Head and neck carcinoma: Anyone get a second opinion at Mayo Clinic?
My wife currently has squamous cell carcinoma in her neck. We have dealing with our doctors for two years and feel now we are going backwards we looking into second opinion is there anyone here that has been treated at Mayo Clinic for a similiar situation and how was it for you.
Interested in more discussions like this? Go to the Head & Neck Cancer Support Group.
Hello @pozwex . As a long time patient of Mayo, I want to recommend that their care is priceless in comparison to local doctors. We have found Mayo costs most reasonable over the years. Sharing your information via video visit is a perfect idea and worth any expense. I also have head and neck cancer ( for over 11 years) and see a wonderful oncologist there, Dr. Katharine Price. We drive 10 hours from Ohio to Rochester,Minnesota and it is worth every minute spent traveling. Best of luck to you. You have a battle ahead, but stay strong and positive to get you through.
How are you doing, @pozwex?
Doing OK. Thanks for asking.
Fortunately, I found 2nd opinions right here in the DFW area so I am no longer seeking a 2nd opinion from the Mayo Clinic. The Mayo Clinic was great and easy to communicate with, but it isn't easy to handle all the issues from 1,000 miles away.
I now have additional "input" that I wanted and we are moving forward.
Thanks to all the people at Mayo that offered assistance. It is appreciated.
pozwex