Our Son’s World Has Turned Upside Down – He Will Die Without Your Support
Our Son’s World Has Turned Upside Down – He Will Die Without Your Support
Help Angad fight Duchenne Muscular Dystrophy (DMD), a rare genetic disorder. This is our race against time, and every second counts. Join us in giving Angad a chance at life.
Help Angad fight Duchenne Muscular Dystrophy (DMD), a rare genetic disorder. This is our race against time, and every second counts. Join us in giving Angad a chance at life.
A Parent’s Worst Nightmare
A Parent’s Worst Nightmare
“Mumma, why do I fall so much? Why can’t I walk like other kids?”
“Mumma, why do I fall so much? Why can’t I walk like other kids?”
- Angad, 20 months old
- Angad, 20 months old
- Angad, 20 months old
Two weeks after Angad’s diagnosis, he began to notice the world moving past him. Frequent doctor visits and physiotherapy sessions left him confused and upset. He would look at his mother with questioning eyes, using toddler’s sign language to ask why he couldn’t stand or run like other children.
No parent should ever have to answer questions like these. Yet, here we are—faced with the task of explaining a life-altering condition to our baby boy. DMD doesn’t just steal away a child’s strength; it can eventually claim their life. But with your help, we can turn this around and give Angad the future he deserves.
The Race Against Time
Duchenne Muscular Dystrophy is relentless, but there is hope. With advanced medical care, therapies, and emerging treatments, Angad has a chance to enjoy a more fulfilling life. Unfortunately, the cost of these treatments is overwhelming:
Duchenne Muscular Dystrophy is relentless, but there is hope. With advanced medical care, therapies, and emerging treatments, Angad has a chance to enjoy a more fulfilling life. Unfortunately, the cost of these treatments is overwhelming:
₹26 crore is needed for a revolutionary treatment to halt DMD’s progression.
₹26 crore is needed for a revolutionary treatment to halt DMD’s progression.
₹26 crore is needed for a revolutionary treatment to halt DMD’s progression.
We’re reaching out to kind-hearted people like you to help bridge this gap.
We’re reaching out to kind-hearted people like you to help bridge this gap.
We’re reaching out to kind-hearted people like you to help bridge this gap.
No family can bear this burden alone. With your support, nothing is impossible.
No family can bear this burden alone. With your support, nothing is impossible.
Your Support Can Save a Life
Your Support Can
Save a Life
Donate
Donate
Your generosity, no matter the amount, brings us closer to our ₹26 crore goal. Every rupee matters and contributes directly to Angad’s treatment.
Your generosity, no matter the amount, brings us closer to our ₹26 crore goal. Every rupee matters and contributes directly to Angad’s treatment.
Your generosity, no matter the amount, brings us closer to our ₹26 crore goal. Every rupee matters and contributes directly to Angad’s treatment.
Spread the Word
Spread the Word
Share our campaign on social media, with friends, family, and colleagues. Awareness is power, and the more people know, the stronger our collective impact.
Share our campaign on social media, with friends, family, and colleagues. Awareness is power, and the more people know, the stronger our collective impact.
Corporate Support & CSR
Corporate Support & CSR
If you represent an organization, your sponsorship or CSR contribution can make a monumental difference. We would be grateful for any form of partnership or fundraising efforts.
If you represent an organization, your sponsorship or CSR contribution can make a monumental difference. We would be grateful for any form of partnership or fundraising efforts.
Stories of Kindness and Hope
“I came across Angad’s story and felt compelled to help. Knowing my contribution could save a life was incredibly fulfilling.”
“I came across Angad’s story and felt compelled to help. Knowing my contribution could save a life was incredibly fulfilling.”
– Sarthak Jain
– Sarthak Jain
“As a DMD survivor family, we understand the challenges. We’re proud to support Angad and hope others do too.”
“As a DMD survivor family, we understand the challenges. We’re proud to support Angad and hope others do too.”
– Rishabh Dubey
– Rishabh Dubey
“We pray for Angad. May God bless you with grace to fight this evil disease.”
“We pray for Angad. May God bless you with grace to fight this evil disease.”
– Ramanan M
– Ramanan M
These testimonials serve as a reminder that we are not alone in this fight and that every act of kindness—big or small—makes an impact.
These testimonials serve as a reminder that we are not alone in this fight and that every act of kindness—big or small—makes an impact.
These testimonials serve as a reminder that we are not alone in this fight and that every act of kindness—big or small—makes an impact.
Frequently Asked Questions
What is Duchenne Muscular Dystrophy (DMD)?
What is Duchenne Muscular Dystrophy (DMD)?
DMD is a rare genetic disorder causing progressive muscle weakness and degeneration. Over time, it affects the ability to move, breathe, and live independently.
DMD is a rare genetic disorder causing progressive muscle weakness and degeneration. Over time, it affects the ability to move, breathe, and live independently.
How will my funds be used?
How will my funds be used?
Your donations go directly towards Angad’s medical treatment, including specialized therapies, hospital visits, potential gene therapy, and other supportive care essential for managing DMD.
Your donations go directly towards Angad’s medical treatment, including specialized therapies, hospital visits, potential gene therapy, and other supportive care essential for managing DMD.
Is my donation secure?
Is my donation secure?
Yes. We use a reputable, secure payment gateway to ensure every donation is protected.
Yes. We use a reputable, secure payment gateway to ensure every donation is protected.
Are donations tax-deductible?
Are donations tax-deductible?
This depends on the regulations in your country/region. We are exploring ways to provide tax relief and will update the website once confirmed.
This depends on the regulations in your country/region. We are exploring ways to provide tax relief and will update the website once confirmed.
How can I stay updated on Angad’s progress?
How can I stay updated on Angad’s progress?
We will post regular updates on this website and social media. Once you donate, you can also opt-in for email updates to follow Angad’s journey.
We will post regular updates on this website and social media. Once you donate, you can also opt-in for email updates to follow Angad’s journey.
We’d Love to Hear From You!
Do you have questions or want to learn more about how to help? Reach out to us anytime:
Do you have questions or want to learn more about how to help? Reach out to us anytime:
harmeet.kaur.khurana.1992@gmail.com
standforangad@gmail.com
harmeet.kaur.khurana.1992@gmail.com
standforangad@gmail.com
Phone: +91 7022 90 8055
Phone: +91 7022 90 8055
Address: G 026, Ananth Nagar Phase 1, Electronic City Phase 2, Bengaluru, Karnataka 560100
Address: G 026, Ananth Nagar Phase 1, Electronic City Phase 2, Bengaluru, Karnataka 560100
Follow Angad’s Journey on Social Media
Follow Angad’s Journey on Social Media
Thank you for supporting Angad in his fight against Duchenne Muscular Dystrophy. Your kindness and generosity mean the world to us. Let’s make every moment count.
Thank you for supporting Angad in his fight against Duchenne Muscular Dystrophy. Your kindness and generosity mean the world to us. Let’s make every moment count.