March 2010 Chemo Start

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  • badger
    badger Member Posts: 34,614
    edited October 2010

    Geez Ana, so sorry to hear that, waiting (and worrying) is the pits.  Sending good vibes!!

  • LillyC
    LillyC Member Posts: 64
    edited August 2013

    Ana - Have been thinking so much about you, and have made an appointment with my surgeon on Monday to check out my lump.  Even though the radiologist and the oncologist said not to worry about it, I've decided to let the surgeon check it out after thinking about you.  It's hard to even think that all of that chemo and radiation didn't get everything, but better safe than sorry.  Keeping you in my prayers.

    Also, a new problem...at least it seems to be a problem to me - my nipple is discharging clear fluid. Of course this would happen three days after seeing the oncologist and the radiologist who told me not to give the lump a second thought. I guess it is the fluid in the lump coming out. I will find out on Monday.  Anyone else having this problem? I just noticed it today.  It did happen once during radiation and they were not concerned.

  • badger
    badger Member Posts: 34,614
    edited October 2010

    LillyC - glad you got in so quick to see surgeon, hope that lump turns out to be nothing!

    Anyone else growing a beard? <sigh> it's downy and colorless but a beard nonetheless.

    I'm so hesitant to shave for fear of stubble, or growing back thicker / darker.  {{hugs}}

  • hereandnow
    hereandnow Member Posts: 322
    edited October 2010

    Lilly and Ana, I hope you get those tests back quickly, and can put this behind you soon.

    Badger, I'm not growing a beard yet, though I do have a little soft downy hair on my face, but I always did. I have seen some women on the hair hair hair thread shaved their "beards" and reckon it doesn't come back, I'd be careful of that too, but I'm not sure of the solution.

  • Charley
    Charley Member Posts: 255
    edited October 2010

    NOooooooo!!! Praying for you Ana!  Hopefully they are just being overly cautious!!?? Hang in there and let us know how things go!

    (((Hugs)))

    Charley

  • teemee
    teemee Member Posts: 122
    edited October 2010

    Yes Ana, please let us know how you are and big hugs.

    Toni

  • Charley
    Charley Member Posts: 255
    edited October 2010

    Oh Lily C - Didn't see your post before my last post.  Hopefully it all turns out to be nothing!  Yes, why do things happen just days AFTER you see the dr? AARGH!  I had BMX so I have nothing to add on this. :(

    (((more hugs)))

    Charley

  • staceyt
    staceyt Member Posts: 106
    edited October 2010

    Hello Ladies,

    So sorry to hear Lillyc and Ana - hugs and prayers to you - Charley you look fabulous what a beautiful smile you have.

    Went away for a few days with the DH - took a road trip on the motorcycles to Bath, Maine.  Had a fantastic time and met some great people.  I have a t-shirt that reads - I didn't survive cancer to die of stress and was wearing it there and had a guy come up and ask if he could ask me a personal question - long story short - his wife who was driving by car is going through chemo now and asked if I would speak with her.  We hit it off immediately - God works in mysterious ways does he not? 

    I think and pray for all of us everyday - and I do read everyday also- I have not forgotten my wonderful fellow Marchers.

    My best to all - Stacey

  • LillyC
    LillyC Member Posts: 64
    edited October 2010

    Here's an update - went to the breast surgeon today about the lump and the nipple discharge.  He said it was a seroma, a fluid filled cavity, and aspirated it.  What I was seeing was not actually nipple discharge, but the seroma fluid finding a way out. He sent the fluid to the lab for testing, but said he was only doing that to reassure me as he normally doesn't send seroma fluid for testing.  I should expect that the cavity will fill again and that he will continue to drain it until it stops. Seromas are evidently somewhat commmn, but he was surprised to see one so far out from surgery.  I explained that I have had it for some time, but the radiologist and oncologist just kept saying not to worry about it.  I'm glad that I saw him!

  • hereandnow
    hereandnow Member Posts: 322
    edited October 2010

    oh Lilly, that sounds like good news, and now you have an answer for something that's been troubling you. what a relief.

    Stacy, sounds like your getting in some great road trips. Do you ride a big Hog?

    ANa, hope you're ok and that MRI has been organised quickly. Thinking of you (((hug))),

    Lisa

  • staceyt
    staceyt Member Posts: 106
    edited October 2010

    Lilly - so glad to hear it was something "simple" so to speak.  Lisa - No I ride a Honda -Badger, I'm not sure if I would shave it - for fear it would come back even thicker.

    Fall is here - I love the fall - our peak leaf season has come and gone - oh well - hoping for a nice Indian Summer.

    Hugs and prayers to all - Stacey

  • hmh23
    hmh23 Member Posts: 306
    edited October 2010

    Great news Lily!

    Ana;  A good friend of mine just went through a similar experience and believe it or not, it was a lymph node that had been moved during one of her procedures (I believe it was a mamogram, I've never heard such a thing) but her surgeon removed it for precautionary reasons and she is completely fine.  Keeping you in my thoughts and prayers.

    Thx to everyone for your words of encouragement on rads.  I went for my first appointment of prep for my rads.  Feeling much better about just getting this done and over with.

    To everyone who has completed treatment and now expected to get "back to normal", I think it's important to not only remind yourself but remind others, that the body itself needs time to recover from what its has been through but so does the heart and the mind.  I personally feel that given how quickly everything happened from the diagnosis, through surgery, through chemo etc, we just aren't given the time to grieve everything that we have lost whether it is a breast, or both breasts, part of a breast, our hair, etc.  Our families and friends, need to realize that we need more time to heal emotionally but more importantly, we need to accept this ourselves.

    Fondly, Heather

  • Ana1973
    Ana1973 Member Posts: 88
    edited October 2010

    My wonderful Marchers....thank you for all your prayers, thoughts and encouragement. I finally heard from my Onc today. The first words out of his mouth is that he believes it's scar tissue. Nothing showed up on the mammogram, but the anomaly did show up on the ultrasound. It didn't show any kind of blood flow (food source) and is not palpable. He did suggest to have another ultrasound in 6 weeks to make sure it's not changing. Obviously if there are changes I will need a biopsy and surgery. At this point he is saying he is 98% sure it's scar tissue! Needless to say I will be holding my breath and praying that there are no changes. I truly felt in my soul that this was just scar tissue. I'm satisfied with his assessment and pray for continued health.

    LillyC- I'm thrilled to hear it was nothing to be concerned about :)

    Heather- I couldn't agree more. Especially since I had this scare, I see in myself that emotionally and mentally I am not healed and need more time.

    Thank you ladies. You are always here with encouraging words every time I need them. Now I need a nap, all this stress over the last 5 days has left me exhausted.

    Sending hugs, Ana

  • LillyC
    LillyC Member Posts: 64
    edited October 2010

    Ana, I am so relieved for you.  I have been so concerned and have really felt for you as we all know that the waiting and worrying is the worst.  I think 98% is great news!     

    Love and prayers to all!

  • Yeshua4Me
    Yeshua4Me Member Posts: 77
    edited October 2010

    Ana: I'm so happy the news is positive! I've been worried. It is like each of us are connected and if one of us has a concern, then we all do! We can all breathe easier for now.

    Heather: I'm also doing rads right now. Just had my 11th one. I'm scheduled for 25. This is MUCH easier than chemo. The ladies here gave me confidence when I was told I needed radiation. They taught me what to expect and how to take care of my skin. If you have any questions before you start (or during) rads, just ask us. I'm sure someone will respond.

    As to trying to "get back to normal", it has been hard for me. Although I am still doing rads, I am much better and everyone "forgets" that I am still trying to heal both physically and mentally. It has been 5 weeks since my last chemo but my bones (or muscles?) are very weak and it is hard for me to walk upstairs or bend over without wincing. I see my dr. at the end of this month and will ask him about that but in the meantime, I believe people get annoyed with me. I get the feeling that I am expected to act the way I did before treatment. I really do try. Saturday I slipped in the kitchen and fell. I didn't get hurt at all~in fact, I knew I was going to fall so I went down very slowly. The problem was that I couldn't get back up again! No one was home but me and I laid there, on the floor, for about 15 minutes before I could roll over and crawl to a chair to help pull myself up. It was ridiculous! I didn't tell my family until Monday and when I did, I told it as a funny story. I don't want them to worry about me when I'm home alone. But now, I keep my cell in my pocket all the time just in case.

  • Charley
    Charley Member Posts: 255
    edited October 2010

    So glad for the good news Ana and LillyC!

    And Yes that is terrible!! Hoping strength will be returning to you soon! Keep your cell phone close ... at least until you are stronger.

    ((hugs to all))

    Charley

  • frosty1
    frosty1 Member Posts: 420
    edited October 2010

    NORMAL is a state of mind ... and I have adjusted my idea of what normal is ... it makes life a whole lot easier!

    Glad to hear everyone is moving along and progressing.  Hair growing -- even if it isn't all welcome (I'm finding my neck hair starting to get very unruly!).

    Hugs to all.

  • hereandnow
    hereandnow Member Posts: 322
    edited October 2010

    I'm so glad Ana - bloody hell, just what you needed hey, a scare like that, I agree with Yesh that I feel connected with all you lovely women, I was holding my breath too.

    As to others expecting us to be good to go, we will all take our own time and in our own ways to build up our physical and emotional armour.  I think we have to be gentle on ourselves, and not feel bad about ourselves when we don't meet up to others unrealistic expectations, and perhaps our own.

    Yesh you scared me about the kitchen floor story. Wishing you strengthening muscles from afar.

    Badger, how's your beard coming along?

  • badger
    badger Member Posts: 34,614
    edited October 2010

    Hey all - just back from a conference in Cleveland Ohio.  Not sure it was the most productive use of my time but it's good to get away from the office once in a while.  Got in a visit to the Rock & Roll Hall of Fame.  Highlights for me were seeing Jerry Garcia's guitars and John Lennon's piano.  Wish I would've had time to visit the Great Lakes Science Center.  

    Yeshua4Me, good you could make light for your family but that's a scary story, sending healing thoughts your way!

    Lisa, I am still a (lightly) bearded lady. DH doesn't mind it and he actually said don't shave, you'll get stubble. I'm thinking about waxing but that hurts and I'm pain-averse.  I need a haircut soon so will talk to my hairdresser and see what she recommends.

    Take care everyone and {{hugs}} to all.

  • marilyn7
    marilyn7 Member Posts: 86
    edited October 2010

    Yeshua - It took me about 6 or 7  weeks post-chemo before I could walk up a flight of stairs without strong heart palpitations and muscle soreness in my thighs. The stamina came back first and slowly my muscles became stronger.  Still not 100% of course, but at least I can do most of my day to day functioning and get a good walk in on most days. (it's been 3 months).

    Ana / Lilly - Sorry you had such a scare.  I agree with Ana, this has made us feel more vulnerable. Pre-cancer, whenever I had a scare of any sort I assumed it would all work out - post-cancer I find myself a bit more pessimistic - I hope that changes.

    I'm on day 2 of hormone therapy - only 1,823 more to go  - LOL!! I'm assuming I'll stop counting very soon.  So far, so good, but I assume there will be some cumulative effect at some point.  I'm on a generic Aramidex (Anastrozole).

    My hair is FINALLY coming in - but this chicken fuzz is a lot less attractive than my bald head - some have advised shaving this first batch but I waited so long to get it that I don't have the heart to see it go.  I went the whole summer bald and proud, now that I have the fuzz - and it's getting cold, I've gone back to the wig.

    Big hugs to everyone.  Marilyn 

  • badger
    badger Member Posts: 34,614
    edited October 2010

    "Shave and a haircut, two bits"

    Anyone remember that little ditty?  It's been on my mind since this afternoon.  Stopped in to the hairderssers to see about a trim around the ears.  She was able to squeeze me in (not much hair = not much time LOL) and also took the clippers to my downy beard.  She's a naturally fuzzy-faced person which normalized it for me.  She clips hers and I've never noticed stubble on her face, so I figured it was OK and we went for it.

    Marilyn, I've only ever trimmed my hair, like you I didn't want to give up ANY.

    Hope everyone has a good weekend!  Sending good thoughts and {{hugs}} to all

  • hereandnow
    hereandnow Member Posts: 322
    edited October 2010

    Kayne, just checking did you have your liver biopsy yet? Hope those liver enzymes have settled down. Marilyn congrats on the chicken fluff, there'll be no stopping it now. Badger, I'll be interested in how the facial fluff goes now you've clipped. To all Marchers having Rads, I hope you're all going ok.

    hugs to all, Lisa

  • Yeshua4Me
    Yeshua4Me Member Posts: 77
    edited October 2010
    Well, only 2 weeks left of rads! I'm so excited. I can finally see the end of this thing. So far no skin reactions to the radiation and I do keep my breast slathered with aloe vera. After rads is over, I'm finished. No pills or anything for me because I am triple negative. I just see my oncologist every 3 months for a year or so for a blood test. Hopefully this thing never comes back! I mentioned before that I tested positive for BRCA 2 gene which means that my breast cancer was inherited. At that time I was told my 3 children had a 50% chance of inheriting the gene from me. None of my children wanted to be tested. I have 2 boys and 1 girl. Well, my daughter told me last week she decided to get tested. I think because her and her boyfriend have become VERY serious and they are talking marriage. She will be 24 next month. Anyway, I got VERY scared. I don't really want her to have the test because if it comes back positive I will be VERY upset! I didn't say any of this to her. I just smiled, told her I'd make the app, go with her to speak to the genealogist, and be with her for the results. But I am VERY scared. Please, please, not my daughter.......Cry
  • Charley
    Charley Member Posts: 255
    edited October 2010

    Yesh - I'm sorry!  My cousins (all BRCA2+) have the same problems with their daughters.  All are now in the 18-26 age range and scared to do testing! But with knowledge comes power ... if positive she can proactively do something to avoid the problems we have had.  And there are more options now. But still, tough decision ... praying she comes back negative!

    (((hugs)))

    Charley

  • marilyn7
    marilyn7 Member Posts: 86
    edited October 2010

    Yesh - My heart goes out to you.  I have a 16 year old and cross my fingers every day.

    Lots of mixed emotions today. The 3-day BC Walk came through my town this morning - is was a parade of pink. I was standing out there with my fuzzy bald head and my survivor shirt waving everyone on. I've never hugged that many sweaty strangers in my life. Lots of smiles, tears, and hugs. I thought of my fellow March gals and how we have all joined this club, never to look back. We are all part of something much larger than our own journey.

    Sending out lots of warm vibes and sweaty hugs.  Marilyn

  • badger
    badger Member Posts: 34,614
    edited October 2010

    Hi all - just a quick post to mark today's date 10/10/10

    I'm in central time US and it's 10:10 a.m. right now.  :-)

  • badger
    badger Member Posts: 34,614
    edited October 2010

    FYI - did you see the site's going to be down for several hours tonight? Starting

    10:00 p.m. Eastern Time (see my post yesterday is date-stamped an hour late)

    I can't bump up the Moderator Message posted this morning but it says:

    Site will be down starting 10pm, EST

    Our apologies, but beginning this evening at 10pm, EST, we are switching servers. The site will be down for approximately 3 hours. 

    Stay tuned, and we'll be back up, hopefully faster than ever.

    Best,

    The BCO Team 

  • hereandnow
    hereandnow Member Posts: 322
    edited October 2010

    Thanks Badger, I told my supervisors yesterday I just am not ready to present my literature review. We are going to re-schedule it some time in the future. Can't help but feel a little low today about it, but had to be realistic, it just wasn't working (brain and motivation). Have had 2 weeks of good sleep and the flashes are settling - onc gave me ativan and upped the remifemin - just waking at 6 with a flash. Other than that, the weather is beautiful, sun is shining, and Spring is finally here. Hope you're all hanging in there,  Yesh, fingers crossed for your daughters results to be negative.

  • Kayne
    Kayne Member Posts: 103
    edited October 2010

    Anna and Lily:  I am so glad things worked out.  I can't imagine how stressful that was. 

    Yesh:  I too am keeping my fingers crossed for your daughter.

    Lisa:  Don't be so hard on yourself.  Maybe with more time/less stress you will be able to work on it a little bit at a time.  I think we all want to be "normal" again and are trying to do too much.  Oh, thanks for asking about the liver biopsy. 

    Here is the latest:  My onc. reviewed my chart again, charted my blood work and decided I should be done with chemo.  I was not  in agreement.  So she said to think about while she consulted with 3 other onc.   We also spoke to another onc.  So all but one agreed that I have had enough chemo and that it is more important to move onto radiation and hormone therapy.  After speaking to the other onc.  we agreed.   The problem is I felt depressed over it.  Since I physically felt ok on taxol, I actually was comforted by going to chemo.  I also was on a count down.  Now, I have no count down and no celebration.  Very anti-climatic.  Yes, we could celebrate, but it's just not the same.  Anyway, my liver biopsy is scheduled for next Wed. Oct. 20.  We have an appt. with a radiologist this Wed.  I am not to start the tamoxifen until after the biopsy.  Now I am not sleeping, don't know why and still having weird dreams.  How are you ladies on tamoxifen doing?  I just do not feel like any more SE.   

    After my second Pilate's class I was so sore I thought I was getting the flu!!  I think I need to go easier this week, I can not feel like that again.  I was miserable.  I am feeling at the end of my rope with something always hurting me.   And my mental confusion is worse than ever.  All I ever say is "sorry"  I forgot. 

    Oh well, at least I am moving on. 

    Hugs to all,

    Michelle

  • hmh23
    hmh23 Member Posts: 306
    edited October 2010

    Michelle;

    So happy to see your posting.  For some reason I had Oct 4th in my calendar for your liver biopsy. 

    I feel that if you have 3 onc agreeing that you can stop chemo at this point, then just remind yourself that you've done everything they have asked of you and in your case, more.  You got through the majority of it and now you have to walk out of the 'chemo' room and leave it behind.  They still have amunition for you...radiation!!!  I had #2 today of 33. 

    Take good care.

    Fondly, Heather

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