My Great Strides Story
Hal Blackman
Fundraising for Atlanta Great Strides 2026
Hal Blackman
Team IST USA is back for our 15th year of rallying our coworkers, friends, and family nationwide to raise money to help children breathe easier around the world. I'm excited that our IST team will be participating in CFF Great Strides Walks in 38 cities nationwide this year as we gather together and raise money to help kids in need.
I'm also excited to be working at the Kids Zone tents alongside my IST Atlanta team in person at the Atlanta walk again this year on May 16 at Suwanee Town Center as we hand out balloons and sweet treats to walkers and their families.
This year we've added to our ambassador program and are not only walking for Blake and his family but also for Maggie, Hayden and their family. We have so much to do and are excited to get back to doing it!
You can help us to help the kids with CF that need it. Just click the "Donate" button on my page and in less than 2 minutes, from the comfort of your home or office, you can make a quick and easy tax deductible donation online.
Your donation can help go toward medical research to help find a cure for Cystic Fibrosis. Together, we are adding tomorrows to the lives of people living with CF.
I'm also excited to be working at the Kids Zone tents alongside my IST Atlanta team in person at the Atlanta walk again this year on May 16 at Suwanee Town Center as we hand out balloons and sweet treats to walkers and their families.
This year we've added to our ambassador program and are not only walking for Blake and his family but also for Maggie, Hayden and their family. We have so much to do and are excited to get back to doing it!
You can help us to help the kids with CF that need it. Just click the "Donate" button on my page and in less than 2 minutes, from the comfort of your home or office, you can make a quick and easy tax deductible donation online.
Your donation can help go toward medical research to help find a cure for Cystic Fibrosis. Together, we are adding tomorrows to the lives of people living with CF.
Comments