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Brian Wallach ALS Symptoms: Is He Dead or Still Alive? On social media, obituary news of Brian Wallach, an ALS patient and founder of I am ALS, has been circulating. To understand more about the rumor, keep reading the article.

Brian Wallach and his wife Sandra Abrevaya are the founders of the I Am ALS movement, which they created to support ALS patients.

In addition to urging that Congress fully fund #ACTforALS, word of his death is circulating on the internet.

Brian Wallach ALS Symptoms: Is He Dead or Still Alive? Wikipedia Bio

Obituary news of Brian Wallach with ALS is currently circulating on the internet. The co-founder of I Am ALS was yet to be featured on Wikipedia.

He was suffering from amyotrophic lateral sclerosis since 2017, according to sources.

He was given a time of six months for his death nearly two years ago, at the age of 37. On the day his newborn daughter was discharged from the hospital, his doctor informed him that he had the progressive neurodegenerative disease Amyotrophic Lateral Sclerosis, or ALS.

He visited the doctor after he couldn’t stop coughing. It wasn’t a deep or phlegmy cough, but it was so persistent that he frequently struggled to finish a sentence.

It was late July of 2017 when his wife advised him to see a doctor.

ALS is a heinous disease where motor neurons in the brain and spinal cord gradually degrade and die. It causes the patients to eventually lose the ability to move, speak, eat, or breathe.

There is no cure and, with the exception of a few inherited cases, no known cause. When symptoms appear in an arm, leg, or hand, the average survival rate is three to five years. In almost all cases, it is fatal.

Is Brian Wallach Dead or Still Alive?

It’s not clear whether Brian Wallach is dead or still stive, as several obituary news of him are trending on Twitter. He was diagnosed with ALS, a life-threatening disease, in 2017, and was given a six-month life expectancy.

His last post was only yesterday, 21 January, when he wrote, “it makes no difference how you appear on the outside. Whether or not you can walk. Speak up or shut up. Observe or not.

I hate that I have ALS, but I so damn proud to be a part of the ALS community.

Happy weekend all. Put good into the world.

— Brian Wallach (@bsw5020) January 21, 2022

All that matters is who you are on the inside and that you bring that light, love, hope, and vulnerability to the world in order to make us all better.”

He also tweets about how much he despises being an ALS patient and on the contrary how much he enjoys being a part of the ALS community.

However, there are no tweets from him that would indicate his serious health or death to us.

Furthermore, neither his family nor his wife has said or commented anything on the rumor. They have neither denied nor confirmed the news.

We will update you with factual information as soon as the news is confirmed.

Where Is Brian Wallach Wife, Sandra Abrevaya Today

Brian Wallach and his wife, Sandra Abrevaya has founded I AM ALS, a patient-led, patient-centered movement to lead the fight for a cure.

Brian has two wonderful daughters with his wife whose current whereabouts are unknown to us at the moment.

Following his diagnosis, he came to know that in every 4.4 minutes one person in the world is diagnosed with ALS.

Since then he has fundamentally altered how medical advocacy works and how the government approaches medical research.

He was doing everything he could to inspire others and to show his children that their father, even in his short time, did something meaningful.

He didn’t just start an ALS advocacy group, secure more funding for ALS research, he even expand access to treatments for the roughly 15,000 Americans living with ALS.

Even if he is dead as rumored, he will forever be remembered for his great works.

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