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Need To Know > Fitness and health > ‘My three little boys complained of headaches – then they were diagnosed with same rare brain condition’
A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Fitness and health

‘My three little boys complained of headaches – then they were diagnosed with same rare brain condition’

Ria Newman
Last updated: October 17, 2024 9:50 am
Ria Newman Published October 17, 2024
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Remley, Lincoln and Norrin visiting Remley in the hospital. (Jam Press/Whitney Niece)
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A woman has shared her shock after her three young sons were diagnosed with the same rare brain abnormality.

Whitney Niece took sons Lincoln, 10, Norrin, six, and three-year-old son Remley to the doctor after they one-by-one started suffering from headaches, vomiting, and a loss of balance and coordination.

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.

READ MORE: ‘Miracle’ mum takes newborn home after op to remove rare tumour from middle of skull

“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, told Need To Know.

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Lincoln, Norrin, Remley, and their mom, Whitney. (Jam Press/Whitney Niece)

“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.

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Remley on his EVD. (Jam Press/Whitney Niece)

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

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Lincoln before he was going home. (Jam Press/Whitney Niece)

“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.”

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Norrin post EVD placement. (Jam Press/Whitney Niece)

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

Whitney explained: “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 back in June 2022 after he stopped urinating, and an MRI found the malformation incidentally.

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Whitney and Remley. (Jam Press/Whitney Niece)

Lincoln was again incidentally diagnosed, after a doctor spotted his pupils were not the same size, calling for tests in February 2023.

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

The malformations are generally caused by genetic mutations that take shape during foetal development.

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.

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

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Lincoln days after his surgery. (Jam Press/Whitney Niece)

“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.

“Meanwhile, Norrin began complaining of frequent headaches, and we started the testing process for him.

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Norrin right after his EVD was placed. (Jam Press/Whitney Niece)

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

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.

A mother shares her shock after all three of her young sons were diagnosed with the rare brain condition, Chiari malformation type 1, leading to multiple surgeries and recovery.
Lincoln, Norrin, Remley, and their mom, Whitney. (Jam Press/Whitney Niece)

“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!”

READ MORE: Boy, 10, who might not make 20th birthday due to rare disease just ‘wants to be a normal kid’

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TAGGED:BrainchildrenConditiondiagnosedHealthRare conditionshockingsurgery
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