Re: [DIYbio] White House Petition to Reverse FDA decision to bar 23&Me from selling their DNA kits

That link is not open to the public, and the minimum joining fee
without completing their 'scholarship' application is $250. Are there
public archives?

On Wed, Nov 27, 2013 at 4:56 PM, Srihari Yamanoor <yamanoor@gmail.com> wrote:
> Nathan, here goes:
>
> http://lists.participatorymedicine.org/SCRIPTS/WA-SPM.EXE?A0=SPM-MEMBERS
>
> Sincerely,
>
> Srihari
>
>
> On Wed, Nov 27, 2013 at 4:53 PM, Nathan McCorkle <nmz787@gmail.com> wrote:
>>
>> On Wed, Nov 27, 2013 at 11:22 AM, Srihari Yamanoor <yamanoor@gmail.com>
>> wrote:
>> > Sorry my fault. Thanks for correcting me! Also, please note this article
>> > before considering signing the petition. Fans of 23andme might be doing
>> > more
>> > harm than good. Read it carefully, and read the last paragraph. There
>> > is
>> > also another discussion going on at the Society of Participatory
>> > Medicine
>> > listserv.
>>
>> Can you give us the listserv link too? I registered for the
>> PM-ADVOCATES and WHYPM lists here but they're empty:
>> http://lists.participatorymedicine.org/
>>
>>
>> >
>> >
>> > http://www.fiercemedicaldevices.com/story/23andme-digs-fda-wants-test-market/2013-11-27
>>
>> This isn't very informative on the actual claims the FDA makes, to
>> help us understand why they think it's 'diagnostic' and not 'research
>> and educational'.
>>
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>
>
>
>
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--
-Nathan

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