Our Mission

The mission of the CrowdCare Foundation is to improve patient outcomes by removing barriers to a cure.

The CrowdCare Foundation is patient-driven, 501(c)3 non-profit organization that empowers patients with rare diseases at each step of their disease journey - from diagnosis, through education, care and on to a cure.

The Foundation was founded in 2012 by multiple myeloma patient Jenny Ahlstrom to simplify information for patients and encourage them to participate in clinical trials and to proactively support gaps in existing research funding.

Our Strategy
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Support Research-Driven
Patient Needs
Supporting the collaboration of patients and experts to accelerate the best research by crowdsourcing and crowdfunding potential cures.
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Provide Simplified
Patient Education
Offering the the latest research news in language patients can understand.
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Compile Patient
Data for Research
Using data to help patients navigate their disease while inspiring the research community with new insights with a new tool called HealthTree®.
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