The Charles E. Holman Foundation is a grassroots activist organization that supports research, education, diagnosis and treatment of Morgellons Disease. Ultimately, we seek discovery of its cause and cure.
Our organization exists to play an integral role in spreading the understanding of Morgellons Disease to others.
Morgellons Disease Research & Publications
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We are excited to announce that there is now a functional, worldwide Morgellons patient registry. This new registry is named Morgellons Global Data, and is accessible by clicking www.morgellonsglobaldata.org.
Participation in this patient registry will enable us to have an accurate collection of patient data, symptoms, and the impact that Morgellons has had on their lives, both socially and economically. This data is vital in getting Morgellons recognized as a real and devastating condition.
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Jenna RefreshJH2026-03-08 18:35:582026-03-09 19:15:42Advocating for Change: A Day on Capitol Hill for Lyme Disease Awareness
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Charles E. Holman Foundation2026-02-08 10:46:272026-02-08 10:47:00Morgellons Lived Experience Project Update
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Charles E. Holman Foundation2026-02-06 19:17:542026-02-06 19:28:17Persistent Borrelia Infection in Chronic Lyme Disease: A Review of the Medical Literature
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