• 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
  • More
    • 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

BRAD'S STORY

Brad, a rescue specialist with the Canadian Coast Guard, was diagnosed with cold agglutinin disease, changing his life in many ways. Learn how Brad manages his symptoms and navigates life with a rare condition.

SHARON'S STORY

 Because CAD symptoms can be hard for others to see, Sharon’s condition took a back seat to other issues in her life. Hear about her family’s support and the important role it plays in helping her manage her condition. 

JODIE's STORY

  Cold agglutinin disease may be rare, but there are others out there who are finding ways to manage life with the disease. Jodie, a mother of two, learned that she had CAD while she was serving in the military. Learn about Jodie’s diagnosis, how CAD affected her career, and how she manages everyday life with her family.

 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

Copyright © 2025 Cold Agglutinin Disease Foundation - All Rights Reserved.

Privacy & Policies

Powered by

This website uses cookies.

We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.

DeclineAccept