Starting Chemo Feb 2010?

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  • faithfulc
    faithfulc Member Posts: 284
    edited March 2010
    Hugs, Mo!  You will get through this and move on.  You are in my thoughts!
  • retrievermom
    retrievermom Member Posts: 522
    edited March 2010

    Thinking of you, Mo!  Really cruddy that you are going through this.  Hang tight.

  • salsoda62
    salsoda62 Member Posts: 18
    edited March 2010

    So sorry to hear that many of us are struggling, especially Mo, that's terrible that you have to face these issues on top of everything else. We are all pulling for you!

    I too have a nasty cold and hacking cough, which I hoped was getting better, but when I started wheezing yesterday my husband gave me that raised eyebrow look and said he didn't think it was better and in fact thought it was worse. So off to the ONC for antibiotics and an inhaler. Just sitting around waiting for it to take effect!

    My SE's have otherwise been less than the first infusion, which is encouraging. I have felt more tired, though; on Sunday I could barely hold a conversation I felt so exhausted. I guess that is the way it goes. But I'm half way through the AC, so am just trying to keep my eye on the finish line. Hopefully the Taxol will be less of a burden.

    It's a beautiful sunny day here and I hope it is where all of you women are as well. Take care!

  • CinD
    CinD Member Posts: 163
    edited March 2010

    Mo, I am so very sorry you are going thru this!  You've been thru so much, and it's time for you to get a break.  I'm hoping to see you posting soon that it's all figured out and that you're on your way to feeling better. Sending you good, healing thoughts!  I'll be thinking of you!

    I hope those feeling crappy are better soon. Take care of yourselves! Don't forget the medicinal ice cream -- it does wonders.

    Cindy

  • makmak
    makmak Member Posts: 632
    edited March 2010

    Mo, sending good thoughts your way and hoping  you are better real soon!!

    It's 58 and sunny here in Illinois.. so exciting after all the freezing rain!!  My nanny got so excited she and the baby have been gone on a walk for HOURS!!   I am feeling slightly better and more able to breathe.  Last night was really rough but am feeling encouraged now.. Was bummed to miss my Look Good session but was rescheduled for April, and the Onc nurse said I should be able to get treatment tomorrow.. so crossing my fingers.. 

    My work had another lay-off today.. and one of my friends got cut.. as well as a guy in my group.. I worry about the next wave.. being the breadwinner has been a burden enough being healthy... if anything were to happen now.. I am not well enough to go looking for another job.. UGH.. my DH just tells me to focus on getting well for now.. so I read all the posts and try to focus on the ultimate goal!! 

    Hope everyone is feeling OK or recovering well from all these fun things we keep getting!!

    Marina

  • leta17
    leta17 Member Posts: 120
    edited March 2010

    Mo - Thinking of you!! 

    CinD - Yeah halfway through!!  Like Faithfulc I would prefer only 4 TC cocktails vs our 6 but we are all getting there!!  I am enjoying my 2nd week post tx and feeling good and productive all around:)

    Faithfulc - I didn't rest enough after my 3rd...but I am feeling good again now....I'll be thinking of you this week!!

    Teel - Good to hear they found what was going on and you are back on track!!

    Going to a funeral the end of this week, a freak accident took out a young mom of 2 in our town...tree fell on her car while in CT celebrating a sisters birthday...her 3 sisters in the car with her, survived....I got to know her through our PTA and she was just an amazing, friendly, outgoing person...and will be missed.

    Live strong ladies and enjoy life!!!!

  • Ezscriiibe
    Ezscriiibe Member Posts: 598
    edited March 2010

    Donna, I know exactly how you feel about the head shaving. I put it off as long as I could. But the hair was really really hurting my scalp. I had heard people who were hung over talk about having such a bad headache that their HAIR hurt. Now I know exactly what that means! So I took the plunge and shaved it off and have not regretted it a single minute. The pain stopped almost instantly!

    I wasn't sure how I was going to react to all the women in the beauty parlor watching me, but after it was all gone, it didn't bother me at all. I wanted them to see that THIS is what fighting cancer is all about! Doing the treatments that may change how we look, but not our OUTLOOK on life! 

  • ariesrottie
    ariesrottie Member Posts: 260
    edited March 2010

    Ezscriiibe---- God bless you... Thanks for your words... I guess tomorrow is the day since I really don't think that it will last that much longer. I think the beauty parlor is what scare me... Hopefully she will be able to see me her last appointment.  it is really amazing what we have to go through to get well from this disease....Thanks again.

    Saw the breast surgeon today she doesn't want me to see her for another 4 months.... Yeah... One last doctor...

    Hope who every had tx today is ok with little Se. Other sisters please feel good.... The weather  has been good here... Feel like SPRING!!!!!!!
    ((((HUGS)))))

    Donna

  • Ezscriiibe
    Ezscriiibe Member Posts: 598
    edited March 2010

    By the way, Donna, my hairdresser did it for free. I had not expected it to be free, but when it came time for the bill, she made up some silly story about how if you have had a hair cut in the last month, yada yada yada, going shorter is free. . . I was dumbfounded.

    By the way, almost all the other hair dressers came over to hug me when I was ready to leave. They were very sweet. They get lots of chemotherapy (mostly from breast cancer) women in there all the time, apparently.

  • roso88
    roso88 Member Posts: 31
    edited March 2010

    hi ladies,

    sorry i haven't been posting but i've been on this site almost every night laughing, crying and griping with you silently Smile

    mo - keep your head up.  hope things gets better fast.

    burley - what a touching story and what timing!

    writer - glad to the hear the cough is better.  could it be allergies?  i had a whooping cough that wouldn't go away for 2 months right before diagnosis.  went to see allergist as last resort and they said it was environmental.  i've never had allergies in my life.  funny how our bodies can change overnight like that.

    getting my 6th weekly infusion [halfway mark - woohoo] as i write this. 

    worst part has been hair loss.  for the last 3 weeks, i've been putting up with a sore scalp and watching the hairs shed and shed and shed, not to mention vacumming 2-3x a day.  i couldn't stand it anymore and had it buzzed last friday.  immediate pressure relief and felt liberated but now i'm dealing with a new set of challenges.  i washed my wig for the first time.  turns out the natural hair consistency is frizzy [i paid a small fortune for the piece so it was quite shocker; the salon styled it up and made it look great when i picked up so i had no idea].  i spent an hour grooming it last night - ridiculous.  my scalp is also really itchy.  anyone else experiencing this or have any tips to relieve it?  think i will have to find an alternative.  kudos to you brave sisters that can pull off the baldy.  you look beautiful.

    most of my other SE's have been mild but the list is getting long -- some neuropathy & fatigue, diahrrea & constipation, rash on my knuckles, constant runny nose, bloody nose, mild acne breakout.  can't wait to be done with this crap [scream].

    had to let it out.  can go back to being nice & normal again.  have a great rest of week everyone!

    <<warm hug>>

  • Ezscriiibe
    Ezscriiibe Member Posts: 598
    edited March 2010
    roso88, warm hug right back! I know I have to keep telling myself, "This, too, shall pass. . . "
  • mofend
    mofend Member Posts: 140
    edited March 2010

    Hi - back from all the fun of yesterday.  Had a transfusion of four bags (which they tell me is a lot).   Took about all day between the typing of my blood, getting it ordered and then four hours on the drip.  My onc - who is known as the best in the city, said that in his years of practice he has never seen this issue before.  Great - I love being special and unique, just not when it comes to this.  I could tell he was very concerned since my levels had dropped even further prior to the transfusion and he was anxious to get the blood in me.  He had a bunch of consults with various ob/gyn docs, other oncs across the area/country, and they came to the conclusion that I was too compromised to have any surgery (ablation/D&C/hysterectomy) to stop the bleeding.  He felt that I would bleed to death in any surgical situation - woohoo - love hearing that!  Felt very numb at this point and kind of like - holy crap, this is really more serious than I had known.  They came to the conclusion that the only way to stop the bleeding was to give me a shot of Lupron which shuts down your ovaries and puts you into immediate menopause (happy/sad about that - haven't even figured that out yet - just happy to be not bleeding).  So, the shot was no big deal - what's another stick when you've already been stuck about twenty times in the last couple of days.  Came home, felt like I had been run over by a bus and slept for about eleven hours - which is about ten more hours a night than the last week, so I felt good this morning.  The blood apparently takes a bit to mingle with my existing blood and they say that by the end of today I should feel like a new girl - leaping over tall buildings good, so I'm anxious for that to kick in.  No effects from the shot yet, but apparently I'll be getting intense hot flashes and the other fun things that go along with menopause.  I'll take it over bleeding to death any day!  Thanks for all your kind notes and well wishes yesterday - I read them while I was being transfused and it really lifted me up and gave me tears - I'm so thankful for all of you and hope that today's a good day for everyone!  Hugs to all and let's keep on kicking our way through this!  Love Mo 

  • Ezscriiibe
    Ezscriiibe Member Posts: 598
    edited March 2010

    Wow, what an ordeal, Mo!

    I have no idea how forced menopause will be, but the hot flashes can get intense. One of the things that helped me a lot was a small personal fan going all the time. Even in the winter. I carried it with me everywhere.

    And don't worry about mood swings. I think we've all got a carte blanche on mood swings for the next year or two anyway, right?

  • Ezscriiibe
    Ezscriiibe Member Posts: 598
    edited March 2010

    Blech. Just got off the phone with my oncologist's office.

    It's official.

    I have thrush!

    Ugh! The last time I saw thrush was when one of my grandsons was a newborn. 

  • CinD
    CinD Member Posts: 163
    edited March 2010

    Mo, what a day you had!  I'm glad they stopped the bleeding and that you're finally feeling better. The chemo is supposed to throw me into menopause, but I don't know if it's as instant as your Lupron shot. My second period during chemo is 4 days late, so it may be happening. I've had hot flashes every night since chemo began and end up throwing off the covers until they pass. They started at a couple of minutes each but have now worked up to 5 to 15 minutes each. For me, the worst is that they wake me up and it's hard to get back to sleep.  I hope you're feeling great soon! Look out tall buildings!

    Michele, that's crappy about the thrush. Hope it's gone soon.  I just got my first mouth issue today, a mouth sore, but mine was my fault because I got cocky and stopped rinsing with Biotene and salt water. I learned my lesson and am back to it.

    Teel and CAL30, it's good to see both of you posting. Teel, sorry you had pancreatitis. I've heard that is extremely painful. At least you're finally on track now with chemo. CAL30, sorry your 3rd treatment didn't go as smoothly as the others. I hope everything is good now. Just one more to go!  

    Jessica and Leta, thanks for celebrating my halfway point with me! I realize how lucky I am to only be getting 4 and to have had minimal SEs. Going into chemo, I almost put it off because I still felt wiped out from the mastectomy and the ongoing reconstruction process. Now I'm glad I didn't delay, because although I look worn out, at least when it's done, all I'll have left is finishing the reconstruction. Now I seem to be having those fears of the good breast that's left, because they'll want to make sure again that it's fine before finishing reconstruction. I've got to stop jumping ahead in my thoughts or risk going completely bonkers.

    I hope those who have been feeling sick are better. Take care! And Happy St. Patrick's Day! If anybody is out pub crawling, have a Guinness for me, will ya?

    Cindy 

  • writer
    writer Member Posts: 208
    edited March 2010

    Holy cow, Mo, you really dodged a bullet. Here's to new energy soon.

    My hair stylist also buzzed me at no charge, and said she won't accept payment for any haircuts (not that there will be many) until it's grown out to a normal pixie length. She has done that for many clients facing chemo over the years-- I think it's the norm in the industry, and a beautiful thing.

    My hair stylist (who's also a casual friend) stopped by the other day with gifts that she got from another of her clients, who started a business after her year of dealing with breast cancer. Both gifts were fabulous: a white 100% cotton cap just like babies have-- I had searched high and low on the internet to find those for adults and couldn't. All the beanies out there are wool, acrylic, polyester or something that makes me itch. Or they are overly elaborate turbans-- I just wanted a little cap for sleeping. She also has an eyebrow makeup kit for chemo gals. Check it out if you're interested: www.pinxwear.com.

  • lindee629
    lindee629 Member Posts: 61
    edited March 2010

    I haven't been on here for a while, but Mo so sorry about your ordeal!  Hope you are feeling a little bit better. Maybe you won't quite be leaping over tall buildings better, but better nonetheless. Hang in there!  I am still waiting for my period--which is now like a week late. I hope when I do get it, it doesn't come like a flood, ugh.

    For all you ladies struggling with the baldness and newly shaven, I shaved my head (by myself because I didn't want anyone to see me) right after my 2nd round of chemo. It was traumatic, but I look better bald then I did with that horrible thinning hair. I had previously bought 2 wigs and couldn't wait to try them...but after only a few hours of wear, I developed a horrible headache. I can't stand anything tight on my head! I even went back to the wig lady and she adjusted them, but I still find a wig very uncomfortable. So I have my scarves and my hats and caps, I use a scarf and tie it around whatever cap or hat I am wearing, color-coordinate to my outfit for the day, and I have received many many compliments. I don't think I could ever go out in public bald, so kudos to you ladies who have the courage to do so.  Although the free meal at PF Chang's is very tempting....

    So yesterday I finished my 4th and final round of AC yay!!!  I am halfway done!  My Portacath which has always been very positional, was even worse yesterday--unable to get a blood return, or flush it unless I lay on my side with my arm over my head. The nurses were hesitant to run my AC thru the port, so they tried to stick me peripherally twice with no success (they even tried to use my "affected extremity--right arm").  So they eventually managed to get the chemo in thru my port, using blood drawn from the unsuccessful IV start for my bloodwork. Which was great except my hemoglobin is dropping (10.6 from 12.1 last time). Then the doc wanted to send me for a dye scan of the port to check it all out so today I went to radiology, and they accessed my port, injected the dye and guess what! My Portacath is fractured and cannot be used. (so now I am freaking--if the port is fractured then where the hell did yesterdays Adriamysin go??!!!  They assured me it stayed in the vein and didn't leak into my tissues). So I have to meet with my surgeon again and discuss options. This Portacath has to be removed and I think the surgeon wants to put in another one. But the oncologist's office is thinking I would do better with a PICC (peripherally inserted central catheter). And since I have hated my port from day one, maybe a PICC is the way to go, especially since I only have 4 more rounds of chemo to go. Does anyone out there have a PICC line? and if so, how do you like it, any problems??  

    Other than my Portacath problems, the side effects seem to be about the same...don't feel too bad today, just tired and achy. The reflux seems to be a bit better--the time release Prilosec works wonders! And even though I still have tachycardia my Muga scan came back ok with an ejection fraction of 69%, which is only 10% less than my pre-chemo muga, and since I have done nothing but sit on my ass for the last 4 months, I figure that is still pretty good. 

    For all you ladies just who are behind me, I can see the light at the end of the tunnel. Never thought I would be halfway finished, and still (for the most part) feeling pretty decent.

    Take care ladies, and Happy St Patrick's Day to all.  I can't have a green beer this year, so maybe i will have a green tea instead, it's full of antioxidants right?  LOL!

  • burley
    burley Member Posts: 631
    edited March 2010

    Wow, sometimes I read all the posts and am so thankful that my side effects are mild.  I struggle with keeping a positive outlook as it is, so I'm really blessed that I'm not going through massive bleeding, port problems, thrush...kudos to you girls on coping!

    I'm wishing my process was going more quickly-now that I see how well I'm doing after each treatment, I really wish they were every two weeks instead of three.  But I guess the doctor knows best, right?

    I have to wait until chemo is done to have the exchange surgery (tissue expanders to implants), so it seems like it's going to be forever...it will be August before I'm done with chemo, then have the exchange surgery, then I have to wait 3 months to have nipples reconstructed...that puts me into next year-ugh.

    And I SO wish I could have a green beer!  I've been craving beer, of all things.  The weather has been so nice here, it would be awesome to drink a cold one on the back porch...sigh

  • SunnyCoconut
    SunnyCoconut Member Posts: 350
    edited March 2010

    I agree with you Burley, I also have a hard time keeping a perfectly positive outlook but I am so thankful that I haven't had any really bad issues.  I do have side effects - nausea, constipation, headaches, painful feet, etc.  But I guess all in all, it is not as bad as it could be. 

    This morning I had a mental pity party.  I want to be one of the 100 year old ladies on the Smucker jar on the morning news.  I don't want to die of some disgusting cancer.  I hate cancer.  What is it?  Where did it come from?  I hate it!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!  (Side note: I made an appt for the psychologist at the oncologist's office for tomorrow.)  : }

  • ariesrottie
    ariesrottie Member Posts: 260
    edited March 2010

    My love goes out to all my Chemo sisters ......can't mention all of you... But you are ALL close to my heart and in my prayers.....

    Did you know the best and proper way to wear a wig?????? Baldness.... :)::))))))))

    I had no choice. Tomorrow  round 2 of T/C.. Hope it goes good.

    Talk to you tomorrow.....Little or NO SE SISTERS!!!!

    {{{{{Hugs}}}}}

    Donna

  • faithfulc
    faithfulc Member Posts: 284
    edited March 2010

    Had tx #3 today - yeah, half way done. Thanks for thinking of me, Leta. Today was again evnetless. Port was convenient and I feel so lucky. (I do plan to have it taken out as soon as chemo is done, though.)

    Have to watch for the weekend since I was more tired last time. Going in for my Neulasta shot Friday morning - my WBC was good today and RBC was a bit better than right before last treatment.

    Mo, thankfully the doctors are getting things sorted out. Hugs and hope your energy returns soon.

    Lindee, nice picture. Like you, I shaved mine, too. No one really has seen me bald yet - can't bring up the courage.

  • retrievermom
    retrievermom Member Posts: 522
    edited March 2010

    Mo:  Four bags of blood is a lot!  You were in serious shape, as you & your doc realized.  Thinking of you and hoping the infusion will make you feel lots better quickly.  As for the night sweats and hot flashes---darn, but it's so.  I don't have just one fan going at night; in the summer, I have three :)  My DH has always liked white noise, so he doesn't mind that, and he can sleep through my whipping off my sleep shirt (and now hat, too) in the middle of the night.  It's trying to get back to sleep myself that's a bitch.

    Sunny:  Where does it come from?  Can't allow myself to think about that one for too long.  It boggles the mind to think our cells were going along just fine for decades, then took this detour.  And scientists working their voodoo, using the bark from some tree to make a chemo drug?

    Burley:  Thinking of you in Queen Creek (I've been there).  Enjoy the sunshine.  To think this is going to last into next year is mighty hard.  I'm so wanting to go back East to visit family and feel very stuck here.

    As for wigs and feeling self-conscious:  I'm now convinced that others do not look at us as closely as we think.  My wig can't be that good!  People at work keep complimenting me on my new hairstyle and color.  Where I work,  I face glass towards the public.  Someday, I'm going to whip off my wig in front of everyone, cause my office is so blasted hot.

    Round 3 tomorrow.  Hate the way the dexe makes me feel.  Flushed one minute, jittery the next.  Headache and such.  I've got my OTC arsenal for the treatable SE's and am drinking water like mad.  

    All the best to all of you.

  • ariesrottie
    ariesrottie Member Posts: 260
    edited March 2010

    Debbie and Retrtevermo- hope everything went well and goes well on you 3 rounds... You guys are 1 ahead of me... Was up all night from the dexe also.... Make me want to eat all the time..... Wishing you little or NO SE!!!! HUGS to you both and who ever else is having treatment this week.....Girls let me know how it goes... Keeping my fingers cross today for no reaction to Taxotere...Bring on the BENEDRYL

    Michele-----Thanks for the kind words about BALDNESS... Its working... Just got to get used to the wig... No one will see me around my house without something on my head...:) Got to get ready girls ... Enjoy this beautiful weather..

    Courage and Strength,

    Donna

  • SunnyCoconut
    SunnyCoconut Member Posts: 350
    edited March 2010
    Retrievermom:  I triple-dog dare you to whip that wig off in front of everyone!! You made me laugh out loud because I too sit in a glass fish bowl at work!!  Thank you for the visual, I really needed a good laugh today!
  • retrievermom
    retrievermom Member Posts: 522
    edited March 2010

    I'm afraid to scare some childrenSmile  I did whip off the wig in the car coming home the other day.

     I envy those of you who fall asleep from benedryl.  Makes me even more agitated.  My doc has me take my dexe before noon, supposedly so it won't interefere with a night's sleep.  I haven't had one of those in ages....

     Off to the onc

  • lindee629
    lindee629 Member Posts: 61
    edited March 2010

    SunnyCocoanut I totally agree....I always thought I would end up living in my 90's or something, never ever thought I would be facing cancer at age 49. When they told me, I kept thinking to myself, no this is ME! It can't be happening.  And like you, I ask why? What did I do, why did it start, could I have done something to prevent it? It's like my body has turned against me.  But in reality, there is an enemy inside my body and I need to keep focusing on that aspect and tell myself that all these crappy SE's are a good thing because it means my body and I are winning the battle. Of course I could win the battle a little easier if I had a functioning Portacath!!! Meeting with the surgeon today to see what he has to say. And this is my 2nd day after chemo, when I feel the worst, so he better not piss me off.....Good luck to all those facing treatment today, and I hope for lessened SE's for those who are suffering. It's finally a beautiful sunny day here in PA, and I am thinking of summer.....take care all!  

  • leta17
    leta17 Member Posts: 120
    edited March 2010

    Ladies, we are going to make it to our 90's and die of something other than BC!!

  • cbranner
    cbranner Member Posts: 28
    edited March 2010

    I'm thinking maybe something more exotic than BC! Like falling off Machu Picchu at the age of 90!

  • makmak
    makmak Member Posts: 632
    edited March 2010

    So thought I'd share.. not sure if anyone had this reaction yet.. I'm standing at the Natural food store, trying to buy something to help my baby's cold.. YES, I was kind enough to share it with my DH and baby already!!  And two women were discussing how her Sister can't do anything with her thick curly hair.. SO.. I so wanted to take off my wig and say something.. but I didn't.. at least not today!!!  One day I'll be brave enough..

    On a more positive note.. my blood counts were fine and I was able to get treated yesterday.. so far so good on the side effects other than the steroids made me very aggressive and I guess my Mom said I was ready to rip her head off yesterday.. oops...  My exam went well with the Onc.. he said he feels improvement.. I'll take that.. another exam in a month and we'll decide if to scan then or wait another month.. He is hopefull that the improvement in my breast should be indicative of improvement in liver.. but only a scan will tell.. but hopeful is GREAT and makes it easier to go each week for treatments!!

    Take care everyone and no SE's..

    Marina

  • SunnyCoconut
    SunnyCoconut Member Posts: 350
    edited March 2010
    Leta17 and cbranner:  I love it!  I have to come up with one for me.  Maybe when I am turning 100 and am posing for my Smucker's Jar photo, by then I will have traveled the world over, had the greatest love of my life, collected the best friends a person could have, seen everything and done everything, and when they ask me what I attribute my longevity to, I'll say "cold tomato sandwiches with mayonaise on white bread!"  And later on, as I rock slowly in the porch swing on an unseasonably warm evening, I will die gently in my sleep with a smile on my face...   Ok, I'll do that one!

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