U.S. Patients: Register for Information

The Cooley’s Anemia Foundation is here for you.

If you are a person with thalassemia living in the United States, the Cooley’s Anemia Foundation is your partner in improving your care. We want to help you by keeping you informed about new research and care options, as well as opportunities to participate in events that we sponsor for the community.

Please let us know how to reach you by filling out the form below.

If you are a thalassemia patient living outside the United States who would like to be added to our email list, please send an email to sgilbert@thalassemia.org with the subject “Non-U.S. Patient.”

Thank you.

For Parents/Guardians:
By clicking on this box, I give my consent to share this information with the Cooley's Anemia Foundation.

The information gathered on this form will enable the Cooley's Anemia Foundation to stay in touch with you and to better understand the needs of the thalassemia community. This information will not be shared with outside sources.