#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
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#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
Raising ALS | Lou Gehrigs Disease & Parkinsons Disease AWARENESS to the NEXT LEVEL!
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Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
October 17, 2014 10:26 AM
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Bill Gates Ice Water Challenge Spurs IPO Talk From Tobii

Bill Gates Ice Water Challenge Spurs IPO Talk From Tobii | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The founder of a Swedish company that uses eye sensors to help people with disabilities is considering an initial public offering as the business world’s top names draw attention to Lou Gehrig’s disease through an Internet campaign.
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October 15, 2014 9:47 AM
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BrainStorm’s NurOwn Stem Cell ALS Therapy Designated “Fast-track” Product

BrainStorm’s NurOwn Stem Cell ALS Therapy Designated “Fast-track” Product | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Amyotrophic lateral sclerosis (ALS) is a devastating neuromuscular disease that progresses swiftly, causing motor neuron degeneration and subsequent muscle
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October 14, 2014 8:40 PM
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Saints Fans vs. ALS: Gleason Gras 2014 and Pep Rally

Saints Fans vs. ALS: Gleason Gras 2014 and Pep Rally | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Amyotrophic lateral sclerosis (ALS) also know as Lou Gehrig’s disease affects nearly 5,600 Americans every year.  The disease usually starts around the age of 60, but in some cases, such as former New Orleans Saints‘ safety and special teams connoisseur Steve Gleason, ALS can begin at a much younger age. Gleason, now 37, revealed to […]
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October 12, 2014 7:43 AM
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Drama on ALS picks up where Ice Bucket Challenge left off

Drama on ALS picks up where Ice Bucket Challenge left off | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
TAMPA — The nationwide frenzy over the Ice Bucket Challenge has dwindled a bit now that volunteers who invited a dousing have raised more than $115 million to fight ALS.
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October 12, 2014 7:22 AM
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Drug Slowed Progression Of Parkinson's Disease, In New Study

Drug Slowed Progression Of Parkinson's Disease, In New Study | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The drug AT2101 slowed down the progression of Parkinson's disease in mice, in a new study, which if proven effective in humans, would make it the only drug on the market to go beyond merely treating the symptoms of the disease. In the study, which was published in the October edition of Neurotherapeutics, [...]
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September 30, 2014 5:58 PM
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OPENS TODAY! WATCH! You're Not You Movie Trailer | Coming to Select Theatres and On Demand

OPENS TODAY!  WATCH! You're Not You Movie Trailer | Coming to Select Theatres and On Demand | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

It just takes one person to give us hope. Hilary Swank, Emmy Rossum, and Josh Duhamel star in You’re Not You.


Watch the trailer now! 

https://www.facebook.com/video.php?v=324910204335626&set=vb.317241748435805&type=2&theater

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October 3, 2014 6:14 PM
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New 'Theory of Everything' Trailer Shows Stephen Hawking's Struggles

New 'Theory of Everything' Trailer Shows Stephen Hawking's Struggles | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The 2.5-minute trailer for "The Theory of Everything," which came out today (Oct. 1), is the second Focus Features has released to tout the film.
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September 30, 2014 6:51 PM
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Ice Bucket Challenge: Thank You from The ALS Association - YouTube

Via The ALS Association : September 22, 2014

The ALS Association is tremendously grateful for the $115 million received this summer. Ice Bucket enthusiasm continues to translate into local support in communities nationwide. The Association is seeing significantly increased participation in its fall Walk to Defeat ALS® events and other activities.


Given this summer’s unprecedented awareness around ALS, most of The Association’s chapters in both large and small markets, have seen a 30 to 100 percent increase in registrations for their Walks.


The ALS Association Western Pennsylvania Chapter, for example, saw a substantial increase in the total number of walk participants at its most recent even in Pittsburgh: 1,977 participants in 2013 compared to 3,277 people in 2014.


“This is an encouraging sign that people have truly embraced the fight against ALS as a cause they want to support,” said Barbara Newhouse, President and CEO. “We are truly thankful for the public’s continued support of the fight to find treatments and a cure for the disease.”


The Association is actively involved in meeting with key stakeholder groups to provide input into a plan to spend the $115 million in Ice Bucket Challenge donations wisely. The plan, which will be heavily focused on driving ALS research forward, will be voted on by the National Board of Trustees in mid-October.


On Friday, Sept. 19, Barbara Newhouse, President and CEO of THE ALS Association, met with a panel of advisors of people living with ALS. Out of respect for their privacy, health and well-being, The Association has left the decision of sharing their participation directly with these individuals.


“We look forward to continue communicating with all our donors and the public about how this incredible support will fuel the fight against this disease,” continued Newhouse.

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September 21, 2014 3:39 PM
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WSFA : Former pro's battle with ALS highlighted as Prattville champions honored

WSFA : Former pro's battle with ALS highlighted as Prattville champions honored | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
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September 18, 2014 2:58 PM
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A Beautiful Song for ALS | Kiss My ALS

A Beautiful Song for ALS | Kiss My ALS | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
This song “Paradise” written, produced and performed by Daniel Pulver was created for the ALS community and is extremely heartwarming. It is a beautiful tribute to those who stick by our side through the difficult journey this disease brings. It takes unconditional love, support and selflessness. So if you’re a caretaker, friend, family or significant other that gives... Read More
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September 15, 2014 2:26 PM
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After the Ice Bucket Challenge | Steve Gleason and Bill Gates

After the Ice Bucket Challenge | Steve Gleason and Bill Gates | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Steve Gleason is a former NFL player with ALS. He met with Bill Gates and shared with him what it will take to stop the disease and what he’s doing to fight it.
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September 13, 2014 3:33 PM
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Lawmakers: ALS patients hurt by new Medicare policies

Lawmakers: ALS patients hurt by new Medicare policies | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The disease has gained national awareness after the viral "Ice Bucket Challenge."
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September 9, 2014 7:02 PM
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Ellen Meets Anthony Carbajal | Via ALS Association

Ellen Meets Anthony Carbajal | Via ALS Association | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
His ALS Ice Bucket Challenge changed the way we all saw the viral trend. He was here for Ellen’s premiere show to tell her his story.



Via ALS Association: Yesterday, 26-year-old Anthony Carbajal, who was diagnosed with #ALS this year, appeared on the season premiere of the Ellen DeGeneres Show. Anthony has familial ALS and discussed the disease with the comedian and audience members, which included his mother who also has the disease. Watch the video here:


Ellen Meets Anthony: http://www.ellentv.com/videos/0-7risr5ch/


DONATE: ALSA.org

ALSA Facebook: https://www.facebook.com/alsassociation



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October 16, 2014 7:13 PM
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Why Do Eye Muscles Function in ALS While Other Muscles Waste Away?

Why Do Eye Muscles Function in ALS While Other Muscles Waste Away? | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
As the first ice-bucket challenge funds are disbursed, researchers also hope to solve the puzzle of why certain muslces escape the ravages of amyotrophic lateral sclerosis, a detail that might lead to new treatments
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October 12, 2014 7:50 AM
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FDA Grants Fast Track Designation to NurOwn for the Treatment of ALS

FDA Grants Fast Track Designation to NurOwn for the Treatment of ALS | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
BrainStorm Cell Therapeutics Inc., a leading developer of adult stem cell technologies for neurodegenerative diseases, announced that the United States Food and Drug Administration (FDA) has designated NurOwn as a Fast Track product for the treatment of amyotrophic lateral sclerosis (ALS, or Lou Gehrig's Disease).
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October 12, 2014 7:46 AM
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Second Thoughts on Out-of-Favor Parkinson’s Disease Treatment

Second Thoughts on Out-of-Favor Parkinson’s Disease Treatment | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
A small number of patients who underwent fetal-cell transplants are thriving two decades later.
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October 12, 2014 7:33 AM
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Young Woman's Video Goes Viral, Galvanizing Right-To-Die Movement

Young Woman's Video Goes Viral, Galvanizing Right-To-Die Movement | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
HARTFORD — Sara Myers understands 29-year-old Brittany Maynard's decision to end her life next month, a choice the terminally ill California woman has shared with the world in a YouTube video that has gone viral in recent days.
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October 10, 2014 12:16 PM
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Fighting Like Hell-Steve Gleason | The MMQB with Peter King

Fighting Like Hell-Steve Gleason | The MMQB with Peter King | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Four years after his diagnosis, Steve Gleason is working to assemble an ALS research project bigger than any that's ever been done before. And if the reaction of a small crowd in a Manhattan hotel is any indication, he could become a movie star along the way
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October 7, 2014 6:31 PM
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Emory ALS researchers to receive funds from ice bucket challenge

Emory ALS researchers to receive funds from ice bucket challenge | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The ALS Association has announced an initial commitment of $21.7 million from this summer¿s ice bucket challenge to support six programs to expedite the search for treatments and a cure for ALS, amyotrophic lateral sclerosis. Jonathan Glass, MD, director of the Emory ALS Center and professor of neurology and pathology at Emory University School of Medicine, is one of the U.S. investigators for Project MinE, one of the initiatives that will receive funding.
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October 3, 2014 6:11 PM
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One of their own was diagnosed with ALS | What his fellow firefighters did to support. Watch their amazing story.

One of their own was diagnosed with ALS, and what his fellow firefighters did to support him is nothing short of incredible. Watch their amazing story.
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September 27, 2014 6:23 PM
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Bid on a One-of-a-Kind Autographed Ellen Rock to Benefit ALS!

Bid on a One-of-a-Kind Autographed Ellen Rock to Benefit ALS! | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Ellen sent Anthony Carbajal to the iHeartRadio music festival, and while he was there he had tons of rock stars sign it, including Taylor Swift, Usher, Macklemore, Chris Martin, Ryan Seacrest, and more! Bid here for your chance to take home this…
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September 20, 2014 3:27 AM
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The Vincina Protocol - ALS Documentary Film - PreProduction | ● Kickstarter ●

The Vincina Protocol -  ALS Documentary Film - PreProduction | ● Kickstarter ● | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Vincina was 1 of 7 ALS cases in Conneaut Ohio. We show her husband's battle with City Hall over the toxic dumps linked to the deaths.
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September 17, 2014 11:32 AM
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Robin Mower - ALS survivor continues to beat the odds

Robin Mower - ALS survivor continues to beat the odds | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
A Toledo woman is beating medical odds, and she's celebrating a rare milestone with the help of the Toledo Roadrunners Club.
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September 13, 2014 3:44 PM
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Medicare tightens coverage of speech generating devices

Medicare tightens coverage of speech generating devices | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Glenn Asbury spends the first few hours of each day on the Internet, and usually some more in the afternoon. The five to 10 emails he sends daily carry particular importance, as they’re his only means of communicating with anyone who isn’t standing next to him. Since being diagnosed with
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September 10, 2014 9:57 PM
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He Had ALS. She Was His Nurse. This Is Their Love Story

He Had ALS. She Was His Nurse. This Is Their Love Story | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Adam and Hollie first met at a doctor's office in Thousand Oaks, California in November 2009, when Adam was getting treated for Lyme disease and Hollie was his nurse.

The pair met for treatments three hours a day, two to three times a week for a y...
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