Having gone thru radiation, 29 treatments, and chemo, 3 infusions for hpv tonsil cancer in 2024, I'd be more concerned about the after effects than 7 weeks in a motel.
I couldn't even take the full 35 radiation sessions due to severe sinus congestion. Toward the end I didn't sleep for week. The mucus was so bad I thought I was going to strangle. To be fair, not everyone experiences that.
I had to have a feeding tube put in prior to treatment. During the next 6 weeks I lost about 40 lbs. I had swallowing therapy and lymphatic massage therapy.
Today, 16 months after treatment I am cancer free but my taste is still altered and my saliva is much reduced. This causes some swallowing problems and requires frequent fluoride treatments to my teeth. Saliva protects them from deterioration.
Proton treatment wasn't available nearby for me but I considered going to Atlanta for two months where it's available. My medical team here put fear into me about delaying the start of my treatment due to potential metastasis so I elected to stay here.
If I had to do it over again, knowing what I know now, I would have elected proton therapy.
I am starting my 6th week of 7/35 proton radiation treatments and what looks like it will be 6 cisplatin infusions. My radiation oncologist is very happy with my response to treatment and so my medical oncologist is happy with stopping at 6 infusions. I am living in a hotel 300+ miles/an hour flight from home. I specifically chose proton after doing extensive research prompted by my local radiation oncologist informing me that he was going to order a prophylactic feeding tube and that with luck, I might be eating by December. He did not tell me about Proton Treatment. In the course of my research I arranged consultations with Mayo, MDAnderson, Florida Proton in Jacksonville, the Maryland Proton Treatment Center, the New York Proton Center in Manhattan and Memorial Sloan Kettering. Not one advised a prophylactic feeding tube. Yes, it is easier to get nutrition when the road gets rough, but swallowing can be impaired and they now have data that points to delayed swallowing difficulties years later with feeding tubes. I understand they can be necessary but my treatment center has other strategies.
Now, I am in the worst part of treatment. I have had minimal trouble with mouthsores. I do have a very raw throat. I do have terrible mucous. I am consuming only liquids like protein shakes. I am not on opiods. I was put on gabapentin in the 2nd week and will need to be weaned off this following treatment. I have no taste, except bad taste. Truthfully, I, unlike many, have had more issues with tolerating the chemo as time has gone by. I am led to believe that recovery will be quicker under Proton. I'll find out soon. I am glad I am getting Proton and would do it again.
By the way, Medicare pays for 80% of Proton Treatment. I hope this helps.