CLF in the news

Sun, 30 Aug 2015

Aayushi Pratap
htmetro@hindustantimes.com

Fellow patients to share rare drug with Pakistan teenager

A group of patients, who attended a gathering on Wilson’s Disease at the Tata Memorial Hospital, have volunteered to give her (Saba Ahmed) the tablets after learning about her struggles.
DR ABHA NAGRAL

MUMBAI: Doctors at Jaslok Hospital, Peddar Road, will finally be able to give Pakistan citizen Saba Ahmed a new drug after she was unable to tolerate the standard drug given to most Wilson’s Disease patients.

Source/ Reference : http://timesofindia.indiatimes.com/city/mumbai/Pak-girls-health-improvin...
TNN | Aug 30, 2015
Mumbai: Saba Ahmed, the 15-year-old Pakistani girl who was rushed to Mumbai due to complications of a rare genetic disorder, was well enough within a week to attend a support group meeting on Saturday.

Ordinary Mumbaikars raised over Rs 3.5 lakh through a crowd-funding effort to help the teenager fly into Mumbai last week from Karachi for treatment of Wilson's Disease. Her mother Nazia said, "We found out she had Wilson's disease 18 months ago. When doctors back home told me that Saba would never again speak or walk, we came to Mumbai."

Wilson's Disease is a rare genetic disease linked with copper depositing in the tissues and cells of the diagnosed. This disease turns untreatable in the later stages, but it is curable if it is detected early.
 
Dr. Aabha Nagral, presently treating around hundreds of patients suffering from Wilson's disease, defined WD. as an unexplainable chronic disease, which needs to be monitored well by experts.
This disease can be identified easily in patients.
 

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