Three Years, and Counting
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
Comments
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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.
Larry0 -
Awesome Baby!!!!!!!!!!!!!CajunEagle said: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
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!!!
Greg0 -
Whoop, Whoop!!!!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
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.0 -
WHOOOO HOOOOOO!!!
Wonderful news, Kent!! Now I want to dance YOU around the kitchen ...
Believe...Believe...BELIEVE!!!!0 -
Congratsfisrpotpe 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
So uplifting to read those words. 3 years is quite a milestone.
Many more to come!
Tommy0 -
This makes me so optimistic!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
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!!!0 -
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
Leo0 -
LeoLeoS2323 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
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.
kcass0 -
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.
Mike0 -
Congrats KentCrazymom 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!
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,
Steve0
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