2012 sisters

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  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited October 2012

    No its not too bad its just a quick pinch. Even though I'm numb I still close my eyes just so I don't see them inject. All it is, is a butterfly needle. Quick stick. Your PS might be able to write a script for it. My husband is a medic and he got it from work. It's the most amazing thing to have. I will tell you seeing your boobs grow instantly is awesome. Not to sound weird or anything I've been taking pics of mine just so I can see the end results.

    Lol

  • teeballmom
    teeballmom Member Posts: 322
    edited October 2012

    Barbara: Welcome to our group. You will get a lot of support here. Everyone here is wonderful and it's a great place to vent, cry and talk with those who understand what you are going through. The support I've received has been invaluable for my emotional well-being.



    Take care everyone!

  • Scottiee1
    Scottiee1 Member Posts: 2,329
    edited October 2012

    Hi Barbara ......welcome and sorry you have to join our group. I'm close in age, being 65

    and it shook my whole world when given the news. I have been given So much support here and have actually met some beautiful women face to face. These are the only people who will ever truly get what you are going through.

  • stride
    stride Member Posts: 470
    edited October 2012

    Barbara, we're here with you, even if only in cyberdom. Feeling down and scared is natural, just remember those feelings will pass. (((Hugs)))

  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited October 2012

    Hi Barbara welcome to the group. We've all been in or in the same place you are with your emotions. So sorry you have to join but this is a great place for encouragement great advice and laughter.

  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited October 2012

    Hi Barbara welcome to the group. We've all been in or in the same place you are with your emotions. So sorry you have to join but this is a great place for encouragement great advice and laughter.

  • SusannahW
    SusannahW Member Posts: 470
    edited October 2012

    Barbara, we all support you through this scary time-sometimes it feels like the ocean is pounding in your ears, often there are tears. It get's better, please remember that.

    Love and hugs to you.

  • juneaubugg
    juneaubugg Member Posts: 951
    edited October 2012

    Barbara: welcome to our group... So sorry you find yourself needing to be here, but glad you found us.



    So I'm trying to enjoy vaca with my DHs family but between the hot flashes, stomach cramps, and other issues from my Crohns, and rinsing and swishing from the mouth thing in really struggling. I find myself asking myself questions I shouldn't; like 'why am I bothering with all this again?'; my odds haven't been good so far (1 in 8 it's 'nothing'); fuck my life....



    **sigh*** I'm just so tired of constant physical discomfort.... Fuck!

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    Juneaubugg, are you still on AC chemo?   It's rough.  Give yourself huge credit for just being there and taking care of yourself.  And just think, every woman who survived BC did so after losing that "1 in 8" lottery. 

  • Scorchy
    Scorchy Member Posts: 240
    edited October 2012

    Juneau, thinking about you and trying to project as much positive energy as I can!  You will prevail.

    Barbara, Sorry you have to be here.  It will sink in eventually.  All of th support here will help you get through the process.  Be your own advocate, though.  

    Scorchy

  • juneaubugg
    juneaubugg Member Posts: 951
    edited October 2012

    Thanks Scorchy. Yes, Ann still on the AC. last round on oct 10 and then I'm through with chemo altogether. Someone please tell me when the hot flashes, restless legs at night and never ending insomnia dissipate; not to mention the (slowly becoming unbareable) back ache that I've had for years as my mid back muscles just can't stretch enough and my core muscles seem to weeken from being more sedentary. Seriously this is what 44 looks like?! How will I ever survive my "golden years"?! ;'(



    I am trying really REALLY hard to stay positive but this 3rd round of AC KICKED MY ASS. Im exhausted physically now too since I've barely been able to sleep since last Tuesday night before we left.



    Ladies, send me your positive vibes please....!



    (Ramols; keep thinking about you too. How are you hanging in with that cough and the little ones and work?! I think we will complete AC on just about the same day.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2012

    Hey Juneau - been thinking about you too. Sorry to hear you are struggling so much and not in the comfort of your own home. I have to say - round 3 of AC is kicking my ass too. The exhaustion really creeps up on you. My kids were real troopers this weekend, as I spent the bulk of the weekend lying down and resting. Thankfully my mom was here to help entertain them for a good amount of the time. My cough seems to have subsided a bit - but still achey in my abdomen. Who knows what the deal is. I think chemo gives your body a lickin and you just have to grit your teeth and remind yourself that all of this will pass. Right now, I am sitting at my desk in my home office pondering how I'm going to pretend to work today - as all I can think about after the simple morning routine with the kiddies and my shower - is climbing back into bed and not getting back out. And - I have to go for my 2nd muga scan today, which for some reason is causing me a bit of anxiety. But - like you, Juneau - come 10/10, my last round of AC will be in my body. Woo Hoo! Will still have taxol after that, but hopefully it'll be a cakewalk comparatively. Ok - off I go to make a day of things. Sending you all big hugs and wishes for a great day. Hang in there ladies!

  • allurbaddayswillend
    allurbaddayswillend Member Posts: 355
    edited October 2012
    juneau, I get the idea that everyone's different but that third round of AC was hell for me too. I have been having fewer and fewer hotflashes, I'm 4 weeks into my Taxol treatment. Last night, I think I only threw the covers off once and yesterday I just had a couple of them in the daytime. +~+~+~+~+~+~+~+~+~+~+  <- positive vibes

    Barbara and anyone else newish I haven't addressed in person - I'm so sorry you are joining this group. This is a great place for us though since we all need people who understand.

    +~+~+~+~+~+~+~+~+~+~+ <- some for ramols too
  • websister
    websister Member Posts: 1,092
    edited October 2012

    Good morning all

    Juneaubug and Ramols - sending those good vibes; I went for my labwork this a.m. to see if I am OK'd for my third FEC which is the equivalent of AC but has 5FU thrown in for good measure. It will be good to get that part over with and move on to Taxotere and Herceptin but it looks like I should plan on lots of rest.

    I too have been having the 'chemopause' symptoms, last night was the worst so far, pretty well constant and soaking wet from sweat. How is a person supposed to hydrate extra prior to chemo when their body is sweating out that much fluid? ;)

    The weekend was a good one, I was able to relax and let others pick up the slack and I was OK with imperfection and just letings things be. I walked the 5 km in the Run for the Cure, very moving experience - two of my boys ran the 5K and then came back and walked and caught up to us for the last 2 km of the walk. Our city raised 1.5 million, proud to be part of it.

    Barbara - as others have said, we are here for you. It can all be overwhelming - this is a great place to come to - welcome.

    Off to another appointment and then I will attend a meeting at work and go get in some groceries for my post chemo week.

    Take care everyone

  • KarenZ0305
    KarenZ0305 Member Posts: 487
    edited October 2012

    Agh those hot flashes! My poor hubby suffered through those over the summer with me and our house was like the scene in Father of the Bride 2 with Steve Martin in a parka and the house freezing!



    For those on AC it kicked my butt around treatment 3 too and hung on till after taxotere. But on my good days I made up for the bad and yes there are some good days in between treatments.



    Hang in there baby!🌈❄(a little coolness for the hotness!)

  • liefie
    liefie Member Posts: 2,440
    edited October 2012

    Back from Vegas, and had such a good time. I'm not a gambler at all, just to experience that place for the first time was thrilling enough. The sheer scale of everything, the throngs of people, the magical shows . . . enough said.

    I did not read all the posts, but Juneaubugg, for me round 3 was also the worst. I had a very tight chest and cough, could not breathe properly, and had zero energy for anything. Pretty much spent those 3 weeks on the couch. Moving required that I had to breathe, which was hard to do. Round 4 was much better, probably because I drank much more water than with the previous rounds to flush the beast out of my system. The fact that it was the last chemo also helped a lot. About the tight back muscles: I had that for seven years after a bad fall on ice. The muscles healed, but shortened in the process, so often I would injure it again, and be in pain for days, getting physiotherapy, taking pain medication, etc, etc. It got steadily worse over time with painful episodes every few weeks. It became more and more debilitating. The last straw was in July 2011 when I had simply leaned forward to pick up a cup of coffee from the coffee table, and was out of commission for days. That's when I decided to try yoga for my tight back muscles. I have been going to a 'gentle stretch' yoga class twice a week since then, and my back has NEVER bothered me again. During cancer treatment from January till July this year I did not do yoga or any other exercise apart from walking now and then - did not have the energy - and never had another back episode during all that time. I started gentle stretch yoga again a month ago. Apart from the benefits for my back and the rest of my body, it is also very relaxing and calming. There is no competition in yoga; everyone does just what they are able to do, never forcing anything, and gradually you loosen up, and become able to stretch further. I wish I had started yoga earlier in my life. Will never stop. It is so good for you. Try it, Juneaubugg. You won't be sorry. 

    Websister, my son and his fiance also took part in Run for the Cure yesterday in Calgary with you guys! He ran for me, and she ran for her mom who also had a BMX in 2011. I did not know that they were planning to do that, and was moved to tears by this beautiful gesture from my children. I sincerely hope your labs are good, and that you can get that chemo out of the way. For the nightsweats, a fan might really help. I have one that runs on its lowest setting all night. The moment I feel hot, I throw off the covers, have a drink of water from the tall glass next to my bed, and the fan cools me down quickly. It doesn't bother my DH at all - he just huddles deeper under the covers. I hear you about being okay with imperfection. During this last year I have also learnt that perfection is an illusion, and I finally became able to say 'good enough'. It is very liberating, actually.

    Everybody else and the new ones here, good wishes to you all. THIS WILL PASS. Trust me.   

  • halfcan
    halfcan Member Posts: 253
    edited October 2012

    I would love to join this forum of sisters!   My story started in June when I found the "lump".  Then, amazingly the mammogram could not see the 2.5cm+ tumor, but the ultrasound and biopsy confirmed the ugly lump.  So here I am.... mastectomy done ...port placed Friday (ouch!) ... now it is only a few more days wait till my first chemo on Thursday.  I am so thankful for these forums!  When I find myself pacing the floor and my nerves are getting the best of me I come here and read others stories.  I find it comforting and I learn a lot, so thank you to all who are willing to come here and talk about this crap in our lives we all share.   If all goes well with chemo and I stay on the 3 week schedule X6, I will finish mid January.  And then the new chapter is rads and harmone therapy.  Sigh.....  (((Hugs and best wishes to all)))   

  • liefie
    liefie Member Posts: 2,440
    edited October 2012

    A hearty welcome to you from Vancouver Island, halfcan! I love your name, and hope that can is half full - LOL! This is the best place to share your ups and downs, and find comfort among those who are there, or has been there. Best wishes for the first chemo on Thursday! (((Hugs!)))

  • halfcan
    halfcan Member Posts: 253
    edited October 2012

    Thank you liefie.  I love Van. Island!!!   It just so happens that I was in Duncan on a weeks vacation when my cell rang 2 days in and I was told to get back to the mainland for a biopsy the following morning.   Maybe I will get back there next summer!  Smile 

  • Tazzy
    Tazzy Member Posts: 2,546
    edited October 2012
    Welcome halfcan. Glad you found us, sorry you had to. Where in BC are you from - long as you dont mind me asking. On this site you only share what you are comfortable with.

    Welcome to all the new ladies.

    Juneau/ramols: hope those SE's diminish soon. Rest up ladies.

    Websister - happy to hear that you did the 5k walk.. me too. Found it a very moving experience. Great fundraising too for your area... Kelowna raised over $253,000 and that's rising. And so far over $30 million raised across Canada.

    Liefie... glad you had a good time in vegas. Like you I have enjoyed yoga in my life, but have not done it since treatment. I am going to ask my MO on Thursday if I am OK to start again.

    Hi to all I have missed - thinking of you as always.

    Hoping for a calm, peaceful Monday for you all.
  • MrsCich
    MrsCich Member Posts: 409
    edited October 2012

    Well, I did get my first fill. 50cc in each and it was not pleasant at all. I didn't watch but it sure felt like a knitting needle was being inserted into my ports.



    It seems I will need another surgery as well. 😔 My nips are attached nicely but there is an area on each that is open and raw. My right is much worse than my left. My PS wants to cut out the open areas and sew them closed. I will have 5 or 6 stitches on either side he said. The nips will be a bit deformed looking but he said we can fix that later. However, I really don't care if they are deformed looking. No one sees them but me and my husband and he's already said he doesn't care what they look like. His reason for cutting out the areas is because with my chemo infusions the likelihood of them healing on their own is going to be slow. I'm good with his decision since I'm just tired of all of it



    BC really is the gift that keeps on giving, huh? I don't want to be cut on again and poked and prodded. Ugh.



    Still no real side effects on day 3 post chemo. Thankfully.



    Hugs to all. I have my private wig fitting in a bit. Then I may just go to sleep.

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited October 2012

    Hey Tazzy, halfcan is from Abby, I already beat you to it! She and I seemed to be on similar paths with her a bit ahead but not a race of course. Had my abdominal CT this morning with 3 more pokes to get the IV in and same last Thursday; 3 pokes for the bone scan. Luckily it was at MSJH and the ER was not too busy and they got an ER nuurse to come and even then it was two goes for him. But it is DONE and only an hour until we go the Cancer Agency for the afternoon and yes I am excited. Not because I am looking forward to anything that I will be doing ahead but because we are moving forward. liefie, mrscich, juneau and all of you, I will post lots tonight but now time to go! Oh and here is a good one; my cousin and his wife live a block from VGH and so only a 10 minute walk to the Fairmont Bldg. where overflow from the Cancer Agency now goes and my cousin is giving us a fob so we can come and go from secure underground parking for the duration. Sure helps with parking in that crazy area!

  • Tazzy
    Tazzy Member Posts: 2,546
    edited October 2012

    Well maybe I will need to do a visit to the lower Mainland next year... to meet all you ladies.    There's so many from the Canadian boards I'd love to meet too.

    MrsCich... happy to hear no SE's set in yet.  Have fun with the wig fitting.  Sorry about the more surgery - sux !

  • Nkb
    Nkb Member Posts: 1,436
    edited October 2012

    AC #3 was my worse one by far also. I felt poisoned and told my DH that i couldn't do #4 unless I got a lot better. It was a week of really feeling bad. #4 was much better. Not sure if it was because it was the last one.

    Seems like so many people thought #3 was the worse-so be assured the worse one is done.



  • halfcan
    halfcan Member Posts: 253
    edited October 2012
    Thanks for the welcome Tazzy.  I just love your profile pic!  That big smile makes me grin for some reason.  lol   I see you are NED...that is frickin awesome!!!  You have been going through this journey all year!  I see Marian told you I was from Abbotsford.  Smile   i haven't been to Westbank or anywhere near it but would love to do a road trip and hit all the provinces. 
  • Tazzy
    Tazzy Member Posts: 2,546
    edited October 2012

    Yay... BS gave me clear margins when I got my path report from the surgery.   Still waiting for rads... next Thursday is my 'dry' run.   Not sure if I was being premature with the NED... far as I am concerned I am  Laughing

  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited October 2012

    mrscich- did you ask your PS about lidocaine jelly for future fills? It saves A LOT of the sting from the injection. I carry mine in my purse now, because I never know when he's going to fill again.

  • shockd
    shockd Member Posts: 68
    edited October 2012

    Well I am up for my 3rd round AC next Tuesday (as long as my labs are good this friday).  You all have me worried about how it's gonna go... cross your fingers for me, please!  I am looking forward to getting through this AC, not necessarily looking forward to the Taxol, but hoping it will be less toxic.  

    Hello to all you Canadian sisters, I am originally Canadian, born in Vancouver, raised in Ontario, moved to the US 19 years ago now.  Sorry you have to be here but thankful that there's a place where we can go and get some sympathy when we need it, right?

    Websister - good luck with your labs.  Hugs to all.

  • halfcan
    halfcan Member Posts: 253
    edited October 2012

    shocked2behere...I am originally US and moved to Canada 7 years ago.  We are opposites. lol   Sorry, I start chemo on Thursday so can't answer your questions. 

    Just wanted to say "Hi" and wish you and everyone else a stress free evening. ((hugs)) 

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    Hi shocked2behere, not sure if this will give much comfort, but for me AC #2 and AC #4 were the worst.  I barely remember AC #3.  I think #2 caught me off guard because #1 was pretty easy, I was expecting #3 to be rough based on #2, but it was pretty easy, then again #4 was a surprise since #3 had been ok.  Glad they're behind me now!

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