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donate blood, donate life
1. * Thalassemia describes a group of inherited
disorders characterized by reduced or absent
amounts of hemoglobin of the blood , the
oxygen-carrying protein inside the red blood
cells.
2.
3. * fairly common blood disorder worldwide.
* Thousands of infants with beta thalassemia are
born each year.
* Beta thalassemia occurs most frequently in
people from Mediterranean countries, North
Africa, the Middle East, India, Central Asia, and
Southeast Asia.
4.
5.
6. * Regular monthly blood transfusion of blood
* Iron chelating
* Bone marrow transplant
7. It’s hard to know that your only little 2-
year old son must be provided with blood
regularly…its harder to know that your
blood doesn’t match with his blood… and
we can’t even imagine the sorrow of how
hard is to know beside all the difficulties
you will face in finding blood your son has
an O- blood group…
HOPE
11. * Average Lifespan of a Red Blood Cell is 120 days
* The Blood loss will be replaced within 4-8 weeks.
* Therefore Blood donations can be given every 2 months.
* Completely SAFE
19. 1-Providing steady blood supply for Thalasemic
patients :
* starting from three universities:University of
Sulaimani,AUIS,Hawler medical Universities in
Sulaimani and Hawler
* Collecting students to become blood donors on
a regular basis.
20. 2-*Spreading awareness about Thalasemia,the patients
and their needs,
* focusing on public education
* Providing knowledge about the disease, and the impact
of the proper treatment on improving the patients
lives.
* Encouraging tests to detect carrier genes of the
disease.
21. 3. Motivation for
blood donation,
* Clarifying the myths
regarding blood
donation.
* Making blood
donation a familiar
good deed.
Hinweis der Redaktion
The Maldives has the highest incidence of Thalassemia in the world with acarrier rate of 18% of the population. The estimated prevalence is 16% in people from Cyprus, 1% in Thailand, and 3-8% in populations from Bangladesh, China, India, Malaysia and Pakistan. There are also prevalences in descendants of people from Latin America and Mediterranean countries (e.g. Greece, Italy, Portugal, Spain, and others). A very low prevalence has been reported from people in Northern Europe (0.1%) and Africa (0.9%), with those in North Africa having the highest prevalence. Ancient Egyptians suffered from Thalassemia with as many as 40% of studied predynastic and dynastic mummies with the genetic defect. Today, it is particularly common in populations of indigenous ethnic minorities of Upper Egypt such as the Beja, Hadendoa, Saiddi and also peoples of the Delta, Red Sea Hill Region and especially amongst the Siwans.