Melanoma & Skin Cancer support: Introduce yourself and connect
Welcome to the Melanoma & Skin Cancer support group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet others living with skin cancer or caring for someone with skin cancer, including melanoma, basal cell carcinoma (BCC) squamous cell carcinoma (SCC), dermatofibrosarcoma protuberans (DFSP), Merkel cell carcinoma, sebaceous carcinoma, and their treatments. Let's learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
Take these steps to participate in the group:
- Follow the group.
- Browse topics.
- Use the group search to find answers to your questions.
- Introduce yourself.
Pull up a chair and chat. Why not start by introducing yourself? What is your experience, or your loved one’s experience, living with melanoma or skin cancer (i.e., what type, how long since diagnosis, how it’s managed)?
Do you have a question, tip or story to share?
Interested in more discussions like this? Go to the Melanoma & Skin Cancer Support Group.
Connect

@grammato3
The dermatologist and surgeon indicates most of my nose will need to be removed with reconstruction as a forehead flap. According to the surgeon, the surgery will be very challenging and hard and reconstruction and recovery will be long. I am horrified. Is there not any other treatments other than this major surgery?
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2 Reactions@vickiegoins: So to be sure I understand correctly, it's not so much your age that's worrying you, it's the extent and complexity of the surgery and perhaps the cosmetic results that are concerning you, is that it?
As to your question again about alternative treatment, I just need to be sure you understand that this is first and foremost a forum where you can meet others with similar health issues, however, it is not a place to get professional medical advice. We can learn a lot from participants who share their experiences and exchange information with others. We as mentors often post research and documentation from Mayo and other reputable sources to support medical topics, such as the one I referenced earlier that explained how and why malignant melanoma is treated by excision. As a patient myself who went on to have metastatic melanoma, I have been actively involved in organizations dedicated to the treatment of this condition, such as AIM at Melanoma Foundation https://www.aimatmelanoma.org/stages-of-melanoma/stage-i/. To my knowledge, there is no other alternative at this time for initial intervention. (And, I have to add, my immunotherapy for that condition has been successful to date in the two years since it was discovered). However, I need to underscore that I am not a medical provider or an expert in the field.
It's understandable you have concerns. Keeping in mind that time may play a role in not delaying interention too long, have you considered getting a second opinion?
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5 Reactions@vickiegoins Had MOHS performed couple years back on left ear. Took 1 month, 3 visits. Good luck.
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4 Reactions@grammato3 I merely replied duration of my mohs for my melanoma procedure to someone who was opposed to getting a nose flap . There is no choice to get that mohs. Melanoma killed my entire family, now knocking at my door
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5 Reactions@00hjabl72: I'm so sorry to hear about your family's history with melanoma. Years ago, this diagnosis had carried a 10 year survival rate of approximately 5%. These days, the success rate for metastatic melanoma (cases where melanoma has spread to distant organs) has reached or surpassed 50% . For localized melanoma, such as in cases where it's detected on the skin and has not spread and treatment such as Mohs or WLE is performed, the rate of 5 year survival reaches 99%. This does indeed underscore the need for prompt detection and early intervention. In the scheme of things, trading a scar for a cure would tend to be the ultimate goal to achieve, however, it is a major life change and may require the intervention of a therapist to arrive at such acceptance if there is difficulty in coming to this type of conclusion especially if it involves the prospect of mortality.
Did you find it challenging to accept this when you had been given the diagnosis in light of your family history? If so, what steps did you find helpful in moving forward?
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