#Fight2EndALS campaign-Katie’s Story

Join the #Fight2EndALS campaign.

This is Katie’s story, and with her story, we will fully fund ACT for ALS!

Federal and State policy makers have the power to decide the future for all ALS patients, their carers, and families.
There are a number of funding opportunities in the balance at the beginning of this year and it’s important we keep ALS funding at the top of the political agenda. Legislators are currently considering federal funding for important bills that could help people living with ALS gain access to therapies and advance the science.
We need your help right now, before it’s too late and we miss out on critical 2024 funding.
Share this film and ‘tag’ your representatives to remind them how important it is to fund ALS treatments and research.
We’ve made it easy.  All you have to do is fill out this form and we will automatically create a social media post that shares this film and ‘tag’ your US senators and representative.

The tweet: @Representative, watch Katie’s story https://youtu.be/oej5ResnKPQ, and make sure ALS doesn’t rob anyone else of their mother by fully funding ACT for ALS #EndALS #Fight2EndALS

If you have another persuasive ALS story that needs to be told, submit your story and photographs and we’ll consider it to be part of the #fight2enALS social media campaign. Follow the step-by-step instructions on this form to get the process started. 

#Fight2EndALS #EndALS

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Join us for the 2024 Community Summit!

Join us in Washington DC from May 29th - June 2nd for the 3rd annual ALS Awareness Month flag display and inaugural Community Summit.

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