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.

New normal?

Forums Cutaneous Melanoma Community New normal?

  • Post
    MrG
    Participant
      Hi All,

      I just returned from my 6-month derm appointment and he removed a small 2mm mole from my back. I’ve been going to this derm for over 3 years and religiously a follow up every six months. More often than not, something gets cut out during each visit. So far I’ve had one severely atypical mole which needed to get a WLE and another 4 removed which varied from nothing to moderately atypical. Given the size of the mole, and my history, is this the new normal for me? When do you watch and wait as opposed to biopsy? I didn’t get a chance to ask the derm but as someone who doesn’t have a family history, not a sun worshipper, and is approaching his mid-40s, do I go for mole mapping or just dread the biannual appointment waiting to get something else removed?

    Viewing 0 reply threads
    • Replies
        slholmdahl
        Participant
          You need to have confidence in your doctor. If you feel like he is doing to many biopsies, by all means find a new doctor. I am almost five years out with with bi-annual skin checks and my doctor never has done a biopsy. There are ranges with each doctor. You have to fee comfortable, if you have doubts try a new dermatologist, someone who has some experience with melanoma.
      Viewing 0 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