Starting Chemo in June 2005

Options
1404143454674

Comments

  • Watson
    Watson Member Posts: 1,490
    edited September 2005
    Jenster,
    I felt the same way about the interview. I waited all week and was a little disappointed. It seemed like Oprah kept cutting her off from details of her BC which is what I wanted to hear about.
    Her chemo description was strange. I know we're all different and I know I got off easy with AC, but three months of extreme pain like none she'd ever known? huh?

    Well, she looked good and had a nice sassy 'do! There's hope!
  • Jenster
    Jenster Member Posts: 267
    edited September 2005

    Yeah. I haven't heard anyone here complain of extreme pain for three months. She did look good, though. And what she did manage to get out was that there is so much hope. That was just plain nice to hear!

  • danahollis
    danahollis Member Posts: 161
    edited September 2005
    Hi all...

    I had my first Radiation treatment yesterday. I also got my port removed yesterday afternoon. It was a day surgery (operating room) for me. They didn't put me completely under but they gave me enough "loopy juice" that I don't remember any part of the actual procedure. That's the way I like it! (That's the way uh huh, uh huh I like it, uh huh, uh huh... )

    Anyhow, ooh... HOT FLASH.... gotta open the window! Ok, that's a bit better! I am so SICK, SICK, SICK of these hot flashes. They just make me miserable. They happen so often and I actually get weak and a little sick to my stomach if I'm on my feet doing something when they happen. I sure hope that I can do something to alleviate them soon. Those of you that are getting them... I feel for ya... I really do!

    Oh darn it... I just missed Melissa Etheridge on Oprah! Shoot!

    JoMac... I know it's tough to set aside those fears. But you are here, very much alive, and if you let yourself get caught up in the what if's, you're robbing yourself of too many precious moments. I know those are tough words... but they are what I tell myself to pull me up when I go to that place. Sometimes we need a good kick in the pants, ya know? I get scared and have a good cry... and then I pick myself up and do my darndest to move on. The way I see it is this... I'll be really disappointed in myself if I wallow in misery for the next 60 years worried about dying before my time! Please PM me if you'd like to chat. I'd be happy to give you a call and we could talk for real. I'll hold your hand if you need it... even if it is from a distance!! (Besides... I like to have my hand held, too!)

    Cathi.... ya know, funny you mention the cramping feeling. Just last night (Or maybe it was this morning) I was laying in bed thinking I felt like I was going to maybe start my period soon. I had those same crampy feelings... and then I got a little worried given my past cervical issues... but with those I had no idea there was anything wrong. So, my thoughts went back to starting my period. But then I thought this would seem way too soon and I am having HOT FLASHES constantly so I just don't know what it could be. Maybe I had gas! Ok, I'm rambling....

    Anyway, I better go for now.

    Lotsa HUGS to you all!
  • cindanbob
    cindanbob Member Posts: 16
    edited September 2005

    I also saw Oprah today. Melissa Etheridge was inspiring, and the song she sang made me cry a little. But her descriptions of chemo scared me! I'm just diagnosed with IDC on Sept. 13,05. Surgery is Oct. 10. I still don't know whether it'll be chemo or just rads after. So hearing about her chemo treatment terrified me. I don't know what to expect if I do have chemo, but I hope it won't be anything like that.

  • danahollis
    danahollis Member Posts: 161
    edited September 2005
    CindyM.... Welcome! In your free time (LOL!!!) you could read back through our posts. Chemo is no fun... but all of us here have been through it. Some are done (like me) and others are getting close to be being done. It was not as bad as most of us thought it would be. If you have to have it, you'll get through it. Some days are worse than others, but there are still some pretty decent days in between! Don't be terrified!

    HUGS!
  • LizFL
    LizFL Member Posts: 377
    edited September 2005
    From your post Nancy...today was your last chemo? If so, CONGRATULATIONS!

    CindyM...we are all making it through...like Dana said...good days and bad, but it's doable!

    Liz
  • danahollis
    danahollis Member Posts: 161
    edited September 2005
    Oh my gosh... I missed that!

    CONGRATS NANCY... WOOHOOO... Yipeee!!!!! Let the hair growing begin!!!
  • Jenster
    Jenster Member Posts: 267
    edited September 2005
    CindyM - I haven't heard anybody say they were in excruciating pain the whole time they went through chemo. That was a first for me. So I wouldn't let that worry you. No doubt you'll come through without so much as a hiccup! Well, maybe a hiccup or two. But I'm sure you'll do fine.

    Jen
  • nosurrender
    nosurrender Member Posts: 2,019
    edited September 2005
    Hello Girls,
    I missed Melissa Ethridge not once but twice- I missed the re-run they have on at 7PM as well as the regular Oprah time.

    I just felt that I needed to say that although you are all almost finishing up - your Snowflake status does not melt away....

    For Cindy, I like to remind everyone that there is not one type of breast cancer. For as many girls that have it- 2 MILLION LIVING WITH IT AS SURVIVORS!- that makes 2 million different types of BC. Make that 2,000,001 including you!

    Everyone has an their own body chemistry and immune system, everyone has a different tumor with separate and distinct characterists, so like a snow flake, there are no two women alike- and no two cancers alike.

    We can share our experiences, and many are similar, but some may get one side effect where others don't feel a thing. Melissa Ethridge said she was in bed for six months? And in pain? Well, I don't know because I didn't see it- but I once told everyone that chemo can sometimes activate underlying or dormant problems you may have that you didn't know about. One is Arthritis. I know that is how I discovered I had arthritis. But after the chemo it went back into its little hiding place.

    Plus, she may have an extremely low threshold of pain and any ache or bump knocks her for a loop. That just means that it happened to HER- it isn't a prediction of what will happen to you in the future. FAR FROM IT!

    And for everyone feeling different now that treatment is finishing, remember that everyone processes things in their own unique way. Some people can be chipper and up beat the whole time- And some people feel what is happening to them at the time it is happening.

    You see- all of this has to be processed and worked out in your mind and spirits...Let's face it, YOU HAVE BEEN THROUGH A LOT! And maybe when the hustle and bustle of treatment ends some of the chipper girls may feel a bit at sea - that is NORMAL. It happens when you allow yourselves to FEEL what just happened to you. You may have some down days to work through- but you do get past that.

    Some girls are terrified at this point. You are being told to stop fighting. It may feel like you are being told to give up- but the FACT IS: You won. There is nothing left to kill. No more chemo - no more rads- you are done. You conquered and beat back the Beast.

    I was one of the girls who felt everything as it was happening. That is fine too. It was my way of getting through it.

    So as a Snowflake you will find your Post Cancer Comfort Zone... and the BEST part about that is- the longer you go the more COMFY you get. Give yourselves a time to heal inside- not just the scars and hair growing back. Give yourselves a big break.

    Cindy, I just want to reassure you of one thing:
    EVERYTHING IS GOING TO BE OK. Really. Look at these girls- they are there and back and in one piece. You will be able to not only handle what lies ahead- but you will take it on and attack it so you can get your life back as soon as possible.

    The secret now is to NOT PROJECT. Take everything one day at a time, one proceedure at a time. The rest will all fall into place. And before you know it- you WILL be done. And you will be yourself again. Right now you are in the WORST part. The unknown, the what-ifs.... It all gets better from here.... here is my test- I joined these magnificent women when they first were starting their battles. I told them when they were at your stage it was the worst stage and it gets better- as they learn what they needed to learn, took things one step at a time- they would think back now and say- wow I made it!

    So JUNESTERETTES??? What have you got to tell Cindy?
    Am I right? Wasn't where she is now the worst part? And here you are strong Towandas who made it one piece? Let's let our new sister know!

    And one last thing Cindy-

    NO SURRENDER.
    (It's been four years for me...
  • NancyM
    NancyM Member Posts: 289
    edited September 2005
    Yesterday as I was getting my final Taxol, I was feeling really happy, and when the onc said I didn't even need a final Neupogen I was practically giddy! I pictured myself out in the parking lot, clicking my heels together as I headed to my car!

    Imagine my surprise when I ended up practically bursting into tears when the nurse brought me a "champagne" bottle of sparkling apple cider to take home for a celebration. Gosh, I was so embarrased! What was this all about? I was suddenly feeling like "oh, man...look what I've been through!" and I felt almost like I wanted to mourn the chemo process! No more having to be brave, trying to be strong. I could just let it all out. (But I didn't.)

    It was weird that all the times I had been there for chemo and the place was packed...yesterday I was the only patient left for the last hour so it felt kind of lonely! Just the two nurses were there, they gave me hugs and thanked me for the donuts I had brought in. They told me to ring the large bell next to the door on my way out of the room. I had noticed the bell before, but never saw anyone ring it! So, they told me to ring it loud enough so the receptionists could hear it, too! On my way out of the lobby they called out "Congratulations!!" I love symbolic stuff like that.

    So now I have my radiation consultation on the 5th. A new phase!

    I hope you all are doing well, and I'm glad we're all still together in this!
  • rmmom
    rmmom Member Posts: 168
    edited September 2005
    Hey Cindy we're all here for you. The hardest part was the beginning-the unknown-it was like that each time something new started. We won't kid you there were days you just want to pull the covers over your head and sleep until it is better. So we did and it got better. Me I just called my mom-I bet she would make Melissa Etheridge look like a strong kick butt Towanda! I remember one time when I was just tired, not really enjoying eating and just whiny I called and and she talked about her painful HANG NAIL the whole time-not a word about how I was doing!! One hour of HANG NAIL pain I am not kidding. By the time we were done I felt better because I was so mad at her She still does does it to me. My favorite lines are: "You can't begin to understand pain." and "You really don't want to get old." WHO IN THEIR RIGHT MIND WOULD SAY THAT TO A CANCER SURVIVOR! (by the way she is young-only 62) I could have my mom call you-she makes EVERYTHING less scary.
    I am happy-my surgeon called today she doesn't feel I need radiation she she is going to check in things for me.--See Cindy about worrying each step of the way. But it really is doable. And we all are here when you need us.
    Take care all
    Bev
  • rmmom
    rmmom Member Posts: 168
    edited September 2005
    Opps I meant to do the happy dance for Nancy :grin
  • Watson
    Watson Member Posts: 1,490
    edited September 2005
    Happy Dance for everyone!

    As some of you may remember, I've been whining about my back for a while. I had a clean bone scan in June, but last week my onc made me do an x-ray 'just to be sure'. Well with the hurricane and all, they just got around to calling me and telling me it's okay!
    I was at Lowe's buying a new hot water heater when they called me. I hugged the poor kid helping me with copper hoses! He'll never be the same having a bald woman with Taco Bell sauce dripped down her shirt hugging him in the middle of the store. I sure hope the other guys don't tease him!
    Have a great weekend! Even though my back still feels like it's been put in a vice, I know it will go away when this is all over.
  • danahollis
    danahollis Member Posts: 161
    edited September 2005
    Watson... that's great news! Now maybe you can feel a bit more calm. I'm so happy for you.
  • Jenster
    Jenster Member Posts: 267
    edited September 2005
    Yay, Watson!! And thanks for the laugh! lol.


    Jen
  • Jenster
    Jenster Member Posts: 267
    edited September 2005
    Hey!! I just got up from a nap a little bit ago and while I was washing my hands I noticed I could tell from my wayward hair which side I was sleeping on!!! How exciting is that??

    So it's only a couple of gray hairs that seem to be growing much faster than the rest of it. It was still fun for me.

    I'm really starting to get used to my hair thickening up and getting longer. I think I'll be much more disappointed if I lose it again than I was the first time.

    Jen
  • Scout
    Scout Member Posts: 76
    edited September 2005
    Watson, that's great news!
    Congrats to all that are towards the end! I have 4 more Taxotere left...whew!
    Had my biopsy, on the left side, today. It was an MRI guided one, so I had to lay with my arms up...and they started to cramp up right before the end. Over all, it wasn't bad, but I had it at 10am and it's 5:30pm and the holes are still bleeding...sigh. My other biopsy didn't have this problem.
    I should know on Monday or Tuesday what the results are. Keep your fingers crossed that I'm not starting this journey all over on the left!
  • danahollis
    danahollis Member Posts: 161
    edited September 2005
    Scout... keeping you in my thoughts and prayers and hoping all turns out ok.

    Hugs!
  • minerva
    minerva Member Posts: 36
    edited September 2005
    Susan - I am so glad you are finished and on to the next stage. I cried while I read your post on leaving the chemo room for the last time. I hope that someday soon you, Rebecca and I will be able to meet.

    Jenster - LOL on the hair doo! Enjoy your Christmas lights!

    Watson - So happy for you!, the poor kid, lmao.

    Scout - I hope that you only receive good news. I will pray for you. Happy dance for you!

    NoSurrender - Thanks always for your positive input and strength. You always know what to say to help us through this hard time.

    I will be having my last chemo on Oct 13th. Last time it had to be delayed because my CBC came back to low, but this time I will not allow my body take over! I am ready to be done, but also scared. I have been a little weepy the last few days, but I believe that it is because I am being close to being done. I agree that it has been tough being strong for so long. My surgery is scheduled a month after chemo and then rads start a month after that. Just a few more hurdles and I will finish the race.

    Cindy - keep coming back because there ladies are wonderful and strong. They will help you so much.

    Take care all. Hugs
  • nosurrender
    nosurrender Member Posts: 2,019
    edited September 2005
    Minerva- Cry all you want- you earned it! You can even cuss too! You all have been so incredibly strong, once you let your guards down you will feel confused, a little scared, and then a wave of pure relief washes over you.

    Nancy- I tried to PM you but they wouldn't let it through...
    But I wanted to tell you YAY!!!!! Congratulations!

    And Scout- hoding you close in prayers - you are going to be ok, I just know it. This weekend give yourself a break. There is nothing you can do to change what the sample is doing in the lab over the weekend so take a little trip on De-Nile and don't think about it...


    Watson - I am so happy for you! and who knows? you may have given the young man a thrill!

    It feels like fall here. I am not ready for that yet. So I am refusing to put my moccasins away...that way indian summer can still come!
  • Fi_in_oz
    Fi_in_oz Member Posts: 49
    edited October 2005
    I'm so very very tired of people starring at me

    If I wear a hat, they stare
    If I wear a scarf, they stare
    If I wear sunglasses, they stare even more
    If I wear a bald head, they stare
    If I use my "smile", they stare
    If I give them a "what are you starring at" look, they still stare.
    If I catch their eye whilst they are starring, they wait till they are 1/2 way past me and then turn for another look, am I supposed to have tunnel vision just because I'm bald?

    people really can be so very very rude without even uttering a word.

    yippee I have another 6 months until I have decent hair.

    But a beautiful thing happened to me today, I ran into a girl I went to school with 20 years ago, she greeted me with a rub on the head and said "chemo huh?"...
    her mum is a breast cancer survivor...
    that one gesture took all the "annoyance" of all the stares away.

    Perhaps we need to educate the world that the majority of breast cancer endurers during treatment may not actually look "sick", just bald and beautiful.

    Food for thought

    Fi
  • LizFL
    LizFL Member Posts: 377
    edited October 2005
    Scout...add me to those praying for you! Hope you find something to keep you busy and chase away the worry.

    Hugs,
    Liz
  • Watson
    Watson Member Posts: 1,490
    edited October 2005
    Scout,
    Fingers, toes, and eyes are crossed for good news!

    Fi,
    I'm sorry people stare. Other than maybe the quick double take some people give me, I really don't seem to notice the stares. I'm probably in denial!
    I had lunch yesterday with four women I"ve 'met' on this site via the discussion boards or live chat. We were having margaritas and I got a Hot Flash. I whipped off my wig right there at the table and put on a baseball cap!
    I am just soooooo over being bald. Gotta say it looked pretty funny with my 'hair' sticking up out of my purse!
  • danahollis
    danahollis Member Posts: 161
    edited October 2005
    Fi... ya know, I find I notice bald women even more than I used to. I also feel something completely different when I look at them now and I'm guessing I may even look longer at them than I would have before BC. I feel so much more compassion and I guess I just want to see what's in their eyes... ya know???

    I think you are very brave for going bald!

    HUGS!
  • Fi_in_oz
    Fi_in_oz Member Posts: 49
    edited October 2005
    Thanks Watson and Dana,

    ~s~ I know its not just me noticing, a girlfriend who came away with me for the first radiotherapy week noticed it too, and commented by about day 4 that she didn't know how I handled it so well in public.

    I really think perhaps it just gets too me later in the week as I get more tired. Then I come back home and play hermit in my house, down on the beach, out at the farm and the frustration goes away.

    Dana, I wish I could say I'm being brave, but in all honesty I'm just being pratical, my head overheats even with a scarf and hat, and well a wig, just wasn't in my "Priorities budget" when this is all done I won't have worked my regular job for 10 months, there were simply more essential things to spend money on.

    Thanks for the positive thoughts ladies

    Best wishes

    Fi
  • danahollis
    danahollis Member Posts: 161
    edited October 2005
    Hi everyone,

    I went back to work today... part time... 4 hours a day while I am doing Radiation. It was nice to see everyone and do something "normal."

    How is everyone??? I hope you all are doing well. I have nothing interesting to report so I'll be brief.

    HUGS to you all!
  • Jenster
    Jenster Member Posts: 267
    edited October 2005
    Good for you, Dana!

    I'm doing pretty good, though I broke a tooth yesterday. I have to go get labs tomorrow morning to make sure I can go to the dentist to get the tooth fixed. Which I'm pretty sure my WBC is going to be low so I don't know what they're going to do. The tooth doesn't hurt (thank goodness for the filling), but it's jagged and hurts my tongue.

    Oh, for the days when I can just go to the dentist without anyone else's permission!! Can't wait to be normal like you, Dana!!

    Jen
  • danahollis
    danahollis Member Posts: 161
    edited October 2005
    Oh Jen... sorry to hear about your tooth... that's a BUMMER! Hopefully you'll be able to get it fixed very soon! I'll think good WBC boosting thoughts for you!

  • LizFL
    LizFL Member Posts: 377
    edited October 2005
    Jen...I chipped a tooth last week. Oncologist said it would be ok as long as dentist didn't have to do anything invasive. He filed tooth down and bonded it...I was in and out of there in no time.

    Congrats on your return to work Dana!

    Liz
  • Jenster
    Jenster Member Posts: 267
    edited October 2005
    Liz - That's good to know. I'm sure my dentist can do something, if only temporary.

    Dana - thanks for the WBC well wishes!! lol

    Jen

Categories