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Vote/like my ALS essay on social media to send me to the Mayo Clinic Social Media Conference
Lou Gehrig's disease is a fatal disease that claims more than 5000 lives a year, and currently has no known treatment. Urge the National Institutes of Health to increase funding for Lou Gehrig's research in order to find effective treatments and ...
The ALS Association encourages scientific research to find a cure for ALS, heightens awareness of the nature of the disease, stimulates volunteerism and activism, and increases awareness of government leaders to encourage support of research and... The ALS Association is grateful to have received funding to support this new groundbreaking research from the following: The Kanter Family ALS Research Fund and The ALS Association Greater Philadelphia Chapter The Jeff Kaufman Fund and The ALS Association Wisconsin Chapter The Wallace Genetic Foundation and Mrs. Jean Wallace Douglas The George Yardley Company, the family of George Yardley, and The ALS Association Orange County Chapter Contributors to the Lou Gehrig Challenge campaign of The ALS Association
Via TEAM Cure ALS Foundation|www.TeamCureALS.com|Find us on Twitter:@TEAMCUREALS, Rosa Silveira
Those watching Super Bowl XLVII on television last night didn’t see it, but just before kickoff, the jumbotron at the Superdome was alit with a gripping nonprofit PSA.
A Purdue University biochemist has determined the function of a gene that when mutated leads to a genetic variation of amyotrophic lateral sclerosis, or Lou Gehrig's disease.
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Rescooped by
Susan Speranza
from ALS
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Tickets for Laugh Your ALS Off in Pittsburgh from ShowClix. "Laughter is the best medicine".
Dr. Timothy Miller is director of the Christopher Wells Hobler Lab for ALS research. “We can do go in a technique called antisense oligo nucleotides and take that small mistake in those RNA instructions and like a small eraser and go in an erase that mistake and fix it.” said Dr. Timothy Miller. Washington University made history this year by conducting the first ever human trials. The first phase focused on whether the drug called antisense oligo nucleotide was safe.
Via TEAM Cure ALS Foundation|www.TeamCureALS.com|Find us on Twitter:@TEAMCUREALS
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Help Tommy Help His Mom Patch.com Seven-year-old Tommy Swift of Warren recently decided that he would commit some of his time to helping his mother, Natalie, who has Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig's disease.
Physicist Stephen Hawking visits LA stem cell lab USA TODAY LOS ANGELES (AP) — Stephen Hawking on Tuesday toured a stem cell laboratory where scientists are studying ways to slow the progression of Lou Gehrig's disease, a neurological disorder that...
BrainStorm Cell Therapeutics said the Mayo Clinic in Minnesota has agreed to conduct a clinical trial of the company's adult stem cell treatment for ALS. The Mayo Clinic is the third leading U.S. clinical site to sign a letter of understanding, following the University of Massachusetts and Massachusetts General, BrainStorm said
Via TEAM Cure ALS Foundation|www.TeamCureALS.com|Find us on Twitter:@TEAMCUREALS
Thomas Byrnes of Manlius, NY suffers from ALS or Lou Gehrig. ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and the spi...
A Purdue University biochemist has determined the function of a gene that when mutated leads to a genetic variation of amyotrophic lateral sclerosis, or Lou Gehrig's disease.
The Northeast ALS Consortium (NEALS) has launched their new website devoted to supporting clinical research of Amyotrophic Lateral Sclerosis (ALS) and other motor neuron disease (MND).
Tickets for Laugh Your ALS Off in Pittsburgh from ShowClix. "Laughter is the best medicine".
As a tribute to Pam, who lived with ALS from 2006 until her death in February of 2012, Healin' Wheels LLC has established the Friends of Pam Scholarship Fund to assist dependents and primary caregivers of ALS patients who plan to continue their education in college or vocational school programs. Renewable scholarships are offered each year for study at an accredited institution of the student's choice.
Our Neurologic Diseases Registry is a collection of different types of materials and information related to degenerative neurologic conditions, such as ALS, PLS, the HSPs, the dementias, Parkinson disease, the ataxias and the muscular dystrophies. It includes blood, DNA, ceribrospinal fluid, skin samples and brain and spinal cord tissue, as well as clinical, environmental and family histories. We maintain this information very carefully so.......
Via TEAM Cure ALS Foundation|www.TeamCureALS.com|Find us on Twitter:@TEAMCUREALS
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