@Bezawada_Alludu Garu,
Respect. 👏
Many people tweet for a day and move on, but you backed your words with action by traveling from Chennai to Delhi.
The best part is that you may support a political party, you're not afraid to question it when it's wrong. That kind of honesty and consistency is rare. Keep raising your voice.
Hear out
Emotional Bangalore school principal voice
లాస్ట్ కి "It's not my country" అనే దాకా తెచ్చారు
Not only her, today morning మా సొసైటీలో బ్లైండ్ గా మోడీ భజన చేసే భక్తులు కూడా భూతులు తిడుతున్నారు
Only Accountability matters, nothing will side track this issue...
. @naralokesh Anna ❤️
Asalu oka page lo English inko page lo Telugu aa thought ki hatsoff anna ❤️
Quality Books
6 th Class Nunchi AI 👌
Oka student ki inthakanna em kavali.
I saw someone post on here claiming that Ganguly’s only career highlight was waving his shirt at Lord's. This video is for anyone who needs a reminder of who actually transformed the Indian cricket team into the world-beaters we see today.
@SGanguly99 #indiancricketteam
@ChikouTrader - Thank you very much, sir. 🙏
We are deeply touched by your generous contribution and by the effort you've taken to spread awareness about my son's fundraiser through your official platforms.Your support means more to our family than words can express.
Words cannot express our gratitude. We will remain forever grateful.
@MusicThaman - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@vamsi84 - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@tarak9999 - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@JanaSenaParty - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@brahmaninara@ntrtrust - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@revanth_anumula@TelanganaCMO - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@manabalayya@Nandamurifans - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@KTRBRS - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@JaiTDP - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@naralokesh@AndhraPradeshCM@ncbn - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@PawanKalyan@APDeputyCMO - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@ncbn@naralokesh - A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight.
https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease #Luxturna #GeneTherapy #SaveVision #RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836
@HeroManoj1 -
- A rare genetic eye disorder (RPE65 Gene Mutation – Retinal Dystrophy) is slowly taking away Karthikeya's vision. The only treatment, Luxturna gene therapy, can help save his eyesight, but it costs nearly ₹7 crore—far beyond family's means. We humbly seek your support in giving him a chance to see. An RT from you will greatly help increase the reach of the fundraiser and give him a chance to save his eyesight. https://t.co/G3i8ataNaa
https://t.co/MBXHkjfQVO
#RaraEyeDisease
#Luxturna
#GeneTherapy
#SaveVision
#RPE65
👁️ A 3 Year Old Child May Lose His Vision. We Can Still Help. 🙏
One of our subscribers, Naresh, has reached out to me for help with a fundraising cause.
This is for a 3 year old child, Karthikeya, who is battling a rare inherited retinal disease caused by an RPE65 mutation. The child needs Luxturna gene therapy, and this fundraiser is being done to help preserve his eyesight.
Just imagine a child who has not even fully seen the world yet, slowly losing the ability to see it. 💔
At this age, children should be running, playing, learning colours, recognising faces, and seeing their parents smile.
But this family is fighting something no parent should ever have to fight alone.
I am sharing this here purely out of compassion. 🙏
I want to clearly mention that I am not taking any cut,
commission, benefit, or percentage from this fundraiser.
I am only posting this because a subscriber requested support, and I felt this cause deserves visibility.
I have personally contributed a small amount to this cause, and I will also be contributing a portion of my revenue towards supporting this baby. 🙏
Sometimes charts, markets, profits, targets, and trades can wait.
When a child’s vision is at stake, even a small contribution from many people can become life changing support for the family.
If you are in a position to help, please contribute whatever amount is comfortable for you. Even ₹100, ₹500, or ₹1,000 can matter when many hearts come together. ❤️
Also, if any of you are able to connect this family with any organisation, company, NGO, trust, foundation, hospital support group, or CSR team that can support through CSR funds or medical assistance, I sincerely request you to please help.
Even one right connection can make a huge difference.
Fundraiser link:
https://t.co/kVJw5ZE9gZ
Please contribute only after doing your own verification and only if you genuinely wish to support.
Let us show that this community is not only about markets, but also about humanity. 🙏
Contact: Naresh
9676485836