We did it! Marcy Dunne completed her goal of running a Fluid Running marathon on September 8, and it was a huge success. We raised over $150,000 for ALS and our dear friend and fellow Fluid Runner, Michelle Kram. Our amazing community showed up in full force, getting a great workout while supporting a great cause. Although the event is over, it’s not too late to give! Let’s keep pushing to raise even more for such an important cause. Read Michelle’s story!
Making Waves for ALS
Thanks to the generosity of so many friends and family members we have raised over $150,000 for ALS far surpassing our ambitious original goal of $100,000. But let’s not stop there! You can still make a contribution. You will see a list of organizations that Michelle has specifically chosen because each one has played a unique and crucial role in supporting her on her journey. Click the arrow button to learn more about how each organization has helped make a difference for Michelle. No matter which organization you choose to support, all proceeds will go directly to that organization.
Total Raised To Date: ~$150,000
ALS Association
The largest and most well know.
They have provided me with great information on the disease, especially when I was first diagnosed. I have taken advantage of their virtual support groups and a few other resources.
Les Turner ALS Foundation
Strong focus on research and equipment.
This is a Chicagoland support organization, affiliated with Northwestern Hospital. I am in a ALS clinical drug study with NW now. They have a strong focus on research and local support with equipment and other services.
ALS United of Greater Chicago
Support for those in Chicagoland.
Branched out from the ALS Association to provide more local support for those living with ALS. They have supported me with equipment not covered by insurance such as walking rolaters, canes and wheelchairs.
Team Gleason
Focus on technology based resources
New Orleans Saints ex football star Steve Gleason has been bravely fighting this disease since 2011. He founded Team Gleason and their strong focus is on technology based resources to make living with ALS more manageable. One resource they have provided to me at no cost was the ability to “bank my voice” to use at a later date if I can no longer speak. I will be able to use my computer to communicate in my own voice. How cool!
I AM ALS
Strong legislative advocates.
Founded by local Chicagoan Brian Wallach and his wife Sandra Abrevaya. Their organization has provided so much great resource information early on when I was first diagnosed. They have been very strong legislative advocates with their Washington connections (worked for the Obama administration) to pass important laws and increase legislative funding for ALS. Watch their powerful documentary on Amazon Prime – For Love and Life, No Ordinary Campaign.