We need 'One Nation, One Blood
THE WEEK India|October 06, 2024
Anubha, a thalassaemia major patient, is fighting for the rights of thousands like her.
Mohit Sharma
We need 'One Nation, One Blood

An advocate herself, she demands a 'One Nation, One Blood' law from the government. In an interview, she talks about the challenges of the disease and the way forward. Excerpts:

Do you think there is a lack of awareness about thalassaemia?

Yes, and I think the reason is that there is no national-level control or prevention programme like for polio or tuberculosis or even sickle cell anaemia, which is also a disability under the Rights of Persons with Disabilities Act 2016, just like thalassaemia. The situation is very strange.

Do you think the medical fraternity is doing justice to thalassaemia patients?

I would not doubt the intention of the medical fraternity at all because the very fact that I am sitting here in front of you means that I have been taken care of. The medical fraternity is trying to do their best. We have devoted doctors. But they can only do as much as the infrastructure allows them to.

What is the government's response so far and what are your expectations?

Their are certain policies for thalassaemia but their implementation needs to be better. I would like to talk about a blood law, which is absolutely necessary. When I talk about thalassaemia, our most primary requirement is that of blood.

この記事は THE WEEK India の October 06, 2024 版に掲載されています。

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この記事は THE WEEK India の October 06, 2024 版に掲載されています。

7 日間の Magzter GOLD 無料トライアルを開始して、何千もの厳選されたプレミアム ストーリー、9,000 以上の雑誌や新聞にアクセスしてください。

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