#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
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HARK'S Hope on the Horizon Documentary Trailer

Through this film Hark will change the way the world views ALS, increase awareness of this fatal disease and raise funding to provide resources to ALS patients and their families that need assistance in facing a challenge far greater then the White Mountains.
Look for the completed film coming soon!

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#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
Raising ALS | Lou Gehrigs Disease & Parkinsons Disease AWARENESS to the NEXT LEVEL!
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Michael Lopez Jr. Celebration Of Life - Saying Good Bye to All American "Magic Mike" RIP: 1/13/2013 - In Loving Memory of Michael - Forever in Our Hearts #19

★ Final Farewell To Mike Lopez Jr.★

It is hard to imagine anyone who followed football in Oregon in the 1980′s not remembering his name. It struck fear into many an opponent and his #19 was called and shouted often at Oregon State where he did some legendary things. He was one of the greatest athletes to every come out of Oregon and was an All American and named Gatorade Player Of The Year. The 1981 Graduate of Aloha was truly special in every way and was known by those closest to him as “Magic Mike”! ♥

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Inspirational & Unique | One of a Kind | Sterling Silver Jewelry | Hand Stamped-Made in Oregon | USA

Inspirational & Unique | One of a Kind | Sterling Silver Jewelry | Hand Stamped-Made in Oregon | USA | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

*Our Unique & Inspirational Jewelry can be customized especially for you or as a gift*

Be CREATIVE! Design your own Unique Piece of Inspiration|Each Piece is Handcrafted In Oregon|Sent to you with Hope-Inspiration-Strength-Courage.

Help TEAM UP for A CURE!

To Order, Visit: www.TEAMCureALSfundraiser.com 

 #TEAMMikeLopez #TEAMUp4ACure

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Pennsylvania Father of 6 with ALS Is Fighting for ‘Right to Try’ Legislation: ‘Failure Is Not an Option’

Pennsylvania Father of 6 with ALS Is Fighting for ‘Right to Try’ Legislation: ‘Failure Is Not an Option’ | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Frank Mongiello fights for Right to Try legislation on behalf of those with terminal illnesses, including ALS
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First Trial Begins Testing Drug in People with GBA Mutation | Parkinson's Disease

First Trial Begins Testing Drug in People with GBA Mutation | Parkinson's Disease | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
This study is a major step for PD research as it is the first drug trial where one's genetic information determines eligibility and is testing a potential therapy to slow or stop disease progression.
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ALS is slowly robbing ex-linebacker Tim Shaw of his muscles. But he won't let that stop him from living.

ALS is slowly robbing ex-linebacker Tim Shaw of his muscles. But he won't let that stop him from living. | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Three years after being diagnosed with ALS, Shaw's goals are simple -- but even more meaningful, he says.
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Eye tracking technology will change these 4 domains

Eye tracking technology will change these 4 domains | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Thanks to advances and breakthroughs in hardware, software and artificial intelligence, eye tracking technology has progressed immensely in the past year, and is now drawing the attention of tech industry’s biggest players. The acquisition of eye tracking companies EyeFluence and Eye Tribe by Google and Facebook respectively, as well as the move toward mobile eye …
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‘Joost, you’re a hero’: MND sufferer describes how visit from rugby legend helped him to keep fighting

‘Joost, you’re a hero’: MND sufferer describes how visit from rugby legend helped him to keep fighting | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
When Deon was diagnosed with MND in 2004, doctors told him that he may only have months to live – but he is still holding on.
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VocaliD - Tobii Dynavox

VocaliD - Tobii Dynavox | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
VocaliD is on a mission to humanize the voice within AAC devices. Founded by Dr. Rupal Patel in 2014, VocaliD leverages its Human Voicebank of over 15,000+ members from over 110 countries that together have contributed upwards of 6 million sentences and the company’s proprietary voice blending technology to create unique vocal persona for every AAC use
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Press Release - BrainStorm

Press Release - BrainStorm | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

HACKENSACK, N.J. and PETACH TIKVAH, Israel, Feb. 6, 2017 /PRNewswire/ -- BrainStorm Cell Therapeutics Inc. (NASDAQ: BCLI), a leading developer of adult stem cell technologies for neurodegenerative diseases, announced today that Chaim Lebovits, Chief Executive Officer, will provide a corporate overview at BIO CEO & Investor Conference, being held on February 13-14, 2017 at the Waldorf Astoria in New York City.

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Mark Zuckerberg's Research Hub Just Gave 47 Scientists $50 Million to Fight Diseases

Mark Zuckerberg's Research Hub Just Gave 47 Scientists $50 Million to Fight Diseases | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The Chan Zuckerberg Biohub, launched by Facebook CEO Mark Zuckerberg and wife Priscilla Chan, has awarded $50 million to 47 scientists
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This Year’s 10 Biggest Advances in ALS Research

This Year’s 10 Biggest Advances in ALS Research | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
In 2016, a significant number of ALS research discoveries, advances in clinical trials, collaborations and strategic initiatives all accelerated the pace of discovery in finding treatments and a cure for ALS. We’ve pulled together what we think are 10 of 2016’s biggest advances in ALS research that gave us, and people living with ALS,…
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Controlling Alexa With eyegaze to speech

I have ALS so I am mostly paralyzed and use my eyes to communicate. I have a smart home and now can use my eyes to type commands through my Microsof
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A Dying Man's Wish with ALS to Save Others Hits Hospital Ethics Hurdle | care continuum, leadership, legal, management, policy, quality.

A Dying Man's Wish with ALS to Save Others Hits Hospital Ethics Hurdle | care continuum, leadership, legal, management, policy, quality. | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
An ALS patient wanted to donate his organs when he died. He asked to be admitted to the hospital specifically to end his life. And despite the planning, his request made some people uncomfortable.
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NFL hero leads charge against ALS in acclaimed documentary ‘Gleason’

NFL hero leads charge against ALS in acclaimed documentary ‘Gleason’ | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
“Gleason” is an acclaimed documentary spotlighting former New Orleans Saints player Steve Gleason and his courageous battle with amyotrophic lateral sclerosis (ALS). TODAY correspondent Jenna Bush Hager talks to Gleason about his story full of love and hope.
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Ralph Delius's curator insight, Today, 1:19 PM
If you have not already seen this movie, put it on your list.  Warning, it's a tear jerker.  It gives us an insight in ALS on a daily basis.
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Video: ALS WARRIOR FRANK MONGIELLO'S FIGHT FOR ALL TERMINALLY ILL AMERICANS

Produced by:Loving Life Productions Website: http://www.lovinglifeproductions.net/ Facebook: https://www.facebook.com/lovinglifeproductions/
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Support The MND/ALS Emergency Hotline. Every Disease Requires The Proper Care And Knowledge

Support The MND/ALS Emergency Hotline. Every Disease Requires The Proper Care And Knowledge | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
My Concern for MND/ALS Protocol and MND/ALS Hotline In the past several months I have experienced some very important concerns of ALS patients being admitted into local hospitals under pneumonia and other Flu like symptoms. Over 17 ALS patients in the past 4 months have died. In many cases th
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BrainStorm seeks early approval for stem cell treatment in Canada

BrainStorm seeks early approval for stem cell treatment in Canada | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Israel's BrainStorm Cell Therapeutics is seeking early approval in Canada for its adult stem cell treatment for patients with amyotrophic lateral sclerosis (ALS), a neuro-degenerative disease, even before it completes late-stage clinical trials.
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Microsoft app helps people with ALS speak using just their eyes

Microsoft app helps people with ALS speak using just their eyes | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
A smartphone app called GazeSpeak uses eye movements to predict the words you want to say, allowing people with motor disabilities to communicate faster
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Moulton introduces bill to speed benefits to those with ALS

Moulton introduces bill to speed benefits to those with ALS | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
SALEM — Salem Congressman Seth Moulton has helped introduce a bipartisan bill to accelerate benefits for those diagnosed with amyotrophic lateral sclerosis, or ALS.
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Blood test might make Parkinson's diagnosis easier

Blood test might make Parkinson's diagnosis easier | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
A blood test may be as accurate as a spinal fluid test for differentiating Parkinson's disease from atypical parkinsonism disorders, according to a new study.
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Creating Personal Voices For All-Voice Banking

Creating Personal Voices For All-Voice Banking | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

The ModelTalker System is a revolutionary speech synthesis software package developed by the Nemours Speech Research Laboratory and designed to benefit people who are losing or who have already lost their ability to speak. It allows people who use a Speech Generating Device (SGD) to communicate with a unique personal synthetic voice that is representative of their own voice.

To learn more, see the FAQ section under Help, or select an option under our Voices menu to get started right away!

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Michael Maloney, top ALS treatment advocate in WNY, dies at 65 - The Buffalo News

Michael Maloney, top ALS treatment advocate in WNY, dies at 65 - The Buffalo News | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
June 7, 1951 – Feb. 3, 2017 Michael J. Maloney, who worked closely with families as he helped lead some of the region’s top senior living communities, and who became known in recent years for his advocacy and fundraising for ALS research and treatment, died early Friday from a complication of the neurodegenerative condition, also known as Lou Gehrig’s disease. He…
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Parkinson’s disease: Hallan two key neuroprotection and natural increase of dopamine

Parkinson’s disease: Hallan two key neuroprotection and natural increase of dopamine | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Ramón Cacabelos, one of the best specialists in the world in the neuro-degenerative disorders and genomic medicine, and his team have completed preclinical and clinical studies with a nutraceutical…
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The man who beat Lou Gehrig’s disease

The man who beat Lou Gehrig’s disease | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Ted Harada made medical history and brought hope to others who have been diagnosed with a terminal illness.
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IBM's Watson supercomputer discovers 5 new genes linked to ALS

IBM's Watson supercomputer discovers 5 new genes linked to ALS | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
IBM Watson discovered five new genes linked to ALS, which means the supercomputer could make discoveries in research of other neurological diseases.
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Former Saints player Steve Gleason visits his old stomping grounds

Former Saints player Steve Gleason visits his old stomping grounds | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Steve Gleason revealed in 2011 that he has ALS; since then, he has promoted awareness for the disease and vowed to lead a life of purpose.
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