#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
162.6K views | +0 today
#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
Raising ALS | Lou Gehrigs Disease & Parkinsons Disease AWARENESS to the NEXT LEVEL!
Your new post is loading...
Your new post is loading...
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 28, 2013 5:12 PM
Scoop.it!

Scientists identify amyotrophic lateral sclerosis disease mechanism

Scientists identify amyotrophic lateral sclerosis disease mechanism | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Researchers have tied mutations in a gene that causes amyotrophic lateral sclerosis (ALS) and other neurodegenerative disorders to the toxic buildup of certain proteins and related molecules in cells, including neurons.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 27, 2013 3:34 PM
Scoop.it!

A Stem Cell Cure is it Embryonic Stem Cell or Adult Stem Cell Therapy

A Stem Cell Cure is it Embryonic Stem Cell or Adult Stem Cell Therapy | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

Of the trillions of cells in the human body, there are over 200 cell types, each having their own function. Yet, a sub set of those cells are considered to be “start ups” and are either embryonic or adult stem cells. Both have regenerative potential to immediately repair human tissue their.................

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 24, 2013 9:30 PM
Scoop.it!

Portland Metro Walk: TEAM Lopez Warriors - Walk to Defeat ALS®| WALK*Donate*Join the TEAM!

Portland Metro Walk: TEAM Lopez Warriors - Walk to Defeat ALS®| WALK*Donate*Join the TEAM! | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

WALK*DONATE*Join Lisa's TEAM!

WALK to DEFEAT ALS Oregon! 

 

http://web.alsa.org/site/TR?pg=team&fr_id=9236&team_id=255561

 

#MEbecomesWe #TEAMMikeLopez #TEAMCureALS #fight4theCure 

 

 

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 24, 2013 6:53 AM
Scoop.it!

Study identifies new culprit that may make aging brains susceptible to neurodegenerative diseases

Study identifies new culprit that may make aging brains susceptible to neurodegenerative diseases | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Study identifies new culprit that may make aging brains susceptible to neurodegenerative diseases
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 23, 2013 10:27 PM
Scoop.it!

Parkinson's Central Smartphone App

Parkinson's Central Smartphone App | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
National Parkinson Foundation
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 23, 2013 9:51 PM
Scoop.it!

Linda Ronstadt Discloses Her Battle With Parkinson’s Disease

Linda Ronstadt Discloses Her Battle With Parkinson’s Disease | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
EntertainmentLegendary singer Linda Ronstadt, 67, told AARP today that she “can’t sing a note” because she suffers from Parkinson’s disease. Diagnosed eight months ago, Ronstadt began to show symp...
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 22, 2013 4:24 AM
Scoop.it!

Sensors, motors help people with tremors hold spoon steady

Sensors, motors help people with tremors hold spoon steady | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The U.S. maker of a so-called smart spoon says it will help stabilize tremors in people with Parkinson's disease and related disorders.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 20, 2013 6:39 PM
Scoop.it!

One woman's push to raise awareness of ALS

One woman's push to raise awareness of ALS | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
A South Burlington woman is pushing herself to the limits,
fighting to raise awareness for a rare and devastating disease that for her,
hits close to home.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 18, 2013 6:35 PM
Scoop.it!

Phil Timp's voice is weak but his smile can still brighten a room | Book: Moments That Took My Breath Away

Phil Timp's voice is weak but his smile can still brighten a room | Book: Moments That Took My Breath Away | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Two years after being diagnosed with Lou Gehrig's disease, it has robbed the use of Timp's legs, his right arm and now attacks his diaphragm and his ability to breathe, eat and speak.

 

With his voice fading, a new book - Moments That Took My Breath Away - speaks for him, telling others of his journey with this disease and episodes good and bad with daughter's Beth's Rett Syndrome, a severe neurological disorder of the brain.

"The book is something I started writing before I got my diagnosis and it was about our life with Beth. When I got the diagnosis, I had to reformat the whole story and add another huge mountain to climb," Timp said last week. "It's been very inspiring to many people who've already read it. I've gotten amazing responses from many people."

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 16, 2013 3:03 PM
Scoop.it!

A New Wrinkle in Parkinson’s Disease Research

A New Wrinkle in Parkinson’s Disease Research | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Scientists have discovered that a drug in an over-the-counter skin cream slows or stops the effects of Parkinson’s disease on brain cells.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 15, 2013 6:13 PM
Scoop.it!

OJ Brigance honored by Touchdown Club of Houston

OJ Brigance honored by Touchdown Club of Houston | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Fighting amyotrophic lateral sclerosis (commonly known as ALS or Lou Gehrig's disease) for more than six years, he is still part of the Ravens organization and was a source of inspiration during the team's run to a championship last season.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 8, 2013 7:10 PM
Scoop.it!

Race matters when a patient needs a stem cell or marrow transplant

Race matters when a patient needs a stem cell or marrow transplant | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
It’s harder for members of minority groups get the right genetic match; cultural factors add to the difficulty.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 7, 2013 6:28 PM
Scoop.it!

Did Someone say: "SOLD OUT"! You Betcha! #TEAMCureALS 7th Annual Golf Tourney

Did Someone say: "SOLD OUT"! You Betcha! #TEAMCureALS 7th Annual Golf Tourney | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

Did Someone say: "SOLD OUT"! You BETCHA!

T.E.A.M. Cure ALS Foundation 7th Annual Memorial Golf Tournament is SOLD OUT!
Full Field for a Memorable Day to Come!

#19 Magic Mike is so Proud for the Love & Support in his Memory!
We can see that beautiful *SMILE* every time we close our eyes!


#MEbecomesWe #TEAMMikeLopez #TEAMCureALS #ALS #LouGehrigsDisease 


--->>STAY TUNED to find out how you can TAG & WIN! <<-----

Win Beaver and Duck GEAR For your Photo TAGS on Golf DAY! 

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 27, 2013 8:09 PM
Scoop.it!

The United States of Football The USOF | Screenvision| Find a Showing in Your Area

The United States of Football The USOF | Screenvision| Find a Showing in Your Area | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The United States of Football is a must-see documentary that explores the cumulative effect of repetitive trauma in football. “Should my kid play?”
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 27, 2013 3:27 PM
Scoop.it!

Linda Ronstadt, Michael J. Fox Soften Parkinson's 'Cruel' Hand

Linda Ronstadt, Michael J. Fox Soften Parkinson's 'Cruel' Hand | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Linda Ronstadt's celebrity status, as well as that of Michael J. Fox, who in 1991 was diagnosed with early-onset Parkinson's at the age of 35, shines a spotlight on a disease that is still poorly understood and for which there is no cure.
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 24, 2013 4:21 PM
Scoop.it!

DRIVE - Art exhibit by Steve Dezember II to benefit ALS research

I'm honored and excited to share this new project with you. On August 24th at the Kai Lin Art Gallery in Atlanta, we will be hosting a one-night art show titled…
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 23, 2013 11:59 PM
Scoop.it!

Dr.Craig Oster|One man's mission to fight disease with proper nutrition. [video]

One man's mission to fight disease with proper nutrition.

 

"Dr. Oster" PBS Documentary is Now on YouTube!

Raising ALS awareness, from a wellness perspective. Please share it to help my life be used to give millions inspiration, people with all kinds of tough challenges.

 

YouTube: http://www.youtube.com/watch?v=v63wOe5F2_c&feature=c4-overview&list=UUkLBWd6sIF5dE_gHAO9XbJQ



PBS is planning on filming for a follow up story in the Fall. A special thanks to Hollywood producer Troy Anthony Garriga and Garriga Tribe Pictures for the great footage which PBS used for B-roll when someone was talking. Troy has changed my life. A Wider World is a show with heart and the Executive Producer Jim Saliba is first-rate. A Wider World made my world wider in a great way, I believe the series is viewed by about 600,000 people. Thank You God!

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 23, 2013 10:02 PM
Scoop.it!

20/20 Stem Cell Predictions for the Year 2020

20/20 Stem Cell Predictions for the Year 2020 | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

Can we make 20/20 (i.e. accurate) predictions for where the stem cell field will be that far down the road?

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 22, 2013 4:34 AM
Scoop.it!

I'm A Killer...(PSA)

Actor: Christian Carey (www.kids4cure.com) Director: Brad Burns
No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 22, 2013 3:50 AM
Scoop.it!

ALS Research Program: Targeting Drug Discovery| Via ALSA

Lucie Bruijn, Ph.D., The ALS Association. Dr. Bruijn is the FY13 Integration Panel Chair for the DoD Amyotrophic Lateral Sclerosis Research Program (ALSRP).

 

Via ALS Assoc.: This is a great insight into the Department of Defense (DOD) ALS Research Program. Watch The ALS Association's Chief Scientist discuss it here. Our nation's veterans develop ALS at twice the rate of civilians, regardless of branch of service or combat duty witnessed.

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 20, 2013 12:47 AM
Scoop.it!

"There is only one way to succeed in anything & that is to give it everything" Each of you did just that & MORE! Thank You!

"There is only one way to succeed in anything & that is to give it everything" Each of you did just that & MORE! Thank You! | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

*THANK YOU! to the multitude of Sponsors, Donors and Volunteers that donated to the 7th Annual T.E.A.M. Cure ALS Foundation Memorial Golf Tournament.

"There is only one way to succeed in anything and that is to give it everything."...........Each of you did just that & MORE! Thank You!

#19 Magic Mike is truly Proud!

 

www.TEAMCureALS.com

www.TEAMCureALSfundraiser.com



‪#‎MEbecomesWe‬ ‪#‎ALS‬ ‪#‎LouGehrigsDisease‬ ‪#‎TEAMCureALS‬ ‪#‎TEAMMikeLopez‬

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 16, 2013 3:37 PM
Scoop.it!

ALS BOB

Throughout his life, Bob Deyan struggled to find his place in the world. Leaving his father's trade as a young man, Bob set out to find a new calling. After meeting his wife Debra, the two set off on an ambitious journey to build a successful business. Finding he had quite a talent for audiobooks Bob and Debra carved a solid place for themselves in that industry, and the trajectory of Bob's life finally seemed set on the right path. Just when it seemed like he had made it, his life was thrown completely off course when diagnosed with ALS (Lou Gehrig's Disease). Never one to let adversity stand in his way, Bob found a new calling. END ALS for good. Join him and support him by watching and sharing this heartfelt documentary.

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 16, 2013 1:19 PM
Scoop.it!

*ALS Steals Your Body, Not Your Soul*

*ALS Steals Your Body, Not Your Soul* | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

Meet Rob Boulton..................


Do you want to be a part of something big? Want to help spread awareness and inspiration? Peace Ragz will make a donation to ALS for every shirt sold. You pick any color and remember sizes like XXXL are available if not listed. My motto celebrates the spirit shared by many with this devastating disease. Share with friends, family, groups, coworkers and neighbours. We can make a difference in many lives and look great doing it! Please share this post - let's do some good and show we are all Soul Warriors. Peace Ragz will ship to Canada or U.S. If you have any questions Peace Ragz will address them.
http://www.peaceragz.com/step-2/?message=13


Besure to stop by Rob's Facebook Page and Give it a "LIKE" | Leave Rob a message of Support!


"Take it All But-Leave My Soul"....................Rob Boulton

https://www.facebook.com/TakeItAllButLeaveMySoul


No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 13, 2013 3:45 PM
Scoop.it!

The ALS Association Announces $4.3 Million in Research Grants for Global Fight Against ALS -MND

August 13, 2013

The ALS Association announced today that it has awarded $4.3 million in new research grants. These awards are part of its Translational Research Advancing Therapy (TREAT ALS ™) program, through which The Association funds a diverse portfolio of amyotrophic lateral sclerosis (ALS) research to find treatments and a cure for the disease.

“These awards will drive research on several emerging fronts in the quest to understand and find treatments for ALS,” said Lucie Bruijn, Ph.D., Chief Scientist for The ALS Association. “The generosity of our donors and supporters makes these grants possible. We are very grateful for that generosity and the opportunity it provides to make these awards for this important research.”

The awards will go to scientists in laboratories in 14 states in the United States as well as in the United Kingdom, Ireland, Belgium, Canada, Argentina, France and Italy. These awards will support 35 new research projects.

Financial support from the following organizations and individuals enabled The ALS Association to fund these new research grants: Greater Philadelphia Chapter; Greater New York Chapter; The Jeff Kaufman Fund of the Wisconsin Chapter; Greater Chicago Chapter; Texas Chapter; Golden West Chapter; Greater Sacramento Chapter; Orange County Chapter; Greater San Diego Chapter; The Motor Neuron Disease Association of the United Kingdom; and Jay and Toshiko Tompkins. 

The ALS Association funds both Investigator-Initiated Awards,

for...................http://www.alsa.org/news/archive/fall2013-grants.html

No comment yet.
Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
August 8, 2013 5:41 PM
Scoop.it!

Speak for ALS | Donate Your Voice

Speak for ALS | Donate Your Voice | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
We asked four people with ALS what they wanted to say, and now YOU can help them say it. Go to SpeakforALS.org and donate your voice today!
No comment yet.