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.

Miriam Kadosh

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      Miriam Kadosh
      Keymaster
      Thank you, Ed. As a heads up, we are moving up the patient forum to be higher up on the homepage with greater visibility. Additionally, the Patient Forum is linked under [Patient Care] as a dropdown option. If there is any other feedback on how we can continue to make sure this forum is thriving please do reach out to me at education@melanoma.org.
      Miriam Kadosh
      Keymaster
      Thanks, Ed! Would you be able to post in the facebook group for me? send me an email at mkadosh@melanoma.org for more info! Thank you so much!

      Miriam

      Miriam Kadosh
      Keymaster
      Great to hear from you and glad to hear you are doing well! Thank you for sharing your hope!
      Miriam Kadosh
      Keymaster
      Hi! Please get in touch with me as we are happy to help support or host this forum. education@melanoma.org
      Miriam Kadosh
      Keymaster
      General guidance for congenital nevi (CMN) in children: unless there are melanoma specific features or features worrisome for melanoma, we do not recommend prophylactic removal of CMN during childhood or adolescence (or at any time), especially for those of smaller size; The risk of melanoma developing in a small sized, or smaller sized medium CMN is very low, over one’s lifetime, albeit it is no zero. When melanoma does develop, based on the current literature, it is more likely to develop in later decades of life, like the 60’s, and develops at the borders of the lesion, like a typical adult melanoma.
      Most melanomas develop de novo, in general, in fact, meaning from a spot of normal skin and not a mole someone has had all their lives.
      Checking CMN once a year at the PCP is recommended and if there are concerning changes or symptoms, definitely see a dermatologist right away (ideally a pediatric one until he is closer to 18).
      Miriam Kadosh
      Keymaster
      Thank you all for your insights here. We also have a treatment center finder here if you need additional help finding a center near you: https://melanoma.org/treatment-center-finder/

      The MRF will be doing a patient and caregiver symposium with Dr. Hamid on February 7th. If anyone is in the area we would love to have you register and join! Reach out to me at mkadosh@melanoma.org.

      Thanks!

      Miriam

      Miriam Kadosh
      Keymaster
      We are so excited you are joining us, Jenn! @lucas I reached out to you via private message- check it out!
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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.

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