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To bring about a dramatic and wide reaching change in conditions and attitudes for the rare disease community. Creating engaging awareness solutions. RARE-Rev-inar. Join us and experts to find out more about the importance of shared decision making, the role of multi-disciplinary teams and more.
For our next RARE Rev-inar we will be joined by experts in the field of cold agglutinin disease. CAD is a rare auto-immune disease requiring treatment and life changes. Sponsored by @Sanofi
Join us to find out more https://bit.ly/Sanofi-UnderstandingCAD
‘Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens’ is the topic of our next RARE-Rev-inar. Join us and experts to find out more about the importance of shared decision making, the role of multi-disciplinary teams and more.
Register free here:
What is cold agglutinin disease and how is it diagnosed? Find out more about the acute symptoms and long-term chronic impact at ‘Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens’ webinar.
Register free here:
Pleased to have Prof Catherine Broome join our panel discussion on Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens. Sponsored by @Sanofi
Register at:
Jörg is a busy retiree living in Rhineland-Palatinate, Germany. He has been living with cold agglutinin disease for more than six years now, but it took several years before he was diagnosed. Join Jörg and our expert panel for ‘Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens’. Register at:https://bit.ly/Sanofi-UnderstandingCAD
The CAD Foundation is one of the few patient organisations worldwide supporting people living with CAD. Join Pat Watson, president of the CAD Foundation as part of our expert panel on ‘Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens’ as we look at the biggest challenges for people living with CAD. Register at:
We are delighted to welcome such a knowledgeable and expert panel on ‘Understanding cold agglutinin disease (CAD) from a multi-stakeholder lens’ as we look at the biggest challenges for people living with CAD. Sponsored by @Sanofi. Register at https://bit.ly/Sanofi-UnderstandingCAD
Week in RARE is just around the corner, and we couldn't be more thrilled to welcome attendees from all over.
Join us and attend the 2023 Global Genes Week in RARE event encompassing two rare advocate-facing events, the RARE Health Equity Forum and the RARE Advocacy Summit. The events are taking place between September 18-21 at the Sheraton San Diego Hotel & Marina! Elevate your rare disease advocacy learnings with sessions that will provide you with insights about the latest in rare disease innovations, transforming the rare disease landscape and advancing health equity, best practices for advocating on an individual and organizational level, and actionable strategies you can take home and implement immediately to accelerate change. Join us for networking, learning, and inspiration. Learn More.
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Contact Us: info@cadfadvocacy.org
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