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Apple a Day Isn't Enough, Speak out against discrimination of Medical & Health Rights Learn More

 

Uday Foundation's Storyteller Program :Our storyteller program is an immersion program that offers volunteers story telling and book reading opportunities for students, professionals, celebrities and anyone to read stories to little patients at bedside of children ward in the hospital.. Click Here

RareBloodGroups.Org :Arranging rare blood group is always a tough task as awareness on these ailments is still low and usually getting started on the search for rare blood groups draws a blank with most people. RareBloodGroups.Org : India’s 1st online registry of rare blood type donors including AB Negative, A Negative, B Negative, O Negative and Bombay Blood Type . learn more.

Anorectal Malformation and Associated Congenital Defects : This project is supported by World Anorectal Malformation Association with common goal to support children with anorectal malformation and associated birth defect. Learn More.

Intersex / DSD ( Disorders of Sex Development) : Uday Foundation is devoted to systemic change to end shame, secrecy, and unwanted genital surgeries for children born with an anatomy that someone decided is not standard for male or female. In India Intersexuality is primarily a problem of stigma and trauma, not gender. Learn More

Congenital Heart Defects : 3-8 children out of every thousand live births are born with heart disorders and two-thirds of them are liable to die before they cross their first birthday. Key Result Area of this project is to to give underprivileged children in India born with heart diseases appropriate treatment. Uday Foundation aims to assist early diagnosis and availability of monetary assistance for diagnostic purposes and surgical interventions. Learn More

 

The other key result area of the Uday Foundation are :-

To impart and promote the imparting of awareness and support on birth defects and registry of Rare Blood Groups Donors.

To promote the rights of new born and children with birth defects through the influence of public policy and social awareness.

To develop partnerships and initiate programmes which empower and improve the well-being of children with birth defects, malformation & associated anomalies

To sustain our initiatives on awareness about birth defects through the development of a sound financial and knowledge support base.

To provide essential information & support on birth defects & associated problems

To create awareness about importance of voluntary blood donation.

To represent a valid working tool for the clinicians, to be an important source of information for lay people (affected individuals, their families and the community)

To maintain Registry of RH Negative Blood Donors including AB Negative , B Negative , O Negative and A Negative ( All Rare Blood Type ).

To provide Rare Blood Donors to critically ill patients , children with congenital defects , surgery , pregnant women , Anemia , Road Accident , Excessive Destruction of Red Blood Cells , Thalassemia , Sickle Cell Anemia , Hemophilia ,Leukemia , Bone Marrow Transplant ect ( incase of rare blood groups types . i.e AB Negative , O Negative , B Negative and A Negative ) .

To initiate and execute project relating to AIDS awareness through the respective Governments and Non-Government Organisations for the welfare and benefit of the people and the society.

To initiate and execute any project relating to social and areal development through the respective Governments and Non-Government Organisations for the welfare and benefit of the people and the society.

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