February 2014 Starting Chemo Club

Options
1252628303151

Comments

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Jules,

    Hang in there sister.  The Taxol should be much better!   If I wasn't dealing with some serious anemia right now (fatigue and winded), I would be tolerating the Taxol quite well.   Keep in mind that there is only one AC left!  

    I blog about AC/Red Devil.  If you would like to read: you may relate

    http://jbokland.wordpress.com/

  • tangandchris
    tangandchris Member Posts: 1,855
    edited April 2014


    Jbokland-I just read your blog about the chemo...sheesh you are sooo right on the way you described the weekend after AC. I've completed 3 and have 3 more to go and I have and continue to think I just don't know if I can do this again. It is a dark time those first few days after, but I keep holding on because eventually it gets better.

    ((hugs))

  • 3doglady
    3doglady Member Posts: 50
    edited April 2014

    The AC was pretty bad.  My first week was a haze.  My second week, things seemed to return to normal - at least as normal as life is now.  I def had and still do have the feeling "I dont want to do this." But I do.  Im on taxols now; today is #2 of 12 total.  Anxiety creeps in as I approach.  Hang in there.  Time will pass quicker than you think. 

  • tangandchris
    tangandchris Member Posts: 1,855
    edited April 2014


    I left a message for my MO's nurse about my back pain. *sigh* why do I always feel like I'm being a pain in a$$ when I call with an issue? It's not them, it is me.

    Hope everyone is holding up today, as well as can be expected. I've got the fatigue today big time! ((hugs))

  • Sicilian
    Sicilian Member Posts: 49
    edited April 2014

    Feeling like garbage right now. Still running a low-grade fever. Been on antibiotics since Sunday night. The Doc said my white count is still within normal range, but it dipped from 7.6 to 4.7, so I have to go back and get it checked again on Thursday. Hopefully, it stays consistent and doesn't dip any lower.

  • h0pe
    h0pe Member Posts: 125
    edited April 2014

    Post 11 days from dd AC #4 and felt the most fatigued out of all the chemo days. Not sure if it was from a long day yesterday of hanging out with friends and lack of sleep, but I could hardly stand today. Exhausted. 

  • Njmom3
    Njmom3 Member Posts: 143
    edited April 2014

    Had my #4 dd AC and I say good riddance to the red devil!  I am wiped out not sure if I didn't sleep good last night or what but usually this fatigue stays away till the next day...  Last nuelasta tomorrow, wow two milestones in a week YES!  And my RBC count stayed the same after the last blood transfusion and chemo so yet another plus!  Waiting for the other shoe to drop as they say!  Taxol in 2 weeks then on my way for weeklys...  My port didn't want to play today had to recline all the way back and put my knees up and turn my head opposite of it to get draw back, it was ok for infusions but not draw backs, odd.  Even yesterday I had to have it flushed twice for labs. The nurse said even a few pound weight difference could affect it, great something to worry about....

    As for the Claritin with nuelasta is just regular Claritin not the D.  I have the redi tabs that melt and have no problems with pain, my onc did approve them.  Hope to keeps working for my last one!

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    You know what ladies, I love the group on this posting!  It good to have sisters on similar schedules and journeys to compare notes with and encourage each other!  

    I only wish there were "like" buttons to a way to comment back directly to someone's post   (I guess I am a true FaceBook girl). 

    I will share that when I hit my lowest point of feeling defeated and decided to have a pity party for myself, the universe saved me.  That same day I was advised of another patient in my MO office that was just 24 years old with stage III, no health insurance and minimal family support.   I stuck my chin up at that moment and was reminded of perspective.   BTW, I made it my mission to befriend this beautiful young budding artist and took her to lunch today.  I am trying to mentor her through some of this craze.

    Good riddance to the Red Devil and F$ck Cancer. 

  • princessrn
    princessrn Member Posts: 370
    edited April 2014

    jb...you're the best egg ever!!

  • Jules_NY
    Jules_NY Member Posts: 276
    edited April 2014

    jb- I wish there was a like button too!!!!! Lol. And thank you so much for sharing your blog, the obituary to the boobs was hysterical. I look forward to reading more!

    You are right no matter how hard this is, it can always be worse!

    Sicilian-hoping your numbers are good!

    My last red devil is tomorrow!!!!!!! I'm not looking forward to it at all because I still haven't fully recovered from the last one. Make of this what you will, but on my way to my last 3 treatments the song Titanium played on the radio. I was never really a big fan of the song but now it's kind of my anthem. As I was having a little pity party on the way home from work today, It came on again. And lifted my spirits a bit. 

    This crap can shoot us down, but we won't fall, we are TITANIUM!!

    Love and hugs sistas!!!!!

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Thanks Jules...I appreciate you reading my blog and your compliment!

    Funny - I went to see a dermatologist today and had to fill out the history form.  One of the questions was "Do you use IV drugs?".  I said yes!

  • Njmom3
    Njmom3 Member Posts: 143
    edited April 2014

    Congrats Jules on that last red devil, I am so glad to be done with it, I don't care how crappy I feel!  I love titanium as an anthem, yes!

    Jb I wish there was a like button as well!  What a great thing to do for that young woman!  At 47 I usually feel like the youngest in the joint, which is depressing, until yesterday a young boy in his early 20's, if that, was across from me and alone.  I felt bad for him...  Everyone has a story, that's for sure!

  • Jules_NY
    Jules_NY Member Posts: 276
    edited April 2014

    jb-I would have hit the like button on that last post about the IV drugs. That's hysterical!!

  • tangandchris
    tangandchris Member Posts: 1,855
    edited April 2014


    I've also thought that I wish there was a "like" button here :)

    So, I've got a weird question maybe....

    When you get blood work done prior to your treatment, does your MO go over any of it with you. I'm wondering if there are any "markers"  on the blood work that might show if the chemo is working or not. I'm not sure why I'm thinking about this tonight, but I am. When do we get scans again, after chemo and rads or between the 2?

    I know this is something that I need to talk to MO about, I just wondered if anyone had any info on this.

    MO's nurse called me about my back yesterday. She said it was possible that it was the Nuelasta shot causing the pain and that I should try to take it as easy as possible. She also said to take pain pill as needed.

    ((hugs))

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Tang

    No, there are no markers to know the success of the chemo during treatment of breast cancer.    

    I know what it's like...you fart too much and convince yourself it's now spread to your colon! 

    My MO and RO explained to me that if the first PET was clear before chemo another one is not typically indicated. Unnecessary radiation is not a g good idea.  Blood test after treatment to monitor liver enzymes and inflammation markers will help them keep an eye out for any new issues.

    Are you using the Claritan D to help with the bone pain? I had to use Advil, too. It wasn't to bad for me , but some people it hits harder. Mine was across my lower back an. d hips. 

  • jujubee83
    jujubee83 Member Posts: 30
    edited April 2014

    jbokland

    I know what you mean about putting things in perspective.

    A couple weeks back I wanted to quit. I had gotten a virus and was admitted to the hospital. The stomach pain was so bad...As bad as natural labor. In those days I really thought about giving up. I felt I wasn't strong enough to continue. The next day someone had posted a video of a young girl (maybe 6) ringing the bell for her last chemo.  She had leukemia and endured 2.5 years of treatment.  I cried like a baby.  I felt like an @$$. How could this little previous girl have to go through this and have to deal with such grown up problems and I'm overt here feeling bad for myself and wanting to give up. My treatment is only 5 months,  she did 2.5 years! It is hard living through this day to day and sometimes I just gotta cry and let it out, but there are so many that have to go through this a lot longer or indefinitely. 

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Jujubee,

    Great story!  I think the universe will send us a message (or a slap in the face), just when we need it. 

    We just have to listen.

    I spend a fair amount of time volunteering and fund raising for a local breast cancer organization that provides free mammograms and care for uninsured/underinsured women.   There are so many women out there who are young moms, single or no support going through surgery and treatment alone.----I feel VERY fortunate that I am surrounded by love and support so I try to pay it forward.

  • lago
    lago Member Posts: 17,186
    edited April 2014

    tangandchris I specifically asked my onc when I first met her how do we know if this stuff is working. She said "we don't." Then she explained that in my specific case that there was a 40% chance that all I needed was surgery... but the problem is they have no way of knowing. There are lots of studies going on now to see if they can do tests to figure this out but we are a long way from that. Tumor markers are unreliable. They work for some people and not for others. My thought on this is... unless someone tells me there is a problem I am not going to worry about it. Below are 2 of my infamous "speeches" I have posted here:

    seat belt speech:


    You don't assume you will get into a car accident every time you
    get in your car. You do put on your seat belt and drive carefully. Same
    with breast cancer. Eat right, maintain a healthy weight, exercise,
    and take your hormone therapy (if prescribed). No reason to think you
    are going to get mets until you actually have a symptom.


    shit happens speech:

    Some people win the lottery and become millionaires too but do you
    really think that's going to happen to you? Shit happens. Sometimes
    good shit, sometimes bad shit, but most of the time shit doesn't
    happen. Don't assume shit is going to happen to you.

    *Seriously most of us early stage folks make it and never have to deal with this distant mets.

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Lago

    You are SO right! 

    I just saw this video last night, which I found absolutely fascinating and truly insightful.   Its of Anita Moorjani, a woman who had a near death experience and recovered from end stage cancer.   If it is beyond your belief, watch it anyway....her message is POWERFUL for living to your fullest, especially during cancer:

    http://m.youtube.com/watch?v=vvmABrII35c

  • tangandchris
    tangandchris Member Posts: 1,855
    edited April 2014


    Ladies!! Lot's of love you to this morning! Juju, Jk and Lago...all what I needed to hear. It's so easy to get caught up in this crap, I just want to enjoy the good of today. We are going to do an early wedding anniversary this weekend, our 10th is next Thursday and that is also my next tx day. I just want to be in the moment the next few days and not wondering what if, why me, or how come. That is my prayer for us all! ((hugs))

  • lago
    lago Member Posts: 17,186
    edited April 2014

    I still want the winning the lottery and become a millionaire shit to happen though. 

    I never played the lottery but have a few times since after I was finished with treatment... no luck yet Loopy

  • tangandchris
    tangandchris Member Posts: 1,855
    edited April 2014


    Dang me too....dh plays every once in awhile..nothing yet!

  • lago
    lago Member Posts: 17,186
    edited April 2014

    Oh and by the way there is a "like" emoticon:

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    Enjoy your early anniversary Tang.  Live in the moment this weekend and everyday.  I tried worrying once...it didn't change a thing!  It on my robbed me of being present. 

  • Sicilian
    Sicilian Member Posts: 49
    edited April 2014

    Thank you, ladies, for the perspective and pick-me-up.

    Had my blood checked again today. White count is down to 1.1, so I am getting shots of Neupogen. Getting it approved by insurance was quite the merry ride, so I have to go to the local hospital and get the shots there. Pain in the butt, but there are worse things.

    Hugs to all!


  • Jules_NY
    Jules_NY Member Posts: 276
    edited April 2014

    good riddance AC, Red devil, draino!!!!! Kiss my arse!!!!!!!!!!! I feel like no matter how bad the next few days are I can take it, knowing I am done with the EVIL meds!!!!!

    Sicilian so sorry to hear about your counts! Hoping the shot does the trick!

    I started out the day feeling good, despite the fact I never completely recovered from the last treatment. I was almost excited to get my chemo and end this phase. I had to space out my appts because my daughter had her spring show today so I had my vitals and blood work, saw the MO and had an hour before chemo to go to my daughters school. But the MO wanted me to get a sono on a lump in my arm to rule out a clot (no clot thankfully). I lost it on the sono table, when this messes with my kids I can't take it. I was already missing my sons first hockey game of the season. It took awhile but I realized that I'm doing this so I don't miss stuff in the future. Those moments are going to come but we can't let them overcome us!!! My husband told me he asked the coach to have my son play defense, he knew if I missed his first goal he'd probably have to commit me, lol!

    Tang I never thought about what you are going through. With IBC I have to have chemo first because of how the tumor grows, kind of in sheets and it invades the skin, and because of how aggressive it is. The chemo hopefully shrinks it into a ball, or ideally until it is gone. so when I have my surgery they can get clean margins. It is def shrinking I can feel it and so can my MO. It basically took up my whole breast. I would think the same way if I had surgery first!!! Pour your worries out on this board we got your back!!!!!!

    I thank my lucky stars everyday for you guys!!!! Love and hugs

    Jb you are a pisser!!!!!!!

  • jbokland
    jbokland Member Posts: 890
    edited April 2014

    I'm not sure if I posted this before, (I will use the chemo brain card if I did)...but I still crack up when I think of this.  We had fun in the mall...we called this "Where's Baldo?"

    image

  • Gardengirl66
    Gardengirl66 Member Posts: 93
    edited April 2014

    Happy dance...last chemo today for me...and yes I was excited. 

    Congratulations to the other ladies finishing as well and to all the other women doing their best and getting closer to finishing.  I know I will have some rough days ahead, but my body is getting better,especially  in three time when I will not be having chemo again...it will continue to recover and get better from all the side effects.

    Radiation consultation on the 22 , then decide from there what will be next on this adventure.

    Thank you to all the great women in this group , could not have done it with out you...wish I could meet you all and thank you in person.  Sending lots and lots of hugs to everyone !! 

    Thinking of all of you , especially all the women who first had to do chemo 30  years ago, making it easier for me today. So thank you  and feeling thankful !

  • Holeinone
    Holeinone Member Posts: 2,478
    edited April 2014

    garden girl.......happy dance all night long....I was so relieved & so scared when I went in for my last chemo. Still there, 4  1/2 months later and I'm kinda stuck in the time, emotional warpath of trying to move on,  but its not really happening. I start a survivorship class next week. ( I hate that word survivor ship ) I did not go to war, protect our wonderful, country. And yet here I am, tearful, trying to be a tower of strength, feel like a fraud....

    Bottom line, a long slow processes for some of us....Radiation should be easy compared to chemo...

  • lago
    lago Member Posts: 17,186
    edited April 2014

    Congratulations to all those who are finishing! Now stop watching for your hair to grow. It's like watching paint dry. You have to give it several weeks. 

Categories