: Covid-19 pose additional challenges for patients with Gaucher #IndiaNEWS #CORONAVIRUS New Delhi, Oct 28 | The Covid-19 pandemic has ushered in a new normal the world over and has thrown up challenges

Covid-19 pose additional challenges for patients with Gaucher #IndiaNEWS #CORONAVIRUS
New Delhi, Oct 28 | The Covid-19 pandemic has ushered in a new normal the world over and has thrown up challenges of varying magnitude. In the healthcare domain, India is grappling with various challenges especially when it comes to the field of rare diseases.
One of the reasons, these challenges appear insurmountable especially during a pandemic is due to the lack of guidelines in the absence of a rare disease policy. This is further compounded by low disease awareness amongst patients and lack of accessibility to specialists. This along with other critical factors make the rare disease patients even more vulnerable.
Every year, during World Gaucher Month, doctors treating rare diseases come together to reiterate their commitment to raise awareness about Gaucher disease in India. Gaucher disease (GD) is the most common disorder among Lysosomal storage disorders (LSD) worldwide and in India.
Under Lysosomal Storage Disorders India has been witnessing the prevalence of Hunter Syndrome, Gaucher Disease and Fabry Disease amongst other treatable rare diseases.
Enzyme replacement therapy is profoundly expensive which makes it unaffordable for many patients. In Rajasthan, for example, the awareness about rare diseases remains low with many medical centers not even having proper facilities for diagnosis and treatment. In Jaipur, only two hospitals namely J K Lone Hospital and SMS hospital have the ability and the facility to diagnose rare diseases.
According to Dr Ashok Gupta, Professor of Pediatrics and In-charge Rare Diseases, Superintendent J K Lon Hospital SMS Medical College, Jaipur said, Gaucher disease is quite prevalent in Rajasthan. Although, no statistical data is available till date. There is an urgent need for early diagnosis, and timely intervention so that patients can lead a near-normal life.
The only treatment available for Gaucher patients is enzyme replacement therapy. Therefore, we need urgent intervention by the government in the form of the reintroduction of the National Policy for Treatment of Rare Diseases. As we are learning to adapt to the new normal, we are now being able to send test samples more frequently and more easily but still the patients fear coming to the hospital for their treatment. I would like to advice Gaucher patients to continue with their enzyme replacement treatment and take proper nutrition, failing which their condition can further deteriorate making them more prone to complications.
In 2017, the National Policy for Treatment of Rare Diseases (NPTRD) was announced by the Government with a corpus of Rs 100 crore, to provide financial assistance for the treatment of rare disease patients. In November 2018, was put on hold.

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