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.

Young Adults Diagnosed With Ocular Melanoma

Forums Ocular Melanoma Community Young Adults Diagnosed With Ocular Melanoma

  • Post
    laurenmarie0623
    Participant
    Hi Guys!

    My name is Lauren Marie, and I am currently a 5-year Ocular Melanoma survivor. According to my last scan in January, I am thankfully still cancer-free with no evidence of disease. I was diagnosed in 2016 at the age of 21 and am now 26 years old, working as a behavioral health specialist at a children’s psychiatric hospital.

    I recently started a support group for young adults who have been diagnosed with OM. I started the group a few years ago after searching on various support websites and realizing that it is very uncommon to find someone in their late teens, ’20s, or 30’s diagnosed with this. I created two groups: one on Facebook and the other through a text message group. We will occasionally get together through facetime or zoom to chat with everyone and see how they are doing and give support if needed. If you are a patient or know someone in this age group who wants to join, please have them reach out to me by email or send me a message on Facebook. I am excited to get to know anyone who decides to join the group :)

    I hope everyone on this forum is doing well and never forget to keep fighting and always keep your spirits up :)

    If you would like to reach out via email: [email protected].

    Loading spinner
  • 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.