Advocacy partner:
Cold Agglutinin Disease Foundation Inc.
About the CAD Foundation
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]
Resources
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.
Upcoming events
About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.
Recent Posts
- Attending church can be challenging for this CAD patient
- Cell therapy helps woman with rare combination of 3 diseases
- National ‘That Sucks’ Day reminds me of all this weary CAD warrior endures
- Chemotherapy triggers cold agglutinin disease in woman with breast cancer
- I am ready to cluck about CAD, ‘The sky is falling! The sky is falling!’
- Making a pattern in needlework prepared me for my CAD diagnosis
- Bacterial lung infection sparks CAD, kidney injury for woman
- How I’m like Mr. Spock: Cold logic and cold agglutinins
- Blood stem cell transplant complicated by temporary CAD in donor: Case report
- After a trip to the ER, I’m figuring out how to strengthen my immune system
