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Our Champions

Brian Wallach

Brian Wallach is an ALS Warrior on a mission to win this ALS fight, to unlock critical breakthroughs for not just ALS, but Parkinson’s, Alzheimer’s, Frontal Temporal Dementia, and beyond and save the lives of millions of people. He founded I AM ALS in January 2019 with every intention of making this dream a reality, and is committed to working alongside Augie’s Quest and the entire ALS community to find a cure, and not in the next 20 years, but in the next three.  

A practicing attorney, former U.S. Attorney and staffer for President Obama, Brian recently testified before Congresswoman Rosa DeLauro, Chair of the House Labor, Health and Human Services, Education, and Related Agencies Appropriations Subcommittee on the underfunding of ALS research during the subcommittee’s Public Witness Day.

“I sit here filled with hope. Why? Because we can actually cure ALS. How? By fully and boldly funding the fight against ALS,” Brian says in his opening comments. “The research that this subcommittee has funded over the last decade enables me to say, and truly believe, that it is no longer a question of if we can cure ALS, but when.”

Brian is a man after Augie Nieto’s own heart – and one we’re extremely excited to work alongside (be sure to check out a recap of our time together with Orangetheory Fitness at Wrigley Field). It is going to take a village to #EndALS, and having Brian as a dynamic leader and partner is key to our success. Read and see more about Brian’s story in his own words (also available via


This is an ALS Story. It happens to be my story. But it could be your story. Your spouse’s story. Your child’s story.

I was diagnosed with ALS in November 2017. I was 37. With two girls under three. And I was told then that this disease will take my life. Rob my daughters of their father. And my wife of her husband.

That, however, is not how my story will end. Why? Because, together we are going to cure ALS. The first time I heard the words “ALS” from my doctors was on August 14, 2017. As those words crashed around her office, my family and I asked questions. Trying desperately to make sense of this diagnosis.

Wasn’t I too young to have ALS? How could I have it if we have no family history of ALS? Aren’t there parts of my symptoms that suggest something else, anything else?

The answers didn’t come that day. There is not yet a test to diagnosis someone with ALS. Instead, it is a diagnosis that is reached when all other options are exhausted. What doctors call a diagnosis by exclusion.

And as we were waiting for that diagnosis we read everything we could find about ALS.

Let me start with the punchline: there is no cure right now for ALS.

  • Every 4.4 minutes someone in the world is diagnosed with ALS.
  • Every 4.4 minutes someone dies of ALS.
  • In the time it takes you to read this document someone’s son will have been diagnosed with ALS and someone’s mother will have died from ALS.
  • ALS is a disease that turns your body against itself. It causes your body to attack itself. To wear out its muscles until you can no longer move your hands. Your arms. Your legs. Eat. And ultimately breathe.
  • Lou Gehrig had ALS. So did Stephen Hawking.
  • So do nearly 500,000 people around the world.
  • One out of every 500 Americans will be diagnosed with ALS. Those diagnosed are young and old, male and female, and every skin color.
  • ALS doesn’t discriminate. It can affect anyone.
  • 90% of the people diagnosed with ALS have no family history of ALS. 90%
    On average, they will live 2 to 5 years after being given this diagnosis. 

So this story, my story, is actually our story—because if ALS can affect anyone, curing it takes everyone. The good news is that our story can have a happy ending.

That’s because ALS is not an incurable disease; it is an underfunded one. Indeed, even though ALS research is badly underfunded, researchers are closer to finding a cure than ever before having identified over 40 genes connected to ALS.

In fact, the tools are in place to defeat ALS. The ALS community has the necessary building blocks of a movement for a cure: patients, advocates, and organizations striving for new recognition, new commitments, and new breakthroughs. They remain hopeful, driven, inspiring and inspired.

What is missing from the fight right now is a patient-led, patient-centric movement that can empower those in the fight and bring those not affected by the disease into our struggle.

So that’s what we have built with I AM ALS.

A patient-led, patient-centric movement that will drive collaboration, build and provide critical missing resources for the ALS community, organize and empower the ALS community, and drive increased awareness of ALS in order to generate millions of dollars in new funding to accelerate finding a cure. 

Thank you for joining us—the patients, caregivers, advocates, and doctors at the helm of I AM ALS—in this fight. As I sit here typing these words, I am filled with hope because I truly believe that I will live to see a cure for ALS. A cure that will allow me to raise my girls with my wife. To be there for the father-daughter wedding dance. A cure that will change the lives of tens of thousands by ensuring that no patient ever has to be told, “you have ALS, get your affairs in order.”

Please join I AM ALS and Augie’s Quest to Cure ALS – like, follow, share and sign up for the latest in news and efforts to #EndALS.


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