
Why AI Matters for HFA and the Community
By Brent Tritt, Vice President of Information Technology, HFA AI isn’t just a buzzword for technology companies’ offerings and efforts,
Dateline contains the latest news and touching stories about the people in our vibrant community. Discover what’s happening on the state and national level, the latest in gene therapy and advancements, as well as valuable information that impacts the quality of life for the bleeding disorders community.

By Brent Tritt, Vice President of Information Technology, HFA AI isn’t just a buzzword for technology companies’ offerings and efforts,

In early July of this year, Congress passed H.R. 1 — nicknamed the “One Big Beautiful Bill Act.” It’s a

By Skyler Tulley When Skyler Tulley laces up his running shoes, he’s not just preparing for another long run—he’s pushing

By Dana Kuhn, Ph.D. To the Bleeding Disorders Community, As a legacy leader in this community, especially during the tumultuous

At Hemophilia Federation of America, our strength lies in the people behind the mission—individuals who bring purpose, empathy, and relentless

By David Huskie, Board Member, HFA In 1985, my wife and I were dealing with the medical and insurance challenges

The Louisiana Hemophilia Foundation (LHF) is based in Louisiana. Currently, it operates with a dedicated team of two staff members

HFA Launches New Online Learning Platform to Provide Innovative Learning to Patients, Caregivers & More By Emily A. Roush, HFA’s

By Brent Tritt, Vice President of Information Technology, HFA AI isn’t just a buzzword for technology companies’ offerings and efforts, but there’s a growing role

In early July of this year, Congress passed H.R. 1 — nicknamed the “One Big Beautiful Bill Act.” It’s a sweeping law that rewrites large

By Skyler Tulley When Skyler Tulley laces up his running shoes, he’s not just preparing for another long run—he’s pushing against the limits that his

By Dana Kuhn, Ph.D. To the Bleeding Disorders Community, As a legacy leader in this community, especially during the tumultuous years (1990-1995) where this community

At Hemophilia Federation of America, our strength lies in the people behind the mission—individuals who bring purpose, empathy, and relentless drive to every aspect of

By David Huskie, Board Member, HFA In 1985, my wife and I were dealing with the medical and insurance challenges for a two-year-old with severe

The Louisiana Hemophilia Foundation (LHF) is based in Louisiana. Currently, it operates with a dedicated team of two staff members and 12 core volunteers who

HFA Launches New Online Learning Platform to Provide Innovative Learning to Patients, Caregivers & More By Emily A. Roush, HFA’s Learning Central Manager Since 2020,
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