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Author Topic: Save This Child's Life - URGENT!!! NO DONATIONS. JUST A SIGNATURE  (Read 3634 times)
AT101ET (OP)
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December 26, 2013, 12:04:19 AM
 #41

It means, it will now be reviewed by White House officials.
They have the final say and will either give it the all clear or reject it.
drb0n3z
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December 27, 2013, 10:14:37 AM
 #42

Hi Guys,
Before you close the tab, this isn't a charity plea!
This was sent to me in an email asking me to sign a petition to help save this Child's life.

Refael Elisha Cohen, a six year old from Houston TX, was diagnosed with brain cancer. He has gone through many treatments and unfortunately, doctors have now given him one last resort.
The only possibility of saving his life is  by giving him Antineoplaston therapy. However, this therapy is currently under FDA inspection and it'll be too late for him when it is finally approved.
The FDA has the power to approve a "compassionate use exemption" so Refael Elisha can undergo this therapy before it is fully approved to try and save his life.

I know that the community here is large. We have thousands of users of different cypto-currencies here. All I ask is that you take a minute out of your schedule to sign this White House Petition to help give this brave and strong child a chance of life.

The petition can be found here: https://petitions.whitehouse.gov/petition/authorize-fda-grant-compassionate-use-exemption-refael-elisha-cohen-antineoplaston-therapy/BVSP1ZkW

Another 46000 signatures are needed by January the 2nd.

We alone on bitcointalk have the power to ensure that the petition reaches 100k signatures in order to save this Child.

Please spread the word, and post below if you have signed it. No matter what race or religion you are, we are all humans and we all have the right to live...

Many Thanks

- AT101ET

https://petitions.whitehouse.gov/petition/authorize-fda-grant-compassionate-use-exemption-refael-elisha-cohen-antineoplaston-therapy/BVSP1ZkW


Just looked a the petition and it's over the needed amount! Good job
jackjack
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December 27, 2013, 12:18:32 PM
 #43

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The FDA also observed that Burzynski had denied patients informed consent by not informing of extra costs that they might incur during treatment and that he could not account for his stock of the investigational drug. Lastly, the FDA observed: "Your [...] tumor measurements initially recorded on worksheets at baseline and on-study treatment [...] studies for all study subjects were destroyed and are not available for FDA inspectional review," meaning that there is no way for the FDA to verify either initial tumor sizes or any effect that the antineoplastons might have had.
Classy

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