My 3 little boys complained of headaches – then a devastating brain disease left their skulls crushing their spines --[Reported by Umva mag]

A MUM has shared her shock after her three little boys were diagnosed with the same rare brain condition. Whitney Niece took sons Lincoln, 10, Norrin, six, and Remley, three, to the doctor after they started suffering from bizarre symptoms one-by-one. Lincoln, Norrin, and Remley were diagnosed with a rare brain condition one after the otherJam Press/Whitney Niece Jam Press/Whitney NieceAll three were struck with bizarre symptoms like headaches and balance issues – picture with mum Whitney Niece[/caption] Jam Press/Whitney NieceRemley was the first to be diagnosed with Chiari malformation type 1[/caption] Remley during a shunt tapping procedure to relieve pressureJam Press/Whitney Niece They were struck with headaches and vomiting, as well as a loss of balance and coordination. At first, doctors dismissed their symptoms as being caused by a virus. But the three youngsters were found to have Chiari malformation type 1 – a condition which occurs when the lower part of the brain pushes down into the spinal canal, triggering worrying symptoms. “Our lives felt like a whirlwind – it seemed like one challenge after another hit our family,” their 38-year-old mum, a marketing coordinator from Indiana, US, said. “I felt defeated before we had answers. “It was always chalked up to being a viral issue, yet no one else was sick. “So finding the cause for their problems was a strange feeling. “I felt relief but then also nervousness because I had no idea [of] anything about the condition. “Remley’s diagnosis was unexpected, as all prenatal tests failed to detect it. “Then, Lincoln’s diagnosis was another shock, leaving me to wonder about the odds of having two children with the same condition. “I suspected Norrin might have it too based on his symptoms, but that didn’t lessen the impact of discovering that all three of our boys shared the same diagnosis.” The boys’ symptoms had presented slightly differently and at different ages. Whitney said: “Lincoln and Norrin’s were mainly headaches and vomiting, while Remley had the loss of coordination – he would walk and just fall, typically face first since he was so little.” Little Remley was first diagnosed in June 2022 after he stopped urinating, and an MRI found the malformation incidentally. Lincoln was again diagnosed by chance, after a doctor spotted his pupils were not the same size and called for tests in February 2023. Finally, Norrin was diagnosed in December 2023 after battling headaches for three months. Jam Press/Whitney NieceLincoln right before Chiari decompression surgery – he was the second to be diagnosed[/caption] Norrin post decompression surgery – he was diagnosed lastJam Press/Whitney Niece Jam Press/Mackenzie Miller PhotoThe boys have been in and out of hospital for surgeries[/caption] Whitney, Ron, and their kids Lincoln, Norrin, and RemleyJam Press/Mackenzie Miller Photo The malformations are generally caused by genetic mutations that take shape while babies develop in the womb. While not life-threatening, the diagnoses still came as a shock to the parents – and have led to a string of hospital stays, including decompression surgeries to help ease the symptoms. The procedure involves removing a small piece of bone from the base of the skull or top of the spine to reduce the pressure on the brain and allow the fluid in and around the brain and spinal cord to flow normally. Whitney said: “In March 2023, Lincoln underwent a decompression surgery and fortunately was out of the hospital within three days. “Around the same time, Remley began to show more symptoms, prompting his neurosurgeon to request further imaging to determine if he also needed surgery. “He was decompressed that August but developed a cerebrospinal fluid leak just 10 days later. “He required emergency surgery to insert an external ventricular drain, which he had for 10 days until a ventriculoperitoneal shunt was placed at the end of the month.” This is a thin plastic tube that helps drain extra cerebrospinal fluid from the brain. The mum went on: “Meanwhile, Norrin began complaining of frequent headaches, and we started the testing process for him. “In January, he was also decompressed, facing the same CSF fluid leak, EVD drain, and shunt that Remley had experienced months earlier.” What is a Chiari malformation? A Chiari malformation is where the lower part of the brain pushes down into the spinal canal. There are four main types, but type 1, called Chiari I, is the most common. In someone with Chiari I, the lowest part of the back of the brain extends into the spinal canal. This can put pressure on the brainstem and spinal cord, and obstruct the flow of fluid. The severity of Chiari malformations can vary f

Oct 17, 2024 - 13:50
My 3 little boys complained of headaches – then a devastating brain disease left their skulls crushing their spines --[Reported by Umva mag]

A MUM has shared her shock after her three little boys were diagnosed with the same rare brain condition.

Whitney Niece took sons Lincoln, 10, Norrin, six, and Remley, three, to the doctor after they started suffering from bizarre symptoms one-by-one.

three young boys laying in a hospital bed with one wearing a spiderman shirt
Lincoln, Norrin, and Remley were diagnosed with a rare brain condition one after the other
Jam Press/Whitney Niece
a woman is holding three children and one of them is wearing a shirt with smiley faces on it
Jam Press/Whitney Niece
All three were struck with bizarre symptoms like headaches and balance issues – picture with mum Whitney Niece[/caption]
a child is smiling in a hospital bed with a blanket that says sesame street on it
Jam Press/Whitney Niece
Remley was the first to be diagnosed with Chiari malformation type 1[/caption]
a baby is being examined by nurses in a hospital room
Remley during a shunt tapping procedure to relieve pressure
Jam Press/Whitney Niece

They were struck with headaches and vomiting, as well as a loss of balance and coordination.

At first, doctors dismissed their symptoms as being caused by a virus.

But the three youngsters were found to have Chiari malformation type 1 – a condition which occurs when the lower part of the brain pushes down into the spinal canal, triggering worrying symptoms.

“Our lives felt like a whirlwind – it seemed like one challenge after another hit our family,” their 38-year-old mum, a marketing coordinator from Indiana, US, said.

“I felt defeated before we had answers.

“It was always chalked up to being a viral issue, yet no one else was sick.

“So finding the cause for their problems was a strange feeling.

“I felt relief but then also nervousness because I had no idea [of] anything about the condition.

“Remley’s diagnosis was unexpected, as all prenatal tests failed to detect it.

“Then, Lincoln’s diagnosis was another shock, leaving me to wonder about the odds of having two children with the same condition.

“I suspected Norrin might have it too based on his symptoms, but that didn’t lessen the impact of discovering that all three of our boys shared the same diagnosis.”

The boys’ symptoms had presented slightly differently and at different ages.

Whitney said: “Lincoln and Norrin’s were mainly headaches and vomiting, while Remley had the loss of coordination – he would walk and just fall, typically face first since he was so little.”

Little Remley was first diagnosed in June 2022 after he stopped urinating, and an MRI found the malformation incidentally.

Lincoln was again diagnosed by chance, after a doctor spotted his pupils were not the same size and called for tests in February 2023.

Finally, Norrin was diagnosed in December 2023 after battling headaches for three months.

a young boy in a hospital gown holds a stuffed animal
Jam Press/Whitney Niece
Lincoln right before Chiari decompression surgery – he was the second to be diagnosed[/caption]
a young boy is laying in a hospital bed with a tablet and a stuffed animal
Norrin post decompression surgery – he was diagnosed last
Jam Press/Whitney Niece
three young boys are sitting in the grass and smiling for the camera
Jam Press/Mackenzie Miller Photo
The boys have been in and out of hospital for surgeries[/caption]
a family poses for a picture in a field with a dog
Whitney, Ron, and their kids Lincoln, Norrin, and Remley
Jam Press/Mackenzie Miller Photo

The malformations are generally caused by genetic mutations that take shape while babies develop in the womb.

While not life-threatening, the diagnoses still came as a shock to the parents – and have led to a string of hospital stays, including decompression surgeries to help ease the symptoms.

The procedure involves removing a small piece of bone from the base of the skull or top of the spine to reduce the pressure on the brain and allow the fluid in and around the brain and spinal cord to flow normally.

Whitney said: “In March 2023, Lincoln underwent a decompression surgery and fortunately was out of the hospital within three days.

“Around the same time, Remley began to show more symptoms, prompting his neurosurgeon to request further imaging to determine if he also needed surgery.

“He was decompressed that August but developed a cerebrospinal fluid leak just 10 days later.

“He required emergency surgery to insert an external ventricular drain, which he had for 10 days until a ventriculoperitoneal shunt was placed at the end of the month.”

This is a thin plastic tube that helps drain extra cerebrospinal fluid from the brain.

The mum went on: “Meanwhile, Norrin began complaining of frequent headaches, and we started the testing process for him.

“In January, he was also decompressed, facing the same CSF fluid leak, EVD drain, and shunt that Remley had experienced months earlier.”

What is a Chiari malformation?

A Chiari malformation is where the lower part of the brain pushes down into the spinal canal.

There are four main types, but type 1, called Chiari I, is the most common.

In someone with Chiari I, the lowest part of the back of the brain extends into the spinal canal.

This can put pressure on the brainstem and spinal cord, and obstruct the flow of fluid.

The severity of Chiari malformations can vary from person to person, but generally:

  • Chiari I malformations are not considered life-threatening
  • Some people experience painful headaches, movement problems and other unpleasant symptoms but many people will not have any symptoms
  • There’s a chance of developing syringomyelia (where a fluid-filled cavity called a syrinx develops in the spinal cord), which can damage the spinal cord if not treated promptly
  • Surgery can usually stop the symptoms getting worse and can sometimes improve them, although some problems may remain

Many people with a Chiari I malformation will not have any symptoms.

Sometimes they’re only found after an MRI scan of the brain is carried out for another reason.

If symptoms do develop, they can include:

  • Headaches – these are usually felt at the back of the head and may be brought on or made worse by coughing, straining, sneezing or bending over
  • Neck pain
  • Dizziness and balance problems
  • Muscle weakness
  • Numbness or tingling in the arms or legs
  • Blurred vision, double vision and sensitivity to light
  • Swallowing problems
  • Hearing loss and tinnitus
  • Feeling and being sick
  • Insomnia and clinical depression

Treatment will depend on how severe the symptoms are.

Painkillers can help relieve any headaches and neck pain.

But if your headaches are severe or you have problems caused by the pressure on your spinal cord – such as movement difficulties – surgery may be recommended.

Source: NHS

Whitney says the health issue has been difficult for her and husband Ron, 41, to navigate – but that things have started to calm down.

She said: “Financially, we felt overwhelmed, trying to juggle caring for our kids, managing jobs, and caring for the other two who were not in the hospital.

“Thankfully, life has settled down significantly since then.

“While we still deal with headaches weekly, they are now manageable with medication at home.

“Lincoln was cleared by his neurosurgeon and is no longer under neurosurgical care.

“Norrin and Remley will have annual check-ups for their VP shunts, but their futures look bright – and hopefully healthy!”




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