Three Years, and Counting

Kent Cass
Kent Cass Member Posts: 1,898 Member
Got my PS/CT results today- all clean.

My ENT, whose name is Tomek and a Wake Forest alumn, and whom I am really, really, glad he is my ENT, was showing an Intern around. He had to summarize my case, and told this Intern that because of my unknown Primary they had to "double dose" my treatment, which is the first I'd heard about the severity of my regiment- nevermind that they unloaded all their ammo right from days #1-#5 of treatment. Wouldn't have had it any other way, now, though at the time I'm not so sure...Yeah, I am. All in, aka Come What May. Three years, Folks. Worked another 10-hour shift tonight, and smiled a lot. Oh yeah!

Believe

kcass
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Comments

  • osmotar
    osmotar Member Posts: 1,006
    CAN YOU Say Wonderful
    Way to go...reading your post made my morning. Congrats!!!!

    Linda
  • CajunEagle
    CajunEagle Member Posts: 408
    Way to go, Kent.
    My 3 year treatment completion date is in June. Suppose I'll have a PET scheduled towards the end of May, and hopefully all is well. Amazing how we've all come such a long way........so CONGRATULATIONS, fella.

    Larry
  • Greg53
    Greg53 Member Posts: 849

    Way to go, Kent.
    My 3 year treatment completion date is in June. Suppose I'll have a PET scheduled towards the end of May, and hopefully all is well. Amazing how we've all come such a long way........so CONGRATULATIONS, fella.

    Larry

    Awesome Baby!!!!!!!!!!!!!
    Kent,

    You da Man! Great news Brother! Cause of this piece of news, I'll be smiling a lot today as well. Take the day off, play 18 holes, watch the Cubs/Cards game - Enjoy!!!

    Greg
  • Tonsil Dad
    Tonsil Dad Member Posts: 488
    Greg53 said:

    Awesome Baby!!!!!!!!!!!!!
    Kent,

    You da Man! Great news Brother! Cause of this piece of news, I'll be smiling a lot today as well. Take the day off, play 18 holes, watch the Cubs/Cards game - Enjoy!!!

    Greg

    Whoop, Whoop!!!!
    Way to go kent,
    Congrats on your three years,
    May you have many, many, many more ahead.
    News like this makes my day.

    KEEP CALM and CARRY ON.
    God Bless

    Tonsil Dad
    Dan.
  • phrannie51
    phrannie51 Member Posts: 4,716
    WHOOOO HOOOOOO!!!
    Wonderful news, Kent!! Now I want to dance YOU around the kitchen :)...

    Believe...Believe...BELIEVE!!!!
  • fisrpotpe
    fisrpotpe Member Posts: 1,349 Member
    Wow!
    Wow! great news. congrats

    had to post with a different w since many before took all the other w words

    have fun and take time to celebrate.

    john
  • tommyodavey
    tommyodavey Member Posts: 727 Member
    fisrpotpe said:

    Wow!
    Wow! great news. congrats

    had to post with a different w since many before took all the other w words

    have fun and take time to celebrate.

    john

    Congrats
    So uplifting to read those words. 3 years is quite a milestone.

    Many more to come!

    Tommy
  • ditto1
    ditto1 Member Posts: 660
    Dear MR CLEAN
    Congrat Ken, You were one of the 1st I read on my post "Ready for the Fight? You were there to tell me yes it was worth the fight, and reading your post today just gives me that much more insentive to do just that. God Bless You.
  • Skiffin16
    Skiffin16 Member Posts: 8,305 Member
    Sweet.....
    WTG brother.....

    John
  • Hondo
    Hondo Member Posts: 6,636 Member
    Hi Kent

    I am just soooo very happy for you my brother, I pray that you will be NED for at least another 100 years or until we see our Lord coming for us who Believe.

    God Bless
    Hondo
  • KRBigFish
    KRBigFish Member Posts: 25
    Hondo said:

    Hi Kent

    I am just soooo very happy for you my brother, I pray that you will be NED for at least another 100 years or until we see our Lord coming for us who Believe.

    God Bless
    Hondo

    This makes me so optimistic!
    Congratulations! I guess I should put in a picture of me and my Big Fish so you know who I am. I am a cancer survivor, but every news of another one beating the C backs helps in my anxiety waiting on my 5th biopsy result. Woot Woot for you!!!
  • D Lewis
    D Lewis Member Posts: 1,581 Member
    Happy Dance!
    Doing the happy dance in my kitchen! Great news! Happy Third Anniversary and may you have many many more!

    Still believing!

    Deb
  • Hal61
    Hal61 Member Posts: 655
    When you're smilin'
    The whole board smiles with you. Great to hear Kent.


    best, Hal
  • patricke
    patricke Member Posts: 570
    Great news Kent, and I'm
    Great news Kent, and I'm doing the Happy Dance" for you too! Work hard, and play harder, and keep those great reports coming!

    PATRICK
  • LeoS2323
    LeoS2323 Member Posts: 160
    Congrats / unknown primary
    Hi Kent

    Firstly c
  • LeoS2323
    LeoS2323 Member Posts: 160
    Congrats / unknown primary
    Hi Kent

    Firstly congratulations on the fantastic news, love reading your posts - keep those shifts coming!!

    I was interested in what you said about your unknown primary treatment that they attacked it straight away. What grade was it? There seem to be different approaches to this - I am in the early stages after diagnosis with the first step for me being a neck dissection. But I also have an unknown primary, which wasn't apparent on a PET scan. They are going to take a tonsil out and try to find the primary when I have my dissection, but if they don't then I guess I might have a decision to make - wait and see if it shows or have a go at it with chemo.

    I am inclined to attack it whilst it is small and before it has a chance to develop! I know obviously the treatment is incredibly tough but I will get through that and I just want to do whatever gives me the best chance of long term cure, no matter how difficult it is in the short to medium term. I am Interested in the approaches of others who were in an 'unknown' situation - especially those like you who have won the fight and continue to be free of it.

    All the best

    Leo
  • Kent Cass
    Kent Cass Member Posts: 1,898 Member
    LeoS2323 said:

    Congrats / unknown primary
    Hi Kent

    Firstly congratulations on the fantastic news, love reading your posts - keep those shifts coming!!

    I was interested in what you said about your unknown primary treatment that they attacked it straight away. What grade was it? There seem to be different approaches to this - I am in the early stages after diagnosis with the first step for me being a neck dissection. But I also have an unknown primary, which wasn't apparent on a PET scan. They are going to take a tonsil out and try to find the primary when I have my dissection, but if they don't then I guess I might have a decision to make - wait and see if it shows or have a go at it with chemo.

    I am inclined to attack it whilst it is small and before it has a chance to develop! I know obviously the treatment is incredibly tough but I will get through that and I just want to do whatever gives me the best chance of long term cure, no matter how difficult it is in the short to medium term. I am Interested in the approaches of others who were in an 'unknown' situation - especially those like you who have won the fight and continue to be free of it.

    All the best

    Leo

    Leo
    Stage-3, NPC. Had been living with night sweats and weight loss for some 7 months before the two enlarged lymphs showed on the left side of my neck.

    And yes, there are different attack plans. Being NPC, which is notorious for showing up in distant sites, like the lungs, etc., I went thru two Biopsy Ops and scoping all that could be scoped, and the PS/CT didn't help, either. Only place they got a Positive was the one lymph they sampled. Tomek decided the try and eliminate it in any other place it could be, which essentially kept it from growing into an identifiable Primary. I had a major windpipe medical history going into this, so maybe that was part of his reasoning for "heading it off at the pass."

    Different H&N Cs likely have different characteristics/risks, Leo, and a few different attack plans. Waiting would allow them to better find definite targets for the rads, but also brings with it risks, in my opinion. Our C is spread via the lymph system, which runs far and wide thru the body. I got a real problem with the notion of letting the C spread, especially with NPC, so I'm very glad I was treated as I was. Seems to me we've all heard that the earlier one catches the C the better, you know, and the less it has spread the better.

    We talk a lot about the severity of treatment, here, and perhaps rightly so. It has been said that only Renal C has a harsher treatment, in general. Thing is, the severity of H&N varies from one Patient to another, also. But even in the extreme cases that don't involve Surgery, it is not bad at all on a comparable basis. I'm not aware of any side-effects that are not manageable, Leo, with meds, and maybe therapy. I was amazed at how well my body tissue healed, though it did take a little time. And when one considers the alternative...

    I would advise you to speak at length with your Drs about the risks with waiting, and specifics of your type of C. As with all of us, the fact that C has developed means the defense system our body has came up short in preventing C to form. And, without treatment there's nothing that's really gonna stop the C cells from replicating, as they do, and that leads to you-know-where. The worst case involves Surgery with removal, Leo, which is to say C&R is a better option than an Op which physically alters one.

    kcass
  • Mikemetz
    Mikemetz Member Posts: 465 Member
    3 years, too!
    I got my 3-year NED scan just two weeks ago, so we're on pretty much the same schedule. Congratulations! Not related to my recent scan, I also had one of those "Well, no one told me that before" moments a little while ago. My wife is really good at remembering things the docs have told me along the way, but even she didn't know this very important particular fact about my dx, which now explains my ORN side effect from the rads.

    So, even when the doctors explain things verbally and when you've asked all the questions you can think to ask, sometimes you still don't get the whole story. Looking back, I should have asked for all written records about my dx after each and every diagnostic event and consultation.

    Mike
  • Crazymom
    Crazymom Member Posts: 339 Member
    Great News
    Thanks for the post. It made my day! I feel like I can get through this now. I just finished my radiation 2 weeks ago and it has been a bit tough...but it will be worth it!
  • hawk711
    hawk711 Member Posts: 566
    Crazymom said:

    Great News
    Thanks for the post. It made my day! I feel like I can get through this now. I just finished my radiation 2 weeks ago and it has been a bit tough...but it will be worth it!

    Congrats Kent
    Kent
    So glad you are traveling with NED !!! I am at 2 yrs and go in soon for the PET. Just wanted to thank you for sharing your good news, made my day.
    all the best,
    Steve