The Pfizer Patient Engagement Team helps connect patients living with a rare disease to educational resources. Members of the team are field-based employees of Pfizer and, if you choose, will provide you with educational resources for awareness and management of your rare disease. Some of the ways a contact can help patients and their caregivers include:
Connect with advocacy groups that can provide resources and support
Provide educational resources about living with a rare disease
Supply helpful information and answer questions about Pfizer programs and resources
Pfizer Patient Engagement contacts are not able to provide medical advice. Questions about treatment and management of a rare disease should be discussed with your health care provider. Pfizer Patient Engagement contacts do not share personal or contact information in order to promote Pfizer products and do not contact patients or caregivers without their consent. Even if you choose not to opt-in for Pfizer Patient Engagement support, you may still access all other Pfizer patient support offerings for which you are eligible.
The Smart Patients Pediatric Alopecia Community’s online support complements CAP’s work by creating a network of patients (18 and older) and their parents who can share information and support.
From the Publisher of, Head-On, Stories of Alopecia the Top Alopecia podcast, Alopecia Life – The Alopecia Roadmap is a resource designed to be informative, easy to complete, and practical! Now offering a course just for parents and caregivers.
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