Match sickle cell status, not horoscopes before marriage, say experts in Odisha
Headline by Prism · from 1 report
Health experts in Odisha are urging families to prioritize medical screening for sickle cell disease over horoscopes when considering marriage to manage the condition's impact and reduce social stigma.
The HinduThe brief
Written by software from the 1 report below.
- Sickle cell disease is a prevalent genetic disorder affecting over ten percent of the population screened in Odisha.
- Experts advise that individuals living with the condition can maintain healthy marriages if partners are screened to ensure they do not carry the sickle cell trait or disease.
- Significant social stigma persists, often causing families to conceal diagnoses or fail to disclose medical history during marriage negotiations.
- Government initiatives like the National Sickle Cell Anaemia Elimination Programme aim to manage the disease as a public health issue by 2047.
What to watch next
- Future impact of the National Sickle Cell Anaemia Elimination Programme on public awareness
- Developments in social stigma reduction initiatives by the National Alliance for Sickle Cell and Thalassemia Control
The points restate the reports; where one says why it matters, that is Prism's reading, not a reported fact.
Who said what
4 quotes · 1 outlet
Only words found exactly in the article are shown, attributed and linked to the line they came from.
R. K. Jena
haematologist
1 quote · 1 outlet
“The programme is one of India’s largest initiatives to control a genetic disease and is being closely watched internationally because of its scale and comprehensive community-based approach. Besides medical interventions, we also need to address the taboos and social stigma surrounding the disease. People living with SCD themselves must take the lead in creating awareness about the condition”
In the article
…launched the National Sickle Cell Anaemia Elimination Programme (NSCAEP) on July 1, 2023, across 17 high-prevalence states, including Odisha, with the goal of eliminating SCD as a public health problem by 2047. “ The programme is one of India’s largest initiatives to control a genetic disease and is being closely watched internationally because of its scale and comprehensive community-based approach. Besides medical interventions, we also need to address the taboos and social stigma surrounding the disease. People living with SCD themselves must take the lead in creating awareness about the condition ,” said Professor R. K. Jena, a renowned haematologist. Experts, including Ruby Khan, Deputy Director of the National Health Mission, Madhya Pradesh, and Manoranjan Mohapatra, Head of the Department of Haematology at…
Ruby Khan
Deputy Director of the National Health Mission
1 quote · 1 outlet
“Kundli milao ya na milao, lekin sickle cell reports milana zaruri hai”
In the article
…at AIIMS, Delhi, advised patients and their families that people living with sickle cell disease can lead a healthy married life if their partner does not have either sickle cell trait (SCT) or sickle cell disease. “ Kundli milao ya na milao, lekin sickle cell reports milana zaruri hai (Match horoscopes or not, but matching sickle cell medical reports is a must). Pregnant women should also undergo prenatal diagnosis, while screening of family members should be carried out as a preventive measure,”…
Manoranjan Mohapatra
Head of the Department of Haematology at AIIMS, Delhi
1 quote · 1 outlet
“Not every patient will require a bone marrow transplant. Patients must follow the advice prescribed by their doctors and overcome their fears”
In the article
…should be carried out as a preventive measure,” said Dr. Khan. Prof Mohapatra said that, unlike thalassaemia, people with SCD can lead normal lives and that, not every patient requires a bone marrow transplant. “ Not every patient will require a bone marrow transplant. Patients must follow the advice prescribed by their doctors and overcome their fears ,” he said. Although medicines such as hydroxyurea, which helps reduce the frequency and severity of pain episodes, are available at government hospitals, and haematology departments have been opened at several…
Debarpita Mohanty
scientist
1 quote · 1 outlet
“In Kandhamal district, where we are studying the social stigma attached to blood disorders, we have found that some people collect medicines from places far from their homes to conceal their condition from neighbours. Marriages also take place without families disclosing the medical condition of their sons or daughters”
In the article
…are available at government hospitals, and haematology departments have been opened at several government and private hospitals, patients and their families continue to face social stigma associated with the disease. “ In Kandhamal district, where we are studying the social stigma attached to blood disorders, we have found that some people collect medicines from places far from their homes to conceal their condition from neighbours. Marriages also take place without families disclosing the medical condition of their sons or daughters ,” said Debarpita Mohanty, a scientist at the ICMR’s Regional Medical Research Centre, Bhubaneswar. Published - September 27, 2026 07:08 am IST…
Coverage
1 outlet
All filed from India
NamedIndia · Mahanadi Coalfields Limited · AIIMS · Asish · Debarpita Mohanty · ICMR · Malini · Manoranjan Mohapatra · National Alliance for Sickle Cell and Thalassemia Control · National Health Mission · Odisha Haematology Association · Regional Medical Research Centre · R. K. Jena
The 1 report is listed beside the record.
Corrections and versions
A correction says what was wrong and why. Every earlier headline and brief of this record is kept.
Something wrong?
Say what, and it arrives with this record's address filled in. A correction is welcome.
Ask this story
Answers cite the 1 report above, or say they can't.