KellyCDM
REGISTER
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.

KellyCDM

Forum Replies Created

Viewing 1 reply thread
  • Replies
      • September 16, 2020 at 3:19 am
      KellyCDM
      Participant
        I guess also I have been worried that maybe this bad unusual nausea could be a sign that the melanoma is spreading.
        • September 16, 2020 at 3:17 am
        KellyCDM
        Participant
          Thank you so much for replying, John. You are so right. I think I have been playing it down but inside I am worried. And maybe the nausea is all the anxiety I am hiding. I think when I get back to work and busy, I won’t have as much time to worry. Also, waiting for results can be frustrating and stressful.
          • August 25, 2020 at 6:06 am
          KellyCDM
          Participant
            Thank you tkoss. I assume you did not have the lymphedema complication then? And because you needed further treatment, the cancer was found in your lymph nodes as a result of the SLNB surgery?
            • August 25, 2020 at 5:59 am
            KellyCDM
            Participant
              I can’t thank you all enough for taking the time to respond to my post. Your answers do ease my mind regarding the necessity of the SLNB. And Celeste, I did peruse your blog, including the very pertinent articles about the procedure and the studies. It is amazing that you gather all that info to make it easier for people like me – confused and a bit scared. Thank you!
          Viewing 1 reply thread
          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.