Monica cells revealed the fight with rare muscle disease, myasthenia gravis

Tennis champion Monica sales are first speaking about their fight with a rare, incurable muscle-disease disease.

MyAsthenia Gravis (Mg) is a chronic neuromuscular disease that causes weakness in “voluntary muscles” according to the national neurological disorder and strokes.

Voluntary muscles are those that connect to bones, face, throat and diaphragm. They contract to move weapons and legs and are essential for breathing, swallowing and facial movements.

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“My MG Yatra has not been an easy in the last five years,” Slesce said in a press release that the immunology company announced his cooperation with the company Argonx.

“I felt isolated and defeated, because many of the activities I enjoyed were no longer possible for me.”

The purpose of the selection partnership with Argenx is to raise awareness and understanding about MG and add people affected by available equipment and resources.

What do you know about MySthenia Gravis

Jackson-Madison County General Hospital in Jackson, Tenasi, a board-certified neurologist Dr. According to Ernest Lee Murray, MySthenia Gravis is classified as an autoimmune disease.

This means that the body’s own defense system attacks the relationship between the veins and the muscles.

“I felt isolated and defeated, because many of the activities I enjoyed were no longer possible for me.”

Murray told Fox News Digital, “MySthenia Gravis is different from other neuromuscular diseases, which often signs of patients.”

Overall, symptoms are very light double vision and the decline of eyelids to difficulty in walking, breathing and swallowing.

The doctor said, “Some patients who start only with mild eye symptoms can progress more severe symptoms in the first few years of their diagnosis.”

However, some patients experience only eye issues.

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Summer, such as summer season or hot rainfall, according to experts, can make the symptoms worse. As physical exertion can also increase symptoms, Murray said that patients should speed up themselves.

Some health conditions-as the Kovid-19, can trigger a severe deteriorating of infection-laxations of the flu or urinary tract, called the “mysthanic crisis”, which is often hospitalized for close respiratory monitoring.

It is important to tell patients to their physicians that they have mysthenia gravis before starting a new drug, Murray said, as some drugs, including antibiotics, can spoil the symptoms.

“If there is any question, patients can always examine with their neurologists,” he advised.

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Doctors usually manage MG in two ways. First of all, they can prescribe a drug like pyridostigmin, according to the Mayo Clinic, which can temporarily reduce muscle weakness.

They can also prescribe drugs that calm the immune system to prevent nerves and muscles from attacking.

In the past, this immunity was done with steroids such as repression prednisone. Now, there are new drugs that target the disease directly. These targeted remedies can work well, according to Murray and cause less side effects.

While MG could be serious, the doctor insisted that this is not the end of the road.

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“Most patients live a normal life in both individual and professional,” he said. “With close management and a neurologist, familiar with MG, can suit treatment to adapt to the quality of patients.”

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Anyone who sometimes experiences dual vision, eyelid dropping or weakness that worsens with fatigue, should talk to your doctor about testing, dead.

Diagnosis usually involves blood tests, neurological tests and a neurological assessment.

Murray said that symptoms such as breathing, swallowing or holding the head require immediate emergency care.