Being born with blood related genetic disorder is a curse in our country. More so because of the high cost of treatment, medication compounded with straitened financial conditions of the patients.
In December 2013, when the parents of an eight-year-old thalassaemic boy wrote to Delhi High Court seeking its intervention to get free blood transfusion treatment and bone marrow transplant, the problem of unavailability of free-of-cost blood to those requiring repeated blood transfusions came into notice.
As per the National AIDS Control Organisation guidelines, those suffering from thalassaemia, haemophilia, sickle cell anaemia and any other blood-related ailment are authorised to get blood free of cost from all blood banks. But is it actually being followed?
Indira Venkaraman, secretary Haemophilia Federation India, says, private blood banks are obviously charging money from the patients and it is really expensive. |
“However, patients who are registered with our society are being provided blood at subsidised rates. The main cost is of transfusion only.”
Notably, the society which is run and sustained by public donation, has a tie-up with Rotary Blood Bank and Red Cross Society for blood supply.
Talking about its collaboration with the Rotary Club, she says, “If Rotary is selling the blood to us at Rs 1,200 then we are providing it at a subsidised rate of Rs 600 to the patients registered with us which is inclusive of the transfusion cost. Also, patients get free treatment. No consultation fee is being charged.”
According to her, government hospitals are also supportive of the cause. “They are providing blood to the patients who require repeated transfusion.
There are three hospitals where blood has to be distributed to haemophilic patients free of costs.
LNJP Hospital has been supportive of the cause whereas in the other two hospitals, kin of the patients are being asked to pay for blood units.
Even to get blood from All India Institute of Medical Sciences, patients have to take a donor along with them.”
On the other hand president of the society, Dr VK Garg, washed his hands of the issue by saying, “I just treat haemophilia patients.”
Given that the treatment of haemophilia depends upon blood and blood components, the availability etc the doctor’s evasivenesswas inexplicable.
Though haemophiliacs need blood at the time of injury or surgery as their body is genetically unable to facilitate blood clotting, patients of thalassaemia, on the other hand, require blood transfusion every 20 days.
“Thalassaemic patients require blood transfusion every month, as their body cannot make haemoglobin which is an essential part of the blood,” says Monisha Gogoi, project manager at the National Thalassaemia Welfare Society.
“There are more than 3,000 children in the City who are thalassaemic and in every government hospitals there are thalassaemic wards which cater to these kids.”
The society helps the patients by organising blood camps, collecting the blood and then giving it to government blood banks that, after processing and different tests, provide it to the needy.
When asked about the private blood banks, she clearly says, “They don’t give the blood for free. Patient take along with them a donor, as well pay for the
blood or the required component. Even the price is also steep.”
Enquiring about the cost at which blood is made available to these patients, Metrolife spoke to Dr RN Makroo, Director, Transfusion Medicine, Apollo Hospital.
“We have 50 to 60 thalassaemic patients registered with us. We don’t ask them to bring donors along with them,” he says.
Ask him specifically about the amount charged for one transfusion, Dr Makroo tries to skirt from the issue, “I don’t remember,” is his straight-faced reply.
“People come to the hospital as per their affordability. Some people prefer going to government hospitals, some to private hospitals while there are people who go
abroad for the treatment,” he says.
Undoubtedly a practical statement, but cruel and insensitive to those whose every minute of life is dependent upon donated blood.
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