“Yawning 100 times a day?”…I said I was tired, but what happened to ‘this incurable disease’?

The story of a woman who learned that her habit of yawning about 100 times a day was a symptom of a fatal disease was revealed. (Photo = Capture from British media Mirror report)

The story of a woman who learned that her habit of yawning about 100 times a day was a symptom of a fatal disease was revealed.

Recently, according to the British media Mirror, Nikki Davis yawned often but did not think it was a big deal. They thought it was due to simple fatigue or the aftereffects of COVID-19. Before being diagnosed with Motor Neurone Disease (MND) in July of last year, Nikki lived with a yawn. I yawned close to 100 times a day.

In addition, Nikki visited the hospital when symptoms of slurred speech and headaches appeared. Nikki explained, “I thought I yawned about 100 times a day as a result of the COVID-19 infection,” and “But the symptoms continued, and I stuttered and had a headache.”

Nikki fell into despair after being confirmed at the hospital that she had motor neuron disease. This disease has no cure and can shorten life expectancy. Although he spent two weeks crying after his diagnosis, he began receiving treatment with hormone replacement therapy.

Even now, Nikki is having trouble with her daily life, feeling tired easily and having difficulty eating. Nevertheless, it is said that he is trying not to lose his positive mind. “It’s hard to eat because my tongue doesn’t work properly, and I get tired easily, so it’s hard to do the activities I like,” he said. “But I try to look at life positively.” He added, “If you think something is wrong with your body, please seek neurologist treatment.”

A disease in which brain nerve cells, known as motor neurons, gradually stop functioning… Swallowing food and breathing become difficult.

Motor neuron disease, which Nikki was diagnosed with, is a disease in which brain nerve cells called ‘motor neurons’ gradually stop functioning. As muscles gradually weaken, breathing becomes difficult and physical movements become uncomfortable. You may fall easily or have difficulty climbing stairs.

Like Nikki, you may find it difficult to swallow food. As the disease progresses, you may frequently sneeze or cough when eating. As the patient progresses, his or her limbs become thinner, making it difficult to fasten buttons or lift objects.

The cause is not clearly known, but it is presumed that genetics, immune system problems, infection, and nerve microfiber dysfunction play a combined role in its development. It is known that the incidence is mainly higher in people over the age of 40 and that men are more likely to suffer from it than women.

There is no cure…even if the only approved drug is used, the likelihood of death is high in the end.

Unfortunately, there is no cure, so treatment is done in ways that prevent the progression of symptoms, such as physical therapy or speech therapy. You can also try the drug riluzole, which is the only drug approved to treat this disease. However, the patient eventually has difficulty moving, swallowing, and breathing, so oxygen must be artificially injected, and there is a high possibility of death. There are reports that 20% of all patients survive up to 5 years after diagnosis.

For motor neuron disease, conservative treatment to prevent complications and improve quality of life is of utmost importance. Like the woman in the story, efforts to avoid stress and regular respiratory function tests are needed.

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Source: kormedi.com