Living with PoTS and dysautonomia

Perhaps more than any other aspect of chronic illness I have ever had to deal with, including chronic unrelenting pain, dysautonomia has the ability to throw your entire life into disarray, permeating every single aspect of your life in ways that can be as invisible to the casual bystander as they are devastating. Is there a bright side, things we can learn, ways of living with it better?

Should you really wear cushioned shoes with hypermobility issues?

When you can trust your feet, when you can feel the earth beneath you and when your body knows it can really trust where it is putting its weight down, your whole body relaxes, you become more instinctual in the way you walk, your balance improves, your left and right hemispheres get toned in their relationship with one another as you walk out in nature, and you come back feeling happier, healthier and as though you have had an all-round therapy just from putting one foot in front of the other. We need to use this...its foundational for good health!

What would I be without “all that”?

"Without pain, I would be a neurodiverse hypermobile person (which is both to think and move outside the box…) with exceptional skills of insight and sensitivity, who knows how she likes to be and work and with whom and how to follow her best, most balanced, guidance through life." Excavating the gifts of diversity beyond a paradigm of struggle.