August 2011 chemo, anyone w/ me?!

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  • Flautalee
    Flautalee Member Posts: 118
    edited September 2011

    Justina, wow!  I will check it out.  I reread my portacath post-op directions.  I can't swim until next Friday, so no swimming in the ocean this beach trip because we will be coming back Wed. AM.  So is the store called "Just for You?"  Thank you for your help.  Best to you.

  • jbagley
    jbagley Member Posts: 102
    edited September 2011

    Hi, I'm jenn, stage 3 bc, 38 yrs old.



    I lost most all of my hair by day14 and day15-16 after first and second treatment.it was really hard for me. My 9yr old said to me" mommy we will still love you even if you don't have any hair" course that made me cry harder. She actually shaved my head once it started falling ojt. She had a grand ole time" shaving mommy's head" I can laugh about it now, but for a week I cried. Women are suppose to have hair. Anyway, it does get a little easier. I don't walk around the house anymore with a cap on.



    Jenn

  • edyem
    edyem Member Posts: 38
    edited September 2011

    Wow! I started tx in late July, but most of you will finish before I do.  I have my 3rd AC next week, and 1 more 3 weeks later.  Then I have 12  weekly tx of Taxol!  I am stage IIIc, though so that is probably why.  I also have 6 weeks of daily radiation following that.  

    Justina - I believe we have the same treatment regimen as far as chemo goes.  I'm going to ask my Onc about the shortage of Taxol that I've been hearing about.  Have you asked your doc about that?  I'm wondering what the solution is if there is none available.  

  • celina2011
    celina2011 Member Posts: 29
    edited September 2011

    im new to the site. I will have minesept 9 withACT and hercepten, still battling to have a port or pic line pls help

  • celina2011
    celina2011 Member Posts: 29
    edited September 2011

    hows your adriamycin do yor have a port too

  • celina2011
    celina2011 Member Posts: 29
    edited September 2011

    we have the same treatment but I will have herceptin as antibody

  • Taylor777
    Taylor777 Member Posts: 141
    edited September 2011

    Chrys..so far I'm getting some leg pain , some fatigue and I'm not really sleeping at night. Thanks for the idea of the journal. I had my neulasta shot given by my nurse and I cant beleive were supposed to inject the others ourself ughhhh!!! Hope your doing ok and no S/E's..

  • Taylor777
    Taylor777 Member Posts: 141
    edited September 2011

    I'm getting 8 treatments but 7 now to go thats a big booo for me Yell

  • Taylor777
    Taylor777 Member Posts: 141
    edited September 2011

    Hi Celina ..I have a port it was a little uncomfrotable for about 6 days but now I dont feel a thing and I love it!!

    Hi Jbagley..I know it sucks that after all we have to do to beat this is lose our hair too!! And our such young children have to be apart of this makes me angry!!!!

  • vtellen
    vtellen Member Posts: 345
    edited September 2011

    Hey Chrys- so this will be day 4 w/ steroids for me. I could feel some pains flittering around last night. As per onco I also upped ativan to 11/2 mg (or pills) He said I can take 2 at night to help w/ sleep during the bone pain, and i slept pretty well last night. Am also taking Aleve.

    Taylor- are you taking anything to help w/ sleeping? Ativan, ambian,etc? I

    I can def see the advantage of a port. Nice achy bruise on my inner left elbow, I am ready to get tough w/ the next blood taker who acts as though that is the only spot from which to draw blood. They are going to have to get creative and hopefully not jab the heck out of me in the process!

  • dianamaps
    dianamaps Member Posts: 50
    edited September 2011

    Shortage of drugs:   Seems like this is going to affect a number of us.  A friend's young daughter with leukemia in California is being impacted too.  Here in central NY Taxol is in very short supply and I've been told there likely won't be enough for me, so I'll be given Taxotere instead.  The onc says it'll have the same chemo-effect in terms of disrupting/killing cancer cells, but I seem to get mixed message about the different SE of the two.  Some things I've read say Taxotere will be worse.  I'm supposed to take it once/week for 12 weeks.   

    Any others know yet how the shortages might affect them? 

  • jbagley
    jbagley Member Posts: 102
    edited September 2011

    Hi



    Taylor777--i have port too, its the best thing.



    Vtellen--will you be getting a port? One stick for blood draw then off for infusion. No bruising.



    Dianamaps--i haven't heard about the shortaage of taxol, (Maine) but will find out when I go to Lafayette Cancer Center on tuesday when I go for my last A/C. I am due for 4 rounds of taxol. We will see.



    After I take my neulasta, my neck and shoulders are the only place I hurt. Tingly, prickly feeling in my skin, then it settles into my muscles and shoulders. This is the only time I use my oxycodone and ativan, though ativan I take at bedtime to help me sleep. It doesn't always help though. I am feeling pretty good today. Only to start over on tuesday.



    Thanks everyone for the support. Jenn

  • Robyn6463
    Robyn6463 Member Posts: 167
    edited September 2011

    No drug shortages here that I'm aware of...just water. (Water main breaks during the flooding after Irene). They've cancelled all non-urgent surgeries, but I've not been told no chemo yet! I'm off to number 2 in about an hour!

    Hoping this port starts to feel better eventually! Taylor, you give me hope! I really didn't mind the needle sticks so bad! 

  • Lowrider54
    Lowrider54 Member Posts: 2,721
    edited September 2011

    Morning!  Haven't seen a September 2011 chemo sisters thread yet...sooo, I start today.  I am nervous.  I had chemo 13 years ago but this is so different - I am taking the chemo class since things have changed so much with drugs and se's and stuff. 

    robo47 - wishing you luck today too. 

    Update when I get done and perhaps on a Sept 2011 thread! 

    We will all get through this!

    Hugs

    LowRider

  • dianamaps
    dianamaps Member Posts: 50
    edited September 2011

    jbagley:  I have the exact same reaction to the neulasta.  Very sore and sensitive upper back and shoulders.  Seems to only last for 2-3 days after the shot.

    Wishing us all some zero-to-mild SE today. 

  • vtellen
    vtellen Member Posts: 345
    edited September 2011

    I only have 2 more treatments, and plenty of good alternate veins, so no port for me. And BTW, I have seen a Sept chemo group starting up. Taxotere is a bit tougher, I would not want to have it every week! Wonder why the different schedules for dosing?

  • vtellen
    vtellen Member Posts: 345
    edited September 2011

    Robyn- Salisbury ( my little piece of Vt. was relatively untouched) Sorry about your troubles, do you have water in Bennington? Boiling?

    I am having some pretty debilitating cramps. Why and any suggestions? I have some of the usual C, but actually better than last time. Anyone else have this problem?

  • capinva
    capinva Member Posts: 138
    edited September 2011

    Treatment went well yesterday but took a nap when I got home. This was 2nd round of a/c. Anyway vomitting started and the onco nurse said I wouldn't need to take my pills until today. So I took a pheghan (sp?), didn't help then popped the ativan. That helped and I slept all evening and night. Today is better. Going for my shot in a few mins. My last shot wasn't too bad, only pain in hips and upper thighs but advil helped. Hoping the throwing up is over and the rest of the week is zero s/e. Hope everyone else has a zero s/e day.

  • Taylor777
    Taylor777 Member Posts: 141
    edited September 2011

    Robyn..I promise the port is going to start feeling better..It hurt like hell that first night had to go back to the hosipital the next morning cause it felt like I had knives in my neck, I ended up being allergic to the tape and it took 6 days and I sometimes forget the port is there.

  • Taylor777
    Taylor777 Member Posts: 141
    edited September 2011

    Good luck low rider and to all other's going for treatment today!!

    Hoping for a side effect day for everyone!!!

    Happy Friday everyone!!Smile

  • summergirl1
    summergirl1 Member Posts: 182
    edited September 2011

    Hair is shedding a lot now its freakin me out Im so sad think this will be the hardest/Scariest  thing I have had to deal with in my life, but other than that I feel great TG

    Dianamaps Sry about your daughter being upset thats gotta be hard , My kids are grown up so they wont be freaked out, My son is gonna shave my head I pity him LOL as I know I will be a mess but he wants to do it, and from my experience of Taxotore I found it to be ok just about 2-3 yukky days no sickness just flu type sympoms and no other SE's at all. I am actually looking forward to round 2 next week as I feel I will be getting closer to the end. Good Luck

    Good Luck to any of you having TX today and cant wait for the day we are all taking abot our last TX and getting back to our lives again. 

  • Justina
    Justina Member Posts: 53
    edited September 2011

    Edyem, I will ask my onc about the Taxol shortage when I see him this Thursday.  I've read about Taxotere having worse side effects, so am a little apprehensive.  I have to wonder - if we hadn't read about the shortage on this site, how would we know? 

     Hope everyone has a side-effect-free holiday weekend!

  • dianamaps
    dianamaps Member Posts: 50
    edited September 2011

    At my onc's office they were giving out reprints of this article, 

    http://www.nytimes.com/2011/08/20/health/policy/20drug.html

    that talks about the chemo drug shortages.  

  • isa702
    isa702 Member Posts: 12
    edited September 2011

    Hello ladies!!! Gud luck to everyone having Tx today and wishing everyone a minor to none side effect day today...

    Today is my day #3 of 1st A/C tx, just feeling a minor headache and kind of like some nausea but not quite :/ ...

  • MaryjRN
    MaryjRN Member Posts: 130
    edited September 2011

    Hi ladies,

    Just got back from an accupuncture session.  Started them because of low back pain; can't say for sure that it's helping my AC side effects.  Will report back to you later.  The Ambien is not helping my 2am insomnia.  Can't seem to get back to sleep.  I have some Ativan lying around from my sister's death 3 years ago.  Will try that tonight.

    Happy se-free days to all my bc friends!

  • koalakid39
    koalakid39 Member Posts: 42
    edited September 2011

    My steroids don't have me pepped up like usual. I'm really tired today and it didn't help that I had to take hubby back up to the ER. They found 2 more broken ribs that they somehow missed last week after his accident???!! My hair is getting thinner by the day. I thinks it's time to go take a nap!

    I hope everyone has a great weekend with minimal se's! HUGS

  • Robyn6463
    Robyn6463 Member Posts: 167
    edited September 2011

    Sigh. Site where the installed the port is infected, so now I've got antibiotics to help mess up my stomach. Then it took 2 1/2 hours to flush the port in order to use it today. Once we FINALLY got started, the infusions went very well. I dozed through the taxotere this time! Still a little sinus burn from the cytoxin, but nothing major. I go back Tuesday to recheck the port and have the neulasta shot. Now that there's an infection present they won't mess around. Ugh. A very nice Reiki therapist came through and provided some treatments today. She was fun! Feeling pretty good, drugged and tired, so I agree koalakid, good time for a nap. Cranky with my boys, (17 yo son, 6 yo grandson) they drank all my stuff while I was gone! I'll have to find a hiding place!

    On another note, I got to watch the Red Cross land a couple of helicopters outside the window. They're delivering cases of water bottles to the hospital, town water main is broken. It was pretty cool. They were HUGE! I'm fortunate to have a well, so I don't have any problems, but will be sharing with friends as they need it! Thanks for asking Ellen! 

  • zanoza
    zanoza Member Posts: 40
    edited September 2011

    Celine - I see you're HER+ which means a year of Herceptin, so port is a really good solution for you. PICC lines work for the short term cycles. I just had my port in today, so far so good, they even didn't prescribe any pain-killers, looks like in Canada we're getting less drugsFoot in mouth

    Good luck for everybody getting treatment today, pray for as little SE for all of us as possible! I'm day 10 after the first tx and STILL nauseatedYell

  • Vivie
    Vivie Member Posts: 52
    edited September 2011

    Hello there!

      Hair loss is continuing here..*sigh* 

     Grimbol happy late anniversary , and glad that you feel better! 

      BOO , I have only 7 more tx's to go thru..#2 is Tuesday..I go in Monday for blood draw and check...but I wonder how I'll get THAT done..as I had done a CAT scan ( chest area ) and the CAT tech decided it was a fine day to destroy my veins..I have a bruise at the crease of my elbow...it hurts! ( 3 sticks to get a VEIN , ugh ) and the other arm is a no go bc of the MX side..

     I should have demanded an port...*sigh* kinda late now , but I'm not a big fan of getting searched for veins ALL the time.

  • Flautalee
    Flautalee Member Posts: 118
    edited September 2011

    Celina2011 - Welcome to our group. This is a wonderful site where we can learn from each other and the post moderators. I know that I feel supported and not alone because we are here for each other. I'm really surprised that you are having to "fight" for a PIC line or Port unless your veins are way better than most of ours are (mine are terrible). One of the really hard things about "before" treatment is the waiting for each step. When my oncologist decided what my treatment was going to be, then things started moving a lot faster. I am grateful to a few unnamed patients in my Onc's practice who changed around their treatment day or time so that I could start my chemo on 8/26. If your veins are good, maybe this is a way for you to start your chemo sooner. Best!

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