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What is Multiple Myeloma?

Multiple Myeloma is a type of cancer that affects plasma cells, which are a type of white blood cells that produce antibodies. In this condition, abnormal plasma cells accumulate in the bone marrow and interfere with the production of healthy blood cells.

How is Multiple Myeloma diagnosed?

Multiple Myeloma can be diagnosed through several tests and procedures, including:

Blood tests: These tests can detect the presence of abnormal proteins or other substances that may indicate multiple myeloma.

Urine tests: Similar to blood tests, urine tests can detect the presence of abnormal proteins.

Imaging tests: X-rays, CT scans, MRIs, or PET scans can help detect bone damage or growths.

What is the cost of Multiple Myeloma Treatment?
  • Bone Marrow Transplant          Rs.666000 to Rs.888000
  • Bone Marrow Cancer   Rs.754800 to Rs.1006400
  • Haplogenic Bone Marrow Transplant   Rs.1110000 to Rs.1480000
  • Autologous Bone Marrow Transplant   Rs.532800 to Rs.710400
  • Allogeneic Bone Marrow Transplant     Rs.976800 to Rs.1302400
  • Leukemia Treatment    Rs.799200 to Rs.1065600.

    USD 6431 TO 8575

Who is the right doctor to consult for Multiple Myeloma?

An oncologist or hematologist, who specializes in the diagnosis and treatment of cancers and blood disorders, is the right doctor to consult for Multiple Myeloma. They have expertise in managing this specific type of cancer and can guide you through the treatment process.

What technology is used during Multiple Myeloma treatment?
  • Advanced imaging technologies like PET-CT scans to detect and evaluate myeloma lesions.
  • Laboratory testing for genetic abnormalities and specific biomarkers associated with Multiple Myeloma.
  • Newer targeted therapies and immunotherapies that leverage advances in biotechnology and precision medicine.
What are the after treatment precautions?

After multiple myeloma treatment, it is important to follow certain precautions to promote healing and overall well-being. Here are some common after treatment precautions:

Follow-up appointments: Regularly attend follow-up appointments with your healthcare team to monitor your progress and address any concerns.

Medication adherence: Take all prescribed medications as directed by your doctor, including chemotherapy drugs, immunomodulatory agen

What are some key tests to be done after the treatment?

After multiple myeloma treatment, several key tests may be performed to monitor your response to treatment, detect any potential relapse or complications, and assess your overall health. Here are some common key tests:

Complete Blood Count (CBC): This test measures the levels of different blood cells, including red blood cells, white blood cells, and platelets. It helps assess overall blood cell counts and detect any abnormalities.

Imaging Tests: Imaging tests, such as X-rays, computed tomography (CT) scans, magnetic resonance imaging (MRI), or positron emission tomography (PET) scans, may be done to evaluate bone damage, check for any signs of disease progression, or monitor treatment response.

Bone Marrow Biopsy and Aspiration: These procedures involve taking a small sample of bone marrow from the hip bone to examine the presence of myeloma cells, assess treatment response, and evaluate the bone marrow environment.

Kidney Function Tests: Multiple myeloma can affect kidney function. Tests such as blood urea nitrogen (BUN) and creatinine levels help evaluate kidney function and detect any renal complications.

It's important to note that the specific tests and frequency may vary depending on individual circumstances and treatment protocols. Your healthcare team will determine which tests are most appropriate for your situation and establish a monitoring plan accordingly.

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Frequently Asked Questions

Yes, congenital heart disease can be passed down from a parent to a child. If one or both parents have a congenital heart defect, there is an increased risk of their child having the condition as well. However, it is important to note that not all congenital heart defects are inherited and some can occur due to other factors such as infections during pregnancy or exposure to certain medications or substances.

The initial treatment process for a child with congenital heart disorder depends on the type and severity of the condition. This could include medications for visible symptoms and monitoring with regular checkups.

The tests for congenital heart disorders do not always require hospitalization. Many of the tests can be performed on an outpatient basis, which means the patient can leave the hospital or clinic on the same day. However, some tests may require a short hospital stay, particularly if the patient is an infant or young child.

The treatment options for congenital heart disease may depend on the type and severity of the condition. These options may include medications or procedures like cardiac catheterization.