I discovered a story about a little boy by the name of David
Vetter, known to many as “the boy in the bubble.” David was born with severe
combined immune deficiency (SCID), and after his birth, he had to immediately
placed in an incubator because he could not be exposed to germs (The New York
Times, 2015). His disease prohibited him from living in an unsterile
environment. David spent his life in the Texas Children’s Hospital living in an
incubator that continued to grow and expand as he aged. Many Doctor’s and human
rights groups were concerned about the fact David was being housed in a plastic
box (The New York Times, 2015). It was not until 1977, NASA researchers built
a special suit for David to venture outside into the world. Allowing him to go
outside play, be held by his mother, and go to the movies. All the things that
most people take for granted.
David
disease was very rare back in the 1970s, and he needed a bone marrow transplant
because his bone marrow did not produce immune cells. Researchers were unable
to find a matching bone marrow. As a result, his medical decided to used
donated bone marrow from David’s sister, but her bone marrow contained the
virus lymphoma that ultimately led to his death (The New York Times, 2015). David’s
life was documented and captured for many to watch on their television. David’s
mother understood the risk related to her son’s condition and was willing to follow
the guidance and recommendation of David’s medical team. So much medical
research was gathered over the span of David’s life about SCIDs. Due to the notoriety of David’s journey with SCIDs;
it helped to boost awareness and research into the disease. Today fetuses can
be tested and treated for SCID in the womb.
References:
The New York Times. (2015, December 15). The Boy in the
Bubble | Retro Report | The New York Times [Video file]. Retrieved from
https://www.youtube.com/watch?v=pJa6KVLwl9U

