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.

Samroberts4

Forum Replies Created

Viewing 2 reply threads
  • Replies
      Samroberts4
      Participant

        First of all, thanks so much for all of your mindful comments and support.  To update you on my condition, I have a 6 mm deep melanoma and am in stage IIb.  The mitotic rate was high, although I don't remember the exact figure because the doctor was hitting me with a barriage of negative information at a faster rate than I was able to absorb it. The margins were also wide.  Yesterday, the plastic surgeon cut out a large chunk from the side of my right bicep, which required him to graft a significant amount of skin from my right quadricep to patch the wound.  He also did a sentinel-node biopsy to see if the melonoma has reached the lymph nodes in my armpit.  I am on pins and needles waiting for the result, which will come tomorrow or Friday.  However, three things cause me to remain hopeful: a manual check by the doctor revealed no lumps or swelling under the armpit; the alkaline phosphatese test indcated normal levels; and the LDH were normal, meaning that cancer has proabably not spread to other organs.

        I elected to go with a plastic surgeon because he worked primarily on melonoma for ten years when he was in New York and Philly.  When he was in upstate New York, he was the only doctor who worked on melanoma cases within a 60-mile radius, which comprised 60% of his cases.  I also live in Montana, where we aren't exactly close to melonoma specialists, and the doctor felt at the rate the tumor was growing, I needed to act fast.  I don't know if it's because melonoma comprises such a small amount of cancers, but when my doctor took a proactive approach to seek out oncologists who could treat melonoma in the event it is found in the lymph nodes, nobody in Missoula, MT. was comfortable treating it. My doctor said he contacted his friend from med school who lives in Kalispel, and he has quite a bit of experience in lymph-node dissection, which is a bridge I hope I don't have to cross.

        I'll let you all know how things turn out in a couple of days. In the meantime, I will be taking percocet, tramadol, heaps of antibiotics, and sponge baths.  On the bright side, I'm glad that my arm is so heavily bandanged that I don't have to see the giant hole that I know is there. If you all have any thoughts on where I'm at, or what my next step should be in the event that the lymph nodes are involved, I look forward to reading them.

          Samroberts4
          Participant

            P.S. the melanoma is not ulcerated, which is another good sign.

            Samroberts4
            Participant

              P.S. the melanoma is not ulcerated, which is another good sign.

              Samroberts4
              Participant

                P.S. the melanoma is not ulcerated, which is another good sign.

              Samroberts4
              Participant

                First of all, thanks so much for all of your mindful comments and support.  To update you on my condition, I have a 6 mm deep melanoma and am in stage IIb.  The mitotic rate was high, although I don't remember the exact figure because the doctor was hitting me with a barriage of negative information at a faster rate than I was able to absorb it. The margins were also wide.  Yesterday, the plastic surgeon cut out a large chunk from the side of my right bicep, which required him to graft a significant amount of skin from my right quadricep to patch the wound.  He also did a sentinel-node biopsy to see if the melonoma has reached the lymph nodes in my armpit.  I am on pins and needles waiting for the result, which will come tomorrow or Friday.  However, three things cause me to remain hopeful: a manual check by the doctor revealed no lumps or swelling under the armpit; the alkaline phosphatese test indcated normal levels; and the LDH were normal, meaning that cancer has proabably not spread to other organs.

                I elected to go with a plastic surgeon because he worked primarily on melonoma for ten years when he was in New York and Philly.  When he was in upstate New York, he was the only doctor who worked on melanoma cases within a 60-mile radius, which comprised 60% of his cases.  I also live in Montana, where we aren't exactly close to melonoma specialists, and the doctor felt at the rate the tumor was growing, I needed to act fast.  I don't know if it's because melonoma comprises such a small amount of cancers, but when my doctor took a proactive approach to seek out oncologists who could treat melonoma in the event it is found in the lymph nodes, nobody in Missoula, MT. was comfortable treating it. My doctor said he contacted his friend from med school who lives in Kalispel, and he has quite a bit of experience in lymph-node dissection, which is a bridge I hope I don't have to cross.

                I'll let you all know how things turn out in a couple of days. In the meantime, I will be taking percocet, tramadol, heaps of antibiotics, and sponge baths.  On the bright side, I'm glad that my arm is so heavily bandanged that I don't have to see the giant hole that I know is there. If you all have any thoughts on where I'm at, or what my next step should be in the event that the lymph nodes are involved, I look forward to reading them.

                Samroberts4
                Participant

                  First of all, thanks so much for all of your mindful comments and support.  To update you on my condition, I have a 6 mm deep melanoma and am in stage IIb.  The mitotic rate was high, although I don't remember the exact figure because the doctor was hitting me with a barriage of negative information at a faster rate than I was able to absorb it. The margins were also wide.  Yesterday, the plastic surgeon cut out a large chunk from the side of my right bicep, which required him to graft a significant amount of skin from my right quadricep to patch the wound.  He also did a sentinel-node biopsy to see if the melonoma has reached the lymph nodes in my armpit.  I am on pins and needles waiting for the result, which will come tomorrow or Friday.  However, three things cause me to remain hopeful: a manual check by the doctor revealed no lumps or swelling under the armpit; the alkaline phosphatese test indcated normal levels; and the LDH were normal, meaning that cancer has proabably not spread to other organs.

                  I elected to go with a plastic surgeon because he worked primarily on melonoma for ten years when he was in New York and Philly.  When he was in upstate New York, he was the only doctor who worked on melanoma cases within a 60-mile radius, which comprised 60% of his cases.  I also live in Montana, where we aren't exactly close to melonoma specialists, and the doctor felt at the rate the tumor was growing, I needed to act fast.  I don't know if it's because melonoma comprises such a small amount of cancers, but when my doctor took a proactive approach to seek out oncologists who could treat melonoma in the event it is found in the lymph nodes, nobody in Missoula, MT. was comfortable treating it. My doctor said he contacted his friend from med school who lives in Kalispel, and he has quite a bit of experience in lymph-node dissection, which is a bridge I hope I don't have to cross.

                  I'll let you all know how things turn out in a couple of days. In the meantime, I will be taking percocet, tramadol, heaps of antibiotics, and sponge baths.  On the bright side, I'm glad that my arm is so heavily bandanged that I don't have to see the giant hole that I know is there. If you all have any thoughts on where I'm at, or what my next step should be in the event that the lymph nodes are involved, I look forward to reading them.

                  Samroberts4
                  Participant

                    Thanks, Mark. To answer your question, my tumor was not ulcerated and was on the right  side of my arm where the bicep meets the tricep.  The doctor felt that the reason the tumor did not spread was due to the lack of ulceration.  I think you're right about the depth of skin in the heel aiding in the lack of spread, even if the tumor was not ulcerated, which was apprently the case with yours. 

                    I'm so happy that we were both able to get past this dreaded disease. Take care and stay NED forever!

                    Cheers,

                    Sam

                    Samroberts4
                    Participant

                      Thanks, Mark. To answer your question, my tumor was not ulcerated and was on the right  side of my arm where the bicep meets the tricep.  The doctor felt that the reason the tumor did not spread was due to the lack of ulceration.  I think you're right about the depth of skin in the heel aiding in the lack of spread, even if the tumor was not ulcerated, which was apprently the case with yours. 

                      I'm so happy that we were both able to get past this dreaded disease. Take care and stay NED forever!

                      Cheers,

                      Sam

                      Samroberts4
                      Participant

                        Thanks, Mark. To answer your question, my tumor was not ulcerated and was on the right  side of my arm where the bicep meets the tricep.  The doctor felt that the reason the tumor did not spread was due to the lack of ulceration.  I think you're right about the depth of skin in the heel aiding in the lack of spread, even if the tumor was not ulcerated, which was apprently the case with yours. 

                        I'm so happy that we were both able to get past this dreaded disease. Take care and stay NED forever!

                        Cheers,

                        Sam

                    Viewing 2 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