In Patiala, Punjab, a couple was allegedly attacked by a pitbull while visiting a property with a real estate dealer.
The husband and wife had gone to inspect the house when the dog suddenly lunged at them after they rang the doorbell.
Local residents intervened, but both suffered multiple bite injuries and were taken to a private hospital for treatment.
Hi @HappiestMinds team,
I am working as the Technical Lead at this company,
I am writing to request your assistance. My friend’s son is suffering from SMA type 1 disease. The cost of the required injections is ₹17 crore. If you are able to contribute, I would be grateful.
💔 "We Put the Nation First. Now, Our Child is Left Behind."
We are a proud, middle-class, tax-paying couple from Andhra Pradesh. When leaders like Chief Minister N. Chandrababu Naidu garu, urged families to have more children for the nation’s future, we listened. We welcomed our second child, ready to raise another honest, contributing citizen.
Today, our world is shattered. Our beautiful baby has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1 - a fatal genetic condition. The life-saving treatment costs crores, a sum impossible for any middle-class family to afford.
The Heartbreak of Honest Taxpayers
We have knocked on every door, only to find a devastating truth: Neither the State nor the Central Government has a functional policy or funding mechanism to fully support and save SMA Type 1 children.
We ask our leaders with the utmost respect: How can citizens confidently keep the Nation First when the nation's policies leave our children unprotected?
1. We paid our taxes honestly.
2. We answered the call for a stronger demographic future.
3. Yet, in our darkest hour, we are left in a complete policy vacuum.
Our Urgent Plea as Parents
We are not asking for a handout; we are begging for our child's right to live. SMA Type 1 moves rapidly. Our baby is running out of time.
We humbly appeal to the Prime Minister’s Office, the Ministry of Health, and the Andhra Pradesh Government for immediate, emergency intervention. If you want us to build India’s future, please help us save our children today.
Please share our story. Let it reach those in power.
@PMOIndia@MoHFW_INDIA@NCBN@AndhraPradeshCM@JPNadda@PMOIndia@MoHFW_INDIA@NCBN@AndhraPradeshCM@JPNadda@naralokesh@OfficeofNL
#SaveOurBaby #SMAType1 #RareDiseasesIndia #TaxpayersOfIndia #AndhraPradesh #PopulationPolicy #ChandrababuNaidu #SaveShyam
💔 "We Put the Nation First. Now, Our Child is Left Behind."
We are a proud, middle-class, tax-paying couple from Andhra Pradesh. When leaders like Chief Minister N. Chandrababu Naidu garu, urged families to have more children for the nation’s future, we listened. We welcomed our second child, ready to raise another honest, contributing citizen.
Today, our world is shattered. Our beautiful baby has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1 - a fatal genetic condition. The life-saving treatment costs crores, a sum impossible for any middle-class family to afford.
The Heartbreak of Honest Taxpayers
We have knocked on every door, only to find a devastating truth: Neither the State nor the Central Government has a functional policy or funding mechanism to fully support and save SMA Type 1 children.
We ask our leaders with the utmost respect: How can citizens confidently keep the Nation First when the nation's policies leave our children unprotected?
1. We paid our taxes honestly.
2. We answered the call for a stronger demographic future.
3. Yet, in our darkest hour, we are left in a complete policy vacuum.
Our Urgent Plea as Parents
We are not asking for a handout; we are begging for our child's right to live. SMA Type 1 moves rapidly. Our baby is running out of time.
We humbly appeal to the Prime Minister’s Office, the Ministry of Health, and the Andhra Pradesh Government for immediate, emergency intervention. If you want us to build India’s future, please help us save our children today.
Please share our story. Let it reach those in power.
@PMOIndia@MoHFW_INDIA@NCBN@AndhraPradeshCM@JPNadda@PMOIndia@MoHFW_INDIA@NCBN@AndhraPradeshCM@JPNadda@naralokesh@OfficeofNL
#SaveOurBaby #SMAType1 #RareDiseasesIndia #TaxpayersOfIndia #AndhraPradesh #PopulationPolicy #ChandrababuNaidu #SaveShyam
Urgent plea for my son 2 months old battling SMA Type 1. The ₹16Cr life-saving injection is far beyond my family's reach. Requesting @naralokesh anna & @AndhraPradeshCM to step in with the same compassion shown during #ProjectPunarvika. Please save another innocent life! 🙏
Urgent Appeal My 2-month-old son has been diagnosed with SMA Type 1, a rare & fatal genetic disorder. He needs the life-saving Zolgensma injection (₹16+ Crores) immediately. We are helpless and going through so much mental pressure as well. Every rupee can help save his life and a moral support to go through this tough phase. Please donate & share widely:
https://t.co/ZVLvgutv5Z
@Moneypurseadv@daytradertelugu@drprashantmish6 sir — please help amplify this life-saving appeal. #SaveBabyFromSMA #SMAawareness #CrowdfundingIndia
📍IMT Manesar, Gurugram, Haryana: While parking a scooty, an overhead electric transformer mounted on a pole fell and struck one person. The pillion rider had already gotten down.
Overhead infrastructure failure poses serious risk.
Avoid standing close to poles/transformers; stay alert while parking.
It started on November 14 2013..
SACHIN TENDULKAR's final Test
The last dance of the man who defined Indian cricket.
It was the day a part of my childhood started saying goodbye..
#ThankYouSachin