Eric Den In his first video, his ALS diagnosis with fans and a new campaign for the cure for the cure for the disease is completely weaker with fans.
"I am Eric. An actor, a father and now a person living with ALS," says Den (42) In Instagram Video Monday, September 7, was divided on Monday.
The Gray's anatomy Alam vowed, "Together, we will renew the Landmark Law Act for ALS, promising treatment of thousands of patients like me.
Den, who declared her ALS Diagnosis AprilSlowly spoke and had some slur with some of his words in the video, which was concerned about watching something. Periodically all over the video, the actor's weapons can be seen uncontrollable.
According to ALS, the actor's speech and involuntary spams are both common symptoms of ALS, which is a nervous system, a nervous system that affects the nervous system of the brain and spinal cord and has no cure.
"There's more to learn more. We need to do more and do it right now," Den has asked to see the link below for his followers "to donate. Get involved and be part of pressing for progress."

Although many fans praised the actor for the desire to raise awareness about the disease and to find out the cure, others had the opportunity to ask questions in the comment section to understand the actor's diagnosis better.
"I don't know much about ALS, by admitting, someone can tell me whether Eric's speech difference is a part of the diagnosis." A user wrote in the comment section. "It seems blurred as if he's fighting with talking. It is absolutely heartbreaking to see how fast he has changed for the worst."
I responded to the ALS, "Yes; Also affects all the muscles in the body with vocal vocals and neck muscles."
When the other user mentioned that Den's "There is a twitch in his arm" seemed to be, the company replied, "Yes. Aloes are a brutal disease."
Dane Shared its ALS diagnosis publicly in April Man At that time, "We are grateful to get my loving family by my side as well as navigating this next chapter."
Dane, who shared the daughter Billy (15) and 13 -year -old Georgia with wife RebeccaHe mentions that he will continue to work as much as possible. (Gehart, 54, and Den were married 14 years before filed for divorce in 2018. In March, he Filed to dismiss his divorce From Den, however, the pair Not romantically back together.)
In June, Dane sat down with Diane Sawer For His first interview From the declaration of his diagnosis. He revealed the time that the illness reached a level where he began to lose its functioning of his organs.
"I have a functional arm. ... my left side is working my right side, (which is my dominant side), fully stopped working," Den said at the time. "(My left arm) is running. I think probably a few months, a few more months and will not be left. ... I'm concerned with my legs."
Despite many unknown about his future, Den said to Sawer 793 years old She is leaning toward Ghert And his family.
"I'm fighting as much as I can. There is a lot about it beyond my control," he shared. "I am angry because you know, when I was a kid, my father was taken from me and now I have a very good chance I will be taken from my girls at a very young age. At the end of the day, what I want to do is spend time with my family and I want to do something if I want to do it."
Although Dane 2025 AMi Missing the Award Sunday, September 7th, where he was ready to take the stage with a colleague Gray They Jesse WilliamsHis presence in the ALS video on Monday showed some hope for fans - and concern for others.
The I ALS community, however, expressed tensions about being such a visible spokesperson to promote the disqualified disease.
“We declare ProgressALS is a groundbreaking promotion to secure $ 1 billion for Federal funds for ALS, to accelerate ALS research, and over the next three years, "I have given the caption of the video on his personal Instagram page.
The message continued: "I am the ALS - 'the most successful patient of the 21st century Advocacy Movement - it is now launching this campaign because the ALS is at a tipping point. New treatment is within reach, but thousands of people living with ALS will lose access unless we take action.
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