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Wednesday, 20 June 2012

Anger


Many specialists will wade in on this issue with confusing double talk that might explain it but could simply confuse the hell out of you and leave you more enraged.  I made issue with the show “Golden Girls” and Stella back in my signs and symptoms section for a reason.  It is now common knowledge amongst the scholars that the last part of the brain to develop and often the first part of the brain to go as we age, is located in the frontal region.  This part is responsible for many things, behavior being one and another is planning.  We often wonder why our children act brain dead and take such dangerous risks that could kill them and the reason is that the wires have not fully developed where they start to take stock in the right and wrong of any given situation.  An example is staying out late on the dangerous streets at night because it is cool or skate boarding without helmets and making the bold statement that it’s my body and if I want to do it then I will.  They do not factor in that if they fall on their head and become incapacitated then society, the distraught parents pay the ultimate price by having to care for them forever.  They do not factor in the cost to their parents, of possibly wiping out their savings and retirement all for the selfish reason of it’s my body and I’ll do with it what I want.  This is normal behavior and fortunately it too does pass and as parents we give a big sigh of relief if they along with us survive until those neurons finally connect and a decent young adult emerges.
            Now think about this for a moment.  If you were to meet me I would look like an average guy.  There are no telltale signs that I am brain injured.  Most psychologists would aptly diagnose my anger as easily managed with some basic coping skills.  If he was not aware of my previous brain injury he would apply the same treatment on me as he would a non-brain injured individual and that would be his first mistake.
            My anger is not an issue that comes from the norm of a bad upbringing where I was beaten but rather because the pathways that once led to my frontal brain have been altered or completely severed.  Many problems are happening simultaneously to a brain injured person and the caregiver needs to fully appreciate this.  Those coping skills of life have to be re-introduced and rewired in many cases.  The time it takes a non-injured person to learn new coping skills will be a great deal shorter than that of a brain injured.  It is a Pandora’s Box of emotions from crying, to depression, to despair, to elation and of course anger.  All of which need to be addressed and it is no easy task.  One cannot separate anger from the rest of the issues.  Anger is a result of the many internal problems that a brain injured is facing.  He/she is angry because they recognize that they cannot speak properly, can’t find the words quickly enough, forget constantly, their balance is lost and the list goes on.  The caregiver has no coping skills to deal with this scenario and may accidentally remark, why can’t you remember and that triggers an anger outburst the likes you’ve never seen before.
            My point is this, the brain injury and anger is very complex.  One cannot separate anger without identifying all the triggers that bring on the outburst in the first place.  This will take months of testing and rehabilitation.  We have to rebuild the pathways and re-educate the brain injured so that he/she has an understanding of what the triggers are and how to better deal with them.  It is imperative that the care giver learn as much about the brain injury as possible if they are to survive this ordeal in tact.  You will employ the same techniques for dealing with the brain injured as for the non-injured however if the instructor is not familiar with brain injury he or she may alienate the TBI patient.  Remember the TBI survivor may be dealing with memory issues or permanent damage to the frontal lobe.  The anger may not be easily controlled as a result and therapy may take many months and not just a weekend retreat that might be prescribed for non injured counterparts.

Wednesday, 13 June 2012

Half Full is a great starting place

I may have been hard hitting in my last blog with regards to fellow TBI survivors who feel they can make it on their own.
Allow me to clarify my position for you.
In life we do not get to where we are without feedback and help.  We start with our parents guiding us, enrolling us in sports, school, music and from there we begin to network.
We gain employment through our efforts and referrals.
From those referrals we learn of better career choices and climb the ladder of success.
We also have setbacks along the way from scraped knees to broken hearts and someone is always there to help us back onto our feet.
Why should we think it should be any different when we are suddenly brain injured?
After the brain injury it should not matter why or whose fault it was but rather how we can overcome and what resources will we need to tap into to ensure the best outcome for me.
Why in your time of your greatest need would you abandon all that have used in the past, your networking skills, and choose to go it alone?
Yes, it is a new endeavor and yes it is frightening or even embarrassing to admit you need help from the last place you thought you would ever be, however it is a resource and you will benefit.
Let's face it, brain injury will conjure up the "One Flew Over The Cuckoo's Nest" mentality in some less educated people.
Mental health in general has some pretty negative overtones that can frighten some people.  This is born from a lack of understanding.  Some friends may abandon you out of this reason.  Not to worry because throughout life you will gain some friends and lose others. Why would you think it would be any different now?
The new friends will understand your needs and stand by you rather than toss your aside.
You are not a freak show.  You are simply brain injured.  You may have speech, memory or mobility issue but you are still you and are desperately important to your family so you owe it to them and moreover to yourself to at least give it your all.
It is in the end, a new career choice, fraught with all the uncertainties, like riding the bike for the first time or the new job or getting your driver's licence.  Look at it like it is, a challenge, one you will overcome, and most important it is one you will master to the best of your ability.
Is your cup half full?
It is incumbent on you to see that it is because so much is riding on your recovery and your loved ones are counting on you to have great hope for the future like you did before the accident took place.

Sunday, 10 June 2012

Help! I have a TBI!

The sooner you can get help for your TBI survivor the better.  I have rarely met a survivor who jumps at the opportunity to join or attend a Brain Injury Group.  Ego being the mother of missed opportunity, will cause your loved one, time when it comes to recovery.

If he, and I mean he because 9 out of 10 times it is the male who will argue, I am not as bad as them why do I need to attend?
This bravado is a defense mechanism.  I actually joined in hopes to help other survivors because it had been 15 years since I had been injured.
To my surprise I learned more about myself in the process and enjoyed my time so much I eventually became President of our Brain Injury Society.
It offers support for the caregivers and lets you know that you are not alone.  The society will also have resources both locally and provincially or state wide, that you can tap into.
Things like attorney's who specialize in brain injury.
Why do I need an attorney trained in TBI?
Some lawyers will settle a case from an MVA, and state that the person will be healed up in 2 years and so you are compensated for 2 years and no clause for long term disability was considered.
What if scar tissue builds up and another surgery is required?

So help is most crucial at every turn.

I found that it was so nice to attend a group where I could contribute to with suggestions like the ones on this blog and in turn receive suggestions that might just work for me.
Yes there are people in the group that are far more injured than yourself and there are those who are less affected. The great thing is you will feel like you belong.  It is a place where we don't mind if you stutter, have mobility issues or anger issues.
The mere fact that when you arrive you are accepted as is, will make you feel at peace.  You don't have to explain yourself each and every time you forget. It's understood.

For the caregiver, it will be a place to network and a shoulder when things get tough.  Our group has assisted from giving food and clothing to getting the right medical assistance for you or your loved one.

If there is not a group in your town then check online to see where one is.  You might even decide to start one.
Ours started out of a home with a handful of people and now has hundreds of clients and is partially funded by the provincial government.  The only thing I can warn you about is that when you decide to start one get ready to be overwhelmed by how many respond.

What if my TBI survivor refuses to attend?

Well there is nothing from stopping you.
Second:  Get him to read this page.
MY SPECIA;L NOTE TO MR. TBI.

I like you are brain injured.  You have everything to gain and nothing to lose by attending your local brain injury support group.  If you truly want to heal, have a productive life, not lose your wife, avoid the 90 percent divorce rate that your fellow brain injured survivors enjoy, then if that is nothing for you to lose continue on with your head in the sand and have a great life.
If you can appreciate the fact that your wife is standing by you trying to help you back on your feet, don't you think you owe her a little respect for all she is sacrificing for you?
Don't hesitate and Join today! It may just save your marriage let alone your life.

Did you know that now that you have suffered from a brain injury you are twice likely to suffer a second before someone suffers their first?  Lets keep it to one and learn how to cope.

Thursday, 7 June 2012

Brain Injury...Forever....

The title sounds like a death sentence, but in fact it doesn't have to be.  It is a matter of is your cup half empty or half full?
Obviously there will be many challenges and there will be many triumphs along the way.  Here is my question to you, Does this last sentence define life itself?   We all have challenges we must overcome.  We all have moments of great elation and those all come with a dose of cold hard reality that sometimes have us gasping for a reprieve and then the cycle repeats itself.
I stated in previous writings, that is is how we train our brains to keep our expectations in check that help us mitigate the more challenging moments in our life.  If we set the expectation bar just a little lower then obviously the reaction to not meeting that expectation will be easier to accept.
We have to build up our tool box of coping skills.  In the last blog I mentioned this along with anger management being one of those benefits along with accepting your new limitations.

It is not to say that your limitations will be permanent because there will be healing over the first couple of years.  Re-assessment is crucial as you travel the path of recovery.
I couldn't write a full sentence back in 1977, however I now have overcome that obstacle.  Most of my writing skills returned after the initial surgery along with my spelling.  The part that has remained a challenge is my short term memory which I can say without any hesitation is permanently damaged.
My recall of memory is also challenged and some days I remember or recall an event or a name immediately and on other days it is a write-off.
Yesterday started like any other for me.  I got up at 5am tinkered around the house and while I was shaving heard the phone ring.  When I went to see who called I realized it was the Physio Therapy office informing me that I had missed that morning's appointment.  I called them and was raked over the coals because this was the second time in a row that I had forgotten.  What they do not appreciate or understand and I forgive them for it, is this is normal fare, for me.  It is a new event.  I suck at new events because they are not a part of my daily routine.
I had forgotten to add the appointment into my cell phone calendar and was not warned at a timely manner as I usually am.
I left there and got home.  I took my truck to the repair shop and my wife and I walked the dogs, grocery shopped and returned home.  I had an appointment with my boss and went to the meeting that ran a little over and though my alarm sounded about my new afternoon appointment I ended up being about 8 minutes late.  Again I was scolded by the Therapy staff.
I left and went home for a nap as my brain was on overload.
I awoke and decided to go to the store.  I got to the store and low and behold my wallet was back at home.
I usually place it in my hat when I nap and when I got home I realized my hat was still at the physio office.
This explained why I had forgotten my wallet. A simple step or coping skill failed when I left my hat elsewhere and things began to snowball as a result.I have several hats and so I replaced the lost one with a new one.
The point of this exercise is to inform you the reader and possible TBI survivor, that this is a regular occurrence for me.  I am 34 yrs past my injury and still with all good intentions aside, with the memory  prosthesis (cell phone), I still forget.
I am far beyond the point where I let it get the better of me but it still pisses me off when, the medical staff have no understanding (physio), and I spend money in the form of fuel to only have to repeat the trip because my wallet was left behind.
The lesson I want you to take from this is rooted firmly in the title, brain injury is permanent.
How you deal with this new reality will determine whether your trip back will be easy or hard.  In fact you will determine by your action on how tough you want to make it on yourself.
Your cup will have to be half full if you want peace of mind.
The sooner you adopt this attitude the healthier it will be for you.  you stand to drive all your friends, loved ones away which will only go the enhance a negative outcome for you.
I kind of think you do not want a divorce added to your mounting problems.  I am sure you do not want to be alienated  by your friends.
You have so much to gain by a positive attitude.
Will it be easy?
Of course not.
The antithesis of a happy go lucky approach however is a lonely, frustrated and dejected person who has alienated all those who loved and supported him.
Slow and easy helps to win the race.  Next I will explore the area of Help.

Tuesday, 5 June 2012

Where do I begin?

There are the obvious steps from initial brain injury to when all the fanfare ends and everyone abandons you figuratively, that you soon discover yourself left to your own devices.  This happened to me right after surgery when my Neurosurgeon signed off on the case and said have a nice life.  That of course was in 1977-78.
I was told not to go to school for one year and take it easy and allow the brain to heal.

I was not referred to any other facility, nor were my parents educated on what to expect of their brain injured son.
To them, (my parents), I was cured.  It was like I had a broken arm and in my case it was a broken brain that I had survived, I should be blessed and carry on with life like nothing had happened.

Was that ever a narrow minded view.  Fortunately we have become more aware of the complexity of brain injury and have some techniques in place to assist those suffering from such a tragedy.

I wish to cover the latter scenario, of after you have discovered you have multiple injuries to your brain and what you personally can do or not do to enhance your situation.

I say multiple brain injuries like I am some kind of expert.  Considering that my case is 34 years old and as I muddled through my life discovering several key injuries, I think I am qualified enough to share my findings with you.  When I say multiple, I truly mean more than one and in fact I challenge anyone living with a brain injury to prove to me that they only have one such injury or disability.
The brain like a computer is complex.  If you delete a little code from the hard drive chances are many programs will be affected.  The same can be said with the brain.  Alter speech and see if the the recall ability is not altered.

A brain injury is complex however the way we approach it can make a huge difference in how the disability affects our daily life.

I had the surgery.  My speech was reduced to one syllable words.  The speech came back quite quickly but my spelling took a lot longer.  I also found it hard to keep up with a conversation because I would forget what I was about to say.  My patience took a major blow.  I became easily frustrated and would "lose it" and frighten people by my volatility.

Little did I know that this was directly to my short term memory deficit.  When you are working on assembling a BBQ or installing a ceiling fan and as you fumble for the tool that you forgot where you put it, you start to get annoyed at yourself and then the colorful language appears.  You may toss the tool, punch a wall or even worse take it out on your loved one.

This is why I am writing this installment.

Where does one begin?  If you are brain injured, I highly recommend an anger management course.  I have recommended this before but lets face it.  Even if you do not have an anger management issue yet, you just might and even if you don't there is a greater issue that Anger Management courses will teach.
Coping skills.
When you become brain injured, you are in another world.  What once worked for you no longer holds water so to speak.  You need to learn to analyze yourself when you act or react to a situation inappropriately and learn to find a better response when that same situation occurs again.
Believe me, it works miracles.  You become calmer and better in control of the outcome.

The next tool is acceptance.  Boy is this a hard one to overcome.  I still catch myself getting frustrated at my "incompetence" for forgetting.  I have to remind myself that I am not incompetent but rather I am and will be forgetful so get used to it.
I inform my co-workers of my memory and we get a good laugh at how short it is.  So rather than getting down on yourself, the sooner you can accept your disability or should I say your limitations the sooner the world will accept you as you are and not what you ought to be.

Coping tools.  This is an important one and can play on your ego especially if you are a male where you should be able to perform simple tasks such as installing a light fixture.
I tried this time and time again, whether a light, or assemble a bike or BBQ, I soon learned that the family would head for the hills because it was going to become a gong show.
What did I do.
I surrendered to my limitations and hired someone to do it for me.  It was great!  He could build the deck, he could install the dishwasher, he could install the light or paint the house and I had more time for myself and family.
Sure you can argue the cost but believe me it costs more to lose a family, it costs more to replace that light that you broke out of frustration then it does to have an expert come in and do it for you.

Try it some time you might just like it.  Simply park your ego at the door, invite the repair man in and go outside in the back yard sit back have a beer and watch the grass grow.  It is quite relaxing.  Did I mention that it helps with your sex life too.  Have you ever approached your wife after a day from hell and ask her for some nooky?  It doesn't go far now does it?  It might if your are calm and relaxed.  She might just appreciate you a little more.

Look, the simple fact is, you are still you.  If you have a cast on your foot, you are not going to play soccer anytime soon.  You are not going to run a marathon.  The same goes for your brain.  You may never run the brain marathon like you did before the injury.  If you can accept a cast on the foot and know that there are certain thing you can't do and will need help with,  like cutting the lawn or cleaning out the gutters, then take that same approach to your brain injury.  The only difference is that you may be wearing that cast on your brain forever and not just a few weeks.
It is amazing how helpful people are when they understand your limitations.  My clients call me to remind me to key in an order for them.
I use my cell phone to key in appointments so that I can be reminded on the day of and it alerts me.
This is a good start.  I will examine this and more in my next blog.

Thursday, 31 May 2012

Detective Advocate....Caregivers...That's You


At the outcome of any brain injury the role of the caregiver is paramount to the quick diagnosis and treatment of the afflicted loved one.  My hat goes off to these unsung heroes whose job becomes overwhelming, challenging, and fraught with anxiety, tears and eventually resolve.  Your responsibility is nothing less than pure unadulterated, selfless, sacrifice that very few are either prepared or trained for.  Thusly this book will try to alleviate some of the frightening and often confusing factors that plague the caregiver.
I feel there are two roles amongst many that stand out namely the detective and the advocate.  Both roles go hand in hand as you try to disseminate and translate what the doctor has told you and then try to advocate for your loved one ensuring they get the best treatment and rehabilitation possible.  At this juncture I’d like to say good luck!  I say that with some cynicism because chances are, depending upon your coverage, you’ll be banging your own head against a wall to a point of becoming brain injured yourself.
            There is a progression one goes through with regards to any traumatic injury to a loved one.  There is the shock where the world seems to spin out of control.  The doctor may say things to you that you can’t comprehend or understand and or you will be lulled into a false sense that all is right with the world and the loved one will be just fine in a few days or weeks.
            Initially your world will spin and finally after the shock wears off there is a tendency to rely on the words of your doctor.  BIG MISTAKE!  I do not want to cast any dispersions on the medical community, however, many are not prepared nor educated on brain injury in general and furthermore the role of a neurosurgeon is that of patching your loved one up and not that of educating you, the caregiver.  This is why your role is so important.  You have to ask the pertinent questions.  What is in store kind of questions?  Where do we go from here kind of questions?
            One should never downplay any kind of brain injury.  Look at me.  I had 7.5 hours of brain surgery that should have sent up red flags to all the medical staff.  I should have received rehabilitation.  I had a traumatic brain injury where the x-rays show that my brain is atrophied and the left hemisphere is tilted.  It is difficult to explain this clearly, but let me give it a try.  If your loved one receives any surgery to the brain….that is a serious invasion of that organ and therefore it is traumatic in nature and follow up is imperative.  If your loved one has surgery and shows no outward impediment, like memory loss or speech or mobility problems, the injury is still traumatic and should still be treated seriously and follow up is imperative.  If your loved one receives trauma to the face, skull, is knocked out or suffers from whiplash, then the injury is traumatic and should be treated equally to one that requires surgery.  If the trauma is a concussion, a broken nose with no loss of consciousness, the injury is still traumatic and follow up should be imperative.
            In other words all trauma to the head or neck is of great concern and one should not jump for joy if the injury seems less than spectacular in nature.  Never downplay any trauma to the head…period.
            You may run into some detractors in the medical community that say you are over reacting.  Give them a copy of this book because they obviously have their heads up their rear ends and need a lesson in the reality of dealing with the long term affects of brain injury.
            Your second role is that of a detective.  Besides finding the resources available within the community there is yet another important aspect of the detective and that is doing the boring stake out.  It is being the quiet observer of the loved one after the brain injury.  Taking notes and comparing them to the mental ones of how your loved one behaved prior to the injury with those new notes taken after.  You have to paint a picture that can be presented to your doctor spelling out in detail, the differences you have noticed in your loved one.  A doctor cannot examine your loved one in a 10 minute office visit and discover all that might be wrong with your loved one.  Your observations will be of great assistance to getting the right rehabilitation.  Some of the traits may show up immediately after the trauma while others are more transparent and show up gradually over time.  Your loved one will have a moment of momentous healing shortly after the injury as swelling subsides.  Then the finer details of the injury will present itself.  I had anomia prior surgery, couldn’t do math and had quite a temper.  After the surgery those aspects reduced or went away.  The obsessing, the short term memory and to a lesser degree the anger subsided or remained constant in nature.
            Your observation of the changes as listed in the chapter signs and symptoms will make a big difference in the overall outcome of your loved one.  In the less obvious injuries, the behavior may be an increased frustration assembling products.  A sense of mental exhaustion that requires an increased amount of sleeping may be one of the signs.  Depression, lower level of concentration at school or work may be another.  If the performance at the work place or in school decline then one needs to look at testing and follow-up with a specialist.
            I have given a list in the chapter “Getting Help After Brain Injury” however one must know finer details which I will cover here.  Recently on any one of those many trauma style T.V. shows, I often see brain injury patients who show bleeding on the brain but require no surgery.  The prognosis is that he/she will be fine in a few days and as long as there are no medical complications like seizures we’ll (the hospital) will release the patient.
            No one asks the doctor what the long term affects will be.  Let us examine it a little closer.  The loved one suffered a trauma that caused bleeding on the brain.  It stopped and all is right with the world.  We know that brain injury can occur at microscopic levels and here on the MRI or CAT scan we see bleeding which means a little inflammation, contusions usually located in two regions of the brain.  If the front is bleeding then there is a good chance that the exact opposite side will be injured to a lesser degree but nonetheless still injured.  If there is an obvious sign such as blood then the injury is very serious regardless what the doctor states.  If it was your brain and it was bleeding you would take it more seriously than just a cursory glance.  You would probably be deeply concerned and demand all tests available to determine the next preferred action to take in the full recovery of yourself.  This will take 2 neuropsychological tests spaced between 6 months and maybe a third at a year and a fourth at the 2nd anniversary.
            If there was a procedure for post care with regards to all brain injuries the following would occur.  The patient would not fall through the proverbial cracks.  The divorce rate with brain injured would decline by 40% to the national average of 50%.  The crime rate would decline.  Violence to females and children and people in general would decline.  The prison population would decline by up to 90%.  The street crime and the homelessness situation would be greatly impacted and reduced.  With a little preventative education these levels would fall even further.  This means fewer murders, less alcohol and drug dependency and the savings to society would be immeasurable.  In Canada alone the savings would be well over 2 billion dollars annually.
            In the mean time we have this book to assist those who continually fall through those cracks and end up becoming one of those horrific statistics.

Once your loved one has been diagnosed with a brain anomaly of any kind, demand answers.

1)      I am informed that brain injury may occur at cellular level therefore scans are insufficient and I would like additional tests.
2)      I would like a neuropsychological test similar to the Structures of Intellegence (SOI) http://www.soisystems.com/index.html
3)      You want tests to determine their Figural, Symbolic, Semantic, Comprehension, Memory, Evaluation, Problem solving, Creativity, Arithmetic, Math, Reading, Reading Readiness, Reading Concepts, which is even broken down further to the following:

EFU Visual discrimination-judgement skill

CFS Coping Skill-difficulty dealing with change-eg furniture rearranged, papers moved dishes rearranged etc.

CFT Locating and transferring skill, locating objects, reading maps transferring information from one idea to another ie) finding car in parking lot, locating papers, clothing, keys, wallet etc.

NFU divergent thinking- may display an inability to require an alternative point of view.  May obsess or simply quit the activity.

MSUv and MSSv Visual memory skills

MSU & MSSa Auditory Memory Skills

CMUr Vocabulary

The test results may come back in medical jargon the likes you will have difficulty digesting let alone interpret and therefore it is incumbent on you to ask the tester, usually a neuropsychologist, the following questions:  What does this mean?  How will this impact of the patient with regards to daily living?  What can we do to improve on this weakness or disability?  If they cannot tell you what can be done then run don’t walk from his office and find someone else who can.  There are definitive exercises that will improve every aspect of the brain.  After a brain injury, the sooner rather than later you begin the rehabilitation the quicker the recovery.  The brain can and will try to heal on its own.  It will grow new neural pathways around the damaged area and may utilize another secondary region to replace the lost or damaged area.  Naturally there are no guarantees on the final outcome and it may take a long time for the healing to take place.  My 1978 and 1995 tests show that my disability is permanent however I adopted coping skills that have diminished those negative affects.  If I had been treated with rehabilitation and specific treatment focusing on the weak areas, I may have not experienced many of the setbacks that prevailed in the next 25 years.  I may have had better control of my anger if I was made aware of my weaknesses early on.  I would have adopted better coping skills to reduce those frustrations born of a damaged memory.  My auditory dyslexia traits would have indicated my inability to listen properly which caused me to lose my kids because I forgot where they said they went.  Now that they are teenagers I find there are times I wish I hadn’t learned how to remember where they went and would lose them again.  O.K., so I throw in a little levity in a deep subject but I often wonder why I was not informed and placed my children at great risk as a result of not knowing.  A self imposed coping skill evolved from this fear of where the children were by having them tell me and then write down the info so that mom would be satisfied.
            You have to be assertive and virtually move mountains.  If the alleged injury is the fault of another person then a suitable lawyer trained in brain injury needs to be contacted.
A small warning should prevail in the form of common sense when your loved one is tested and that is some and not all results may be a related to the actual brain injury. If you know the individual had learning disabilities, was poor in speech, math or other areas of education then one would be jumping to conclusions if after this first test all negative results were thought to be a direct cause of the brain injury.  How can one tell if it is or isn’t a cause of the injury?
You really can’t, however it is important to factor the past behavior of the patient into the mix so that a realistic view emerges.  I may have had a hearing difficulty before the injury until I look at the region of the brain affected and what its primary functions are and compare that with the results of the test.  It is pretty basic police work that your doctor should be able to perform if they are brushed up on the brain’s basic functions.
Here is a picture and the definitions follow.



                                 
                   Frontal Lobe
Initiation                                                        Smell
Planning/anticipation                                   Motor Planning
Follow through                                              Personality
Impulsivity                                                     Emotional (Affect)
Judgement                                                   Speaking (word Finding)
Reasoning                                                    Integration of thought and emotion
Abstract Thinking                                         Self Monitoring

Temporal Lobe
Memory
Hearing
Understanding Language

Parietal Lobe
Intellect
Sense of touch
Differentiation: Size,Shape color
Spatial Perception
Visual Perception

Occipital Lobe
Vision

Cerebellum
Balance
Coordination
Note: The Parietal and Temporal Lobes have a left and right side.
Many doctors may try to downplay the brain injury for many reasons including lack of funding and long waiting lists in Canada, to poor coverage or that some insurance companies may refuse to cover such testing.  One must factor the motivating factor of the doctor.  It may not be in his best interest to refer you.  The days when doctors put the needs of the patient first are long gone and profits take precedent.

If your loved one was injured in a MVA or at work then your chances are better in receiving the utmost care and prompt response to your request for testing.  This is why a lawyer trained specifically in Brain Injury is critical in receiving both the best treatment and of course compensation.  One cannot expect to discover all the injuries and deficits overnight.  It may take months and months and still complications arise.  Your loved one may go home and be completely fine and then 2 years later, scar tissue grows and seizures begin.  Do not think for a moment that there is clear sailing ahead and end up shooting yourself in the foot when in 10 years post original brain injury, a complication occurs.  Unfortunately you took the buy out or your doctor’s word and the case was closed 2 years post injury and you have no legal recourse and the medical costs wipe you out.

Will this injury cause scar tissue to build up?
Will this trauma cause an onset of Parkinson’s condition (not disease)  caused from trauma to the lower brain stem.
Will this memory problem cause an onset of Alziemers disease?

Most doctors will say the injury will not cause this.  Unfortunately for us there is little support either way.  I was going to name this book “The Final Frontier” and truly it is.  We may have a better understanding now than ever before but it is far from being fully understood.  The veil of uncertainty has definitely been lifted and we now appreciate the fact that what once seemed hopeless no longer holds true.  The brain begins to compensate and heal immediately after the trauma and in many cases reverses several of the conditions caused by the initial injury.  We now know that new neural pathways grow and bypass or re-attach to the damaged region.  We know that increased oxygen to the brain improves its healing properties and now even employ the use of hyperbaric chamber to assist in recovery.

The problem lies in the approach.  We should be tackling brain injury before it occurs.  We should educate in every area of life where brain injury may occur such as sports, work and most important in motor vehicles so that we can prevent the injury before it happens.
We should draw attention to the potential of the brain injury by reclassifying all head and neck injuries as that of a potential brain injury.   We should reclassify whiplash, concussion, broken face bone, jaw, nose, and skull as traumatic brain injuries and scrap the term mild or moderate brain injury.  By retraining the medical staff to be cognizant of the potential for a brain injury and raising its likelihood to the forefront, one might reduce the misdiagnosis of it drastically.  I cannot for the life of me understand why in the 20th and 21st centuries, we are even having this conversation?  By diverting away from the whole to a part of the body we risk death.  This was taught to me in first aid and we could lose our first aid ticket if we didn’t treat the whole body and diagnose on the side of the worse case scenario.  In the hospital we throw out that approach and become desensitized to the potential and would be mocked if we tried to treat beyond the obvious.  It’s a broken nose.  The treatment for a broken nose is this.  Let’s not assume that the sinuses may be damaged or that the brain and the frontal lobe may have been seriously compromised by the force that was sufficient enough to break a facial bone.

It is impossible to list all questions without knowledge of the individual brain injury however there are crucial ones you should have in your arsenal and they are:

1) How severe is the brain injury?
2) Where is the damage located?
3) What brain functions will this injury affect?
4)Who would you recommend as a referral for follow up treatment?
    (Neurosurgeon, Neuropsychologist, rehabilitation center, family therapist, support    groups for survivors and caregivers)
While you wear your advocacy hat, one should research the referrals made to you and don’t hesitate to ask the specialist you’ve been advised to see to supply his or her own references.  Ensure that some are from patients.  Most agencies and doctors will gladly make available a list of former clients/patients who have benefited from their treatment programs.  If not go online and enter a chat group and see if there is anyone who has used this specific doctor, therapist or center and make a decision from that.
Some therapies, or medicines may assist in treatment but the side affects may bring about another set of circumstances.  Research the drugs or treatment before embarking on a prescribed regimen that you may possibly regret.
I was recently prescribed by a doctor a medication to aid in quitting smoking.  The medication is not recommended for stroke victims.  Good thing one does research or this book would have never been written and I’d be pushing up daisies.
   Do not fret if one treatment fails or a medication causes a bad side affect.  Each patient will react differently and brain therapy will be fraught with many such set backs and then many more gains.  One has to experiment in a safe manner and by arming yourself with information you and your doctor can make an informed decision on what path to take and truly hope for the best.  Remember this is new ground for both of you, the patient and in most cases for the doctor or therapist.  What works miraculously for one may be the antithesis for another.  I have mentioned Bob in previous pages and he is the flagship for this trial and error.  His medication has been altered more times that I can count.  Sometimes the adjustment is great and Bob responds well, with a new zeal and energy and progress is made in his therapy.  The next adjustment sets him back several steps.  He becomes lethargic and depressed wishing he was dead.  The next month the drugs have been balanced and he is perky and full of humor.  It is this dance of healing that we must continue to engage that can at times seem hopeless.  It is two steps forward and one step back and when you entertain the prospect of dealing with a brain injured person you better like a lot of dancing because you are going to put Fred Astaire to shame.






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Wednesday, 30 May 2012

Mild Brain injury if there ever was one?

As you know I am not a fan of qualifying brain injuries and my reason being, EVERY BRAIN INJURY IS SERIOUS, having said that I want to address a area greatly overlooked by the medical community and hopefully others will copy this page and present it to their local hospital....It might just save a life or two.

When a person comes to an emergency ward they are soon questioned about what is wrong.  It's a good place to start, however it ends up classifying your injury into scale of minor or serious.  Obviously we need to triage our patients and treat the most critical first.
It is referred to the "Golden Hour", that first hour post injury, if left untreated, reduces the survival rate dramatically.
When it comes to trauma to the face head or neck a weird anomaly occurs.  We look at the patient and determine that he/she has a bleeding nose.  Recently my 12 year old grandson presented with this very scenario and guess what?
The exact thing I feared occurred.  He was not sent to the hospital by the soccer staff and went for a sleepover at a friends.  His mom saw him the next day with the two shiners and asked what had happened and he said he broke his nose playing soccer.
That was the sum total of his treatment.

What is worse is if he had gone to the hospital he would have been informed that his nose was broken and sent home with an ice pack and that would have been the end of the journey.

If you have a concussion, the rattling of the brain, bringing on temporary loss of consciousness, you are given a list of what to watch for by the medical staff and if a headache ensues or he does not awake easily then you are instructed to return to the hospital.

If you are punched or hit by a base ball or soccer ball, fall off your bike, are in a MVA and suffer whiplash, your are classified by the hospital as Whiplash, broken nose, broken jaw, skull fracture and the list goes on.

NOT ONE CLASSIFICATION MAKES MENTION OF THE FACT THAT ANY TRAUMA TO THE HEAD THAT RENDERS ONE TEMPORALLY UNCONSCIOUS, HAS A FORCE SUFFICIENT TO FRACTURE A BONE IN THE HEAD, OR CAUSES WHIPLASH IS SUFFICIENT ENOUGH TO CAUSE BRAIN INJURY!

All head injuries should be reclassified as a broken nose and possible brain injury.  Every broken jaw should be classified as broken jaw and possible brain injury. Every concussion should be classified as concussion and possible brain injury.  Every skull fracture should be classified as skull fracture and possible brain injury.

To not bring attention to the most crucial organ in the body, the brain, has me questioning the medical community as to why they could overlook this crucial error in judgement?

If we drew attention to the potential of a brain injury we could encourage the loved ones to pay attention to the behavior of the injured and see if there are any signs or symptoms when the patient is released from the hospital.

Brain bleeds can occur from trauma to the neck or head.  This may be a mild bruise however they are now seeing long term affects on sports personnel who have suffered several concussions and their brain has lesions and the entire brain becomes diseased.
The person becomes violent or suicidal later in life from such trauma.
We may not be able to prevent a concussion in sports however we may be able to prevent a second or third by having the person quit the sport before it becomes a life sentence.

It is up to us as individuals to be proactive when it comes to brain injury before it happens.   By wearing helmets, not heading a soccer ball in the younger leagues, and taking all head trauma as a potential brain injury can save someone their life.

Be aware of the fact that head and neck trauma may result in brain injury.

I hope the Doctors in your emergency department will read this and reclassify all head and neck trauma to include potential brain injury.  It may not change the treatment but at least you will be made aware of the potential long term affects of multiple traumas to the head and maybe reduce how many one receives by modifying ones behavior.