Jo Banta, Vice President of the CAD Foundation, describes the foundations efforts to raise awareness of the condition among the public and with health care providers.
Two of those affected by CAD, Jo and Beth, relate their experience with the disease sudden onset and lasting symptoms.
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Whether you are a CAD patient, family member or a care partner, we want to hear from you! Sharing real life experiences is essential to raising awareness about the issues facing those who live with CAD.
Contributing stories is a way of bringing the CADdy Community together and can help each member to know he/she is not alone!
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