Just a "zebra" trying my best to live life to the fullest with EDS and POTS...and loving the ride.

This is all I got…

Written by Katie. Posted in Ehlers-Danlos Awareness

I came across a couple of interesting blog posts by eye doctor, Diana Driscoll about EDS and POTS, and the possible MS connection.  You can read them here.  (It makes more sense to read the second one first and then scroll up to read the first one.)

I’m running real low on “spoons,” and this is all I have in me for tonight.

Five for Friday will be a day late.  It’s off to bed for this girl!

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