Attack Life Sloan Foundation

Attack Life Sloan Foundation The Foundation was established to assist the Sloan family as they continue their journey with ALS.

Additionally, the Foundation serves the ALS community of patients and caretakers with equipment purchases, home remodeling, and much more. Our "why" - Support the ongoing needs of families diagnosed with ALS. On September 8, 2020 Nick Sloan was diagnosed with amyotrophic lateral sclerosis (ALS) commonly referred to as Lou Gerhig's disease. Nick, a Marine Corps veteran himself, was surprised to dis

cover that veterans are 2.5 times as likely to be diagnosed with ALS. The Foundation, a 501c3 nonprofit organization, was established in September 2020 to support the Sloan family's ever changing needs. Despite the fact that veterans are 2.5 times as likely to be diagnosed with ALS, the VA has set the standard of care for ALS patients and caretakers. Our hope is to stand in the gap for all ALS patients and caretakers by Advocating for the ALS community legislatively; Living along side the patients and caretakers as they come to grips with the reality of this disease; and Serving the unmet needs of ALS patients, assisting with home remodeling and renovations.

advocate

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05/24/2026

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ALS treatment research is continuing to evolve as an experimental oral therapy recently received FDA fast track designation: https://bit.ly/4dF9RpH

Read more about how researchers are approaching nerve cell communication in ALS, and why this update is gaining attention in ongoing ALS clinical trials and experimental treatment development. Researchers are continuing to explore new pathways that could shape future ALS treatment options, adding to broader conversations around research, symptom progression, and emerging therapies.

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05/04/2026

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BREAKING NEWS: On the first day of the Senate version of the ACT for ALS Reauthorization Act (S.4472) has officially been introduced.

This bipartisan legislation would help build on the progress being made to accelerate ALS research, expand access to investigational therapies, and strengthen the infrastructure helping move promising research and treatments forward.

Reauthorizing ACT for ALS means continuing to invest in what is working and ensuring we do not miss this moment when we are on the cusp of real breakthroughs.

Tell Congress to support the ACT for ALS Reauthorization Act: alsnetwork.quorum.us/campaign/152857/

02/05/2026

Appropriations bill H.R. 7148 has passed, increasing federal funding for ALS research by $45M for a total of $313M – the most we’ve ever had!

This happened because of your advocacy and continued efforts. Community is powerful!

🙏Thank your senators and representatives today who voted "yes" for passing this bill.

01/10/2026

For the first time, amyotrophic lateral sclerosis has a treatment shown to slow underlying nerve damage. A landmark clinical trial found that Tofersen reduced biomarkers of motor neuron injury and slowed muscle decline in patients with ALS caused by the SOD1 gene mutation.

ALS has long had no therapies that directly alter disease biology. Tofersen works by targeting the genetic source of toxic SOD1 protein buildup, reducing stress on motor neurons rather than only addressing symptoms after damage occurs.

While the treatment applies only to a subset of ALS patients with this specific mutation, researchers describe it as a historic step forward. It represents the first credible evidence that ALS progression can be slowed, opening the door to future therapies for broader forms of motor neuron disease.

Source/Credit: The New England Journal of Medicine — Tofersen ALS clinical trial
Shared for informational/Educational purpose only

12/11/2025
12/11/2025

We at Attack Life Sloan Foundation are grateful to have be able to support families and individuals this year. We have gifted almost $20,000, helping with medical and personal expenses for families affected by ALS. We are small, and not super flashy. I don’t take pictures or make giant checks, but I want you all to know your donations have made a difference.
If you prefer to donate to larger organizations there are several options. I will continue to share information about them on our page.
Again thank you all
~Shanda

12/11/2025
12/10/2025
As we move toward the fall, and the start of school, three Sloans will be attending college! As exciting as this is, it ...
07/03/2025

As we move toward the fall, and the start of school, three Sloans will be attending college! As exciting as this is, it also comes with some major expenses. Throughout the year Attack Life Sloan will start hosting micro fundraisers. The thought is if a lot of people give a small amount it will help in a big way! Our first one starts today.
Please share! This money will go directly to tuition costs
THREE DOLLAR THURSDAY!

07/03/2025

Tell Congress to Oppose NIH Funding Cuts

Address

Sunnyvale, TX
75182

Telephone

+12143251455

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