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Stage IIIA patients doing yervoy vs watch and wait.

Forums General Melanoma Community Stage IIIA patients doing yervoy vs watch and wait.

  • Post
    mybelle
    Participant

      Looking for some feedback from other stage IIIA patients who are making the decision to watch and wait or try yervoy. Son diagnosed with IIIA, 1.1mm on right arm, micro one node, 23 other nodes negative. He is leaning more toward boosting his immune system naturally through healthy living due to the side effects of yervoy. Appreciate hearing from other patients in a similar situation.

    Viewing 17 reply threads
    • Replies
        jennunicorn
        Participant

          Hi, sorry your son has to go through this. I am 29, stage 3b, and doing Yervoy. I chose Yervoy over watch and wait for myself due to knowing that I need to feel like I am physically doing something, plus, I am young and healthy so if any side effects came up I'd be able to take care of them quickly. I have done 3 rounds of treatment so far, and the only side effect I have experienced is fatigue. No one knows how a drug will react with their body until they try it, and I am definitely very glad I have been able to get this far with no major side effects at all. 

          It is a very personal decision. Whatever decision he is most comfortable with will be the best decision for him. 

          I hope all the best for your son.

          -Jenn

          jennunicorn
          Participant

            Hi, sorry your son has to go through this. I am 29, stage 3b, and doing Yervoy. I chose Yervoy over watch and wait for myself due to knowing that I need to feel like I am physically doing something, plus, I am young and healthy so if any side effects came up I'd be able to take care of them quickly. I have done 3 rounds of treatment so far, and the only side effect I have experienced is fatigue. No one knows how a drug will react with their body until they try it, and I am definitely very glad I have been able to get this far with no major side effects at all. 

            It is a very personal decision. Whatever decision he is most comfortable with will be the best decision for him. 

            I hope all the best for your son.

            -Jenn

              mybelle
              Participant

                Hi Jenn. Thank you for the feedback. I'm so happy for you that you are tolerating yervoy well. He is young and otherwise healthy like you so his oncologist thinks he would probably tolerate it well. Tough decision and I don't think there is a right or wrong decision. Just a personal decision for him to make. He and I have been curious about how many other 3A patients are opting for yervoy. He wants to still be able to work and finish his degree. I wish you the very best also. It helps to talk to other patients going through this.

                jennunicorn
                Participant

                  I am both in school and working too. I have gone down to part time work rather than my usual full time, just because of the fatigue and my doctor told me I shouldn't overexert myself. I know other people who have mentioned that they continued to work while doing treatments, it's definitely not as debilitating as some older forms of treatment were, which is really nice. I know it can really help hearing positive stories to balance out the negative ones. 

                  jennunicorn
                  Participant

                    I am both in school and working too. I have gone down to part time work rather than my usual full time, just because of the fatigue and my doctor told me I shouldn't overexert myself. I know other people who have mentioned that they continued to work while doing treatments, it's definitely not as debilitating as some older forms of treatment were, which is really nice. I know it can really help hearing positive stories to balance out the negative ones. 

                    jennunicorn
                    Participant

                      I am both in school and working too. I have gone down to part time work rather than my usual full time, just because of the fatigue and my doctor told me I shouldn't overexert myself. I know other people who have mentioned that they continued to work while doing treatments, it's definitely not as debilitating as some older forms of treatment were, which is really nice. I know it can really help hearing positive stories to balance out the negative ones. 

                      mybelle
                      Participant

                        Hi Jenn. Thank you for the feedback. I'm so happy for you that you are tolerating yervoy well. He is young and otherwise healthy like you so his oncologist thinks he would probably tolerate it well. Tough decision and I don't think there is a right or wrong decision. Just a personal decision for him to make. He and I have been curious about how many other 3A patients are opting for yervoy. He wants to still be able to work and finish his degree. I wish you the very best also. It helps to talk to other patients going through this.

                        mybelle
                        Participant

                          Hi Jenn. Thank you for the feedback. I'm so happy for you that you are tolerating yervoy well. He is young and otherwise healthy like you so his oncologist thinks he would probably tolerate it well. Tough decision and I don't think there is a right or wrong decision. Just a personal decision for him to make. He and I have been curious about how many other 3A patients are opting for yervoy. He wants to still be able to work and finish his degree. I wish you the very best also. It helps to talk to other patients going through this.

                        jennunicorn
                        Participant

                          Hi, sorry your son has to go through this. I am 29, stage 3b, and doing Yervoy. I chose Yervoy over watch and wait for myself due to knowing that I need to feel like I am physically doing something, plus, I am young and healthy so if any side effects came up I'd be able to take care of them quickly. I have done 3 rounds of treatment so far, and the only side effect I have experienced is fatigue. No one knows how a drug will react with their body until they try it, and I am definitely very glad I have been able to get this far with no major side effects at all. 

                          It is a very personal decision. Whatever decision he is most comfortable with will be the best decision for him. 

                          I hope all the best for your son.

                          -Jenn

                          Kenny
                          Participant

                            Hi Mybelle,

                            I started out in almost the same place as your son just under 2 years ago.  At that time I was offered interferon, clinical trial, or watch and wait.  I was not accepted for the trial so I chose the watch and wait.  I did change my diet and exercise (walk 3.5 miles) 6 days a week.  So far so good.  I have a CT scan and blood work next week and meet with my oncologist the following week.  Tough choice but I am sure he will make the right one for him.

                            Take care,

                            Ken

                            Kenny
                            Participant

                              Hi Mybelle,

                              I started out in almost the same place as your son just under 2 years ago.  At that time I was offered interferon, clinical trial, or watch and wait.  I was not accepted for the trial so I chose the watch and wait.  I did change my diet and exercise (walk 3.5 miles) 6 days a week.  So far so good.  I have a CT scan and blood work next week and meet with my oncologist the following week.  Tough choice but I am sure he will make the right one for him.

                              Take care,

                              Ken

                              Kenny
                              Participant

                                Hi Mybelle,

                                I started out in almost the same place as your son just under 2 years ago.  At that time I was offered interferon, clinical trial, or watch and wait.  I was not accepted for the trial so I chose the watch and wait.  I did change my diet and exercise (walk 3.5 miles) 6 days a week.  So far so good.  I have a CT scan and blood work next week and meet with my oncologist the following week.  Tough choice but I am sure he will make the right one for him.

                                Take care,

                                Ken

                                  mybelle
                                  Participant

                                    Hi Ken,

                                    thanks for your post. So good to hear positive stories. This has really been quite a ride since his diagnosis. I appreciate everyone communicating. We have had some low moments with all this and are trying to remain positive. I think that my son and all melanoma patients are some courageous people. I wish you continued good health.

                                    mybelle (Michelle)

                                    mybelle
                                    Participant

                                      Hi Ken,

                                      thanks for your post. So good to hear positive stories. This has really been quite a ride since his diagnosis. I appreciate everyone communicating. We have had some low moments with all this and are trying to remain positive. I think that my son and all melanoma patients are some courageous people. I wish you continued good health.

                                      mybelle (Michelle)

                                      mybelle
                                      Participant

                                        Hi Ken,

                                        thanks for your post. So good to hear positive stories. This has really been quite a ride since his diagnosis. I appreciate everyone communicating. We have had some low moments with all this and are trying to remain positive. I think that my son and all melanoma patients are some courageous people. I wish you continued good health.

                                        mybelle (Michelle)

                                      ed williams
                                      Participant

                                        Mybelle, if you haven't already read the EORTC trial 18071 findings on Ipilimumab they might be helpfull in making a decision. Just Google Ipilimumab and EORTC and Prof Alexander M M Eggermont of the Gustave Roussy Cancer Campus. It is a very big decision to make especially with the risk of grade 3 or 4 adverse advents being so high. The two approved Pd-1 drugs are already starting to show up in small adjuvant trials and have a much lower rate of grade 3-4 reactions. While waiting and watching is still considered the standard of care for 3A, it is very hard to do when faced with possible progression. Which ever direction your son choose to go he should know that the advancement in Melanoma research are trully amazing during the last 3 to 4 years. If you choose to wait make sure that you are being followed by a good Oncologist that is willing to scan on a regular basis to check for progression. Wishing you the best in your journey!!!!! Ed

                                        ed williams
                                        Participant

                                          Mybelle, if you haven't already read the EORTC trial 18071 findings on Ipilimumab they might be helpfull in making a decision. Just Google Ipilimumab and EORTC and Prof Alexander M M Eggermont of the Gustave Roussy Cancer Campus. It is a very big decision to make especially with the risk of grade 3 or 4 adverse advents being so high. The two approved Pd-1 drugs are already starting to show up in small adjuvant trials and have a much lower rate of grade 3-4 reactions. While waiting and watching is still considered the standard of care for 3A, it is very hard to do when faced with possible progression. Which ever direction your son choose to go he should know that the advancement in Melanoma research are trully amazing during the last 3 to 4 years. If you choose to wait make sure that you are being followed by a good Oncologist that is willing to scan on a regular basis to check for progression. Wishing you the best in your journey!!!!! Ed

                                          ed williams
                                          Participant

                                            Mybelle, if you haven't already read the EORTC trial 18071 findings on Ipilimumab they might be helpfull in making a decision. Just Google Ipilimumab and EORTC and Prof Alexander M M Eggermont of the Gustave Roussy Cancer Campus. It is a very big decision to make especially with the risk of grade 3 or 4 adverse advents being so high. The two approved Pd-1 drugs are already starting to show up in small adjuvant trials and have a much lower rate of grade 3-4 reactions. While waiting and watching is still considered the standard of care for 3A, it is very hard to do when faced with possible progression. Which ever direction your son choose to go he should know that the advancement in Melanoma research are trully amazing during the last 3 to 4 years. If you choose to wait make sure that you are being followed by a good Oncologist that is willing to scan on a regular basis to check for progression. Wishing you the best in your journey!!!!! Ed

                                              mybelle
                                              Participant

                                                Hi Ed

                                                Thank you for the info. We have read the IPI trial. Have also found a great melanoma specialist at Mayo in Jvlle Fl. to guide his care and scan on a regular basis. I have been trying my best to help him through this ordeal using every resource I can find. Now he just has to decide yes/no on adjuvant treatment. The PD1 drugs sound much more appealing. I will go to the link you provided and read that article as well. I appreciate the support.

                                                 

                                                mybelle
                                                Participant

                                                  Hi Ed

                                                  Thank you for the info. We have read the IPI trial. Have also found a great melanoma specialist at Mayo in Jvlle Fl. to guide his care and scan on a regular basis. I have been trying my best to help him through this ordeal using every resource I can find. Now he just has to decide yes/no on adjuvant treatment. The PD1 drugs sound much more appealing. I will go to the link you provided and read that article as well. I appreciate the support.

                                                   

                                                  mybelle
                                                  Participant

                                                    Hi Ed

                                                    Thank you for the info. We have read the IPI trial. Have also found a great melanoma specialist at Mayo in Jvlle Fl. to guide his care and scan on a regular basis. I have been trying my best to help him through this ordeal using every resource I can find. Now he just has to decide yes/no on adjuvant treatment. The PD1 drugs sound much more appealing. I will go to the link you provided and read that article as well. I appreciate the support.

                                                     

                                                  mkirkland
                                                  Participant

                                                    Hi – I am also taking ipi for stage 3A. I started in December and will be going for my 3rd dose Monday. I am only taking the 3mg dosage though and not the 10mg. So far I've really only experienced fatigue and it's mostly during the first week. I have had a few episodes of diarrhea but nothing too bad. Could have even been something I ate it was so minimal. I work full time and have a 6 year old and 18 month old so life is pretty tiresome anyways. 🙂  I have read people have no side effects, minimal to horrific so it's really just depends on how it effects that person. Best wishes in making a decision. I know how difficult it was for me and I'm sure y'all are in the same boat. 

                                                     

                                                    Misty 

                                                    mkirkland
                                                    Participant

                                                      Hi – I am also taking ipi for stage 3A. I started in December and will be going for my 3rd dose Monday. I am only taking the 3mg dosage though and not the 10mg. So far I've really only experienced fatigue and it's mostly during the first week. I have had a few episodes of diarrhea but nothing too bad. Could have even been something I ate it was so minimal. I work full time and have a 6 year old and 18 month old so life is pretty tiresome anyways. 🙂  I have read people have no side effects, minimal to horrific so it's really just depends on how it effects that person. Best wishes in making a decision. I know how difficult it was for me and I'm sure y'all are in the same boat. 

                                                       

                                                      Misty 

                                                        mybelle
                                                        Participant

                                                          Hi Misty. Interesting to hear you are getting the lower dose and my son plans to ask his doctor about this option. From the above posts I can see that several younger people (including you) are opting for yervoy. He is planning to make a decision this week. Thank you for your post. I hope you do very well in the future and glad to hear you are tolerating yervoy without much difficulty. Best wishes.

                                                          mybelle
                                                          Participant

                                                            Hi Misty. Interesting to hear you are getting the lower dose and my son plans to ask his doctor about this option. From the above posts I can see that several younger people (including you) are opting for yervoy. He is planning to make a decision this week. Thank you for your post. I hope you do very well in the future and glad to hear you are tolerating yervoy without much difficulty. Best wishes.

                                                            mybelle
                                                            Participant

                                                              Hi Misty. Interesting to hear you are getting the lower dose and my son plans to ask his doctor about this option. From the above posts I can see that several younger people (including you) are opting for yervoy. He is planning to make a decision this week. Thank you for your post. I hope you do very well in the future and glad to hear you are tolerating yervoy without much difficulty. Best wishes.

                                                              gregor913
                                                              Participant
                                                                I’m on the 10mg dose of ippi. Just finished 2nd dose a week ago. Side effects so far was a little tired after infusion. The way my doctor put it was he wanted me to do systemic treatment. He feels like they got it all but if they didn’t he would rather be treating 100 cancer cells vs a billion cancer cells. Greg
                                                                gregor913
                                                                Participant
                                                                  I’m on the 10mg dose of ippi. Just finished 2nd dose a week ago. Side effects so far was a little tired after infusion. The way my doctor put it was he wanted me to do systemic treatment. He feels like they got it all but if they didn’t he would rather be treating 100 cancer cells vs a billion cancer cells. Greg
                                                                  gregor913
                                                                  Participant
                                                                    I’m on the 10mg dose of ippi. Just finished 2nd dose a week ago. Side effects so far was a little tired after infusion. The way my doctor put it was he wanted me to do systemic treatment. He feels like they got it all but if they didn’t he would rather be treating 100 cancer cells vs a billion cancer cells. Greg
                                                                    mybelle
                                                                    Participant

                                                                      Thanks Greg. Glad to hear its going well.

                                                                      mybelle
                                                                      Participant

                                                                        Thanks Greg. Glad to hear its going well.

                                                                        mybelle
                                                                        Participant

                                                                          Thanks Greg. Glad to hear its going well.

                                                                        mkirkland
                                                                        Participant

                                                                          Hi – I am also taking ipi for stage 3A. I started in December and will be going for my 3rd dose Monday. I am only taking the 3mg dosage though and not the 10mg. So far I've really only experienced fatigue and it's mostly during the first week. I have had a few episodes of diarrhea but nothing too bad. Could have even been something I ate it was so minimal. I work full time and have a 6 year old and 18 month old so life is pretty tiresome anyways. 🙂  I have read people have no side effects, minimal to horrific so it's really just depends on how it effects that person. Best wishes in making a decision. I know how difficult it was for me and I'm sure y'all are in the same boat. 

                                                                           

                                                                          Misty 

                                                                          keepthefaith11
                                                                          Participant
                                                                            If he decides to go the natural route, with no medication, I would get him on a curcumin supplement as well as co q10. Reishi mushroom is also beneficial. 14 years ago my mother had stage 3 triple negative breast cancer with 7 nodes involved. She went through with the chemo but also changed her diet and I had her on a bunch of different supplements including these. I firmly believe this is at least partially why she is well today and never had a recurrence. My dad is currently on these supplements as well. Also matcha green tea is excellent! I am kind of a combination alternative and conventional medicine type person. I believe for the best results both might be needed. Oh, & a good probiotics is important as well as high dose of vitamin D. I have found the Biotics brand vitamin D works the best. Let us know what he decides to do.
                                                                            keepthefaith11
                                                                            Participant
                                                                              If he decides to go the natural route, with no medication, I would get him on a curcumin supplement as well as co q10. Reishi mushroom is also beneficial. 14 years ago my mother had stage 3 triple negative breast cancer with 7 nodes involved. She went through with the chemo but also changed her diet and I had her on a bunch of different supplements including these. I firmly believe this is at least partially why she is well today and never had a recurrence. My dad is currently on these supplements as well. Also matcha green tea is excellent! I am kind of a combination alternative and conventional medicine type person. I believe for the best results both might be needed. Oh, & a good probiotics is important as well as high dose of vitamin D. I have found the Biotics brand vitamin D works the best. Let us know what he decides to do.
                                                                              keepthefaith11
                                                                              Participant
                                                                                If he decides to go the natural route, with no medication, I would get him on a curcumin supplement as well as co q10. Reishi mushroom is also beneficial. 14 years ago my mother had stage 3 triple negative breast cancer with 7 nodes involved. She went through with the chemo but also changed her diet and I had her on a bunch of different supplements including these. I firmly believe this is at least partially why she is well today and never had a recurrence. My dad is currently on these supplements as well. Also matcha green tea is excellent! I am kind of a combination alternative and conventional medicine type person. I believe for the best results both might be needed. Oh, & a good probiotics is important as well as high dose of vitamin D. I have found the Biotics brand vitamin D works the best. Let us know what he decides to do.
                                                                                  cavsnut
                                                                                  Participant

                                                                                    Hi Mybelle,  I had a 2mm tumor on my right calf, 4 nodes taken out in the SLNB with one possitive with .9mm micromet…I chose watch and wait with ultrasound and routine scans, that was in August 2014…NED so far , just personally didn't want to do the immunatherapy that was available at the time with such a small amount in one lymp node with the chance I may never have to deal with melanoma again…Best of luck to your son in the choice he makes…

                                                                                     

                                                                                    Craig

                                                                                    mybelle
                                                                                    Participant

                                                                                      thanks so much to everyone for the comments. In regard to the most recent posts, I have already started him on vitamin supplements and turmeric. Anything he can do to boost his immune system naturally. Craig's comment above encouraging. Really tough decision and after he meets with his doctor again this week at Mayo he will decide. I'm just trying to research and give him all the info he needs so it will be an informed decision. My best wishes to all the people fighting melanoma out there. Your support means a lot. thank you.

                                                                                      mybelle
                                                                                      Participant

                                                                                        thanks so much to everyone for the comments. In regard to the most recent posts, I have already started him on vitamin supplements and turmeric. Anything he can do to boost his immune system naturally. Craig's comment above encouraging. Really tough decision and after he meets with his doctor again this week at Mayo he will decide. I'm just trying to research and give him all the info he needs so it will be an informed decision. My best wishes to all the people fighting melanoma out there. Your support means a lot. thank you.

                                                                                        mybelle
                                                                                        Participant

                                                                                          thanks so much to everyone for the comments. In regard to the most recent posts, I have already started him on vitamin supplements and turmeric. Anything he can do to boost his immune system naturally. Craig's comment above encouraging. Really tough decision and after he meets with his doctor again this week at Mayo he will decide. I'm just trying to research and give him all the info he needs so it will be an informed decision. My best wishes to all the people fighting melanoma out there. Your support means a lot. thank you.

                                                                                          cavsnut
                                                                                          Participant

                                                                                            Hi Mybelle,  I had a 2mm tumor on my right calf, 4 nodes taken out in the SLNB with one possitive with .9mm micromet…I chose watch and wait with ultrasound and routine scans, that was in August 2014…NED so far , just personally didn't want to do the immunatherapy that was available at the time with such a small amount in one lymp node with the chance I may never have to deal with melanoma again…Best of luck to your son in the choice he makes…

                                                                                             

                                                                                            Craig

                                                                                            cavsnut
                                                                                            Participant

                                                                                              Hi Mybelle,  I had a 2mm tumor on my right calf, 4 nodes taken out in the SLNB with one possitive with .9mm micromet…I chose watch and wait with ultrasound and routine scans, that was in August 2014…NED so far , just personally didn't want to do the immunatherapy that was available at the time with such a small amount in one lymp node with the chance I may never have to deal with melanoma again…Best of luck to your son in the choice he makes…

                                                                                               

                                                                                              Craig

                                                                                            DZnDef
                                                                                            Participant

                                                                                              I'm sorry you've had to find yourself here, mybelle.  It's a good group with lots of different experiences and opinions with the same disease so you'll get a good variety for making a decision.  First, I want to emphasize that there is no right or wrong decision.  Your son needs to do what feels right for him and then hope for the best because nothing is guaranteed.  When it comes to Yervoy, your son will either be a responder or he won't be.  There is no way to know which in advance.  If he is a responder to Yervoy, he will also be a responder later IF he advances to stage IV.  If he is not a responder, then it won't make a difference now or later.  

                                                                                              For what it's worth, I believe living a healthy lifestyle IS "doing something".  Our immune system is our number one defense against cancer.  Cancer cannot exist in an environment where our immune system is functioning perfectly.  Even Yervoy, when it works, is using the immune system.

                                                                                              There is a lot of conflicting information out there on what constitutes a "healthy" diet.  My own doctor believes it is not one-size-fits-all but rather that some of us are meat-eaters, some of us more vegetarian and some of us are both.  Wherever you fall on the spectrum, find the cleanest most natural versions of that food as possible (no hormones, antibiotics, pesticides, etc.).  And if you eat animals, make sure those animals ate what they are designed to eat (I.e., cows eat grass, not grains, chickens eat grass, seeds and insects, not corn).  No sugar, flour or processed foods.  There's a lot of junk in our food supply unfortunately.  But also lots of farmers' markets and on-line resources.

                                                                                              I wish you and your son well.  Best of luck making this difficult choice.

                                                                                              Maggie

                                                                                                mybelle
                                                                                                Participant

                                                                                                  Hi Maggie,

                                                                                                  I responded earlier to your post but I don't see it…so will reply again. Thank you so much for your kind reply. It is all sound advice and I will take it to heart. He has already started eating an organic diet. Interesting thoughts on responder vs non-responder. I have tried to gather information for him and I have now stepped back to let him think it through and make his own decision. Worried mom..so it's difficult. I appreciate your support and I wish you the very best.

                                                                                                  mybelle
                                                                                                  Participant

                                                                                                    Hi Maggie,

                                                                                                    I responded earlier to your post but I don't see it…so will reply again. Thank you so much for your kind reply. It is all sound advice and I will take it to heart. He has already started eating an organic diet. Interesting thoughts on responder vs non-responder. I have tried to gather information for him and I have now stepped back to let him think it through and make his own decision. Worried mom..so it's difficult. I appreciate your support and I wish you the very best.

                                                                                                    mybelle
                                                                                                    Participant

                                                                                                      Hi Maggie,

                                                                                                      I responded earlier to your post but I don't see it…so will reply again. Thank you so much for your kind reply. It is all sound advice and I will take it to heart. He has already started eating an organic diet. Interesting thoughts on responder vs non-responder. I have tried to gather information for him and I have now stepped back to let him think it through and make his own decision. Worried mom..so it's difficult. I appreciate your support and I wish you the very best.

                                                                                                    DZnDef
                                                                                                    Participant

                                                                                                      I'm sorry you've had to find yourself here, mybelle.  It's a good group with lots of different experiences and opinions with the same disease so you'll get a good variety for making a decision.  First, I want to emphasize that there is no right or wrong decision.  Your son needs to do what feels right for him and then hope for the best because nothing is guaranteed.  When it comes to Yervoy, your son will either be a responder or he won't be.  There is no way to know which in advance.  If he is a responder to Yervoy, he will also be a responder later IF he advances to stage IV.  If he is not a responder, then it won't make a difference now or later.  

                                                                                                      For what it's worth, I believe living a healthy lifestyle IS "doing something".  Our immune system is our number one defense against cancer.  Cancer cannot exist in an environment where our immune system is functioning perfectly.  Even Yervoy, when it works, is using the immune system.

                                                                                                      There is a lot of conflicting information out there on what constitutes a "healthy" diet.  My own doctor believes it is not one-size-fits-all but rather that some of us are meat-eaters, some of us more vegetarian and some of us are both.  Wherever you fall on the spectrum, find the cleanest most natural versions of that food as possible (no hormones, antibiotics, pesticides, etc.).  And if you eat animals, make sure those animals ate what they are designed to eat (I.e., cows eat grass, not grains, chickens eat grass, seeds and insects, not corn).  No sugar, flour or processed foods.  There's a lot of junk in our food supply unfortunately.  But also lots of farmers' markets and on-line resources.

                                                                                                      I wish you and your son well.  Best of luck making this difficult choice.

                                                                                                      Maggie

                                                                                                      DZnDef
                                                                                                      Participant

                                                                                                        I'm sorry you've had to find yourself here, mybelle.  It's a good group with lots of different experiences and opinions with the same disease so you'll get a good variety for making a decision.  First, I want to emphasize that there is no right or wrong decision.  Your son needs to do what feels right for him and then hope for the best because nothing is guaranteed.  When it comes to Yervoy, your son will either be a responder or he won't be.  There is no way to know which in advance.  If he is a responder to Yervoy, he will also be a responder later IF he advances to stage IV.  If he is not a responder, then it won't make a difference now or later.  

                                                                                                        For what it's worth, I believe living a healthy lifestyle IS "doing something".  Our immune system is our number one defense against cancer.  Cancer cannot exist in an environment where our immune system is functioning perfectly.  Even Yervoy, when it works, is using the immune system.

                                                                                                        There is a lot of conflicting information out there on what constitutes a "healthy" diet.  My own doctor believes it is not one-size-fits-all but rather that some of us are meat-eaters, some of us more vegetarian and some of us are both.  Wherever you fall on the spectrum, find the cleanest most natural versions of that food as possible (no hormones, antibiotics, pesticides, etc.).  And if you eat animals, make sure those animals ate what they are designed to eat (I.e., cows eat grass, not grains, chickens eat grass, seeds and insects, not corn).  No sugar, flour or processed foods.  There's a lot of junk in our food supply unfortunately.  But also lots of farmers' markets and on-line resources.

                                                                                                        I wish you and your son well.  Best of luck making this difficult choice.

                                                                                                        Maggie

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                                                                                                    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.

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