She was only alive for eight months, but thanks to her parents’ determination, her memory will live on. Three years ago Marc and Mandy Seymour set out to raise $500,000 to build the Quinn Seymour Chapel inside the University of Minnesota Masonic Children’s Hospital.
Anton is a charming 5-year-old spending about six months in Minnesota to receive a bone marrow transplant at Masonic Children’s Hospital. He was born with a rare skin tissue disorder, epidermolysis bullosa. His whole family traveled from Texas to Minnesota to be with him during the treatment.
Anton Delgado has epidermolysis bullosa. It makes his skin so delicate, it easily blisters or even comes off.
He recently had a bone marrow transplant at the University of Minnesota Children’s Hospital to try to improve his health.
A young boy who came to Minnesota to get help with his rare disease has died.
There are kids that live every day with unimaginable pain. It is a rare disease that tears their skin, just through touch.
A 4-year-old Wisconsin boy with a rare skin disease has received a stem cell transplant in Minnesota.
A 4-year-old Wisconsin boy born without the gene that binds skin together is heading to Minnesota to prepare for a stem-cell transplant that could save his life.