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विनोद चौधरी खुद व्हीलचेयर पर , लेकिन उनके हौंसले से लाखों को सहारा

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00:00The problem of this problem is that it is difficult to challenge the risks of the risk of risks and the risk of risks.
00:07We have problems with the risk of risk of risk and risk of risk.
00:14So in the first place, we have taken one division from the Swahigalbarn Foundation,
00:21the ATS program, which is a high level program.
00:28We have to know how many children are.
00:35We have the muscular dystrophy, which is a muscular dystrophy,
00:39who has a small adult,
00:42and it has become a new disease and it has no kind of symptoms.
00:48This is how we get the pain, the pain, the pain, the pain, the pain, the pain, the pain, the pain.
00:56This is one of the symptoms of my Neurology.
01:01We have to experience the brain and we have to experience the disease.
01:04This is why I started as a school district.
01:07This was a high school district, and as he became a school district,
01:13they began to run by the schools and school district.
01:18At 8.10.
01:21We grew up in the old school.
01:25We had the school district and we had to be a student and still grow.
01:31Now, we have to know about how the children are going to get rid of the symptoms of the brain.
01:41We have to know that this is a muscular dystopia.
01:45We have to know that this is a muscular dystopia.
01:51We have to know that this is a muscular dystopia.
01:57So, you can get into the same thing as the same as the same as the same.
02:10So, here's the same thing as the same as the same as the same as the same.
02:19We have 30 crores of rare disease and in India we have 7 children with rare disease.
02:27But now there is no evidence.
02:29Rare disease is used as 2,000 people.
02:34It's not just 2,000 people.
02:38It's not just 2,000 people.
02:40It's not just 2,000 people.
02:42It's not just 2,000 people.
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