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A dedicated resource for support, education, and community for those impacted by morgellons and lyme disease. Whether you’re seeking information, connection, or guidance, we’re here to help.
Britt Girvan was diagnosed with morgellons and lyme disease two years ago. Today, she is on a mission to transform her experience into purpose.
At What the Morgs, our mission is to support those affected by morgellons and lyme disease. By having meaningful conversations, telling real stories and raising awareness for the community.
Connect with us on Instagram and Facebook or send us a direct message through our contact sheet.
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