Soreness under jaw
I'm coming up on my 6 month check up post treatment June 27th. Three month PET/CT results were NED. Thank the Lord! A few weeks ago the area under the right side of my jaw started feeling sore to the touch. No noticeable swelling and didn't feel any pearl shaped nodes. I was diagnosed with BOT Stage IV Aug 2017 (now stage I under new staging).
Have any of you had the same type of soreness in that area after treatment? TIA!
Joe
Comments
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Yes, mine finally went away
Yes, mine finally went away after about 16 months post. It was combined with my Lymphedema. As the total swelling went down so did the tightness. I found that my neck stretching exercises helped. Basically it was not impossible, but was annoying. When it all sorted itself out it all happened 'pretty quick' if you discount the +year of minimal progress. It came when I was doing a bunch of walking, doing museums in Europe. I was also on a higher protein diet, lots of sausage, cheese, and eggs. Generally I attribute it to increasing activity, tho I am not sure how a year of things like swimming, tai chi, etc. was not activity. But I had tightness and now I don't, tho I wouldn't bet I'll not see it again.
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Thanks for the reply. IAnotherSurvivor said:Yes, mine finally went away
Yes, mine finally went away after about 16 months post. It was combined with my Lymphedema. As the total swelling went down so did the tightness. I found that my neck stretching exercises helped. Basically it was not impossible, but was annoying. When it all sorted itself out it all happened 'pretty quick' if you discount the +year of minimal progress. It came when I was doing a bunch of walking, doing museums in Europe. I was also on a higher protein diet, lots of sausage, cheese, and eggs. Generally I attribute it to increasing activity, tho I am not sure how a year of things like swimming, tai chi, etc. was not activity. But I had tightness and now I don't, tho I wouldn't bet I'll not see it again.
Thanks for the reply. I experienced lymphedema before my last ENT visit. It went away after a week or so and haven’t experienced it since. I’m hopeful this is the same.
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Edgy
I don't know after you have H&N cancer or any other cancer for that matter you are always
edgy about any pain or unusal feelings in the affected area in general.
And in your body overall sometimes.
We can wait a little but not too long always good to get it checked to make sure.
Blessings to all.
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Edgy... I had a fecal sample
Edgy... I had a fecal sample come back with blood in my stool. I switched from the H&N discussion board to Colorectal, spent two weeks reading up on that cancer. Got the first available GI doc appointment, drank ALL the colonoscopy prep solution, got that done, even saw my primary care for the first time in five years.
False positive, come back in 3 to 5 years.
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Same thing!
Sounds like the exact same thing going on with me.
I'm 9 months post-op for BOT stage IV/stage I under the new staging, 6 months post radiation. About 3-4 weeks ago I noticed this one sore spot under my right chin/back closer to the ear. No swelling (besides the lymphedema, which has been pretty significant), I don't have any lymph nodes left in that area anyway; no pain unless I touch it.
Was at the surgeon's for a checkup Monday, he felt around and didn't feel anything, said not to worry about it. As noted, I've been dealing with lymphedema on this side, and notice that when I do my self-massage that sore spot happens to be the point where I rest my thumb.
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