Patient Overview

How Patient Data Helps the Community

Community, meet technology

Through ATHN, the community is in control of its own data. And now that data can start to work for the community.

Using the latest technology, providers will be better able to improve clinical results, prevent disruption in care, support research, and expand collaboration. It will take many patients contributing their information to make the data set meaningful. Community involvement—that is, participation in the ATHNdataset—is key to its value.

There’s strength in numbers. Make your data count.

Treatment centers and patients are already putting the technology to work. By using this technology, the community will ensure that care is more closely managed and seamless—whether routine, during an emergency, or while traveling. And patients, chapters, and others will be able to find the supporting data they need for advocacy efforts.

Among the greatest benefits of the ATHNdataset, however, is its power to begin
addressing questions about bleeding disorders and their treatment that haven’t been answered, simply because there hasn’t been enough standardized data. The ATHNdataset opens the door to new possibilities for the bleeding disorders community, now and for generations to come.

ATHN follows all HIPAA privacy guidelines to keep personal health information confidential.

Ask your treatment center how you can start putting your data to work today.

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