Parents had a "giggled" baby for 17 hours a day who thought he was just happy – before he found that he had a rare brain tumor; cause kidney acceptance.
Gemma and Ed Young from Winscombe, Somerset, found that their son Jack was just happy when he started to make white sounds two weeks after he had been born.
But after being a "rehearsal program," doctors found that hypothalamic hamartoma, an indirect brain tumor that causes "geometric" incidental attacks – also known as a "smile catching".
Two years after excavation, which could be done. The first thing in the morning to the last thing at night was Jack's 10-hour job to take off the removal and stop the strange attacks.
His son's weight, Gemma, 32 said: "There was no breach from him, the sound sound was steady, and for a long time we had no reason why.
"We were tired and so happy when GPs could have been working on Jack at the end of two long years and finished their bad attacks."
Doctors usually explained that one in out of every 1,000 children with brain disease could be rare in captive and absorbing the rapid distress of power, usually in the form of a smile or tears.
After Jack's little birth on May 11, 2014, his son, Thatchers Cider's son, and Ed Ed's 42, project manager of the same company, realized that the boy had taken a long time, 39; think it was just a happy child.
Spinning her sleep, as well as when she was awakened, Gemma says she was a smile; – who would be involved in 30 minutes left but could not stop for 17 hours – he did not wake up.
"To be honest, we thought it was so happy all the time," said Gemma, who also has a son, now nine, from his friendship; has gone past, and she does not want to name.
"It's a bit a bit but it was likely that it was going on, as a record.
"To start with it, I was just a new mother trying to get into a new routine, but after two months it came to a great deal and we had to move Jack down the stairs to sleep in the end , because he also kept his brother, mourning. "
Then, at seven weeks' seven weeks, Jack's health visitor told Gemma that she never heard Jack's charcoal sounds before and she was worried.
"I was really feeling that another woman had noticed this in my baby, and as a mother I should understand," continued Gemma.
She then Jack saw the doctor, who was broken and gave the child to an eyebrower, a nose and a neck (ENT).
"At the moment, we did not have any sleep and I wanted doctors to do something," said Gemma.
"The sound was not accidental and amazing. It was hard to sleep, because I did not think when the sound was going to happen again."
But even the ENT team left to scratch their heads and then talks about the family to look at a neurologist at the Royal Bristol Hospital for Children.
Previously, six months were spent. The family was ruined and frightened about what was wrong with their little boy.
"There was even a nurse in the hospital who thought she was just laughing and disturbing her when she realized she was a laughter & the reason we were & Seeing doctors, "said Gemma.
"People would say to us," Is not he a happy young man? "And he was a little boy happy, but his smile did not smile, it was another thing.
"I did not think what Jack could have been wrong, but I was afraid he would not stop."
Finally, after receiving a MRI scan, his family received a decision in November 2014.
"The doctor said that he had a hypothalamic hamartoma, which meant that an immune brain was immersed in the size of a brain at the base of his brain, which causes the capture of vegetables.
"There was a great relief to find out what was wrong, so it was very difficult to think that he had gone through that. "
Gemma and Ed, who met in the six years ago, would need Jack to have a big job to take away the tumor, but after that the foolish retreats would have gone well.
The totals were added to a waiting list and medications were provided to help reduce the attacks.
But as long as the family was Waiting for his work, he did not move foolish laughter.
"All its development areas were as spectacular as his speech and understanding, but he was laughing all the time," said Gemma.
"He did not affect eating providers at six weeks or at a one-year-old walk – indeed, amazingly, he could walk and smile at the same time.
"It would usually go around a day, but the laughter is too."
Then, two years after he first heard, on June 16, 2016, Jack's successful attack was removing the referee at the Royal Bristol Hospital for Children.
"Seeing Jack to go for the worst day of my life," said his mother.
"I wanted to sign a permit form to complete the procedure and I did not know how I did that, my hand was so big shaking."
From work, Jack, who is four years old, has only one smile attack.
Although his parents admire, they can still be difficult when it rises naturally – because they often play at TV cartoons – they are so grateful that it can be a normal life him.
"The day after the work, we realized that Jack had not hit once, which was a strange feeling," said Gemma.
"We were sitting on waiting for it, but it did not.
"But when we heard it a smile for the first time it was amazing."
Now a little boy, happy, healthy, no one would know that Jack had never been wrong with anything.
Gemma said: "He is a little little boy now and is very successful.
"A little boy is so sad that he, with supremacy, comes out with single-lattices that make us laugh.
"Hypothalamic hamartoma is so rare and I want other parents to know that light is at the end of the tunnel and things are getting better.
"That work changed Jack's life, and ourselves, and we are so grateful."