u/Equal_Quarter6422

Hi All,

I just want to share that if you've struggled with Morgellons and the lack of support from the medical community there's a new website aimed at collecting quantative and qualitative data so that it's available when someone in medicine is ready to research further, there will be plenty ready and waiting for their analysis.

The website is Morgellons Data Registry and maybe a bit of information from each experience can help connect some dots someday.

Best of luck to each of you.