Devlin Brothers Go on a 3,000 Mile Run, 100-day Journey Across America to Stomp Out ALS

PR Newswire — April 10, 2017

NEW YORK, April 10, 2017 /PRNewswire/ — Brothers Mike and Joey Devlin announced
their plans to travel across the U.S. to raise significant research funds for
Project ALS in an effort to try one promising autophagy drug in people with ALS.

Mike Devlin, 27, is an ultramarathon runner who will begin his quest in San
Francisco on Saturday, April 15. Over the course of 100 days, Mike will run
3,000 miles across America, with his younger brother Joey, 23, who will drive
the follow vehicle. They are scheduled to complete their journey on August 1st
in New York City. Mike’s goal is not to break records, but to raise awareness
about this fatal brain condition and raise monies that will directly go toward
fighting and finding a cure for ALS, also known as Lou Gehrig’s disease. 100% of
funds raised from #ProjectRun go directly toward vital research to deliver one
new drug to clinical trial for people with ALS.

Mike and Joey’s schedule is available and will be documented at, along with opportunities for visitors to follow their
remarkable endeavor, as well as make sponsorship or financial contributions. ALS
advocates, families and friends affected by ALS, and those interested in joining
Mike on his runs, are encouraged to come out, meet Mike and Joey, and show their

ALS is extremely personal to Mike and Joey, who lost their grandmother Edna
Devlin to Bulbar ALS in 2014. “Three years ago, we watched as ALS attempted to
strip our Grandmother of her humanity,” said Mike Devlin. “Now, Joey and I want
to focus all of our efforts on fighting this disease and paying it forward, just
as Grandma Devlin would have done. In planning this expedition, we wanted to
align ourselves with an organization that would be both transparent and allow us
to commit all funds raised toward finding a cure for this horrible disease.
Project ALS is this partner – they’ve shown us the research they are focused on,
how they are pushing forward in the fight against ALS, and are allowing us to
dedicate every dollar directly to research, not infrastructure.”

Approximately only 300 people have ever successfully completed their own runs
across America, and Mike will soon join this roster of elite runners. “This
3,000-mile, 100-day run is about showing that you’re capable of more than you
think,” said Joey Devlin. “When something as daunting as ALS confronts you, you
fight whether you’re ready or not. While Mike and I are on the road, we want to
meet those who have been affected by ALS and those who have shown unwavering
strength and courage to help find a cure.”

Devlin’s #ProjectRun and Project ALS have already tapped the expertise of a
dream team of ALS researchers that is testing FDA approved cancer drugs that hit
a cellular process known as autophagy. Autophagy happens in every living cell of
the human body. It’s like waste management for cells. When autophagy works, it
clears unwanted proteins from a cell. When autophagy machinery goes wrong, a
cell becomes overwhelmed with proteins and does not function properly.

“Autophagy is a fancy word for something that happens inside of cells that may
contribute to ALS. The amazing Devlin brothers will raise funds to support the
aggressive testing of a drug that is already FDA-approved to target autophagy,”
said Valerie Estess, director of research for Project ALS.

#ProjectRun Cities (visit for the full schedule):

San Francisco, CA
Sacramento CA
Reno, NV
Lovelock, NV
Salt Lake City, UT
Dinosaur, CO
Loveland, CO
North Bend, NE
Omaha, NE
Des Moines, IA
Hawkeye, IA
Nottingham Woods, IL
Chicago, IL
South Bend, IN
Cleveland, OH
Warren, OH
Rockland, PA
Luthersburg, PA
Liberty, NJ
Morristown, NJ
New York, NY

For Mike and Joey’s full schedule and to donate to #ProjectRun, follow their
journey at,,, and

What is ALS?
ALS is a brain disease that is closely related to Parkinson’s, Alzheimer’s, and
Huntington’s. Also known as Lou Gehrig’s disease, ALS targets brain cells called
motor neurons. Motor neurons send messages from the brain to muscles throughout
the body. In ALS, as motor neurons die, a person progressively loses the ability
to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens
to seniors, and is usually fatal within 2-5 years of diagnosis.

About Project ALS
Founded in 1998, the non-profit Project ALS has advanced ALS research,
accelerating the testing of potential drugs, establishing the world’s first and
only privately funded stem cell laboratory, and developing the first laboratory
models of ALS. Project ALS identifies and funds scientific research most likely
to result in the first effective treatments and a cure. By recruiting the
world’s best scientists and doctors to work together – rationally and
aggressively – Project ALS has developed a better understanding of the ALS
disease process and, in parallel, better therapeutic strategies. Project ALS is
the only ALS organization who has an organized RAB that reviews proposals and
progress. In 18 years, Project ALS has raised over $92 million, directing
between 80-93% annually to research programs. For more information, visit

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