A 2007 Rochester Runner of the Year Series Event 

 

Presented by

 

Medved

Medved 5k to Cure ALS

& 3k Fitness Walk

Father's Day

 Sunday, June 17, 2007

Active.com - part of the Active Network, Inc.

 

2006 Individual Results  

2006 Age-Group results

2006 Team results

Pictures

   
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Race Day 

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2006 Medved 5k to Cure ALS Champions:  Benand Onsare (14:41) of Kenya and Shari Boyle of Toronto (17:56). Onsare led a 1-2-3 sweep by the Hamilton, Ont. based group with former Medved 5k champion Henry Githuka  2nd (14:42) and Simon Njoroge 3rd (14:43). Boyle's Toronto Olympic Club teammate Colleen Hopkins won the Women's masters division in 20:18 while Dave Bischoff salvaged the day for the good ol' USA by winning the Men's Masters division in 17:20.

Kids vs. "Spikes the Mascot" Races

begin at 9:30am

               

 

Press Release 

 

The quest is now for $200,000!

Proceeds from the  Medved Father's Day 5k to Cure ALS  are now over $124,000  and go to help fund an ALS drug screening research project at Harvard University. 

Currently, over 30,000 people are are  afflicted with this non-curable disease, for which there presently exists no treatment and no hope for survival.

Additional tax-deductible donations can be given by a check made out to ALS-TDI and submitted with the race form or dropped off at the registration table on race day.

See a list of 2006 donors to date

Contributions for ALS:

Individuals that raise $50 or more in contributions for ALS will receive free entry to the 2007 race and a commemorative Medved 5k race t-shirt.  Contributions must accompany your entry form either by mail or in person at Medved Running & Walking Outfitters at 3400 Monroe Ave (in the Pittsford Colony Plaza) on Saturday June 17, 2007 from 10 am - 5 pm or in person on the day of the race, starting at 7 am.

ABOUT ALS

TDF IS NOW TDI
COLLABORATION FUNDS HISTORIC $36M ALS DRUG SEARCH
Partnership Combines Vision of Hope and Science to Become
World’s Largest Drug Discovery Program for ALS

CAMBRIDGE, Mass. and TUCSON, Ariz., January 16, 2007 — The Muscular Dystrophy Association (MDA), through its Augie’s Quest initiative, and the ALS Therapy Development Institute today announced they are establishing the world’s largest research program dedicated to discovering drugs to treat amyotrophic lateral sclerosis — ALS, or Lou Gehrig’s disease.
    Under the agreement, the collaboration will be funded by MDA’s Augie’s Quest and by the Institute (formerly the ALS Therapy Development Foundation). MDA will grant at least $6 million a year for the next three years; the Institute will add its $6 million annual budget to the project. Additionally, MDA will provide access to patients through its nationwide network of 225 clinics. MDA’s funding for this collab¬oration is above and beyond its existing ALS research expenditures. The research will take place at the Institute’s 16,000 square-foot facility in Cambridge.
    As a result of the collaboration, the ALS Therapy Development Institute elected Augie Nieto chairman of its board of directors. Nieto also serves as co-chairman of MDA’s ALS Division and is an MDA national vice president. The program also will add a drug discovery team and appoint former Biogen Idec executive, Steve Perrin, Ph.D., as chief scientific officer of the Institute.
    A major goal of the ALS Therapy Development Institute will be to license its intellectual property on relevant pathway and drug leads to biotechnology and pharmaceutical companies for further develop¬ment and commercialization. “Our collaboration with MDA’s Augie’s Quest is an unprecedented initiative of speed, efficiency and focus on drug discovery,” said Sean A. Scott, president of the Institute, who, with Nieto and Sharon Hesterlee, Ph.D., MDA’s vice president of translational research, spear¬headed the collaboration. “With the expansion of our capacity for target validation and the addition of state-of-the-art drug discovery under Dr. Perrin, we’re now able to apply the necessary resources to take the disease apart at the molecular level and target appropriate therapeutics.”
    The ALS Therapy Development Institute combines the passion and dedication of a nonprofit organi¬zation with the entrepreneurial and scientific spirit of a biotechnology company. “This initiative represents a natural fit between two organizations with complementary strengths, a common vision and a relentless entrepreneurial spirit,” explained Nieto. “This shows what can be done when you combine smart money with smart science to focus on an unmet medical need and a potential business opportunity.”
    MDA’s Dr. Hesterlee added, “ALS has been a major part of our program since Eleanor Gehrig first sought MDA’s help in stopping the disease that claimed her husband. We look forward to seeing that promise fulfilled.”
    Dr. Perrin brings to the ALS Therapy Development Institute more than 20 years of experience in genomics and proteomics applied to translational medicine — the “translation” of basic research into medical treatments. Prior to joining the Institute, he spent nearly seven years at Cambridge-based Biogen Idec, Inc., most recently as associate director, responsible for target discovery and biomarker characteri¬zation, using transcription profiling and proteomics for the company’s research and development. Dr. Perrin also was project team leader of Biogen Idec’s ALS initiative.
Uncovering the Cause of ALS
    Through the MDA collaboration, the Institute’s expanded research and drug discovery program will integrate both animal and human research based on cutting-edge bioinformatics, and genomic and proteomic technologies. Applying its expertise in the newest mass profiling and screening approaches to ALS pathology, the Institute’s scientific objectives will be to:

  • Identify physiological pathways and molecules in animal models of disease progression
  • Generate therapeutic hypotheses around these pathways, and modulate the function of key molecules using novel drug delivery strategies to target the central nervous system
  • Create a comprehensive translational medicine initiative to identify ALS biomarkers for disease staging and prognosis, as well as markers of drug efficacy and patient response


About ALS Therapy Development Institute

    The ALS Therapy Development Institute (www.als.net), based in Cambridge, Mass., was founded in 1999 as the ALS Therapy Development Foundation. Re-named in 2006 as a result of its collaboration with MDA’s Augie’s Quest, the Institute continues its mission to discover and develop drugs to treat ALS. A leader in ALS transgenic mouse studies, it excels in identifying novel disease targets, and screen¬ing potential treatments for ALS, as well as related disorders like Alzheimer’s, Parkinson’s and Hunting¬ton diseases.

About Augie's Quest

    Fitness pioneer Augie Nieto started Augie's Quest (www.augiesquest.org) in conjunction with MDA's ALS Division. Nieto is co-founder and former president of Life Fitness of Chicago, and chairman of Octane Fitness. He and his wife, Lynne, serve as co-chairpersons of MDA's ALS Division. Nieto received a diagnosis of ALS in March 2005.

About MDA

    MDA (www.mda.org) is the world’s largest provider of ALS services and funder of ALS research. Over the years, it has expended almost $200 million in this effort. It operates 225 neuromuscular disease clinics across the country and 37 ALS-specific research and care centers.

Media Contacts

Charles Versaggi, Ph.D.
Versaggi Biocommunications®
415/806-6039
cv@versaggibio.com

Sharon Hesterlee, Ph.D.
Muscular Dystrophy Association
520/529-5433
shesterlee@mdausa.org
 

After 134 Years, why is there no Cure for ALS?

For a personal look at ALS, click here to read about the Heywood Family, founders of ALS-TDI

Also, here are some links which provide information about a movie being made of ALS-TDI (www.als.net) which includes some very powerful up-close-and personal stuff about the disease and its impact upon ALS-TDI's founders, The Heywood Family. 

http://www.indiewire.com/people/2006...ity_06_st.html

(http://www.westcityfilms.com/smsf.html)

(http://www.jonathanweiner.com/)

Here is a link that very powerfully details a "real" story of one athlete's life with ALS:
 
http://www.johnsjourney.org/

Trapped Inside of His Own Body

ALS sufferer Jack Parker
Reported By: Keith Whitney
Web Editor: Michael King
Last Modified: 2/3/2006


An early 2006  episode of "ER" highlighted ALS. A devastating illness once known as Lou Gehrig’s disease, ALS literally traps its victims inside of their bodies.

Jack Parker was once a runner’s runner. With 14 marathons to his credit, he put in enough practice miles to circle the globe twice. Then, in 2002, ALS changed his life.

“Three and a half years since I was diagnosed. About 50 percent of the people will die within two years, another 30 percent for a total of 80 percent will die by five years. The average life span is less than three years,” Parker said.

Amyotrophic lateral sclerosis is a fancy way of saying the mind is willing, but the body is unable because of nerve degeneration.

"This one is about to claw up a little bit, whereas this one is still straight. Unfortunately, though this one will follow the path of this one at some time,” said Parker.

The ALS Association of Georgia helps people living with the disease with everything from wheelchairs to computers.

“Very few people know what it is, but when you do -- when you’re touched by it, you never forget it’s a devastating disease, but it’s something our patients are battling,” said Keith Fenton of the ALS Association of Georgia.

If Jack Parker’s body has to become a prison, then he chooses to serve his life sentence with hope.

“There is no cure. There's really no effective treatment, so it's a matter of taking each day and taking what it's worth and what you can do with it, Parker said.

Parker, like many, believes that hope for a cure lies with stem cell research.

 
 
Also, here