Navneet Maheshwar
Child Name:Navneet Maheshwari
Age: 8 Years
Mother’s Name : Preeti Maheshwari
Problem: Atrial septal Defect (ASD)
(ASD)
Treatment at: -Cardiology Department
of G.B Pant Hospital.
With immense pleasure to announce that Navneet Maheshwari has been operated successfully on 11/04/2023 and got discharge on 14/04/2023.
He was admitted on 8th march 2023, but before that his mother Preeti struggled a lot for his treatment. Navneet condition was very critical he couldn’t able to do routine activities as his siblings do normaly.So, PSF submitted the fund for his treatment on 09/01/2023.We got his surgery date after 3 months of submitting the funds. This time was very difficult because in government hospital it takes long waiting time for dates.
We are glad to know that now he is healthy and perfectly fit and fine and doing his routine activities without any difficulty.
Please read below Navneet’s struggle of his life.
Preeti was working in cloth shop as dhaga katne ka kaam, she is having 3 children; 12 years old daughter, 10 years old son and Navneet 8 years old boy was suffering from heart problem.
Navneet 6.5 years old; was suffering with Atrial Septal Defect (ASD) & is under treatment of Dr.Arnima at cardiology department of G.B Pant Hospital, New Delhi.Preeti is staying separately from her husband on rented house and taking care of her 3 children. It wasn’t possible for her to manage his treatment expenses along with other responsibilities.
Doctor advice Preeti for financial support, Preeti can connect to Parivartan Sandesh Foundation, as earlier PSF supported heart surgery in G.B Pant Hospital.
She has applied for support to Parivartan Sandesh Foundation & permitted us to share her family & personal details to explain her situation, so PSF can approach donors to support of her son’s treatment expenses.
Parivartan Sandesh foundation has promised to support as much as possible.
Akanshi
It was the most remembering day for PSF when Shiv Kumar, father of 1 year old Akanshi, came and request to save
her daughter’s life with tears in his eyes. After settee down a bit, he told us about the critical health
condition of Akanshi who was suffering from Congenital Heart Defect (CHD).
Akanshi was born in Delhi and lived in a joint family with her parents. Her father Shiv Kumar works as a peon in
a school at Seema Puri and earns Rs.4000 per month. It was not possible for his family to arrange treatment
expenses and family had no hopes left of seeing their daughter lead a normal life like other children. Suddenly
he came to know about social work performed by the PSF among Leprosy patients at Seema Puri, New Delhi and in
desperation he came at PSF office to seek support.
Next day project coordinator went to meet the doctor who was treating Akanshi after diagnose the defect. The
visit report submit by project coordinator was too shocking as thousands of children were suffering with this
problem at the hospital and from them 80% children belong to deprived section.
After review the need and problem, PSF launch Project “Heart Energize” and Akanshi be the first beneficiary of
this project and surgery conducted free of cost. The prayers of her parents were not left unanswered and Akanshi
was treated successfully on September-2016.
Mahira
Mahira, daughter of Shehzad Alam is a helper at Printing Press who has to feed a family of 5 people. Till the
age of 8 year, Mahira used to fall sick every month and vomit frequently. She also had high fever every second
week ’. She was once rushed to the hospital in the middle of the night when she felt breathless. After a series
of tests Mahira was diagnosed with a hole in the heart- a Congenital Heart Defect. Family was not in a position
to afford the treatment The devastated family reached out to many people for financial help but no one was
forthcoming. Through a patient they came to know about the surgeries being supported by Parivartan Sandesh
Foundation. They Appeal to PSF for her surgery support and she underwent by successful surgery under PSF Project
“Heart Energize”
Sonu
13 year old Sonu is extremely shy but wants to become a police officer when he grows up. The second child of his
parents from the three , he has been pampered by her mother and elder sister. He stays with his family in Delhi
at Jai Prakash Nagar. His father is partially disabled and mother works as packaging labor at a factory in
Gandhi Nagar. They have limited income
Sonu was unlikely to other children fall sick frequently and get tired while perform necessary routine activity,
Very often he felt breathing problem with unusual sweating. Before 2 years of his surgery, his parents misguided
by a local doctor & sonu declared asthmatic.
Day by day his poor health condition force his parents to consult to another doctor and after a number of tests
the doctor advised his parents to consult to cardio doctor. Poor financial condition does not allow them to go
to any private hospital so they visit G.B Pant Hospital, New Delhi where after echo he diagnose with Atrial
Septal Defect (ASD) Heart Defect. However they did not have enough money to pay for immediate surgery. They came
back home with dispirited heart.
His worsening condition took them to hospital very frequently many times he got hospitalised due to critical
condition. After final warning for arrangements of surgery sonu’s mother was crying at hospital corridor when a
staff told her to contact Parivartan Sandesh Foundation, which was already active at the hospital and supported
many children earlier.
With hope in her heart, Sonu’s Mother came to office of Parivartan Sandesh
Foundation to appeal for his treatment support. After one month of her visit at PSF’s office sonu underwent by
successful surgery and now living an normal and healthier life. He is working hard to make his dream alive to
become a Police Inspector.
Simar
Simar is 1 year old. She lives in slums of New Delhi. When she was 7 months old she went for a medical check-up
with a local physician and was diagnosed with a heart problem but due to the lack of resources she was not
diagnosed properly. Her parents took her to government hospital for further treatment, where they get to know
about her problem and expense of treatment. Her father is a Casual worker at Printing Press and earns Rs.4600
per month. He has a family of 5 (including his parents) to support. He cannot afford the cost of surgery and
requested for support from Parivartan Sandesh Foundation
Hamza
Hamza was born with a Congenital Heart Defect. His heart condition was not noticed until he was 8 months old.
When his parents noticed hamza having too much of difficulty while breathing, they also noticed an increased
bluish discoloration on his lips and fingernails. They then started visiting hospitals for treatment. All the
doctors advised them to consult a heart specialist. Since they did not have any money to visit any private multi
specialist hospital they started his treatment at G.B Pant Hospital where he diagnosed with the problem and
needed to undergo an device closure implantation. Due to lack of financial resources his father started
searching for help and his search ended at Parivartan Sandesh Foundation. Hence the child underwent successful
surgery by Dr. Sanjeev Kathuria and living a joyful life with his family.
Rehmat
Rehmat 13 years old, She lives with her parents and 5 siblings in slum at Faridabad mall village. Rehmat is a
charming girl and helps her mother with house work at home. Her father, Aasmohumad, is a labourer earning about
Rs.7500 per month and her mother
Rehmat’s family was aware of her heart problem from an early age. They took her to local medical Institute in
Faridabad where they conducted a Cath Test and found that she needs a surgery. However, due to their financial
conditions they couldn’t get the surgery done and started looking for philanthropic support. Meanwhile they kept
visiting G.B Pant Hospital with the hope of treatment and kept Rehmat under medical management.
One day a PSF Program Officer meet her at G.B Pant Hospital and gather all relevant information about her. After
a week Rehmat get saviour heart pain and difficulty to breath get admitted at local hospital. Where the doctor
suggest to get the surgery done soon & PSF appealed to Fortis Foundation to support her treatment to get surgery
done as soon as possible. And within 7 days Rehmat has a successful surgery at Fortis Faridabad
