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Join the Fight ALS Film Fest
Thanks to the hard work of many people in the ALS community, we are proud to host the 3rd Annual Fight ALS Film Fest this ALS Awareness Month.
Register Now
Join the Fight ALS Film Fest
Thanks to the hard work of many people in the ALS community, we are proud to host the 3rd Annual Fight ALS Film Fest this ALS Awareness Month.
Register Now
About the Fight ALS Film Fest
This ALS Awareness Month, join us on Monday nights for a panel discussion on these incredible ALS films. This series is being hosted by The ALS Therapy Development Institute (
ALS TDI
) and
Her ALS Story
. Our emcee for the events will be Sunny of
SunnyStrong
. Thank you to our incredible sponsor
Mitsubishi Tanabe Pharma America
for supporting this program!
Please note, by registering for the film festival, you will receive weekly email reminders two hours before the event with login information for each of the four panel discussions.
We ask that all participants watch the films before the panel to have sufficient background knowledge for the discussion.
Week 1 5/6 at 7:30 CT - Gleason
After he is diagnosed with ALS, former professional football player Steve Gleason begins making a video diary for his unborn son, as he, his wife, and their friends and family work to raise money for ALS patients as his disease progresses.
Panel Discussion: 5/6 7:30 CST
Panel Participants: TBD
Week 2 5/13 at 7:30 CT - TBD
More information to come
Week 3 5/20 at 7:30 CT - TBD
Go On, Be Brave
is a film about Andrea Lytle Peet's race against time - a diagnosis of ALS and an attempt at the impossible: to be the first person with ALS to complete a marathon in all 50 states.
How to watch:
https://goonbebravefilm.com/
Panel Discussion: 5/20 7:30 CST
Panel Participants: Andrea and Dave Peet, Filmmakers Miriam McSpadden and Brian Beckman
Week 4 5/27 at 7:30 CT - TBD
More information to come
Register to Join the Fight ALS Film Fest
About ALS TDI
The ALS Therapy Development Institute (ALS TDI) and its researchers quickly discover and validate potential treatments for ALS. It is the world's first and largest nonprofit biotech focused 100 percent on ALS research. Led by drug development experts and people with ALS, ALS TDI understands the urgent need to slow and stop this disease.
ALS TDI is recognized as an international leader in preclinical and translational ALS research, and partners with pharmaceutical companies and biotechs around the world. Awarded the highest nonprofit rating – four stars – on Charity Navigator, ALS TDI spends 87 cents of every dollar raised on finding effective treatments and cures for
ALS
.
Donate to ALS TDI in honor of the Fight ALS Film Fest
About Her ALS Story
A group of women diagnosed with ALS before their 35th birthdays to challenge the stereotype that ALS is an older white man's disease. Her ALS Story fosters an open dialogue about their declining health in female-centric media outlets; cultivates relationships with female lawmakers to improve current insurance and Medicare standards and introduce legislation to speed up the drug pipeline; and raises money for the pursuit of unbiased, supercharged ALS research to ultimately end this devastating disease. Funds raised for Her ALS Story from the Film Fest will go towards supporting their 2023 Warrior Weekend!
Donate to Her ALS Story in honor of the Fight ALS Film Fest
About Mitsubishi Tanabe Pharma America
Learn More About MITSUBISHI TANABE PHARMA AMERICA
What is Lou Gehrig's Disease?
Amyotrophic lateral sclerosis (
ALS
), also known as Lou Gehrig's Disease, is a progressive neurodegenerative disease that attacks motor neurons in the brain and spinal cord. This results in the wasting away of muscle, loss of movement and eventual paralysis. There are an estimated 30,000 people living with ALS in the United States at any given time. Every 90 minutes, someone is diagnosed with ALS.
To learn more about Lou Gehrig and the history of ALS research,
click here
.
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