› Forums › General Melanoma Community › NED 2 Years
- This topic has 21 replies, 6 voices, and was last updated 11 years, 4 months ago by Linny.
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- December 26, 2012 at 5:56 am
Hello all, I am happy to announce my 2 year aniversery from being diagnosed stage 3 melanoma. I do not post much here but do check in once in awhile for information and updates on treatments and so forth. This site has helped me cope with this cancer for the last 2 years when I read some of the stories of others on this forum. From the first time I found out I had melanoma and my surgeon told me the survival rates and all I thought i was doomed. I have made 2 more Christmases and also am finally being able to not worry about mel all the time. My family Dr.
Hello all, I am happy to announce my 2 year aniversery from being diagnosed stage 3 melanoma. I do not post much here but do check in once in awhile for information and updates on treatments and so forth. This site has helped me cope with this cancer for the last 2 years when I read some of the stories of others on this forum. From the first time I found out I had melanoma and my surgeon told me the survival rates and all I thought i was doomed. I have made 2 more Christmases and also am finally being able to not worry about mel all the time. My family Dr. just recently told me my chances of reoccurrence is very slim since i made it 2 years now, however the oncologist disagrees with that. Anyhow i am happy to be NED this long and hope it lasts for many more years. Thanks to everyone that posts here for peole to get so much info about melanoma, as i seem to find more answers here than I can at a Drs office. Happy new Years everyone and I hope every person on this site will be here next year to read my third aniversery post.
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- December 26, 2012 at 6:06 am
Congratulations!! Many Many Many more years to come!! What an awesome Christmas present!!
Denise
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- December 26, 2012 at 4:42 pm
Whooo hoooo….Congratulations on this awesome mile marker Denise ! CELEBRATE GIRL !!!
(Listen to your oncologist – Wayne was clean 13 1/2 years before a recurrance – you cannot ever give up vigilance on this monster cancer).
HAPPY HAPPY NEW YEAR and MANY MORE TO COME !
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- December 26, 2012 at 4:42 pm
Whooo hoooo….Congratulations on this awesome mile marker Denise ! CELEBRATE GIRL !!!
(Listen to your oncologist – Wayne was clean 13 1/2 years before a recurrance – you cannot ever give up vigilance on this monster cancer).
HAPPY HAPPY NEW YEAR and MANY MORE TO COME !
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- December 26, 2012 at 4:42 pm
Whooo hoooo….Congratulations on this awesome mile marker Denise ! CELEBRATE GIRL !!!
(Listen to your oncologist – Wayne was clean 13 1/2 years before a recurrance – you cannot ever give up vigilance on this monster cancer).
HAPPY HAPPY NEW YEAR and MANY MORE TO COME !
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- December 27, 2012 at 3:13 pm
Thank you for the update. I was diagnosed stage IIIa in July, and of course my initial reaction was that the world was coming to an end and I had a will drawn up, etc., etc.
Then I found this message board and the wide spectrum of experiences people have had with this disease. I understand now that it is very random and one cannot predict much at all. That uncertainty is one of the difficult aspects for me.
So reading others' success stories give me hope.
Take care – Paul.
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- December 27, 2012 at 3:13 pm
Thank you for the update. I was diagnosed stage IIIa in July, and of course my initial reaction was that the world was coming to an end and I had a will drawn up, etc., etc.
Then I found this message board and the wide spectrum of experiences people have had with this disease. I understand now that it is very random and one cannot predict much at all. That uncertainty is one of the difficult aspects for me.
So reading others' success stories give me hope.
Take care – Paul.
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- December 27, 2012 at 3:13 pm
Thank you for the update. I was diagnosed stage IIIa in July, and of course my initial reaction was that the world was coming to an end and I had a will drawn up, etc., etc.
Then I found this message board and the wide spectrum of experiences people have had with this disease. I understand now that it is very random and one cannot predict much at all. That uncertainty is one of the difficult aspects for me.
So reading others' success stories give me hope.
Take care – Paul.
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- December 27, 2012 at 5:23 pm
Congratulations! We are on about the same timeline.
I was officially diagnosed in December 2010 and had THE worst Christmas, birthday, and New Year's imaginable. The dermatologist I saw had nothing but bad news: having an unknown primary doesn't give you a better prognosis (this, in spite of medical studies I'd read on the topic), the clean scans I'd had two weeks prior to my visit with him didn't mean anything, and the only approved treatment is interferon which is really rough. And, there were no clinical trials for me at Hopkins. Then after all that, he asked me if I wanted to know my prognosis. Are you freakin' kidding me?!? I told him, "HELL NO!!!!!" After I saw this guy I saw the surgeron who was going to be doing my LND and by that time I was emotionally shot, thanks to the grim reaper I'd just seen. She tried her best to lift my spirits by reminding me that my scans were clean and to focus on that. She also told me that there were some trials at Hopkins for which I might qualify but a lot would depend on what she uncovered after the surgery. But the emotional damage was done.
I survived that ordeal and am happy to still be NED and to be able to celebrate another Christmas, birthday, and New Year.
Fortunately I don't have to see that dermatologist on a regular basis. Though, he did have to biopsy a freckle on the sole of my foot about a year ago. He remembered me and asked me how I was doing. I told him, "I'm still here, NED, and in a clinical trial." Boy, did that feel good! LOL
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- December 27, 2012 at 5:23 pm
Congratulations! We are on about the same timeline.
I was officially diagnosed in December 2010 and had THE worst Christmas, birthday, and New Year's imaginable. The dermatologist I saw had nothing but bad news: having an unknown primary doesn't give you a better prognosis (this, in spite of medical studies I'd read on the topic), the clean scans I'd had two weeks prior to my visit with him didn't mean anything, and the only approved treatment is interferon which is really rough. And, there were no clinical trials for me at Hopkins. Then after all that, he asked me if I wanted to know my prognosis. Are you freakin' kidding me?!? I told him, "HELL NO!!!!!" After I saw this guy I saw the surgeron who was going to be doing my LND and by that time I was emotionally shot, thanks to the grim reaper I'd just seen. She tried her best to lift my spirits by reminding me that my scans were clean and to focus on that. She also told me that there were some trials at Hopkins for which I might qualify but a lot would depend on what she uncovered after the surgery. But the emotional damage was done.
I survived that ordeal and am happy to still be NED and to be able to celebrate another Christmas, birthday, and New Year.
Fortunately I don't have to see that dermatologist on a regular basis. Though, he did have to biopsy a freckle on the sole of my foot about a year ago. He remembered me and asked me how I was doing. I told him, "I'm still here, NED, and in a clinical trial." Boy, did that feel good! LOL
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- December 27, 2012 at 5:23 pm
Congratulations! We are on about the same timeline.
I was officially diagnosed in December 2010 and had THE worst Christmas, birthday, and New Year's imaginable. The dermatologist I saw had nothing but bad news: having an unknown primary doesn't give you a better prognosis (this, in spite of medical studies I'd read on the topic), the clean scans I'd had two weeks prior to my visit with him didn't mean anything, and the only approved treatment is interferon which is really rough. And, there were no clinical trials for me at Hopkins. Then after all that, he asked me if I wanted to know my prognosis. Are you freakin' kidding me?!? I told him, "HELL NO!!!!!" After I saw this guy I saw the surgeron who was going to be doing my LND and by that time I was emotionally shot, thanks to the grim reaper I'd just seen. She tried her best to lift my spirits by reminding me that my scans were clean and to focus on that. She also told me that there were some trials at Hopkins for which I might qualify but a lot would depend on what she uncovered after the surgery. But the emotional damage was done.
I survived that ordeal and am happy to still be NED and to be able to celebrate another Christmas, birthday, and New Year.
Fortunately I don't have to see that dermatologist on a regular basis. Though, he did have to biopsy a freckle on the sole of my foot about a year ago. He remembered me and asked me how I was doing. I told him, "I'm still here, NED, and in a clinical trial." Boy, did that feel good! LOL
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