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

#Repost @solacoffee with @get_repost
SOLA HOT MINI 5K is around the corner! March 28th @ 8:30am, we are gathering #togethertoendALS! Run, walk, stroll, cartwheel, volunteer, cheer - all are welcome! Register at solahotmini5k.com 😎

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Sitting outside in January seems fitting for the first meeting of the Alaska production team for our documentary! YOU should come with us! #goonbebrave #alaska #endals


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#Repost @solacoffee with @get_repost
Sola Hot Mini 5K REGISTRATION IS OPEN 🎉 SIGN UP, PEEPS 🏃‍♂️March 28th we will be hosting our 7th annual 5K as we raise funds to end ALS! Link in our bio for registration and more info. More details to come! #TogetherWeEndALS

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Reposting my blog post when I had the privilege of meeting Mickey Shy Tuna Johnston, who touched so many w/ALS through his tiedye tshirt ministry. He lived courageously with ALS for 10 years, all while celebrating life, loved ones, & music. Fly high Shy! http://www.teamdrea.org/2016/05/29/race-for-shy-tuna-part-1/

Breakfast with 🎅 was a success! Thanks to everyone who came out, we were able to raise almost $1,500 which will support ALS research! We are also so grateful for @ChuysRestaurant Cary, Parkside Town Commons, @kiterealtygroup , & our Team Drea elves for making it all happen.


50 marathons x 26.2 = 1310.0 which is the new @AviatorBrew beer for #alesforals supporting @ALSTDI. So very cool of them to help #endALS!

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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.