Almost done but have a few guestions :O)

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Kathy9433
Kathy9433 Member Posts: 61

Hi Ladies!  Just need a little education from all you experts here before my next visit to Dr.  I have finished 4 AC treatments and 3 of the 4 Taxotere (only one more to go YAY!!) My next appt is March 19 and this will be to finish the chemo and to set up appt. with Radiation Onc.  I met with the RO before I started chemo.....What are good questions to ask at this point? 

The nurse said something about "markers" being on the lab slip for my next bloodwork before last chemo; I should have asked her at the time, but I usually just can't wait to get out of there when I'm finished!  Any info on this marker business??

And my last question, for now :O) is when chemo and radiation are finished...what then???  I know there's not much for TN but how have you been followed up after treatments?  Thanks for any and all info...this site is great and I have learned SO MUCH!  All the ladies are wonderful and have given me MUCH in the way of support with humor and understanding and dignity.

OXOXOXOXO  Kathy :O)

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  • thenewme
    thenewme Member Posts: 1,611
    edited February 2012

    Hi Kathy,

    Congrats on being almost done with chemo - there's definitely light at the end of the tunnel!  Did you have surgery before chemo, or will you be doing it afterward?  

    I'd ask the radiologist about specific and risks and benefits for your individual case.  If you've had or will be having surgery/reconstruction, ask about the implications of radiation.  Ask ahead of time if you do decide on radiation, how to best protect your skin and do it faithfully before skin problems happen. Ask if there are any options as far as type/scheduling/duration of radiation for you.

    I have bloodwork about every 6 months to monitor tumor markers, vitamin D level, and CBCs.  The tumor markers are a bit controversial and not necessarily all that accurate, but in some cases they can show a concerning trend or a sudden jump that could indicate a developing problem.  My onc is fairly flexible about my followup.  In general, scheduled scans aren't really recommended if there are no symptoms, but my onc was pretty cautious in the first 2 years, so I had a few PET scans. Also, I had some other problems (hip pain, difficulty swallowing, etc.) that she followed up very thoroughly with a variety of scans and tests.  She was/is very flexible, though, and tailors my followup, at least in part, to how comfortable I am and how much reassurance I want.  

    You're right, there's not much available for TN after surgery/chemo/rads.  For me personally, I've tried to make healthy lifestyle changes and to be as healthy generally as I can.  There is real research  that shows exercise and nutrition to be valuable, so I'm more "health minded" than I was before, although I was pretty darned healthy before.  Have you had your vitamin D levels checked?  If not, I'd ask about it.  Again, it's not a panacea, but there's at least a tenuous correlation between Vitamid D deficiency and breast cancer.  

    I take some dietary supplements, try to eat healthy, try to get exercise and sunshine, minimize stress, sleep well, and try to live my life well.  Of course, these are all general things everybody should do anyway.  

    Anyway, best of luck!  Go easy on yourself - you've been through a huge battle, and it does take time to recuperate. 

    Sorry, I'm rambling again!  

    Best of luck!

  • Kathy9433
    Kathy9433 Member Posts: 61
    edited February 2012

    Thank for the response NEWME!

    I had surgery before chemo; lumpectomy-after receiving a negative BRCA test the surgeon said lump with chemo and rads would be as effective as mastectomy.  No argument from me!  I will add the vitamin D question to my list and ask about supplements.  I already eat fairly healthy (except for the first week after chemo-MUST HAVE POTATOES!!) For some strange reason they taste heavenly!  I'm still unclear about 'markers' so will be asking about that, too.  I know I'm a bit ahead of myself but I function better if I kind of know what to expect and like to be pro-active.  But if I don't have a list of questions prepared and in my hand, well, forget it......it's out the window!  Thanks again for the info--really appreciate anything and everything!

    OXOXO  Kathy

  • thenewme
    thenewme Member Posts: 1,611
    edited February 2012

    Hi Kathy,

    You're very welcome.  Hahaha, I know what you mean about potatoes.  For me it was popcorn!  It reminds me of weird cravings during pregnancy.  I'm a firm believer that during chemo, you do what you need to do to get by!  It's definitely not the time to be a martyr about what you eat.  I agree...I'm an info junkie myself and like to know what to expect.  

    So you've already done surgery - one more hurdle completed and one step closer to closing this chapter that wasn't so much fun!

    Best of luck!

  • Titan
    Titan Member Posts: 2,956
    edited March 2012

    Kathy..believe me.."they" won't let you go... you will probably see your onc every 3 months and your BS every 3 months for a very long time...doctors vary on blood tests, scans etc...you will be followed very closely...and you should be..

    I just enjoy my every 3 months, watch for symptoms and try not to freak out too much...

    congrats on almost done with chemo...that is awesome...

  • Kathy9433
    Kathy9433 Member Posts: 61
    edited March 2012

    Titan--thanks for the response.  I guess that's all we can do after going after this with both guns blazing.  And its nice to know that there's an end in sight!  Sending OXOXOXO...

    Kathy :O)

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