Help to save Little warrior against Naimann pick type A

Help to save Little warrior against Naimann pick type A Help to save a young life from Naimann pick type A

09/01/2026

Help to Save Little Warrior –
Hello, and thank you for visiting our page.
This page is dedicated to our beloved son,, who is bravely fighting a rare and life-threatening genetic disorder called Niemann-Pick Disease Type A.
🧬 Medical Background
Niemann-Pick Type A is a very rare inherited genetic disease. It occurs when both parents unknowingly carry a faulty gene. Sadly, this disease is not caused by lifestyle, food, or infection—it is something that comes by the will of God and genetics.
Our family has a history of genetic illness, which we only discovered after our child became sick.
🏥 What Our Son Is Facing
Due to this disease, our son suffers from:
Severe weakness and delayed development
Recurrent chest infections and breathing problems
Enlarged liver and spleen
Feeding difficulties and poor weight gain
A very low immune system
💔 Winter is especially dangerous for him. Even a simple cold can become life-threatening, and doctors often advise hospital admission, but unfortunately, we struggle with the cost.
👨‍👩‍👦 Parents’ Fight
We are parents just like you—doing everything humanly possible to save our child.
We have consulted doctors, genetic specialists, and hospitals. We are ready to provide:
Medical reports
Doctor prescriptions
Test results
Hospital documents
This page exists for awareness, honesty, and hope.
🤍 Why We Need Support
Treatment, frequent hospitalizations, medicines, and tests are very expensive, and we cannot manage this alone. Many parents of rare disease children survive only because of the kindness of others.



💔 A Father’s Cry for Help 💔My little son is suffering from Niemann-Pick disease, a rare and painful illness. Because of ...
18/08/2025

💔 A Father’s Cry for Help 💔

My little son is suffering from Niemann-Pick disease, a rare and painful illness. Because of this disease, fluid keeps building in his small body. The only way to manage it is through albumin treatment, which he needs every month. The cost is around 200 USD monthly, and for us this is extremely difficult to manage.

We belong to a poor country where people do not have resources for such expensive treatment. Every day is a struggle to arrange his medicine on time, and as parents, it breaks our hearts to see our child suffering.
🙏 I am humbly requesting you—please keep my son in your prayers, and if you can, kindly support his treatment or share our fundraising link with your family, friends, or community. Even the smallest help or a simple share can bring hope for my son’s life.

👉 Fundraising Link https://whydonate.com/en/fundraising/-urgent-appeal-save-a-young-life-from-niemannpick-disease

I am also tagging Niemann-Pick related groups in hope that more kind hearts will see this and help. Please, together we can give my little boy a chance. 💙




Ateeq Khalid Needs Your Help | As a devoted father from Pakistan, I'm reaching out with a desperate plea for help to save my 1.5-year-old son's life. Diagnosed with Niemann-Pick disease, h...

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Islamabad
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