Re: - LDN News from LDN Research Trust

[Guest guest]

hi

can you do the same thing in australia. naltexone isn't an narcotics blocker it's alcohol blocker used here and you need to be an alcholic

-------Original Message-------

From: low dose naltrexone

Date: 11/13/04 08:08:42

MSWatchers

Cc: LDN group; Spotlight_LDN

Subject: [low dose naltrexone] - LDN News from LDN Research Trust

----- Original Message ----- From: Managers of MS Friends

Members of MS Friends

Sent: Friday, November 12, 2004 04:35

Subject: MS Friends Announcement - LDN News

Announcement from Managers of MS Friends

Reply

Exciting news! We have the Registered Charity No.1106636. , and I completed the Charity Commissions registration forms on 4th September, registration was granted yesterday 8th November. The red tape was endless as we had to prove that research was charitable but after several weeks of jumping through the right hoops we have finally made it:)We now need as much publicity as possible. We have contacted numerous National and Local Newspapers, TV & Radio Stations this morning, we really need your help if you live in the UK. Local media are interested in LDN if it is of interest to their readers, we need people that are prepared to be interviewed and say how LDN is working for them and that clinical trials are needed. Is this YOU? Would you like to get involved and help? If you’re happy to do so, please email me with your full details. I will contact your local media and add your name to the list for the national media. Together we can get LDN into Clinical Trials, it’s a case of team work.The next challenge is to get funding, if you have an ideas please let us know. The more ideas we get the better.Best Wishes to you all,

Attached is the press release.

LDN Research Trust

Registered Charity No.1106636

LDN to be trialled as a treatment for MS

The LDN Research Trust established in May 2004, has come a long way in a short time, registering as a Charity, assisting eminent Neurologist Dr Alasdair Coles and Dr Lawrence with proposals to trial LDN as a treatment for MS.

The function of the LDN Research Trust is to raise £500,000 to fund clinical trials. This amount will be staggered as several trials are proposed. Trustees, Elsegood, and Rebello, work tirelessly without payment or numeration. Every penny given goes towards trials, only the actual day to day running expenses are drawn. To date £103 has been deducted, this includes the cost of the web site. www.ldnresearchtrust.org

Low Dose Naltrexone (LDN) has been used as a treatment for MS in the USA since 1985 but is relatively new in the UK. LDN was devised and developed by Dr Bernard Bihari, who is qualified in Neurology, Psychiatry and Internal Medicine in New York. His website is www.low dose naltrexone.org

How LDN Works: The benefits are due to the temporary inhibition of brain endorphins (a natural pain-killer, produced in the brain). Consequently this leads to an increase in the production of natural endorphins, helping stop the progression of MS, reducing painful symptoms and an increase sense of well-being. A 3 mg capsule of LDN is taken nightly for 4 weeks and then a 4.5 mg capsule thereafter, sometimes the dosage needs adjusting slightly.

In the recent LDN survey 97% of people with MS said they experienced symptom relief such as Fatigue, Bladder Urgency, Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm, and Numbness etc. Many people with MS are unable to try LDN because the medical profession are concerned that it has not been trialled for MS. Numerous desperate people have had no choice but to source and fund LDN themselves from the USA. Prices range from £17.50 - £26 for one months supply including delivery.

Naltrexone is freely prescribed on the NHS, as an opiate blocker for Heroin addicts, in doses of 50mg often 3 times a day.

Mainly it is symptoms of MS that are treated and often with drugs that have not been clinically trialled for MS. LDN is no miracle drug and not a cure but anecdotal evidence suggests LDN helps stop progression and for many, improves symptoms and at such a low dose there are few to no side effects, any that might appear are normally gone within the first week or two.

The LDN Research Trust needs your help. To find out how you can help; Telephone 01603 279508 or email contact@... or write to The LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are waiting to hear from you today!

[Guest guest]

I saw no real changes until almost the seventh month.

[Guest guest]

hello i am french began ldn 21 days ago at 3mg ldn/per day and note no change what do you think about thisin 9 days i 'll take 4,5mg/per dayi 'll be happy to get your comment> ----- Original Message ----- From: Managers of MS Friends >Members of MS Friends >Sent: Friday, November 12, 2004 04:35>Subject: MS Friends Announcement - LDN News>Announcement from Managers of MS FriendsReply >Exciting news! We have the Registered Charity No.1106636. , and I completed the Charity Commissions registration forms on 4th September, registration was granted yesterday 8th November. The red tape was endless as we had to prove that research was charitable but after several weeks of jumping through the right hoops we have finally made it:)We now need as much publicity as possible. We have contacted numerous National and Loca

l Newspap

ers, TV & Radio Stations this morning, we really need your help if you live in the UK. Local media are interested in LDN if it is of interest to their readers, we need people that are prepared to be interviewed and say how LDN is working for them and that clinical trials are needed. Is this YOU? Would you like to get involved and help? If you’re happy to do so, please email me with your full details. I will contact your local media and add your name to the list for the national media. Together we can get LDN into Clinical Trials, it’s a case of team work.The next challenge is to get funding, if you have an ideas please let us know. The more ideas we get the better.Best Wishes to you all,>Attached is the press release.> > LDN Research TrustRegistered Charity No.1106636 LDN to be trialled as a treatment for MS The LDN Research Trust established in May 2004, has come a long way in a short time, registering as a Charity

, assisting eminent Neurologist Dr Alasdair Coles and Dr Lawrence with proposals to trial LDN as a treatment for MS. The function of the LDN Research Trust is to raise £500,000 to fund clinical trials. This amount will be staggered as several trials are proposed. Trustees, Elsegood, and Rebello, work tirelessly without payment or numeration. Every penny given goes towards trials, only the actual day to day running expenses are drawn. To date £103 has been deducted, this includes the cost of the web site. www.ldnresearchtrust.org =0

D

Low Dose Naltrexone (LDN) has been used as a treatment for MS in the USA since 1985 but is relatively new in the UK. LDN was devised and developed by Dr Bernard Bihari, who is qualified in Neurology, Psychiatry and Internal Medicine in New York. His website is www.low dose naltrexone.org How L

DN Works:

The benefits are due to the temporary inhibition of brain endorphins (a natural pain-killer, produced in the brain). Consequently this leads to an increase in the production of natural endorphins, helping stop the progression of MS, reducing painful symptoms and an increase sense of well-being. A 3 mg capsule of LDN is taken nightly for 4 weeks and then a 4.5 mg capsule thereafter, sometimes the dosage needs adjusting slightly. In the recent LDN survey 97% of people with MS said they experienced symptom relief such as Fatigue, Bladder Urgency, Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm, and Numbness etc. Many people with MS are unable to try LDN because the medical profession are concerned that it has not been trialled for MS. Numerous desperate people have had no ch

oice but to source and fund LDN themselves from the USA. Prices range from £17.50 - £26 for one months supply including delivery. Naltrexone is freely prescribed on the NHS, as an opiate blocker for Heroin addicts, in doses of 50mg often 3 times a day. Mainly it is symptoms of MS that are treated and often with drugs that have not been clinically trialled for MS. LDN is no miracle drug and not a cure but anecdotal evidence suggests LDN helps stop progression and for many, improves symptoms and at such a low dose there are few to no side effects, any that might appear are normally gone within the first week or two. The LDN Research Trust needs your help. To find out how you can help; Telephone 01603 279508 or email contact@... or write to The LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are waiting to hear from you today!

---------------------------------------------------------------- <Publicité>JOUEZ AVEC NEUF TELECOM ! Découvrez un nouveau jeu des bestioles: elles détestent les offres Internet chères et détruisent tout sur leur passage ! Où çà ? Sur leur nouveau site internet à découvrir absolument : http://www.laccesinternetquivousrendbeauetcelebre.com

[Guest guest]

you must go on, sometimes the improvements are very slow.

Alain

"ferfasse@..." <FERFASSE@...> wrote:

hello

i am french began ldn 21 days ago at 3mg ldn/per day and note no change what do you think about this

in 9 days i 'll take 4,5mg/per day

i 'll be happy to get your comment

>

----- Original Message ----- From: Managers of MS Friends

>Members of MS Friends

>Sent: Friday, November 12, 2004 04:35

>Subject: MS Friends Announcement - LDN News

>

Announcement from Managers of MS Friends

Reply

>Exciting news! We have the Registered Charity No.1106636. , and I completed the Charity Commissions registration forms on 4th September, registration was granted yesterday 8th November. The red tape was endless as we had to prove that research was charitable but after several weeks of jumping through the right hoops we have finally made it:)We now need as much publicity as possible. We have contacted numerous National and Loca l Newspap ers, TV & Radio Stations this morning, we really need your help if you live in the UK. Local media are interested in LDN if it is of interest to their readers, we need people that are prepared to be interviewed and say how LDN is working for them and that clinical trials are needed. Is this YOU? Would you like to get involved and help? If you’re happy to do so, please email me with your full details. I will contact your local media and add your name to the list for the national media. Together we can get LDN into

Clinical Trials, it’s a case of team work.The next challenge is to get funding, if you have an ideas please let us know. The more ideas we get the better.Best Wishes to you all,

>Attached is the press release.

>

> LDN Research Trust

Registered Charity No.1106636

LDN to be trialled as a treatment for MS

The LDN Research Trust established in May 2004, has come a long way in a short time, registering as a Charity , assisting eminent Neurologist Dr Alasdair Coles and Dr Lawrence with proposals to trial LDN as a treatment for MS.

The function of the LDN Research Trust is to raise £500,000 to fund clinical trials. This amount will be staggered as several trials are proposed. Trustees, Elsegood, and Rebello, work tirelessly without payment or numeration. Every penny given goes towards trials, only the actual day to day running expenses are drawn. To date £103 has been deducted, this includes the cost of the web site. www.ldnresearchtrust.org

=0 D Low Dose Naltrexone (LDN) has been used as a treatment for MS in the USA since 1985 but is relatively new in the UK. LDN was devised and developed by Dr Bernard Bihari, who is qualified in Neurology, Psychiatry and Internal Medicine in New York. His website is www.low dose naltrexone.org

How L DN Works: The benefits are due to the temporary inhibition of brain endorphins (a natural pain-killer, produced in the brain). Consequently this leads to an increase in the production of natural endorphins, helping stop the progression of MS, reducing painful symptoms and an increase sense of well-being. A 3 mg capsule of LDN is taken nightly for 4 weeks and then a 4.5 mg capsule thereafter, sometimes the dosage needs adjusting slightly.

In the recent LDN survey 97% of people with MS said they experienced symptom relief such as Fatigue, Bladder Urgency, Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm, and Numbness etc. Many people with MS are unable to try LDN because the medical profession are concerned that it has not been trialled for MS. Numerous desperate people have had no ch oice but to source and fund LDN themselves from the USA. Prices range from £17.50 - £26 for one months supply including delivery.

Naltrexone is freely prescribed on the NHS, as an opiate blocker for Heroin addicts, in doses of 50mg often 3 times a day.

Mainly it is symptoms of MS that are treated and often with drugs that have not been clinically trialled for MS. LDN is no miracle drug and not a cure but anecdotal evidence suggests LDN helps stop progression and for many, improves symptoms and at such a low dose there are few to no side effects, any that might appear are normally gone within the first week or two.

The LDN Research Trust needs your help. To find out how you can help; Telephone 01603 279508 or email contact@... or write to The LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are waiting to hear from you today!

---------------------------------------------------------------- <Publicité>JOUEZ AVEC NEUF TELECOM ! Découvrez un nouveau jeu des bestioles: elles détestent les offres Internet chères et détruisent tout sur leur passage ! Où çà ? Sur leur nouveau site internet à découvrir absolument : http://www.laccesinternetquivousrendbeauetcelebre.com

Créez gratuitement votre avec 100 Mo de stockage !

Créez votre

Le nouveau Messenger est arrivé ! Découvrez toutes les nouveautés pour dialoguer instantanément avec vos amis.

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[Guest guest]

thank's a lot Alain may be i know u>you must go on, sometimes the improvements are very slow.>Alain> >"ferfasse@..." wrote: hello i am french began ldn 21 days ago at 3mg ldn/per day and note no change what do you think about thisin 9 days i 'll take 4,5mg/per dayi 'll be happy to get your comment>> ----- Original Message ----- From: Managers of MS Friends /DIV>0A>>Members of MS Friends >>Sent: Friday, November 12, 2004 04:35>>Subject: MS Friends Announcement - LDN News>>Announcement from Managers of MS FriendsReply >>Exciting news! We have the Registered Charity No.1106636. , and I completed the Charity Commissions registration forms on 4th September, registration was granted yesterday 8th November. The red tape was endless as we had to prove that research was charitable but after several weeks of jumping through the right hoops we have finally made it:)We now need as much publicity as possible. We have contacted numerous National and Loca l Ne

wspap ers

, TV & Radio Stations this morning, we really need your help if you live in the UK. Local media are interested in LDN if it is of interest to their readers, we need people that are prepared to be interviewed and say how LDN is working for them and that clinical trials are needed. Is this YOU? Would you like to get involved and help? If you’re happy to do so, please email me with your full details. I will contact your local media and add your name to the list for the national media. Together we can get LDN into Clinical Trials, it’s a case of team work.The next challenge is to get funding, if you have an ideas please let us know. The more ideas we get the better.Best Wishes to you all,>>Attached is the press release.>> >> LDN Research TrustRegistered Charity No.1106636 LDN to be trialled as a treatment for MS The LDN Research Trust established in May 2004, has come a long way in a short time, registering as

a Charit

y , assisting eminent Neurologist Dr Alasdair Coles and Dr Lawrence with proposals to trial LDN as a treatment for MS. The function of the LDN Research Trust is to raise £500,000 to fund clinical trials. This amount will be staggered as several trials are proposed. Trustees, Elsegood, and Rebello, work tirelessly without payment or numeration. Every penny given goes towards trials, only the actual day to day running expenses are drawn. To date £103 has been deducted, this includes the cost of the web site. www.ldnresearchtrust.org

=0 D =0

D

Low Dose Naltrexone (LDN) has been used as a treatment for MS in the USA since 1985 but is relatively new in the UK. LDN was devised and developed by Dr Bernard Bihari, who is qualified in Neurology, Psychiatry and Internal Medicine in New York. His website is www.low dose naltrexone.org Ho

w L DN Works: The benefits are due to the temporary inhibition of brain endorphins (a natural pain-killer, produced in the brain). Consequently this leads to an increase in the production of natural endorphins, helping stop the progression of MS, reducing painful symptoms and an increase sense of well-being. A 3 mg capsule of LDN is taken nightly for 4 weeks and then a 4.5 mg capsule thereafter, sometimes the dosage needs adjusting slightly. In the recent LDN survey 97% of people with MS said they experienced symptom relief such as Fatigue, Bladder Urgency, Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm, and Numbness etc. Many people with MS are unable to try LDN because the medical profession are concerned that it has not been trialled for MS. Numerous desperate people h

ave had n

o ch oice but to source and fund LDN themselves from the USA. Prices range from £17.50 - £26 for one months supply including delivery. Naltrexone is freely prescribed on the NHS, as an opiate blocker for Heroin addicts, in doses of 50mg often 3 times a day. Mainly it is symptoms of MS that are treated and often with drugs that have not been clinically trialled for MS. LDN is no miracle drug and not a cure but anecdotal evidence suggests LDN helps stop progression and for m

any, improves symptoms and at such a low dose there are few to no side effects, any that might appear are normally gone within the first week or two. The LDN Research Trust needs your help. To find out how you can help; Telephone 01603 279508 or email contact@... or write to The LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are waiting to hear from you today! /

TBODY>---------------------------------------------------------------- <Publicité>JOUEZ AVEC NEUF TELECOM ! Découvrez un nouveau jeu des bestioles: elles détestent les offres Internet chères et détruisent tout sur leur passage ! Où çà ? Sur leur nouveau site internet à découvrir absolument : http://www.laccesinternetquivousrendbeauetcelebre.com

[Guest guest]

Bonjour,

If you read through the messages you will see that everyone reacts

differently. I think that you should not give up. I certainly do

not intend to and I'm still trying to find what is best for me. I'm

curious to know where you get your LDN from. Did you find a doctor

to prescribe it? I'm also in France but get my supplies in the

USA. My neuro and my doctor were not willing to help out. Hang in

there! and let us know how you're doing.

Best regards

Joanne

> hello

> i am french began ldn 21 days ago at 3mg ldn/per day and note no

change what do you think about this

> in 9 days i 'll take 4,5mg/per day

> i 'll be happy to get your comment

>

>

> >

> ----- Original Message -----

> From: Managers of MS Friends

> >Members of MS Friends

> >Sent: Friday, November 12, 2004 04:35

> >Subject: MS Friends Announcement - LDN News

> >

>

> Announcement from Managers of MS Friends

>

>

>

>

> Reply

>

> >Exciting news! We have the Registered Charity No.1106636.

, and I completed the Charity Commissions registration

forms on 4th September, registration was granted yesterday 8th

November. The red tape was endless as we had to prove that research

was charitable but after several weeks of jumping through the right

hoops we have finally made it:)

>

> We now need as much publicity as possible. We have contacted

numerous National and Local Newspapers, TV

> & Radio S

> tations this morning, we really need your help if you live in the

UK. Local media are interested in LDN if it is of interest to their

readers, we need people that are prepared to be interviewed and say

how LDN is working for them and that clinical trials are needed. Is

this YOU? Would you like to get involved and help? If you're happy

to do so, please email me with your full details. I will contact

your local media and add your name to the list for the national

media. Together we can get LDN into Clinical Trials, it's a case of

team work.

>

> The next challenge is to get funding, if you have an ideas please

let us know. The more ideas we get the better.

>

> Best Wishes to you all,

>

>

>

> >Attached is the press release.

> >

> >

> LDN Research Trust

> Registered Charity No.1106636

>

> LDN to be trialled as a treatment for MS

>

> The LDN Research Trust established in May 2004, has come a long

way in a short tim

> e, regist

> ering as a Charity, assisting eminent Neurologist Dr Alasdair

Coles and Dr Lawrence with proposals to trial LDN as a treatment for

MS.

>

> The function of the LDN Research Trust is to raise £500,000 to

fund clinical trials. This amount will be staggered as several

trials are proposed. Trustees, Elsegood, and

Rebello, work tirelessly without payment or numeration.

Every penny given goes towards trials, only the actual day to day

running expenses are drawn. To date £103 has been deducted, this

includes the cost of the web site. www.ldnresearchtrust.org

>

> Low Dose Naltrexone (LDN) has been used as a treatment for MS in

the USA since 1985 but is relatively new in the UK. LDN was devised

and developed by Dr Bernard Bihari, who is qualified in Neurology,

Psychiatry and Internal Medicine in New York. His website is

www.low dose naltrexone.org

>

> How LDN Works: The benefits are due to the temporary inhibition of

brain endorphi

> ns (a nat

> ural pain-killer, produced in the brain). Consequently this leads

to an increase in the production of natural endorphins, helping stop

the progression of MS, reducing painful symptoms and an increase

sense of well-being. A 3 mg capsule of LDN is taken nightly for 4

weeks and then a 4.5 mg capsule thereafter, sometimes the dosage

needs adjusting slightly.

>

> In the recent LDN survey 97% of people with MS said they

experienced symptom relief such as Fatigue, Bladder Urgency,

Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm,

and Numbness etc. Many people with MS are unable to try LDN because

the medical profession are concerned that it has not been trialled

for MS. Numerous desperate people have had no choice but to source

and fund LDN themselves from the USA. Prices range from £17.50 - £26

for one months supply including delivery.

>

> Naltrexone is freely prescribed on the NHS, as an opiate blocker

for Heroin addicts, in doses of 50mg o

> ften 3 ti

> mes a day.

>

> Mainly it is symptoms of MS that are treated and often with drugs

that have not been clinically trialled for MS. LDN is no miracle

drug and not a cure but anecdotal evidence suggests LDN helps stop

progression and for many, improves symptoms and at such a low dose

there are few to no side effects, any that might appear are normally

gone within the first week or two.

>

> The LDN Research Trust needs your help. To find out how you can

help; Telephone 01603 279508 or email contact@l... or write to The

LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are

waiting to hear from you today!

>

>

>

>

>

[Guest guest]

Joanne,

I just sent you my dr and pharmacy' addresses in Paris.

Best regards

AlainJoanne <jo.comissiong@...> wrote:

Bonjour,If you read through the messages you will see that everyone reacts differently. I think that you should not give up. I certainly do not intend to and I'm still trying to find what is best for me. I'm curious to know where you get your LDN from. Did you find a doctor to prescribe it? I'm also in France but get my supplies in the USA. My neuro and my doctor were not willing to help out. Hang in there! and let us know how you're doing.Best regardsJoanne> hello > i am french began ldn 21 days ago at 3mg ldn/per day and note no change what do you think about this> in 9 days i 'll take 4,5mg/per day> i 'll be happy to get your comment> > > > > -----

Original Message ----- > From: Managers of MS Friends > >Members of MS Friends > >Sent: Friday, November 12, 2004 04:35> >Subject: MS Friends Announcement - LDN News> >> > Announcement from Managers of MS Friends> > > > > Reply> > >Exciting news! We have the Registered Charity No.1106636. , and I completed the Charity Commissions registration forms on 4th September, registration was granted yesterday 8th November. The red tape was endless as we had to prove that research was charitable but after several weeks of jumping through the right hoops we have finally made it:)> > We now need as much publicity as possible. We have contacted numerous National and Local Newspapers, TV > & Radio S> tations this morning, we really need your help if you live in the UK. Local media are interested

in LDN if it is of interest to their readers, we need people that are prepared to be interviewed and say how LDN is working for them and that clinical trials are needed. Is this YOU? Would you like to get involved and help? If you're happy to do so, please email me with your full details. I will contact your local media and add your name to the list for the national media. Together we can get LDN into Clinical Trials, it's a case of team work.> > The next challenge is to get funding, if you have an ideas please let us know. The more ideas we get the better.> > Best Wishes to you all,> > > > >Attached is the press release.> > > > > LDN Research Trust> Registered Charity No.1106636> > LDN to be trialled as a treatment for MS> > The LDN Research Trust established in May 2004, has come a long way in a short

tim> e, regist> ering as a Charity, assisting eminent Neurologist Dr Alasdair Coles and Dr Lawrence with proposals to trial LDN as a treatment for MS.> > The function of the LDN Research Trust is to raise £500,000 to fund clinical trials. This amount will be staggered as several trials are proposed. Trustees, Elsegood, and Rebello, work tirelessly without payment or numeration. Every penny given goes towards trials, only the actual day to day running expenses are drawn. To date £103 has been deducted, this includes the cost of the web site. www.ldnresearchtrust.org > > Low Dose Naltrexone (LDN) has been used as a treatment for MS in the USA since 1985 but is relatively new in the UK. LDN was devised and developed by Dr Bernard Bihari, who is qualified in Neurology, Psychiatry and Internal Medicine in New York. His website is

www.low dose naltrexone.org> > How LDN Works: The benefits are due to the temporary inhibition of brain endorphi> ns (a nat> ural pain-killer, produced in the brain). Consequently this leads to an increase in the production of natural endorphins, helping stop the progression of MS, reducing painful symptoms and an increase sense of well-being. A 3 mg capsule of LDN is taken nightly for 4 weeks and then a 4.5 mg capsule thereafter, sometimes the dosage needs adjusting slightly. > > In the recent LDN survey 97% of people with MS said they experienced symptom relief such as Fatigue, Bladder Urgency, Concentration, Depression, Balance, Mobility, Muscle Strength/Spasm, and Numbness etc. Many people with MS are unable to try LDN because the medical profession are concerned that it has not been trialled for MS. Numerous desperate people have had no choice but to source and

fund LDN themselves from the USA. Prices range from £17.50 - £26 for one months supply including delivery.> > Naltrexone is freely prescribed on the NHS, as an opiate blocker for Heroin addicts, in doses of 50mg o> ften 3 ti> mes a day.> > Mainly it is symptoms of MS that are treated and often with drugs that have not been clinically trialled for MS. LDN is no miracle drug and not a cure but anecdotal evidence suggests LDN helps stop progression and for many, improves symptoms and at such a low dose there are few to no side effects, any that might appear are normally gone within the first week or two.> > The LDN Research Trust needs your help. To find out how you can help; Telephone 01603 279508 or email contact@l... or write to The LDN Research Trust. PO box 1083. Buxton. Norwich NR10 SWY. They are waiting to hear from you today!> > > >

>