World Thalassemia Day Information For Students

World Thalassemia Day 8 May: Federation, Celebration and Theme

World Thalassemia Day is celebrated every year on 8th of May to increase the awareness about this disease among common public all through the world. Celebrating World Thalassemia Day on 8th of May was established by the World Health Organization in order to raise the public awareness about this disease, prevention measures and measures to avoid its transmission.

World Thalassemia Day: 08 May

According to the statistics, around 19% of the total population is the carrier of Thalassemia gene in the Saudi Arabia Kingdom. Thus world thalassemia day is celebrated there as a big event by organizing variety of preventive programs to increase awareness and reduce spread of this genetic disease. This event celebration promotes and encourages the common public for the pre-marriage test to reduce the genetic problems among families.

8th of May has become a very special day for the people suffering from the thalassemia as it brings a chance for them to get diagnosed earlier. The day is dedicated to commemorate the thalassemia patients and give them a special chance to live like a normal person as well as prevent this disease to spread in the community, society, state, country and finally world.

Overview:

A blood disorder involving lower-than-normal amounts of an oxygen-carrying protein. Thalassemia is an inherited blood disorder characterized by less oxygen-carrying protein (haemoglobin) and fewer red blood cells in the body than normal. Symptoms include fatigue, weakness, paleness and slow growth. Mild forms may not need treatment. Severe forms may require blood transfusions or a donor stem-cell transplant.

Rare:

Fewer than 1 million cases per year (India)

World Thalassemia Day Date:

World Thalassemia Day will be celebrated by the people all over the world on

  • 2024: 8th May 2024 (Wednesday)
  • 2025: 8th May 2025 (Thursday)
  • 2026: 8th May 2026 (Friday)

What Is Thalassemia?

Thalassemia is an autosomal recessive blood disorders which gets inherited from parents to the children through genes. It is a blood disorder causes weakening and destruction of the red blood cells, affects the formation of hemoglobin in the body and causes mild or severe anemia. It causes complications like bone deformities, iron overload, cardiovascular illnesses, heart palpitations, enlarged liver, jaundice, enlarged spleen, enlarged bones of cheeks or forehead, delayed puberty and etc.

Around 3.4% of the people are carrier of the thalassemia and around 7000 to 10,000 children are born with thalassemia per year in India. It can be of any type such as alpha thalassemia, beta thalassemia, delta thalassemia and combination of other hemoglobinopathies (hemoglobin C, D, E and S).

It is seen among children of one or two years of life. Mild thalassemia sometimes does not show any symptoms thus can be un-diagnosed until blood test (complete blood count, CBC test). It can be treated through the blood transfusion, B group vitamins supplements, iron chelation therapy and blood and bone marrow stem cell transplantation to maintain the normal level of haemoglobin and healthy RBCs.

Since, it is an inheritable disease so cannot be prevented completely however, it can be lessen through the prenatal tests which helps in the early detection and cure before the child birth. It is requested to all the carriers of thalassemia gene to meet a genetic counselor as soon as possible to get proper treatment before being a parent of child or prevent the gene to get inherited to their child.

Why World Thalassemia Day Is Celebrated?

World Thalassemia Day is celebrated all across the world to help people suffering from the thalassemia and its complications in their daily life. Thalassemia is a genetically inheritable blood disorder which can affect people of any age group. It is a disease which having ability to destroy the whole nation and world by affecting a child. Children are the most important asset of the country and world who have capability to lead their nation and world thus it has become the big responsibility of the government of each country to prevent children, country and world from this fatal inheritable disease. Some of the objectives of world thalassemia day are mentioned below:

  • It is celebrate to increase the awareness about the disease among common public.
  • To develop a most effective prevention measure to have control on the disease.
  • To motivate and encourage the common public especially youths for the blood donation in order to prevent the people suffering from thalassemia.
  • To motivate doctors and other health professionals to take care of the patients especially what they need.
  • To promote the people suffering from it to come to the hospital for the early detection, prevention and cure.
  • To motivate the youths for the pre-marriage test to get diagnosed about this problem and prevent this disease to get inherited among new generations.
  • To make the community, society, nation and world free of thalassemia and other inheritable diseases.
  • To give them (people having thalassemia) equal chance of living like a normal and well being person.
  • To encourage government organizations to develop more heath care facilities in the vulnerable area.
  • To reduce the death rate of people all over the world on international level because of the thalassemia.
  • To increase the number of healthy people without thalassemia or other fatal diseases in the country and world.

How World Thalassemia Day Is Celebrated?

World thalassemia day is celebrated by organizing various activities and events in the public places, schools, colleges and other educational institutions to make it more effective. Patients and their families are encouraged to actively take part in the celebration to get all the knowledge about the thalassemia.

The Thalassemia International Federation (TIF), which is a non-profit and non-governmental patient-driven organization, actively involves in organizing the event celebration with its associated associations and members in many countries. World Health Organization and other health bodies all through the focuses on the patients basic rights to encourage more people with thalassemia.

Variety of activities like debates on the health related subjects, discussion over the thalassemia patient’s quality of life including health care services. Posters and banners activities are also done to aware people about this disease.

Varieties of other awareness campaigns are launched by the TIF aiming to spread the information and awareness about hemoglobinopathies, haemoglobin disorders and iron deficiency among common people especially amongst the young people. Educational materials are also distributed to the young students to raise awareness among youths.

Red Day Activities are also organized by the TIF at many places when students wear red T-shirts indicating the cartoon characters of red-blood cells showing the requirement of thalassemic patients.

World Thalassemia Federation:

Thalassemia International Federation is a non-profit and nongovernmental organization having 108 member associations all over the world in 55 countries and officially has relation to the WHO and other major health-related agencies since 1996. TIF is responsible for improving the quality of life, health and the life expectancy of the thalassemic patients and patients with other inherited congenital haemoglobin disorders. It involves in many activities such as:

  • It provides supports to other health organizations in increasing the health awareness all though the world.
  • It helps in establishing some new health organizations for better health care of the patients.
  • It supports and encourages other national health authorities in developing an effective and efficient national health control strategies, prevention measures and clinical management of the disease.
  • It organizes educational campaigns for the patients and their families, parents, health specialists, and other medical professionals to raise awareness.
  • It organizes local, regional, national and international level conferences, seminars, workshops and campaign of distributing educational materials and books in order to provide up-to-date information to people, web visitors and its members.
  • It also helps in promoting the national health control programmes in the European countries.
  • Collect and promote the updated and accurate epidemiological data for diseases.
  • Create European Reference Centres and collaborative networks between the medical professionals and patients communities.

Theme:

This special day is celebrated every year using a particular theme to make it very effective and encourage patients for getting appropriate treatment to enhance their quality of life. Some of the year wise themes are listed below:

  • 2024: Empowering Lives, Embracing Progress: Equitable and Accessible Thalassemia Treatment for All.
  • 2023: Be aware. Share. Care.
  • 2022: Be Aware. Share. Care: Working with the global community as one to improve thalassaemia knowledge.
  • 2021: Addressing Health Inequalities Across the Global Thalassaemia Community
  • 2020: The dawning of a new era for thalassaemia: Time for a global effort to make novel therapies accessible and affordable to patients
  • 2019: Universal access to quality thalassaemia healthcare services: Building bridges with and for patients.
  • 2018: Thalassaemia past, present and future: Documenting progress and patients’ needs worldwide
  • 2017: Get connected! Share knowledge and experience and fight for a better tomorrow in thalassemia
  • 2016: Access to Safe & Effective Drugs in Thalassaemia
  • 2015: Enhancing partnership towards patient-centered health systems: good health adds life to years!
  • 2014: Economic Recession: Observe – Joint Forces – Safeguard Health
  • 2013: The right for quality health care of every patient with Thalassemia: major and beyond
  • 2012: Patients Rights Revisited
  • 2011: Equal Chance to Life
  • 2010: Thalassemia: Knowledge is Strength
  • 2009: Together industry. We Care.

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