देश के विकास के लिए जरूरी कदम उठाए गए उसके लिए हम दिल से प्रधान मंत्री जी का आभार व्यक्त करते है

आदरणीय प्रधान सेवक महोदय,आजकल देश के कुछ राज्यो में महिलाओं के आत्म सम्मान के साथ खिलवाड़ किया जा रहा है,चूँकि प्रधानमंत्री एक मुखिया होता है देश का ।क्या प्रधानमंत्री जी देश के किसी भी राज्य सरकार को कार्यवाही का आदेश नही दे सकते। क्या राज्य सरकार की शक्तियां केंद्र सरकार से ज्यादा है? राज्य अपनी राजनीतिक लाभ के रूप में इस घटनाक्रम का उपयोग कर रहे है। क्या महिलाओं का कोई सम्मान,सुरक्षा नही होगी अब देश मे जहाँ नारी को देवी के रूप में पूजा जाता है।

namasthe most respected PM ji, sir in INDIA our kids are having academic year from JUNE to MARCH. I personally feel that schools must be given monsoon holidays rather than summer holidays. Half days in summer should not be there sir. during monsoon kids get infected so fast from kid to kid due to seasons diseases, and special care is needed during summer in HOT SUN kids are coming home where sometimes kids are getting fainted also. if full day is RUN during summer kids will have healthy quality time in school sir. please look into our INDIAN education system Academic year. You are the only person whom we can rely on to BRING change in the kids life.

Sir, I'm Niyant Patel from Bhavnagar, Gujarat. My friend Jeet Bhatt is a patient of Friedreich's ataxia. It gradually push the person from Chair to Wheelchar and then wheelchair to Bed. Friedreich's ataxia (FA) is a crippling Rare genetic disease that shortens life quality. Patient faces lot of physical health challenges including walking, speaking and unable to support themselves as disease progresses. It's doesn't affects their cognitive skills. Please bring the only approved first medicine named Skyclarys to India and help Indian patients get it as currently its available only in USA. Also, bring clinical trials to India. AIIMS Delhi well is aware of such patients' existence and struggles. They are also trying hard to get in touch with MoHFW to include this disease in National Rare Disease Policy.. The efforts are still on.. We request you to help them in their efforts to get the disease listed in National Policy of Rare Disease if possible Regards Niyant Patel

माननीय श्री नरेंद्र मोदी जी आपसे विनम्र निवेदन है कि देश में Malnutrition की बडी समस्या है और गरीब बच्चे इसके शिकार हो रहे है कृपया इस विषय पे आप अपनी मन की बात मे बात जरूर करे और उसका समाधान भी करे

Hi sir, Am Pradeep Kumar from Bangalore Nowadays I can see many young people are addicted in betting apps in India ,am also the one of the person in that category, In my life I did big mistake,I was very good in studies ,I completed my MBA in Mysuru with out anyone support,in that time I working part time jobs in hotels ,after that I got job in HPI and DXC technology,they recognised my work and they sent Canada ,France and other countries for work ,but after lock down someone suggested me Pari match betting app ,initially I was not interested but I started to play and I last more than 40 lakhs , I suffered so much , I given so much problems to my family ,now I lost everyone in my life ,all are saying ,your waste fellow ,you don’t deserve to live ,go and die , now I have good job in genpact,but mentally am unable to concentrate my work ,am lossing everything in my life ,don’t know what to do ,I want my life back ,I want my normal life ,there is no one is there to support me.

Dear Sir, I'm Bhargav from Bhavnagar. My brother-in-law Jeet Bhatt is a patient of Friedreich's ataxia. It gradually push the person from Chair to Wheelchar and then wheelchair to Bed. Friedreich's ataxia (FA) is a crippling Rare genetic disease that shortens life quality. Patient faces lot of physical health challenges including walking, speaking and unable to support themselves as disease progresses. It's doesn't affects their cognitive skills. Please bring the only approved first medicine named Skyclarys to India and help Indian patients get it as currently its available only in USA. Also, bring clinical trials to India. AIIMS Delhi well is aware of such patients' existence and struggles. They are also trying hard to get in touch with MoHFW to include this disease in National Rare Disease Policy.. The efforts are still on.. We request you to help them in their efforts to get the disease listed in National Policy of Rare Disease if possible Regards Bhargav

Sir, I'm Viraj Shah from Ahmedabad. My friend Jeet Bhatt is a patient of Friedreich's ataxia. It gradually push the person from Chair to Wheelchar and then wheelchair to Bed. Friedreich's ataxia (FA) is a crippling Rare genetic disease that shortens life quality. Patient faces lot of physical health challenges including walking, speaking and unable to support themselves as disease progresses. It's doesn't affects their cognitive skills. Please bring the only approved first medicine named Skyclarys to India and help Indian patients get it as currently its available only in USA. Also, bring clinical trials to India. AIIMS Delhi well is aware of such patients' existence and struggles. They are also trying hard to get in touch with MoHFW to include this disease in National Rare Disease Policy.. The efforts are still on.. We request you to help them in their efforts to get the disease listed in National Policy of Rare Disease if possible Regards Viraj Shah

Greetings to the Prime Minister of India. My hearty congratulations for nice initiatives and success in Digital India of India. This not only facilitates transparency but also encourages the participation of citizens and leads to data-driven decision-making. In order to achieve this effectively Centralized Skill Based Education System (CSBE) is needed for this hour. Essential skills utilisng online citizen services introduced under your leadership, Electrical Restoring Technique, electronic equipment repairing, electric vehicle repairing, Health services like first aid/injection/ dressing,, river irrigation management , disaster management etc. So 12th pass students should have skills , ready to get job where as current education system is lacking of it. It also motivates our future generation on right path right carrier with ethics taught by our ancestors

Sir, I'm Shreya Bhatt. My brother Jeet Bhatt is a patient of Friedreich's ataxia. It gradually push the person from Chair to Wheelchar and then wheelchair to Bed. Friedreich's ataxia (FA) is a crippling Rare genetic disease that shortens life quality. Patient faces lot of physical health challenges including walking, speaking and unable to support themselves as disease progresses. It's doesn't affects their cognitive skills. Please bring the only approved first medicine named Skyclarys to India and help Indian patients get it as currently its available only in USA. Also, bring clinical trials to India. AIIMS Delhi well is aware of such patients' existence and struggles. They are also trying hard to get in touch with MoHFW to include this disease in National Rare Disease Policy.. The efforts are still on.. We request you to help them in their efforts to get the disease listed in National Policy of Rare Disease if possible Regards Shreya