Starting Chemo in June 2005

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  • Analemma
    Analemma Member Posts: 1,622
    edited November 2005

    Bev, I've had Sporanox for toenail fungus before, a long time ago.

  • Fi_in_oz
    Fi_in_oz Member Posts: 49
    edited November 2005
    oohh how time is dragging now, and I can't believe it I'm "nesting" all over again.

    Starting Taxol finally on friday the 25th Nov, and I'm starting to get nervous, oh well,this too shall pass.

    For those who are on TimTam's Forum, I've filled in some time with updating my page with lots more "phases"..

    Kinda got knocked for six the other day when I learnt that one of the ladies I met at the "look good feel better" day only a few months back had passes away, she was a lung cancer patient, not breast cancer. Its floored me (yet again) though at how quick cancer can take people.

    That's two people that I know personally who have passed on since I started chemo back in June, the other was an aunt who in six weeks went from diagnosis to passing.

    Perhaps a discussion on "survivors guilt" would be beneficial right now.. who knows.

    Take care all of you, so glad you are coming closer and closer to finishing treatment..

    best wishes,

    Fi
  • minerva
    minerva Member Posts: 36
    edited November 2005
    Watson - So sorry to hear about your troubles from your port. I am glad you are able to have your last one next week through IV though. After all we have been through, what is one more obstacle? Speaking of nails, I had 4 nails that threatened to fall of after my Taxol, but never did. They are back to normal and stronger than they have ever been.

    Jenster - Glad you had a good weekend, but sorry to hear about DH bronchitis.

    I had to postpone my visit with radiation doc per my surgeon, because my incision from my mast is not healing as fast as it should. The surgeon wants me to wait for 6 weeks after surgery. In a way I am happy that I won't be gone from home the whole month of December. I wanted to be able to bake cookies and do other holiday events with my grandsons. When I do my radiation I will be 200 miles from home. I will be staying in a motel and be able to come home on the weekends, weather permitting.


    I hope everyone has a great holiday!
    Hugs to all!
  • Jenster
    Jenster Member Posts: 267
    edited November 2005
    Fi - I'm so sorry about the loss of these ladies. I know it's kind of like a kick in the gut, isn't it? Good luck with Taxol. I'm sure you're going to do great.

    My in-laws and parents came over last night to celebrate my end of chemo. We ordered Chinese food and had already brought home yummy cupcakes with pink ribbons from my favorite baker. While every male in the house was off picking up the Chinese, I was hit with a horrible migrain. From out of nowhere! I ended up on drugs, in my bed except for the time I was throwing up everything in my stomach. I actually laughed. Six months of chemo and never once did I throw up. Until last night. And it wasn't even chemo-induced, though I think it may have been exacerbated by chemo. Anyway, how ironic!

    Everyone else had a nice party, though. lol. I'm much better today and I've got some Chinese in the fridge with my name on it. Literally!!

    Hope you all have a great Thanksgiving!!

    Jen
  • Jenster
    Jenster Member Posts: 267
    edited November 2005
    Hey!! My family took me to the mall today for a last-chemo surprise. My husband had bought sound chips (or whatever) for a Build-A-Bear and he and the kids each made one for me this morning while I was in the shower. Then they took me to Build-A-Bear and I got a cute, white bear with the sound chips in her that talk about how happy they are I'm finished with chemo, etc.

    Anyway, I'm going to try to post a picture (DH had to take a ton of photos - how embarrassing!) I've never done this before on this message board so we'll see what happens.

    Oh! BTW - I named my bear Towanda! lol


    [image]image[/image]
  • Watson
    Watson Member Posts: 1,490
    edited November 2005
    Thanks for the sympathy ladies!

    But I got some great news today that overshadows my disappointment over not gettinch chemo today.

    I had my first mammogram and surgeon appt since diagnosis and..................
    ALL IS GOOD! I was so dreading this appt that I almost cancelled it yesterday when I got my no chemo news. I'm so glad I went. Now I really have something to be thankful for!

    Jen, great pic!

    Happy Thanksgiving all~

    Watson
  • LizFL
    LizFL Member Posts: 377
    edited November 2005
    Great news Watson! Taxotere has done something to my taste buds too...it's been a month and I still don't have full taste back...not that it stops me from eating.

    Jen...I love your picture...you have so much hair! It will probably be months before I have even half of that. Towanda is the perfect name for your bear. That sure is a cute surprise.

    Minverva...I think it worked out well that the radiation is delayed so that you get to be home for the holidays. Hope that incision starts healing quickly.

    Fi..good to hear you are doing well. We are all making progress and have a lot to be thankful for.

    I will be leaving Friday for Tampa and will be away on the cruise for TWO weeks. Work was crazy today and to top it off I have been having some swelling in my ankles. Chemo nurse said it's not related to chemo and sent me to my primary. I thought I was done with doctors for a little while. Anyway, nothing serious, adding a few meds to my ever growing collection and they want to do an ultrasound when I return. Since I met my maximum out of pocket expense on my insurance a while ago, may as well cram in as much as possible before the end of the year!

    HAPPY THANKSGIVING TO EVERYONE!

    Liz
  • nosurrender
    nosurrender Member Posts: 2,019
    edited November 2005
    Fi, I am so sorry about your losses. I went through something similar when I was just finishing rads. At first, I felt scared to death- why them and not me? And then when I realized they had children and I had none I felt that it SHOULD have been me instead.

    There is a dark side to this disease that we don't like to think about and this is part of it. Sometimes people don't do well. Are they like us? Maybe they have the same lifestyle- two kids a house and a golden retriever, but what is inside them, deep inside their cell's DNA really separates us from each other. We cannot compare ourselves to another cancer patient. Just like here- you girls have had some similar experiences with chemo and some totally opposite- and all of your diagnoses have been different.

    We must remember that breast cancer is not one disease - it is several. And some people get worse kinds than we do.

    Life can seem unfair. Jane doesn't make it and Mary is fine. Mark was late to work that Tuesday and Kevin was sitting at his desk in the World Trade Center at 8:46 AM. Some areas of New Orleans are gone forever and some are opened for business.

    On this day of Thanksgiving here in the US, we sometimes have to stop and say to God or our higher power or whatever it is you worship that we cannot begin to understand the reason WHY He chooses to have happen the things He does... but we are thankful he chose to let us live to love again, laugh again, cry again, mourn our friends, play with our kids and live our lives again.

    We cannot ever know the WHY. All we can do is see what we have in the NOW. And if we are finishing up one of the most difficult times of our lives, and we are now seeing we are at the other side and on our way back to being US- then we just have to breathe and say thanks.

    It hurts to lose people. It is frightening. But it has nothing to do with us. Just because we also had cancer doesn't make us responsible. We all have cars- yet we don't feel responsible for everyone who has a fatal car accident do we?

    It is good to feel sad and mourn someone who has left us, we know her better than anyone. I think of the girls that went before us as our very own angels. I like to think of them whispering ideas into the researchers ears bringing them closer to that day when no one is lost again.

    You girls have either completed or are just about to complete your battles. My Junesterettes have proven themselves to be a migthy fighting force. I am so proud of each and every one of you. I have NEVER seen the courage, grace, and warmth and genuine caring as you have all shown in my life. I feel so lucky to have been able to hang with you.

    I was telling a friend last night in an email that once you are a survivor, every day is Thanksgiving.

    I am thankful for all of you, for all of your successes, for becoming victors and for beating back that beast for good.

    What's next?

    You life is waiting- just like I told you... it is still there but it better be ready for the inner Towanda that is coming back!

    Love to you all
    and
    Happy Thanksgiving!

    NOSURRENDER!!!
  • Fi_in_oz
    Fi_in_oz Member Posts: 49
    edited November 2005


    Jenster,
    thank you for the encouragement, absolutely appreciated.

    LizFL
    Thank you too.

    No Surrender,
    what can I say, your post was just what I needed to be reminded of, thank you so very very much. You have been amazing support during these last almost 6 months.

    I think we need to adopt thanksgivings day here in Australia !

    Update on my result waiting:
    I got interesting news from last weeks ultrasound, at this stage its (the new lump) not looking suspicious, but its not looking the opposite enough either to forget about it.
    If its still there in 3-4 weeks without signs of reduction or other substantial change, its another ultrasound, followed by a biopsy.
    So, I'll take all the prayers I can thanks ladies, from whichever source you pray to.

    Best wishes to all of you

    Fi
  • kimBe
    kimBe Member Posts: 101
    edited November 2005
    Prayers are with you Fi.....I am going to try to be more actively supportive to those of you who have "bumps" in the road. Every day I am thankful that I have had it so easy and pray and think of all of you. I am one week out from my last chemo and my mental attitude the last two days has been SO much better than the last month I can't believe it. Take care and have a good weekend.
    KimB
  • NancyM
    NancyM Member Posts: 289
    edited November 2005
    Fi, I am so sorry to hear about your lump. I pray that it is benign! I hope your Taxol treatment goes smoothly. Please let us know!



    NoSurrender, it's so good to read your posts again!



    Jenster, your family is so cool, and you are a cutie patootie in you picture!



    Kim, I'm glad you are feeling better - it's so great to have chemo over with!



    Hi, hi, hi to everyone else!



    I was talking to a co-worker who took part of my caseload until I get more energy back. She told me she had put me on her church's prayer list. I thanked her, and then said how much I appreciated her taking on extra work to help me out. She said "I don't think this cancer is a trial only for you. It was given to all of us, to allow us to serve you in your time of need." Wow, that really choked me up. This is a woman who has had severe financial problems lately, and her husband has a lot of health problems himself. I can't get over how some people who have serious problems have it in them to give so much to others. I feel really, really humbled by her attitude and faith. I just wanted to share that with you all.



    I hope everyone is having a peaceful Thanksgiving weekend.

    Love you all,

    Nancy
  • Jenster
    Jenster Member Posts: 267
    edited November 2005
    You're almost there, Watson!!! In just a couple more days you can say, "NO MORE CHEMO!!!" AND you get your port out soon, too. Lucky you!

    I hope everyone had a good Thanksgiving. Mine was fine, even if I was a bit tired. Still ate good - though my taste wasn't as sharp as I would have liked. And then slept even better. lol.

    I had DH buzz my head yesterday. I've been shedding for three weeks! It's starting to drive me nuts. I wish it would either stop or fall out again completely. It's definitely thinned a lot, but I still have quite a bit.

    Now that I'm finished with chemo, we're starting to work on moving. We won't be listing the house until January, but we've had one Realtor out to tell us what we need to do and what we can ask and I've got two more coming out this week. Yikes. I've kept the whole moving thing on the back burner because I just wanted to get through chemo. Now I have to turn up the heat and it's a bit overwhelming.

    I'm so looking forward to 2006. And being settled in a house with nothing more to concern myself with than taking care of my family. And maybe seeing if I can actually keep a garden alive. Oh, and getting a new and improved chest (forgot about that one).

    I'm just rambling here. I'll stop before I put you all to sleep.

    Jen
  • Watson
    Watson Member Posts: 1,490
    edited November 2005
    Nancy,
    Thanks for the inspiration this morning!

    Jen,
    My hair is growing and falling out at the same time! It's gross. I re-shaved my head about a month ago? Now I've got 1/4 to 1/2 inch hairs sprinkling down again. My sister really liked my Ally Sheedy/Breakfast Club imitation at the Thanksgiving table! lol

    I'm taking my anti biotics like a good chemo victim. Hopefully they'll let me have my LAST chemo on Wednesday. Even though my port has never really bothered me, I am very excited to get it out.

    Have a nice week!
  • Jenster
    Jenster Member Posts: 267
    edited November 2005
    Ally Sheedy! LMAO!!! Hopefully you didn't do that imitation while the food was on your plate! ) OH! And when I get my new boobs maybe I can do the Molly Ringwold/Breakfast Club/lipstic thing!! That can be my new talent. What a pair we would make.

    So how long have you been shedding then? I was surprised at how much hair DH buzzed yesterday. We used the #2 setting on the clippers and there was still a lot of hair. I'm definitely thinned out, though. Oh well. I do know this will eventually pass. Just wish it would hurry up!!

    Hey! Doesn't hair grow faster when it's cold? I guess that's a good thing, seeing as how it's winter. Even though Arkansas hasn't quite figured that out, yet. Flamin' 70 degree weather and tornadoes yesterday. How was your weather? I think we got what you started out with.

    Jen
  • Jenster
    Jenster Member Posts: 267
    edited November 2005
    Here's wishing and praying for Watson today!! Hope the very last chemo treatment EVER goes well!!

    Jen
  • danahollis
    danahollis Member Posts: 161
    edited November 2005
    Hi Junies...

    Good luck Watson!!!

    I had/have to take a little break from the boards for a bit. I was finding myself getting way too "into" this cancer thing. Ya know? I need to move on a bit. I've been spending a bit more time at my favorite scrapbooking website... TwoPeasinaBucket.com... and it feels really good to be more "normal"... but with a new perspective.

    I'm feeling pretty darn good. Update on my back... still a bit sore... but getting much better. My guess is that the stupid Rad table through it out, then combined with a very sedentary lifestyle for the past MANY months and also the little dent in my bed mattress from sleeping so much during chemo... phew!... it's no wonder my back hurts! Anyhow... my fears of it being caused by METS are slowly fading.

    I'm having my hysterectomy Dec. 21. I'm nervous... but will be so happy to have all my "stuff" done. I'm tired of being the sick one!

    I'll check in on you all often! But I'm NOT going to read any other posts. I'm feeling a bit too fragile and need to focus on FUN stuff!

    Hugs to you all!

    image
  • Watson
    Watson Member Posts: 1,490
    edited November 2005
    Drumroll please...........................

    Woo Hoo! I had my last chemo and they used my port!
    Boy that feels good to have behind me! Thanks for all your good thoughts!

    My cupcakes were a big hit even though they fell over in the car and looked less appetizing! They ate them anyhow. One nurse couldn't see the last line of cupcake words, so all she saw was

    CHEMO
    SUCKS
    NURSES

    lol!

    She didn't see the whole phrase was Chemo Sucks, Nurses Don't. I told all of them I never wanted to see them again unless it was at the grocery store!

    Jen, can't wait to do a re enactment of The Breakfast Club with you!

    Dana, it's good to take a break! (if you're reading this! ) lol

    Take care ladies! Now on to radiation!

    Watson
  • Jenster
    Jenster Member Posts: 267
    edited December 2005
    YAY WATSON!!!!

    I kept checking to see if you got it. And they used your port?? Great! Are you still getting it out tomorrow??

    "Chemo sucks nurses". Hm. That's quite a great quote. I'll have to pass it on. LOL!

    So glad that's all over for you.

    Jen
  • Watson
    Watson Member Posts: 1,490
    edited December 2005
    The port is getting yanked tomorrow morning at 8am!

    Watson
  • rmmom
    rmmom Member Posts: 168
    edited December 2005
    Watson so happy for you! I go in a week to find out when I get my port out.
    We had a great Thanksgiving! I enjoyed seeing #1 son. We miss him so much.
    My nails aren't hurting as much, I have been keeping them super dry and trying not to lift anything. They mean it when they say "don't lift!" Ouch!
    I am losing hair too. All the hair that stayed around on my arms is jumping ship-now when it is cold and I need it:(
    And I find tiny hairs in the tub from my head. I wonder if it has anything to do with me not having hair until I was two when I was baby? My sister was born with more hair than I had (April) then at my birthday I had enough for a ponytail(June) I wonder if I got headaches from hair growing that fast? Hope it starts growing fast now. Still no lashes LOL
    Take care
    Bev
  • JoMac
    JoMac Member Posts: 192
    edited December 2005
    I took a break from the boards too. My treatment is all done. I am having my ovaries out on Dec. 16th.
    I have been feeling very very achy in all my joints. It hurts to make a fist. Even my tiniest joints hurt.
    I called my oncologist about this. He hasn't called in two days. I should have called him today but I had the chance to have lunch with my daughter so I put all my energy into that instead.
    Is anyone else having the "weepies". I see my girl and I just tear up. I look at my husband and I feel my throat get all hot and tight.
    I treasure them and instead of feeling delight ....I feel something dark and scary.
    The truth is I feel the two opposite things at the same time. I treasure them and fear loosing them.
    This is not helpful behavior so I give my self a good talking to and try to loose myself in some kind of task like removing lint from my sweater.
    This is a very weird time.
  • Analemma
    Analemma Member Posts: 1,622
    edited December 2005
    Jo, I too am achy all over! When I wake up in the morning I dread having to get up because ALL my joints hurt, but especially knees, ankles, feet, and hands. Oh, and hips and back occasionally, shoulders too. I've never heard about this as a side effect, but it started during chemo and has gotten worse with radiation, and the change to cold weather doesn't help, either. I've totally switched from showers to a hot bath every night.

    I'm feeling kind of lost since I'm a triple negative, so no more treatment for me. It's kind of scary, to have to be passive in this fight. Has everyone finished chemo, now that Watson is done? I've lost track.......

    Good luck to you ladies who have surgeries coming up. Jo, will your daughter be home for the holiday when you have your surgery? If not, she will be home soon after to take care of you.

    It's so gray and dark in Cleveland in the winter. Hard to stay positive, especially not going out to a job every day. I need sunshine!!
  • JoMac
    JoMac Member Posts: 192
    edited December 2005
    Brenda, I have used one of those lamps that mimic sunshine for years. I put it on for about 20 minutes a day. I don't know if it helps but I know it doesn't hurt anything.
    I get on my treadmill with the sunlamp on and the fan too keep me cool and pretend it is spring or summer time while I walk for about forty minutes. It is my "mini" vacation from the long Vermont winter.
    My daughter will be home the same day that I have surgery. seeing her will be all the medicine I need.
    Sorry to hear you are achy too.
    I decided to imagine the aches are the regenerating tissue that got killed by the chemo this summer coming back to life.
    That at least makes me feel more mentally positive about it.
    It must be so hard to be triple positive.They just have to get something more to help that catagory.
    Hang in there as the days get shorter.
    I haven't even made a wreath for the door.
    By now I am usually up to my chin in projects and crafts.
    I did pot up some paperwhites and amaryliss bulbs. They should be in bloom in two weeks. I have that to look forward to.
    Yeah....I know I am grasping at straws here....(work with me people).
  • Scout
    Scout Member Posts: 76
    edited December 2005
    There you all are! I thought you all dropped off the face of the earth and I felt soooooo alone!
    I am finished with chemo too....onc. let me finsh early because the side effects were so bad. I also found out on Monday that I won't need radiation either...yipee!
    I had my mast. on the 15th and developed a staph infection, so they had to take one of the implants out.
    Gotta run to bed now (anyone else as tired as I am??) I will catch up with the posts tomorrow.
    So glad I found all of you!
  • JoMac
    JoMac Member Posts: 192
    edited December 2005
    I just spoke to my oncologist who sounded completely suprised at my aches and pains.
    It got me stirred up.
    I wanted him to say "Oh., of course we see this all the time no big deal....."
    But "no" He sounded flumuxed (is that a word) .
    so now I am worried.
    Arghh......and I thought I was feeling pretty centered today.
  • rmmom
    rmmom Member Posts: 168
    edited December 2005
    JoMac-I have aches too. I only get pain in my knee before a big storm and two days before the Thanksgiving snow here I had to take pills-didn't need them the whole time I was on Taxol! I think you were right about the tissues regenerating -It makes sense to me. And your doc! I don't think they know as much as they think. My Dr. Flake doesn't but I feel better about myself after seeing the lady in the wheel chair who was on oxygen being "blown off" by her(in the waiting room). I thought now there is a sick lady and still Dr. Flake isn't taking her problems seriously"
    Scout I am so glad you are done:)!!!!
    Three weeks out I finally feel almost like my old self. I can go out and do two maybe even three things before I need to rest. It feels great. Glad you don't need rads either. Although it is a gray NE Ohio day I feel suuny with your news.
    Take care
    Bev
  • danahollis
    danahollis Member Posts: 161
    edited December 2005
    Ok... had to check in on you guys AGAIN today!

    I have found that my oncologists don't really know about ALL the side effects... either that or they just won't admit to their existance!

    Aches and pains... oh yeah... I've got them too! Weren't you all listening when I was WHINING about my back???? Well... in addition to my back (rightish side)... my right hip hurt too.... oh gees and now my neck gets so sore... I feel my bones get all creaky VERY often. It drives me NUTSO! I get so worried... but my common sense tells me it's just all related to the stress I put my body through making darn sure I killed any renegade cancer cells.

    My latest pain is in my "BAD" boob... it's very achey and it doesn't help that I'm constantly "feeling myself up" to see if there's "anything suspicious" there... which there isn't... just the same old scar tissue that has been there all along. It seems harder now... but I think I was told that would happen.

    So ya see... girlies... you AIN'T alone.

    FYI... I came directly to our thread and did not read anything else... now I'm going to leave and not read anything else. Feel free to email me if you'd like...you know I want to hear from you all. I just can't keep FREAKING myself out by reading some of the stuff here. Ya know?

    HUGS!!!!! (dmiron@charterDOTnet) get it... replace the DOT with a period...

    image
  • NancyM
    NancyM Member Posts: 289
    edited December 2005
    Brenda, I'm a triple neg also! I think Dana is, too. And NoSurrender. Anyone else in this category? Let's plan on getting old together...we can still post from the nursing home, right?

    Watson, I loved the "chemo sucks" message! That cracked me up. Congratulations on finishing chemo!!

    Scout - sorry that you felt alone - we didn't mean to leave ya! Congratulations on finishing chemo!! I'm sorry to hear about the staph infection. I hope your incision heals well. Get better soon!
    *****sending Towanda beams your way*****

    Dana, you made me realize how many photos I have that are just collecting dust. I need to start scrapbooking again, now that I can concentrate on projects!

    Last week I met the friend of a friend, and my friend had already told this woman about my diagnosis. The FIRST thing this woman says to me is how a young woman she worked with died of BC a year after she finished chemo. OH THANKS, THANKS A LOT! YOU ARE SO FLIPPING HELPFUL...PLEASE BE ON MY SUPPORT TEAM!!

    Only 4 rad boosts left! I think I'll do my imitation of Mary Tyler Moore, only instead of a jaunty beret, I'll toss my jaunty wig up in the air!

    Have a good weekend, y'all!
  • Scout
    Scout Member Posts: 76
    edited December 2005
    Nancy, don't you just love people like that??? What are they thinking???? Or maybe I should say, why don't they think before they talk!!!!!!!!!!!!!!!!
    Saw the PS today. She said the healing was great and even took some stiches out and the right drain! Yipee!!!! The left should come out on Monday. She is scheduling the surgery (to put the implant back in) at the beginning of January. The think that sucks is this puts me back to square one again. I have another week before I can drive (and it's Christmas time!) and then in Jan I get to do it all over again (4 to 6 weeks recover).
    Can't wait for Feb!! I will be over most of this and I can start winter sowing my seeds...yea!
    I have to keep the port in until next year due to the Herceptin. I think I will have my "finished" party then.
  • JoMac
    JoMac Member Posts: 192
    edited December 2005
    I must have been in "la la" land. Until about four weeks ago I was only focused on the stage of my cancer not the type of tumor it was.
    I didn't even "get" what triple negative meant. ( I am er/pr+)
    I do understand it now.
    It makes me realize how different we are and yet are still under the same umbrella.
    I only come to this one safe place on the board these days. Then I scoot away to a fun site like televisionwithoutpity.
    I guess I feel the need to connect and not feel completely isolated...then skitter off like a cockroach when the light comes on.
    I will have to learn to live with the aches and pains and take lots of advill.
    As far as hearing about other people dying of this disease ...nosurrender's analogy is working for me. She said up thread
    " We all have cars yet we don't feel responsible for everyone who has a fatal car accident do we? "

    That really made sense to me.
    These days I am trying to take lots of deep cleansing breaths. Then get really really busy on some task that involves thinking.
    Maybe I could take up juggling.

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