ICE BUCKET CHALLENGE Revival for Mental Health Sparks Controversy between the ELA community

The ice cube challenge has returned, but this time for a new cause.

Als’s ice bucket challenge that became mega-viral in the summer of 2014 had more than 17 million people on social networks, and even celebrities in interview programs, throwing ice water on their heads.

The challenge, supported by the ALS Association, intended to raise awareness about the disease. Finally, he raised $ 115 million for ALS’s research and patient care.

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Eleven years later, the ICE Bucket Challenge has been revived by USC Mind, the mental illness of the University of Carolina needs a discussion club.

In support of a foundation called Active Minds, the largest non -profit organization in the country for teenagers and young adults, the USC group launched the #Speakyourmind Ice Bucket Challenge.

The challenge is to take off on social networks and has raised almost $ 400,000 at the event collection site.

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The rebirth of the trend has caused some controversy for taking attention to ALS (amyotrophic lateral sclerosis), Also known as Lou Gehrig’s disease, a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord.

The average life expectancy after ELA’s diagnosis is typically two to five years, according to the Als association.

Brooke Eby, a patient and influencer of the ELA, published a video on social networks with the legend, “seeing people steal the ice cube challenge for a different cause when Als still does not have a cure and is 100% fatal. Hume.”

Michael Stone, another content creator and patient with ELA, talked about the impact that the challenge had on the ELA community.

“It’s more than a trend,” he printed in an infographic. “The challenge of the ice cube als changed lives.”

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“Knowing awareness about the ELA is crucial because it leads to financing, and financing leads to research,” Stone wrote. “What began as a viral challenge became something much greater: a worldwide effort that is financing the research that changes life and giving hope to those affected by this devastating disease.”

Brian Frederick, Marketing and Communications Director of the ALS Association, shared the organization’s support for revived movement.

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“We are delighted to see young people assume the spirit of mental health activism, but we also want people to know that Als is still fatal and urgently needs a cure,” Frederick said in a statement to News Digital.

“Mental health is an important issue in the ELA community, given the devastating physical, emotional and financial tolls that Als assumes entire families.”

Frederick commented that Als Ice Bucket’s original challenge “drastically accelerated” the fight against ALS, which led to “new genes discovered, new treatments in the pipe” and a significant increase in care services.

Since the challenge, the Als Association has invested more than $ 150 million in ALS investigation, followed by almost $ 1 billion in additional research funds of ALS, according to Frederick.

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“We still have a long way to go to move from Fatal to habitable and cure it, but we are grateful to everyone for taking the challenge of ice cubes and raising awareness about ELA and mental health,” he added.

Cathy Cummings, CEO of the International Alliance of Associations of ALS/MND, said that many people with ELA and their caregivers can face “serious mental health challenges”, such as depression and anxiety.

“Using the ice cover challenge to raise awareness about mental health also supports our community,” Digital’s News told News. “We would like to maintain space for the experiences of several people, without choosing, which is more deserving.”

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In a press release on Thursday, both the ALS Association and the active mentality announced that they are being associated in this new ice cube challenge for the month of May, which is both the month of awareness of mental health and the month of awareness of ALS.