Apex Systems & Stratacuity
On February 18th, 1999, Stratacuity co-founder Patrick Marshall’s nine month old daughter Kate was diagnosed with Cystic Fibrosis (CF). The diagnosis of a rare disease is incredibly painful for any family. Thankfully, fellow CF dad and NFL Hall of Famer Boomer Esiason offered three pieces of advice that changed everything: (1) learn everything possible about CF science and become your daughters' advocate; (2) rally everyone possible to raise money to buy research; and (3) use your talents and gifts to personally make a difference. Mr. Marshall used this advice to partner with Rob Patten to cofound Stratacuity with the mission of finding scientists who would play a part in discovering a cure for CF. Since then, we have witnessed unprecedented scientific advancements for people with CF and many other diseases. Stratacuity is proud to be part of this process by providing support and resources for biopharmaceutical companies learning more about diseases and creating new treatments and cures. We know so much more needs to be done and there is no time to waste.
Stratacuity was purchased by ASGN in 2017 and is part of the Apex Ssytems, LLC Segment. The entire Apex Systems, LLC Segment immediately joined us in our mission, bringing many more people to the fight against CF and expanding our fundraising reach nationwide.
Join our Team for the Great Strides Walk!
Since 2001, our company has participated in Great Strides. Please join the 2020 Stratacuity Great Strides Walk team either in person at the event or in spirit by donating money to our team for the Cystic Fibrosis Foundation. Having you on our team is the best way to make a difference to anyone who suffers from CF by supporting the Foundation's mission to cure CF and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.