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.

melanoma cures

Forums General Melanoma Community melanoma cures

  • Post
    Nebr78
    Participant

      I have had a very good friend of mine says that he knows of two people that went somewhere in Mexico and got cured of Melanoma.  Of course you never know if you are cured.        It cost a lot of money $25,000.      This friend is not barking up a tree.   He is from Iowa and I am from Nebr.  We were in service together in Korea (1951.       Does anyone know if any of our Cancer research people have looked into this.   I would think they would and give an evaluation. &

      I have had a very good friend of mine says that he knows of two people that went somewhere in Mexico and got cured of Melanoma.  Of course you never know if you are cured.        It cost a lot of money $25,000.      This friend is not barking up a tree.   He is from Iowa and I am from Nebr.  We were in service together in Korea (1951.       Does anyone know if any of our Cancer research people have looked into this.   I would think they would and give an evaluation.     There is a fox in the chicken house somewhere.    Ipilimumab was supposed to be approved in Dec. 2010 and then in March 2011, and so far hasn't.    Is there any good reason for this.  I have 2 lumps in lung (4 cent. and 2 cent) and what I have been getting does no good.   Is reasearch really being done?????????????????

       

    Viewing 1 reply thread
    • Replies
        MichaelFL
        Participant

          Ipilimumab (also known as MDX-010 or MDX-101) which was developed by Bristol-Myers Squibb and was FDA approved in the United States on March 25, 2011, and is now marketed as Yervoy. If you scroll down, you can read other posts concerning Yervoy, costs etc.

          Be wary of these so called cures in Mexico.

          Michael

            Nebr78
            Participant

              I am wary of treatment in Mexico but I wonder if anyone in research field has looked to see what they are.???

              Surely someone has.  I am going to try Am Cancer Society and National Cancer Society but really don't think they know a heck of a lot.

              Nebr78
              Participant

                Micheal:    You said to scroll down to get cost, etc for this Yervoy.  It will not scrool down on your reply.   I tried everytrhing I know (which isn't much) but cannot comeup with anything.     Do you mind sending me some more instructions. 

                Thanks,        Nebr78

                EmilyandMike
                Participant

                  Just google Ipilimumab and you will see all the news from Friday when it was FDA approved.  Michael meant scroll down the forum posting.

                  http://www.bloomberg.com/news/2011-03-25/bristol-myers-squibb-wins-u-s-fda-approval-for-new-melanoma-medicine.html

                  The mexico thing is probably Gerson therapy – google that also.  It is heavy juicing and enemas.  It is probably really good for you but it is not a cure.

                  Best,

                  Emily

                   

                   

                  EmilyandMike
                  Participant

                    Just google Ipilimumab and you will see all the news from Friday when it was FDA approved.  Michael meant scroll down the forum posting.

                    http://www.bloomberg.com/news/2011-03-25/bristol-myers-squibb-wins-u-s-fda-approval-for-new-melanoma-medicine.html

                    The mexico thing is probably Gerson therapy – google that also.  It is heavy juicing and enemas.  It is probably really good for you but it is not a cure.

                    Best,

                    Emily

                     

                     

                    dian in spokane
                    Participant

                      Nebraska, you have to go back to the main list of topics to see all the topics, then pick out the ones involving Ipililmumab. There are several of them over the last few days. You could also just plug Yervoy into your Google and it will bring up many news articles on the topic from the last few days.

                      And listen..about that Mexico cure. IT is MOST LIKELY BOGUS!

                      This is not to imply that your friend is lying, he may have had a remission. Many of us go through periods of time when we feel like our melanoma is GONE. NED..no evidence of disease, can be a result of surgery or even spontaneous remission.

                      If there were a CURE for melanoma out there, anywhere, it would be shouted from the rooftops. If Mexico had a cure, they'd be selling that cure to people all over the world. Think of the money that company would be making if they had a cure.

                      I know it's attractive to want to believe in such a thing.

                      I hope you are seeing a good melanoma specialist somewhere here in the US. Have you considered MD Anderson? Nebraska is not that far from Texas…

                       

                      good luck to you.

                      Dian in Spokane

                      waltzing with melanoma since 1983

                      dian in spokane
                      Participant

                        Nebraska, you have to go back to the main list of topics to see all the topics, then pick out the ones involving Ipililmumab. There are several of them over the last few days. You could also just plug Yervoy into your Google and it will bring up many news articles on the topic from the last few days.

                        And listen..about that Mexico cure. IT is MOST LIKELY BOGUS!

                        This is not to imply that your friend is lying, he may have had a remission. Many of us go through periods of time when we feel like our melanoma is GONE. NED..no evidence of disease, can be a result of surgery or even spontaneous remission.

                        If there were a CURE for melanoma out there, anywhere, it would be shouted from the rooftops. If Mexico had a cure, they'd be selling that cure to people all over the world. Think of the money that company would be making if they had a cure.

                        I know it's attractive to want to believe in such a thing.

                        I hope you are seeing a good melanoma specialist somewhere here in the US. Have you considered MD Anderson? Nebraska is not that far from Texas…

                         

                        good luck to you.

                        Dian in Spokane

                        waltzing with melanoma since 1983

                        Janner
                        Participant

                          Nebr78:

                          Michael was just telling you to scroll through the other questions that had been posted.  In the last 3 days, there have been many postings about Yervoy/Ipilimumab.  It has been FDA approved so now it may be possible for you to get that treatment if you are interested.  Since it is new, there are still questions on insurance, etc, but it appears that from most of the info out there, insurance will probably cover it.

                          Here's a link to the bulletin board again, and you can just scroll down through all the replies looking for the info on Yervoy..

                          http://www.melanoma.org/community/mpip-melanoma-patients-information-page

                          Janner
                          Participant

                            Nebr78:

                            Michael was just telling you to scroll through the other questions that had been posted.  In the last 3 days, there have been many postings about Yervoy/Ipilimumab.  It has been FDA approved so now it may be possible for you to get that treatment if you are interested.  Since it is new, there are still questions on insurance, etc, but it appears that from most of the info out there, insurance will probably cover it.

                            Here's a link to the bulletin board again, and you can just scroll down through all the replies looking for the info on Yervoy..

                            http://www.melanoma.org/community/mpip-melanoma-patients-information-page

                            Nebr78
                            Participant

                              Micheal:    You said to scroll down to get cost, etc for this Yervoy.  It will not scrool down on your reply.   I tried everytrhing I know (which isn't much) but cannot comeup with anything.     Do you mind sending me some more instructions. 

                              Thanks,        Nebr78

                              Nebr78
                              Participant

                                I am wary of treatment in Mexico but I wonder if anyone in research field has looked to see what they are.???

                                Surely someone has.  I am going to try Am Cancer Society and National Cancer Society but really don't think they know a heck of a lot.

                              MichaelFL
                              Participant

                                Ipilimumab (also known as MDX-010 or MDX-101) which was developed by Bristol-Myers Squibb and was FDA approved in the United States on March 25, 2011, and is now marketed as Yervoy. If you scroll down, you can read other posts concerning Yervoy, costs etc.

                                Be wary of these so called cures in Mexico.

                                Michael

                            Viewing 1 reply thread
                            • 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