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Concussion Awareness Law, in North Carolina, Signed by Governor Bev Perdue

posted by SK Brain Injury    |   August 24, 2011 20:48

On Thursday, June 16th, Governor Bev Purdue signed into law a bill to protect North Carolina middle and high school student-athletes against concussions. This piece of legislation, known as the Gfeller-Waller Concussion Awareness Act, is designed to raise awareness of the significance of concussion injuries, as well as emphasize the importance of safety in sports.

Matthew Gfeller died in August 2008 after sustaining a head injury during a high school football game in Winston-Salem. He played for R.J. Reynolds High School.  Jaquan Waller, a football player at J.H. Rose High School in Greenville, died in September 2008, after sustaining a head injury during a game. Waller suffered from Second Impact Syndrome, a condition that occurs when a person sustains multiple concussions in a short period of time.

The key points of this bill include:

1. Mandatory concussion education is required for all parents, coaches, administrators,  and athletes to read & sign annually.

 2. If an athlete displays any signs or symptoms of concussion during competition or practice, they are immediately removed from play and not allowed to return-to-play that day.  Prior to returning to sport, they must be evaluated and cleared by a medical provider with training in concussion management.

3. A venue-specific Emergency Action Plan is required for each facility hosting athletic events. 

 The act currently applies to all public middle and high schools, and will begin 2011-2012 school year.

 CFPSM would like to thank our providers, staff, patients and their families who helped by contacting their local representatives in the House and Senate to support this act. The multiple letters, emails, and phone calls for this act were heard, appreciated, and made a difference in the lives of the student-athletes across North Carolina.

 CFPSM’s Carolina Sports Concussion Clinic was established in August 2008. Our mission is to educate the community on concussion prevention, recognition, and proper management. To date, our providers have evaluated and managed over 500 concussions.  Dr. Josh Bloom is also a member of the North Carolina High School Athletic Association’s Athletic Safety Task Force Committee.

 For more information on the Carolina Sports Concussion Clinic, please visit: http://www.carolinasportsconcussionclinic.com/

 To read the full article regarding passing the Gfeller-Waller Concussion Awareness Act, please visit: http://www.highschoolot.com/content/story/9734410/

 

Source: http://bit.ly/pRJ8Ib

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School Sports: Concussion Testing

posted by SK Brain Injury    |   August 24, 2011 20:44

Cary, NC – Ready or not, Fall is around the corner and once again school will be in session. That means many teens are already practicing for their school sport, whether it’s football, soccer, cheerleading or any other physical activity.

As parents, we make sure that our children are well prepared for school and sports by providing all the equipment needed. But, what about preparing for the possibility of a future head injury? 

Gfeller-Waller Concussion Awareness Act

Now you can have a baseline ImPACT test done for all high risk athletes before a head injury like a concussion occurs.

In June, Governor Bev Purdue signed into law a bill to protect North Carolina middle and high school student-athletes against concussions. This piece of legislation, known as the Gfeller-Waller Concussion Awareness Act, is designed to raise awareness of the significance of concussion injuries, as well as emphasize the importance of safety in sports.

Matthew Gfeller died in August 2008 after sustaining a head injury during a high school football game in Winston-Salem. He played for R.J. Reynolds High School.  Jaquan Waller, a football player at J.H. Rose High School in Greenville, died in September 2008, after sustaining a head injury during a game. Waller suffered from Second Impact Syndrome, a condition that occurs when a person sustains multiple concussions in a short period of time.

What exactly qualifies as a concussion?

A concussion is so much more than just a bump in the head, or getting one’s “bell rung.”  A concussion is a mild traumatic brain injury and results in a wide variety of symptoms.

These symptoms fall into four categories:

  • Physical
  • Cognitive (those that affect thinking & concentration)
  • Emotional
  • Sleep related

These symptoms are a result of either a direct blow to the head, or a blow to another part of the body which transmits a force through the head resulting in the brain being shaken, compressed, or twisted within the skull.

When the brain is functioning normally, there is a nice, steady balance of impulses shooting from one cell to the next.  When this balance is disrupted, a change in emotional responses occurs and these symptoms become apparent.

Measuring Head Injury

Since this metabolic imbalance cannot be seen on imaging such as CT scan, or MRI, how can the severity of these injuries be measured?  Healthcare professionals used to rely solely on the description of symptoms provided by the athlete.

An athlete could say “I have a headache” or “I feel dizzy when I turn my head from side to side” but it was difficult to measure the cognitive deficit that had likely occurred.

Now, there are options and ways to measure neurocognitive function using a computer-based test. In Cary, physicians at Carolina Family Practice & Sports Medicine (CFPSM) developed the Carolina Sports Concussion Clinic.

This clinic, in addition to obtaining a thorough medical history and asking specific questions regarding symptom patterns, has added the use of ImPACT testing to its toolbox. ImPACT helps providers make appropriate clinical recommendations based on an athlete’s composite scores in four categories:

  1. verbal memory
  2. visual memory
  3. visual motor speed
  4. reaction time

In the Fall of 2008, CFPSM provided baseline ImPACT testing for all high risk athletes in the Wake County Public High Schools.  Once these baseline tests were established, athletes were then referred to CFPSM after sustaining a concussion and a repeat test was performed as part of the athlete’s office visit.

Once an athlete was evaluated, his or her ImPACT scores were also taken into account in making a diagnosis of concussion as well as developing an individualized plan for each athlete’s recovery.

Can I get a baseline test for my child?

Each year, CFPSM has added new schools and organizations to its baseline testing pool.  Student-athletes at Campbell University, St. Augustine’s College, Cardinal Gibbons High School, East Coast Eagles Hockey, and various youth sports programs have initiated baseline ImPACT testing as part of their pre-participation standards.

Other area schools like Cary Academy are considering implementing baseline testing for the 2011-12 school year. Check with your school to make sure they offer this test to their student athletes.

If you or your child is in an extracurricular sport, you can get the whole team tested. Baseline testing can be done in a group setting, takes less than an hour to complete, and is reasonably priced.

As athletic participation remains a popular recreational choice for youth, adolescents, and adults alike, concussion awareness will continue be to at the forefront of the Carolina Sport Concussion Clinic’s presence in the Wake County community.

 

Source: http://bit.ly/oLS6dt

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Students, coaches act pre-emptivey against concussions

posted by SK Brain Injury    |   August 15, 2011 19:10

 

Right before halftime several years ago, a Council Rock North football player approached athletic trainer Mike Horan with a strange complaint. He couldn’t remember the first quarter of the game.

When Horan performed a sideline evaluation for signs of a concussion, the player had no problems with balance, dizziness, headaches and his eyes were fine. He also remembered all the words that Horan asked him to repeat.

A few minutes later, Horan did the tests again, and the only problem was that the player did not remember the first quarter.

Not satisfied, the trainer involved a team doctor, who suspected a concussion and held the boy out the rest of the game. The next day, a computer test confirmed a mild concussion.

With head injuries, one symptom is one too many, trauma experts say. But the signs of a concussion can be subtle and sometimes take hours, days, even weeks to appear, increasing the risk of a second, life-threatening head blow because the player is not benched.

One tool for diagnosing a concussion is a computer-based neurocognitive test players take before a head injury that provides a baseline for memory, reaction time, speed and concentration. But not all area high schools use ImPACT testing, and those that do, may not use it consistently, though that could soon change.

Pending legislation in the Pennsylvania Assembly would create standards for managing concussions and trauma brain injuries involving student athletes, bench students who show symptoms of a concussion, require student athletes to undergo baseline testing and sport coaches to undergo concussion education training.

Meanwhile, for this upcoming school year, the Council Rock and Neshaminy school districts will require high school athletes who participate in contact sports to undergo ImPACT testing as part of a pilot project.

Student athletes will also be required to attend an educational program on concussions prior to testing. The coaches at participating schools will attend a training program on preventing concussions and recognizing their signs.

More than 700 fall athletes in the three high schools schools will be tested this month and another 600 will be tested throughout the school year, said Kim Everett, trauma prevention coordinator for St. Mary Medical Center in Middletown, which with the Bucks County Intermediate Unit’s Brain STEPS team and Princeton Brain and Spine Center brought the testing pilot to the districts.

Earlier this week, 466 athletes were tested including cheerleaders, football, soccer and field hockey players, Everett said. Another 75 to 100 kids at each school still needed to be tested as of Thursday. Monday is the first day of the fall sports season.

Only about 10 of the nearly 70 of Council Rock High School North football players failed to attend testing Tuesday, athletic trainer Mike Horan estimated. A makeup session will be held Monday, and students who miss it will be barred from practice until the test is administered.

“This is that important of an issue to us,” Horan added.

INVISIBLE INJURY

The human brain is a soft organ protected by a hard skull. Normally the fluid around the brain protects the organ from banging into the skull, but if the head or body is hit hard enough, the brain can shift, resulting in injury.

The Centers for Disease Control and Prevention estimates that U.S. emergency departments annually treat 135,000 sports- and recreation-related traumatic brain injuries, including concussions, among children ages 5 to 18.

Any sport involving a high rate of movement and sudden stops can result in a concussion, and most — 80 percent to 90 percent — are considered mild, meaning the person did not lose consciousness, according to the CDC.

But a mild concussion is a potentially serious injury that, if not treated properly, can result in brain damage, doctors emphasize.

Emerging research suggests that an athlete who has a concussion is more susceptible to a second one, and some studies have connected repeated concussion injuries with depression, Parkinson’s disease and amyotrophic lateral sclerosis, also known as Lou Gehrig’s disease.

The greatest health risk is second-impact syndrome, which carries a high risk of death and permanent brain damage. It occurs when the brain has not adequately healed from an initial concussion and an athlete returns to play and has another concussion.

St. Mary Medical Center’s trauma unit is seeing an increase in the number of concussions among young athletes, Everett said. But too often the injuries are not immediately diagnosed or followed up on.

Kids today are physically larger than in previous generations, which creates a higher risk for concussions during contact sports and play, said Dr. Raymond Talucci, director of trauma services at St. Mary Medical Center.

“These hits can be quite violent at times,” he said.

A delay in diagnosis can occur because a diagnostic imaging scan may not show any immediate brain damage, though symptoms emerge later. This is the reason why observing how a person behaves and functions after a head blow is a better indicator of a concussion, Talucci said.

“If the CT is negative it does not mean the child is not injured,” Talucci emphasized. “If a kid has a bad enough injury to require a CT, he’s in trouble.”

INCONSISTENT TESTING

The way that ImPACT testing works is, when a concussion is suspected, the original test results are compared with a post-injury retest. The test not only can help diagnose a concussion and its severity, but show when a player has recovered enough to return to play.

Many Bucks and eastern Montgomery county districts use ImPACT testing to some extent, but they’re not using it as effectively or widely as they could, Everett said. The main reason is a lack of staff to administer the test to all athletes participating in contact sports, Everett said.

Since 1999, Council Rock North has required ImPACT testing for its football team, which averages about two player concussions a year, Horan said. Six years ago, the school added mandatory testing for all other contact sports teams. Council Rock High School South added the student athlete testing last year.

For the last two years, Council Rock North students had been allowed to take on online version of the ImPACT test at home, and provide proof they took it. But a home environment doesn’t allow for the test control conditions necessary for a true baseline score, he said.

Neshaminy High School has offered ImPACT testing since 1999, but it has not been consistently used, athletic director Bryan Schendlinger said. Last school year, for example, only about one-quarter of football players were tested.

Neshaminy High School athletes had one or two serious concussions last year, but fewer minor concussions than the prior year, Schendlinger said. Where he is seeing more head injuries isn’t with football, it’s girl’s lacrosse.

Students typically will tell him or a coach if they are hit hard enough, but sometimes it can depend on the game situation, Schendlinger said.

“Some kids will turn other kids in,” he added.

Council Rock North senior Ferguson Amo, 18, plays football and runs track. Concussions are something he frequently thinks about.

He had one before, when he fractured his frontal sinus cavity after he was accidentally kneed in the head during gym class.

While coaches emphasize safer tackling techniques, head blows happen, the Upper Makefield teen added. That is why he thinks requiring the testing is a good idea.

“It’s going to be helpful. Nobody wants to end up like (the brain damaged football player) in the video we watched,” he said

Newtown Township resident A.J. Garboski, 17, plays football, hockey and baseball, all high-risk contact sports. He has been hit in the head, but doesn’t worry about concussions much.

About seven years ago he had a mild concussion after a head blow during a Pop Warner football game, but he hasn’t had a problem since, he said. But he agrees with the new testing requirement.

“It is good knowledge we all need to learn about,” he said. “It’s about our safety.”

Source: http://bit.ly/orAX77

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Living within the system: The story of two women battling to overcome the complexities of social assitance

posted by SK Brain Injury    |   August 11, 2011 19:01

SBIA is a member of DISC and hopes that the SAID program will be implemented as soon as possible.

BY A.J. BASSETT
SACL COMMUNICATIONS COORDINATOR

For many people with disabilities, life is a constant battle for survival to make ends meet. The same things that many Canadians take for granted, a heated home, a vehicle, food in the fridge, a telephone and a computer, are often out of reach for many Canadians with a disability.
According to a recent report by the Council of Canadians with Disabilities, more than 16% of adults with disabilities lives in poverty. It’s an issue that’s often overlooked for a variety of reasons, mainly due to a lack of knowledge or understanding about the issue.

In late spring, I sat down with two persons with disabilities, Gayle Dixon and Jana Friel, both of whom have struggled to live a quality life within a system that tends to perpetuate poverty. I was also joined by Judy Hannah, SACL Project
Coordinator for the Grassroot Alliance, and one of the key individuals behind the Disability Income Support Coalition

(DISC):
Gayle’s Story:
Now in her early 50s, Gayle has a warm disposition, her eyes bright and cheerful. From Gayle’s laugh and smile, one would have little idea that in reality, life for Gayle has been a constant battle of making ends meet while struggling with her emotional disability including chronic depression.
It’s a disability that Gayle has endured for most of her life.
Gayle thinks back to the years following her mother’s death, which happened in the mid-90s. “I had a fear of leaving my house by myself, and friends had to take me shopping and to appointments, and my nerves were really bad,” said Gayle.

“I was really depressed, and I just wasn’t coping with life very well.”

A salvation of sorts came about for Gayle 11 years ago by happen stance when she watched a television show featuring service dogs. The dogs are highly trained to provide support to persons with disabilities such as visual and hearing. Service dogs also guard diabetic owners, and have known to have saved numerous lives of diabetics who go into diabetic shock.

“After I saw the show, I went to my doctor and asked if maybe a service dog might help me, and she said why not?” said Gayle. After a long search for a suitable dog and a huge community effort where more than $5,000 was raised to pay for service dog training, Gayle got Murphy, a young Black Labrador. Murphy, as it turned out, would be the first service dog in Saskatchewan to provide support for an emotional disability.

Gayle’s situation is slightly more unique than others who are on social assistance. She owns her own small house – an inheritance from her mom. She also owns her own car, albeit very old and used, which helps her make frequent trips to the leash-free park to exercise her service dog. Gayle’s fortune of having a house, however, is offset by the system which has penalized her for having property. It’s an issue that Judy has been working for years to change.

“Because Gayle has her own house, Social Assistance covers the taxes and utilities, but reduces her allowance so that she receives only $473 a month to live on.”

“After her basic housing expenses are paid for, Gayle has $58 a week to use to pay for everything. Her food, clothing, entertainment, car repair ... everything” says Judy.

The bond between Judy and Gayle has grown over the years. Gayle’s experience with the system has given Judy a disturbing glimpse into living life on the bare edge of existence.

“I remember one time last winter you had a cold”, said Judy as she turned to Gayle and smiled. “You had a few colds last winter and you called me and said you wanted to buy a box of Kleenex because you had a cold. I told her ‘well, go buy a box of Kleenex then!”

“Do you remember what you said? You said it would cost $1.29 to buy a box of Kleenex and when you’re living on so little money you have to always think twice if you’re going to buy a box of Kleenex, you know?”

Gayle nods her head. “I’m barely surviving. Barely surviving. The price of food has gone up and I mean, you go grocery shopping and it doesn’t go as far as it used to. And you can’t buy really healthy food, and so you buy a lot of Kraft Dinner and macaroni because that’s cheaper.”

As Gayle can testify, being on social assistance means not only a question of living on the edge of existence; it’s also a question of dignity. Every main expenditure must be tracked and explained to a social assistance worker in the Ministry. Failure to account for how money received is spent can mean a reduction of benefits, or loss of the assistance altogether.

Gayle is still haunted by a harrowing experience she had with her furnace, which had unexpectedly broken down. “I phoned Sask Energy and told them my furnace wasn’t working. I had to explain that I owned my house but was on social assistance.”

Because the furnace breakdown was an unforeseen expense, Gayle required special permission from her social assistance worker to approve a visit from Sask Energy. However, her frantic attempts to contact her worker before the end of the day were unsuccessful. “I had to spend that night without heat. It was very cold but I didn’t have any choice, I couldn’t get help.”

Judy nods. “You have to ask for everything from your social assitance worker. If you need anything special or extra you have to ask.”

“For those of us who don’t depend on assistance, we never do that. If we need the furnace fixed, we just get it done.” Gayle’s experience is hardly uncommon for those who have long-term disabilities and have little option other than social assistance to survive. One of the major drawbacks for persons with disabilities who are on social assistance is they are severely restricted by any attempts to plan or save money for the future.

Constantly managing every precious penny, Gayle once decided to set aside her GST tax credit for savings and investment, if only to plan for her future and give herself a cushion for unexpected expenses, like maintaining her old car.

“I was saving my tax credits so I could keep it for things like repairs for my car,” says Gayle. “Went I went to report to my social assistance worker, they saw that I was setting aside money for savings.” “It wasn’t a lot of money, but when they found out, it was a big problem. I came really close to getting kicked off of social assistance and if that had happened, I’d have no options left to survive.”

Gayle’s harrowing experience from her attempts to save money has played a big role in motivating her to become involved in reforming the system. She was one of the first people involved in the now-established Disability Income Support Coalition (DISC), and she has helped to lobby for Saskatchewan Assured Income for Disability, or SAID program.

“I started coming to meetings and getting interested in trying to make a difference,” said Gayle. “I’ve been on Social Assistance for over 10 years, so I know what it’s like and I know how the system can be very difficult for people who depend on support.”

“I like coming to the DISC meetings, because we’re all of one mind. We’re all working for the same thing which is to get people onto the SAID program.” The SAID program, which following years of planning, meetings and lobbying,
was established in 2008. The program is unique in that it provides assistance for people with significant and enduring
disabilities, and gives individuals who receive the assistance greater control over how the money is spent.

“SAID’s reporting structure will be much less restrictive,” says Judy. “It gives recipients greater control over their lives, and it won’t force them to report every single expenditure for approval.”

Also unlike social assistance, SAID doesn’t punish its recipients for saving money says Judy.

“Here Gayle was, being responsible by trying to put her tax credit money aside and the system wouldn’t let her do that.” “When it’s fully developed, SAID would allow for money to be set aside and nobody would question her about it.”

“If you’re on welfare you’re not allowed to save for the future. On SAID, Gale can set money aside for home maintenance, and if she does, nobody will threaten to cut her off. “

“SAID is gonna be great because there’s so many people with disabilities that are just barely surviving,” says Gayle.

“We need the government to really listen to us and to be able to meet with DISC to understand why we need the SAID program.”

Judy quickly interjects. “What Gayle is asking for is just to be able to live, really. And social assistance doesn’t allow that, plus the lack of dignity from being on welfare, and she has to go every year for intake where people with disabilities are asked ‘do you still have a disability?’”

“That’s something that will change when they go on to SAID. They will have to report in every three years. But these disabilities never disappear – if anything your condition often deteriorates over time, so it will give more dignity to their lives, and even the people who are on it already have said it feels different.”

Judy remains very positive that the SAID program will soon be expanded to include more persons with disabilities.

“Kudos to the government,” says Judy. “They launched SAID and they got people in residential care on the program.”

Ironically, even with her long-term debilitating disability, Gayle has yet to be approved for the SAID program, due largely to backlogs and red tape. Still, she holds out hope that within a year or two, she’ll finally be approved.

“They got people in residential housing on SAID 18 months ago,” says Judy. “Since that time, nobody else has gotten on. Right now the government is testing an assessment tool, and the hope is that they’ll finish testing by the end of this summer and start getting more people like Gayle on SAID this fall and winter.”

Gayle is adamant that not being on social assistance will provide her with a precious feeling of dignity and control. “If I get on SAID I’ll feel like I have respect for myself. I’ll feel like I’m not just existing and that I’m actually able to live.”

“I’ll feel like I’m worth something.”

Jana’s Story:
Jana Friel is a 29 year old woman with an intellectual disability. Born and currently residing in Regina, Jenna has lived independently for the past 8 years at an independent living apartment in the city.

I met Jana recently at an SACL Self- Advocacy forum. Warm and engaging, Jana immediately directs us to a meeting place. She does not lack independence and assertiveness. Indeed, Jana has lived a great portion of her life independently, extending all the way back to when she entered the work force at a tender 16 years of age.

“I started working while I was still going to school. I was at home and I like to go out but I was also bored. So I asked my mom if I could work and she took me in to talk to the manager, and they hired me on the spot.”

Because of Jana’s disability, she depends on social assistance to help cover her basic living expenses. The system, however, has very strict rules for the amount of money people can earn while working. Up until February of this year, the Ministry penalized individuals who earned more than $150 a month. 75% of any monthly earnings over the $150 amount were deducted off of her assistance check.

Jana wasn’t generally affected by the penalty – working reduced part-time hours, Jana’s earnings were under the cap. However, with her employer issuing paychecks every other week, there are two months out of every calendar year where three pay stubs are issued.

The combined total of the stubs exceeded the earnings cap, and as a result, Jana’s social assistance benefits were penalized.

“I felt sad when they took money away,” says Jana. “I worked hard for my money but I had no more in my bank account. I have to have enough money for rent, the phone bill, groceries and other things to live on. I didn’t have any money to do other things like go to a movie or go out with friends.”

“I worked hard for my money but I had no more in my bank account.”

Jana wasn’t only sad. She was angry.

With the help of Judy and the DISC, Jana managed to meet Social Services Minister June Draude face-to-face about the penalty.

“I met with Minister Draude last summer and I talked to her about how I once got three pay stubs in a month, and asked her what do I have to do to keep my money?”

“She said that wasn’t right.” Indeed, following that meeting, Minister Draude enacted an adjustment a few months later which raised the earnings cap by $125 to $275 a month.

For Jana, her big wish right now is to work more hours, perhaps even getting a second job. “I would like to work on the days I don’t have anything to do, like three or four days a week and work 16 or 20 hours a week.”

“The problem is,” says Judy “if she were to work more hours, she would still lose money, because the earnings exemption isn’t very high.”

“We’re working on raising that further. Jana deserves to keep the money she’s earning.”

For Jana’s parents, Shirley and Mark Friel, the concerns they share for Jana go beyond making ends meet month- to-month (which often, she can’t). They think about Jana’s long-term future, and what supports will be there to ensure she will be taken care of after they’re gone.

“Every month we have to subsidize Jana for things like clothes, and some groceries and cleaning supplies,” says Shirley. “It really doesn’t take very long for her money to be used up.”

“Exactly,” says Mark. “I’ve talked face to face with people from Social Assistance who issues these checks and they know that all the parents are providing some help to their children. The big question is how would Jana survive if

Shirley and I weren’t here?”

Right now the Friel’s are putting money away through the Registered Disability Savings Program (RDSP), where money can be put away until the recipient reaches the age of 59.

Still, Shirley and Mark don’t stop worrying about Jana’s future.

“Prior to the RDSP, which I think is phenomenal, the long-term is helped a little, but Jana needs to look at the pure long-term,” says Mark. “If I last until I’m 80 years old, and I can keep putting money in yearly into a RDSP, and look after any shortfall, then that’s okay.”

“But what if I don’t live until I’m 80? It’s on my mind every day.”

“We know that while we’re alive we make sure that she’s got things she needs in her apartment,” says Shirley. “But we know if we were to be gone suddenly from the picture that the system would probably take over, and Jana might not be able to retain that independence and live on her own.”

While advances like the RDSP have been made in helping to provide greater security for the future of individuals with disabilities, Shirley and Mark are still haunted by pessimism.

“Are things moving fast enough? No. Hell no,” admits Shirley.

“But are they moving forward? Yes. And hopefully for those who come after as we look back on the days of integration and mainstream integration that we fought so hard for with Jana to stay and remain in her neighborhood schools.” “What has happened in the years to follow has been to benefit parents bringing very young children into
schools, and finding programs in place, and supports in place that weren’t there when we enrolled Jana.”

Shirley’s voice dims. “Things are moving forward, but there are still a lot of issues. Right now Jana can’t earn much more than a couple hundred dollars of her own money before they start clawing back on what is already a very low income.”

“Will we live long enough to see persons with disabilities have enough money to live a quality life? I’m not sure.”

“I don’t think we’ll see it in our lifetime.”
........................................................................
A few weeks later, I happened to meet Gayle again, this time she’s beaming with her new service dog, Angel. We sit down and talk about how things are coming along – matters are up and down. Her car is acting up, and she fears that she might have to get expensive repairs done. With Angel at her side though, I sense that Gayle feels like things will turn out alright.

We talk about her future. I ask Gayle what her life dreams are.
Gayle pondered my question for a bit. “I’d like to be able to buy treats for my dog. She works so hard for me that I wish I could buy something for her in return.”

“I’d love to be able to buy Christmas presents for my friends. I try every year to make things for my friends just to say thanks for all they do to help me.”

“I’d like to go to a movie if I saw one that I thought was good. I have a friend that lives on the other side of the river and we don’t see each other very often because it costs so much for transportation.”

“I’d love to phone her up and say ‘hey, can we meet for coffee or something?’”

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Head injuries the most serious injury when kids are on wheels

posted by SK Brain Injury    |   August 10, 2011 22:39

Safe Kids Canada: Helmets can reduce the risk of head injuries by 85 per cent.

Toronto, Ontario – May 31, 2010 – With spring in full swing and summer just around the corner, the number of kids enjoying wheeled activities like cycling, in-line skating, skateboarding and scootering is about to rise. But before hitting the streets this year, parents need to know one key thing: helmets save lives. Various injuries can occur from a fall, but the most serious are those to the head. Head injuries can often lead to death for kids on wheels – particularly in those children not wearing helmets. According to a Safe Kids Week research review, helmets can reduce the risk of head injury by 85 per cent.

The benefits of wearing a helmet during wheeled activities have long been touted by injury prevention experts. According to Transport Canada, in 2007 alone, over 1,000 children under the age of 15 were injured while riding their bikes. Other serious injuries include broken bones, facial injuries and serious skin abrasions that require grafts. Traumatic brain injuries account for eight per cent of emergency room visits by cyclists, four per cent of visits for both skateboarders and in-line skaters and six per cent of emergency room visits for injuries related to scooter riding in children under 19, according to the Public Health Agency of Canada.

“Serious head injuries are most often caused by falls; even seemingly minor incidents may cause short or long term brain damage,” says Pamela Fuselli, executive director of Safe Kids Canada, the national injury prevention program of The Hospital for Sick Children. “A child’s skull is only one centimeter thick and is easily fractured by a fall - even at slower speeds. When kids are on wheels, wearing a helmet can save their lives.”

Children riding bicycles are more likely to be admitted to hospital with an injury, but according to the Public Health Agency of Canada, traumatic brain injuries account for four per cent of emergency room visits for skateboarding and in-line skating related injuries, and six per cent of emergency room visits for scootering related injuries for children under 19.

According to a new Leger Marketing/Safe Kids Canada survey on helmet safety, more than a third of parents polled (35 per cent) say they are not concerned about their child having a cycling-related injury.
Cap off your wheeled activities with a helmet

Children are most likely to get hurt when they are beginners and just learning how to ride; when they ride or skate near cars and traffic; when they do not use safety gear and when they go too fast or try stunts.

“It’s important to select a helmet which is approved for the activity you’re doing,” says Dr. Charles Tator, neurosurgeon and founder of ThinkFirst Canada, a national non-profit organization dedicated to the prevention of brain and spinal cord injuries. “Bicycle helmets are good for people on bicycles, scooters and in-line skates, but skateboarders need a different helmet that protects the back of the head.” A less obvious, but equally important, difference between bicycle and skateboard helmets is in the construction. “Bicycle helmets are intended to offer the best protection against a single, forceful crash, after which it must be replaced,” Dr. Tator explains, “but skateboard helmets don’t offer this kind of protection. They work best against multiple, less intense impacts most common in skateboarding. So wearing the right helmet for the right activity really can make a difference.”

Become a ‘Roll’ Model

Most parents (73 per cent) say their child always wears a helmet when cycling. But when it comes to setting an example, both mom and dad could brush up on their helmet use. Overall, 31 per cent say they never wear a helmet when cycling.

“One of the best ways to get kids to wear their helmets when riding or gliding is by setting a good example,” reminds Fuselli. “Children who see their parents wearing helmets while cycling or gliding are more likely to wear their own helmets on a regular basis.”

Making headway with new laws

Head injury rates among child and youth cyclists are approximately 25 per cent lower in provinces with helmet laws, compared to those without. Currently Quebec, Manitoba, Saskatchewan, Newfoundland and Labrador and the Territories do not have mandatory bicycle helmet legislation for children under 18.

“We believe there should be a harmonized approach to helmet use for Canadian children,” adds Fuselli. “We’re advocating for helmet legislation for children in Quebec, Manitoba, Saskatchewan, Newfoundland and Labrador and the Territories to ensure all Canadian children are protected equally.”

The majority of Canadians polled (90 per cent) support legislation that mandates bicycle helmet use by children riding on public roads, and 81 per cent support legislation that mandates bicycle helmet use by children and adults. Almost two thirds of Canadian parents (63 per cent) consider helmet legislation as important as seatbelt legislation.

Top five tips to protect your child’s head

  • Ensure your children wear a helmet every time they ride.
  • Get the right kind of helmet. Choose a bicycle helmet for cycling, in-line skating and scootering. Skateboarders need a special skateboarding helmet that covers more of the back of their head.
  • Ensure the helmet fits your child. The helmet should rest two finger widths above the eyebrow. The side and chin straps should be snug.
  • People of all ages should wear a helmet when they ride. Remember: You are your child’s best role model.
  • Children under 10 should not ride on the road. They do not have the physical and thinking skills to handle themselves safely in traffic. Children over 10 need to practice before they can ride on the road.

Today marks the start of the 2010 Safe Kids Week – Got Wheels? Get a Helmet! – which runs from May 31 – June 5, 2010 and is sponsored by Johnson & Johnson.

Spokespeople across Canada

Safe Kids Canada has local expert spokespeople in Toronto, Montreal, Halifax, Calgary, Edmonton and Vancouver who are available for interviews.

Got Wheels Get a Helmet Pamphlet
Safe Kids Canada and Johnson & Johnson are offering a free educational pamphlet on helmet safety for parents and caregivers. Visit www.safekidscanada.ca to download your copy.

About Safe Kids Canada
Safe Kids Canada’s mission is to lead and inspire a culture of safety across the country in order to reduce unintentional injuries, the leading cause of death among children and youth in Canada. As a national leader, Safe Kids Canada uses a collaborative and innovative approach to develop partnerships, conduct research, raise awareness and advocate in order to prevent serious injuries among children, youth and their families. Our vision is Fewer Injuries. Healthier Children. A Safer Canada. Safe Kids Canada is the national injury prevention program of The Hospital for Sick Children. Across Canada, Safe Kids Canada partners are conducting Got Wheels? Get a Helmet! events this week, educating families on helmet safety. To learn more about Safe Kids Canada and child safety, visit www.safekidscanada.ca or call 1-888-SAFE-TIP.

About Johnson & Johnson
Johnson & Johnson is the founding sponsor of Safe Kids in North America (Canada, U.S., and Puerto Rico), and in 17 other countries around the world. The company also sponsors Safe Kids Week, Safe Kids Canada’s largest annual public awareness program designed to help reduce the frequency and severity of preventable childhood injuries, the leading cause of death and disability of Canadian children. Caring for the world, one person at a time inspires and unites the people of Johnson & Johnson. Johnson & Johnson embraces research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. Johnson & Johnson has more than 250 operating companies in 57 countries around the world, employing 115,500 people and selling products in more than 175 countries. Johnson & Johnson worldwide headquarters is in New Brunswick, New Jersey, USA

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Donated CFL brains show concussion-related disease

posted by SK Brain Injury    |   August 7, 2011 12:44

Two of the four deceased CFL players whose brains were donated to the Canadian Sports Concussion Project suffered from a neurological disease linked to concussions, preliminary results show.

The brains of Bobby Kuntz, Jay Roberts, Peter Ribbins and Tony Proudfoot, who all suffered from repeated concussions, were examined as part of the project at the Krembil Neuroscience Centre in Toronto Western Hospital.

The results show that Kuntz and Roberts suffered from a neurological disease known as chronic traumatic encephalopathy (CTE), an abnormal buildup of a protein in the brain.

Kuntz, a former linebacker for the Toronto Argonauts and Hamilton Tiger-Cats, and Roberts, an Ottawa Rough Riders tight end, also displayed other degenerative changes.

"While both of these men appeared to have pathological signs of CTE, they also suffered from other serious neurological and vascular-related diseases," said Dr. Lili-Naz Hazrati, a neuropathologist who performed the autopsies.

The study, the first of its kind, was conducted at Toronto Western by a collection of concussion experts, including Dr. Charles Tator, Dr. Richard Wennberg and scientists from several other Canadian institutions.

Patients who suffer from CTE can experience memory impairment, emotional instability, erratic behaviour, depression and problems with impulse control. The condition can also advance into dementia.

"There are still so many unanswered questions surrounding concussion and the long-term consequences of repeated head injuries," Tator said. "We are trying to determine why some athletes in contact sports develop CTE and others don't, as well as how many concussions lead to the onset of this degenerative brain disease Also, we need to develop tests to detect this condition at an early stage and to discover treatments."

Kuntz died in February 2011 at age 79 after a long battle with Parkinson's disease and diffuse Lewy body disease — a condition that overlaps with Parkinson's and Alzheimer's disease. Roberts, 67, passed away in October 2010 after suffering from dementia and lung cancer.

The results from the autopsies done on Ribbins and Proudfoot did not show signs of CTE. Ribbins, a receiver and defensive back with the Winnipeg Blue Bombers, died at age 63 of Parkinson's disease. Proudfoot, an all-star defensive back with the Montreal Alouettes, lost his battle with amyotrophic lateral sclerosis (ALS) this year at 61.

Dr. Hazrati emphasized the exact link between concussions and neurodegeneration need to be examined by further research.

"Right now we have more questions than answers about the relationship between repeated concussions and late brain degeneration," he said. "For example, we are still trying to understand why these two players acquired CTE and the other two did not."

Ribbins and Proudfoot played in an era when tackling by leading with the helmet was common. Known as a hard-hitting defensive back during his 12-year career, Proudfoot experienced repeated head trauma, according to the CFL's Alumni Association.

Mary Kuntz, wife of the late Bobby Kuntz, believes more players who donate their brains for research will help athletes in the future.

"We've always had questions about Bob's health, because there were so many conflicting medical opinions," she said. "We knew there must have been some effect from all of the concussions over the years, and this was an affirmation that concussions did have a part in his health problems.

"Young players should know the risks of concussions. When you are young, you can't believe what can happen to you when you are older, but we have lived though it. What is good about this study is that there will be more evidence and information for players."

"We were very happy to be involved in this and it has brought us a sense of closure."

Jay Roberts's son Jed and his sisters recognized the earlier signs of their father's memory loss after he recounted the same stories.

"My dad had numerous concussions, although they were undocumented, and I think he knew there was something was wrong, which is why he wanted to help find answers that would hopefully protect future football players," said Jed, a former CFL player with the Edmonton Eskimos. "I think it is really important that we create awareness around this issue, so that players can live healthy, productive lives beyond the game."



Read more: http://www.cbc.ca/sports/football/story/2011/07/26/sp-cfl-players-study.html#ixzz1UN0MOGn3

 

Source: http://bit.ly/nJU47l

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Sask. needs safety culture

posted by SK Brain Injury    |   August 4, 2011 16:55

For a province with a small population, Saskatchewan seems to frequently be among the national leaders, but not always in a good way.

As some recent figures from the Canadian Institute for Health Information and from the province's Workers Compensation Board reveal, whether at play or work, Saskatchewan residents are among the leaders in Canada when it comes to paying a heavy price through wholly avoidable injury or death.

For instance, propelled in part by Saskatchewan's newfound wealth that allows families to buy bigger and faster toys, and in part by some ingrained recklessness that contributes to riders eschewing basic safety gear such as helmets and eye protection, and forgoing so much as a safety course in handling high-powered equipment, this province has become a national leader in ATV injuries over the past decade.

Lagging only the richer, and apparently higher risk-taking Albertans, Saskatchewan rocketed to an ATV injury rate of 22.1 per 100,000 residents in 2009-10, according to CIHI, compared to nine injuries per 100,000 in 2001-02.

Among the problems involved with curbing reckless and/or inebriated riders is the fact that Saskatchewan is lone among the provinces in not requiring the registration of these vehicles, which makes it tougher to report offenders even if it's to save their lives.

The agency released its findings just before the August long weekend because summer holidays are the prime time for injuries not only from ATV-related events but also from other outdoor leisure activities, with falls and collisions involving bicycles the most common.

While horrific ATV injuries can range from broken bones and nerve damage to paralysis, predominantly involving young men aged 15 to 24, bicycle-related injuries in young people under age 20 are by far the most common, accounting for almost half the hospital admissions from recreation-related events.

Even though head injuries from bicycle accidents can have a permanent and debilitating impact, Saskatchewan cities have yet to follow the lead of places such as Vancouver and implement mandatory helmet use laws.

Rather than treat helmet use as a case of individual responsibility, it's time that the provincial government took the lead in sending a strong message by mandating their use. While the decline nationally in head injuries among cyclists during the past eight years as the number of injuries remains fairly constant suggests that more people are wearing helmets, even one serious brain injury prevented by mandating helmet use is worth the effort. And with Saskatoon having among the highest proportion of cyclists per capita in Canada, such a law is bound to pay dividends by preventing some heart-wrenching injuries.

The objective necessarily isn't to punish offenders as much as it's to make it part a safety culture in a province that sorely needs an attitude adjustment on safety.

After all, despite a decades-long law on seatbelt use, the number of injuries and deaths involving unbuckled motorists, especially in rural areas and on reserves, remains depressingly high.

As the WCB's annual report keeps noting year after depressing year, even though Saskatchewan is making gains in reducing workplace injuries, our rate remains near the top of injury rankings at nearly twice the national percentage.

None of these are areas where Saskatchewan wants to lead Canada. Let's leave that to our universities and athletes.

 

Source http://bit.ly/nDcKex

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Why are so few adults wearing bike helmets?

posted by SK Brain Injury    |   August 1, 2011 20:55

 

Every day in Canada, 36 people end up in hospital from bicycle injuries. That rate hasn't changed much in the last decade, according to new data. But even with more kids wearing helmets when they cycle, the number of adults who insist on riding helmet-free holds stubbornly steady.

Data from the Canadian Institute of Health Information show that the number of Canadians ending up in hospitals from bike accidents remained fairly unchanged between 2001 and 2010 -- about 4,300 a year.

The number of cycling-related head injuries decreased significantly in that decade: from 907 to 665. But among the most severe injuries -- those ending up in trauma units -- 78 per cent were not wearing a helmet.

"That data suggest that perhaps helmets are helping and it is a shame that people are not hearing the message about wearing helmets," says Claire Marie Fortin, CIHI's manager of clinical registries.

When CTV News cameras headed out to some popular cycling trails in Toronto, it wasn't hard to find adults who weren't wearing helmets.

"Why didn't I wear a helmet? Because I am a fool. I don't think it will happen to me," cyclist Kevin Boland said.

Another cyclist said he doesn't wear a helmet out of convenience, because he doesn't like taking the helmet on and off. Others told us helmets were too uncomfortable.

Across Canada, many provinces have laws requiring kids under 18 to wear helmets when cycling. But only four -- British Columbia, New Brunswick, Nova Scotia and Prince Edward Island -- require all cyclists to protect their heads with helmets.

"Some of our provinces have zero legislation even for children can you believe that?" says concussion expert Dr. Charles Tator of Toronto Western Hospital.

"So we have a big job to do to convince our legislators and to convince the public that we should have comprehensive legislation right across the country for bicycles, scooters and inline skates and on our road."

But it is a tough battle. The British Medical Journal has just published a survey showing that two thirds of its readers voted against mandatory bike helmets -- and many of those readers would have been health care workers.

In Vancouver, where bike helmets are mandatory, there are plans for a legal challenge of the helmet law that's scheduled for mid-August. Many of those fighting the law say making helmets mandatory infringes on their rights.

Some even call the law discriminatory against cyclists, noting that drivers who are also at risk in an accident don't have to wear helmets. They note there are only a few hundred hospitalizations for head injuries among cyclists. By comparison, in 2004, there were close to 6,000 hospital admissions for head injuries in car crashes.

The cyclist who is challenging the law argues in his court filings: "Bicycle helmet legislation is discriminatory as it applies, with demonstrable justification, only to individuals who ride bicycles without being equally applied to individuals who drive automobiles or walk."

With a report from CTV's medical specialist Avis Favaro and producer Elizabeth St. Philip

 

Source: http://bit.ly/pKD2Kp

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Head injury dementia link

posted by SK Brain Injury    |   July 25, 2011 17:15
A study conducted by researchers at the Southern General Hospital in Glasgow and the University of Pennsylvania is thought to be the first to find a physical abnormality in the brain tissue of people who have had a head injury.

A previous link had been established between dementia and sports where repetitive blows to the head are common, such as boxing and football.

However, this study has revealed a similar link with people who have suffered other kinds of head injury.

Dr William Stewart, head researcher of the Glasgow team said: "We know from clinical studies that there's a link between sustaining a head injury and developing dementia, and what we're interested in is trying to understand what might be happening in the brains of these patients," reported the BBC.

The link was established when researchers examined the brain tissue from 39 people who had recovered from a brain injury, and 39 people who had never had a brain injury.

Abnormalities were found in one third of those who had had an injury.

Dr Stewart said: "What's quite remarkable, and causing much excitement, is that the patients who'd had a head injury had quite large numbers of proteins – or abnormalities – in their brain.

"That's very similar to what we'd see in older patients and, in particular, people with Alzheimer's, yet these patients were in their 40s and 50s and the only thing which marked them apart from the control group was that they'd had a head injury."

Significantly, the study suggests a brain injury could kick-start a process in which the brain is damaged in other ways. Dr Stewart hopes that this finding will lead to further research to uncover how and why dementia develops.

"Part of the challenge in dementia is that a lot of the work we do is with people who already have it.

"What we don't understand is how they get to that stage and what sets off the process in their brain. What we might be able to do is to study patients after a head injury and work out what's happening inside their head."

Veterans study

A large study on older veterans has raised fresh concerns about mild brain injuries and concussions that hundreds of thousands of troops have suffered in recent wars.

The studies, reported at the Alzheimer's Association International Conference in France, challenge the current view that only moderate or severe brain injuries put people at a higher risk of dementia.

The veterans study was led by researchers at the San Francisco VA Medical Center.

Dr Kristine Yaffe, a University of California professor and director of the Memory Disorders Clinic at the Medical Centre who led the study said: "It's by far the largest study of brain injury and dementia risk. It's never been looked at in veterans specifically."

As reported at yahoo.com, researchers reviewed medical records of 281,540 veterans who got care at Veterans Health Administration hospitals from 1997 to 2000 and had at least one follow-up visit from 2001-2007. All were at least 55 and none had been diagnosed with dementia when the study began.

As the dementia risk is more common with age, the large number of cases studied was needed to compare those with and without brain injuries.

Records showed that 4,902 of the veterans had suffered a traumatic brain injury, or TBI, ranging from concussions to skull fractures. Over the next seven years from 2007, more than 15 percent of those of those who had suffered a brain injury were diagnosed with dementia versus only 7 percent of the others. Severity of the injury made no difference in the odds of the developing dementia.

Despite evidence that even a concussion or a mild brain injury can put you at risk, said Laurie Ryan, a neuropsychiatrist who used to work at the Walter Reed Army Medical Center, William Thies, the Alzheimer's Association's scientific director told people not to panic, as this doesn't mean that every soldier or student athlete who has had concussion is in danger. He said: "Pro-football players and boxers "are almost a different species from us" in terms of enduring repeated blows they take to the head."

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Governor General and Mrs. Johnson have become patrons of BIAC

posted by SK Brain Injury    |   July 24, 2011 12:08

OTTAWA – The Brain Injury Association of Canada is proud to announce that Their Excellencies the Right Honourable David Johnston, Governor General of Canada and Mrs. Sharon Johnston, have agreed to be Patrons of the organization. The board, volunteers and staff of the Brain Injury Association of Canada are very honoured by this timely announcement, prior to our Annual Conference in August in Prince Edward Island. "We are particularly pleased that the Governor General and Mrs. Johnston have agreed to be Patrons of the Brain Injury Association of Canada. The Governor General's vocal recognition of the value of volunteerism and philanthropy to the quality of Canadian communities is important to the brain injury community. Active support of volunteering and philanthropic giving are key contributions to our nation’s social, cultural, and economic prosperity makes this a strong partnership," said Harry Zarins, Executive Director of the Brain Injury Association of Canada.

In an instant a life is changed, forever. Every day we participate in activities that produce endless risks for sustaining a brain injury: car accidents, a fall from a bike, or a blow to the head. It is estimated that thousands of Canadians incur a traumatic brain injury (TBI) and mild traumatic brain injury (mTBI), also known as a concussion, each year, the majority being young adults. Statistics indicate that the incidence of brain injury is two times greater in men. The Brain Injury Association of Canada (BIAC) strives to raise awareness of the incidence of acquired brain injury (ABI) in Canada.

A brain injury may make it necessary for the injured person to require full time assistance. Families often become the primary caregiver and support person. Many families are left to cope on their own. They sometimes have little understanding of the effects of the injury and the demands that will be made of them by an injured family member. Families need support from others who understand the effects of acquired brain injury.

The Brain Injury Association of Canada (BIAC) provides a shared forum for the support of both families and survivors. BIAC also advocates for the enhancement of support services. Prevention through public education, and safety legislation is the key to the reducing the occurrence of ABI amongst Canadians. The Brain Injury Association of Canada engages in extensive public education initiatives through its many local community associations across Canada. Neuroscience and injury prevention research is another key to addressing ABI. The Brain Injury Association of Canada endeavours to support and promote research in Canada and internationally.

At the founding meeting in July 2003 in Montreal, members from brain injury associations from across Canada, representing survivors, families, medical and research professionals identified the need to create the Brain Injury Association of Canada. Our mandate is to improve the quality of life for all Canadians affected by acquired brain injury and promote its prevention. BIAC is dedicated to the facilitation of post-trauma research, education and advocacy in partnership with national, provincial/territorial and regional associations and other stakeholders. BIAC is incorporated as a national charitable organization under the Canada Corporations Act and the Canada Revenue Agency.

 

SOURCE: www.biac-aclc.ca

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