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Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS). |
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08-02-2015, 09:22 AM | #1 | ||
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I've had this for about a year after jarring my head biking. It gets better and worse depending on how much activity I do.
My functional neurologist wants labs done. Should I get them? He says anemia and blood pH imbalances are things he sees a lot. The therapy hadn't made me feel much better. But my pupils are a lot smaller and the same size now. Thanks for any help! |
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08-02-2015, 03:50 PM | #2 | ||
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Legendary
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How often does it happen ?
Do you take niacin supplements ? Anxiety can cause this symptom. There are many different causes. Google 'burning face.' |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-02-2015, 04:06 PM | #3 | |||
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The whole face? burn /stinging or more of warming flush?
Maybe - TMJ??/ jaw pain issues Pinched nerves? Occipital Neuralgia and other Cranial Neuralgias ? - http://neurotalk.psychcentral.com/forum105.html Trigeminal Neuralgia ? - http://neurotalk.psychcentral.com/forum26.html
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-02-2015, 05:50 PM | #4 | ||
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Yes, the whole face, but most intense on the top part. it is warm and sometimes stings when really intense. If it's a neuralgia, thankfully it's not terrible. It is very tolerable, but gets worse when doing lots of activity.
I do take niacin, but this started happening long after i started taking it. It's not anxiety. Thanks for the ideas guys! |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-02-2015, 09:20 PM | #5 | ||
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Quote:
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-02-2015, 10:39 PM | #6 | |||
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Magnate
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People with TBI do sometimes report burning sensations. The issue is most common in female patients between 40-59.
As TBIs are often the result of whiplash, nerve damage, as others have mentioned, could be the problem. Are you taking any medications? |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-03-2015, 10:20 AM | #7 | ||
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It could be nerve related, but I'm not sure. I take abilify.
Sure thing tbi survivor. Send me a private message, but don't be afraid to make your own thread too! More responses. |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-03-2015, 07:17 PM | #8 | ||
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JB,
I don't know about Abilify but ssri's can have tolerance withdrawals that produce similar things in some folk. Bud |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-14-2015, 05:24 PM | #9 | ||
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I had a burning sensation around my left cheek bone (this is where I got hit when I got my concussion) for over two years after my injury. I think it was mostly anxiety-related sensation, but sometimes it would be there even when I wasn't anxious. It eventually subsided and went away.
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12/02/2012 - Light concussion at boxing practice. Ended up having PCS for about 3 months. March 2013 - Thought that since most of my symptoms resolved I could start having fun again. Went snowmobiling once (didn't hit my head) and concussion symptoms returned and got even worse than before. June 2013 - accidentally bumped my head against a deck railing, and had a month-long setback. November 2013 - drove to work after a big snowstorm and the roads were very rough, ended up having another setback. 2014 - Having setbacks after coughing/sneezing too much, or someone slapping me on the back, or any other significant jarring. Feb 2014 - Started seeing Atlas Orthogonal chiro - most helpful doc so far. June 2014 - Two months of physical/visual therapy - no noticeable improvement. September 2014 - Diagnosed with Perilymph Fistula in right ear. November 2014 - Fistula surgery (switched to left ear before the surgery after additional testing). January 2016 - Quit work to "work" on figuring out PCS, so far it seems that eyes/vision issues are the most contributing factor, especially computer work. Current symptoms are: inconsistent sleep patterns, headaches, vertigo/dizziness, anxiety/panic attacks, mental fog/problems with concentration, problems with computer screens. |
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"Thanks for this!" says: | DejaVu (08-15-2015) |
08-15-2015, 08:35 PM | #10 | |||
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Sounds like your functional neurologist has some valid concerns. Why not get the labs done? Is there a barrier to getting them done? Lack of insurance coverage, other concerns that cause you to hesitate? Warmly, DejaVu |
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