Tony Proudfoot donates brain, spinal cord to research

ALLAN MAKI

From Tuesday’s Globe and Mail
Published Tuesday, Jan. 11, 2011 12:09AM EST

It was the last act of a compassionate man. Before he died last month, Tony Proudfoot considered his three-year fight against Lou Gehrig’s disease and knew what he had to do. He had to help find a cure, the reason behind his affliction. So he did one last thing.

He donated his brain and spinal cord to researchers.

Tony Proudfoot, a former CFL all-star who once employed a staple gun to give his team an edge in the Grey Cup's storied ``Ice Bowl,'' has died. He was 61. Proudfoot, who had been fighting Lou Gehrig's Disease for the last three years, is photographed at his home Tuesday, August 24, 2010 in Montreal. - Tony Proudfoot, a former CFL all-star who once employed a staple gun to give his team an edge in the Grey Cup's storied ``Ice Bowl,'' has died. He was 61. Proudfoot, who had been fighting Lou Gehrig's Disease for the last three years, is photographed at his home Tuesday, August 24, 2010 in Montreal.

On the second last day of 2010, Proudfoot passed away from amyotrophic lateral sclerosis, leaving behind a wife and three children and too many former Montreal Alouettes teammates and admirers to number. What he also left behind was a tangible means of examining ALS and the possibility he believed in: that the disease bore a connection with repeated head trauma. The kind he endured as a hard-hitting defensive back in the Canadian Football League.

Proudfoot and his family’s decision to donate his brain and spinal cord is another constructive step in trying to diagnose the brain and what affects it. Tissue samples of Proudfoot’s 61-year-old brain have been taken to Montreal’s Neurological Institute and Hospital and passed along to pathologists in Toronto.

Those who will assess and discuss the findings include Toronto neurosurgeon Dr. Charles Tator and Dr. Angela Genge, ALS director at the Montreal Neurological Institute. Genge had worked with Proudfoot after he was diagnosed in 2007.

“It really does [speak to his character],” Genge said of Proudfoot’s decision to fight ALS in every way he could, even in death. “He turned even this into something good. Not everyone will do that.”

Genge said the study of head trauma and concussions needs not just damaged brains to research but those from former athletes who have passed away through natural causes. The plan is to compare subjects and their experiences. It may be a mix of factors that leads to ALS and it’s something the medical community is eager to explore.

“On the science side, there are different things happening,” Genge said. “One is looking at the long-term potential risk facing football players who were exposed to recurrent head trauma. Another is, were there any toxic issues? Like pesticides used on fields. That’s not been proven at all. But is there a combination of factors?”

Former Winnipeg Blue Bomber Leo Ezerins is doing his part for research too. As head of the CFL Alumni Association, Ezerins has been soliciting brains for Tator and others at the Krembil Neuroscience Centre at Toronto Western Hospital.

Ezerins secured Jay Roberts’s brain before the 67-year-old former Ottawa Rough Rider died of lung cancer last October. Roberts suffered several concussions in his career, including one where he had no memory of what he’d done over a period of 72 hours.

“I was told the biggest challenge was to find brains,” Ezerins explained. “I said, ‘I’m sure our guys would be interested.’ Any guy I’ve talked to has said, ‘Not a problem.’ It’s part of a legacy. … The doors just opened up with Jay Roberts.”

Ezerins is a member of a group that includes neurosurgeons, pathologists and psychologists looking into postconcussion syndrome in professional athletes. Genge said it’s critical that athletes and their leagues get behind the science of the brain and what can be done to protect those who take the greatest risks.

“Some [leagues] are just plain afraid,” Genge said. “That’s a normal response. They’re afraid of the consequences, and in the business of professional sports, some organizations are afraid to be sued. … The quest to understand recurrent head injury trauma should be most important.”

Proudfoot played 12 seasons in the CFL and was also renowned for his life-saving efforts during the 2006 shootings at Dawson College, where he was a teacher. He helped raise more than $500,000 for ALS research before his death.

http://www.theglobeandmail.com/sports/football/tony-proudfoot-donates-brain-spinal-cord-to-research/article1865047/ 

Tony Proudfoot, CFL Alumni, relying on his team to fight the battle

 

 Tony Proudfoot, CFL Alumni, relying on his team to fight the battle.

ALS has forced Tony from the field to the sidelines, but he refuses to go quietly.

Montreal (November 20, 2009) Amyotrophic Lateral Sclerosis (ALS)—also known as Lou Gehrig’s Disease—is devastating.  For Tony Proudfoot, former Alouettes and BC Lions player, he knows the impact all too well. “In 2007, I was diagnosed with ALS and from that moment on my life changed forever,” says Tony. “I never thought that I would be forced to stand on the sidelines so early in my life.” But Tony refuses to stand quietly. As with his football career, he is fighting to win this one but he needs to recruit a committed team.

“Team Proudfoot Inspired Mosaic.”

“With this team I am asking for people to help raise awareness surrounding ALS,” says Tony. “With the Inspired Mosaic all those touched by ALS, no matter how they communicate, what their mobility or strength is, can take part.”

Awareness breeds knowledge, knowledge fosters change. The desired outcome: enhanced research, improved clinical care, upgraded services. Be part of this team, we have a significant challenge in front of us!

Since Tony became public with his diagnosis, he has inspired thousands of people coast to coast through his words, his actions, and his positive outlook on life. It has now been two years since he was diagnosed with ALS. “I am continuing to slide downhill, communicating only with the aid of my computer, eating with a feeding tube (I have lost 50 lbs, and counting) and struggling to breathe even on the smallest of exertions,” he says. “Luckily I can still move about and I keep on doing the activities that I love with the people I care about. I enjoy my association with the Alouettes, working as an adviser and I writing about football on CJAD’s website.”

As the hype for the Grey Cup nears, Tony welcomes the opportunity to “talk” football, “talk” about living with ALS and/or “talk” about “Team Proudfoot Inspired Mosaic.”

 For information, contact:

 Tony Proudfoot:  tonyproud24@hotmail.com (text message: 514-919-2093)

Claudine Cook, Executive Director, ALS Society of QC: ccook@sla-quebec.ca , mobile 514-298-0540

Dr. Angela Genge:  Director of the ALS Clinic, Montreal Neurological Institute Hospital 514-398-3868
What is ALS?

Amyotrophic Lateral Sclerosis is a rapidly progressing, neuromuscular illness that is always fatal. Known in France as Charcot’s Disease – after the neurologist who first described it 130 years ago – and in America as Lou Gehrig’s Disease – after the famous baseball player who died of it in the 1940s, it is characterized by the progressive degeneration of the neurons controlling the motor muscles, gradually leading to total paralysis of the body while leaving the intellectual faculties untouched. ALS can strike anyone, regardless of age, sex or ethnic origin. Although ALS generally develops between the ages of 50 and 75, it can occur in people as young as 20. ALS usually leads to death within three to five years of the diagnosis, although for some unknown reason, 10 to 15% of patients survive about 10 years after they have been diagnosed.

How to be part of “Team Proudfoot Inspired Mosaic” 

To be part of “Team Proudfoot Inspired Mosaic” only takes a few minutes. Simply upload a photo and send a message to Tony, someone touched by ALS, a loved one or to someone who has inspired you. The photo then becomes a permanent part of the tapestry of the “Inspired Mosaic” and a lasting tribute to caring individuals who are or have been touched by ALS.

To upload a picture and message:

1.go to: http://www.sla-quebec.ca/mosaic/?lang=en (english) or

             http://www.sla-quebec.ca/mosaic/?lang=fr (french)

2. Follow the easy steps … then watch Team Proudfoot and our Inspired Mosaic build!

3. You can view the Inspired Mosaic by visiting http://www.sla-quebec.ca (click on the icon)

4. With a donation of $50 or more, donors will receive a print of the Inspired Mosaic   autographed by Tony Proudfoot