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


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Old 01-18-2013, 02:15 PM #21
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Default I can relate

This is my first concussion and it is devastating on the body & soul all together....Liar I been called in my search of a over a year for diagnosis! I got very angry and went on a one way ticket to hell....Luckily I stayed alive and free to get off that ticket to finally find one Dr that had a piece of compassion for me....

After I went into numerous Dr offices sounding Drunk (but was sober) and sent home empty handed, no hope, no direction, simply maybe some addictive prescription in hand that I would tear up and flush down toilet.....these Dr's basically were telling me to get back on my impulsive one way ticket being a threat to my soul.

Now in result from this I am emotionally a wreck amongst the long list! "But I suppose to make this positive change to get better" or to make therapies have a better result....

Well I think the hardest part is letting go of all these Dr's that helped me become a worse mess then just a straight diagnosis of a TBI/PCS!

The first thing I have learned in this new life of a month is "If it's not their problem, no one cares" Sad but true reality of life in any kind of situation!!

I am not trying to be a negative Nancy at all....I as well have had a horrible week with this "new"life....But at the end of the day I have to say thank you to all of this support group because we are all humans still and we all can relate to this complex syndrome....I do not know what I would do if I did not find you!

Rio I hope today goes better then before....and be strong to keep fighting with whatever result good or bad....I will be looking for your result post
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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~*~
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Old 01-18-2013, 05:56 PM #22
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Default Results post

Today I saw my usual family doctor as opposed to the one that I've been dealing with from the start, who was quite frankly, a cow. I was under the impression that I had to see the MD that first started the WCB claim. (I am not sure that's true but I get confused) I'm very glad I got to see my regular doctor today.

ANYWAY. My regular doctor remembers how I was versus how I appear now. She said very bluntly, "this is way over my head. You need to see a neurologist and you're off work until those reports come back. Having you get reassessed every 2 weeks is pointless pressure."

So... I guess that's the news. I believe she is referring me to a neurologist, from what I gather. I think that's perhaps progress? Not sure how to feel, I was so overloaded by the bright, crowded, noisy waiting room that I was burnt right out during the appointment. I'm relieved that I don't have to face working at a loud busy casino at least for a little while longer.

Although I want my life back, and my career, I also want to be allowed the best chances to heal to whatever degree is achievable.
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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!
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Old 01-18-2013, 07:33 PM #23
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Default

That sounds like good news! I didn't realize you weren't seeing your normal physician. Having someone that knows you is obviously a big difference! I'll be interested to see how long it takes to see a neurologist. I wonder if workers comp will speed that up at all? You could have a few months of not having to worry about anything and just healing!!

At 1 month my doctor made an appointment with a neurologist and it was for 5 months later!!! I got on a cancellation list and was able to see her the next week... she said then that she doesn't normally see concussion patients until around 6 months so that's why the appt was so long away. She was useless at 1 month as she believed I was going to recover any day. Now it's been 6 1/2 months and I could maybe use her advice more now!

Let us know when you get your neurologist appt. In this case I think you'll be better off if it's a long way off, to give you time to heal worry free from WCB harassment, unless there's symptoms that you think you need her help with.

Thanks for the update. I hope you feel calmer now.

CC
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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!
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Old 01-19-2013, 12:14 AM #24
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Yay!! So good to have someone who has seen the before and after. That really can make all the difference in the world with brain injury. And so nice that you will have longer between assessments, too. Hope that will give you some time to relax and heal!
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mTBI and PCS after sledding accident 1-17-2011

Was experiencing:
Persistent headaches, fatigue, slowed cognitive functions, depression
Symptoms exacerbated by being in a crowd, watching TV, driving, other miscellaneous stress & sensory overload
Sciatica/piriformis syndrome with numbness & loss of reflex


Largely recovered after participating in Nedley Depression Recovery Program March 2012:

.


Eowyn Rides Again: My Journey Back from Concussion

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Old 01-19-2013, 01:19 AM #25
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Good news about your doctor. Hope the neurologist adds something!

Keep on keeping on! It gets better....slowly, but it does!
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