Rare diseases are defined as diseases that affect a small percentage of the population. Because of the rarity of each disease itself, much remains unknown about many rare diseases. Lack of awareness coupled with the health authorities’ attitude towards rare diseases lead to many undiagnosed cases or the diagnoses come after the disease has done fatal damages.
The Organization for Rare Diseases India (ORDI) was founded in 2014. The non-profit organization, which serves an umbrella organization for rare disease patients and other stakeholders in the country, aims to improve the health of patients with rare diseases in India through awareness and advocacy.
Rare Disease Day: Living With a Rare Disease
February 28 is designated as Rare Disease Day to intensify research for treatment of rare diseases.
February 28 is designated as Rare Disease Day to intensify research for treatment of rare diseases.
According to him, a lack of awareness about rare diseases among patients, doctors and policy makers and the absence of public policy on rare disease are the major problems in India. There is also a need to create a national database on rare diseases. "A lot of work has to be done in this field," he said. Excerpts from the interview:
1. Can you share statistics of rare diseases in India?
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The incidence of these rare diseases is very rare among the general population. Some of them are genetic in origin, while the etiology of the others remains unknown
The incidence of these rare diseases is very rare among the general population. Some of them are genetic in origin, while the etiology of the others remains unknown
All rare diseases taken together affect about 6–8% of the world's population. About half of the rare diseases affect children causing significant social and economic burden while the other half manifest in adulthood.
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Since there are very few cases of rare diseases reported in India, health ministries do not make an effort to know about them, says APJ Abdul Kalam, former President of India.
Since there are very few cases of rare diseases reported in India, health ministries do not make an effort to know about them, says APJ Abdul Kalam, former President of India.
2. What are the biggest challenges facing patients with rare diseases in India?
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Lack of awareness
There is a significant lack of awareness about rare diseases among the public, and even among doctors in India. The health care training and education system in our country are more focused on training physicians and health care personnel to treat common diseases such as infectious diseases. This has led to a pronounced dearth of trained physicians and healthcare personnel to care for patients with rare diseases.
Lack of infrastructure
Inadequate training and facilities to diagnose rare diseases in a timely manner is another disadvantage. If it takes an average of 7 years to diagnose a rare disease in developed nations like the USA, the average time to diagnose is likely to be greater in developing countries. The average time taken to diagnose a rare disease in India is unclear and indefinite. There is a lack of adequate statistics and data on incidence as well as prevalence of rare diseases in India. The availability of such basic information is essential for use by policy makers, physicians, scientists, drug or device manufacturers, patients and the community at large.
Prohibitive costs
A majority of patients with rare diseases in India cannot afford the high costs of treatments even when available. Most orphan drugs are not curative but palliative and need to be administered regularly. These drugs are highly expensive and inaccessible to the majority of the Indian population affected by rare diseases.
Cultural influences
The incidence of rare diseases is believed to be higher in India compared to western countries due to the practice of consanguineous marriages in many communities. Social stigma for physically challenged individuals and patients with rare diseases continue to be a societal challenge that can only be addressed with education and awareness.
Government initiatives
There is no specific push for research and development in the field of rare diseases in India, although the programs by funding agencies like the ICMR, Department of Science and Technology (DST), Council of Scientific and Industrial Research (CSIR) as well as the Department of Biotechnology (DBT) are noteworthy.
The Government should encourage and fund Indian academic research laboratories as well as pharmaceutical and biotechnology industries to take up scientific research work leading to the development of diagnostics and drugs for rare diseases.
ORDI would persuade and assist the government:
(i) To enact an act similar to the Orphan Drugs Act (ODA) of USA, and
(ii) To create a fund to support work related to rare disease research, education and treatment by institutions that are prepared to take up this work.
The Government has already started funding such work in a small way, but we believe that a lot more needs to be done. A national plan for rare disease research needs to be developed.
Funding
The lack of significant public funding for rare disease research is another critical impediment in creating the much-needed momentum for education, diagnosis and treatment of rare diseases in India
3. Can you tell us about rare diseases identified in India that need more attention from policymakers and doctors?
In the absence of a patents registry or database, it is very difficult to list top diseases and any number presently available may not be justified. ORDI believes that ‘No Human Life Should Be Judged by a Statistic'.
4. Do we have a national government policy to tackle rare diseases? If no, what should policy makers do to develop a national policy?
We do not have a Government Policy for Rare Diseases. The Government needs to have a Task Force and involve all the stakeholders to discuss and debate the need for Rare Disease policy. ORDI being an umbrella organization and has already brought various stakeholder together and can be engaged along with other disease-specific support groups.
ORDI is already in the process of developing a Rare Disease Patient Registry. The registry can enable government policy making through various statistics for prioritizing focus and budget allocation.
5. Tell us about major initiatives of ORDI to help patients with rare diseases.
In last two years, we have undertaken various initiatives to address some of these challenges.
- 24*7 Rare Disease Helpline - This is India's 1st ever helpline which will address the need for relevant information and will connect the public to appropriate resources. The number: (+91 8892 555 000)
- Conducting awareness programs for both Medical Professionals and other stakeholders.
- Organizing medical camps across India to screen rare genetic diseases.
- Rare Disease Care Coordination Center, which serves as a nation-wide hub to gathers patient information.
References:
1. http://ordindia.org/2. https://en.wikipedia.org/wiki/Rare_disease
Source-Medindia
