Elliot Preddie was born with sickle cell disease, an inherited blood disease which leads to blockages that prevent blood from reaching parts of the body.
INDIANAPOLIS — Elliot Preddie isn’t your average 12-year-old boy.
“He just couldn’t enjoy life as a kid,” said his mom, Tremesha.
Elliot was born with sickle cell disease, an inherited blood disease which leads to blockages that prevent blood from reaching parts of the body.
We first met Elliot last year at Riley Hospital for Children at IU Health.
“Because of sickle cell, Elliot was always a kid who struggled with energy level and stamina and he got dehydrated very easily,” said his mom.
He was getting a stem cell transplant from a matching donor.
“When I was younger, I played sports a lot, but then I got too cold from my sickle cell. That’s why I started quitting all my sports. My baseball and soccer,” said Elliot as he sat on his back porch next to his family.
One year later, Elliot is now free of sickle cell disease.
“I’m really thankful that things are getting back to some sense of normalcy for all of us,” said Elliot’s father, Terry.
Elliot’s doctor said he will continue to be monitored.
“Now it’s at a point where he’s really just coming in for monthly checks with our stem cell transplant team,” said Dr. Seethal Jacob, sickle cell program director at Riley Hospital for Children at IU Health.
Jacob said the challenge was finding matching bone marrow and matching blood donors.
“Elliott was on chronic blood transfusions every month before he went to transplant and he really needed blood that matched him well enough so that he would not react to it,” said Jacob.
About 3,000 Americans die each year because they can’t find a matching donor. African-Americans have about a 25 percent chance of finding an unrelated donor, compared to about 75 percent of whites.
Elliot’s 4-year-old brother Carter was also born with sickle cell disease.
“The way it shows up in Carter is massively different from the way that it used to show up in Elliot. He largely maintains. He’s done well with his one or two maintenance medications that he takes. He does have severe pain episodes, but they are not so common that we’re at a place where it makes more sense for us to risk stem cell for him,” Tremesha said.
Carter continues to go to Riley for checkups.
His mother said she’ll continue to push for more funding and education about the disease, especially what’s called the “sickle cell trait’ – something she didn’t know she had until she was five months pregnant with Elliot.
Both parents must have the sickle cell trait in order to pass the disease on to their children. Terry and Tremesha said sickle cell trait is often misunderstood or mistreated.
“I could not get a lot of doctors to believe me that I was having pain, even though I had very visible evidence of a pain crisis on several occasions. The assumption is, ‘Oh you have (sickle cell) trait, so there’s no complications,’ but that’s not necessarily true,” Terry said.
The Preddies said some people don’t know they have it.
“I’m hoping that as research keeps progressing, people look into trait,” Terry said.
As for Elliot, he said he can’t wait to get back to playing the sports he once loved.
“His future is really bright in ways that it wasn’t potentially before,” said Tremesha.
“I’m hoping I can play one of them again,” said Elliot.
For more information on sickle cell disease, log onto www.sicklecelldisease.org.
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