Ali Zaib Blood arranges blood camps at various Colleges, Factories, Public places, etc. for the collection of blood for the Thalassaemic and Hemophilic Patients. The volunteer donors are screened for the serious diseases like Hepatitis B, Hepatitis C, HIV, Malaria syphilis etc. before the blood collection.
Ali Zaib Blood is providing its 24/7 services to the patients in six major cities of Punjab province through its transfusion centers. Thousands of patients are being provided free of cost blood transfusion facilities every month. The organization provides a pleasant patients friendly environment and air conditioned transfusion rooms. Its laboratory is equipped with all necessary innovative equipments where the pathologists and laboratory technicians are following standard operating procedures aiming at the provision of safe blood and reliable medical investigations which is necessary to ensure proper treatments of the patients. Highly qualifies staff serve the patients with the passion to redress the grievances of the patients.
The blood bank of Ali Zaib Blood is fully equipted with highly qualified staff alongwith innovative blood screening, processing and storage machanism that ensures the availablity of safe blood to the patients. Blood and its componets such as Packed Red Cells, Fresh Frozen Plasma (FFP), Platelets and Crioprecipitates are available 24/7 at the blood bank. This facility is available for all the patients regadless of disease and the hospital where the patients have been treated.
A large number of patients from small cities and rural areas approach Ali Zaib Foundation for medical treatment and blood transfusion facilities every day. In an attempt to redress their grievances, Ali Zaib Foundation is providing them with transport facilities from Bus stop and railway Stations to its blood transfusion center at zero cost.
In an attempt to spread awareness about Thalassaemia, and Hemophila, Ali Zaib Foundation organizes awareness walks and seminars in various cities. It also arrange awareness workshops at Universities, Colleges and Technical & Vocational Training Institutes so that the youth of the nation could be aware of these serious diseases.
Ali Zaib Foundation serves the Pakistan as a large group of non-profited organization they also serve the children who suffered from thalasemia and now is a Thalassemia Center in Pakistan.
Thalassemia is a bunch of hereditary disorders characterized by reduced or absent amounts of haemoglobin, the oxygen-carrying macromolecule within the erythrocytes. There are 2 basic teams of hypochromic anemia disorders: alpha hypochromic anemia and beta hypochromic anemia. These conditions cause varying degrees of anemia, which may vary from insignificant to life threatening. All kinds of thalassemias are supposed of quantitative diseases of hemoprotein, because the amount of hemoprotein created is reduced or absent. Usual adult hemoprotein is formed of 3 components: alpha simple protein, beta simple protein, and heme. Thalassemias are classified according to the globin that is affected, thus the names alpha and beta hypochromic anaemia. Although each categories of hypochromic anaemia have an effect on identical protein, the alpha and beta thalassemias are isolated diseases that disturb the body in numerous ways.
Normal Hb conjointly referred to as Hb A, has four macromolecule chains two alpha simple protein and 2 beta simple protein. The 2 major sorts of hypochromic anemia, alpha and beta, are named once defects in these macromolecule chains. Four genes (two from every parent) are required to form enough alpha globin protein chains. Alpha hypochromic anemia attribute happens if one or two of the four genes are missing. If more than 2 genes are missing, moderate to severe anemia happens. The foremost severe type of alpha hypochromic anemia is named alpha Thalassemia major or hydrops fetalis. Babies who have this disorder typically die before or shortly after birth. Two genes (one from every parent) are required to form enough beta globin protein chain. Beta hypochromic anemia happens if one or each gene is altered. The severity of beta hypochromic anemia depends on what proportion one or each genes are affected. If each genes are affected, the result is moderate to severe anemia. The severe type of beta hypochromic anemia is thought as thalassaemia or Cooley's anemia. Thalassemia has an effect on males and females. The disorders occur most frequently among folks of Italian, Greek, geographic region, Southern Asian, and African descent. Severe forms typically area unit diagnosed in time of life and area unit womb-to-tomb conditions. Doctors diagnose thalassemias victimization blood tests.
Both types of Hemophilia A and B are caused by a hereditary imperfections present on the X DNA. (Hemophilia C is innate in an unusual manner.) Regarding 70 percent of all citizens with hemophilia type A or hemophilia type B innate the disease. Other 30 percent extend from an impulsive hereditary transmutation. The consequent concepts are imperative to understanding the heritage of these disorders. All humans have two DNAs determining their sexual category: The difference between males and females with respect to chromosomes is XY and XX respectively. Since the part of chromosome also known as trait is accepted only on the X chromosome, it is also known as "sex-linked chromosome" The chromosome's defective unit is referred to the factor. Both genes 1st are factor VIII and 2nd is factor IX are formed by hereditary faults of the X chromosome, so both types of hemophilia are sex linked. Since a feminine kid all the time receives two X DNAs, she almost always will be given at least one usual X DNA. Consequently, even if she receives one defective X chromosome, she still competent to produce an enough amount of factors c and IX to evade the signs of hemophilia. An individual who has one defective DNA and this person has not suffered from hemophilia its mean he is carrier. He carries the defected gene and can transfer it on to his children. If, yet, he has a son who receives his defective X DNA, he will not be capable to make the right amount of genes VIII or IX, and he will also endure some types of hemophilia.
In the case of severe blood disease, the primary hemorrhage event sometimes happens before eighteen months older. In some babies, blood disease is suspected directly, once a routine circumcision (removal of the foreskin of the penis) ends up in remarkably serious hemorrhage. Toddlers are at explicit risk, as a result of the fall often, and will bleed into the soft tissue of their arms and legs. These little bleeds end in bruising and noticeable lumps, however do not sometimes would like treatment. As a baby becomes a lot of active, hemorrhage could occur into the muscles; a way a lot of painful and enervating downside. These muscles bleeds end in pain and pressure on the nerves within the space of the bleed. Harm to nerves will cause symptom and attenuate ability to use the gashed limb.
In Pakistan Ali Zaib Foundation is one of the largest group of non-profited organization they serve the children who suffered from hemophilia and today is a Hemophilia Centre in Pakistan.
Hemophilia may be a rare hemorrhage disorder that stops the blood from coagulates properly; therefore an individual who has it bleeds over somebody without haemophilia does. It is a hereditary condition, which implies it's the result of a modification in genes that was either familial or occurred throughout development within the female internal reproductive organ. The normal mechanism for coagulation could be a complicated series of events involving the interaction of the injured vessel, blood cells (called platelets), and over twenty completely different proteins that additionally circulate within the blood.
When a vessel is out of action during an approach that causes harm, platelets collect over the injured space, and form a brief plug to forestall additional harm. This temporary plug, however, is simply too disorganized to function a semi permanent solution, thus a series of chemical events occur, leading to the formation of a more reliable plug. The ultimate plug involves tightly woven fibers of a fabric known as protein. The assembly of protein needs the interaction of many chemicals, particularly a series of proteins known as clotting factors. A minimum of 13 completely different clotting factors are known.
In general, someone with milder bleeder's disease might only bleed excessively once during a while, whereas severe bleeder's disease puts somebody at risk for having hemorrhage issues rather more typically. Most of the peoples with hemophilia discover they need the condition once they are babies or young once when they. Generally the disorder is thus mild that a bloke does not even recognize he has it till he has surgery like obtaining his tonsils or appendix out and it's found in blood tests that doctors perform before surgery.