Advocacy partner:
Cold Agglutinin Disease Foundation Inc.

A non-profit foundation dedicated to creating healthier lives for the CAD community of patients, and committed to educating them, their care partners and the medical profession about this rare disease.

CAD Foundation’s purpose is to foster and increase public awareness and education regarding the diagnosis, management and treatment of this rare disease, which in turn will enhance the quality of life of those diagnosed or treating patients with CAD.

Contact: Pat Watson – President
Phone: (770) 605-4276‬
Email: [email protected]

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Understanding Cold Agglutinin Disease: A Conversation with Dr. Roy Smith

Speaker: Dr. Roy Smith
Host: Adele Fogle

Dr. Roy Smith answers questions from the CAD community about living with the effects and symptoms of Cold Agglutinin Disease.

Welcome to CADdy CHATTER FB Group

CADdy CHATTER is a private Facebook community for people living with CAD, their care partners, families, and advocates. Join us to connect with others who understand the journey, find support, share experiences, ask questions, and stay informed about CAD, treatment options, research, and the latest community news.

Whether you’re newly diagnosed or have been part of the CAD community for years, we’re glad you’re here. Together, we’re building a stronger, more connected CAD community through education, support, and hope—because no one should navigate CAD alone.

CAD Foundation Newly Diagnosed Package

Newly diagnosed with Cold Agglutinin Disease (CAD)? This six-page printable package offers practical tools to help you feel more informed and prepared, including essential questions for your doctor, lab cards, checklists, a blood test tracker, and a symptom journal.

Download your free newly diagnosed package now!

About Advocacy Partners

The information above is provided by our partner. Learn more about our advocacy partners here.