8 May Thalassemia's World Day and Pakistan........

All over the world every year the world day is celebrated on May 8 thalassemia۔are different seminar held in reference to save the people of consciousness thalassemia is highlighted thalassemia disease is a persecutor included in the red blood due to the formation of undesirable quantity named protein۔is to shift in the form of poor blood ownership is the most common disease۔some people also say it thalassemia patient the remainder expressed by some other diseases can۔as light 46, hunger, JAUNDICE, ANEMIA i.e. heart diseases and liver disease is a Genetic disorder which is the increased etc.۔nor do not wash the food nor bacterium It is discouraging to۔LINEALLY is transferred from the parents of children is necessary for the prevention of this۔parents during pregnancy before birth to approach the doctor thalassemia ancestral disease like most victims of Asia, Africa and Mediterranean Sea linked countries are three types of۔ are present in thalassemia thalassemia thalassemia minor and thalassemia major, in which۔Inter media۔ Thalassemia minor throughout the world moss thalassemia minor the patient is neither any pain nor it is no sign obviously spend a complete healthy life۔such people are confirmed only if it is only possible to test ۔spend a normal life itself But his illness can shift in their children which is essential for the protection of۔۔ Peen Thalassemia major most dangerous thalassemia contains so little blood in patients of major prepared that patient to every two to four weeks after the blood in the form of not to assess lima۔his body paralyzed ۔their lives is started blood bank is dependent۔are neither the healthy people can play کوود nor can live at the top of the educational field۔such patients suffering from his entire life in the phenomenon keeps that they died due to blood and many diseases are also by the parents of these children۔ And family financial resources are also facing۔unsuitable because of treatment facilities is located in the majority of the patients early death thalassemia major takes birth then when the mother and father also contains the both parents i.e. thalassemia۔if both mother and father I am children are also creating normal۔if any one thalassemia minor contains 50 percent if your child can create normal minor and 50 percent۔if both are capable of minor 25 contains of 25 rd being discriminated against percent children can be created۔if both mother and father thalassemia major be of great then compulsory all children will create only contains the major۔according to a cautious estimate more than ten daily throughout the world And the annual thousand children are capable of thalassemia major۔throughout the world as more than million۔Thalassemia are scored in Pakistan was not a survey on government level۔but cautious estimates of more than one million in Pakistan are minor thalassemia thalassemia major of more than one laky contains۔while patients are in annual six thousand growing that it is a congenital disease, which was not complete till date treatment۔a flash this treatment is also done bone marrow operation is quite expensive in Pakistan in this operation has spent approximately one million that after which are to rid the disease while 30 percent70percent possibility that even death occurred There is no complete this disease may۔i.e. treatment could not be discovered in poor country like Pakistan۔so expensive is not possible for any kind of treatment for this is the work of the most awareness so that people can be saved from this deadly inheritable disease۔came from those countries this disease in our country in Greece, Italy, and cypress are in the ratio of thalassemia major today is nil۔apart from many countries in the world has kept on this disease awareness and legal actions because of other Muslim countries like Iran today is under control and in Turkey Thalassemia screening test before marriage legally compulsory that is the reason that these countries in thalassemia major The ratio of the patients has been considerably reduced۔Pakistan also need timely such steps. TV and other media in the Pakistan government unfortunately the net works with reference to this should be to broadcast messages۔awareness in addition to this marriage before the thalassemia screening as a compulsory and legal process so that the poor and uneducated people should give ۔ancestral disease could be saved from this phenomenon plate۔in Pakistan and many organizations are working on private level because of which the deadly Genetic disorder people of Pakistan is being informed about the disease in Pakistan۔Thalassemia major patients the average age 10 to 15 years in which it was due to the various organizations of their awareness and aid Who is increasing till now has been regular subscribers 30۔these organizations and institutions to mention here is also very important because of the Munnu Bhai۔named Sndas Foundation labor thalassemia patients throughout Punjab Pakistan especially today and the second is to provide aid to blood۔Similarly Kashif Iqbal center also in Karachi the thalassemia patients is to provide facilities of life۔besides this jihad for zero thalassemia, Khidmat foundation, Umair Sana foundation, Fatima foundation and individually Yasmeen Rashid and others to end this inheritable disease and humanity are performing their duties as the head is also very important to mention here۔struggle foundation, because of which the awareness seminar the invitation cards The less knowledge me this dreadful inheritable and deadly disease discovered the whole truth about the young۔struggle Foundation President Talha Naseer a organizational meeting۔met after which I know that how many different stepping up a large congenital disease and thalassemia Is increasing day by day and after which the struggle۔foundation and Talha Naseer promised to inform the people about the deadly disease and Genetic disorder for their part will definitely boughs۔readers struggle foundation is that it is based on the entire organization youth and the whole of Punjab are prevalent in the educational institutions in various universities who۔Thalassemia are held regarding the awareness of the functions۔ especially universities of the students who are near the marriages they are giving awareness about thalassemia test۔besides this struggle is the unity of the foundation named Sndas foundation and other treatment of installing۔named Sndas Foundation blood work while struggle foundation throughout Punjab In addition to the awareness of work to reduce the excess iron patients and blood camp to provide pumps blood also provide etc are part of the struggle of awareness works۔struggle of other members Nauman Rasool, Maheen and Bilal etc. the dedication and enthusiasm of watching every Pakistani heart will surely truly commendable and performance of God the day when every young Pakistani their daily life out a few moments part of such welfare work will contribute۔readers requested that thalassemia about their ancestral and deadly disease close people must inform۔so that the innocent children can be saved from this dreadful Genetic disorder disease۔Pakistan Zinda Bad