HPV P16 positive cancer
Hello, I am reaching out to see if anyone in this group is diagnosed with HPV P16 positive cancer We have unknown origin and are being treated for head and neck cancer. Anyone else with similiar presenation?.
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@anybody10, the radiation treatments usually begin showing their harsh effects a few weeks ahead of where you are presently at on the timeline. Please read my past entries for experiences and tips. Look up red-light therapy, and buy an inexpensive wand. Begin shining it inside mouth, back of throat, and the outside of neck.
Every day before radiation treatment, I waved the wand around slowly for about ten minutes. Research has shown very positive results on radiated tissue when subjected to this type light. Hang in there!
Did you receive the standard 70 grey of radiation & where did you receive treatment? We are looking for low dose to minimize long term side affects.
My boyfriend freaked out from the mask as well!! His Drs gave him a prescription for Ativan to help him & it worked like a charm! I’m very surprised the Drs won’t help you with this!
You get to see your grandchildren longer.
I finished radiation & chemo treatment (35 rad & 7 wks chemo) Nov. 5, 2021, for HPV-stage 2; surgery not an option. Toughest treatment due to area, stay positive and stick with it.
Was doing very well after treatment from Nov through July, 2022. August began choking on simple sips of water & it progressively got worse, Neck described as "woody"; hard & stiff & reflected inside of throat. Swallow test showed narrowing in a section of esophagus, so had it stretched (Sept 2022) which helped a little. In this brief period of time, my body defense has developed an extreme case of Radiation Fibrosis (scare tissue), making eating a worse challenge than going through treatment. Had throat stretched for 2nd time (Feb, 2023), but not very successful. Doctor suggests doing again but in the hospital vs. his surgery center, where he will have more options; will schedule. Learning I am not alone because some have developed latent scare tissue even many years later. If anyone has Radiation Fibrosis and any other "family" related illnesses, please reply. I also have classic symptoms of scaladerma (Hands, feet & digestive issues) though tested negative for it many times, but my sister has it so it runs on the family.
I received 35 standard radiation treatments in Portland Oregon @ Knight Cancer Center - part of Oregon Health & Science university I also only received two rounds of chemo. I’m now 6 months post treatment and I am feeling better, gaining weight, & cancer free. Some dry mouth from time to time and my taste is off a bit.
Yes I have the exact same thing. I went through 35 radiation treatments. And 5 chemo treatments, both at the same time.
I’ve been done. With treatment for
15 months. But the side effects are still very active.
I had 35 radiation treatments and 5 chemo all at the same time. RDiation was 5 days a week. I’m 15 months out from treatment. But drinking water is the worst ! My saliva is a constant sour taste. I can only drink water that has a powdered flavor in it.
Food is still such a struggle. Sometimes it won’t go down when I swallow. My mouth and esophagus are too dry. I’m wondering by now is this permanent ?
What is the Ativan for ?
It calmed him down to be able to wear the radiation mask & be bolted to the table without panicking. It’s a lifesaver!