Showing posts with label als. Show all posts
Showing posts with label als. Show all posts

Wednesday, August 27, 2014

Cold cash just keeps washing in from ALS challenge

In the couple of hours it took an official from the ALS Association to return a reporter's call for comment, the group's ubiquitous "ice bucket challenge" had brought in a few million more dollars.

In this photo taken on Tuesday, Aug. 26, 2014, Ten Pocket iNet corporation employees, from left,including Terri McMakin, Don Gibbard, weargin hard hat, and Jake Tegtmeier, right, take the ice bucket challenge at the Walla Walla Regional Airport in Walla Walla, Wash.to benefit ALS research. The water was poured from two lift trucks. Gibbard said he wore his hard hat to protect from the ice cubes and took the brunt of dousing because "I was pulled back!": In this photo taken on Tuesday, Aug. 26, 2014, Ten Pocket iNet corporation employees, from left,including Terri McMakin, Don Gibbard, weargin hard hat, and Jake Tegtmeier, right, take the ice bucket challenge at the Walla Walla Regional Airport in Walla Walla, Wash.to benefit ALS research. The water was poured from two lift trucks. Gibbard said he wore his hard hat to protect from the ice cubes and took the brunt of dousing because "I was pulled back!"

Approaching $100 million, the viral fundraising campaign for the ailment better known as Lou Gehrig's Disease has put the ALS group into the top ranks for medical charity donations. Since the end of July, the money has been sloshing in at a rate of about $9 million a week. Last year, from July 29 to Aug. 26, the group raised just $2.6 million.
It's caught everyone off-guard, none more so than the ALS Association folks. But they know this is likely a one-off phenomenon, and the group now faces the task of spending all that money wisely. Research, care and advocacy are the group's three main missions — but officials say they don't know yet exactly how they'll use the astonishing windfall.
"I think even if I or any PR person at either a non-profit or a for-profit company had all of the PR dollars in the world to invest, no one would have come up with this idea," says Carrie Munk, the association's spokeswoman. "We realize there are responsibilities that come with being good stewards of these dollars."
In this Friday, Aug. 22, 2014 file photo, people pour ice water over themselves during an "ice bucket challenge" fund raising event in Bangkok. About a thousand people turned out to raise money for the fight against ALS, or Lou Gehrig's Disease.
Part of what's surprising is that ALS — or amyotrophic lateral sclerosis — is one of those "orphan" diseases. It is a neurodegenerative disease that causes paralysis and death, and the association estimates that about 5,600 new cases are diagnosed in the U.S. each year.
This campaign hasn't exactly put the charity in the same neighborhood as giants like the American Cancer Society, the American Heart Association or Susan G. Komen for the Cure — which raised $889 million, $529 million and $310 million last year, respectively. But it's moving into the same ZIP code now.
"People who have been in this space for a long period of time feel like it's a dream come true," says Munk.
In case you've been under the proverbial rock, here are the basic rules: Someone issues a challenge — that you allow yourself to be doused with a bucket of ice and water, like winning coaches along the sidelines. Then, the challengee has 24 hours to make a $100 donation to the ALS Association or submit to the water torture.
In the last month, everyone from Microsoft co-founder Bill Gates to former President George W. Bush has been doused. The Internet and airwaves are awash in videos of people taking the challenge — even if they fully intend to write the check.
Jonah Berger, author of the book "Contagious: Why Things Catch On," says it's like a modern-day chain letter — except, in this case, everyone will know if you break the chain.
"It has a lot of the key ingredients that often make people want to share things," says Berger, a marketing professor at the University of Pennsylvania's Wharton School. "It gives people lots of social currency to be part of it. It makes you look good. It makes you look smart and in the know; you know what's going on. And it's always hard to back down from a challenge."
And now others are co-opting the bucket challenge for their own causes.
Actor Matt Damon, for instance, dumped toilet water over his head to call attention to his passion — safe drinking water. Actor Orlando Jones of the television series "Sleepy Hollow" showered himself with bullets in the wake of black teenager Michael Brown's shooting death by a white police officer in Ferguson, Missouri.
"I'm challenging myself to listen without prejudice, to love without limits and to reverse the hate," he said. "So that's my challenge — to me. And, hopefully, you'll accept this challenge, too."
But the success for ALS is the kind of thing you can't really replicate — even if you did it first.
In late June, about a month before the ice bucket challenge exploded, University of Arizona woman's basketball coach Niya Butts took the "cold water challenge." After being doused with a 10-gallon plastic cooler, Butts gave her Pac-12 coaching rivals 48 hours to do the same or donate $250 to the Kay Yow Cancer Fund — named for the North Carolina State University coach who succumbed to the disease in 2009. That challenge — #Chillin4Charity — has raised only about $75,000 so far.
"We didn't raise millions," Butts told The Associated Press on Wednesday. "But we raised awareness of millions."
The campaign has had more than 80,000 tweets, 100,000 retweets more than 215 million Twitter reaches, said Susan Donohoe, the Yow fund's executive director.
The Chronicle of Philanthropy says the ALS Association has, in this short period of time, raised more than many of the charities included on its Philanthropy 400 list.
"Right now, we're really focused on reaching out to and acknowledging and thanking the over 2 million donors that have come to the ALS Association," said Munk, the association spokeswoman. "And also working to put a process in place to make the best decisions to spend these dollars."
The American Institute of Philanthropy's CharityWatch gave the group a B+ rating for spending about 73 percent of their cash budget on programs. Analyst Stephanie Kalivas has no reason to believe that rating will need to be downgraded.
"We will definitely be keeping an eye out for them," she says. "Hopefully, they won't be wasteful with it."
Dr. Richard Bedlack, who runs the ALS clinic at the Duke Institute for Brain Sciences in Durham, North Carolina, knows how he would allocate the money. While the temptation might be to plow it all into the search for a cure, he says the biggest strides have been made in patient care and quality of life, and that would be his No. 1 priority.
"The chances of one of these research studies really finding meaningful disease-modifying therapy is very small," he says. "We're shooting in the dark. So, of course we've got to keep trying. But the bottom line is we've got to understand this disease better before we're going to be able to fix it in most people."

Tuesday, August 26, 2014

Man stricken with ALS suspected of killing 2 women

Accused: ex-Dane County sheriff's deputy Andrew Steele, pictured, is accused of killing his wifeWhen Andrew Steele retired as a sheriff's deputy, his career cut short by the advance of ALS, he had no bigger cheerleader than his wife. Ashlee Steele spearheaded a drive to raise $75,000 for his medical care, and her Facebook feed is filled with the shrieks and laughter of the cold-water challenges the couple's family and friends were eager to accept.
Now, Andrew Steele is a suspect in the killings of his wife and her sister, Kacee Tollefsbol, at the Steeles' home in suburban Fitchburg, Wisconsin on Friday. Steele himself is being treated for an apparent suicide attempt that, police say, they never saw coming.
"Nobody closely aligned with Andy and his family expected something like this to occur," Dane County Sheriff Dave Mahoney told The Associated Press on Monday. "We believe his diagnosis had an impact on the family but they were moving forward."
Mahoney said Steele, 39, had been a deputy since November 1998. He had worked for the past several years in the county jail but resigned in June after he was diagnosed with amyotrophic lateral sclerosis, better known as ALS, or Lou Gehrig's disease. ALS attacks nerve cells and can lead to complete paralysis and death. The average life expectancy is two to five years after diagnosis.
Police said Ashlee Steele, 39, and Tollefsbol, 38, of Lake Elmo, Minnesota, were shot.
It was unclear when prosecutors might charge Andrew Steele. Dane County District Attorney Ismael Ozanne didn't immediately return a phone message Monday, and Fitchburg Police Lt. Todd Stetzer said he had no information to release on the case.
Before Friday, Mahoney said deputies had been talking with Steele about joining the family's "Tough as Steele" effort to raise money for his medical care and other family expenses. The Steeles have two children while Tollefsbol was the mother of four.
"We're trying to understand what could possibly have gone wrong and resulted in the death of two young women and the fact that there's now six children without a mother," Mahoney said.
Steele's family started the "Tough as Steele — Taking Down ALS" campaign via the website GiveForward.com. The site said the loss of his income had been crushing to the family. As of Saturday, supporters had raised nearly $23,000 toward their $75,000 goal, the Milwaukee Journal Sentinel reported. The campaign appeared to have been removed from the site over the weekend.
Ashlee Steele's Facebook page contains several videos of law enforcement colleagues and other friends taking the ALS Ice Bucket Challenge in Steele's honor. They include Madison Police Chief Mike Koval offering prayers and firefighters from three departments cheering as a ladder truck hoses them down.
"I never would have expected the type of reaching out people have done," Andrew Steele told WMTV earlier this month. "People that have donated, people that I don't even know very well, I haven't seen or talked to in years. It's hard to describe that."
Ashlee Steele had taught 3-year-olds in the preschool at Christ Memorial Lutheran Church in Fitchburg, staff coordinator Elsa Gumm said.
"She was very organized, just full of joy in general," Gumm said. "She was so great at being hands-on with the kids. She just made kids and parents alike feel at ease."
Gumm said she had never met Andrew Steele and couldn't offer any insights into why he would have hurt his wife.
"That's the big question in our minds as well," she said. "What we keep turning to is we may not get answers to those questions, so we just cling to our hope in Jesus Christ."

Wednesday, August 20, 2014

Former Titans LB Tim Shaw 'overwhelmed' with support after revealing his ALS diagnosis

Tim Shaw knew, sooner or later, he had to go public that he had ALS.
As the Ice Bucket Challenge phenomenon to raise awareness and money to fight the disease and find a cure swept the country, the former Titans linebacker and special teams captain knew the time had come. Shaw had been living with ALS since April, and on Wednesday shed light on his decision.

"It was very difficult to go public," Shaw said. "But it was made very clear to me that the time was right. I had waited for months, and needed to process it on my own and figure out what my message was going to be. Because if I had just come out right away, I wouldn't have known much about it. I wouldn't have known what I am really going to stand for against this in my life."

Following training camp practice on Wednesday, every Titans players and the coaching staff accepted that Ice Bucket Challenge, collectively dumping ice water over their heads as Shaw smiled while watching. He was then greeted with hugs and words of encouragement by many of his former teammates.

"I am overwhelmed just by the support," said Shaw, 30, a seven-year NFL veteran who played for the Titans from 2010-12. "It has been unbelievable. I have always loved attention, but not this kind of attention. I knew it was something that I needed to do. I knew it was something that would be beneficial, not for me, but for the cause.

"So, that's why I did it. It has been amazing support, an amazing response. The human race is so powerful in what we can do when we pull ourselves together and put our minds to something. It's really amazing."

Commonly referred to as Lou Gehrig's Disease, Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. There is no cure for the debilitating disease that often leads to paralysis and/or death.

According to the ALS Association website, it has received $31.5 million in donations as of Wednesday as a result of the Ice Bucket Challenge. That compares to $1.9 million raised during the same time period last year. Donations have come from existing donors and 637,527 new donors.

"It's an important cause," Titans coach Ken Whisenhunt said. "It's a terrible disease. I have a lot of respect for Tim. It's horrible that he has to go through this. But anything we can do to raise awareness for it, to help get a cure, that's important."

Shaw said he started feeling symptoms of the disease in late 2012 and early 2013. He was released by the Titans during training camp last year when the team made its final roster cut to 53 players. A 2007 fifth-round draft pick of the Panthers, he also played for the Jaguars (2008) and Bears (2009), before playing 48 games in three seasons with the Titans.

"It showed itself in my muscles," Shaw said of early ALS symptoms. "You could see my legs twitching, my muscles twitching. And it showed itself in weakness in my muscles, and it showed itself in loss of some athletic ability that I have always had. Those were the early signs."

Following the end of the 2012 season and leading to training camp in 2013, Shaw worked with Titans staff and doctors trying to find a cause for his ailments.

"While I was playing here, that whole 2013 offseason, the Titans' staff were analyzing me for different things and trying to figure out what sports injury I was suffering from and to just no avail," Shaw said. "I don't blame anyone. It's just something that you don't think about. There were tests done, and there were doctors seen. So, it just never crossed anyone's mind to go that direction."

Titans linebacker Derrick Morgan was Shaw's teammate all three seasons he played for the Titans. He said today it was difficult to see Shaw and what he was going through, but also expressed admiration for how Shaw is handling the disease.

"I have been praying for him ever since I found out," Morgan said. "Tim is such a good guy, so you hate to see somebody who's a good guy with a good heart going through something that harsh. It really hurts to see him, but his resolve has been very impressive.

"He is remaining positive and making the most out of his opportunity and his platforms that he has. We have to keep encouraging him, keep him in your prayers, and hopefully a miracle will happen and he will get healed."

Shaw said that he does not blame playing football and its physical nature as a factor in having ALS.

"I love the game of football," Shaw said. "From the time I first played it as a 12-year-old, this game was for me. No doubt about it in my mind, not a single regret. The game of football has given me so much. It's brought me so many different places and so many avenues and opportunities, I wouldn't take it back."

But Shaw said that the game of football at all levels needs to improve its approach when it comes to prevention, diagnosis and care for all kind of injuries, including those to the brain.

"I do think that we need to get smarter as we continue with this game," Shaw said. "I think we do need to learn more about what it is doing to our bodies and heads and things like that. I don't blame the game. I'm not a doctor. I don't know. People get this disease who never play football."

Shaw said that he is currently taking an approved drug to slow symptoms of the disease. He also meets with physicians every three months, but vows to continue to living life as he always has.

"It's the hardest thing I ever had to hear," Shaw said of learning he had ALS just a month after turning 30. "So, every thought runs through your mind. But as a man, you have a choice. What are you going to do? Are you going to stand up and fight for your life? Or are you going to accept what someone else tells you is reality and just fade away?

"And so, as staggering as that news was and as shocking as it is to hear and to say, I made that choice to stand up and live life to the fullest like I believe I always have."