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.

Stage IV NED since May 2001

Forums General Melanoma Community Stage IV NED since May 2001

  • Post
    Dana R.
    Participant

    We recently celebrated my husband's "NED anniversary". 13 years ago, I was on the MPIP almost daily as my husband endured bio chemotherapy. This site was a life-line.  We are so thankful to all of the people from this site who helped us figure out how to deal with side effects and gave us moral support. May God bless you all as you battle this disease.

Viewing 11 reply threads
  • Replies
      JoshF
      Participant

      Dana-

      So happy for you!!! Being Stage 4 myself it gives hope.

      Curious as to what treatment your husband did…assuming IL-2?

       

      Josh

      JoshF
      Participant

      Dana-

      So happy for you!!! Being Stage 4 myself it gives hope.

      Curious as to what treatment your husband did…assuming IL-2?

       

      Josh

        Dana R.
        Participant

        In 2001, Dr Sewa Legha was doing trials at MDA on a bio chemo protocol: cisplatin, vinblastine, dacarbazine, high dose IL-2, and interferon. It was brutal. We elected to do this off-study, because our youngest was 2 years old at the time, and we wanted as much time together as a family as possible. At that time, we were told that 5 year survival was about 3-5%. After 4 cycles, Steve's lungs were clear. Our onc then recommended an immunotherapy protocol that was in trials at JWCI. It was specifically for bio chemo follow-up. More IL-2, GM-CSF, more interferon…monthly cycles, 12 months worth. Quality of life was pretty good after the initial blast of high dose IL-2. We even traveled some during that year. Did a cross-country "see America" trip with our 4 kids with a cooler of IL-2 and interferon for daily injections. 

        Praying that melanoma finds you to be a disagreeable host and LEAVES!

         

        Dana R.
        Participant

        In 2001, Dr Sewa Legha was doing trials at MDA on a bio chemo protocol: cisplatin, vinblastine, dacarbazine, high dose IL-2, and interferon. It was brutal. We elected to do this off-study, because our youngest was 2 years old at the time, and we wanted as much time together as a family as possible. At that time, we were told that 5 year survival was about 3-5%. After 4 cycles, Steve's lungs were clear. Our onc then recommended an immunotherapy protocol that was in trials at JWCI. It was specifically for bio chemo follow-up. More IL-2, GM-CSF, more interferon…monthly cycles, 12 months worth. Quality of life was pretty good after the initial blast of high dose IL-2. We even traveled some during that year. Did a cross-country "see America" trip with our 4 kids with a cooler of IL-2 and interferon for daily injections. 

        Praying that melanoma finds you to be a disagreeable host and LEAVES!

         

        Dana R.
        Participant

        In 2001, Dr Sewa Legha was doing trials at MDA on a bio chemo protocol: cisplatin, vinblastine, dacarbazine, high dose IL-2, and interferon. It was brutal. We elected to do this off-study, because our youngest was 2 years old at the time, and we wanted as much time together as a family as possible. At that time, we were told that 5 year survival was about 3-5%. After 4 cycles, Steve's lungs were clear. Our onc then recommended an immunotherapy protocol that was in trials at JWCI. It was specifically for bio chemo follow-up. More IL-2, GM-CSF, more interferon…monthly cycles, 12 months worth. Quality of life was pretty good after the initial blast of high dose IL-2. We even traveled some during that year. Did a cross-country "see America" trip with our 4 kids with a cooler of IL-2 and interferon for daily injections. 

        Praying that melanoma finds you to be a disagreeable host and LEAVES!

         

      JoshF
      Participant

      Dana-

      So happy for you!!! Being Stage 4 myself it gives hope.

      Curious as to what treatment your husband did…assuming IL-2?

       

      Josh

      shanemcdonald99
      Participant

      Thats fantastic !

       

      thanks for the update !

       

      peace

      Shane

      shanemcdonald99
      Participant

      Thats fantastic !

       

      thanks for the update !

       

      peace

      Shane

      shanemcdonald99
      Participant

      Thats fantastic !

       

      thanks for the update !

       

      peace

      Shane

      cpeters2498
      Participant

      So happy for you.

      I was diagnosed stage IV in January we need to hear these types of success stories!

      I plan on being one of them.

      Charlie

      cpeters2498
      Participant

      So happy for you.

      I was diagnosed stage IV in January we need to hear these types of success stories!

      I plan on being one of them.

      Charlie

      cpeters2498
      Participant

      So happy for you.

      I was diagnosed stage IV in January we need to hear these types of success stories!

      I plan on being one of them.

      Charlie

      Jahendry12
      Participant

      AWESOME! Thanks for coming back and sharing. 

      Jahendry12
      Participant

      AWESOME! Thanks for coming back and sharing. 

      Jahendry12
      Participant

      AWESOME! Thanks for coming back and sharing. 

Viewing 11 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