Know Better About Child Heart Foundation

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ANANTIKA, 9 Yrs Was diagnosed with congenital
heart block, revision of Pacemaker was required.
Is a healthy happy child now
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ABOUT US

• Child Heart Foundation is a registered Trust ,
  under Trust Act 1882
• CHF was started with an idea by parents who have
  been through similar situations and have gotten
  over with their tough part of life and now want
  to contribute to the underprivileged families

Ayman Wani, 1 Year needs an ASD Device Closure
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Our statutory governance
Ishika, 9 Years had undergone VSD Closure
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ORGANISATIONAL BACKGROUND

• We work with children diagnosed with congenital
  heart defects, born in underprivileged families
• Our focus is to help the families who are
  indigent or needy and cant meet the financial
  requirements for heart surgery or intervention.

Mishti when she had surgery
Misthi, now 4 years old after
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Congenital Heart Disease is any heart
abnormality present at birth
On an average 1,75,000 CHD children born in
INDIA every year

• Congenital heart disease affects 1 child in every
  100 live births in INDIA
• Only approx 15,000 heart surgeries are performed
  every year

YUVAAN has got treated AYMAN, 3.5 years old, is
waiting for funds
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OUR VISION

• Early diagnosis of child heart disease (CHD) in
  India,

• To have regional Pediatric Cardiac Centers in all
  states where economically challenged patients can
  seek best of treatment and free of cost

• Pediatric cardiac treatment should be within
  reach of every child, irrespective of
• their financial, gender, caste, religion or
  social and economic background

Zohair, 4.5 Years needs an ASD Device Closure
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OUR MISSION

• To educate the next generation of leaders in
  child health
• Define and cascade steps for pediatric cardiac
  centers in all the cities of India which works
  specifically for under privileged people

• To become a helping hand for the Government
  bodies for the treatment of marginalized children
  born with congenital heart disease

DIVYANSHI, 1.5 year old, needs a TOF repair, also
DOWN Syndrome patient
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OUR VALUES
DIVYANSHI, 1.5 year old, needs a TOF repair, also
DOWN Syndrome patient
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Hard facts

• We have only 250 trained pediatric cardiologists
  in India
• Only 15 doctors are getting trained per year
• We require 1 pediatric cardiologist/ District

Viraaz, 6 Months Undergone Balloon Aortic
Valvuloplasty
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Hard facts

• Most of the congenital heart patients require
  treatment in first year of their life
• Poor parents find it impossible to raise funds
  for treatment which can run into lakhs. They end
  up losing their children

Vineet, 5 Year Had undergone an open heart
surgery and is healthy now
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Hard Facts
Angshu, 1 Year Needs a PDA Device Closure

• The waiting period at Government hospitals is too
  long as the patient load is too high.
• Lack of specialized infrastructure required for
  treatment.

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Our Project SDG

• CSR Act
• SDG 3 (good health and well being)
• SDG 4( Quality education)
• Schedule 7, Clause 4 ( reducing child mortality)
• Clause 2 ( promoting education)

Ishika, 9 Years had undergone VSD Closure
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OUR PROJECTS
Ritik, 1 Year Requires BT Shunt
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OUR PROJECTS
Viraaz,6 Months Undergone Balloon Aortic
Valvuloplasty
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Our other commitments
Pihu Jaiswal, 3 Years has undergone TOF Repair

• Advocacy in child right
• Child Heart Foundation had a major role to play
  in bringing back the Furoped, a very important
  cardiac medicines for infants in the market after
  the manufacturing was stopped due to price
  capping by NPPA

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OUR IMPACT
AYMAN, 1 Year Needs an ASD Closure
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OUR IMPACT
Anantika, 9 Years Leading a healthy life Post
surgery
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For further queries

• Ms. Sunita Harkar Shalla
• sunita_at_childheartfoundation.com
• 91-9999142268 011-40519163
• Address 130 Uday Park,New Delhi 110049
• Email info_at_childheartfoundation.com
• Website www.childheartfoundation.com
• www.facebook.com/childheartfoundation/

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Join hands with us to create a whirls with
healthy and happy children !!!
Sanatan
Abir
Kartik
Yuvaan
Mishti
Anantika
Pihu
Monica