{"id":16496,"date":"2026-08-25T14:36:32","date_gmt":"2026-08-25T14:36:32","guid":{"rendered":"https:\/\/koshalsambada.in\/?p=16496"},"modified":"2026-08-25T14:36:32","modified_gmt":"2026-08-25T14:36:32","slug":"a-second-chance-the-uncertainty-struggle-behind-indias-organ-transplant-boom-india-news","status":"publish","type":"post","link":"https:\/\/koshalsambada.in\/?p=16496","title":{"rendered":"A second chance: The uncertainty & struggle behind India’s organ transplant boom | India News"},"content":{"rendered":"


\n<\/p>\n

\n
\n
\n
\n
\n
\n
\n
\"A<\/div>\n<\/div>\n<\/div>\n
Organ transplant in India. Photo credit: AP<\/span><\/div>\n<\/section>\n<\/div><\/div>\n<\/div>\n

India\u2019s transplant system has grown rapidly, from 4,990 transplants in 2013 to 20,138 in 2025. But for a patient, a transplant is far more than a surgical procedure. It is a journey through medical tests, clearances, documentation, waiting, uncertainty, organ matching and, eventually, surgery and lifelong follow-up.Transplant hospitals and coordinators are at the centre of this system, working within the wider network of the National Organ and Tissue Transplant Organisation (NOTTO), Regional Organ and Tissue Transplant Organisations (ROTTOs) and State Organ and Tissue Transplant Organisations (SOTTOs).Yet statistics and institutional structures can obscure what the process actually feels like for the person waiting for an organ. For recipients such as Hemant Kumar Thakur and Shrishti Sinha, the reality is one of uncertainty, exhaustion and fear \u2014 followed by the possibility of a second chance at life.<\/p>\n

\n
\"India's<\/p>\n

India’s organ transplant system works through a three-tier hierarchical network coordinated by NOTTO, ROTTO, and SOTTO<\/p>\n<\/div>\n<\/div>\n

<\/p>\n

The journey begins before surgery<\/h3>\n<\/p>\n

A patient with advanced organ failure is first evaluated at a registered transplant centre. The assessment can involve blood tests, imaging, organ-specific investigations and evaluation by a multidisciplinary team. If found medically suitable, the patient is registered in the relevant transplant system.Being on a waiting list, however, does not simply mean waiting in chronological order. Allocation depends on the organ and applicable rules, including factors such as medical urgency, compatibility and, for some organs, time spent on the list. NOTTO\u2019s framework also provides for urgent and super-urgent categories. For kidney patients, for instance, time on dialysis is among the factors considered.<\/p>\n

\n
\"Percentage<\/p>\n

Live Kidneys lead India\u2019s transplant numbers. <\/p>\n<\/div>\n<\/div>\n

NOTTO coordinates the system nationally, while ROTTOs and SOTTOs connect regional and state-level transplant activity. The State Appropriate Authority separately oversees regulatory compliance, including the registration of transplant centres and adherence to legal and ethical requirements.For recipients, however, the elaborate network can feel much simpler: a long wait, a stream of tests and paperwork, and the constant question of what happens next.<\/p>\n

\u201cThe process is not smooth\u201d<\/h3>\n<\/p>\n

Hemant Kumar Thakur, from Jamshedpur, Jharkhand, underwent a kidney transplant at Apollo Hospitals in Kolkata, with his wife, Kanchan Mala, donating a kidney. For him, the hardest part was not the operation but navigating the process beforehand.Because he lived in Jharkhand while the transplant took place in West Bengal, Hemant had to deal with inter-state approvals and paperwork.\u201cBecause the procedure involved two different states \u2014 Jharkhand and West Bengal \u2014 I had to obtain No Objection Certificates (NOCs) from both states before the transplant could proceed,\u201d he said.<\/p>\n

\n
\"The<\/p>\n

The transplant journey begins long before the operating room, with a long road of tests, paperwork and waiting.<\/p>\n<\/div>\n<\/div>\n

Despite the difficulties, Hemant was fortunate to have a compatible donor within his family.\u201cThe process is not smooth; it is quite challenging. I was lucky that the match was found within my own family, with my wife,\u201d he said.His experience also made him aware of the uncertainty faced by patients without a matching family donor. He recalled seeing patients who had found donors and completed much of the paperwork, only for the donor to later withdraw.\u201cAfter going through the entire process, they were back where they had started \u2014 back to square one,\u201d he said.<\/p>\n

Consent can change the course<\/h3>\n<\/p>\n

India\u2019s transplant framework is governed by the Transplantation of Human Organs and Tissues Act, 1994 (THOTA) and related rules. Organ donation must be voluntary and free from commercial dealings, while transplantation is permitted only through authorised institutions.Dr Ankur Garg, GI Surgeon and Liver Transplant Specialist at Paras Health in Gurugram, says legitimate organisations and transplant coordinators play an important role in educating patients, facilitating listing and supporting families when brain-stem death is declared.But he warns that patients can also be targeted by unscrupulous intermediaries.\u201cThere will always be unsocial elements, touts, agents in society luring needy patients and families and giving false hopes and promises of early organ allocation, lesser waiting times and so much extra,\u201d he said.Consent can also change during the donation process. Dr Garg explains that once brain-stem death has been declared and the family consents to donation, the process of identifying eligible recipients begins. But consent can still be withdrawn before organ retrieval.\u201cBefore wheeling into the operation theatre where organ harvesting happens, anyone can withdraw consent, and the whole process will stop,\u201d he said.For recipients, that possibility can mean losing an organ they had been preparing to receive and returning to the uncertainty of the waiting list.<\/p>\n

\n
\".\"<\/p>\n

Once an organ is allocated, the recipient is prepared for surgery and then closely monitored for complications and organ function<\/p>\n<\/div>\n<\/div>\n

<\/p>\n

Living donation<\/keyword>: another route, but not a simple one<\/h3>\n<\/p>\n

Not every patient has to depend on a deceased donor. Certain organs, particularly kidneys and part of the liver, can be donated by living donors after medical, legal and ethical evaluation.The donor\u2019s compatibility and health are assessed, while the legal process depends partly on the relationship between donor and recipient. Near-relative donations follow the applicable framework, while other living-donor relationships may require scrutiny by an Authorisation Committee.Dr Garg says a patient cannot simply register at multiple centres and wait for whichever offers an organ first.\u201cAs per the rule, any patient is allowed to register at one place only. Under NOTTO guidelines and Indian transplant regulations, a patient cannot be registered on a deceased donor waiting list at multiple hospitals or centres simultaneously,\u201d he said.He said the listing process requires a medical summary, blood group, relevant reports and valid Aadhaar or national identification.<\/p>\n

\n
\".\"<\/p>\n

Following the surgery, transplant centres also continue monitoring recipient information and clinical status.<\/p>\n<\/div>\n<\/div>\n

<\/p>\n

The surgery is only the beginning<\/h3>\n<\/p>\n

Once an organ is allocated, the recipient is prepared for surgery and then closely monitored for complications and organ function. But leaving the hospital does not mean leaving the transplant journey behind.Recipients must take prescribed immunosuppressive medicines consistently, attend follow-up appointments and undergo regular investigations. Transplant centres also continue monitoring recipient information and clinical status.Hemant said his own transplant was comparatively smooth once the approvals and paperwork were completed, but the financial and medical commitments continued.He spent approximately Rs 15\u201320 lakh on the transplant and related treatment in 2020.\u201cI do not have any additional complications. I just go for routine check-ups every six months and have to take medication for the rest of my life,\u201d he said.He currently spends around Rs 7,000\u20138,000 a month on medicines, although he noted that aftercare and medication costs vary between patients.Hemant also contrasted the long-term experience of the recipient with that of his living donor, his wife.\u201cThe donor has to take medicines for about three months after the transplant and can lead a normal life,\u201d he said.<\/p>\n

The emotional toll of transplantation<\/h3>\n<\/p>\n

Shrishti Sinha, an engineer who now works as a freelancer in Delhi, describes her transplant journey through a different lens: uncertainty, gratitude, fear and the possibility of rebuilding a future.\u201cThere are many moments of uncertainty. There are medical tests, clearances, waiting for updates and constantly wondering what comes next,\u201d she says.Even hope was fragile.\u201cNot completely. As if one moment hope was rising, the next it was gone. There were cases more severe than mine, or someone who had a higher percentage of surviving,\u201d she recalls.Shrishti underwent treatment at R&R Hospital in Delhi and remembers her doctors as a source of encouragement.\u201cIt was R&R Hospital, Delhi, and the doctors were positive and kept trying to cheer me up,\u201d she says.When she finally realised she would receive an organ, her response was deeply personal.\u201cI was crying and feeling grateful that I was going to live, that I would get to spend more time with my husband and create a future,\u201d she recalls.<\/p>\n

Recovery brings a new set of challenges<\/h3>\n<\/p>\n

The transplant did not instantly restore normal life. Shrishti found recovery difficult, from eating and drinking to physiotherapy.\u201cRecovery was not straightforward. There were challenges with eating, drinking and physiotherapy. Seeing the scar for the first time was scary,\u201d she says.There were unexpected experiences, too.\u201cThe weirdest thing was having strange cravings that I never used to have,\u201d she recalls.Five years later, however, she says the biggest change is her ability to think beyond her illness.\u201cThe biggest change is that I can think about the future again. Before the transplant, so much of my life revolved around my health and whether my condition would deteriorate further.\u201d<\/p>\n

\n
\n
\n

Share your thoughts in the comments<\/p>\n<\/div>\n