Article in my local paper - LDNNow meets with the Prime Minister / NIHR

March 17, 2010

Feel free to post 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

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.

Recommended Posts