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    • Home
    • Welcome
    • CAD & Treatments
    • Donation
    • Resources
    • Webinar Resources
    • Register Web Series
    • Latest News & Articles
    • Clinical Trials
    • Specialists
    • Media
    • Our Stories
    • Stay In The Know
    • Medical Advisors
    • Contact Us
    • Privacy & Policies
    • E-Learning Education
    • Rare Disease Day
    • Observational Study
    • New Members
  • Home
  • Welcome
  • CAD & Treatments
  • Donation
  • Resources
  • Webinar Resources
  • Register Web Series
  • Latest News & Articles
  • Clinical Trials
  • Specialists
  • Media
  • Our Stories
  • Stay In The Know
  • Medical Advisors
  • Contact Us
  • Privacy & Policies
  • E-Learning Education
  • Rare Disease Day
  • Observational Study
  • New Members

OUR STORIES

Karger - patient perspectives

Advocacy and Awareness for Cold Agglutinin Disease

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.

Living with Cold Agglutinin Disease

Two of those affected by CAD, Jo and Beth, relate their experience with the disease sudden onset and lasting symptoms.

 VIDEOS ARE PRODUCED BY SANOFI 2020 - ALL RIGHTS RESERVED 

share your story

Are You Interested In Writing Your CAD Story

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! 

Email your story

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