He has what? How do you spell that?
These are questions that you never want to think about upon your child’s birth.
However, when Jackson Gabriel Silver was born in October of 2007, Jamie and Alex Silver heard the doctor utter six words that would change their lives forever: “I think he has Epidermolysis Bullosa.”
Jackson had a routine heel prick and the nurse placed a band-aid on his heel. When the band-aid was removed the next day, all the skin on his tiny foot tore off with it.
Since that day, the Silvers have made it their mission to support the brilliant research focused on finding a cure for EB that will give Jackson, and other children afflicted with EB, a chance at living pain-free lives.
Jackson has Recessive Dystrophic Epidermolysis Bullosa (RDEB), one of the most severe forms of EB. After that first hospital incident, EB continued to rear its ugly head intensely. In the neonatal intensive care unit (NICU), Jackson’s skin began to tear and blister with increased frequency. His tongue blistered and his mouth bled when he drank from a bottle. The elastic in his diapers tore up his thighs. By the time the Silvers took Jackson home after two weeks in the NICU, his body was covered in bandages.
At the time of Jackson’s birth and currently, there is neither a treatment nor a cure for EB. The only way to “manage” the disease is to wrap Jackson’s body in non-adhesive dressings to try to reduce the chance of injury and infection.
In spite of this serious diagnosis, Jackson has thrived beyond doctors’ expectations. With the proper protective bandages, he is able to play with his peers, though it is rare for him to make it through a day without sustaining a painful injury. His hands are scarred from repeated blistering, his knees, heels and elbows are always bandaged and, all too often, his esophagus tears from eating, but it does not dampen his spirit.
During his daily bandage changes, the Silvers witness how much Jackson’s little body has to endure. No toddler should have to sit through lengthy bleach baths or fear that food will hurt him when he swallows. No child should have to worry that if he falls, his palms will become giant blisters filled with blood. No four-year-old should have to know about needles and syringes.
The Jackson Gabriel Silver Foundation is working with the research community to ensure that Jackson and all other children inflicted with this disease can lead long and happy lives, free of the burden of EB.
But for now, EB is today’s reality. With your support, we can make it tomorrow’s past. Learn how you can help.