Re: European Parliament Petition - encouraging news!

[Guest guest]

[LDNandIBD] European Parliament Petition - encouraging news!

Thought I'd share with all that I have received a letter from the European

Parliament re our petition. They had a panel discussion on 27/28 January

and have agreed to ask the European Commission to further research into LDN,

continue the examination of Low Dose Nalterexone and as soon as they reach a

decision they will write back to me.

The door hasn't been slammed in our faces, so please folks, continue to

support the LDN petition to the European Parliament - it really is important

and don't forget, don't fund the petition link. All that's needed is your

signature and support. This really is of vital international importance and

anyone can sign anywhere in the world. Please click here

http://www.ipetitions.com/petition/ldnnow/

I can't stress the importance of this. Please cross reference to other

groups as you see fit. Appreciate this.

Many thanks!

Jayne Crocker

LDNNow logo the one to use

www.LDNNow.com

<http://www.ipetitions.com/petition/ldnnow/> Important! Please sign our

LDN petition to the European Parliament by clicking here

tel: +44 (0) 7877 492 669

<

Dr Steele MBE, talking

about LDN

LDNNow, a patient and friend led organisation (so not a charity) with no

funding and no affiliation to any company or organisation, but rather a

group of concerned individuals focussed on improving the health of those who

suffer from the many diseases and conditions that LDN treats.