KK Women’s and Children’s Hospital (KKH), in collaboration with Temasek Foundation, has introduced a groundbreaking genetic screening programme. It’s for couples planning to start a family or those already expecting. This free screening, available from 2024 to 2027, empowers parents to make informed decisions about family planning. Through this, they can identify potential risks of passing on severe genetic disorders.
Why Genetic Screening Matters for Families
For parents-to-be, the idea of having a child brings joy, but it can also come with concerns about ensuring their baby is as healthy as possible. KKH’s new genetic screening programme aims to address these worries by offering a proactive approach to family planning. The programme screens for more than 80 genetic disorders that are particularly relevant to the Asian population, including conditions like spinal muscular atrophy and primary bile acid synthesis disorder.
Imagine knowing ahead of time that both parents are carriers of a specific genetic disorder. This knowledge can make a big difference, allowing families to plan early and explore their options. With up to 1 in 250 couples potentially at risk of being carriers, this screening provides couples with valuable information that could shape their family’s future.
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What Does the Programme Cover?
Parents who sign up for this programme will undergo a simple blood test or cheek swab to check for genetic disorders. The programme is open to Singaporean citizens or permanent residents and is completely voluntary. Screenings can be done before or during pregnancy, and self-referrals are welcome. Those attending obstetric appointments at KKH can also be referred to the programme.
One of the standout features of this initiative is the comprehensive list of over 80 genetic disorders, many of which are common in Singapore but not covered by traditional tests. For instance, while screening for conditions like Thalassemia major has reduced the incidence of the disorder, many other recessive genetic disorders have flown under the radar.
Counselling and Support for At-Risk Couples
Finding out that both partners are carriers of a genetic disorder can feel overwhelming. But KKH’s programme doesn’t stop at diagnosis. Couples identified as at-risk will receive thorough genetic counselling. Specialists will explain the risks, help them understand the implications of the results, and discuss family planning options in a compassionate, supportive manner.
It’s not about making decisions for couples but about giving them the knowledge and choices to navigate their journey to parenthood with confidence. From understanding risks to exploring advanced fertility options, parents will be fully supported every step of the way.
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How to Join the Programme
Parents-to-be can easily make appointments through a self-referral process by emailing [email protected] or reaching out via WhatsApp at 6394 3998. The screening is set to roll out in phases, starting with couples planning to start a family, followed by those in the early stages of pregnancy.
This pilot programme aims to screen approximately 40,000 eligible couples over the next three years. Based on the results and feedback, KKH will assess how to scale the programme beyond 2027.
Why This Matters to You
For any couple planning a family, this programme offers an invaluable opportunity to get ahead of potential health concerns. Parenthood is a beautiful journey. But it can also be tough. By taking part in KKH’s genetic screening programme, you can gain peace of mind and help ensure the best possible start for your future child. This is not just about preventing disorders; it’s about giving your family the healthiest, happiest life possible.
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