Questions regarding Sloan or Vanderbilt
1. Has anyone gone to Sloan? What was your experience like? Did you use a hepatic pump? I understand that Sloan is one of the few hospitals that will use this. Do you happen to have the name of an oncologist and liver surgeon there?
2. Has anyone visited Vanderbilt? Do you happen to have any contact info for an oncologist and liver surgeon there? Do they utilize the hepatic pump as well?
Thanks guys,
Jon
Comments
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Jon and Vanderbilt......
I went to Vandy for my colorectal surgery and there was a team of Drs who took great care of me. It is a teaching hospital along with being a clinical trial hospital. It is considered the 14th best hospital in the nation MD Anderson being #1. I will pm you the # and you may asked to be transferred to the correct surgeon or oncologist. You will probably speak with the Nurse Practioner of the colorectal unit but she will transfer you to who you need to speak with. It is by far an outstanding hospital with everyone from the top biomedical engineers to the janitors wear a constant smile on their face and are very congenial...along with being great in their work.....Good Luck to you in your journey, Clift0 -
Memorial-Sloan Kettering
Jon,
I was diagnosed in November 2008 during the scheduled c-section of our third child. I had 5 bilobar liver mets. In February of this year I had my liver resection and had an HAI pump installed. Since then I have been doing adjuvant therapy (chemo in both the HAI pump as well as systemic). I will complete my last treatment early November (God willing).
The HAI treatment consists of having FUDR put into the pump every 5 weeks. Refer to this thread (http://csn.cancer.org/node/174161) for more information regarding my experience with the HAI pump. Additionally, there are others on the board (Phillieg and ADker) who have also had the pump therapy.
I do go to Memorial-Sloan Kettering and I do love the facility. The doctors and nurses are at the top of their game and everyone on staff knows your name and even though it's a larger facility it feels very personal. I highly recommend Sloan Kettering. I meet people in the waiting room (one floor is dedicated to colon cancer and melanoma) that travel from all over the country (even world) to go there for treatment. My oncologist is http://www.mskcc.org/prg/prg/bios/123.cfm. She is considered the "queen" of the HAI therapy. My liver surgeon was http://www.mskcc.org/prg/prg/bios/708.cfm. He was a phenomenal surgery and one day years from now I hope to tell him as well as my oncologist "thank you" for saving my life.
I have read studies that indicate that the HAI pump is very successful in both getting patients to operable status as well as preventing additional liver mets. My surgeon told me that liver recurrence was 50% likely but with the HAI therapy it was only 30% likely. I will take that. As of right now I have been NED for almost 7 months. My next scan is in November which will be 9 months from my surgery.
I know not many places do the pump implantation as it truly requires a skilled liver surgeon to do the placement. You want someone doing it who has done hundreds before. I believe that MSK does on the order of 200-300 per year. If you have any other questions about MSK or the pump, PM me or post here. Philieg and ADker are also patients at MSK. I am sure they will post later.
All the best,
Amy0 -
Sloan-Ketteringmom_2_3 said:Memorial-Sloan Kettering
Jon,
I was diagnosed in November 2008 during the scheduled c-section of our third child. I had 5 bilobar liver mets. In February of this year I had my liver resection and had an HAI pump installed. Since then I have been doing adjuvant therapy (chemo in both the HAI pump as well as systemic). I will complete my last treatment early November (God willing).
The HAI treatment consists of having FUDR put into the pump every 5 weeks. Refer to this thread (http://csn.cancer.org/node/174161) for more information regarding my experience with the HAI pump. Additionally, there are others on the board (Phillieg and ADker) who have also had the pump therapy.
I do go to Memorial-Sloan Kettering and I do love the facility. The doctors and nurses are at the top of their game and everyone on staff knows your name and even though it's a larger facility it feels very personal. I highly recommend Sloan Kettering. I meet people in the waiting room (one floor is dedicated to colon cancer and melanoma) that travel from all over the country (even world) to go there for treatment. My oncologist is http://www.mskcc.org/prg/prg/bios/123.cfm. She is considered the "queen" of the HAI therapy. My liver surgeon was http://www.mskcc.org/prg/prg/bios/708.cfm. He was a phenomenal surgery and one day years from now I hope to tell him as well as my oncologist "thank you" for saving my life.
I have read studies that indicate that the HAI pump is very successful in both getting patients to operable status as well as preventing additional liver mets. My surgeon told me that liver recurrence was 50% likely but with the HAI therapy it was only 30% likely. I will take that. As of right now I have been NED for almost 7 months. My next scan is in November which will be 9 months from my surgery.
I know not many places do the pump implantation as it truly requires a skilled liver surgeon to do the placement. You want someone doing it who has done hundreds before. I believe that MSK does on the order of 200-300 per year. If you have any other questions about MSK or the pump, PM me or post here. Philieg and ADker are also patients at MSK. I am sure they will post later.
All the best,
Amy
As Amy indicated, I am also treated at Sloan-Kettering. I travel far (5 hours) and only go to Sloan every 4 weeks, plus for CT scans, etc. I had liver mets far more extensive than yours at diagnosis. An HAI pump was implanted at the same time as my colon resection. Together with aggressive systemic chemo, my liver became resectable within 6 months.
The HAI pump is of course more effective before your tumors become resistant to chemo. It also may not be offered to you if the cancer metastasizes further. With your history of repeated recurrence in the liver, I really believe that it would be a great idea for you to do a full consult at Sloan, particularly since systemic chemo does not seem to have gotten the job done for you.
I do not have the same warm fuzzies as Amy about my experience at Sloan, probably because I am not there as often and I was not referred by a friend of the oncologist. Communication is difficult. I spend a fair amount of time obtaining copies of the oncologist's office notes so that I will know what she is thinking and what her plan is. I need the help of my brother who is a doctor to get copies of radiologists' reports of my scans before my appointment so that I can understand the 2-3 sentences that usually constitute my conversations with my oncologist. While there are no negative statements, the closest thing to an encouraging statement that anyone at Sloan has made to me was earlier this year, upon the discovery of a met, that at least things were much better than a year ago. I try to find ways to work around the impersonal treatment and inconveniences. I look elsewhere for emotional support. I firmly believe that I would be dead or dying without the medical care that I have received there. I don't really need warm fuzzies. I need top-notch medical care that is particularly well-suited to my circumstances and that is what I receive from Sloan-Kettering.0 -
My Liver Guymom_2_3 said:Memorial-Sloan Kettering
Jon,
I was diagnosed in November 2008 during the scheduled c-section of our third child. I had 5 bilobar liver mets. In February of this year I had my liver resection and had an HAI pump installed. Since then I have been doing adjuvant therapy (chemo in both the HAI pump as well as systemic). I will complete my last treatment early November (God willing).
The HAI treatment consists of having FUDR put into the pump every 5 weeks. Refer to this thread (http://csn.cancer.org/node/174161) for more information regarding my experience with the HAI pump. Additionally, there are others on the board (Phillieg and ADker) who have also had the pump therapy.
I do go to Memorial-Sloan Kettering and I do love the facility. The doctors and nurses are at the top of their game and everyone on staff knows your name and even though it's a larger facility it feels very personal. I highly recommend Sloan Kettering. I meet people in the waiting room (one floor is dedicated to colon cancer and melanoma) that travel from all over the country (even world) to go there for treatment. My oncologist is http://www.mskcc.org/prg/prg/bios/123.cfm. She is considered the "queen" of the HAI therapy. My liver surgeon was http://www.mskcc.org/prg/prg/bios/708.cfm. He was a phenomenal surgery and one day years from now I hope to tell him as well as my oncologist "thank you" for saving my life.
I have read studies that indicate that the HAI pump is very successful in both getting patients to operable status as well as preventing additional liver mets. My surgeon told me that liver recurrence was 50% likely but with the HAI therapy it was only 30% likely. I will take that. As of right now I have been NED for almost 7 months. My next scan is in November which will be 9 months from my surgery.
I know not many places do the pump implantation as it truly requires a skilled liver surgeon to do the placement. You want someone doing it who has done hundreds before. I believe that MSK does on the order of 200-300 per year. If you have any other questions about MSK or the pump, PM me or post here. Philieg and ADker are also patients at MSK. I am sure they will post later.
All the best,
Amy
I had this guy for my liver surgeon, he was great!
http://www.mskcc.org/prg/prg/bios/348.cfm
We have the same Oncologists.
A+ facility in my book. I really can no think of anything I had problems with on their end at all.
I left more info on another post http://csn.cancer.org/node/176241#comment-712077 along with the link to my scan so you can see the pump inside me.
http://csn.cancer.org/node/1750050
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