That's awesome news, congrats to you and Pete! And continued wishes for good luck.

-Chip

NJF, glad to hear you didn't just take your first oncologist's opinion as gospel, and decided to better educate yourself on options. Honestly, even if a patient turns out not to be a candidate for HAI...Sloan Kettering is either the #1 or #2 cancer center in the U.S., so you can't go wrong by gettin...

Plain and simple, HAI at Sloan Kettering saved my life. It's not always a possibility with lung mets, but sometimes it is. More than half my liver was cancerous 8 years ago, yet I now have no evidence of it in my body. And frankly, it has always bothered me - and continues to bother me - that so few...

Hi there. I'm also an HAI patient, it worked miracles for me (still here, and technically NED 8 years after stage IV dx with massive tumor load). Intense chemo did a job on my liver and bile ducts, but I can't complain. Technically I think I had a recurrence after I stopped HAI...but frankly they ne...

You may want to consider looking into HAI / hepatic pump, especially if your met(s) is/are liver-limited. It can really have dramatic results, and it's the main reason I'm still here today. Most oncs that don't know much about HAI will discourage looking into it, voicing doubts on effectiveness. How...

You may want to consider looking into HAI / hepatic pump, especially if your met(s) is/are liver-limited. It can really have dramatic results, and it's the main reason I'm still here today. Most oncs that don't know much about HAI will discourage looking into it, voicing doubts on effectiveness. How...

You are right not to give up...certainly not after just one opinion. Upon dx I had metastasis to my liver...also too many spots to count - as well as my hepatic portal lymph nodes. Thanks to the miracle workers at Sloan Kettering in NYC (and HAI hepatic pump treatment), I am still here - with no evi...

Hi, just responding to a comment from Mariane...I have no idea if Dr. Kemeny is or isn't taking new patients right now; I was assigned to the very capable care of Dr. R seven(!) years ago, and I never even asked about Dr. K. Just wanted to make clear that the docs at MSK all work well together as a ...

I traveled from Central Mass once a month for 2.5 years during HAI treatment (and for occasional follow-up care afterward). My advice in a nutshell - just do it! I was able to get my pump drained and refilled with saline every other week at my local hospital, and they also gave me my bi-weekly syste...

Sorry you had to join the club. I got my stage IV (with over half my liver cancerous) "terminal" diagnosis seven years ago. Not long thereafter, I found this and other CRC discussion boards, heard about HAI (hepatic arterial infusion), and got a third opinion from Memorial Sloan Kettering ...

Congrats Mike, glad things look promising for you with MSK/Kemeny/HAI. Just a few quick responses: 1 - once you start HAI chemo (maybe about a month after install), you'll get FUDR (essentially 5-FU) in the pump for a 2-week slow-drip. Likely you will do systemic (in your case, maybe FOLFIRI, with o...

Hi Maddie, always good to see you active on the board and (presumably) doing well! I certainly agree with your concern regarding proposed reduction in NIH and cancer research funding. I'll try to leave politics out of this, but I must say this negates much of the optimism I felt when VP Biden briefl...

Hi there. Forgive me for the unsolicited advice, but since no one has mentioned it on this thread- Have you considered HAI (hepatic pump) treatment? I'm not sure what your physical situation is, but for people with mets limited to the liver, it can be an excellent option for many. I won't swamp you ...

I went to MSK for the pump install (and colon primary resection), didn't have Dr K as my onc, but a colleague of hers who was fantastic (as were the colon and liver surgeons I had.) I was lucky to live less than 4 hours away, but knowing what I now know, I would have gladly taken a plane if I needed...

Yes, it's the Oxaliplatin in FOLFOX that could cause permanent neuropathy, though it's rare to get permanent debilitative neuropathy. In my case, I had 12 txs of FOLFOX, the last 3 were slightly reduced. Frankly, knowing what I know now, I may only have done about 8 or so txs of OX, and 2 reduced. A...