Bone Marrow Transplant in Hyderabad
A bone marrow transplant — also called a stem cell transplant, or BMT — replaces the blood-forming cells that a blood cancer or marrow-failure condition has stopped making. At CION the indicative cost is ₹8–15 lakh. And a transplant is not always the answer — many people are treated well without one. This page tells you, honestly, when a transplant is usually needed and when it usually is not.
- Indicative ₹8–15 lakh · a real estimate for your case
- A second opinion before you commit to anything
- Follow-up close to home across Telangana & AP
What a bone marrow transplant costs in Hyderabad Indicative
| Type of transplant | Indicative cost | Typical stay | Usually used for |
|---|---|---|---|
| Autologous Your own stem cells | ₹8,00,000 – ₹11,00,000 | About 3–4 weeks | Multiple myeloma; some relapsed lymphomas |
| Allogeneic Matched sibling donor | ₹11,00,000 – ₹15,00,000 | About 4–6 weeks | Acute leukaemia, aplastic anaemia, thalassaemia, MDS |
| Haploidentical / unrelated Half-match or registry donor | Assessed case by case | About 6–8 weeks | When there is no matched sibling donor |
Indicative cost estimator
Pick your situation for an indicative range, then request an exact estimate for your case.
What this figure does not include
Almost no hospital tells you this, and it is the part that catches families out — particularly families travelling in from a district.
- Accommodation in Hyderabad for an attendant, typically four to six weeks — someone has to stay.
- Travel, for the patient and for the family.
- Lost earnings — for the patient, and usually for the family member attending.
- Medication after discharge, which continues for months.
- Follow-up blood counts and transfusions after discharge — these, at least, CION can do at your nearest centre.
What bone marrow actually does
Bone marrow is the spongy tissue inside your bones, and it is a factory. It makes the three things your blood is built from: red cells that carry oxygen, white cells that fight infection, and platelets that stop bleeding.
In a blood cancer, that factory starts producing abnormal, immature cells that crowd out the healthy ones — which is why people become tired, bruise easily and catch infection after infection. A transplant is a way of replacing the factory.
Almost everything else on this page follows from that one idea. It is why the old marrow has to be cleared before new cells go in, why blood counts fall to nothing for a couple of weeks afterwards, and why recovery is measured in months rather than days — a factory takes time to start up.

Do you actually need a transplant?
Often, no. A transplant is not the standard treatment for every blood cancer, and it is not something to agree to simply because it has been mentioned. Whether it is right for you depends on your exact subtype, your genetic and molecular results, and how the disease has responded to treatment so far. Here is where a transplant usually sits for each condition — and where it usually does not.
Acute myeloid leukaemia
Not a foregone conclusion. Whether transplant is advised depends on the leukaemia's genetic risk group and how completely it responds to first treatment. Many favourable-risk patients in remission never need one — which is exactly why the molecular and cytogenetic results matter so much.
Acute lymphoblastic leukaemia
Many people — children especially, and many adults — are treated with chemotherapy alone and never need a transplant. It is generally considered for higher-risk genetics, disease that does not clear with initial treatment, or a relapse.
Chronic myeloid leukaemia
If you have been told you need a transplant for CML, get a second opinion. Most people today take a daily tablet at home and live many years with the disease well controlled. Transplant is now reserved for the few who don't respond to targeted therapy.
Lymphoma (Hodgkin & non-Hodgkin)
Most lymphomas are treated with chemotherapy and immunotherapy, and most people never need a transplant at all. Where it comes in, it is usually an autologous transplant considered when the lymphoma returns or does not respond.
Multiple myeloma
An autologous transplant is a standard part of care for many who are fit for it — but it comes after an initial course of drug therapy, and it aims to deepen and prolong remission, not to cure. It can give years of good-quality life.
Aplastic anaemia
Not a cancer — the marrow simply stops producing enough cells. For a younger patient with severe disease and a matched sibling, allogeneic transplant is frequently the preferred first treatment rather than a last resort.
Thalassaemia major
For a child, transplant is the only treatment that can end lifelong transfusions and iron chelation. Outcomes are meaningfully better when done young, before iron overload accumulates — one of the few situations where delay itself carries a cost.
Myelodysplastic syndrome
Lower-risk MDS is often managed supportively for years. For higher-risk MDS, allogeneic transplant is the only treatment aimed at eliminating the disease — but it is demanding, and whether someone can tolerate it depends on age and organ function.
The tests that decide whether a transplant is right — and safe
Diagnostic & evaluation services we offer — book any of these:
Bone marrow biopsy
A small marrow sample to confirm the diagnosis and check how the disease is responding.
HLA typing (blood test)
A simple blood test for you and potential family donors to find a match. It commits no one to anything.
Molecular & cytogenetic testing
Genetic risk-group testing that decides whether a transplant is actually needed for your subtype.
PET-CT / staging scans
Imaging to stage the disease and check the extent before a transplant decision.
Organ-function assessment
Heart, lung, liver and kidney checks to confirm your body can safely tolerate conditioning.
Haematology tumour board
Your reports reviewed together by haematology, medical oncology and pathology — an honest recommendation.
The four types of transplant — and who can donate

Autologous — your own cells
Your own stem cells are collected before high-dose treatment, stored, and given back afterwards. There is no donor to find and no risk of the graft attacking your body. Mainly used in multiple myeloma and lymphomas that have returned.
Allogeneic — a matched sibling
Stem cells come from a brother or sister who is a full HLA match. A full sibling has roughly a one in four chance of matching. The donor's immune system also helps attack any remaining cancer — part of why this works.
Haploidentical — a half-match
Stem cells come from a parent or a child, who is always at least a half-match. This is the option that changed everything: a family without a matched sibling is no longer a family without a donor.
Unrelated donor or cord blood
Where no family donor is available, a matched unrelated donor may be found through a registry, or stem cells may come from banked umbilical cord blood. The search takes longer, and the cost is higher.
Why a sibling match is 1 in 4 — and why a parent always works
Everybody quotes the one-in-four figure; almost nobody explains it. Your HLA type — the set of markers a donor has to match — comes in two halves. You inherit one half from your father and one half from your mother. Each parent has two halves to give, so there are four possible combinations a child can end up with. Two siblings match fully only when they happen to draw the same combination — hence one in four.
But look at what the same arithmetic says about parents. Since you got exactly half your HLA type from your father and half from your mother, a parent is always a half-match. So is a child. Not usually. Not if you are lucky. Always. That is why haploidentical transplant matters so much, and why "we have no matching brother or sister" is not the end of the conversation families believe it to be.

What actually happens — start to finish
The transplant itself is not a surgery. There is no operation, no scalpel and no general anaesthesia. The stem cells go in through a soft tube into a vein, much like a blood transfusion — the patient is awake, sitting up, and it takes a few hours.
What makes people unwell is the conditioning chemotherapy in the days beforehand, and the weeks of very low immunity afterwards — not the transplant.

Evaluation
1–2 weeks. Tests confirm a transplant is right for you and that your body can withstand it.
HLA typing
1–3 weeks. A blood test for you and potential family donors. The step families dread — and it is only a blood test.
Collection
1–5 days. Usually apheresis — blood out of one arm, through a machine, back into the other. No surgery.
Conditioning
5–10 days. High-dose treatment clears the old marrow to make room. The hardest part of the process.
Day 0 — infusion
A few hours. The stem cells go in through the central line. Patients are often surprised how ordinary it feels.
Engraftment
2–4 weeks in protected isolation, while the new cells settle in and start producing blood.
Discharge & follow-up
3–6 months and beyond. Home, with careful monitoring as the immune system rebuilds.
Only one step on that list is outside your control, and it is the one families get stuck on: finding a donor. That is the next question — and it is where the most damaging misunderstanding in this whole process lives.
Where stem cells actually come from
Across Telangana, families believe bone marrow is taken from the spine, and that donating leaves a person permanently weak — unable to lift, unable to farm, unable to work. Siblings refuse to be tested because of it.
It is not true, and it has cost people their lives.

“They take it from the spine.”
No. Nothing goes into the spine, ever. Most donors today give stem cells through apheresis — blood drawn from one arm, passed through a machine that separates out the stem cells, and returned through the other arm. It is closer to donating platelets than to any operation. Where actual marrow is collected, it is drawn from the hip bone with a needle, under anaesthesia.
“He'll be weak for life.”
No. The body replaces donated stem cells within a few weeks — that is what these cells do. Donors are typically back to normal activity within days of apheresis, and within a week or two after a marrow harvest. Farmers farm. Labourers work. There is no permanent loss of strength.
“It will affect her fertility or marriage.”
No. Donating stem cells does not affect fertility, does not affect the ability to have children later, and leaves no lasting mark. An unmarried sister who donates is in exactly the same position afterwards as before.
“Donating might give him cancer.”
No. Donating stem cells does not cause cancer and does not increase a donor's risk of it. The donor's marrow simply makes more cells to replace the ones given.
Who in your family could be a donor?
About a 1 in 4 chance of a full match
Each full sibling has roughly a one-in-four chance of being a complete HLA match; with more than one sibling, the odds that at least one matches go up. Finding out costs nothing more than a blood sample. Testing is not consent to donate — it is simply information.
Always at least a half-match
A parent or a child is always a half-match — arithmetic, not luck. Half-matched (haploidentical) transplant is now well established and performed routinely. If you have a living parent or an adult child, you have a potential donor.
Test the siblings first
A fully matched sibling is generally the preferred donor, so siblings are typed first. If none match — and three times in four, none will — a parent or child is always a half-match. With both available, you are very unlikely to be left without a donor at all.
Still not out of options
Harder, but not the end. Matched unrelated donors can be found through registries, and umbilical cord blood is another source. It costs more and takes longer, so book a haematology consultation now rather than concluding from a search result that nothing can be done.
Transplants & treatments we coordinate
Book a consultation for any of these:
Autologous transplant
Your own stem cells collected, stored and returned — mainly for myeloma and relapsed lymphoma. No donor needed.
Allogeneic (matched sibling)
Stem cells from a fully matched brother or sister — for acute leukaemia, aplastic anaemia, thalassaemia and MDS.
Haploidentical (half-match)
A parent or child as a half-matched donor — the option for families with no matched sibling.
Stem cell collection (apheresis)
Cells collected from the arm through a machine — no surgery, and you are awake throughout.
Chemotherapy & immunotherapy
For the many people whose blood cancer is treated well without a transplant at all.
Second opinion & tumour board
An honest review of whether a transplant is even needed, with full molecular and cytogenetic review.
Risks, GvHD, and what the odds honestly are
Graft-versus-host disease — and its other side
In a donor transplant, the arriving cells bring the donor's immune system with them. Sometimes that immune system treats the recipient's body as foreign — attacking the skin, gut or liver. This is graft-versus-host disease (GvHD): the complication families fear most and understand least. It can be mild, and it can be severe. It is monitored closely, and it is treatable.
Here is what is rarely explained. The same donor immune system that can attack your tissue also attacks any cancer cells left behind — the graft-versus-tumour effect, and a large part of why a donor transplant works at all. The goal of treatment is not to switch the donor's immune system off, but to hold it in the right place.

The other risks
- Infection. The most immediate danger, and the reason for the isolation weeks.
- Bleeding, while platelet counts are low.
- Organ effects on the liver, kidneys, lungs or heart, from the conditioning treatment.
- Fertility. Conditioning can affect fertility, often permanently. If this matters to you, raise it before treatment starts — options exist, but only beforehand.
- Graft failure, where the new cells do not establish themselves.
- Relapse. A transplant reduces the risk of the disease returning. It does not remove it.
About "success rates"
You will find success-rate figures quoted freely online, and you should treat almost all of them with suspicion. Outcomes vary enormously with the condition, the patient's age, the type of donor, and — above all — how well the disease had responded to treatment before the transplant. A twelve-year-old with thalassaemia and a matched sibling is in a completely different position from a sixty-year-old with leukaemia that has already returned once. A single headline percentage that ignores all of that is close to meaningless, and we are not going to put one on this page. A haematologist who has read your reports can give you figures that actually apply to you.
Recovery — and follow-up close to home
Why the isolation weeks happen

Then comes the part nobody warns you about
Discharge is not the end. In the first year after a transplant, a patient typically needs thirty or more follow-up visits — blood counts, transfusions, medication reviews, checks for GvHD and infection — twice weekly at first, then weekly, then fortnightly, tapering over months. If you live in Hyderabad, that is inconvenient. If you live in Nizamabad, Suryapet, Vikarabad or Srikakulam, it is a serious problem: thirty-odd journeys, several hours each way, made by someone whose immune system is still rebuilding.
This is what CION's network is actually for. Your transplant happens at an accredited partner transplant centre in Hyderabad. Your follow-up — the counts, the transfusions, the supportive care — happens at your nearest CION centre, in your own town, reviewed by the same haematology team.
A single-site transplant hospital, however good, cannot offer you this. It is the one thing they cannot build.
Getting back to normal life. Most people are out of hospital within four to six weeks. The immune system takes months to rebuild, and the first three to six months at home mean real care around crowds, raw food and infection. Many people return to work, study and family life — how well and how quickly depends on your condition, your age, the type of transplant, and whether complications occur.
Financial support & Aarogyasri
Cost should not decide whether a family even comes in. Under Aarogyasri and PMJAY, eligible treatment at empanelled centres may be supported, and private insurance is accepted cashless where applicable. Our counsellors help check eligibility and map out what you will actually pay — often a more workable picture than the advertised range suggests. If you cannot afford this, come in anyway and say so plainly: it is a more common conversation than you think.
Transplant in Hyderabad. Follow-up in your own town.
We're never more than 30 minutes away. Same panel of specialists at every centre. Same tumour board reviews. Same NCCN protocols. Pick the closest one and call directly — or let us pick for you.
Not sure which centre fits best? Tell us where you are — we'll suggest the closest one with the right specialists.
Help me pick the right centre35+ centres across Telangana & Andhra Pradesh
Travelling for treatment? We may have a centre right where you are.
Don't see your city? Call 18002028726 — we'll find your nearest CION partner centre.
Your transplant is planned by a team, not one doctor.
Haematology, medical oncology and pathology review every blood-cancer case together — part of 17+ senior specialists across CION.
Dr. C. Raghavendra Reddy
MBBS(Gold Medal), DNB(General Medicine), DM(Medical Oncology)(Gold Medal)
Dr. Bharati Devi Gorantla
MBBS, MD(General Medicine), DM(Medical Oncology)(Adyar,Chennai), ECMO, MRCP SCE(UK)
Dr. Owais Mohammed
MBBS, MD (General Medicine), DrNB (Medical Oncology), ECMO, MRCP SCE (Medical Oncology) (UK)
Dr. Muralidhar Muddusetty
MBBS (AIIMS), MS (Surgery) (AIIMS), DNB (Surgical Oncology), MRCS (Edinburgh)
Dr. Vinay Mamidala
MBBS, MS(General Surgery), M.Ch(Surgical Oncology), FMAS, FARIS(Ongoing)
Dr. Mohammed Imran
Dr. Vajja Sandeep Kumar
MBBS, MS (General Surgery), DrNB (Surgical Oncology), FALS Oncology
Want a specific doctor for your case? Mention them when booking.
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With acute leukaemia, time is the one thing you cannot recover.
Before you commit to a transplant — or conclude nothing can be done — let CION's haematology team review your reports and tell you honestly whether you need one, and what it would really cost.
The questions families actually ask — answered
Asked quietly, usually after the doctor has left the room. Here are honest answers to the ones we hear most in Telangana.
Why CION for a bone marrow transplant
We are specific about what we do and what we coordinate, because you deserve straight information rather than marketing language. Your evaluation, haematology care, transplant decision and follow-up are led by CION's team; the transplant itself is performed at accredited partner transplant centres.
Indicative ₹8–15 lakh
Against a Hyderabad market that commonly quotes ₹10–35 lakh. Indicative — and we give you a real figure for your case.
A second opinion before you commit
Full molecular and cytogenetic review before any decision. Some people who arrive expecting a transplant turn out not to need one.
Follow-up in your own town
Thirty-plus visits in year one — do them at your nearest centre, not on a bus to Hyderabad while immunosuppressed.
A dedicated haematologist
Dr. Basudev Pokhrel — JIPMER and CMC Vellore. Not a general oncologist covering blood cancers as a sideline.
Every case to a tumour board
Haematology, medical oncology and pathology review your case together, not in sequence.
Care in accredited environments
The transplant is delivered at accredited partner transplant centres, to recognised protocols, with CION managing your case throughout.
15,000+ patients chose CION. Hear from them directly.
These aren't paid endorsements or written reviews. These are video testimonials from real patients and families — recorded on their own phones, in their own words. Pick any one. Watch it. Then decide.
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Start Your Story. Book Free Consultation.The support around a transplant
A transplant is not only a medical event. It is months of low immunity, long stretches away from home, and enormous strain on a family. These are part of the plan, not afterthoughts.
Nutrition counselling
Eating safely while immunity is suppressed — keeping weight and strength up through conditioning and recovery. Learn more
Psychological support
For the patient through weeks of isolation, and for the family carrying the fear and the cost. Learn more
Genetic counselling
Where an inherited condition such as thalassaemia is involved, or a family predisposition is suspected. Learn more
Rehabilitation
Rebuilding strength and stamina after weeks in a bed and months of low immunity. Learn more
Palliative & comfort care
Symptom and comfort support at any stage — alongside active treatment, not instead of it. Learn more
Financial counselling
Aarogyasri, PMJAY and cashless insurance guidance so cost never silently blocks care. Learn more
Bone marrow transplant in Hyderabad — frequently asked questions
What does a bone marrow transplant cost in Hyderabad?
Bone marrow transplant in Hyderabad is commonly quoted between ₹10 lakh and ₹35 lakh depending on the centre and the type of transplant. At CION the indicative range is ₹8 lakh to ₹15 lakh: roughly ₹8–11 lakh for an autologous transplant using the patient's own stem cells, and roughly ₹11–15 lakh for an allogeneic transplant from a matched sibling donor. Half-matched and unrelated-donor transplants are assessed case by case. These figures are indicative and are not a quotation, and do not include family accommodation, travel, or medication after discharge.
Is a bone marrow transplant a surgery?
No. There is no operation, no scalpel and no general anaesthesia for the transplant itself. The stem cells are given as an infusion through a central line — a soft tube placed into a large vein — in much the same way as a blood transfusion. The patient is awake and sitting up, and it takes a few hours. What makes people unwell is the conditioning chemotherapy given in the days beforehand, and the weeks of low immunity afterwards, not the transplant.
Is bone marrow taken from the spine? Will the donor be paralysed or weakened?
No. Bone marrow is never taken from the spine, and donating does not cause paralysis or permanent weakness. Most donors today give stem cells through apheresis — blood is drawn from one arm, passed through a machine that separates out the stem cells, and returned through the other arm. There is no surgery and nothing goes into the back. When marrow itself is collected, it is taken from the hip bone, under anaesthesia, through a needle. The body replaces the donated cells within a few weeks, and donors return to normal work and normal life.
Does my family member actually need a bone marrow transplant?
Possibly not. Transplant is not the standard treatment for every blood cancer. Many people with lymphoma are treated with chemotherapy and immunotherapy alone and never need one. Most people with chronic myeloid leukaemia today take a daily tablet at home and rarely need a transplant. In acute myeloid leukaemia, whether a transplant is advised depends heavily on the genetic risk group of the disease and how it responds to first treatment. Before committing, it is entirely reasonable to ask for a second opinion with full molecular and cytogenetic review.
We have no matching brother or sister. Is there no hope?
There is. A full sibling has roughly a one in four chance of being a complete HLA match, so most families do not have one. But a parent or a child is always at least a half-match, because you inherit half of your HLA type from each parent. Half-matched, or haploidentical, transplant is now well established. A family with no sibling match is not out of options, and unrelated donor registries exist as well. Start with a haematology consultation rather than assuming the worst.
What are the types of bone marrow transplant?
There are four, named by where the stem cells come from. An autologous transplant uses your own stem cells, collected and given back. An allogeneic transplant uses cells from a fully HLA-matched sibling. A haploidentical transplant uses a half-matched parent or child. An unrelated-donor or cord-blood transplant uses cells from a registry donor or banked umbilical cord blood. The type determines the cost, the risks and the length of stay.
How does HLA matching work, and why is a sibling only a 1 in 4 chance?
Your HLA type — the set of markers a donor must match — comes in two halves, one inherited from each parent. Each parent has two halves to give, so there are four possible combinations a child can inherit. Two siblings match fully only when they happen to inherit the same combination, which is why the chance is about one in four. The same arithmetic explains why a parent or child is always exactly a half-match.
What is a haploidentical (half-matched) transplant?
A haploidentical transplant uses stem cells from a parent or a child, who is always at least a half-match because you inherit half your HLA type from each parent. It is now well established and performed routinely, and it is the reason a family with no matched sibling is not a family without a donor. If you have a living parent or an adult child, you have a potential donor.
Is bone marrow transplant covered under Aarogyasri or insurance?
Under Aarogyasri and PMJAY, eligible treatment at empanelled centres may be supported, subject to eligibility, and private insurance is accepted cashless where applicable. Coverage for transplant varies by scheme and by case, so the honest step is to have our counsellors check what applies to your specific situation and map out what you would actually pay, rather than assuming either that everything is covered or that nothing is.
Why is the patient kept in isolation? Can the family not visit?
Isolation is not a hospital rule made for convenience — it is the reason the transplant survives. The conditioning therapy clears the old bone marrow, so for roughly two weeks the patient has almost no infection-fighting white cells at all. In that window an ordinary cold, or a common stomach bug carried in on a visitor's hands, can become life-threatening. Once the new stem cells engraft and blood counts recover, restrictions ease. The team explains exactly when and how you can visit, and video calls are almost always possible throughout.
What is graft-versus-host disease (GvHD)?
In a donor transplant, the arriving cells bring the donor's immune system with them, and it can sometimes treat the recipient's body as foreign — attacking the skin, gut or liver. This is graft-versus-host disease. It can be mild or severe, it is monitored closely, and it is treatable. Importantly, the same donor immune system also attacks any remaining cancer cells (the graft-versus-tumour effect), which is a large part of why a donor transplant works at all.
Will receiving another person's bone marrow change who the patient is?
No. What is transplanted is the blood-forming system — the part of the body that produces red cells, white cells and platelets. A person's brain, memory, personality, character and identity are entirely unaffected. The one real change is that the recipient's blood group may gradually become the donor's, because blood group is determined by the marrow. It is a medical treatment for one organ system, not a transformation of the person.
Is donating stem cells safe? Does it affect fertility or cause cancer?
Donating stem cells is safe and well tolerated. It does not affect fertility, does not affect the ability to have children later, and does not cause cancer or increase a donor's risk of it. The body replaces donated cells within a few weeks. Most donors return to normal activity within days of apheresis, or within a week or two after a marrow harvest, including physical work.
How long does recovery take, and how many follow-up visits are needed?
Most people are out of hospital within four to six weeks, but the immune system takes months to rebuild. In the first year a patient typically needs thirty or more follow-up visits — blood counts, transfusions, medication reviews and checks for GvHD and infection — twice weekly at first, then weekly, then fortnightly. CION can carry out much of this follow-up at your nearest centre so you do not have to travel to Hyderabad repeatedly while your immune system is still recovering.
Can a person live a normal life after a bone marrow transplant?
Many people do return to work, study and family life. Recovery is gradual rather than sudden: most people are out of hospital within four to six weeks, but the immune system takes months to rebuild and follow-up continues for a year or more. During the first few months, crowds, raw food and infection risk have to be managed carefully. How well someone recovers depends on their condition, their age, the type of transplant and whether complications occur.
Does CION perform the transplant itself?
Your evaluation, haematology care, transplant decision and follow-up are led by CION's own team. The transplant itself is performed at accredited partner transplant centres in Hyderabad, under a formal arrangement, with the same haematology team managing your case throughout. This is stated plainly so you know exactly what CION delivers directly and what it coordinates — and it is also why routine follow-up can happen close to your home.
What is the success rate of a bone marrow transplant?
Outcomes vary enormously with the condition, the patient's age, the type of donor and — above all — how well the disease had responded to treatment before the transplant. A young person with thalassaemia and a matched sibling is in a very different position from an older person with leukaemia that has already returned. A single headline percentage that ignores all of that is close to meaningless. A haematologist who has read your reports can give you figures that actually apply to you.
Can Ayurveda or home remedies treat blood cancer instead of a transplant?
Traditional practices may bring comfort, and many families find real meaning in them. But with blood cancers — acute leukaemia in particular — time is the one thing that cannot be recovered, because it can progress over days and weeks, not months. Using traditional remedies instead of treatment spends exactly the window in which treatment works best. If you want to continue a traditional practice alongside medical treatment, tell your haematologist: some are safe alongside treatment and some interfere with it.
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Talk to a haematologist first
Bring your reports, or come in for a fresh evaluation. Before you commit to a transplant, it is worth finding out whether you need one — and what it would really cost in your case. Consultations in Telugu, Hindi or English.
