Schwartz, is a woman who suffers from a such a rare disease So far, experts have not been able to identify it. But now he is one of the first patients to be treated at the first unnamed syndrome clinic, located in Great Britain.

However, the woman spent most of her teenage years traveling with her parents in hopes of finding them cure their ailments. However, he said tests showed nothing.

“Your parents heard that, they don’t think the doctor was wrong, because they did all those tests. So the diagnosis must be you making it up,” he said.

A hope for Schwartz

Over the years, Schwartz has presented several health complications, for that he decided again to find a solution to his problem. He finally received a partial diagnosis of mitochondrial disease in 2005, a group of conditions caused by defects in important parts of the body’s cells.

Also He was diagnosed with three other “very rare disorders”: neurological diseases, other diseases affecting the immunology and movement disorders, dystonia. As well as losing her hearing and sight, she has balance problems and can’t feel her hands or anything under her knees.

Nonetheless, he is confident that this will change with the help of the experts working on it the first national syndrome clinic without a name from the United Kingdom, is located in Cardiff, the capital of Wales, about 240 kilometers east of London, and is where he was born.

Experts predict that there may be more than 8 thousand rare diseases and that children are the most disadvantaged, because 50% of it disease it rarely affects children, and nearly a third of them will die before the age of 5 years.