Nerve damage effecting tongue, muscle, swallowing.
Hello, Back in 2015 /2016 I had tonsil cancer after going though chemo & radiation. (I'm cancer free :)) but I do have nerve damage from the first time I had radiation 🙁 my hold body is affected. My neurologist explain to me, it's like a extension cord the treatment I had went through all the protective layers of the ext. cord. How I explain this is like you body is a sleeping fleeing, like your foots or arm is a sleep and you shake to wake it up. My question is now after 7 yrs or so the nerve damage is now effecting my speech, nerves in tongue and the muscle in swallowing. Please has anyone going though this ?
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@lilypilly I have been thinking about getting one. Eating when I’m alone is dangerous!
Have you had to use it?
Jody
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1 Reaction@mojo244 Hi Jody...luckily I have not needed to use.
I do fell better knowing it's available.
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3 Reactions@cskippy
Hey Skippy, Wow you've got a lot going on, as a cancer patient I think we all do and share an experience or better said a journey. Skip I would Like to ask you if you did get to go thru your Electrical Stimulation Acupuncture therapy and to know if it helped you in anyway? I might have this as an option to assist with my pain but I don't know. If so would you recommend? would like to hear from you and hope things are coming along. Thank You.Stephin001
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1 Reaction@stephin001, welcome. What type of head and neck cancer do you have? Have you completed treatments?
Hi,
I am sorry to hear about your challenges. I am about 2 1/2 years out from my treatment, and the symptoms you described I started to get about 18 months after my treatments. I also experience my hands turning blue and brain fog. I have dysphagia, and I have noticed how tired I am/inflammation, and a correlation to my swallowing and speech.
I have tried multiple things, such as acupuncture, compression, and an anti-inflammatory diet, to help manage the neuropathy.
Please feel free to DM me if you would like to discuss.
Best,
Eric
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1 ReactionHello Eric I read your response and even if it was not for me I felt I needed to reach out. I am 18 months out of diagnosis and 15 months post treatment. I have 35 radiation and 3 chemo.
So far I have improved a great deal but still dealing with many issues.
I am unable to swollow without some water or liquid to chase. I suffer greatly from dry mouth and my tongue is still swollen.
Any advice at all as to what may help? I wear a compression mask for neck/throat lymphedema with regular massage.
I use xylitol for dryness and also a dry mouth spray.
However I am so frustrated and just looking for some normalcy in life. Thank you Allison
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4 Reactions@lilypilly have you tried a mouthwash for dry mouth? Manuka honey helps with some symptoms. What type of compression mask do you use?
@hrhwilliam Thank you for sharing your experience and for so many suggestions. I and many others here look to you for support . We are lucky that you help us so much.
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1 Reaction@lizzyj58 yes....I have tried all of it. Manuka....mints...mouthwash...gum...pickles to mention a few.
Nothing seem to help. Nights are really horrible.
I have a custom compression mask. However it does control the swelling a bit. Still swollen when I wake up. Thank you
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1 Reaction@lilypilly I'm so sorry you are going through all this !
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