It first appeared as blisters all over Joel’s body. Tammy Greaves, Joel’s mother, was familiar with the symptoms. After all, she has seen it once before, when Joel had chicken pox months back.
Photo credit: Caters News Agency
When she took her son to the doctors, her hunch was validated when the doctors diagnose little Joel with the chicken pox. When his condition got worse, however, the doctors realized their mistake.
It wasn’t chicken pox; it was Steven Johns Syndrome.
READ: A severe allergic reaction caused his skin to separate from his body
Stevens-Johnson Syndrome is a rare but life-threatening allergic reaction caused by certain medication or an infection.
It was believed that Joel’s reaction had stemmed from the medication he took four croup—an inflammation of the larynx, said reports from the Daily Mail.
Photo credit: Caters News Agency
The doctors put Joel in the intensive care for five days. SJS kills one-in-five people who have it, and so the doctors told Tammy to prepare for the worst.
“[The doctors] had no idea if he was going to survive,” Tammy recalled the heartbreaking moment. “But we just had to hope and pray he’d pull through.”
After his transfer to a specialist burn unit, Joel was wrapped in bandages to help prevent infections and help his skin recover.
READ: Ibuprofen turned this baby’s skin back in an allergic reaction that nearly killed him
“Joel was unrecognizable as his body was so swollen and he had to undergo an eight-hour operation to remove all the dead skin.”
Thankfully Joel is among the lucky few who are able to pull through the syndrome and survive. After a grueling eight-hour operation, Joel, all bandaged up, was allowed to return home with his parents Tammy and Richard.
Photo credit: Caters News Agency
The Greaves said they they had never heard of Steven Johns before, and now that it’s happened to them, they want to raise awareness to the disease.
“Joel was one of the lucky ones but if this condition isn’t diagnosed and treated quickly enough it can be fatal,” Tammy said.
What is SJS
According to Mayo Clinic, Stevens-Johnson Sydrome (SJS) is a rare disorder that starts with with flu-like symptoms. But soon they are followed by a painful red or purplish rash that spreads and blisters.
A form of Toxic Epidermal Necrolysis, SJS is a a reaction to a drug or an infection that can be lethal. Treatment focuses on addressing the underlying cause, controlling symptoms and minimizing complications.
Recovery time can take anywhere from weeks to months, depending on how severe the syndrome is.
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