Merkel Cell Carcinoma: I'd like to hear from others
I am new here, and just last month my mom was diagnosed with Merkel Cell. She had a large tumor on her face. I am looking for the Merkel Cell group to get more information and hear others stories. I know Merkel Cell Carcinoma is a very rare form of skin cancer, so I know there may not be many in the group. Any help would be greatly appreciated!
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Hello @maryluph1953
I was thinking about you and wondering how your appointment went today. Did you get information about your plan for chemo? I hope you feel confident about the treatment plan.
Will you post an update when you have an opportunity?
Hello Mary, I'm Roger, 82 year old male, married 63 years and diagnosed with Merkel in August 2023. It showed up as a purple-colored small sore under my left eye. I had surgery to the left side of my face and the area removed with very little scaring. Merkel cells were found in a lymph node in the cheek so that moved it to Stage Three. I underwent 25 radiation treatments ending January 11th, 2024, and 22 immunotherapy infusions using OPDIVO.
The radiation was not pleasant and resulted in damaged salivary glands and tastes buds still not functioning properly but there has been no spread of the Merkel according to PET scans.
After 22 infusions there were complications that caused fluid buildup in both lungs. Immunotherapy was ceased and I am still undergoing steroid and antibiotic treatment that appears to be improving my breathing and oxygen levels.
There are difficulties in dealing with this rare cancer but the good news is I am still grateful to have life and love and beauty. Every day we have is a gift and there are folks who will go through it with you so you will never be alone.
Let me know if you have any questions.
Sending you hugs.
Thank you for sharing your story. Wishing you many more years! God Bless!