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.

MixtaJones

Forum Replies Created

Viewing 5 reply threads
  • Replies
      MixtaJones
      Participant

        Hello Christian,

        Although I wish no one ever had to find this forum I am glad you did. I am fairly new to melanoma (about 5 months) and have found this board very helpful. I would first find out if them can still do a sentinal node byopsy. This will help them tell if it has made it to your lymph nodes. From there they will know a lot more. I would say the most important thing is to ask any and all questions you can think of. If you don't understand there explination ask them to explain it again. Not a lot of doctors are well versed in Melanoma so it is important to get to a melanoma specialist as soon as you can to make sure you know all your options.

        I hope you are one of the lucky ones who caught it early and it was just the mole and has not spread. If not you will find tons of support and information here.

        Best of luck!

        MixtaJones
        Participant

          Hello Christian,

          Although I wish no one ever had to find this forum I am glad you did. I am fairly new to melanoma (about 5 months) and have found this board very helpful. I would first find out if them can still do a sentinal node byopsy. This will help them tell if it has made it to your lymph nodes. From there they will know a lot more. I would say the most important thing is to ask any and all questions you can think of. If you don't understand there explination ask them to explain it again. Not a lot of doctors are well versed in Melanoma so it is important to get to a melanoma specialist as soon as you can to make sure you know all your options.

          I hope you are one of the lucky ones who caught it early and it was just the mole and has not spread. If not you will find tons of support and information here.

          Best of luck!

          MixtaJones
          Participant

            Hello Christian,

            Although I wish no one ever had to find this forum I am glad you did. I am fairly new to melanoma (about 5 months) and have found this board very helpful. I would first find out if them can still do a sentinal node byopsy. This will help them tell if it has made it to your lymph nodes. From there they will know a lot more. I would say the most important thing is to ask any and all questions you can think of. If you don't understand there explination ask them to explain it again. Not a lot of doctors are well versed in Melanoma so it is important to get to a melanoma specialist as soon as you can to make sure you know all your options.

            I hope you are one of the lucky ones who caught it early and it was just the mole and has not spread. If not you will find tons of support and information here.

            Best of luck!

            MixtaJones
            Participant

              Thank you all for the advice and words of wisdom. For those of you who are wondering about why I think I am stage 4 and why things don't add up read below

              My Melanoma backstory is not typical I would assume. the mole that started this was a level 4 on the Clark scale and .97 on the Breslow scale. It was taken out in July by my primary care doctor (AKA Dr. Dumb Ass) and when biopsied it came back Melignant. The doctor thought that since the margins were clear there was nothing to worry about. he did not take out the sugested 1cm margin though. He never did a SND or even checked my lymph nodes.

              8 month later I found a large lump under my arm. After a few doctor that couldn't figure out what it was I ended up at a surgeon to have what was believed to be a cyst removed. He was the one that put everything together and realized it could be Melanoma from the mole removed 8 months prior. After a few tests and a PET scan he realized it was very involved in the Axila. He did surgery and removed everything he could get to but could not get ones in my color bone area.

              Oncologist number 1 said that those nodes are technically a different group and therefore he feels that that would classify me as Stage 4 but not as bad as if it was in other parts of my body. In my mind I am still stage 3C but I see what he means by it being a different group. I also think he wants to clasify me as stage 4 so I have no problem getting medication and posiibly getting into clinical trials.

               

              MixtaJones
              Participant

                Thank you all for the advice and words of wisdom. For those of you who are wondering about why I think I am stage 4 and why things don't add up read below

                My Melanoma backstory is not typical I would assume. the mole that started this was a level 4 on the Clark scale and .97 on the Breslow scale. It was taken out in July by my primary care doctor (AKA Dr. Dumb Ass) and when biopsied it came back Melignant. The doctor thought that since the margins were clear there was nothing to worry about. he did not take out the sugested 1cm margin though. He never did a SND or even checked my lymph nodes.

                8 month later I found a large lump under my arm. After a few doctor that couldn't figure out what it was I ended up at a surgeon to have what was believed to be a cyst removed. He was the one that put everything together and realized it could be Melanoma from the mole removed 8 months prior. After a few tests and a PET scan he realized it was very involved in the Axila. He did surgery and removed everything he could get to but could not get ones in my color bone area.

                Oncologist number 1 said that those nodes are technically a different group and therefore he feels that that would classify me as Stage 4 but not as bad as if it was in other parts of my body. In my mind I am still stage 3C but I see what he means by it being a different group. I also think he wants to clasify me as stage 4 so I have no problem getting medication and posiibly getting into clinical trials.

                 

                MixtaJones
                Participant

                  Thank you all for the advice and words of wisdom. For those of you who are wondering about why I think I am stage 4 and why things don't add up read below

                  My Melanoma backstory is not typical I would assume. the mole that started this was a level 4 on the Clark scale and .97 on the Breslow scale. It was taken out in July by my primary care doctor (AKA Dr. Dumb Ass) and when biopsied it came back Melignant. The doctor thought that since the margins were clear there was nothing to worry about. he did not take out the sugested 1cm margin though. He never did a SND or even checked my lymph nodes.

                  8 month later I found a large lump under my arm. After a few doctor that couldn't figure out what it was I ended up at a surgeon to have what was believed to be a cyst removed. He was the one that put everything together and realized it could be Melanoma from the mole removed 8 months prior. After a few tests and a PET scan he realized it was very involved in the Axila. He did surgery and removed everything he could get to but could not get ones in my color bone area.

                  Oncologist number 1 said that those nodes are technically a different group and therefore he feels that that would classify me as Stage 4 but not as bad as if it was in other parts of my body. In my mind I am still stage 3C but I see what he means by it being a different group. I also think he wants to clasify me as stage 4 so I have no problem getting medication and posiibly getting into clinical trials.

                   

                  MixtaJones
                  Participant

                    Janner,

                     

                    thanks for the response. I guess I sm wondering if this mole was caused by the original one the removed or if it is its own "starting point". All the nodes in that area are removed so it has nowhere close to go. The yervoy was very effective on my so I am hoping it has kept things contained to this small site 

                    MixtaJones
                    Participant

                      Janner,

                       

                      thanks for the response. I guess I sm wondering if this mole was caused by the original one the removed or if it is its own "starting point". All the nodes in that area are removed so it has nowhere close to go. The yervoy was very effective on my so I am hoping it has kept things contained to this small site 

                      MixtaJones
                      Participant

                        Janner,

                         

                        thanks for the response. I guess I sm wondering if this mole was caused by the original one the removed or if it is its own "starting point". All the nodes in that area are removed so it has nowhere close to go. The yervoy was very effective on my so I am hoping it has kept things contained to this small site 

                        MixtaJones
                        Participant

                          I will ask my onc about the supliments affecting tumors. One of the odd things is it was slightly low before I even started yervoy and dropped a bit more after starting it. I am only 30 so age shouldn't be a factor. 

                          MixtaJones
                          Participant

                            I will ask my onc about the supliments affecting tumors. One of the odd things is it was slightly low before I even started yervoy and dropped a bit more after starting it. I am only 30 so age shouldn't be a factor. 

                            MixtaJones
                            Participant

                              I will ask my onc about the supliments affecting tumors. One of the odd things is it was slightly low before I even started yervoy and dropped a bit more after starting it. I am only 30 so age shouldn't be a factor. 

                              MixtaJones
                              Participant

                                I don't focus on this too much but I do have a law suit open against the GP who didn't follow through on the mole. In California the big thing they look at in settlements is if you went from 50% or higher chance of survival to 49% or lower because of the missed diagnosis. If I was stage 3A or higher when the mole was discovered and am now stage 4 it would make a big impact

                                MixtaJones
                                Participant

                                  I don't focus on this too much but I do have a law suit open against the GP who didn't follow through on the mole. In California the big thing they look at in settlements is if you went from 50% or higher chance of survival to 49% or lower because of the missed diagnosis. If I was stage 3A or higher when the mole was discovered and am now stage 4 it would make a big impact

                                  MixtaJones
                                  Participant

                                    I don't focus on this too much but I do have a law suit open against the GP who didn't follow through on the mole. In California the big thing they look at in settlements is if you went from 50% or higher chance of survival to 49% or lower because of the missed diagnosis. If I was stage 3A or higher when the mole was discovered and am now stage 4 it would make a big impact

                                Viewing 5 reply threads
                                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