BECOME AN HAE ADVOCATE
Learning about hereditary angioedema (HAE) is an essential part of living with the condition.That’s why it’s so important for friends and family members of those diagnosed with HAE to have a true understanding of the condition. Although it is an inherited disorder, family members often go untested.
Because the symptoms of HAE often mimic those of other diseases, misdiagnosis is common. Spreading awareness can help ensure that those with the condition receive an accurate--and early--diagnosis. It can also help friends and family of those who have the condition to recognize symptoms as well as understand and avoid potential attack triggers.
A helpful solution for supporting HAE patients
With the Patient Service Center (PSC), available through the CINRYZESolutions® Programs, patients who have been prescribed CINRYZE® (C1 esterase inhibitor [human]) can work with a Patient Care Coordinator (PCC) to simplify and facilitate insurance authorizations, financial assistance, and other matters related to CINRYZE therapy.
To learn more about what the CINRYZESolutions Programs can do for you, be sure to speak with a PCC at 1-877-945-1000 or send an email to firstname.lastname@example.org.
If you have not been prescribed CINRYZE, visit www.cinryze.com for resources and information about hereditary angioedema and CINRYZE.