I am so proud of my wife for her strength. There is so much further to go until underrepresented illnesses have the treatments they need, but the work moves forward ever more quickly. We will not back down until it's done.
Reposted from
Emalyn Lindeman
I was born with a genetic illness called Hypermobile Ehlers-Danlos Syndrome (hEDS). Spending my entire life in pain, it was not until I was 19 years old, that I got my hEDS diagnosis, giving me clarity as to where my pain is from. Two years later I am still at the beginning of my healing journey.
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