Deprecated (16384): The ArrayAccess methods will be removed in 4.0.0.Use getParam(), getData() and getQuery() instead. - /home/brlfuser/public_html/src/Controller/ArtileDetailController.php, line: 73
 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php. [CORE/src/Core/functions.php, line 311]
Code Context


        trigger_error($message, E_USER_DEPRECATED);

    }
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 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php.'
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deprecationWarning - CORE/src/Core/functions.php, line 311
Cake\Http\ServerRequest::offsetGet() - CORE/src/Http/ServerRequest.php, line 2421
App\Controller\ArtileDetailController::printArticle() - APP/Controller/ArtileDetailController.php, line 73
Cake\Controller\Controller::invokeAction() - CORE/src/Controller/Controller.php, line 610
Cake\Http\ActionDispatcher::_invoke() - CORE/src/Http/ActionDispatcher.php, line 120
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Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
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Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\AssetMiddleware::__invoke() - CORE/src/Routing/Middleware/AssetMiddleware.php, line 88
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Error\Middleware\ErrorHandlerMiddleware::__invoke() - CORE/src/Error/Middleware/ErrorHandlerMiddleware.php, line 96
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Http\Runner::run() - CORE/src/Http/Runner.php, line 51
Cake\Http\Server::run() - CORE/src/Http/Server.php, line 98

Deprecated (16384): The ArrayAccess methods will be removed in 4.0.0.Use getParam(), getData() and getQuery() instead. - /home/brlfuser/public_html/src/Controller/ArtileDetailController.php, line: 74
 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php. [CORE/src/Core/functions.php, line 311]
Code Context


        trigger_error($message, E_USER_DEPRECATED);

    }
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 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php.'
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deprecationWarning - CORE/src/Core/functions.php, line 311
Cake\Http\ServerRequest::offsetGet() - CORE/src/Http/ServerRequest.php, line 2421
App\Controller\ArtileDetailController::printArticle() - APP/Controller/ArtileDetailController.php, line 74
Cake\Controller\Controller::invokeAction() - CORE/src/Controller/Controller.php, line 610
Cake\Http\ActionDispatcher::_invoke() - CORE/src/Http/ActionDispatcher.php, line 120
Cake\Http\ActionDispatcher::dispatch() - CORE/src/Http/ActionDispatcher.php, line 94
Cake\Http\BaseApplication::__invoke() - CORE/src/Http/BaseApplication.php, line 235
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\RoutingMiddleware::__invoke() - CORE/src/Routing/Middleware/RoutingMiddleware.php, line 162
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\AssetMiddleware::__invoke() - CORE/src/Routing/Middleware/AssetMiddleware.php, line 88
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Error\Middleware\ErrorHandlerMiddleware::__invoke() - CORE/src/Error/Middleware/ErrorHandlerMiddleware.php, line 96
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Http\Runner::run() - CORE/src/Http/Runner.php, line 51
Cake\Http\Server::run() - CORE/src/Http/Server.php, line 98

Warning (512): Unable to emit headers. Headers sent in file=/home/brlfuser/public_html/vendor/cakephp/cakephp/src/Error/Debugger.php line=853 [CORE/src/Http/ResponseEmitter.php, line 48]
Code Context
            if (Configure::read('debug')) {

                trigger_error($message, E_USER_WARNING);

            } else {
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
&lt;/div&gt;
&lt;div align=&quot;justify&quot;&gt;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;,
	&#039;disp&#039; =&gt; &#039;&lt;div align=&quot;justify&quot;&gt;-The Hindu&lt;br /&gt;&lt;br /&gt;&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;&lt;br /&gt;Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;&lt;br /&gt;What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;&lt;br /&gt;Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;&lt;br /&gt;As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;&lt;br /&gt;Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;&lt;br /&gt;&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;&lt;br /&gt;When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;&lt;br /&gt;&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;&lt;br /&gt;On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&amp;nbsp;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&lt;em&gt;The Times of India, 12 October, 2015, please &lt;a href=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot; title=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot;&gt;click here&lt;/a&gt; to access &lt;/em&gt;&lt;br /&gt;&lt;/div&gt;&#039;,
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
&lt;/div&gt;
&lt;div align=&quot;justify&quot;&gt;
&amp;nbsp;
&lt;/div&gt;
&lt;div align=&quot;justify&quot;&gt;
&lt;em&gt;The Times of India, 12 October, 2015, please &lt;a href=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot;&gt;click here&lt;/a&gt; to access &lt;/em&gt;&lt;br /&gt;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians..."/>
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                <strong>Indians crowdfund Pakistani girl&#039;s medical treatment -Malathy Iyer</strong></h1>
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                <div align="justify">-The Hindu<br /><br /><em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br /><br />Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br /><br />What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br /><br />Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br /><br />As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br /><br />Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br /><br />&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br /><br />When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br /><br />&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br /><br />On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br /></div><div align="justify">&nbsp;</div><div align="justify"><em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms" title="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br /></div>               </font>
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;,
	&#039;disp&#039; =&gt; &#039;&lt;div align=&quot;justify&quot;&gt;-The Hindu&lt;br /&gt;&lt;br /&gt;&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;&lt;br /&gt;Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;&lt;br /&gt;What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;&lt;br /&gt;Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;&lt;br /&gt;As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;&lt;br /&gt;Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;&lt;br /&gt;&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;&lt;br /&gt;When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;&lt;br /&gt;&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;&lt;br /&gt;On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&amp;nbsp;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&lt;em&gt;The Times of India, 12 October, 2015, please &lt;a href=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot; title=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot;&gt;click here&lt;/a&gt; to access &lt;/em&gt;&lt;br /&gt;&lt;/div&gt;&#039;,
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians..."/>
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                <strong>Indians crowdfund Pakistani girl&#039;s medical treatment -Malathy Iyer</strong></h1>
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                <div align="justify">-The Hindu<br /><br /><em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br /><br />Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br /><br />What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br /><br />Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br /><br />As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br /><br />Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br /><br />&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br /><br />When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br /><br />&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br /><br />On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br /></div><div align="justify">&nbsp;</div><div align="justify"><em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms" title="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br /></div>               </font>
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
&lt;/div&gt;
&lt;div align=&quot;justify&quot;&gt;
&amp;nbsp;
&lt;/div&gt;
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&lt;em&gt;The Times of India, 12 October, 2015, please &lt;a href=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot;&gt;click here&lt;/a&gt; to access &lt;/em&gt;&lt;br /&gt;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;,
	&#039;disp&#039; =&gt; &#039;&lt;div align=&quot;justify&quot;&gt;-The Hindu&lt;br /&gt;&lt;br /&gt;&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;&lt;br /&gt;Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;&lt;br /&gt;What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;&lt;br /&gt;Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;&lt;br /&gt;As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;&lt;br /&gt;Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;&lt;br /&gt;&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;&lt;br /&gt;When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;&lt;br /&gt;&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;&lt;br /&gt;On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&amp;nbsp;&lt;/div&gt;&lt;div align=&quot;justify&quot;&gt;&lt;em&gt;The Times of India, 12 October, 2015, please &lt;a href=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot; title=&quot;http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms&quot;&gt;click here&lt;/a&gt; to access &lt;/em&gt;&lt;br /&gt;&lt;/div&gt;&#039;,
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-The Hindu&lt;br /&gt;
&lt;br /&gt;
&lt;em&gt;MUMBAI: &lt;/em&gt;Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.&lt;br /&gt;
&lt;br /&gt;
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed&#039;s treatment for Wilson&#039;s disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &amp;quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&amp;quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.&lt;br /&gt;
&lt;br /&gt;
What makes Saba&#039;s story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &amp;quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson&#039;s disease, &amp;quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.&lt;br /&gt;
&lt;br /&gt;
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.&lt;br /&gt;
&lt;br /&gt;
As Saba&#039;s condition deteriorated in Karachi, more Indians stepped in to help. &amp;quot;When Saba&#039;s condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&amp;quot; said Shabia Walia of Bluebells Community.&lt;br /&gt;
&lt;br /&gt;
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;We spread Saba&#039;s story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,&#039;&#039; said Walia.&lt;br /&gt;
&lt;br /&gt;
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,&#039;&#039; said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &amp;quot;Saba is on two capsules a day, but it should be stepped up to five soon,&#039;&#039; said Dr Nagral, who took the teenager to eat out in Bandra. &amp;quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,&#039;&#039; said Nagral.&lt;br /&gt;
&lt;br /&gt;
On what Saba or her mother Nazia felt, the doctor said, &amp;quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&amp;quot; said Dr Nagral.&lt;br /&gt;
&lt;/div&gt;
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&amp;nbsp;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni&#039;s face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...&#039;
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians..."/>
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                <strong>Indians crowdfund Pakistani girl&#039;s medical treatment -Malathy Iyer</strong></h1>
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                <div align="justify">-The Hindu<br /><br /><em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br /><br />Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br /><br />What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br /><br />Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br /><br />As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br /><br />Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br /><br />&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br /><br />When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br /><br />&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br /><br />On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br /></div><div align="justify">&nbsp;</div><div align="justify"><em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms" title="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br /></div>               </font>
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		'title' => 'Indians crowdfund Pakistani girl's medical treatment -Malathy Iyer',
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-The Hindu<br />
<br />
<em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br />
<br />
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br />
<br />
What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br />
<br />
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br />
<br />
As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br />
<br />
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br />
<br />
&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br />
<br />
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br />
<br />
&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br />
<br />
On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br />
</div>
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&nbsp;
</div>
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<em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br />
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...',
	'disp' => '<div align="justify">-The Hindu<br /><br /><em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br /><br />Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br /><br />What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br /><br />Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br /><br />As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br /><br />Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br /><br />&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br /><br />When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br /><br />&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br /><br />On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br /></div><div align="justify">&nbsp;</div><div align="justify"><em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms" title="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br /></div>',
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	'title' => 'Indians crowdfund Pakistani girl&#039;s medical treatment -Malathy Iyer',
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-The Hindu<br />
<br />
<em>MUMBAI: </em>Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.<br />
<br />
Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. &quot;Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba,&quot; Jaslok hospital CEO Dr Taran Gainchandani said on Monday.<br />
<br />
What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. &quot;But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, &quot; said liver specialist, Dr Aabha Nagral, who has been treating the teen.<br />
<br />
Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement.<br />
<br />
As Saba's condition deteriorated in Karachi, more Indians stepped in to help. &quot;When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help,&quot; said Shabia Walia of Bluebells Community.<br />
<br />
Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan.<br />
<br />
&quot;We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia.<br />
<br />
When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease.<br />
<br />
&quot;But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. &quot;Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. &quot;Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral.<br />
<br />
On what Saba or her mother Nazia felt, the doctor said, &quot;Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter,&quot; said Dr Nagral.<br />
</div>
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&nbsp;
</div>
<div align="justify">
<em>The Times of India, 12 October, 2015, please <a href="http://timesofindia.indiatimes.com/city/mumbai/Pak-girl-returns-after-web-funded-med-care/articleshow/49328782.cms">click here</a> to access </em><br />
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-The Hindu

MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians.

Some Indians...'
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Indians crowdfund Pakistani girl's medical treatment -Malathy Iyer

-The Hindu MUMBAI: Around the time that Shiv Sainiks were blackening Sudheendra Kulkarni's face on Monday morning, a Pakistani girl and her mother were getting ready to leave Mumbai with warm memories of a 49-day stay and gratitude for Indians. Some Indians had, after all, contributed almost Rs 13 lakh to finance 15-year-old Karachi resident Saba Tariq Ahmed's treatment for Wilson's disease, a disorder that results in poisonous accumulation of copper in the body, at Jaslok hospital. "Saba and her mother, Nazia, boarded an afternoon flight for Karachi. They were extremely happy about how well the treatment worked for Saba," Jaslok hospital CEO Dr Taran Gainchandani said on Monday. What makes Saba's story special is that Indian citizens reached out not once, but twice between April and October, to help her financially. The first time was in April-May, when an NGO, Bluebells Community, raised Rs 7 lakh from Mumbaikars to help Saba. "But Saba did not respond too well to the regularly prescribed medicines for Wilson's disease, " said liver specialist, Dr Aabha Nagral, who has been treating the teen. Dr Nagral added that Saba needed a change of medication, as well as physiotherapy to regain her movement. As Saba's condition deteriorated in Karachi, more Indians stepped in to help. "When Saba's condition started worsening on her return to Karachi in May, Nazia contacted me, seeking help," said Shabia Walia of Bluebells Community. Thus, the online crowdfunding effort started on Independence Day to collect Rs 10 lakh for a three-month treatment with an alternative medication that is not freely available in India or Pakistan. "We spread Saba's story so far and wide that we got an American NGO, Rachel and Drew Katz Foundation, contributing Rs 4 lakh and a London-based NGO promising free supply of medicines,'' said Walia. When Bluebells Community volunteers received Saba at Mumbai airport on August 24, she was wheelchair-bound, could not speak and had tremors and abnormal involuntary movements due to the severity of the disease. "But we started her on physiotherapy as well as the alternative drug, Trientine (which helps remove copper accumulation from the body,'' said Dr Nagral. Procuring the drug was not easy as it is not manufactured in India and 100 capsules cost Rs 84,000. "Saba is on two capsules a day, but it should be stepped up to five soon,'' said Dr Nagral, who took the teenager to eat out in Bandra. "Saba is a fan of Salman Khan and wanted to meet him, so I took her to this theme restaurant that is inspired by the actor,'' said Nagral. On what Saba or her mother Nazia felt, the doctor said, "Nazia said she had been warned that things would not be smooth in India, and she was happy that her fears did not come true. She said Mumbai had been full of warmth and happiness for her and her daughter," said Dr Nagral.   The Times of India, 12 October, 2015, please click here to access