Fw: Article About Meeting With UK Prime Minister

[Guest guest]

[LDN_RaisingAwarenessUK] Article in my local paper re our meeting with

the Prime Minister

I hope you enjoy the read

http://www.westerntelegraph.co.uk/news/5066532.LDN_campaigners_meet_with_the_PM/\

#

<http://www.westerntelegraph.co.uk/news/5066532.LDN_campaigners_meet_with_the_PM\

/>

Feel free to show your support by posting any comments.

I would also like to take this opportunity of letting everybody know that our

efforts with the NIHR in Southampton are paying off and they are now working

‘with’ us instead of ‘challenging’ us to further research/trials into

LDN – how the tables have turned! So we’re quite excited about that. Also

my partner had his annual check up with his neuro on Monday who two years ago

wrote a letter saying ‘trials for LDN is a no brainer’ – it’s always

good to have something in writing, and this year he’s been very supportive of

our campaign and agrees ‘LDN on the NHS is a no brainer’. He did mention

the challenge with LDN is that it is such a controversial drug and our response

was, “what drug isn’t� He agreed and gave us some very good

advice/pointers. He was very pleased with for his SPMS who has now been

taking LDN for 18 months.

Best wishes,

Jayne Crocker

Chairperson

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.

[Guest guest]

[LDN_RaisingAwarenessUK] Article in my local paper re our meeting with

the Prime Minister

I hope you enjoy the read

http://www.westerntelegraph.co.uk/news/5066532.LDN_campaigners_meet_with_the_PM/\

#

<http://www.westerntelegraph.co.uk/news/5066532.LDN_campaigners_meet_with_the_PM\

/>

Feel free to show your support by posting any comments.

I would also like to take this opportunity of letting everybody know that our

efforts with the NIHR in Southampton are paying off and they are now working

‘with’ us instead of ‘challenging’ us to further research/trials into

LDN – how the tables have turned! So we’re quite excited about that. Also

my partner had his annual check up with his neuro on Monday who two years ago

wrote a letter saying ‘trials for LDN is a no brainer’ – it’s always

good to have something in writing, and this year he’s been very supportive of

our campaign and agrees ‘LDN on the NHS is a no brainer’. He did mention

the challenge with LDN is that it is such a controversial drug and our response

was, “what drug isn’t� He agreed and gave us some very good

advice/pointers. He was very pleased with for his SPMS who has now been

taking LDN for 18 months.

Best wishes,

Jayne Crocker

Chairperson

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.