Credits: Wikimedia Commons, Sky News
A woman was airlifted to a London hospital after suffering a sudden relapse of atypical Haemolytic Uremic Syndrome (aHUS), one of the rarest diseases in the world. She is a British Journalist named Deborah Haynes. The rapid coordination between local volunteers, doctors, and the NHS ensured her survival, highlighting both the dangers of the condition and the critical importance of swift diagnosis.
Atypical Haemolytic Uremic Syndrome is an ultra-rare disorder that affects only about one in two million people each year. The condition occurs when part of the body’s immune system—known as the complement system—becomes overactive and begins attacking healthy cells instead of infections.
This immune malfunction leads to the destruction of red blood cells, damage to blood vessels, and the formation of tiny clots. These clots can block blood flow to the kidneys, causing acute renal failure, and may also affect other organs, increasing the risk of heart attack or stroke.
Without treatment, the prognosis can be severe. According to experts, between 10–15% of patients die during the initial episode, while up to 70% may develop end-stage kidney failure requiring lifelong dialysis.
The latest relapse occurred while the Haynes was holidaying on Sark, a car-free Channel Island with limited medical infrastructure. Initially dismissed as seasickness or food poisoning, symptoms quickly worsened. Persistent vomiting, fatigue, and shivering raised the suspicion of a relapse of aHUS.
Sark’s only general practitioner, Dr Bruce Jenkins, conducted a urine test that showed dangerously high protein levels, a clear sign of kidney distress, as reported in Sky News. With blood tests unavailable on the island, he initiated an urgent evacuation.
The patient was transported on an ambulance cart pulled by a tractor—a reminder of the island’s unusual transport system, before being taken by the “Flying Christine” marine ambulance to Guernsey. From there, a specialist medical plane flew her to Luton airport, followed by an ambulance transfer to University College Hospital (UCH) in London.
Remarkably, the entire journey from Sark to intensive care took just 11 hours.
Specialist teams at UCH, led by experts in rare blood disorders, were already on alert. Immediate treatment included eculizumab, a breakthrough drug that blocks the overactive part of the immune system. The patient also required blood transfusions and dialysis support.
Eculizumab, though extremely expensive, has transformed outcomes for people with aHUS since its introduction in 2013. By effectively shutting down the malfunctioning immune response, the drug prevents further damage and significantly reduces the risk of kidney failure.
Doctors note that aHUS may be triggered by infections, pregnancy, or even food poisoning, though in some cases the cause remains unknown. The condition is often linked to genetic mutations, which can remain dormant for decades before suddenly activating.
The symptoms often appear similar to common illnesses—such as nausea, fatigue, or stomach upset—which makes quick recognition vital. Any delay in diagnosis or treatment can prove fatal.
Following nearly two weeks of hospitalization, including time in intensive care, Haynes was discharged and is expected to make a full recovery. Her case underscores the life-saving role of coordinated medical networks, advanced treatment options, and the dedication of both professionals and volunteers.
While rare, the condition serves as a reminder of how quickly a health emergency can unfold—and how crucial early diagnosis and specialist care are in combating ultra-rare diseases like aHUS.
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While you may have heard of the gut-brain connection, did you know it could also signal neurodevelopmental disorders? A study has found children with autism are far more likely to have ongoing stomach and digestive issues than other children.
A new study from the UC Davis MIND Institute found a strong link between these gastrointestinal (GI) problems and other daily challenges, including difficulties with sleep, communication, and behavior.
The study followed 475 children between the ages of 2 and 12, with 322 of them having autism. The researchers talked to the families multiple times over the years to track the kids' health. They found that children with autism were not only more likely to report stomach problems like constipation and diarrhea, but they also tended to have several of these symptoms at once.
Even more importantly, these issues often lasted for years, unlike in other children where they usually went away quickly. What's surprising is that many of these problems didn't have an obvious medical cause. This suggests that doctors and parents need to pay closer attention to these symptoms, even when the reason isn't clear.
Your brain and your gut are constantly communicating, a connection you've probably felt before. This is why you get "butterflies in your stomach" when you're nervous or why a bad feeling about something is called a "gut feeling." This link is a two-way street: your brain can affect your gut, and your gut can influence your brain.
In fact, the gut and the brain are like best friends. They talk about everything, from how you're feeling emotionally to how your body is working physically. More information travels between these two than any other body part. Your gut even has a huge number of nerve cells, second only to your brain. The conversation between your gut and brain influences many of your body's functions, including:
The researchers looked at nine common stomach and digestive symptoms and found that they were strongly connected to other difficulties. Children with more frequent gut problems also had more trouble with sleep, were more anxious and irritable, and struggled more with communication, sensory issues, and repetitive behaviors.
This study reinforces the idea that the brain and the body are deeply connected. When a child feels stomach pain, it's not just a physical problem. It can also influence their mood, how they sleep, and how they interact with the world around them. The researchers stress that treating a child’s gut health is an important step toward improving their overall quality of life.
The researchers pointed out that many of these gut issues are treatable, even if there isn’t a clear medical diagnosis. They hope that doctors, teachers, and families will become more aware of this connection and work together to get children the care they need. They believe that addressing gut health as part of a complete care plan for autism can help children feel better and grow. One of the authors, Christine Wu Nordahl, explained that it's not about finding just one cause for a child's challenges, but about looking at the whole child and helping them in every way possible.
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A simple, 15-minute annual check-up could be one of the most effective ways to protect yourself from dementia. Research now shows that untreated hearing loss is the single biggest risk factor for dementia that you can actually change, even more so than smoking or not exercising. According to Alzheimer’s Research UK, if everyone took care of their hearing, we could prevent seven out of every 100 cases of dementia that occur today.
However, this is not a one-off observation, but other studies have also shown that hearing loss is linked with dementia. A study published in the Lancer showed that treating hearing loss is one of the best ways to decrease risk of dementia.
Interestingly, several studies have shown a significant link between hearing loss and dementia. A recent meta-analysis, which combined data from over 666,000 people, found that individuals with hearing loss had a 37% higher risk of dementia compared to those with normal hearing.
The risk of dementia also increases with the severity of hearing loss. For every 10-decibel drop in hearing ability, the risk of dementia can increase by as much as 24%. This means that even a small decline in your hearing can raise your risk.
In the UK, a staggering one in three people have some level of hearing loss, but many wait a full decade before they seek help. At the same time, nearly one million people are living with dementia, a condition that is the leading cause of death in the country. The Lancet Commission on Dementia found that hearing loss in midlife is the number one modifiable risk factor.
Research suggests that using hearing aids can help reduce the risk of dementia. A review of multiple studies found that people with hearing loss who used hearing aids had a 19% lower risk of mental decline and a 17% lower risk of dementia compared to those who did not.
Another study showed an even more powerful effect, with people at a higher risk of mental decline having a 48% lower chance of their condition worsening into dementia if they wore hearing aids.
These findings suggest that treating hearing loss with hearing aids not only improves a person's quality of life but also plays a key role in preventing or delaying dementia.
The reason for this connection is simple: your brain works much harder when it has to strain to understand conversations, especially in loud places. This extra effort can be exhausting and cause people to pull away from social situations, leading to loneliness and poor well-being. By making it easier to hear, hearing aids help your brain relax and allow you to stay engaged with the world, which is crucial for brain health.
Interestingly, this positive effect wasn't as clear in a group of healthy volunteers who were at a lower risk for dementia. This might be because their mental decline was already slow, so the study's three-year period wasn't long enough to show a major difference.
Scientists think that hearing aids help people at high risk for dementia by doing more than just improving hearing. They might also boost a person's social connections, reduce feelings of sadness, provide more mental stimulation, and make it easier to talk to doctors about medical care. However, more research is needed to fully understand the long term effects.
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A simple eye exam completely changed the life of 29-year-old Rhiannon. A career-loving Occupational Therapist who enjoys traveling, Rhiannon had no idea she was seriously ill. The Brain Tumor Charity shared her story to raise awareness on Eye Health Day.
While she had noticed small issues like a ringing in her ears and feeling tired, she didn't have the typical, more serious symptoms of a brain tumor, such as seizures or severe headaches.
During her eye check-up, Rhiannon's eye doctor noticed an unusual sign: a buildup of pressure around her optic nerve, a condition called papilledema. The doctor suspected this could be caused by a brain tumor and immediately sent her for more tests.
An MRI scan confirmed a mass in her brain. At first, doctors thought it was a less serious tumor, but a biopsy revealed the heartbreaking truth. Rhiannon was diagnosed with glioblastoma multiforme (GBM), also known as a grade 4 astrocytoma. This is an extremely fast-growing and aggressive form of brain cancer that is not curable. To make matters worse, the tumor's location made it impossible to remove with surgery.
According to the American Association of Neurological Surgeons, Glioblastoma (GBM) is a type of brain tumor that grows quickly and aggressively. It invades nearby brain tissue but usually doesn't spread to other parts of the body.
GBMs can either start on their own or develop from a less serious type of brain tumor. In adults, they most often appear in the main parts of the brain, particularly in the front and sides.
This is a very dangerous cancer that, if left untreated, can be fatal in six months or less. It's crucial to get care from experts like a neuro-oncologist and neurosurgeon right away, as immediate treatment can greatly improve a person's chances of survival. The symptoms of a brain tumor can differ depending on where it is located in the brain. Some common signs to watch for include:
Rhiannon is still coping with the shock of her diagnosis. The hardest part for her has been losing her independence. She can no longer work or drive, things she once took for granted. Now, she relies on others for support, which has shown her how truly generous and amazing her loved ones are.
Despite these challenges, Rhiannon is facing her illness with courage. She is taking each day as it comes, finding strength in the moments that matter. She refuses to give in to sadness and holds onto hope that new research will one day lead to a cure.
Rhiannon is sharing her story to highlight how important eye exams can be in finding a brain tumor. She urges everyone not to skip their regular eye appointments, even if they don't have any noticeable problems.
She specifically recommends an OCT (Optical Coherence Tomography) scan, which gives a detailed look at the retina. This test can detect various eye conditions early, some of which may not show symptoms until they are more advanced. In Rhiannon's case, this simple test led to her life-saving diagnosis.
Lorcan Butler, an eye specialist, agrees, emphasizing that many health conditions, including brain tumors, can be spotted during a routine eye exam. If you have any concerns about your vision, he advises you to see an eye doctor right away.
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