We R Both Same type Thalassaemia Carriers

NIPT checks for DNA related conditions like Downs Syndrome, etc. The foetal scan checks for development of the organs. Thalassaemia major is a blood disorder in which the baby’s blood cannot make enough good haemoglobin, which is required to carry oxygen throughout the body to function. This means that in order to live, a baby with thal major will need regular blood transfusions throughout the entire life, or a bone marrow transplant, if suitable. The child will need a fulltime caregiver for quite some time, with regular visits to the hospital. There are also possibilities of complications that may arise from the condition or the transfusions. I think that deciding whether to go for amnio is also a big decision. If a good sample is drawn, you’ll get your answer as to whether your baby’s affected. If the sample’s inadequate, you may need to repeat the test (low chance). But there’s also a 0.5% risk of miscarriage when it comes to doing the procedure, which is probably why you’re also hesitating. So I think you’ll need to have a good talk with your husband.. about what you would do with the results. Will you keep the baby regardless? Would you terminate the pregnancy? Would knowing early help you prepare to make big life changes? Also, are both of you willing to accept the small risks that come with the procedure? This is a tough decision, so I hope you and your husband will be able to find peace in your decision. And I hope you and your baby will continue to be safe and healthy ❤️

Hi, may I know which part did gynae highlight from your blood report that says thalassemia? I just did NIPT and low risk too and received report of my blood works online too. Thanks.

It's advisable to take and confirm it.i think you have to be rational at this moment and decide what is best for both you and your family.

Hello, I’m in the same situation with you now, can I know the route you took? Did you continue with Amino?