› Forums › General Melanoma Community › Hang onto Hope! Still NED at Stage IV
- This topic has 50 replies, 23 voices, and was last updated 13 years ago by Bill G.
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- September 28, 2011 at 8:33 pm
I know we all need to read some good news to balance the bad and sad news that is a reality on MPIP.
I am thrilled to report that I just returned from Moffitt and I remain NED at Stage IV. My profile is up to date and I'll give a brief summary when I sign off this post.
I know we all need to read some good news to balance the bad and sad news that is a reality on MPIP.
I am thrilled to report that I just returned from Moffitt and I remain NED at Stage IV. My profile is up to date and I'll give a brief summary when I sign off this post.
Yes, I've had ups and downs like so many of us. Yes, I have some discomfort from the extensive surgeries. I have challenges with maintaining my weight. Right now I have a rib fracture that was diagnosed on the scan. But I am NED. I wish there was a secret to share. I know many of you are deep in battle and have to be so discouraged.
It was 6 years ago yesterday that I had my liver resection…70% of my liver was removed. I was told at that time that if the surgery was not a success (or any of the very limited treatment options back then) that I had 4-6 months to live.
And I now can go 4 months until my next set of scans.
Thinking of all of you. If I can help in any way, please email me. Thank you so much for all the support you've given and knowledge you've shared over the 7 years that I now have been on MPIP.
Stay Strong
King/Kathie
March 2004 Stage III Unknown primary
April 2004 Left groin lymph node dissection…..NED
May 2004-April 2005 Interferon
July 2005 Liver mets (3.3 cm. Grew to 4.5 cm at time of surgery)
September 2005 Liver resection/Gall Bladder removal….NED
December 2005-November 2006 Phase II Clinical Trial of GM-CSF
March 2008 Peri-Pancreatic Tumor; sub q on left hip/buttock
April 2008 Extensive surgery to remove both areas of mets….NED
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- September 28, 2011 at 9:12 pm
This is great to hear, I am still so down about being diagnosed directly at Stage IV (Brain, Liver & Lung), and to hear people who keep surviving and are NED is what I hope to become!
I have wondered about surgery to remove spots from my lung & liver (basically 1 spot in each), but I do know that if the surgery didn't work on the liver, I'd be basically destroying my chances, since we can't get transplants.
I'm just so worried about the future (I'm in my 1st treatment Yervoy now), and just hoping it shrinks the few spots I currently have. Just want years and years to spend with my 2 young kids!
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- September 28, 2011 at 9:12 pm
This is great to hear, I am still so down about being diagnosed directly at Stage IV (Brain, Liver & Lung), and to hear people who keep surviving and are NED is what I hope to become!
I have wondered about surgery to remove spots from my lung & liver (basically 1 spot in each), but I do know that if the surgery didn't work on the liver, I'd be basically destroying my chances, since we can't get transplants.
I'm just so worried about the future (I'm in my 1st treatment Yervoy now), and just hoping it shrinks the few spots I currently have. Just want years and years to spend with my 2 young kids!
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- September 28, 2011 at 9:24 pm
Hi Kathie!
I was so excited to read your post! You are truly amazing! I remember when I first found this board and you were one of the names I "followed". I was, at the time, stage 1 with practically no reason to believe I would be affected by mel ever again. I stopped visiting, just lurking every now and then. Today I am back after having found a lump in my groin and several surgeries 2010. I had a PET last monday and am following up with a CT tomorrow for a spot behind my knee. Pretty sure it's nothing but better to be safe than sorry with this crazy disease. I hope to be able to reclaim my NED status by next week.
I also consulted Dr Weber when all this started last year (I am north of Orlando). He advised me to NOT do interferon and, against his judgement (I have an auto immune disease too and he said interferon would "kill" me – or was it that he said any doc that would put me on interferon should have their head examined…yeah, that was it!), I worked with my current onc to do it. Of course I had a recurrence and more surgery. I had been NED since Sept of last year. A clear CT tomorrow will confirm one year NED.
Anyway, enough of my personal history…I just wanted to say CONGRATS!!! Lots of scary stuff you've been through on this journey. You've come a long way!
Smiles,
Laurie
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- September 28, 2011 at 9:24 pm
Hi Kathie!
I was so excited to read your post! You are truly amazing! I remember when I first found this board and you were one of the names I "followed". I was, at the time, stage 1 with practically no reason to believe I would be affected by mel ever again. I stopped visiting, just lurking every now and then. Today I am back after having found a lump in my groin and several surgeries 2010. I had a PET last monday and am following up with a CT tomorrow for a spot behind my knee. Pretty sure it's nothing but better to be safe than sorry with this crazy disease. I hope to be able to reclaim my NED status by next week.
I also consulted Dr Weber when all this started last year (I am north of Orlando). He advised me to NOT do interferon and, against his judgement (I have an auto immune disease too and he said interferon would "kill" me – or was it that he said any doc that would put me on interferon should have their head examined…yeah, that was it!), I worked with my current onc to do it. Of course I had a recurrence and more surgery. I had been NED since Sept of last year. A clear CT tomorrow will confirm one year NED.
Anyway, enough of my personal history…I just wanted to say CONGRATS!!! Lots of scary stuff you've been through on this journey. You've come a long way!
Smiles,
Laurie
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- September 28, 2011 at 9:28 pm
Absolutely awesome!!! Looking forward to reading you are 4 MORE months NED in four more months!!!
Jacki
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- September 28, 2011 at 9:28 pm
Absolutely awesome!!! Looking forward to reading you are 4 MORE months NED in four more months!!!
Jacki
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- September 28, 2011 at 9:40 pm
Has it been 6 years now? Wow!!!!
Seems like it has been that long since I have seen you last , but I know it has been over two years now since we met up at Dean's funeral.
Hope you and the hubby are well, and your NED status continues forever.
Keep it up, Michael
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- September 28, 2011 at 9:40 pm
Has it been 6 years now? Wow!!!!
Seems like it has been that long since I have seen you last , but I know it has been over two years now since we met up at Dean's funeral.
Hope you and the hubby are well, and your NED status continues forever.
Keep it up, Michael
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- September 28, 2011 at 9:59 pm
Love to hear this. You help so many and give hope to even so many more!
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- September 28, 2011 at 9:59 pm
Love to hear this. You help so many and give hope to even so many more!
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- September 28, 2011 at 10:56 pm
Kathie,
This is such wonderful news! I just had my last radiation treatment this morning and I thought I was happy then. Now…I am elated. Thank you so much for all of your support and advice over the years. I wish you many, many more years being NED. You are a true inspiration to us all. Go celebrate!
Tricia
P.S. I used to live in Palm Harbor!
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- September 28, 2011 at 10:56 pm
Kathie,
This is such wonderful news! I just had my last radiation treatment this morning and I thought I was happy then. Now…I am elated. Thank you so much for all of your support and advice over the years. I wish you many, many more years being NED. You are a true inspiration to us all. Go celebrate!
Tricia
P.S. I used to live in Palm Harbor!
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- September 29, 2011 at 11:12 am
Kathie,
Great news and it gives us such inspiration. We hope to be like you. Celebrate.
Rebecca and Bob
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- September 29, 2011 at 11:12 am
Kathie,
Great news and it gives us such inspiration. We hope to be like you. Celebrate.
Rebecca and Bob
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- September 29, 2011 at 6:20 pm
That's so great to hear! It's so nice to hear some of the positive stories out there when we are always reminded about the bad news and how horrible this disease can be.
As someone who's a newbie Stage 4 (but currently NED) person it gives us hope!
Thanks for sharing.
Erin
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- September 29, 2011 at 6:20 pm
That's so great to hear! It's so nice to hear some of the positive stories out there when we are always reminded about the bad news and how horrible this disease can be.
As someone who's a newbie Stage 4 (but currently NED) person it gives us hope!
Thanks for sharing.
Erin
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- September 30, 2011 at 3:32 am
Kathie, great news , you are a inspiration and a beacon for hope to all those battling this disease.
best wishes
James
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- September 30, 2011 at 3:32 am
Kathie, great news , you are a inspiration and a beacon for hope to all those battling this disease.
best wishes
James
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