Patients with HAE – Reoccuring Bouts

Patient Worthy is working with a partner agency who is looking to engage with patients living with Hereditary Angioedema (HAE) who have reoccurring symptoms, more than 2 times a month. If chosen, participants will have the chance to take part in a compensated opportunity sharing their experience. Not all interested will be chosen.

Those interested in participating can fill out the form here.

If you have questions about this opportunity, you can get in touch with us at contribute@patientworthy.com.

We value your privacy. To learn more about our privacy policy click here.

 Acknowledgment: This story is promoted through the Patient Worthy Collaborative Content program. We only publish content that embodies our mission of providing relevant, vetted and valuable information to the rare disease community.

PW Collaborator

PW Collaborator

Our mission is to amplify the rare condition voice. One of the ways we achieve that is through collaborations across the community, from patients and caregivers to industry leaders in treatment research and development. To learn more, click here.

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