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By Horror Writers Association
The Horror Writers Association (HWA), the premier organization of writers and publishers of horror and dark fantasy and home of the iconic Bram Stoker Award®, today announced the creation of the Rocky Wood Memorial Scholarship in honor of the...

By Sesame Enable
Head-motion activated technology brings usability and ubiquity of smartphones to previously excluded disabled populations

By Artist Lend Support
Artist Lend Support is a Non-profit, Fine Art Website With Partial Proceeds Going To ALS Services and Research.

By Shittens.com
Company offers $1000 reward in hopes of finding those responsible for cruel ice bucket challenge, soaking autistic boy in urine, feces, and spit.

By Insight Pharma Reports
Understand the market growth of biomarkers, advantages, disadvantages, and validation techniques

By six22
Long Beach, NY based nursing home honors those living with "Lou Gehrig's Disease”

By six22
Bronx, New York Based Nursing Home honors those living with "Lou Gehrig's Disease”

By Frank Groff, Inc.
One of LA’s top fitness instructors, who was forced to trade her spin bike for a wheelchair when she was diagnosed with crippling ALS (Lou Gehrig’s disease), received the surprise of her life when members of the Southern California fitness...

By EGAN Medical Equipment & Supply
EGAN Medical Equipment CEO Peter Egan is asking for your help in helping his company raise money for the Muscular Dystrophy Association (MDA) via the organization's annual "MDA Lock-Up" event.

By Spectrum Athletic Clubs
Special Classes, Memorabilia Auction & Festivities To Mark 2nd Annual “Gettin’ Down With Toni Brown” May 11

By Muscular Dystrophy Association
Warwick, RI—“Making Music for MDA” will take place on Saturday, March 30th, 2013 7pm-10pm at Dave and Buster’s, Providence Place Mall.

By Promixis, LLC
Promixis is providing the automation technology for the Team Gleason House for Innovative Living in New Orleans. PEAC, the automation solution by Promixis, is giving residents independence back where trauma or disease has taken it.

By American Academy of Neurology
SAN DIEGO – Apparent stem cell transplant success in mice may hold promise for people with amyotrophic lateral sclerosis (ALS), or Lou Gehrig’s disease.

By Xcaliber Entertainment & Media
"Be Stil," by Tania L Ramos published through Iuniverse is fiction and is available in softcover, hardcover, Nook, Kindle and Ibook.

By Project A.L.S.
Longtime friends Daniel Rodriguez and Deric Mizokami are bicycling cross-country to raise funds and awareness to support Project A.L.S. research. Project A.L.S. is a non-profit 501©3 devoted to understanding, treating and ultimately curing ALS.

By ALS Society of Canada
Special events at Toronto’s CN Tower, on Parliament Hill and on the Halifax Waterfront will mark the start of ALS Awareness Month (June) in Canada.

By ALS Society of Canada
ALS Society of Canada will be holding its first ALS Yoga Challenge fundraising event on August 18, 2012.

By M4 Publicity
19Events brought out supporters, sports figures, and celebrities alike, to raise money for individuals battling ALS (Amytrophic Lateral Sclerosis) during the Chargers vs Jaguars Monday Night Football Game at Gordon Biersch in Burbank, CA.

All Press Releases

By Horror Writers Association
The Horror Writers Association (HWA), the premier organization of writers and publishers of horror and dark fantasy and home of the iconic Bram Stoker Award®, today announced the creation of the Rocky Wood Memorial Scholarship in honor of the...

By Sesame Enable
Head-motion activated technology brings usability and ubiquity of smartphones to previously excluded disabled populations

By JUSTIN PAGE ALS FUND
Jazz drummer & ALS patient Justin Page with old friends & Jazz greats Kevin Hays, Doug Weiss, Justin Robinson are creating Page's legacy.

By Artist Lend Support
Artist Lend Support is a Non-profit, Fine Art Website With Partial Proceeds Going To ALS Services and Research.

By Zurn Industries, LLC
PHOTO: www.lopressroom.com/zurn/ALS ERIE, PA – The Zurn Wilkins unit of Zurn Industries, LLC recently took up this summer’s national craze, the ALS Ice Bucket Challenge, raising over $1,400 to be used for medical research.

By Shittens.com
Company offers $1000 reward in hopes of finding those responsible for cruel ice bucket challenge, soaking autistic boy in urine, feces, and spit.

By Insight Pharma Reports
Understand the market growth of biomarkers, advantages, disadvantages, and validation techniques

By six22
Flushing, NY based nursing home Waterview Nursing honors those living with "Lou Gehrig's Disease”

By six22
Long Beach, NY based nursing home honors those living with "Lou Gehrig's Disease”

By six22
Bronx, New York Based Nursing Home honors those living with "Lou Gehrig's Disease”

By Shamrock Financial
Shamrock Financial Corp. 75 Newman Avenue 401-438-0202 www.shamrockfinancial.com Contact: Shalimar Albanese Shalimar.albanese@shamrockfinancial.com

By GlobalData
This report is an essential source of information and analysis on the global Amyotrophic Lateral Sclerosis Therapeutics market.

By Frank Groff, Inc.
One of LA’s top fitness instructors, who was forced to trade her spin bike for a wheelchair when she was diagnosed with crippling ALS (Lou Gehrig’s disease), received the surprise of her life when members of the Southern California fitness...

By BookBuzz.net
Dr. Erica Kosal has written a wonderful new inspirational book about her family’s journey through a tough medical diagnosis. Kosal says, “A medical diagnosis can change your life, but how you deal with that news decides your future.”

By EGAN Medical Equipment & Supply
EGAN Medical Equipment CEO Peter Egan is asking for your help in helping his company raise money for the Muscular Dystrophy Association (MDA) via the organization's annual "MDA Lock-Up" event.

By GalaxyMediaUSA
Can this new meditative practice utilizing sound resonance and specially designed music really improve wellbeing of ALS patients?

By Spectrum Athletic Clubs
Special Classes, Memorabilia Auction & Festivities To Mark 2nd Annual “Gettin’ Down With Toni Brown” May 11

By Muscular Dystrophy Association
Warwick, RI—“Making Music for MDA” will take place on Saturday, March 30th, 2013 7pm-10pm at Dave and Buster’s, Providence Place Mall.

By The Kevin Turner Foundation
Citizens of Montgomery, Alabama give record level of support for local hero Kevin Turner at The “American Man” Documentary Screening and Reception, raising close to $120,000 for charity.

By Promixis, LLC
Promixis is providing the automation technology for the Team Gleason House for Innovative Living in New Orleans. PEAC, the automation solution by Promixis, is giving residents independence back where trauma or disease has taken it.

By American Academy of Neurology
SAN DIEGO – Apparent stem cell transplant success in mice may hold promise for people with amyotrophic lateral sclerosis (ALS), or Lou Gehrig’s disease.

By Sentrana Inc.
Sentrana researchers presented their winning research from the Prize4Life ALS Prediction Prize Challenge in a talk entitled "Discovering New Variables and Improving the Prediction of ALS Progression."

By IowaTriBob
Because You Can… That was today’s theme at the 4th annual Walk to Defeat ALS in Cedar Rapids, Iowa. I labeled this article as a race review because that is exactly what the event is, a race to defeat ALS.

By IowaTriBob
I just recently read a post “Rev3 Maine: My Gratitude Race” by Jamie at swimbikerunlive.com and it made me once again realize just how fortunate most of us are. My father passed away from ALS earlier this year.

By Xcaliber Entertainment & Media
"Be Stil," by Tania L Ramos published through Iuniverse is fiction and is available in softcover, hardcover, Nook, Kindle and Ibook.

By Day Care Centers, Inc
Phillie Phanatic helps kids at the Ardsley Community Center take a swing against Amyotrophic Lateral Sclerosis (ALS/Lou Gehrig's Disease) on July 19th between the hours of 11:00a-12:00noon.

By Project A.L.S.
Longtime friends Daniel Rodriguez and Deric Mizokami are bicycling cross-country to raise funds and awareness to support Project A.L.S. research. Project A.L.S. is a non-profit 501©3 devoted to understanding, treating and ultimately curing ALS.

By ALS Society of Canada
Special events at Toronto’s CN Tower, on Parliament Hill and on the Halifax Waterfront will mark the start of ALS Awareness Month (June) in Canada.

By ALS Ontario
ALS Ontario, in conjunction with Bombardier Aerospace and The Marketing Store, will be running the second annual Plane Pull, a fun competition will involve teams, consisting of 10 people, running as fast as they can in 100-metre dash pulling a plane

By ALS Society of Canada
ALS Society of Canada will be holding its first ALS Yoga Challenge fundraising event on August 18, 2012.

By Frank Groff Inc.
Spectrum Athletic Clubs To Raise Funds For Lou Gehrig’s Disease During ALS Month in May With Day of Special Classes/Fitness Sessions Open To Public May 12

By Florida Spine Center
Two stem cell research studies highlight the amazing potential that stem cells hold in the treatment of ALS.

By American Academy of Neurology
The American Academy of Neurology Foundation and The ALS Association are announcing the creation of the Richard Olney Clinician Scientist Development Award in ALS, named after Richard K. Olney, MD, a pioneer in ALS research who died last month of ALS

By Managing Editor Inc.
Managing Editor Inc. (MEI) today announced the release of new XTensions that allow its industry-leading ad-layout solutions to work with QuarkXPress® 9, the latest version of the page-design software.

By Major Hyundai of Stroudsburg
Area cyclists team up to fight ALS in Stroudsburg, PA. Stroudsburg, PA – A group of cyclists and athletes across America has joined together this February for the annual declaration of war against ALS, and the battleground is set at Major Hyundai.

By M4 Publicity
19Events brought out supporters, sports figures, and celebrities alike, to raise money for individuals battling ALS (Amytrophic Lateral Sclerosis) during the Chargers vs Jaguars Monday Night Football Game at Gordon Biersch in Burbank, CA.

By HKA, Inc. Public Relations
A compelling new book, Phyllis A. Langton's Last Flight Out, chronicles three-war veteran George Thomas’ courageous battle with Lou Gehrig’s disease (ALS), an achingly poignant and impossibly funny memoir.

By Kasie Bolling/Out of Her Mind Freelance
Friends and Family of Georgia ALS Patient Plan Charity Event at Smith’s Olde Bar to Raise Funds for John David Keith Medical Relief Fund

By AristoMedia
Check presentation made before Boston Red Sox/New York Yankees game Sept. 1 at Fenway Park

By Kasie Bolling/Out of Her Mind Freelance
Golf Tournament in Cumming to Benefit Local Victim of ALS is Open to the Public

By AristoMedia
With support from dozens of Alabama players and coaches, including legendary Alabama coach Gene Stallings, The Kevin Turner Foundation raised more than $100,000 at its inaugural ALS fundraiser this past weekend.

By AristoMedia
Country artists Ty Herndon and Amber Hayes were on hand this past weekend to help former Alabama and NFL player Kevin Turner raise just over $100,000 at a private Nashville ALS fundraiser event.

By AristoMedia
Country artist Ty Herndon and former NFL football player Kevin Turner have been announced as honorary co-chairs for the 10th annual CVS/pharmacy and ALS Therapy Alliance (ATA) “Researching A Cure” ALS fundraising campaign.

By M4PR
Ronnie Lott's 1st Annual "Drive to Survive" is a two-day fundraiser that aims to raise money for Eric’s Vision (www.EricsVision.org), a nonprofit organization, which was started in memory of Eric Scoggins who passed away from ALS.

By THE ALS ASSOCIATION GREATER CHICAGO CHAPTER
STEALING PIECES-150 mannequin torsos shrouded in black t-shirts commemorating lives stolen by ALS takes center stage in Daley Plaza, May 3rd-5th. This is the most provocative, powerful Midwest ALS Awareness initiative ever undertaken. Do not miss it!

By Managing Editor Inc.
MEI today announced the appointment of Stephen Arbour as Vice President of Technical Services. The 15-year software veteran will oversee a strategic consolidation of several departments.

By Kim Jackson
There are no Hollywood celebrities linked to MSA (Multiple System Atrophy)—just more than 2,300 fans known on Facebook as “Miracles for MSA." The group has designated March as Multiple System Atrophy Awareness Month.

By ALS Society of Canada
Encouraged by its success in 2010, the ALS Society of Canada has once again entered the Giv3’s Great Canadian Charity Contest on Facebook and needs your votes on the Giv3’s Facebook Page

By Melanie Herscovitch
Addgene’s Challenge Award winners were announced this week. The award recognizes laboratories using plasmids from Addgene’s collection in creative ways to advance their research.

By AristoMedia
FUNL Music artist Ty Herndon and former NFL running back Kevin Turner were in Nashville Monday and Tuesday



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