Dawn F.

Thank you so much for your post!

Your wife’s struggles mirror my own in so many ways.

My daughter was diagnosed with EDS almost a decade ago, but the doctor’s in the area considered it a ‘non-illness’, gave us zero information, & zero help.

As both our healths deteriorate, I’m back to looking for answers, solutions, or even  just ideas & direction.

You’ve given me a cohesive way to explain the symptoms to the rhumatologist I go see next month.


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