![](https://play-lh.googleusercontent.com/a-/ALV-UjVCjoQ8zv6yuR0f3BssJngVB4r_t5QN_BRolHtAz_jkaopcNM2k0w=s32)
Jamila Davis
For anyone supporting the EDS community, gets love from me. Some of the information, is not correct, and I deal directly with EDS genetic specialist. One in particular, is that people with African or Asian descendants are more likely to have it, when my European neurosurgeon and other European specialist have told me it's a rare European genetic disorder, due to my European ancestry. It's not the only European disease I have. Do more research or just look on youtube, anyway why does it matter, we are suffering INSIDE!
3 people found this review helpful