Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS).


advertisement
Reply
 
Thread Tools Display Modes
Old 01-31-2013, 11:30 PM #1
MsRriO's Avatar
MsRriO MsRriO is offline
Member
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
MsRriO MsRriO is offline
Member
MsRriO's Avatar
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
Default Seizures?

Anyone have seizures or any type as a complication of concussion or along with other PCS symptoms?

I am going to ANOTHER doctor tomorrow to try to figure this out.

Remember Mark when I said I wake gasping for air (no previous issues before injury) and with throwing ideas around it was brought up that it might be a sleep apnea thing... And apneas can cause seizures while sleeping... I did bring it up to my doctor but it was brushed aside.

Also brushed aside was this: the burnt smell episode was during sleep, about 2 weeks ago. Accompanied by incredible pain and confusion, and later that day extreme exhaustion, troubles getting actual words out (not slurring or stuttering like usual, but actual trouble making sounds), a metal taste in mouth, and a space of 3 hours just unaccounted for, dazed on my couch, felt like 5 minutes.

Ok well another episode last night... This time I woke with my jaw clenched so tight and my eyes open like saucers, drooling out the left side of my mouth... With incredible head and jaw pain. I sat up and couldn't open my mouth and I don't know how long it took before I finally recall getting some water to drink. Metal taste in throat. Had terrible time sleeping with the ache in my jaw. No prior history of jaw clenching or TMJ problems, jaw doesn't make funny sounds, just aches because of that feeling of having a "Charlie horse" cramp.

Today speech was the same as the burnt smell episode. Awful. Also suffered extreme muscular exhaustion so I didn't even get out of bed until 11am though I'd been awake for hours.

Not googling, and not particularly anxious about this. Just wondering if these kinds of episodes have ever happened to anyone here?

Btw I'm on "drug free" recovery thus far, just taking Tylenol.

I'd be glad if doctor would at least do a test but I suspect it will be described and discarded again. I keep living so it's obviously not going to kill me. Lol
__________________
About it: October 26, 2012 I fell backward on an icy parking lot at work. I was on Workers Comp for 9 months. My PCS : everyday headaches became once in a while headaches, and neck pain became manageable. Still have occasional mild dizziness, sometimes fullness in the ears, convergence insufficiency, sequencing struggles, short term memory struggles, verbal processing delays. CT neg, MRI neg. Therapies: prism glasses, acupuncture, icing neck, resting, supplementing, Elavil 20mg at bedtime.

NEW: Completed 12 weeks of physical therapy and returned to work full time.

About me: I'm a marketing manager, a mom with a blended family and wife to a heart attack survivor. I believe my brain injury taught me more than it cost me. I'm grateful to still be me!
MsRriO is offline   Reply With QuoteReply With Quote

advertisement
Old 02-01-2013, 12:24 AM #2
MiaVita2012's Avatar
MiaVita2012 MiaVita2012 is offline
Member
 
Join Date: Dec 2012
Location: N/A
Posts: 685
10 yr Member
MiaVita2012 MiaVita2012 is offline
Member
MiaVita2012's Avatar
 
Join Date: Dec 2012
Location: N/A
Posts: 685
10 yr Member
Default

You know I have lol!The metal burning smells are still trying to be figured out.The seizures I did have post traumatic seizures so I am taking valium.And the jaw yes I went to jaw TMJ MD last April and had too much inflammation so I am going in Few weeks to see what is going to go on with that....before I could not open my mouth and he had to give me steroids and would not see me till after I seen a Neuro....I'll be the lab rat on the jaw thing and let a few people know....but if you could get a MRI of your neck and if there is bulging in C1 or C2...If a cortisone shot is available it will loosen the jaw and face....that is what my physiatrist and physical therapist told me.....
Quote:
Originally Posted by MsRriO View Post
Anyone have seizures or any type as a complication of concussion or along with other PCS symptoms?

I am going to ANOTHER doctor tomorrow to try to figure this out.

Remember Mark when I said I wake gasping for air (no previous issues before injury) and with throwing ideas around it was brought up that it might be a sleep apnea thing... And apneas can cause seizures while sleeping... I did bring it up to my doctor but it was brushed aside.

Also brushed aside was this: the burnt smell episode was during sleep, about 2 weeks ago. Accompanied by incredible pain and confusion, and later that day extreme exhaustion, troubles getting actual words out (not slurring or stuttering like usual, but actual trouble making sounds), a metal taste in mouth, and a space of 3 hours just unaccounted for, dazed on my couch, felt like 5 minutes.

Ok well another episode last night... This time I woke with my jaw clenched so tight and my eyes open like saucers, drooling out the left side of my mouth... With incredible head and jaw pain. I sat up and couldn't open my mouth and I don't know how long it took before I finally recall getting some water to drink. Metal taste in throat. Had terrible time sleeping with the ache in my jaw. No prior history of jaw clenching or TMJ problems, jaw doesn't make funny sounds, just aches because of that feeling of having a "Charlie horse" cramp.

Today speech was the same as the burnt smell episode. Awful. Also suffered extreme muscular exhaustion so I didn't even get out of bed until 11am though I'd been awake for hours.

Not googling, and not particularly anxious about this. Just wondering if these kinds of episodes have ever happened to anyone here?

Btw I'm on "drug free" recovery thus far, just taking Tylenol.

I'd be glad if doctor would at least do a test but I suspect it will be described and discarded again. I keep living so it's obviously not going to kill me. Lol
__________________
What Happened: In 2011 I was in a MVA
.


Symptoms: Physical: I am always cold in any season!!I cannot tolerate anything pressure on my head(sun glasses,hats)longer then a hour,Lock jaw/Displaced TMJ, Dropsey, Hands go numb, Arms go numb, back of head numb (when asleep),Muscle spasms in face & upper body,migraines, concentration headaches, dizziness, nausea, neck and back trauma (from accident), tinnitus, extreme light sensitivity, noise sensitivity, EXTREME fatigue, impaired vestibular system, balance off, Pupils NEVER equal, disrupted sleep cycles,speech problems.

Cognitive: Cognitive Behavior, Brain fog, impulsivity, speech problems, word finding problems, slowed processing speeds, impaired visual memory, impaired complex attention

Emotional: Unable to handle stress or overstimulation without getting extremely irritable or angry, easily overstimulated, MAJOR depression, major anxiety, Panic attacks

Treatment so far: Treatment for PCS,PTSD,Depression & panic,Vestibular therapy, Physical therapy, Vitamin Schedule,Walking,No Dairy, No eggs, No caffeine, No artificial coloring, Sleep with 2 pillows, Very little sugars consumed, Eat healthy,No alcohol, Medications, limit stress and overstimulation.

~*~Learn to treasure yourself and your Divinity. Be willing to accept yourself completely. Be yourself, be graceful, be kind, be wild, be weird ... be true to yourself~*~
MiaVita2012 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
MsRriO (02-01-2013)
Old 02-01-2013, 01:01 AM #3
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,418
15 yr Member
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,418
15 yr Member
Default

MsRrio,

I take gabapentin (Neurontin) before bed to reduce the jaw clenching. I also am very careful with neck position due to C-1 inflammation risks that lead to my Central Sleep Apnea.

Can your husband stay up some night to observe your breathing? My wife did one night and counted my apnea episodes. I stopped breathing 16 times in 1 hour. Most sleep apnea specialists have very little understanding of Central Apnea. The autonomic nerves that control heart beat and breathing are in the C-1 area. When they are compressed by nearby inflammation, the apnea can be a problem.

I have never been able to get a doctor to pay attention to my problems. I have to do my own work at reducing my CSA.
__________________
Mark in Idaho

"Be still and know that I am God" Psalm 46:10
Mark in Idaho is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
MsRriO (02-01-2013)
Old 02-01-2013, 05:04 PM #4
MsRriO's Avatar
MsRriO MsRriO is offline
Member
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
MsRriO MsRriO is offline
Member
MsRriO's Avatar
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
Default

New doc today. Same song.

"Could be migraine aura" .... no attention paid to the sleep apnea thing at all.

How does one learn to cope with being the invisible unheard patient for the rest of time? (Unless I spontaneously heal someday... Lol... Sigh)

__________________
About it: October 26, 2012 I fell backward on an icy parking lot at work. I was on Workers Comp for 9 months. My PCS : everyday headaches became once in a while headaches, and neck pain became manageable. Still have occasional mild dizziness, sometimes fullness in the ears, convergence insufficiency, sequencing struggles, short term memory struggles, verbal processing delays. CT neg, MRI neg. Therapies: prism glasses, acupuncture, icing neck, resting, supplementing, Elavil 20mg at bedtime.

NEW: Completed 12 weeks of physical therapy and returned to work full time.

About me: I'm a marketing manager, a mom with a blended family and wife to a heart attack survivor. I believe my brain injury taught me more than it cost me. I'm grateful to still be me!
MsRriO is offline   Reply With QuoteReply With Quote
Old 02-01-2013, 05:19 PM #5
cyclecrash's Avatar
cyclecrash cyclecrash is offline
Member
 
Join Date: Nov 2012
Location: Ontario, Canada
Posts: 267
10 yr Member
cyclecrash cyclecrash is offline
Member
cyclecrash's Avatar
 
Join Date: Nov 2012
Location: Ontario, Canada
Posts: 267
10 yr Member
Default ugh another bad doc appt....

I know how frustrating it is. I've been through it all before with my fibromyalgia, many doctors with no help or belief, and yet I'm still frustrated every time it happens again! I'm sorry to hear you didn't get any help. It is however quite likely that your last statement is true... you will probably spontaneously heal one day! It probably won't be tomorrow but one day! That, and the help of this wonderful forum will have to be enough to keep us sane!

I hope those events were temporary and you won't have them anymore.

CC
__________________
I'm a 39 year old, female, accountant. On July 2, 2012 I crashed my bike at the end of a 65KM road ride. I was fine that day but woke up the next morning to my current world.

Ongoing symptoms include: dizziness, blurred vision, light and noise sensitivities, cognitive problems, uncontrollable emotions/depression/anxiety, headaches (but they're getting better), mental and physical fatigue, difficulty communicating and sleep disturbances.

Currently seeing a fabulous Neuro Psychologist and vestibular physiotherapist and hoping to soon see a neuro ophthalmologist. I am currently doing 20 minute stationary bike rides daily, 20 minutes of meditating, 15 minutes of Lumosity and lots of resting. I have not been able to work or drive since the accident.

The things that have helped me the most since the accident are vestibular therapy, gel eye drops (for blurred vision, sensitivity and dryness), amitriptyline (10mg), and meditating. I am finally starting to see some slight improvements and am hopeful!

My brain WANTS to heal itself... I just have to let it and stop trying to get better!
cyclecrash is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
MsRriO (02-01-2013)
Old 02-01-2013, 05:46 PM #6
MsRriO's Avatar
MsRriO MsRriO is offline
Member
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
MsRriO MsRriO is offline
Member
MsRriO's Avatar
 
Join Date: Dec 2012
Location: Saskatchewan
Posts: 237
10 yr Member
Default

Thanks cc!

One thing this doctor did say was that I could take Aleve for the pain. Aleve is 220mg naproxen in OTC strength in Canada, for those who don't know.

I've been told up to this point that I could only take Tylenol.

So.... does anyone else take NSAIDs? (Non steroidal anti inflammatory drugs)

Good bad? Ugly? Should I try?
__________________
About it: October 26, 2012 I fell backward on an icy parking lot at work. I was on Workers Comp for 9 months. My PCS : everyday headaches became once in a while headaches, and neck pain became manageable. Still have occasional mild dizziness, sometimes fullness in the ears, convergence insufficiency, sequencing struggles, short term memory struggles, verbal processing delays. CT neg, MRI neg. Therapies: prism glasses, acupuncture, icing neck, resting, supplementing, Elavil 20mg at bedtime.

NEW: Completed 12 weeks of physical therapy and returned to work full time.

About me: I'm a marketing manager, a mom with a blended family and wife to a heart attack survivor. I believe my brain injury taught me more than it cost me. I'm grateful to still be me!
MsRriO is offline   Reply With QuoteReply With Quote
Old 02-01-2013, 06:57 PM #7
rmschaver rmschaver is offline
Member
 
Join Date: Jul 2012
Location: virginia
Posts: 484
10 yr Member
rmschaver rmschaver is offline
Member
 
Join Date: Jul 2012
Location: virginia
Posts: 484
10 yr Member
Default

I take aleve two tabs in morning sometimes two twelve hours later. When headaches or back/neck pain are bad I take oxycodone. BTW I have had seizures at night. I was totally unaware most of the time. My wife witnessed it. Once I woke up with bilateral seizures in my hands and arms. The seizures I had subsided with time so if I am having them I no longer notice. However I have developed a horrendous snoring at times. It wakes both my wife and myself. Pre injury I did not have these issues.
__________________
49, Male Married, PCS since June 2012, headaches, Back pain, neck pain, attention deficit, concentration deficit, processing speed deficit, verbal memory deficit, PTSD, fatigue, tinutitus, tremors.

To see the divine in the moment.
rmschaver is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
MsRriO (02-01-2013), shezbut (02-03-2013)
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Could it be seizures? SpaceCadet Traumatic Brain Injury and Post Concussion Syndrome 5 05-27-2012 10:47 PM
Seizures? daisy.girl Multiple Sclerosis 20 06-12-2010 03:57 PM
seizures babybearcl1421 Children's Health 1 04-04-2009 12:12 PM
seizures and more MrsVal Epilepsy 2 09-28-2008 03:41 PM
Had 2 seizures ... what to do?? Roy Browning Epilepsy 13 01-13-2008 12:15 PM


All times are GMT -5. The time now is 07:17 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.