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Former Syracuse football legend Tim Green says he has ALS. 
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Denali Therapeutics and Sanofi are working to advance in clinical trials small molecules that block the RIPK1 enzyme to possibly treat diseases like ALS.
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A new way to deliver DNA to spinal nerve cells brings us a step closer to a gene therapy for amyotrophic lateral sclerosis
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Nanci Ryder may have lost her ability to use her voice in the four years since she was diagnosed with ALS, but that doesn’t mean the legendary publicist wasn’t heard on Sunday at the LA County Walk…
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A phone camera could transform how organizations help customers with a disability and boost customer service teams within the public and private sector.
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7 mothers who lost their teenage daughters to ALS: It's a disease so rare in kids that the CDC has only counted a handful... now their families are uniting to fight for a cure"...........................
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From
katu
RIDGEFIELD, Wash. (KATU) - A father battling ALS had one wish before he died; he wanted to see his three daughters get married. Akhil Jhaveri's family isn't sure he has enough time left on this earth to see each of his daughters walk down the aisle. We don
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Medicare and Health Care for People living with ALS
Medicare is available for certain people with disabilities who are under age 65. These individuals must have received Social Security Disability benefits for 24 months or have End Stage Renal Disease (ESRD) or Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig’s disease).
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Australian doctors are trialling a new drug they hope will help slow the progress of motor neurone disease, which is on the rise.
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Pat’s words and optimism are what inspire researchers like Pablo to #GoBoldly every day and never stop searching for a cure to end ALS.
Link: https://goboldly.com/als
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Project Revoice is recreating the voices of ALS patients – such as Pat Quinn – so they can embrace the familiarity of their own voices, after the disease takes their vocal chords.
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Hosted by Terance Mathis, the former All-American and Pro Bowl wide receiver,
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Helpful Amyotrophic lateral sclerosis (ALS) information about monitoring and managing ALS for patients and caregivers.
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In this article we take a closer look on cbd & parkinson. Researchers discovered that CBD behaves as an “inverse agonist” when it encounters a protein.................................
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People with End State Renal Disease or Amyotropic Lateral Sclerosis don't have to be 65 in order to qualify for Medicare.
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Researchers from North Carolina State University have identified proteins that may be useful in both earlier diagnosis of Amyotrophic Lateral Sclerosis (ALS) and in more accurate disease prognosis.
Danielle Christian's curator insight,
December 6, 2021 8:20 PM
Diagnosis of ALS could be sped up with the discovery of these proteins!
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The National Amyotrophic Lateral Sclerosis (ALS) Registry allows persons with ALS to fight back and help defeat ALS (Lou Gehrig’s Disease). By signing up, being counted, and answering brief questions about you and your disease, you can help researchers find answers to important questions. The National ALS Registry is a program to collect and analyze data about persons living with ALS.
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From
bidr
Join The ALS Association as we raise funds throughout the month of August through our National online auction in support of people living with ALS.
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There is currently no cure for Amyotrophic Lateral Sclerosis (ALS), but new research published in Nature Communications coming out of the Gibbings lab is bringing us closer.
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Catherine Scott needs your help today! Need accessible furniture 4 Anthony - Our son, Anthony Carbajal, has ALS, also known as Amyotrophic Lateral Sclerosis. He is moving back home - yay!!!, and we are so excited to shower him with love. It has been an incredibly difficult journey for him this past year, but he's on the right track to happiness and joy. We are raisin
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Scooped by
TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
June 6, 2018 3:18 AM
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Dwight Clark, the former 49ers star best known for "The Catch" that won the NFC Championship Game in 1982, has died at the age of 61.
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TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
May 22, 2018 7:01 PM
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The House passed "right-to-try" legislation that would allow the critically ill to bypass the Food and Drug Administration to obtain experimental medications.
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TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
May 22, 2018 6:53 PM
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Scooped by
TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
April 23, 2018 11:05 PM
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To protect, prepare and empower people with Parkinson’s before, during and after a hospital visit, we developed the free Aware in Care kit with tools and information to share with hospital staff during a planned or emergency hospital visit.
