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


advertisement
Reply
 
Thread Tools Display Modes
Old 05-18-2014, 07:14 PM #31
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Default

Think I should call the Dr tomorrow and tell him? Im just nervous he will think im nuts. That and the receptionist is very rude.
Bruins88 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Hockey (05-18-2014)

advertisement
Old 05-18-2014, 10:14 PM #32
Hockey's Avatar
Hockey Hockey is offline
Magnate
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Hockey Hockey is offline
Magnate
Hockey's Avatar
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Default

Quote:
Originally Posted by SarahSmile0205 View Post
I was reading someplace about seizures today and brain trauma and it said that if you smell odd things that it could mean something larger...

That coupled with the staring and fluid coming out of your ear I wonder if you are not losing some sort of spinal fluid...

Smelling odd things can also be a sign of a stroke..

I am not trying to scare you but just trying to think of things that it could be that when you call the doctor tomorrow you can ask... and they can check off the list..
Yes, absolutely do not hold back with your doctor. Consider writing all this stuff down, so you don't forget it when you're in the examination room. If your wife is available, it might be a good idea to take her with you.

That fluid coming out of your ears alarms me, too.

Good luck and keep us posted.
Hockey is offline   Reply With QuoteReply With Quote
Old 05-19-2014, 06:42 AM #33
SarahSmile0205's Avatar
SarahSmile0205 SarahSmile0205 is offline
Member
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
SarahSmile0205 SarahSmile0205 is offline
Member
SarahSmile0205's Avatar
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
Default

I will try and be nice about this but my dear... you need a new doctor or you need to get firm with the one you have...

If the receptionist is rude... in the nicest way possible explain to her that you are suffering from a TBI and she needs to cut you some slack and listen... If she can't do that then she needs to tell you who to ask for as soon as you call since she has zero compassion for those that are struggling.

As for your doctor... Start by telling him or her that you are just looking for some answers or explanations... Your symptoms are scaring you and those around you and then explain what is has happened. If he brushes you off stay firm on getting all the answers... write them down and check them off as you ask... if you don't get an answer at first, ask again until you get one you understand.

Sorry, unresponsive doctors and rude nurses and office staff upset me A LOT... they do not seem to understand that we need help, that is why we are there... we do not have the answers and need them to help us understand what is going on with us...
__________________
The Start: MVA, t-boned, on 1-12-14 (my sons 5th birthday) and did not think anything of it.. my back hurt on site but everything else seemed ok. Lost about 10-12 hours from about 3 hours after the accident to the next day...Experienced terrible brain fog for over a month, plus intense headaches, nausea, dizziness, cognitive difficulties, disorientation, no short term memory, depression and just an overall hangover feeling daily.

Current Situation: I'm about 7 months in and my local neurologist has waived her white flag and therefore I am headed to Dallas to be seen (I have family there). The headaches are still daily. I have nausea, dizziness as well.

Drugs I have been on- Vicodin (off), Naproxen (off), proanolol (off), topamax (off), cataflam (off), Midrin (off), Flexeril (off) and now Namenda XR (off), Nortrptylin (off), Verapamil (off)

Therapy- Osteopath, Vestibular and balance therapy, fuzion/soft tissue massage, acupuncture

Drs- ER (no help), GP, Chiropractor, Neurologist and Osteopath
SarahSmile0205 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Hockey (05-19-2014)
Old 05-19-2014, 08:56 AM #34
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Default

Ok I called. Dr is not in today but she took a message. I just hope they dont think im nuts because five months later and all of a sudden this new weird thing is starting. Lets hope its not seizures. She said they are also still waiting for work comp to approve therapy
Bruins88 is offline   Reply With QuoteReply With Quote
Old 05-19-2014, 09:07 AM #35
SarahSmile0205's Avatar
SarahSmile0205 SarahSmile0205 is offline
Member
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
SarahSmile0205 SarahSmile0205 is offline
Member
SarahSmile0205's Avatar
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
Default

The weird new thing started because he sent you back to work too early and he pushed you too hard...

Do you have more fluid coming out of your ear than normal? If so, I would almost go to the ER... but that is me and I can get paranoid fast and then anxiety sets in and it goes downhill fast
__________________
The Start: MVA, t-boned, on 1-12-14 (my sons 5th birthday) and did not think anything of it.. my back hurt on site but everything else seemed ok. Lost about 10-12 hours from about 3 hours after the accident to the next day...Experienced terrible brain fog for over a month, plus intense headaches, nausea, dizziness, cognitive difficulties, disorientation, no short term memory, depression and just an overall hangover feeling daily.

Current Situation: I'm about 7 months in and my local neurologist has waived her white flag and therefore I am headed to Dallas to be seen (I have family there). The headaches are still daily. I have nausea, dizziness as well.

Drugs I have been on- Vicodin (off), Naproxen (off), proanolol (off), topamax (off), cataflam (off), Midrin (off), Flexeril (off) and now Namenda XR (off), Nortrptylin (off), Verapamil (off)

Therapy- Osteopath, Vestibular and balance therapy, fuzion/soft tissue massage, acupuncture

Drs- ER (no help), GP, Chiropractor, Neurologist and Osteopath
SarahSmile0205 is offline   Reply With QuoteReply With Quote
Old 05-19-2014, 09:25 AM #36
Hockey's Avatar
Hockey Hockey is offline
Magnate
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Hockey Hockey is offline
Magnate
Hockey's Avatar
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Default

Oh, Kev, if you're wrapped up with Workers' Comp, you're going to have to fight tooth and nail to get proper care. They're all about protecting employers, controlling costs and rushing you back to work.

I know that's the last thing you want to hear, when the injury is robbing you of energy, confidence and initiative. However, you need to know that you will need to advocate - hard - for yourself. Remember, you're worth it.

If you're scared, don't wait around for this doctor. Go to the ER. If nothing else, they'll document the ear fluid.
Hockey is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SarahSmile0205 (05-19-2014)
Old 05-19-2014, 09:25 AM #37
Living_Dazed's Avatar
Living_Dazed Living_Dazed is offline
Member
 
Join Date: Jan 2013
Location: Great Lakes area
Posts: 409
10 yr Member
Living_Dazed Living_Dazed is offline
Member
Living_Dazed's Avatar
 
Join Date: Jan 2013
Location: Great Lakes area
Posts: 409
10 yr Member
Default

I was so clueless when this all happened. No knowledge of brain injuries at all. If you feel comfortable after talking to the neurologist, ask him the same question, or ask the nurse. It's worth a try.

I remember only being able to muster, how long til I'm me again.

That was appointment one.

Same for appt. Two I believe.

My family were able to ask more in depth questions which I was oblivious to.

Have someone with you that can follow the conversation, ask pertinent questions, and remember everything.

Peace and wellness,

Jace
__________________

.


*TBI with mild to severe damage November 2012 from car crash. Stroke with hemorage & 4 clots in veins in brain Feb/Mar 2015.

*Vestibular damage, PCS, hypercusis, severe visual processing and tracking issues, short term memory loss, headaches/migraines, occipital neuralgia, cognitive issues, neurological issues, brain fog, brain fatigue when over stimulated, twitching, vertigo, neck issues, nerve issues, PTSD, personality change, Since stroke left side weakness, rage, worsening of vestibular problems, recall, speech, memory.

*Can't drive or work. Have done occupational therapy, cognitive therapy, physical therapy. Learning work arounds, and strategies to be competent in daily life. Change your attitude/perspective changes your life. As TBI survivors this is a vital part of our healing and living.

*Working on getting to know and accept the new me.
Living_Dazed is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Hockey (05-19-2014)
Old 05-19-2014, 09:30 AM #38
Hockey's Avatar
Hockey Hockey is offline
Magnate
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Hockey Hockey is offline
Magnate
Hockey's Avatar
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Default

Quote:
Originally Posted by kevbo887 View Post
Ok I called. Dr is not in today but she took a message. I just hope they dont think im nuts because five months later and all of a sudden this new weird thing is starting. Lets hope its not seizures. She said they are also still waiting for work comp to approve therapy
I think most TBI patients go through self-doubt. I know I did.

You ARE NOT crazy. If anyone tries to tell you otherwise, get away from them - fast!!!
Hockey is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Living_Dazed (05-19-2014), SarahSmile0205 (05-19-2014)
Old 05-19-2014, 09:33 AM #39
SarahSmile0205's Avatar
SarahSmile0205 SarahSmile0205 is offline
Member
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
SarahSmile0205 SarahSmile0205 is offline
Member
SarahSmile0205's Avatar
 
Join Date: Mar 2014
Location: Carmel, IN
Posts: 467
10 yr Member
Default

Quote:
Originally Posted by Hockey View Post
I think most TBI patients go through self-doubt. I know I did.

You ARE NOT crazy. If anyone tries to tell you otherwise, get away from them - fast!!!
AMEN!!! that is what I meant to say... Someone needs to document the fluid coming from your ear!
__________________
The Start: MVA, t-boned, on 1-12-14 (my sons 5th birthday) and did not think anything of it.. my back hurt on site but everything else seemed ok. Lost about 10-12 hours from about 3 hours after the accident to the next day...Experienced terrible brain fog for over a month, plus intense headaches, nausea, dizziness, cognitive difficulties, disorientation, no short term memory, depression and just an overall hangover feeling daily.

Current Situation: I'm about 7 months in and my local neurologist has waived her white flag and therefore I am headed to Dallas to be seen (I have family there). The headaches are still daily. I have nausea, dizziness as well.

Drugs I have been on- Vicodin (off), Naproxen (off), proanolol (off), topamax (off), cataflam (off), Midrin (off), Flexeril (off) and now Namenda XR (off), Nortrptylin (off), Verapamil (off)

Therapy- Osteopath, Vestibular and balance therapy, fuzion/soft tissue massage, acupuncture

Drs- ER (no help), GP, Chiropractor, Neurologist and Osteopath
SarahSmile0205 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Living_Dazed (05-19-2014)
Old 05-19-2014, 10:20 AM #40
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Bruins88 Bruins88 is offline
Member
 
Join Date: Mar 2014
Posts: 410
10 yr Member
Default

Yah, the ear thing has sort of been addressed and he knows about it after the last appt.

I just came back from my normal physician for an annual checkup. They asked how my head was doing ect ect. I told them about the current thing, and as suggested, asked if maybe it was a seizure going on. The dr said she couldnt give me any advice on it since it was a workmans comp case and they dont do that and I have not been under their care for it. BUT, she did highly recommend that I tell the neurologist about it (which I already had) and demand some sort of MRI to look into it, but thats all she would say on it.

My wife has been researching it too after reading this discussion, and she seems to think I could maybe having them as well. Im still not convinced, nor will I be until the neurologist tells me otherwise.

Also with the workmans comp, yah its a hassle. Especially since I was sent back to work part time and now im back out completely. The dr wants me to do stuff like go for walks and cut my grass (small yard) ect ect. I just feel as though if I do, someones watching and waiting to report me. Obviously I know whats going on in my head and the pain im dealing with, but to the naked eye you would never known unless you tried to hold a conversation with me. Slight paranoia I guess.

The pressure in my head this morning has been huge and im catching myself zoning out now. I sort of seem to know what to look for. I get insanely angry or moody, then Ill do something weird like silently scream or start singing a random song furiously, then I zone out. Im noticing though, im frozen in my gaze with my mouth wide open, but im able to think. Usually I can snap myself out of in about 10 seconds. Those first 10 seconds though its just my voice in my head telling me to snap out of it, then finally im able to. Not really sure whats going on, or if its just really my mind playing tricks on me. Usually after this happens I go lay down. Also, when I do it I notice my hands and wrists get really really weak, like I cant hold them up. So I like to say Im doing a velociraptor and limp wristing it. Weird I know.
Bruins88 is offline   Reply With QuoteReply With Quote
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
Saw a neurologist- mrsmith Traumatic Brain Injury and Post Concussion Syndrome 3 09-29-2013 01:30 PM
How Often Do You See Your Neurologist? Wndswptlady Traumatic Brain Injury and Post Concussion Syndrome 10 09-10-2013 12:48 AM
Need a neurologist for PCS NJ/NY PCSNJ Traumatic Brain Injury and Post Concussion Syndrome 5 05-16-2011 10:08 AM
Neurologist! jaynurse05 Myasthenia Gravis 1 03-10-2009 12:05 PM
Went to a different neurologist paula_w Parkinson's Disease 18 07-19-2008 08:55 PM


All times are GMT -5. The time now is 02:44 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.