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My EDS Careteam

Ehlers-Danlos Syndrome type hypermobility (or hEDS) presents many issues outside the party-trick-worthy bendable joints. This means that beyond my killer Mrs Incredible impression, I have complications above and beyond my joints. hEDS seems to affect my entire body, and each system is affected differently. This means I spend a lot of time and money at

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Elimination Diet

I’m about a month and a half into eliminating soy from my diet to try to fix my stomach. But I half assed it for the first two weeks… I see little to no difference. I’m doing this for 3 month, then I’ll add in another weird thing I can’t remember to eliminate. I’ll do

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Ehlers-Danlos Syndrome

I have a genetic disorder that occurs in 1 in 10,000 to 15,000 people. Turns out Daniel does too. Doctors often ask if we met in a support group. It’s called Ehlers-Danlos Syndrome Hypermobility type. This condition is rare (or rarely diagnosed), and many of the symptoms can be lessened with early intervention. I’m hoping

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Nashville Grows

The top photo is from summer of 2013 when we bought the condo (it was stormy) the bottom photo is from today. Even watching Nashville grow every day has been surreal. You can still see the top of the Pinnacle building, the Encore now looks tiny, at the right angle I can still see the

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CMA 2017

I wouldn’t normally write up an adventure for a weekend we spent basically at home, but this weekend was full of too many great stories not to share. Thursday we took a walk and cursed ourselves; we made the mistake of musing to ourselves after our walk that this was the most polite CMA group

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