[Version française]
It's not clear yet whether Emma will participate in person or only virtually.
It's a one-hour virtual event that'll be broadcast on November 20, 2022, at 4 p.m. ET/ 1 p.m. PT. It'll help raise money and awareness for Epidermolysis Bullosa research.
According to ebresearch: "Individuals with EB lack critical proteins that bind the skin's two layers together. Without these proteins, the skin tears apart, blisters, and shears off, leading to severe pain, disfigurement, and internal and external wounds that may never heal. Today, there are no treatments or cures available for EB."
"Details on how to watch this year's show will be released soon"
Source: Harlow
If you have news to share (pictures, infos, scans...), please send an email to eden@emmawatson-updates.com
2 comments:
glad she takes direct action for causes again so happy emma! yay!
I had a friend with this skin disorder she sadly died when she was 17. Its a horrid disorder
Post a Comment