much more comfortable at work. It was less than $40, so I ordered one. I will let you know how it works and looks when I get it.

  • lovlilynne
    lovlilynne Member Posts: 405
    edited June 2015

    GM - I survived pre-game steroids! I had to take them at 9:45 (5 pills - 20mg) and set my alarm for 3:45 AM and take 5 more. Directions said to take with food, but at 9:45, it wasn't that long after dinner, and I decided I wasn't going to wake up enough to choke down some crackers at 3:45, and it was ok - not sure what I'm doing to my stomach???? But, I slept ok! It did take a little while to go back after 3:45 AM pills, but I did and was good until bathroom run around 5.

    First Taxol today, my sister is coming to take me and stay until they get it started. I insisted she then go have lunch with my mom, and she insisted on coming back to drive me home.

    I'll try to check in later to let you know how it went.

    Even though no work - gotta get the kids up and off to school and drive my DD1, so gotta run . . .

    Lynne

  • ThePrincess
    ThePrincess Member Posts: 424
    edited June 2015

    Ladies that go today - good luck!

    I go for first Taxol/Her/Perjeta tomorrow, anxiety is very high!

  • Addie29
    Addie29 Member Posts: 307
    edited June 2015

    good luck lovelylynn. I start my first taxol tomorrow. And littleblueflowers I hear ya about the back issues. I've had them since my surgery and chemo started. Some days my back loves me and others not so much. Like today and last night the whole right side of my back hurt- my muscles are so tight throughout my whole back since ive had these expanders placed. I've been meaning to speak to my ps about seeing a chiropractor but keep forgetting.

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

    Good luck to everyone hitting the chair today! Minimal Side Effects to all!

  • sheshe3
    sheshe3 Member Posts: 70
    edited June 2015

    GL to all visiting the chemo bar today! Wishing all you of low to no se's.

  • Alibeths
    Alibeths Member Posts: 656
    edited June 2015

    Littleblue, can I come over????

    FOllow my page on FB for us survivors!

    https://www.facebook.com/sendBCpacking?fref=ts

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

    Allibeths, For sure! Come over any time! And I love your page..We are survivors. How weird to think that this was killing us at diagnosis, but it isn't any more. Like, we really could have died, but we didn't. Huh. That's brain food right there...

  • Alibeths
    Alibeths Member Posts: 656
    edited June 2015

    Amen sista! : )

  • Alibeths
    Alibeths Member Posts: 656
    edited June 2015

    What do you guys use for DRY EYES????? Visine is NOT cutting it!

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

    I second that...I'm tired of looking like a puffy pink eyed mouse! Help!

  • gingeel
    gingeel Member Posts: 102
    edited June 2015

    Littleblue, what a view, I want to move to Montana! Hope your back is feeling better.

    Scarlett, I realize that some people just don't know how to deal with cancer. My father whom I used to speak to every week, has sort of become a bit distant. We definitely don't talk as often as before.

    Andrea, you should absolutely tell your husband how you feel. He's not thinking of how this is effecting you, and you don't need that. Once in a while is fine, but not every night.

    Congrats KSusan on finishing chemo!

    Addie, you and I both start Taxol tomorrow!

  • GingerChi
    GingerChi Member Posts: 252
    edited June 2015

    Alibeths, I've been using gel lubricant eye drops, and they helped me. I got the generic brand at Walmart.

    Princess, Addie, and gingeel I will join you hitting the chair tomorrow. Taxol + Herceptin #1 for me! I'm nervous too...ugh. My blood pressure will be through the roof. I took my pre steroids this morning, first time I've had to take the pills. I feel ok, kinda tired and jittery at the same time. I feel kinda like I did when getting AC, I wondered how much of my weird feeling was from the chemo and how much from the steroids!

    Lynne, hope all is well after your treatment!

    Allison, congrats on finishing!!!! Love your pictures!! :)

    Kbeee, the ponytail looks neat, let us know how it works for you. Its hitting the mid 90's for the next 10 days here, I have pretty much scrapped the wig and have gone to wearing bandanna type scarves. MUCH cooler.

    Andrea, I can totally understand how you're feeling! If you talk to hubby, hopefully he'll understand your feelings! I probably wouldn't be handling it as well as you are right now! You're a strong woman!

    ksusan, thats so great that you're spending quality time with your mom!!! I've missed mine so much throughout this ordeal, treasure every minute!!

    Hope everyone going thru rotten SE feel better soon!

    Best wishes to everyone hitting the chair this week......may our SE be few!

  • AndreaC
    AndreaC Member Posts: 220
    edited June 2015

    Good day all!

    Thanks all for the support - DH really is amazing, he's so supportive but at times he does feel helpless. We had a good talk about his absences and things should improve. In the meantime, I have been making plans with friends and my daughter...

    Very tired after TC#3 on Thursday. I have been spending much of the day sleeping, aside from going out to get my PICC dressing changed and having coffee with a friend. Speaking of which, I asked my friend to drive me because of the chemo fog. Do other people avoid driving for 5-6 days post chemo? I just think it's prudent. I have a doctor's appt. tomorrow and have another friend driving me, then I will take her out to lunch.

    Littleblue: so glad your back is better! Also, your pics of the landscape around your place are lovely...I think we should all post pictures of where we live. Mine is of my backyard, looking towards the lake and Mt. Prevost (Duncan, BC).

    ksusan: it's so great that your mom is there. Enjoy her company!

    Kbeee: I miss my ponytail too. I have had long hair most of my life and it sucks that I have none now. Post a pic of your new do when you get it!

    imageAndrea


  • ksusan
    ksusan Member Posts: 4,505
    edited June 2015

    #9: I am grateful for a new appointment time that will get my port out a week earlier.

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

    ksusan, hooray for being "deported" sooner!!!!

    Andrea, Glad you were able to have a chat with DH. I have driven myself to the last few chemos and pretty much drive every day. Thankfully I have not noticed problems or chemo fog. I have 3 kids to get here, there, and everywhere. I am not sure what I'd do if I could not drive!

    Gingerchi, Gingeel, Addie, and Princess, we'll all be at the chemo bar for our cocktail tomorrow. Anyone else? I hope everyone getting their first Taxol (or their second or 3rd or 4th)will have an easy time. Tomorrow is Taxol#4 for me...1/3 done with Taxol in 15 hours.

    Lynne, How did Taxol go?



  • starrgirl
    starrgirl Member Posts: 8
    edited June 2015

    Had dose dense taxol #2 today. No complications but really get antsy sitting for 3 hours. My mom and dad took me today so I enjoyed visiting with them. SE that I have been experiencing is extreme bone pain in legs, hips and back that start on day 2 and continue through day 6. Been taking norco for the pain. Appetite has been better and experiencing no nausea. MO said today that with my good counts two weeks post chemo I will probably start radiation a couple weeks after last chemo. I'm definitely ready to move on. Applied for and received LTD so I'm hoping to be back to work in Sept. Good luck to those ladies going in tomorrow and the rest of the week. May you have minimal SE. Thank you for all of your support and valuable information.

  • lovlilynne
    lovlilynne Member Posts: 405
    edited June 2015

    Hi - took my ativan already, so don't know how long I'll last or how coherent I'll be.

    Taxol infusion went well all things considered. They couldn't get a blood return from my port, so took blood from my arm for labs. My numbers were almost unchanged from last treatment, which surprised me because I have been feeling so much more tired and weak and out of breath. But, it means that I don't have to take Neupogen shot tomorrow YAY.

    They had put clot busting medicine in port, so I had to wait another ~30 minutes before they tried to access, and it still would not get a return. ON finally put in another set with a longer needle, and voila. After that, she gave me the Benedryl - 50mg! I felt it almost immediately, and I could not stay awake. They also gave me more Dex. Then another 30 minute wait (she originally said 45) before they started the taxol so that they could be sure that the medicines were through my system. No one had mentioned that. So, it was 12:40 before I had the Taxol going - my poor sister waiting through all of this. I felt nothing, no reaction at all. So, next time I won't have to take premeds, and they may be able to back off my Benedryl too.

    By the time I left - 3:40 PM (got there at 9:45 AM), I did not feel any effects of the Benedryl. My sister drove, and I think I will continue to be driven to and from these, but I feel like I will be fine to drive back to Maine after I get home from next Taxol infusion. I feel fine now, maybe even a little wired, that's why I tool the ativan.

    Oh, I got clarification on the L-Glutamine, I started taking it today, which is the right answer - 3x a day for 3 days, 10mg. I put 2 tsp in a large glass of ice tea and drink it down. It's not bad, but I'll be glad when day 3 is over.

    Also, I have proved my theory that steroids get rid of the mouth sores - did I say that already?

    I'm rinsing still, but is this as much of an issue with Taxol?

    Also, mentioned the cardboard taste buds to NP, and she said she didn't hear much of that, but admitted that Taxol does mess with taste.

    Jeez, guess I had more to say than I thought.

    Thinking of all the chemo-sabes tomorrow - I'll be thinking of those going for 1st Taxol. DD is definitely a LOOONG day.

    So grateful to be on the other side of half way done!

    Lynne

  • ksusan
    ksusan Member Posts: 4,505
    edited June 2015

    Good thoughts for those getting chemo this week!

  • Alibeths
    Alibeths Member Posts: 656
    edited June 2015

    What do you mean that steroids get rid of mouth sores

  • ThePrincess
    ThePrincess Member Posts: 424
    edited June 2015

    Gingerchi, Gingeel, Addie and Lynne? Good luck today! I'm right there with you!

    kbeee! Good luck also - 1/4 way done!!

Categories