Skip to main content

INDIAN PRISONERS SEEKING GOVT.’S MOVE ON RELEASE FROM PAKISTANI JAIL


The Ministry of External Affairs confirmed on Thursday (31October, 2013) that there are 400 prisoners are in Pakistan’s jail and among them 90 prisoners have already completed
their sentence span and are entitled to go home. Among the 400 prisoners 214 are civilian prisoners and 186 are fishermen as told by MEA spokesperson Mr. Syed Akbaruddin. The 90 who have completed their sentence span “should be released according to the India –Pakistan bilateral agreement within one month “In August this year 11 prisoners wrote a letter  to both the Government asking for death sentence to get rid of their woeful life in Pakistan’s prison. They also mentioned that 21 prisoners including four women had been turned unstable due to severe mental and physical torture at Kot Lakhpat prison. It is also known that they have even forgotten their names too. Recently Chief Minister Akhilesh Yadav asked to the Prime Minister to look after the matter of releasing Ghazipur resident Dinesh Vishwakarma who has been suffering in Pakistan prison, though has completed his sentence span.
The CM has arranged one lakh and ten thousand to his family as financial assist and additional Rs.25000 also contributed by the judicial magistrate of Gazipur. Dinesh was working in a private farm in the Alwar district in Rajastan since 2008. Dinesh was missing from 2011. On filling an RTI with Ministry of External Affairs the family came to know that Dinesh had been caught by Pakistani authority in 2012 and he was sentenced to one year rigorous imprisonment according to the Foreigner Act. He was also imposed additional Rs.500 or 15 days imprisonment. He is currently at district jail at Malir in Karachi. Though his sentence has been completed seven months ago, he has not been sent to India. His family consists of his wife Ruckmoni and three children, has earnestly requested the Indian authority to look after the matter. Till now no help has been come from the centre.

Comments

Popular posts from this blog

AYE AYE :THE BAD LUCK OMEN

Aye Aye is one of the rarest animals of the world. It belongs to the mammals groups. This rare creature dwells in globular nest which has a small hole to enter and exit. When this creature rides on the tree, it uses its middle finger to tap the tree. It uses its slender finger to find out the taste insects. Aye Aye also uses the same middle finger to lift out insects. Its eyes and ears are unusually large. Due to its big eyes some consider this creature as the demon. These types of creatures are very sensitive. These rare creatures are generally found in the Madagascar Island.  The native islanders of Madagascar often killed this creature in first sight because they believe this creature as evil omen. Aye Aye are the only primates of the mammal world to depend on echolocation for pursue.But the most astonishing fact is that this species is in great danger. These animals are particularly fond of ceramicist beetle. They even eat insects, nectar, seeds etc. Aye Aye are dark/brown or ...

THE MYSTERIOUS DISEASE HARLEQUIN ICHTHYOSIS

Harlequin Ichthyosis is one of the most mysterious diseases of the world.  It is also called “HARLEQUIN BABY”. It is popularly known as a skin disease. It happens due to the thickening of Keratin in human skin. Due to this disease the skin contains massive diamond shapes and skin takes reddish color. Due to this disease eyes, ear and penis increase abnormally. It is easily attracted by bacteria and it causes infection. Harlequin type generally appears in baby’s face and the serious hyperkeratosis helps to cause diamond shape in skin. It causes serious facial deformities. Ear and nose do not develop normally or some time remain abolish .Eyelid remain everted and the mouth often remain open due to this disease. Due to this disease finger, feet etc always remain in a deform state. Fingers and toes develop abnormally. These are generally abnormal in size. This type of patients cannot grab thing properly. It causes respiratory problem in them . Genetic testing is the most progressive t...

THE RARE FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

It is extremely rare bone disease. In this terrifying disease muscles tendons, ligaments etc turned into bone. In this disease bone begins to originate in place of connective tissue. Autosomal dominant allele in chromosome is responsible for this terrible disease. In maximum cases the unnatural mutation in gametes is the main cause behind this. The people who are suffering with FOP have no children. This disease generally happens to see 1(one) man among 2 million people. The transmutation in the gene ACVR1 is also liable for this disease. The children who have born with FOP have big toes probable no joint. It is a genetic disease and the growth of the bone during this disease starts from the top of the downward. The bone started to grow from neck, shoulder gradually chest arms etc. There are several instances available across the glove of this disease since 1800s.Harry Eastlake is the victim of this disease. His body had completely ossified and he was died in 1973.He donated his body ...