Uttar Pradesh / Campaign to save seven months Anmay from Sitapur paid off an injection worth rs 16 crores

Uttar Pradesh | The campaign to save Anmay, who is battling a rare disease called Spinal Muscular Atrophy (SMA) Type-One, has paid off. Anmay's name has come in the company's lucky draw, after which the company will give free injection of 16 crores to Anmay. Anmay's parents are not capable enough to get an injection of 16 crores, which makes a foreign company named Novartis. There was a campaign to save Anmay on social media. Many appealed to the family to help with the #SaveAnvay hashtag. Sonu Sood also made a touching appeal for help on social media to save Anavay.

Two crore eighty lakh rupees have arrived in Anmay's account through a campaign run on social media. A letter was also written on behalf of the district administration to the government for help from the Chief Minister's discretionary fund. Meanwhile, Anvay's father got a call from Ganga Ram Hospital in Delhi that Anvay's name is included in the lucky draw list. In fact, the company gives free injections to 100 children of the world through lottery. This lucky draw is held every fifteen days. This time Anavay's name is also included in the list. According to the information, Anvay will be examined on Monday at Ganga Ram Hospital in Delhi.

What is Spinal Muscular Atrophy (SMA) Type-One Disease?

There is a gene that makes proteins in the human body. Muscles and nerves survive from this gene. Children who have SMA (spinal muscular atrophy) do not have this gene in their body. Due to this, protein is not made in the child's body. This disease is not detected even in the womb, but it is detected with time.