 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
Rally 09 fundraiser
Raising funds for the LDN research trust
So LDN, what does it stand for?
LDN stands for Low dose Naltrexone. (Wikipedia)
What is LDN?
LDN (Low Dose Naltrexone) is a treatment for MS that has been used in the USA since 1985, but is relatively new to the United Kingdom. This method was devised and developed by Dr Bernard Bihari, a neuro-physician in New York, and he has described the beneficial effects of LDN (Taken from the LDN Research Trust web site).
Read more here (LDN Research Trust site).
LDN Research Trust and it’s goals:
The LDN Research Trust was set up by a small core of people who have Multiple Sclerosis. The primary aim of the Trust is to initiate Clinical Trials of Low Dose Naltrexone.
Whilst working to raise funds for trials, they have helped over 5,000 people to obtain LDN from a General Practitioner or Neurologist, either through the National Health Service or by private prescription. They have also been able to help people, not just in the UK but in countries throughout Europe, as well as USA, Canada, West Indies, Australia, New Zealand, and others. Visit their website and read their downloadable newsletters, you will be able to read the stories of some of these people.
The LDN Research Trust is a non-profit-making Registered Charity, and everyone is a volunteer.
However, they are little different from other charities, in that there are unfunded elements which do ultimately cost them money to maintain and operate. To help them continue their work to bring relief to all people with Multiple Sclerosis, and other conditions they appreciate help with fund raising, either in cash or in kind. You can be sure that all contributions are greatly appreciated, however small.
There are close personal reasons for my choice of charity being the LDN research trust. I hope through this, you too will help sponsor the rally through Europe to raise funds for the trust.
LDN stands for Low dose Naltrexone. (Wikipedia)
What is LDN?
LDN (Low Dose Naltrexone) is a treatment for MS that has been used in the USA since 1985, but is relatively new to the United Kingdom. This method was devised and developed by Dr Bernard Bihari, a neuro-physician in New York, and he has described the beneficial effects of LDN (Taken from the LDN Research Trust web site).
Read more here (LDN Research Trust site).
LDN Research Trust and it’s goals:
The LDN Research Trust was set up by a small core of people who have Multiple Sclerosis. The primary aim of the Trust is to initiate Clinical Trials of Low Dose Naltrexone.
Whilst working to raise funds for trials, they have helped over 5,000 people to obtain LDN from a General Practitioner or Neurologist, either through the National Health Service or by private prescription. They have also been able to help people, not just in the UK but in countries throughout Europe, as well as USA, Canada, West Indies, Australia, New Zealand, and others. Visit their website and read their downloadable newsletters, you will be able to read the stories of some of these people.
The LDN Research Trust is a non-profit-making Registered Charity, and everyone is a volunteer.
However, they are little different from other charities, in that there are unfunded elements which do ultimately cost them money to maintain and operate. To help them continue their work to bring relief to all people with Multiple Sclerosis, and other conditions they appreciate help with fund raising, either in cash or in kind. You can be sure that all contributions are greatly appreciated, however small.
There are close personal reasons for my choice of charity being the LDN research trust. I hope through this, you too will help sponsor the rally through Europe to raise funds for the trust.
This Is The Right Place For Your
Expressive Top-Headline
Expressive Top-Headline