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My name is John Ferman. I am the president of Chronic Pain Partners, a non-profit 501(c)(3) organization. My daughter Deanna and I created the Ehlers Danlos Awareness program in 2011 to help support those with a genetic disorder called Ehlers-Danlos Syndrome (EDS.)
The vision of Chronic Pain Partners is to bring chronic pain support groups and Ehlers danlos support groups to people i....
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Tijdens de hele procedure bleef advocaat rustig en overtuigend. Continue Reading
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Ze wist precies wanneer ze sterk moest optreden zonder drama. Continue Reading
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Geen agressieve aanpak maar toch veel steun gevoeld. Continue Reading
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