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.

Recovery from lymph node dissection?

Forums Cutaneous Melanoma Community Recovery from lymph node dissection?

  • Post
    Christine.P
    Participant

    I recently had two malignant melanomas removed, a SLN biopsy in my right groin, and what turned out to be a full dissection of the lymph nodes under my left arm. This was intended to be a biopsy as well, but as soon as they got in, they could see the cancer had spread. In addition, the melanoma on my leg was large and deep enough that I needed a skin graft. I am currently stage 3 but waiting to do an MRI and PET scan once I heal more from the surgeries

    My question is this. How have others who have had the full dissection under an arm recover from it? My arm is part numb and part "prickly" – as if my arm was asleep and is waking up to pins and needles. The surgeou says it "might" get better – but it may not. It drives me crazy

    Is there somethng I can do to ease the discomfort of the numbness and tingling? . 

Viewing 11 reply threads
  • Replies
      mrsaxde
      Participant

      The entire back of my left arm as well as my armpit has been numb since my lymph node dissection. I just have kind of gotten used to it.

      mrsaxde
      Participant

      The entire back of my left arm as well as my armpit has been numb since my lymph node dissection. I just have kind of gotten used to it.

      mrsaxde
      Participant

      The entire back of my left arm as well as my armpit has been numb since my lymph node dissection. I just have kind of gotten used to it.

      dfeng
      Participant

      I had many surgeries before, there were always something different after. Some slowly went away and some of them, unfortunately, became permanent.

      Try not focus on the discomfort, your body will tune it for you.

      Best wishes. 

      dfeng
      Participant

      I had many surgeries before, there were always something different after. Some slowly went away and some of them, unfortunately, became permanent.

      Try not focus on the discomfort, your body will tune it for you.

      Best wishes. 

      dfeng
      Participant

      I had many surgeries before, there were always something different after. Some slowly went away and some of them, unfortunately, became permanent.

      Try not focus on the discomfort, your body will tune it for you.

      Best wishes. 

      mjanssentx
      Participant

      Christine – I am 10 months after full dissection and still have pain.  The pain was actually pretty modest (except for the 8 weeks with the drain tube) for the for first several months…hardly felt anything around the surgery site.  

      The pain actually increased as I recovered around the dissection area.  (the actual melanoma site gives me no pain…just a 5-6 inch battle scar)  I now have increased feeling (but not normal in much of the dissection surgery site periphery out to 5-8 inches) but that is a double edged sword in that I now have more pain albeit it is now more localized to about 3-4 inches.  I also suspect that a relatively minor case of lymphodema is playing a part as well.

      To be honest…once you reconcile that the feeling will never be the same…you get focused on the treatment side affects and the implications of the scans etc. and the pain at the surgery site becomes a rather minor but annoying inconvenience.

      BTW…once you get the tube out they will give you stretching exercises.  DO THEM…they are simple (maybe 3-4 minutes) and they help immensily with the pain…much more so than OTC pain meds even 10 months later. 

      Best wishes

      Michel

      mjanssentx
      Participant

      Christine – I am 10 months after full dissection and still have pain.  The pain was actually pretty modest (except for the 8 weeks with the drain tube) for the for first several months…hardly felt anything around the surgery site.  

      The pain actually increased as I recovered around the dissection area.  (the actual melanoma site gives me no pain…just a 5-6 inch battle scar)  I now have increased feeling (but not normal in much of the dissection surgery site periphery out to 5-8 inches) but that is a double edged sword in that I now have more pain albeit it is now more localized to about 3-4 inches.  I also suspect that a relatively minor case of lymphodema is playing a part as well.

      To be honest…once you reconcile that the feeling will never be the same…you get focused on the treatment side affects and the implications of the scans etc. and the pain at the surgery site becomes a rather minor but annoying inconvenience.

      BTW…once you get the tube out they will give you stretching exercises.  DO THEM…they are simple (maybe 3-4 minutes) and they help immensily with the pain…much more so than OTC pain meds even 10 months later. 

      Best wishes

      Michel

      mjanssentx
      Participant

      Christine – I am 10 months after full dissection and still have pain.  The pain was actually pretty modest (except for the 8 weeks with the drain tube) for the for first several months…hardly felt anything around the surgery site.  

      The pain actually increased as I recovered around the dissection area.  (the actual melanoma site gives me no pain…just a 5-6 inch battle scar)  I now have increased feeling (but not normal in much of the dissection surgery site periphery out to 5-8 inches) but that is a double edged sword in that I now have more pain albeit it is now more localized to about 3-4 inches.  I also suspect that a relatively minor case of lymphodema is playing a part as well.

      To be honest…once you reconcile that the feeling will never be the same…you get focused on the treatment side affects and the implications of the scans etc. and the pain at the surgery site becomes a rather minor but annoying inconvenience.

      BTW…once you get the tube out they will give you stretching exercises.  DO THEM…they are simple (maybe 3-4 minutes) and they help immensily with the pain…much more so than OTC pain meds even 10 months later. 

      Best wishes

      Michel

      washoegal
      Participant

      Christine,

      Sorry to hear this.  The pain will probably get better.  I think I have had All possible side effects from a CLND and while none fun all can be coped with.  My pain was from a damaged nerve, and yes they do heal themselves (or try to). 6 years later,  I still have occasional sharp pains for no apparent reason but that's a pretty minor annoyance. 

      What you really need to watch for is lymphedema.  If you didn't get a RX for massage therapy already get one next time you see your surgeon.  As soon as you feel a swelling get to a masseuse that specializes in lymphedema.  Also get fitted for a sleeve.  Don't wait on either of these, if it gets out of control it can be a pain but managed early it really isn't bad.

       

      Good Luck,

      Mary

      washoegal
      Participant

      Christine,

      Sorry to hear this.  The pain will probably get better.  I think I have had All possible side effects from a CLND and while none fun all can be coped with.  My pain was from a damaged nerve, and yes they do heal themselves (or try to). 6 years later,  I still have occasional sharp pains for no apparent reason but that's a pretty minor annoyance. 

      What you really need to watch for is lymphedema.  If you didn't get a RX for massage therapy already get one next time you see your surgeon.  As soon as you feel a swelling get to a masseuse that specializes in lymphedema.  Also get fitted for a sleeve.  Don't wait on either of these, if it gets out of control it can be a pain but managed early it really isn't bad.

       

      Good Luck,

      Mary

        Marianne quinn
        Participant

        My husband had the same experience. He saw a lympedema physical therapist who ordered a compression sleeve for him. He is a lot more comfortable and his edema is reduced.,ask your doctor for a physical therapy consult.

        Marianne quinn
        Participant

        My husband had the same experience. He saw a lympedema physical therapist who ordered a compression sleeve for him. He is a lot more comfortable and his edema is reduced.,ask your doctor for a physical therapy consult.

        Marianne quinn
        Participant

        My husband had the same experience. He saw a lympedema physical therapist who ordered a compression sleeve for him. He is a lot more comfortable and his edema is reduced.,ask your doctor for a physical therapy consult.

      washoegal
      Participant

      Christine,

      Sorry to hear this.  The pain will probably get better.  I think I have had All possible side effects from a CLND and while none fun all can be coped with.  My pain was from a damaged nerve, and yes they do heal themselves (or try to). 6 years later,  I still have occasional sharp pains for no apparent reason but that's a pretty minor annoyance. 

      What you really need to watch for is lymphedema.  If you didn't get a RX for massage therapy already get one next time you see your surgeon.  As soon as you feel a swelling get to a masseuse that specializes in lymphedema.  Also get fitted for a sleeve.  Don't wait on either of these, if it gets out of control it can be a pain but managed early it really isn't bad.

       

      Good Luck,

      Mary

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