Our Mission

The Team Drea Foundation supports bold, innovative research to find a cure or effective treatment for ALS.

We see raising awareness about this devastating disease as an opportunity to inspire people to live bravely, love joyfully, and appreciate the gift of life.

Our Founder

Andrea Lytle Peet was diagnosed with ALS in 2014 at the age of 33. In eight months, she went from completing a 70.3-mile half Ironman triathlon to walking with a cane.

Remarkably, she has continued to participate in races. Since diagnosis, she has completed 35+ marathons, half marathons or triathlons on her recumbent trike. Her new goal is to complete a marathon in all 50 states.

Go On, Be Brave. Make A World Without ALS

States + Canada, and the U.K
Donations Raised
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1 day ago

Team Drea Foundation

Do I look cold? I was cold. 🥶 BUT Illinois (state #22) is ✅. And TOTALLY worth it to go with Jodi Klyn 🥰 Thank you Shaw Hipsher for cheering and sherpa-ing and road tripping! #50marathons50states #endALS ...

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1 month ago

Team Drea Foundation

Team Drea does the #solahotmini5k! We dodged a few gates and PNC police looking for tailgaters, but finished with —what else — hot minis! 🍩🍩🍩
We are SO INCREDIBLY GRATEFUL to the Sola community for supporting ALS research and the Luther family! 💚💪 #ibelieveinjeanne

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Medal Monday! On Saturday, I did the Fair on the Square Marathon (#21!) in Danville, IN. The race was fully but thankfully they opened a spot up just for me!! 🙌 ➡️ My new shirt, to which DP said “which part?” 🙄😂 ➡️ Proof we were in Indiana!

Grateful as always to be able to do this...though my knees are really bothering me 😣. We didn’t feel as safe as out west (all of IN needs 😷 wearing lessons...they go OVER your nose 🤦‍♀️). So happy I have 6 weeks til the next ones to rest & re-evaluate 😬.

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About ALS

Amyotrophic lateral sclerosis (aka ALS or Lou Gehrig’s disease) is a progressive neurological disease that affects the nerve cells in the brain and spinal cord. When motor neurons that connect nerves and muscles die, people lose the ability to initiate and control muscle movement. Without stimulation, muscles become weak and atrophy. Most people with ALS become totally paralyzed as they lose the ability to walk, talk, eat, swallow, and breathe.

Every 90 minutes, someone with ALS dies and another person is diagnosed.

The average age of diagnosis is 55; however, cases of ALS also appear in people in their 20s and 30s.

Military veterans are twice as likely to develop ALS as the general population. Athletes also seem to be more susceptible. No one is sure why.

The average life expectancy of a person with ALS is 2-5 years. 20% live 5 years or more; 10% percent live more than 10 years.

The only approved drug for ALS (riluzole), only extends life expectancy by 2-3 months.