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The MRF is dedicated to improving the lives of people impacted by mucosal melanoma. As you know, mucosal melanoma is a rare form of melanoma. We want to help. Please answer these questions to the best of your ability. Thank you, in advance, for your help!

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* 1. Have you or a loved one been diagnosed with mucosal melanoma?

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* 2. What type of information would have helped you right after your diagnosis?

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* 3. What would have been the best method(s) for you to have received that information?

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* 4. How do you prefer to learn about your diagnosis, treatment options, research advances and supportive resources? Please select all that apply.

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* 5. What resources or information would be helpful to you, at this point?

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* 6. What information would you like to see added to the Mucosal Melanoma page on our website?

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* 7. The MRF hosts 8-10 in-person patient symposia throughout the country each year. Would an event like this that is specific to mucosal melanoma be of interest to you, keeping in mind that you would likely have to travel to attend?

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* 8. Do you currently participate in our Phone Buddy program? If so how do you feel this program has offered support to you? If not, would you be interested in participating in a support group such as this?

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* 9. Do you have any other general comments or feedback?

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