Beg Family's 3 precious girls

What is worse than looking in to the eyes of your three beautiful daughters and knowing they are going to die soon.


Abeerah, Khansa and Zahra are diagnosed with Sanfilippo Syndrome also known as MPS-III type B.

MPS is a rare, fatal genetic disorder.

Children with MPS are missing a vital enzyme, which the body uses to break down and recycle dead cells. In results the body is unable to have a proper recycling process. This causes storage of dead cells in every part of the body. Storage of these cells stops proper performance and leaves progressive damage to the brain, joints, vital organs, respiratory and central nervous system.



Children with this disorder begin life normally.
The Beg girls were bright and happy babies and toddlers like any other normal children. By age three, they slowly and subtly started to change. They lost their ability to speak and became hyperactive and difficult behavior. They won't sleep, sometimes they stay awake for days. They have lost hearing and have several dental problems.
Children with the Sanfillipo Syndrome suffer from constant diarrhea, runny nose  and nonstop of chewing anything they can get hold of.




Eventually they will lose their ability to walk, hear, see and even swollow their own food. At some point they start having seizures.


MPS kids lose a little more of their life each day.

After many medical problems, pains and suffering, they can not survive.
Children with Sanfilippo Syndrome do not live past the ages of 11 - 14 years and there is no cure.