It is hard to deny that
parenting is a tough journey and always demanding, yet satisfying. There's
love, responsibility, and a lasting commitment to a child's well-being.
However, when a child is diagnosed with a genetic disorder like thalassemia,
that journey becomes even more complicated and emotionally challenging.
Thalassemia, which is not much talked about, is not just a medical condition
but a lifelong challenge that affects every aspect of a child' development,
health, and quality of life.
This makes it crucial for parents to be fully
informed and aware of the nature of the disorder, the risk it carries, the
available treatment options, and the evolving medical advancements that offer
hope for a better and healthy future.
What is Thalassemia?
According to Dr
MrinaliniChaturvedi, Medical Director of CryovivaLifesciences explains that
thalassemia is an inherited red blood cell disorder that impairs hemoglobin
production and, if left undiagnosed, can lead to serious complications in children.
"It is important for all parents to be aware that both partners can
unknowingly be silent carriers of the condition. Fortunately, advances in
medical science have significantly improved outcomes," says Dr Chaturvedi.
To explain further,
thalassemia is hereditary blood disorder that affecrs the body's ability to
produce normal hemoglobin, the protein in red blood cells responsible for
carrying oxygen throughout the body. Primarily, children with thalassemia
experience chronic anemia, which can lead to several issues like:
Organ damage in severe
cases
"With regular
blood transfusions and iron chelation therapy, many children with thalassemia
can lead longer and healthier lives. In eligible cases, bone marrow
transplantation offers the potential for a cure," reveals Dr Chaturvedi.
Bollywood actors like
Amitabh Bachchan and Jacki Shroff have opened up about their battle with
thalassemia.
Diagnosis of
Thalassemia
One of the most
daunting aspects of thalassemia is that it often comes as a surprise diagnosis.
Many parents discover they are carriers of the gene only after their child is
diagnosed, leading to confusion, guilt, and a frantic search for information. "Understanding
the genetic inheritance patterns, available diagnostic tools, and preventive
measures—such as carrier screening and prenatal testing—is essential for making
informed decisions, especially in families where thalassemia is already
present," suggests Dr Chaturvedi.
In India at least three
to four per cent of individuals are a carrier of thalassemia gene and about 1.5
lakh patients are suffering from thalassemia major. To reduce the burden of
thalassemia, Dr Chaturvedi insists parental decision-making. "It is the
responsibility of healthcare professionals, policymakers, and educators to
ensure that screening is integrated as a routine component of antenatal
care."
Types of Thalassemia
According to Professor
Dr ParinSomani, there are two main types of this condition – thalassemia major
and thalassemia minor. He says children with thalassemia major typically show
symptoms within the first two years of life, including fatigue, paleness, poor
growth, and an enlarged spleen. "These children require regular blood
transfusions to manage symptoms and support normal development," says Dr
Somani.
In the last few years,
treatment for thalassemia has significantly evolved. In addition to lifelong
transfusions, Dr Somani informs that iron chelation therapy is vital to prevent
organ damage caused by excess iron. Bone marrow or stem cell transplants may
offer a potential cure, especially when a matched sibling donor is available.
Gene therapy is emerging as a promising frontier but remains in developmental
stages.
"Public awareness
and early diagnosis are key to managing thalassemia effectively. Parents are
encouraged to seek genetic counselling and ensure timely medical intervention,
offering affected children a better quality of life and access to improved
outcomes," concludes the professor.