ALS still mystifying, nearly decade after Ice Bucket challenge

People participate in the Ice Bucket Challenge, in Boston, U.S., Aug. 7, 2014. (AP Photo)

by Anadolu Agency

Jun 21, 2022 12:07 pm

Back in 2014, before anyone knew anything about a pandemic or coronavirus, a challenge had taken the world by storm – the Ice Bucket Challenge – as people poured a bucket of ice water over their heads to promote awareness of the disease amyotrophic lateral sclerosis (ALS), also commonly known as Lou Gehrig's disease – after the baseball player who was diagnosed with it – and encourage donations for research.

Yet after nearly a decade, ALS is still considered a diverse and decidedly mystifying disease.

Each year, Motor Neuron Disease (MND) associations across the globe mark June 21 as a special day of recognition, acknowledging the impact that MND has on people around the world.

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord that control your muscles, according to the ALS Association.

As your muscles get weaker, it becomes more difficult to do such things as walk, talk, eat and even breathe.

Steve Gleason, a sufferer of ALS, holds his daughter while watching his son throw the ceremonial first pitch of the game between the Chicago Cubs and the Saint Louis Cardinals at Wrigley Field in Chicago, Illinois, U.S., June 2, 2022. (AFP Photo)

"Amyotrophic" comes from the Greek language. "A" means no. "Myo" refers to muscle. "Trophic" means nourishment. So amyotrophic means "no muscle nourishment," and when a muscle has no nourishment, it "atrophies" or "wastes away," according to the definition of the association.

The 2014 ALS Ice Bucket Challenge enabled the ALS Association to increase its annual funding for research around the world by 187%. During this time, ALS researchers made scientific advances, care for people living with ALS expanded and investment in disease research from federal governments grew.

The first symptoms of ALS, which occur with progressive muscle weakness without pain and sensory impairment, usually begin with weakness or thinning in the arms and legs.

Over time, patients develop difficulties in engaging in daily habits such as holding a pencil, buttoning a button and carrying a bag and may stumble while walking. In some people, symptoms of the disease begin with difficulty in speaking and swallowing.

Anthony Carbajal, who is battling ALS, throws out the ceremonial first pitch with the help of a pitching machine prior to a baseball game between the Los Angeles Dodgers and the New York Mets, in Los Angeles, U.S., June 2, 2022. (AP Photo)

While 10% of ALS cases are inherited, the cause of 90% is unknown. ALS mostly occurs between the ages of 45-55 but can also be seen at younger or older ages and is more common in men.

According to Johns Hopkins University, estimates suggest that ALS is responsible for as many as five of every 100,000 deaths in people aged 20 or older. The incidence of ALS worldwide is about one in 50,000 people per year, equating to around 5,760 to 6,400 new diagnoses annually.

If the patients do not receive any care support, they die within three to five years because they also lose their respiratory functions. However, if care support is given in a timely manner, many patients can cling to life and live for more than 10 years.

The Ice Bucket Challenge went viral on social media in the summer of 2014 as a campaign to promote awareness of ALS and encourage donations for research. A person is filmed as a bucket of water and ice is dumped over their head. The individual then nominates a minimum of three people to do the same thing and make a donation to the Amyotrophic Lateral Sclerosis Association.

Last Update: June 21, 2022 15:24