I’m so sad. EDS is absolutely ruining my life and my body. I’m 23 and so many things are being taken away from me because of my body and I just wish I had a different body.
Ehlers-Danlos Syndrome (EDS)
I feel you. I’m having a rough day and I just want to sink into non-existence. (Non in a self harm way, just melty into the floor way) ♥️
I totally feel that. I am 24 and I swear my conditions are getting worse and I don’t even officially have my diagnosis yet. I am supposed to get diagnosed hopefully next month.
This condition is seriously disheartening. Every new issue that comes with countless tests with "normal" results that don't explain anything just beat you down a little more. But then you have to pick yourself up and take it one step at a time. We do what we can. And we're strong and brave for that. You got this ❤️
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