Official pathology report

SnapDragon2
SnapDragon2 Member Posts: 646 Member

Its been an emotional day.  I cried and hugged my surgeon.  Got staples out of my abdomen.  Pathology report states: clear margins, stage IIIB.  I now have 4 months of folfox to go.  Its the last sprint in this marathon to beat cancer!

Comments

  • SandiaBuddy
    SandiaBuddy Member Posts: 1,259 Member
    Staging

    I was a stage 3b as well.  Chemo likely will be a challenge.  Reading the many posts on this board will likely help you prepare, but you will likely have a month or two to heal before chemo.  Congratulations on the good news.

  • suzycruise76
    suzycruise76 Member Posts: 159 Member
    Oh,so great!!!!

    Hi SnapDragon, I so understand you...yes,it is very emotional to get great results. I,personally, cried a few times when getting good results,never cried after being diagnosed with cancer or getting all those scary informations regarding treatment.

    And yes,I too hugged my wonderful surgeon after getting final NED in October 2019,and a few months prior to it I cried and hugged my oncology doctor,when she agreed with me NOT to take an offer of another (mop-out?) chemo because my pathology reports and all other test came completely negative. 

    I see that you are going to be on folfox for 4 months...well,I wish you to get fast and easy through it,and be completely free of treatments (and disease of course) in summer.

    All the best,

    Suzy

  • Trubrit
    Trubrit Member Posts: 5,625 Member
    Good news

    It surley is a roller coaster of emotions. 

    Continue to heal and get your body ready for the onslaught of FOLFOX.  We will be with you all the way. 

    Tru

  • Annabelle41415
    Annabelle41415 Member Posts: 6,715 Member
    Wonderful

    That is awesome news.  Enjoy this news and keep healing.  Remember to walk.  You have to be really relieved at this point, and you can make it through treatment as we are all here with any struggles you might have.

    Kim

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member

    Staging

    I was a stage 3b as well.  Chemo likely will be a challenge.  Reading the many posts on this board will likely help you prepare, but you will likely have a month or two to heal before chemo.  Congratulations on the good news.

    Good morning!  Thank you for

    Good morning!  Thank you for sharing your stage.  I will have to follow you to be more knowlegeable.  My surgeon says I should start chemo within a month to 6 wks of surgery, so ya I was thinking it is going to be rough just from that aspect.  I am going to compliment the folfox with IV vit C to hopefully help with the challenging affects of the chemo.

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member

    Oh,so great!!!!

    Hi SnapDragon, I so understand you...yes,it is very emotional to get great results. I,personally, cried a few times when getting good results,never cried after being diagnosed with cancer or getting all those scary informations regarding treatment.

    And yes,I too hugged my wonderful surgeon after getting final NED in October 2019,and a few months prior to it I cried and hugged my oncology doctor,when she agreed with me NOT to take an offer of another (mop-out?) chemo because my pathology reports and all other test came completely negative. 

    I see that you are going to be on folfox for 4 months...well,I wish you to get fast and easy through it,and be completely free of treatments (and disease of course) in summer.

    All the best,

    Suzy

    Good morning, Suzy!  Thank

    Good morning, Suzy!  Thank you for your note.  I am so happy you are NED!!!!  Its a nice comfort to know I can share things and you all know exactly what I mean.

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member
    Trubrit said:

    Good news

    It surley is a roller coaster of emotions. 

    Continue to heal and get your body ready for the onslaught of FOLFOX.  We will be with you all the way. 

    Tru

    Good morning, Tru!  Thank you

    Good morning, Tru!  Thank you so much for the encouragement.  I am getting myself ready for the onslaught!

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member
    Good morning, Kim!  Thank you

    Good morning, Kim!  Thank you so much.  I (we) are def enjoying the relief of "knowing."  I have been walking every day at least twice.  The weather is not the greatest for it but who cares about a little mud and cold temps :)  I am just happy I can do it.  

  • SandiaBuddy
    SandiaBuddy Member Posts: 1,259 Member
    Xelox/Capox

    You also might want to look at the option of Xelox/Capox (pill plus infusion) as an alternative to the port/pump, if you do not already have the port.

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member

    Xelox/Capox

    You also might want to look at the option of Xelox/Capox (pill plus infusion) as an alternative to the port/pump, if you do not already have the port.

    I was windering about that. 

    I was wondering about that.  I have a port.  I did 5fu and rad before surgery.  I had no idea a pill was an option, was never told about it.  I hated the pump with a passion.

  • AnneO1965
    AnneO1965 Member Posts: 182
    YAY!!!

    So happy to hear that your margins are clear!! Did you end up with the colostomy, or are they going to be able to reverse it for you?  I was also Stage 3B and I did the 4 months of Folfox, I just did mine before the surgery.

    Hopefully the first couple of rounds will be a breeze for you. Just remember that ANY time you start feeling something different, to mention it to your oncologist. Maybe they can adjust your dosage so your side effects aren't that bad.

    I was stubborn about doing the full dosage the whole 8 rounds.. 6 rounds in my doc cut my dosage because of the neuropathy. Said I should of told her sooner because she didn't want to cripple me.

  • SnapDragon2
    SnapDragon2 Member Posts: 646 Member
    AnneO1965 said:

    YAY!!!

    So happy to hear that your margins are clear!! Did you end up with the colostomy, or are they going to be able to reverse it for you?  I was also Stage 3B and I did the 4 months of Folfox, I just did mine before the surgery.

    Hopefully the first couple of rounds will be a breeze for you. Just remember that ANY time you start feeling something different, to mention it to your oncologist. Maybe they can adjust your dosage so your side effects aren't that bad.

    I was stubborn about doing the full dosage the whole 8 rounds.. 6 rounds in my doc cut my dosage because of the neuropathy. Said I should of told her sooner because she didn't want to cripple me.

    HI Anne!  Thank you for

    HI Anne!  Thank you for sharing your stage with me too.  You really helped me prepare for surgery and I am so grateful to you for it.  I do have a perm bag.  I need any and all tips to get thru this folox.  The only thing I have learned for sure thru all of members here is the vit c really helps most.  My surgeon asked to be part of the 4 mths and said its all pretty standard but wants to be included to make sure I am getting everything I need on time and thoroughly.  Mainly I think because my oncologist isn't part of the hosp team I had surgery at.  

  • SandiaBuddy
    SandiaBuddy Member Posts: 1,259 Member

    I was windering about that. 

    I was wondering about that.  I have a port.  I did 5fu and rad before surgery.  I had no idea a pill was an option, was never told about it.  I hated the pump with a passion.

    Pill

    Several board members had to work to overcome the automatic use of a port.  I hate needles and I am fairly insistent, so my doctors gave in pretty easily.  There are old discussions of the profit motive for the port, but I think the reimbursement pattern has changed more recently, so that may no longer be relevant.

  • AnneO1965
    AnneO1965 Member Posts: 182

    HI Anne!  Thank you for

    HI Anne!  Thank you for sharing your stage with me too.  You really helped me prepare for surgery and I am so grateful to you for it.  I do have a perm bag.  I need any and all tips to get thru this folox.  The only thing I have learned for sure thru all of members here is the vit c really helps most.  My surgeon asked to be part of the 4 mths and said its all pretty standard but wants to be included to make sure I am getting everything I need on time and thoroughly.  Mainly I think because my oncologist isn't part of the hosp team I had surgery at.  

    Lots of protein... If you can

    Lots of protein... If you can't manage to eat it, get the drinks like Boost or Ensure. Ask your oncologist to speak to a nutritionist, they can tell you the best things to eat. That being said, you probably aren't going to want to eat, force yourself. You have to keep your blood levels up or they won't give you your treatment.

    REST REST REST  let the house go... Let the laundry go. You will need to sleep. There is a service that offers housecleaning to patients undergoing chemo, I'll see if I can find a link for it.

    https://cleaningforareason.org/