Is There A September 2011 Chemo Group?

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  • Kelliregi
    Kelliregi Member Posts: 138
    edited November 2011

    Yay Bluejay, Terry & Kimberly!!! Congrats for being done! I'm doing my happy dance for you =).

    Belleeast - Sorry it's been a crappy day. I hate those!! 

    I have a stye in my eye and it makes me want to cry!!! It doesen't hurt, but it may cause my chemo to be delayed. Delayed chemo means I won't be done by the end of December as planned =(.

    On the upside, my middle son graduates Airborne next week. My husband is going up to watch his jumps and graduation. This leaves our youngest in charge of getting me to chemo and keeping his eye on me over Thanksgiving (he's 18). I just texted him my schedule and said I know it's a pain in the butt. He said "not for my mother" and "I love you" He's such a good kid. It made me cry.

    Hugs to everyone. Time to close the computer and put the stye goo in my eye. 

  • ccjj
    ccjj Member Posts: 128
    edited November 2011

    Congrats to all of you that are finished!  That is fantastic.  Pinkshirtnow....I will be right there with you.  My last weekly taxol if all stays on schedule will be Jan 27.  Cant wait. 

    My step mom was diagnosed with breast cancer this week.   DCIS.  She wont need any chemo and is trying to figure out her surgery options. Is it possible to have cancer envy? I am so wishing right now as we are all going through chemo that ours would have been found that early.  She is doing well. I think seeing what I have had to go through has put it in perspective for her and she is feeling somewhat fortunate overall. So maybe my experience has helped her a little. Its crazy. In the last year I have known 4 people that were diagnosed. I'm 43. I know I am reaching that age where bad stuff starts happening but man.. it starting to feel like its epidemic. Have any of you been researching life style changes yet.. diet, no alcohol, hormones/estrogen in makeup, etc?  I really haven't yet, but have been thinking maybe I should. 

  • Terry71
    Terry71 Member Posts: 293
    edited November 2011
    kelli that is awesome, my son has came to my last 3 treatments with me he is 20, Hubby came to every one and every Mo app, surgeon app, Picc line insertion app, echo, hes been there every step of the way, my daughter went with DH to meet my chemo nurse before I even knew her name LOL, she has came to almost all my neulasta injections with me, she is limited to the app's she can make as she has my beautiful 3 yr old grand daughter who cannot sit still for any real length of time, you know 3 yr old ahahahahaha..... DONE last treatment today, did the HAPPY HAPPY dance... No bells and whistles or anything but we did have cake :-) Smile and BIG HUGS
  • Sheypres
    Sheypres Member Posts: 35
    edited November 2011

    I am SO jealous of all of you that are done. LOL!  CONGRATS!!!!! I am have 3 more Taxol to go and if all goes well my last one will be Dec 20th.  I am hoping that I get all the SE's in and over by X-mas and my little girls first B-Day on the 28th.  If it follows the pattern of my first it will. The first couple of days of my first Taxol were bliss compared to my AC but then the pain set in.  Still better than all the nausea and crushing headache. The Doc is a bit worried about the pain in my feet but it is gone today.  I have #6 on Tues so at least I will be okay for Turkey day! I am not sure it will be a good idea to do my online shopping while on pain killers.  I guess we will find out..... Good Luck to all of You!!!!   

  • lwarstler
    lwarstler Member Posts: 341
    edited November 2011

    Belle: all I can say is (((hugs))). I'm right there with you (my last day is Jan. 10) and it seems especially long and impossible on these bad days. You can do this and we will get there, all of us, together. Hugs and a tear for you my friend.

    Bluejay, Kimberly, Terry, Jersey, and Rockymm: so incredibly happy for you. I can't wait to start reading about some of your SE's disappearing and your hair coming back. It's a great reminder that this does end.

    Kelli: Your boys are so sweet...when we are well, I'm going to pick your brain for parenting advice for my son :) He's sweet now, but he is only 12.

  • RaeBob
    RaeBob Member Posts: 79
    edited November 2011

    Kimberly, Jersey, Rockymm, Terry, Bluejay: So incredibly happy for you. It's great to see some of our group completing crappy chemo countdown!! Can't wait to hear about your energy and health returning. You all are the lights leading us out of this tunnel. I will be done a day or two after Christmas. Then like PinkshirtNow I will be facing a double mx.



    Cooka: great day for you tomorrow. Another light to shine the way :) Will be glad when we are all out and we can close the miserable tunnel off for good. Keep checking on us we need your encouragement.



    ccjj: I went on this really strict organic diet after my dx and gave up my red wine. Started using all organic body products. Kind of like closing the barn after the horse is out. Then I started chemo and thought it is killing everything in my body so I may as well eat what I want now since the only things I truly crave are all the bad carbs. So decided I will be really good after chemo although I have totally given up my red wine forever. I think the body will need all the good stuff when it is trying to heal and regenerate after chemo. Right now supplements and green stuff only makes me more nauseated. So my body is on chocolate chip cookie time instead. What harm can one little ole cookie do among all the toxins anymore than the good lettuce could do for the same reason. That's my excuse and I am sticking to it :)



    Belle: I feel your pain everyday I wake up and am presented with another new SE. I agree with Kimberly stop sending this crap.



    Kelli: congratulations on your son graduating Airborne school! My husband and kids have all been great through this too. They all take turns doing special little things and since I no longer like to be hugged because of surgery and port they all rub my head we are a touchy feely crowd and the bald head draws em in :) I am just trying to figure out how I am going to keep them showing their appreciation when I am back to my old self lol



    Hugs to all and my tomorrow be a good day for everyone.

  • SCPMadi
    SCPMadi Member Posts: 42
    edited November 2011

    Good Morning up early and dreading the day. #4 today at 9am at least it will be over quickly appartently the Taxotere only takes about an hour. I a really nervous about the SE's with this one espicially the potential swelling or allergic reaction. The good news is the Onc told me not to take the Emend anti-nausea as she was pretty sure I wuld not need it.  I woke up feeling yucky, I felt sort of yucky all day yesterday I attributing it to the steroid I had to take yesterday in prep for today and a difficult time sleeping.

    Nurse came to draw my blood yesterday and checked the PIC. She said the PIC is forming a barrier or scab around the opening and that it is irritating the opening. She reports it is normal for a body to do this similar to the crust a earring hole forms. She did not remove the the scab yesterday said the nurse at the hospital today would remove it and it would stop hurting. 

    Took my blood into the lab and ended up in a argument with the lab tech for half an hour as I had forgot my health card in my Chemo bag and she did not want to take my blood. I finally in a low moment said "Lady I have to go for Chemo tomorrow, I am tired and  bald and not wanting to drive all the way back home with my four year old son in tow to retrieve my health card when I know you can make an exception and just pull it up on your computer." I felt bad using the Cancer card but it worked with a huff she did take my samples and continued to remind me of the importance of bringing my card as if I did it on purpose. 

    Congratulations to the ladies who are done. I am jealous and happy for all of you.For those of you still on the journey Hang in there we will make it through I have faith with all the holiday's in the next 6 weeks we it going to fly by. 

    Have a good day with minimal SE's everyone

    Sarah

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited November 2011

    Morning ladies,



    It's getting cold in Wisconsin with no hair on my head. I have never liked the feeling of a hat on my head but this year it is going to be a must do.



    CCJJ - Yes it is definitely possible to have cancer envy. Let's see. There would be the boob envy, the hair envy, the health envy, the energy envy, the family support envy......even the tastebud envy. I am surprised my skin's not green with all the envy, not to mention the cancer.. Looking at the list of changes I want to make when I get past this last set of SE: I want to increase my exercise and cut the dairy to as close to nil as I can get. I love milk, cheese (every kind of cheese), butter, sour cream. I already liked a lot of healthy foods, it's just that I liked them combined with dairy. It doesn't really make sense for me to be going on Arimidex and still flooding my body with the estrogen and excess fat in the dairy, so.....need to change that, but that's going to be a hard one for me. Need to increase my exercise. At age 35 I could bike 30 miles and not think much of it. 100 pounds heavier at age 50, 1200 steps logged on my pedometer seems like a more active than normal day. LOL. Exercise seems to have an impact on recurrence, so I am going to take that one to heart. And, and, and, I don't think it would be so bad to be boobless were it not for my gut sticking out like a pot belly stove.



    Rae - I think anything you can eat right now that doesn't taste like dirt is okay. May I recommend Edy's Slow Churned Peppermint Chip along with your cookie? Sorry it's painful for you to get hugs. I guess because I'm heavier, the port is in deeper and more protected and I haven't had pain from it. I do find that people are very gentle with hugging me since the breast surgery and I have to give them a tight hug to let them know that they're not hurting me. Somehow a light hug feels like a faint compliment to me, like eating salad instead of steak, something missing, not enough. I like the bear hugs, maybe a little rocking dance with that, an extra squeeze at the end, and a peck on the cheek or forehead afterward. I sure am glad my chest doesn't hurt. I bet the ladies with expanders would scream if they got hugged that way.



    Sarah - Glad the lab tech caved for you. Really, now what were the chances of you being an imposter? Silly really that you got a hard time in the first place. I'm happy to say that at all of my healthcare offices, they only need your card once and after that just ask you if anything has changed, but that's office-based cares where they recognize you and not hospital-based cares.



    Happy Christmas shopping online to all you mothers out there who can afford to shop that way. What's more fun than having little ones that still believe in Santa? All that Christmas decorating can be tiring but it is cheerful with the lights and the smell of a fresh evergreen in the house if you are so inclined.











  • mags20487
    mags20487 Member Posts: 1,591
    edited November 2011

    2 days post AC and just a little nausea...not bad though.  Just got some good news...my BIL does not have cancer...he is the second BIL since i was dx to go thru testing and they both are negative!!..So happy for him and my SIL who is more like a sister to me.  I am just laying around today in my bed and have no desire to do a thing.  The bug guy comes today at 5 so hope the house isn't too messy..haha

    Belle---{{{HUGS}}} to you...it has been a  rough road for you for sure. 

    Maggie

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited November 2011

    Hey Ladies!  Hope everyone is doing well today.  To all those that have finished:  Go girls!  I am so happy for you!  I will be there soon!  December 22 is my last treatment.  Can't wait!

    Had my onc appointment yesterday and once again he was very pleased with the bloodwork.  Everything within normal limits.  And I am feeling so much better today that I did Monday.  Everyday has been a better day for me.  The swelling in my feet has gone and that is a good thing.  My onc told me I could take next week off and he would see me again on my next chemo which is December !.  I was so happy!  Yeah!  I was so excited that I did a little shopping yesterday and I treated my self to supper at IHOP!  Got home late, got my shower, played some games and went to bed.  It was truly a good day!

    Kimberly:  (Waving!)  Here I am girl!  Yes I am quite okay!  Been feeling so much better.  The holidays are coming and they are my most favorite time of year.  Just had to do some shopping! My friend and I are going to do the Black Friday thing on Thanksgiving and I just can't wait. We did it last year too and had so much fun! Should be a blast this year too. Just been so busy around here. Trying to get things together for the chili benefit tomorrow. This will be the last fund raiser for me and I sure hope it turns out as well as the salad luncheon.

    Update on Colby: He is walking more. Unfortunately, he is having to wear an eye patch over his right eye. There has been some nerve damage and he has lost sight in that eye. The left eye is still blurry but he can make people out although I think it's more by their voice. He has amazed everyone!  For a child that we never thought would make it, he has improved, at least to us, by leaps and bounds and stunned everyone including his doctors. I am so thankful!

    I wish each and everyone a great rest of the day and a wonderful weekend. Have to get back to work now, but I will post later.

    HUGS!

  • lwarstler
    lwarstler Member Posts: 341
    edited November 2011

    RJ: glad you are feeling better...too funny...yesterday I went to IHOP and shopping too and it lifted my spirits as well. 

  • bluejay58
    bluejay58 Member Posts: 62
    edited November 2011

    I'm still here and still reading!  THANKS AND HUGS to everyone -- these forums have helped me through this so much I can't even say.

    SCPMadi, your onc warned you about possible swelling/allergic reaction to the Taxol on your fourth treatment?  Mine didn't, and that's what got me Wednesday night!  I took a dexamethasone (steroid) and later a Benedryl (because the dex didn't seem to be doing much).   The swelling really did go down and I was able to go in the next morning to get my Neulasta shot.  The one thing that kept going through my mind through all of this was why did it have to wait until MY LAST TREATMENT?  ARGH.

    But I am much better today and was able to put both my rings back on last night.  :D

    RJ, that really is amazing news about Colby!

    <3<3<3 you all.

  • SCPMadi
    SCPMadi Member Posts: 42
    edited November 2011

    So today went well. The taxotere is a much shorter infusion only an hour and I was out of there. Had a good talk with the Onc. about all the possible side effects. Not looking forward to the possible bone pain or the potential swelling. The nurse cleaned up the pic and is is feeling much better. I am still feeling really good little to no nausea so far. Hooray! Only 2 more rounds to go!

    Bluejay- I am actually on Taxotere. The Onc told me that swelling is a possibility but also said since I am only receiving three rounds it will be minimal. I am taking dexamethasone for one day prior plus day of and one day post to help. Thanks for the heads up though I will defiantly be watching for the swelling and apparently bone pain as well.

    RJ- I am glad your family is receiving such good news. 

    Have a great Weekend everyone!!

    Sarah

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited November 2011

    Belleast:  We do something along those lines here too at Christmas.  We usually hold it the first weekend in December.  It's called Christmas on the square.  All the stores on the square are open and they have refreshments.  We usually have a parade with Santa Claus bringing up the rear with goodies for all the kids.  Live music and the town is all decorated out.  It is really pretty and such an enjoyment.  So sorry you had a crappy day yesterday.

    I think I'm beginning to feel some kind of growth on the old noggin.  Can it be and I'm not even through with treatment yet?  Feels kinda like wirey peach fuzz.  Different than what was there before, you know, the really soft downy fuzz.  Maybe!

    Iwarstler:  Great minds think alike, huh?  I did find something I wanted to get the girls so when I go back for chemo on December 1, I'm going to run by and pick them up.  It is a pair of sleeper socks but they go up to your knees and they have the cutest little balls on a long string hanging from them.  I know my girls would be thrilled to get those for Christmas.  May have to get me some too!  You know:  To RJ From the dogs!  Works for me!

    SCPMadi:  Don't feel bad about using the cancer card.  Sometimes you gotta do what you gotta do!!!

    Hope you ladies have a good evening.  Will "talk" to ya'll later!

    HUGS!

  • cooka
    cooka Member Posts: 278
    edited November 2011

    SCPMadi, so glad to hear your picc feels better and you have knocked out one more round! :)

    RJ, relieved to hear Colby is doing so well. Also, it is encouraging that you are starting to get peach fuzz!! I actually went out a bought a wig after my last tx yesterday because i have to start meeting again soon with clients in my suits and i just can't find a hat or scarf that looks good with a suit. Maybe now that i broke down and bought a wig my hair will come in faster:)

    Hope everyone has a good weekend! 

  • babsbrink
    babsbrink Member Posts: 314
    edited November 2011

    Sorry I haven't been around for so long. I had my fourth round of TC last week. Two more to go. I read up on side effects and thought I was mentally prepared for this journey, but I guess I am much weaker than I thought.The hair loss freaked me out, and I knew it would happen but I still had a breakdown. The pain and nausea last longer and longer after every infusion. I have had vomiting as well. My doctors are trying to help but my body is resisting.Besides the reglan, and dexamethason, I am taking zuplenz in the form of a dissolveable film. I only vomited once this week, so it is helping. But at a price. My copay was $306.00 and I am used to a $4.00 copay. The bone/joint pain has been almost unbearable, so I take oxycodone every three hours for a couple of weeks, then switch to Tylenol for the third week. Xanax during the day, lorazepam at night. And of course senecot s for a few days after infusion, then immodium for the next week or so. I know we are all going through the same thing, and I hate to sound like a cry baby, but when I look into a mirror, and see what I have become, all I do is cry. I want my old life back, but I am smart enough to realize that the woman I was in April is gone forever. This is not the hardest thing I've had to do in my life, the death of my youngest son nine years ago was by far more difficult to live with. I actually see a lot of simularity in the way I feel now, and the way I felt for over two years then. I eventually found a way to go on after Glen died, and I am sure I will find a way again. If you've read this all the way through, then Thank you for listening. I wish all of us a Happy Thanksgiving, and healthy cancer free future.

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited November 2011

    Hi strong ladies, happy Saturday!

    First of all, CONGRATS to everyone who finished their treatments.  I am counting the days on the calendar, and I tell you I would NOT want to be the person to deliver the message to ME that they were going to tack another one on the back end.  Uh uh. 

    I have been off the radar for more than a week.  Tx 4 kicked my butt.  They said the fatigue would be cumulatively worse with each tx but I seriously underestimated that.  My blood counts are still so low even a week after the Neulasta shot, my onc used the "transfusion" word for the first time Friday.  Ugh.  I am just exhausted beyond words.

    Instead of cancer and its crappy side effects that rule my days, I am trying hard to focus on December because I will have both my sons home for most of the month.  My oldest, Casey, is a computer geek for the Navy (stationed in Japan) and he just got promoted  to E4, so he comes home for Christmas a Third Class Petty Officer.  We are so proud!  He will be home 12/5 thru 12/26.  I have tx #5 on 12/1 and #6 on 12/27 so I should be "good" most of the time he is home.  Yay!  (I am thinking positive and assuming the sale!)  And my youngest, Max, will be home from OSU most of the time Casey is home, so I am excited for a month of happy noise at our house.  We are all musicians and play together as a family, and I will have my drummer and bass player home, and life will be as good as I can possibly make it for 3 weeks in December.  Screw cancer!  I can get some normal family actiivity and enjoy my boys.  I am so effing sick of this, I want my life back!

    Re dosages ... I feel so stupid I do not know my dosages, but it is on my question list for next time.  I do know what I take tho ...

    2 Decadron tablets twice a day the day before, of, and the day after chemo (steroids for nausea)

    In my infusion I get:

    Benadryl

    Pepcid

    Emend (sp?)

    Aloxi/Decadron

    Adriamycin (Red Devil; accompanied by a popsicle)

    Taxotere

    Cytoxen

    I have Zofran I take 2x/day the day of and after chemo (for nausea), and as needed.  Plus I have a rx for Phenargan (fast acting nausea and puts you to sleep!) and Xanax (stress and sleep aid) - better living thru pharmaceuticals!)  I have little to no nausea, they throw the kitchen sink at it and whatever the combination, it works.

    Then Neulasta shot the day after chemo.  We all know that is a blessing and a curse.  The claritin/aleve regimen does seem to help with the bone pain.

    After the 1st tx they cut the TAC back 20% and the dosages have remained constant.  (The first treatment damn near killed me.)

    I have my BRCA blood test scheduled for 11/30.  My niece was BRCA1+. 

    I want my digestive tract back.  I used to joke about beer being mashed potatoes in a bottle.  I have traded mashed potatoes in a bottle for mashed potatoes in a cup (so my weight has remained constant since day 1).  Hey, those Bob Evans mac & cheese and mashed potatoes in individual serving size cups - well them's good eatin', yessiree Bob! 

    I made a pumpkin pie for Max when he was home from college two weekends ago.  it was too spicy for me, I could not eat it.  I would die for some Chipotle right now.  I dream about "real" food.  I know how the ghost captain from Pirates of the Carribean felt!  You want to eat everything and can't!  

    I never had much trouble with constipation that a couple Colace would not fix, but for some reason this past week I got really backed up.  Took one of those Senecots you guys talk about, and holy Jesus it was like the scene from Dumb and Dumber where the guy gets slipped the laxative.  Never again.  More fiber drink, more water, more salad.  Oy!

    And how about having to pull out the C card to get a little consideration at the hospital.  Really?  C card, B card, whatever works.  My favorite line from the move Dolores Claiborne is "Sometimes being a bitch is all a woman has to hold on to."  The C card is last resort, but I totally would have played it too. 

    A friend was whining about nothing on her FB yesterday, and it took everything I could not to post "Kristina, whatever is wrecking your day is not cancer, so put your big girl panties on and deal with it."  But I didn't.  People just don't hear themselves whine about nothing.  I have said for years, to give people perspective ... "An INCONVENIENCE is a lump in your oatmeal.  A PROBLEM is a lump in your breast."  I have heard women quote that back to me over the years, and NOW when I say it they REALLY get it.

    Girls ... we are gonna get thru this.  Just hang on in there.  When the spring flowers bloom, so will we!

    Find some joy in the day.  Love you all.

    Debbie 

  • mags20487
    mags20487 Member Posts: 1,591
    edited November 2011

    babsbrink I posted nearly the same venting a few weeks ago..so I understand you as well as the other sisters here.  I am so sorry about the pain you carry in your heart for your son.  I can only imagine how aweful that is.  Stay strong...2 more to go for you...YOU CAN DO IT!!  We all can!.  I have 3 left but I am on just the AC part now as i finished the Taxol already.  BC sucks and we just have to do this to make it thru for ourselves and those we love.  Hang tough...I hate the way my body looks but like my husband says that scar is my battle wound.  HUGS to you

    RJ so happy about the boy's recovery.  Just found out that friends son who died a couple of weeks ago was texting and driving...such a waste and sad loss...Sometimes i think they feel invincible.  Even i did b4 BC.

    Maggie

  • cooka
    cooka Member Posts: 278
    edited November 2011

    Hi Babsbrink,

    For what it's worth, I don't think you sound weak at all. It sounds to me like you are having a very sane response to the horrible stuff that has been thrown at you and you are bravely wading through it. I hope your Thanksgiving is a good one, and I am right with you looking forward to that cancer free future:) 

  • belleeast
    belleeast Member Posts: 653
    edited November 2011

    hi all, went to the hometown xmas, got to see 7 of my grandchildren, visit with my parents and children. didn't win anything but had a good time.

    babsbrink, glad to see you back. hang in there.

    debbie, you,too. enjoyed your post,made me laugh. so glad for you that your boys are coming home, what kind of music do you all play?

  • SCPMadi
    SCPMadi Member Posts: 42
    edited November 2011

    Okay so I am day 3 post #4 Taxotere and I am feeling great. Has anyone else taken this drug? When should I expect all the swelling, bone pain and fatigue to set in?  I am sort of feeling like I am cheating. I guess I should be gratful for a the couple of good days. What a huge difference between this and the Red Devil.

    Hope you are all haveing a good weekend. 

    Sarah

  • cooka
    cooka Member Posts: 278
    edited November 2011

    Hi Sarah,

    I did taxotere/cytoxan but I think my SE's were mostly from the taxotere. My first round was pretty mellow, didn't get hit with the flu-like feeling until day 4, just a few days, then day 7 I had a day where I again felt lousy. Then my WBC's tanked and round 2 I needed Neulasta. That round I had flu from day 3-6 and bone pain day 7 (not everyone gets the bone pain thing though). Rounds 3-4 I got used to the flu feeling and mostly dealt with my legs being super tired even though i have been walking and doing yoga the whole time. I think the fatigue (breathlessness, legs tired) gets progressively worse...but it is very doable! Hope you continue to avoid SE's:)

  • SCPMadi
    SCPMadi Member Posts: 42
    edited November 2011

    Thanks Cooka, I have been living on edge wondering what it might look like this week. I start neupogen tomorrow for 5 days so hopefully can avoid and infection. I wish I was as motivated as some of you I should be doing more exercise. Thanks again.

    Sarah

  • bluejay58
    bluejay58 Member Posts: 62
    edited November 2011
    Sarah, I also did four rounds of Taxotere/Cytoxan.  The side effects from the first treatment didn't hit me until the fourth day.  I never had bone pain, and the swelling didn't strike until the last treatment, but the side effects from the first included sinus pain,  headaches, fatigue, and generally feeling like I'd been hit by a truck.  Everyone is different, though, and you might be one of those who just doesn't get many SEs from the taxotere!  :D
  • mags20487
    mags20487 Member Posts: 1,591
    edited November 2011

    scpmadi..i just told my husband that I too feel like I am cheating my way thru chemo.  I finished taxol and started AC last Wed and my side effects are so minimal I almost feel guilty. 

    Maggie

  • RaeBob
    RaeBob Member Posts: 79
    edited November 2011

    Sarah & Maggie: I am so glad to hear not everyone gets bad SEs from this stuff. I had my 4th round of T/C 3 WEEKS ago and I can't even carry a laundry basket to the next room. My muscle fatigue is so great if I walk from the house to the car I am shaking and out of breath. Even driving I have to hold the steering wheel at the bottom because my muscles start to burn if I hold my arms up too long. I was energetic, held down a full time teaching job, and mothered a big family, could walk trails or shop all day and my teenage daughters would tire first. My kids never saw me sit down now they hardly ever see me sitting up! I can't even grocery shop the first aisle. I have 2 more rounds to go and I am dreading it!

    I hope your SEs continue to be mild you are not cheating, anyone with BC deserves all the breaks they can get. Do you take supplements doing any special exercise, special diet maybe that is helping if so let us know I will give it a try.

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited November 2011

    Good evening ladies,

    Well, true to my word, I'm not skimping on the Percocet for this last round of treatment.  Just had one 1/2 hour ago so feeling somewhat human instead of like roadkill.  When the Perc wears off, ....oh, never mind. Y'all already know. 

    Babsbrink - I wish there were words to comfort you and help you get through it easier.  I think the best we can do sometimes is let you or anyone voice it out loud how miserable it is.  For whatever reason, we don't always feel free to tell our friends, family what this really feels like, either to protect them, or it's too hard to explain, or feeling like an old broken record because this goes on for so long.

    Maggie and Sarah - Don't feel guilty if you feel better than expected.  That's great news and we rejoice with you.

    RJ - I hope the chili benefit was very successful.  I hope it's not too personal to ask...but have you been going through all of this without insurance?

    Belle - Glad you are still able to enjoy Christmas season fun with your family.

    Debbie - I want my effing life back too:)  Sounds like you are going to have a good December.  You go girl.

    Kelli -  Is the medicine for the stye helping?  I know you are so proud of your son.  Maybe you could share a picture of his graduation with us when your husband gets home?

  • belleeast
    belleeast Member Posts: 653
    edited November 2011

    sarah and maggie, don't you dare feel guilty or i'll have to come kick some butt! i think you are more the normal than some of the rest of us who are having worse side effects.

    kimberly, hope you feel better soon. last two days have been better for me,knock on wood!

    raebob, if i could give you a big hug and make it all better i would! HUGS,HUG and MORE HUGS!!!!

    hope everyone is having good days!

  • Rockym
    Rockym Member Posts: 1,261
    edited November 2011

    Tomorrow is the last chemo tx!  Since I finally had my taste buds back the past two days, I've been eating everything in sight.  Went out for Mexican food on Friday night and it was sooooo yummy.  Of course I forgot the possibility of heartburn so there was a price to pay.

    RO appointment in two weeks and I'm a bit nervous about it.  Don't want any permanent tattoos for the alignment.  I also want to want until January to begin.  Hope she agrees.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited November 2011

    Good evening ya'll.  Hope everyone is doing well today.

    Had a good weekend and a very enjoyable chili supper last night.  I have some wonderful friends and family!

    Kimberly:  I dont' mind answering your question at all.  Yes I have insurance but I have to pay 20% of everything until I reach an out of pocket expense of $1500.00.  Just reached the out of pocket in November, so I have had some pretty extensive co-pays through all of this.  Not to mention the added expense of gasoline to travel back and forth to the city 2 to 3 times a week.  That kind of money was just not in my budget!  My good friends and daughters are the ones that have done all the benefits for me and I so appreciate it.  Without them, I know I would have had to file for bankruptcy and I just hated to do that.  So, now I can breathe a sigh of relief and after December 22, move on to the next stage of treatment.  Unfortunately, that will be a new year and once again I will have to meet that 20% and 1500.00 out of pocket expense for this next year.  So I am truly grateful for the financial help.

    Maggie:  Such a tragedy.  Sometimes people just don't get how dangerous texting and driving really is.  I am so sorry for their loss.  Don't feel guilty about minimal side effects.  I am so proud for you!

    Cooka:  When I return to school after the Thanksgiving break, I will be sporting a different wig.  This one is a little longer although basically cut like the one I have but it is a little darker without all the blonde highlights.  I figure since it's getting winter time, time to let the blonde go.  I normally did in the winter anyways.  I really have gray hair but I have kept it dyed for the last 5 years.  And I have to admit, when I started dying it, I did look younger which I very much liked!

    Babs and Debbie:  I am so sorry about your SE's.  I hope that you are better and the last few treatments won't be so bad.  Ya'll go ahead and rant!  We're here to help and yes we know how it feels.  I don't always rant to my family because, well, I don't want them to worry and then of course, I know these damn SE's are only temporary.  Hang in there ladies.  We can do this!

    Belleast:  I am so glad you got to go to your celebration and saw 7 of your grandchildren.  I can hardly wait to get the holidays around here started.  I have always loved Thanksgiving and Christmas.  During the break, I will be hanging my outside Christmas lights and putting up my little plastic figures.  I always have such a good time doing stuff like that!  My grandson is big enough now that he can help and we really enjoy doing this together.

    Sarah:  I am on my 4th Taxotere/Cytoxan treatment and I can say that my swelling came after the 3rd treatment.  Thought maybe I had eaten way too much salt but before my 4th treatment, all swelling had disappeared and I have not seen it since.  I think I'm the one getting all the weird SE's from this combo:  scaling/peeling hands, swelling, constipation, aches/joint pain in spite of taking claritin, etc.  Fortunately,  I have not had the vomiting and other issues that some of the ladies have had.  I, too, feel like I have been hit by a Mack Truck about the 3rd day after receiving the neulasta shot.  That pain seems to get worse with each treatment no matter how hard I try to medicate myself for it.  Rest seems to be the only thing that works for me.

    Get some good rest tonight ladies.  Hope you all have a wonderful evening.  Will "talk" to you tomorrow.

    HUGS!

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