5 down, 5 to go
I had my 5-year follow-up on Monday and I am as unremarkable as ever. Quite boring, actually. Nothing to report other than I will now visit once a year for he next 5 years. Ongoing side effects are pretty much limited to a little dry mouth/throat, and some neuropathy in the hands and feet. Both of which are easily manageable.
For any and all newcomers to the forum, may your treatments be successful, your side affects minimal, and your life a long and happy journey.
Comments
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Mr. Romano, thanks for sharing the wonderful news. There is nothing better for a cancer patient to hear than Boring, Unremarkable, NED, it's the best. I am so glad you got through this all with very light side effects in the end, you are very blessed. So just keep on enjoying life and I am wishing you forever checkups every year that are just plain boooooooring.
We Celebrate with you
Take care, God Bless-Russ
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ERomanO, I was just curious if your reaching the 5-year mark included any scans? I am about 6 months from 5 years and have been getting scoped. I went from every 3 months to 6 months between scopes last year. I believe after this next scope I will be yearly. Thanks
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That's a good question. I had a PET and CT scan 3 months after finishing my treatments. They told me that those would be the last unless there was cause for more. I also had a chest x-ray every year. Follow-ups, which included a scope each time, were every 3 months for the first 2 years, then every 6 months the last 3 years. During the 6 month intervals I saw my ENT every other visit. A nurse practitioner would do the stop the other times and the ENT would view it and write the report.
It sure seems like it's been a lifetime ago since this all started, so I can only imagine how the members feel that have checked in after 10-15 years.
My life is pretty full, and I like it that way. I play guitar and perform 2-4 times a week, and I go to the gym 2-4 times a week to get some cardio and weightlifting in. As I type I'm having my breakfast and will head out to one of the towpath trailheads and go for a 20 mile bike ride (maybe more if I feel up to it). My girlfriend and I are in the process of purchasing a mobile home in SW Florida for the occasional winter getaway. We'll be going out to southern Utah for a vacay in Sept to visit some National and State Parks.
As I said, I feel very blessed and hope everyone else feels the same. The older we get, the more challenging life gets even without having to deal with the after effects of H&N cancer. Even though my side effects. are minimal, I still have to always have my gabapentin on hand and do my darling fluoride treatments. On top of that, I've lost most of my sight in my right eye from glaucoma, but even that doesn't deter me.
Enough of my rambling. Here's a toast (of coffee) to all the good people of the club that no one wants to belong to. But here we are, getting inspiration from those that have been through the wringer before and keep on going, getting a wealth of knowledge from the articles posted my wbcgaruss, and giving words of encouragement to those who just joined.
Cheers!
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Thanks for the info. I did have a pet and a C/T scan of the chest 3 months after treatments. Since I have had scopes only. They said they would not scan anymore unless there was a reason to. I know different doctors have different protocols that’s what I was asking. Thanks
Good luck, keep on keeping on!
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