Ishnoor foundation - For Care & Support

Ishnoor foundation - For Care & Support This is our NGO,We as providing our best.

31.7.26Sunday time with Bravd hearts in PGI ​Our  deepest gratitude to Sonia Madam for her noble and selfless service. W...
31/07/2026

31.7.26
Sunday time with Bravd hearts in PGI
​Our deepest gratitude to Sonia Madam for her noble and selfless service. Waking up every Sunday to prepare fresh, home-cooked food for the patients and families staying at PGI is a profound act of humanity.
​For those who are far from home, battling long illnesses for months and even years, your meals are so much more than just nourishment—they are a source of comfort, hope, and warmth. Your passion, consistency, and kindness bring immense relief to so many souls during their toughest times.
​ Big Thanks to Sangeeta madam, Iqbal ji, Anil kaushal ji, Avnish jain ji, Dr. Sheena jain, Lavneet........ & your families, for being such an inspiration and for serving the community with all your heart. May you always be blessed with good health and happiness.
​With highest regards and respect,
ICS

26/07/2026

26.7.26

Dileep kumar age 31 yrs is again in PGI for treatment of Entefocutaneous Fisula.
An Enterocutaneous Fistula is an abnormal tunnel connecting the stomach or intestines to the skin, causing digestive contents to leak outward. It is primarily a complication of abdominal surgery. The problem is reported after his Intestinal obstruction after surgery (sx) done about 3 yrs ago, wherein a blockage in the small or large intestine that prevents food, fluids, and gas from passing normally through the digestive tract. It is a well-documented and potentially serious complication of abdominal or pelvic procedures.
He needs support for medicines.
ICS

23.7.26Azamit Bi age 18 yrs from J&K is in PGI for treatment of  Myelofibrosis  ( sudden disorder in functioning of her ...
23/07/2026

23.7.26

Azamit Bi age 18 yrs from J&K is in PGI for treatment of Myelofibrosis ( sudden disorder in functioning of her BoneMarrao,)

Myelofibrosis is a rare, chronic blood cancer characterized by the buildup of severe scar tissue (fibrosis) inside the bone marrow. This scarring directly disrupts the body's normal production of blood cells, providing a definitive explanation for the severe anemia and pancytopenia discussed in your previous queries
Pancytopenia is a serious medical condition where your body has abnormally low counts of all three major blood cell types: red blood cells, white blood cells, and platelets.
Severe anemia is a critical medical condition characterized by a dangerously low level of hemoglobin, typically defined as below 8 grams per deciliter (g/dL). Here in her case the Hb level is 3.8 only. At this level, the body's tissues and organs are severely deprived of the oxygen required to function properly.
She needs support for her medicines.
ICS

22.7.26Appeal from Gurvir's Father for help to save his child " Gurvir Singh is just 12 years old. At an age when most c...
22/07/2026

22.7.26

Appeal from Gurvir's Father for help to save his child
" Gurvir Singh is just 12 years old. At an age when most children are focused on school, friends, and dreams for the future, Gurvir is once again fighting a battle for his life.
Five years ago, he was diagnosed with cancer. After months of painful treatment, medicines, and hospital visits, his family believed the worst was finally behind them. Slowly, life began feeling normal again.
But now, the cancer has returned.
Gurvir has been diagnosed with relapsed CML, and doctors at CMC, Ludhiana have advised an urgent bone marrow transplant (BMT), his only chance at survival.

“For years, we lived with fear every single day. When he started recovering, we thought our son had finally gotten his childhood back. We never imagined we would have to watch him suffer all over again,” says his family. The cheerful young Gurvir who once dreamed of returning to school and playing freely with his friends now spends his days inside hospital rooms, surrounded by medicines and uncertainty.
His father works as a car driver, earning just enough to feed them every month. Every day, he drives for long hours trying to support his family, but the cost of saving his son’s life is far beyond anything he can afford.
The bone marrow transplant will cost ₹30 lakhs.

“We are trying everything we can, but every day feels heavier than the last. As parents, all we want is to see our child healthy again,” his father says quietly. Gurvir has already fought cancer once with incredible courage. Now, he is being forced to fight it again before he has even had the chance to truly live his childhood.
He deserves the chance to go back to school, laugh with his friends, and live without fear.
Today, his family is holding on to hope that kind strangers will help them save their son.

Please come forward and help Gurvir get the life-saving transplant he urgently needs.

Ishnoor Charitable Society - ICS

Nine years have passed  since our  Ishnoor left us on this day 22nd July 2017 @ 1.17am , yet the light she brought into ...
21/07/2026

Nine years have passed since our Ishnoor left us on this day 22nd July 2017 @ 1.17am , yet the light she brought into our lives remains as bright as ever.
​Ishnoor’s memory lives on in every quiet moment, every shared story, and the enduring love that time can never fade. She is deeply missed, fondly remembered, and forever held close in our hearts.
We remember the sheer courage she held within their fragile frame, fighting a fierce battle against leukemia with a bravery that left us all in awe.Though her fierce struggle with leukemia took her from our arms far too soon, it could never dim the beautiful spirit, courage, and grace she showed throughout her fight.
​Time has moved forward, but the love we carry for Ishnoor remains frozen in its purity, untouched by the years. We miss her laughter, her warmth, and the bright spark she brought into our world. Though she is taken from us far too soon, Ishnoor’s beautiful spirit remains stitched into the very fabric of our souls—forever loved, never forgotten, and missed more with each passing day.

Ishnoor's Family

16.7.26Appeal from child family: Five months ago, I was counting my baby's fingers and toes. Today, I'm counting the day...
16/07/2026

16.7.26

Appeal from child family:
Five months ago, I was counting my baby's fingers and toes. Today, I'm counting the days I have left to save him from cancer.
Just one month after my son, Sidharth, was born, I noticed a small swelling below his knee. I thought it was something simple that would go away with medicine. Instead, it turned out to be RT Lower Limb Sarcoma, a rare and aggressive form of cancer.
Today, doctors say he urgently needs chemotherapy, surgery, and radiotherapy to survive. His treatment will cost INR 9,19,000.00.
I knew such a huge amount would be impossible for a family like ours....
When Sidharth was born, my husband Rahul and I were overjoyed. He was our first child, and we spent every day dreaming about the beautiful life ahead of him. But within weeks, those dreams were replaced by hospital corridors, sleepless nights, and fear.
We first visited a nearby doctor, who prescribed medicines and creams. When the swelling continued to grow, we rushed him to a bigger hospital. He was admitted for several days, his tiny leg wrapped in heavy bandages, but nothing improved. From there we were sent to another hospital, then another.
Every doctor gave us new medicines, injections, and tests, but no answers.
One hospital believed the wound was filled with pus and tried repeatedly to drain it. Another warned us that his leg might have to be amputated. Meanwhile, my baby's wound became worse. His bandages were soaked with blood, the infection spread, and the smell from his wound became unbearable. After months of moving from one hospital to another, doctors finally discovered the truth.
My baby had cancer.
“This can’t be true…there must be some mistake. Please check him again!”, I begged the doctors, but all they could do was comfort me and tell my husband about the treatment our son was going to need. I couldn’t process any of it. The complex medical terms kept ringing in my head.
What hurts me most is knowing that even after the diagnosis, his treatment was delayed because of repeated referrals and complications. While precious time passed, my son's condition continued to deteriorate.
Today, at just five months old, Sidharth has already endured countless injections, painful dressings, blood tests, and hospital procedures. His delicate skin has begun peeling from repeated treatments, and every day he cries in pain that he cannot even understand.
My husband works as a daily wage labourer, while my father-in-law is a farmer. Together, they earn barely ₹10,000-12,000 a month, and even that income is uncertain. We have already spent nearly ₹2 lakhs on treatment. My husband exhausted all his savings. My mother-in-law sold her gold, and I mortgaged my jewellery.
“Don’t worry beta…we’ll find way to save him,” my mother-in-law tried to comfort me. All I could do was smile faintly, knowing that now was not the time to lose hope.
Today, we have nothing left. We spend most of our days inside the hospital, worrying not only about our baby's life but also about how we will pay for his next treatment.
Before all this happened, we were simply looking forward to watching our son grow. Now, our only dream is to see him recover, come home, and live the childhood every child deserves.
Every contribution, no matter how small, brings Sidharth one step closer to the treatment that could save his life.
Please stand with us and give my little child the chance to grow up free from cancer.

The specifics of this case have been verified by the medical team at the concerned hospital. For any clarification on the treatment or associated costs, contact the campaign organizer or the medical team.
Charity No : 81675561

ICS

14.7.26Muntun paswan has come to PGI, far away from Bihar for treatment of CKD5 . He is on dialysis & has to wait for ki...
14/07/2026

14.7.26
Muntun paswan has come to PGI, far away from Bihar for treatment of CKD5 . He is on dialysis & has to wait for kidney transplant.
He needs support for medicines.

ICS

14.7.26Ashish, now age 8  yrs is suffering from multiple ailments CKD 3D, anemia & Pyonephrosis, leading to his growth f...
14/07/2026

14.7.26

Ashish, now age 8 yrs is suffering from multiple ailments CKD 3D, anemia & Pyonephrosis, leading to his growth failure.

In Stage 3 CKD, kidneys have mild to moderate damage, and they are less able to filter waste and fluid out of blood. This waste when builds up in body, cause to harm other areas, such as high blood pressure, anemia and problems with bones.

Pyonephrosis is a suppurative infection of upper urinary tract due to obstruction of the ureter. It is usually associated with suppurative damage of renal parenchyma and renal function loss.

Ashish had undergone major surgical procedure. With all grace of God, he is responding well . Child needs medical support for next couple of months.

ICS.

14.7.26Asuvendra Gupta came to PGI from UP for treatment of CKD5, when he suddenly came to know that his creatinine leve...
14/07/2026

14.7.26

Asuvendra Gupta came to PGI from UP for treatment of CKD5, when he suddenly came to know that his creatinine level has shooted up to 17, without any major symptoms. He remained on dialysis from 10.6.24 & has undergone kidney tx on 20.2.25 from his wife as a donor.

He needs mefical support after transplant.

ICS

6.7.26This is the post from help mother of baby Vyom, a 2 year child suffering from  very dreadly  RetinoblastomaEvery d...
06/07/2026

6.7.26
This is the post from help mother of baby Vyom, a 2 year child suffering from very dreadly Retinoblastoma
Every day the tumor in his eye keeps growing bigger and more painful! Help him

Baby Vyom is waiting for funds for treatment from Dharamshila Narayana Superspeciality Hospital, New Delhi.
When doctors told me that my 2-year-old son might lose his eye because of a tumor, I felt like the world stopped around me. I could not breathe, I could not think, and I could not accept what I was hearing.
My little boy, Vyom, who should be spending his days playing with his bat and ball, is now fighting a tumor in his eye. Doctors have advised urgent surgery, ICU care, prolonged hospitalization, and intensive monitoring that could cost nearly INR 11,87,000.00!
We have already spent ₹5-6 lakhs and sold all the gold we owned, but my child’s treatment is still far from over.
It all began in January 2025 when I noticed a tiny pearl-like bump on the white part of his right eye. At first, we thought it was a minor infection that would go away with medicines. But one morning, Vyom woke up crying in pain, and the strange bump had become much more visible.
As parents, we were terrified.
We rushed him from one doctor to another, hoping someone would tell us it was nothing serious. Weeks turned into months. We travelled to multiple hospitals, underwent countless tests, and spent whatever little money we had. Yet no one could tell us exactly what was wrong.
Then, in March 2025, we received the news that shattered our family.
Doctors confirmed that the growth inside my son's eye was a tumor.
But the worst moment came when they told us that his eye might have to be removed. “This…this isn’t real right?” I kept asking my husband over and over again.
I remember crying endlessly. How could a two-year-old child lose his eye? How could a mother accept something like that?
Refusing to give up, we continued searching for answers and treatment options. Today, Vyom is admitted at Dharamshila Narayana Superspeciality Hospital, where doctors are trying everything possible to save him.
He now requires surgery under Pediatric Surgical Oncology care, along with ICU support, medicines, investigations, and continuous monitoring. The estimated treatment cost is INR 11,87,000.00.
For our family, this amount is unimaginable.
My husband is a daily wage labourer who earns barely ₹8,000-10,000 a month. Even before Vyom fell sick, providing for our family of six was a daily struggle. Now, because of hospital visits and caregiving responsibilities, he is unable to work regularly.
We have already spent ₹5-6 lakhs and sold every piece of gold we had.
“I’ll do everything within my power to save him. Don't worry,” my husband keeps telling me, trying to console me.
The hardest part is watching Vyom struggle to see properly through his right eye. Whenever he becomes restless or starts crying, we hold him tightly and try to comfort him. He used to love playing with his bat and ball, but now he rarely touches them.
Seeing that change breaks my heart every day.
As parents, we have only one dream: to see our son healthy again. We want him to go to school, study well, and grow up like every other child. Once he recovers, we want to take him to Vrindavan and thank God for giving our son a second chance at life.
Today, I fold my hands before you and ask for your support. Please help us save Vyom’s vision and his future. Every contribution can bring him one step closer to the treatment he urgently needs.
Please help him live without pain.

The specifics of this case have been verified by the medical team at the concerned hospital. For any clarification on the treatment or associated costs, contact the campaign organizer or the medical team.
Charity No : 81675537

The patient is currently at home waiting for the sufficient funds to be raised. Delay in treatment has high risk of spread to other eye & brain.

ICS

Address

Mohali
Mohali

Telephone

+919501043222

Website

Alerts

Be the first to know and let us send you an email when Ishnoor foundation - For Care & Support posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organization

Send a message to Ishnoor foundation - For Care & Support:

Shortcuts

Share