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A Person named Jagadeshwara Rao, who is running dry cleaning shop in city is affected by a failure in both kidneys and for transplantation of kidneys is costing Rs 8,00,000.00( eight lakh rupees only) as doctors said. He is having 2 kids and a wife.

One of His Nearest relative is ready to donate his Kidney, though this family is still struggling for “MONEY” which is necessary for medication and others, hence requesting all to help. Please contact: +91-934 631 3619.

Real Hero — support her in any way — Be Human.

A girl “HARIKA’ by name with her friends “Aayush, Haarika, Ravi, and Rishi” started a society or a platform whatever you may say , in order to support the people who are suffering from the disease of “Cystic Fibrosis”. This is happend because of her own brother “Bharat” is suffering from the same said disease.


Cystic Fibrosis is a rare genetic disease. There many thousands of people in the United States with this condition. The Cystic Fibrosis Foundation ( promotes awareness of Cystic Fibrosis, and raises funds for Cystic Fibrosis related research. The Cystic Fibrosis Foundation has an annual walk called “Great Strides”. Every year thousands of teams participate in these walks and raise funds to help support the on-going research for finding a cure for this disease. Not long ago, most people with Cystic Fibrosis did not live past their elementary school. Now, many Cystic Fibrosis patients are living normal lives and the median lifespan for people with Cystic Fibrosis is well into the forties.

The statistic that shows that most Cystic Fibrosis patients are in Europe and North America is quite misleading. Most of the Cystic Fibrosis cases are not even diagnosed in India and other countries. As a result, most of the patients with this disease die very young and the real cause would never be known. When we discussed some of the infant deaths in our relative’s families in India, we realized that many of those were never completely diagnosed and many of them had the exact symptoms of genetic diseases like Cystic Fibrosis.

Diseases like Cystic Fibrosis are rare. Even with all the support network and work done by the Cystic Fibrosis Foundation, a vast majority of Americans would not know about this disease. One can imagine what kind of awareness exists in countries like India where this mostly not even diagnosed. Many young lives are lost in countries like India because of lack of awareness, testing, and treatment. When we look at Bharat, we realize how dramatic the improvement can be in the lives of cystic fibrosis patients when they are diagnosed and properly treated for Cystic Fibrosis. Early detection is always the key to a better life for cystic fibrosis patients. Fortunately many states in the U.S. now have legislation to screen all newborns for diseases like Cystic Fibrosis.

God blessed her as a Good painter, hence she decided to collect the money by selling her own drawings. so far she sold 3000 self-made greeting cards and collected Rs.400000-00 and donated the same to the foundation..


Contact her :

Local2global  team wish the team a great time …..

I want to live and serve — plzzz help me



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