The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

liver met

Forums General Melanoma Community liver met

  • Post
    bball
    Participant

    3years ned after 2a just found liver met 2.5 cm on right lobe ,where is the best plave to be treated . can go anywhere in the world

Viewing 2 reply threads
  • Replies
      Jahendry12
      Participant

      MD Anderson in Houston texas

      Moffitt in florida

      NIH in Maryland 

       

      Jahendry12
      Participant

      MD Anderson in Houston texas

      Moffitt in florida

      NIH in Maryland 

       

      Jahendry12
      Participant

      MD Anderson in Houston texas

      Moffitt in florida

      NIH in Maryland 

       

        tschmith
        Participant

        I haven't been to either MD Anderson or Moffitt (but would if needed!), however I'm being treated at NIH in Bethesda, Maryland and I can't say enough for the doctors, nurses, even the food!  smiley  Monday I start MAGE TCR  which is a gene transfer therapy.   

        My melanoma specialist, Dr. Evan Lipson from Johns Hopkins is wonderful too.  He has told me that without fail, he has never heard a patient complain about their treatment at NIH. 

        I'm Stage IV and don't know if this will work but I pray, pray, pray and am full of hope.  My doctors are very excited about this new treatment.  I'll be the third person to participate.  Patients one and two are dong well but have not had their follow-up scans yet.

        Faith and Hope!

        Terrie

         

        tschmith
        Participant

        I haven't been to either MD Anderson or Moffitt (but would if needed!), however I'm being treated at NIH in Bethesda, Maryland and I can't say enough for the doctors, nurses, even the food!  smiley  Monday I start MAGE TCR  which is a gene transfer therapy.   

        My melanoma specialist, Dr. Evan Lipson from Johns Hopkins is wonderful too.  He has told me that without fail, he has never heard a patient complain about their treatment at NIH. 

        I'm Stage IV and don't know if this will work but I pray, pray, pray and am full of hope.  My doctors are very excited about this new treatment.  I'll be the third person to participate.  Patients one and two are dong well but have not had their follow-up scans yet.

        Faith and Hope!

        Terrie

         

        tschmith
        Participant

        I haven't been to either MD Anderson or Moffitt (but would if needed!), however I'm being treated at NIH in Bethesda, Maryland and I can't say enough for the doctors, nurses, even the food!  smiley  Monday I start MAGE TCR  which is a gene transfer therapy.   

        My melanoma specialist, Dr. Evan Lipson from Johns Hopkins is wonderful too.  He has told me that without fail, he has never heard a patient complain about their treatment at NIH. 

        I'm Stage IV and don't know if this will work but I pray, pray, pray and am full of hope.  My doctors are very excited about this new treatment.  I'll be the third person to participate.  Patients one and two are dong well but have not had their follow-up scans yet.

        Faith and Hope!

        Terrie

         

        Maureen038
        Participant

        Wishing you the best of luck for your trial Terri!!! My husband and I were extremely impressed with the staff at NIH. There were exceptionally professional, caring and very cautious. Even though he was not a responder to TIL therapy! we feel it considerably slowed down the disease and might be helping with his new trial. The TIL cells are suppose to last in your body for years.

        Maureen

        Maureen038
        Participant

        Wishing you the best of luck for your trial Terri!!! My husband and I were extremely impressed with the staff at NIH. There were exceptionally professional, caring and very cautious. Even though he was not a responder to TIL therapy! we feel it considerably slowed down the disease and might be helping with his new trial. The TIL cells are suppose to last in your body for years.

        Maureen

        Maureen038
        Participant

        Wishing you the best of luck for your trial Terri!!! My husband and I were extremely impressed with the staff at NIH. There were exceptionally professional, caring and very cautious. Even though he was not a responder to TIL therapy! we feel it considerably slowed down the disease and might be helping with his new trial. The TIL cells are suppose to last in your body for years.

        Maureen

        Socks
        Participant

        MD Anderson is very good. My mom went there for her lymphoma, and I know that Melanoma is part of their "Moon Shot" Program. If you have any questions about it, let me know. I don't know much about their melanoma treatment specifically, but Mom and I lived in the hotel owned by MD Anderson (the Rotary House) for four months.

        Socks
        Participant

        MD Anderson is very good. My mom went there for her lymphoma, and I know that Melanoma is part of their "Moon Shot" Program. If you have any questions about it, let me know. I don't know much about their melanoma treatment specifically, but Mom and I lived in the hotel owned by MD Anderson (the Rotary House) for four months.

        Socks
        Participant

        MD Anderson is very good. My mom went there for her lymphoma, and I know that Melanoma is part of their "Moon Shot" Program. If you have any questions about it, let me know. I don't know much about their melanoma treatment specifically, but Mom and I lived in the hotel owned by MD Anderson (the Rotary House) for four months.

Viewing 2 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

Popular Topics