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Cold Agglutinin Disease Foundation Inc, CAD Foundation was created in 2019 as a non-profit, (501)(c)(3) corporation. It is dedicated to the advancement of knowledge about Cold Agglutinin Disease for the medical profession, patients and care partners.
CAD Foundation’s purpose is to foster and increase public awareness and education of
this
Cold Agglutinin Disease Foundation Inc, CAD Foundation was created in 2019 as a non-profit, (501)(c)(3) corporation. It is dedicated to the advancement of knowledge about Cold Agglutinin Disease for the medical profession, patients and care partners.
CAD Foundation’s purpose is to foster and increase public awareness and education of
this rare disease and info from diagnosis, treatment and management of this
rare disease, which in turn will enhance the quality of life of those affected by it by providing a continuously improving system of education, information and opportunities for those diagnosed or treating patients with CAD.
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The goal to serve as a hub of information, support and encouragement for patients and caregivers globally. The facebook.com group, CADdy CHATTER, an outgrowth of the website, was created in 2009 by a CAD patient and is our closed group exclusively for CAD patients and caregivers., They can interact directly with a worldwide membership
The goal to serve as a hub of information, support and encouragement for patients and caregivers globally. The facebook.com group, CADdy CHATTER, an outgrowth of the website, was created in 2009 by a CAD patient and is our closed group exclusively for CAD patients and caregivers., They can interact directly with a worldwide membership of over 1300 very caring CAD patients and caregivers.
In 2007, there was a shortage of information regarding Cold Agglutinin Disease and a significant need to educate and support patients with this rare blood disorder. The founder, a CAD patient herself, with the aid of two others she had met through NORD, created a website dedicated to CAD patients.
The founder in 2019 sought to create the Cold Agglutinin Disease Foundation Non-profit. Recruiting two others, the three founding board members formed the Cold Agglutinin Disease Foundation.
Today, the Foundation has grown through the board and volunteers' efforts to an organization that honours the Mission of CAD Foundation to educate patients, care partners, and the medical community.
On behalf of the CAD Community, we thank everyone who has brought awareness to this rare disease.
Together we harness the power of many vs the power of one.
Your support and contributions will enable us to continue our commitment to serve the community of CAD patients, their families, care partners and medical providers by facilitating communication between patients worldwide and offering:
Your support and contributions will enable us to continue our commitment to serve the community of CAD patients, their families, care partners and medical providers by facilitating communication between patients worldwide and offering:
A rare disease is defined as a condition that affects fewer than 200,000 people. It is estimated that there are approximately 12,000 people diagnosed with CAD in North America, South America, Europe, Australia, and Asia. Cold Agglutinin Disease Foundation, Inc. engages in all permissible fundraising activities and solicitation of grants and donations to meet the goals of the Foundation!
Pat Watson – President, Board of Directors
Pat comes to CADF with a background as a Regional VP in the consumer-packaged goods industry. She has 40 years’ experience in strategic planning, leadership, executive training, and the design of sales and marketing programs. After retiring, Pat used her business background to transition into education as an adjunct college professor where she designs and teaches strategy, leadership, management, and other business courses and works on a team to develop additional bachelor’s programs for the Business College.
Pat earned her MBA, with a concentration in leadership and management, at Kennesaw State University in Georgia and was a member of the Honor Society Phi Kappa Phi. She holds certificates in Coaching, Quality Matters, Critical Thinking, and several online learning platforms.
Pat enjoys her four grandchildren, and her interests include travelling with the grandchildren, genetic genealogy, history, archeology, and others.
Email: president@cadfcares.org
Jo Banta – Vice President, Board of Directors
Jo began her career as a Branch Manager for Kelly Services in Cincinnati, after earning her MBA from Miami University in Ohio. Jo quickly became involved in professional organizations, serving as an officer and board member of the Cincinnati Administrative Management Society. Through the years, Jo moved with her husband and two sons to Indiana, Illinois, and New York. Throughout her journey, Jo's eagerness to explore new opportunities in each location led her to embrace unique roles. Jo made a difference in the field of education by developing and implementing an English as a Second Language (ESL) tutoring program. She dedicated her time to helping special needs young adults as a job coach and built master cohort programs for teachers as a Cohort Coordinator. Additionally, she gained valuable experience as an Administrative Assistant for the Naperville, IL Park District Planning and Development Department.
Now retired, Jo continues to contribute to society through her involvement with P.E.O., a women's educational charity group. Her commitment to empowering women is demonstrated by her active participation in providing grants and scholarships to women seeking post-secondary education. Her interests include gardening, hiking, fishing, and reading.
Jo was officially diagnosed with Cold Agglutinin Disease in January 2020, though she had symptoms for decades. From firsthand experiences, she understands all the challenges patients go through from receiving a diagnosis to lab results to obtaining the correct treatment.
Email: vp@cadfcares.org
Todd Chambley – Treasurer, Board of Directors
Todd is a Senior Vice President at Aon in Atlanta. He has been in the executive benefits and insurance industry for over 28 years. Todd runs Aon’s Executive Benefits Practice, including responsibility for executive benefit consulting operations, sales and marketing, legal and compliance, and client servicing. Since joining Aon, he has held positions such as consultant, IT project management/DBA, controller, and COO. He is currently a member of Aon’s North American Health Solutions leadership team.
Todd has an accounting degree from Lee University and has earned the Chartered Life Underwriter (CLU) and Fellow Life Management Institute (FLMI) designations. He also holds Series 6 and 63 securities licenses and life and health insurance licenses.
Todd is married to Joy, who is a motivational speaker, trainer, and President of Moms with Swords. They have three children. Todd serves as a Board member for Engaging Leaders and volunteers as a coach and treasurer for the Atlanta Vipers Fastpitch Organization. He lives in the Atlanta Metro area.
Email: treasurer@cadfcares.org
Cold Agglutinin Disease Foundation Staff:
Bohdan Jarisz - Social Media/Web-designer/Graphic Artist
Bohdan is a marketing professional with 10 years of experience in web and traditional advertising, promotions, social media, and ad design concepts.
Colleagues know him as a highly creative marketer who can always be trusted to come up with a new approach. He knows that the client’s business comes first, and Bohdan never tries to impose his ideas on others. Instead, he spends a lot of time understanding the business and the audience before suggesting ideas. He can (and often does) work well alone, but he is at his best collaborating with others.
Bridgid and Catherine Connolly - Media/Communication/Writers
Bridgid and Catherine are sisters and medical doctors from Australia.
Bridgid is a Radiology and Nuclear Medicine Consultant, and Catherine is specialising in Pathology and Stem Cell Research.
The sisters became patient advocates for Cold Agglutinin Disease after a family member was diagnosed with the condition. In their spare time, Bridgid and Catherine enjoy outdoor activities such as hiking, running, tennis and cycling.
Kathy Cary – Facebook Content Compliance Manager
Kathy is a Certified Gemologist Appraiser. She has worked in this industry for 45 years and is currently employed by Skie’s Jewelry as a Diamond and Gemstone buyer. She is a graduate Gemologist from the Gemological Institute of America.
In her spare time, Kathy is the Administration Manager for Facebook groups. At present, she reviews for content compliance, not only CAD Foundation’s Facebook Group, CADdy CHATTER, and also manages two art groups. She enjoys painting with watercolors and does calligraphy. Kathy has two sons and is a dog lover. She has three dogs, named Grace, Suze, and Sally Popper, daughter of Susan Popper. She lives in Eugene, OR.
In 2003, Kathy was diagnosed with primary CAD.
Dawn B. Diaz – Patient Advocate for the Newly Diagnosed
Dawn Diaz grew up in Albany, NY and graduated with a BA in accounting from Siena College. She then became a CPA for Coopers & Lybrand straight out of college until becoming Controller for a local builder. Dawn, subsequently, became Director of Internal Audit of Cablevision Industries and eventually, Assistant Direct of Internal Audit at Time Warner, Inc. in New York City and finished her career as a Director of Internal Audit at Ernst & Young, and began volunteering her time soon after marrying Armando Diaz doing pro bono accounting work for local organizations. She lives in Englewood, NJ with her husband and two sons.
Dawn was diagnosed with CAD in 2017 and is happy to share her experience having CAD with other patients and looks forward to helping them to be an advocate for themselves to get the best possible care throughout their disease process.
The Cold Agglutinin Disease Foundation “Family” will forever be indebted to the tireless efforts of Cori Forster who helped build our community and provided support for CAD sufferers and their caregivers. Cori’s legacy lives on in each of us, as we support one another, learn about our conditions and access help through the CADF website and webinar programs she helped to create.
Brad & Cori Forster with Enzo and Griffen
CADdy CHATTER on Facebook.com is our Foundation’s closed group exclusively for CAD Patients and Family, where you can directly interact with over 1000 "CADdy's" from around the world.
Copyright © 2022 Cold Agglutinin Disease Foundation - All Rights Reserved.
Contact Us: info@cadfadvocacy.org