@chnge
CHNGEMeet @Ariana 🦋 a 22 year old woman, who is an advocate and social media content creator breaking the everyday stigmas surrounding unique lifestyles like hers. Ariana, is a college graduate with a B.A in Communications using her obtained knowledge to raise awareness for her painful and extremely rare skin disorder, Epidermolysis Bullosa.About EB:1. Individuals with EB lack critical proteins that bind the two layers of skin 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.2. There are four main types of EB that vary in severity and the location of blister formation. In the more severe forms of EB, life expectancy ranges from early infancy to just 30 years of age. But, with the newest technology and advancements in medical research, people with EB are now exceeding their life expectancy.To donate for a cure and learn more:https://www.debra.org/donateInstagram: @wefighteb
On the profile · Jul 30, 2022