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It is our right

to be seen

and heard!

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Donate!

Provide

support

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Join

Us!

Become

a team member.

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“It is amazing what you can accomplish if you do not care who gets the credit.”

Harry S Truman 1884-1972

MULTIPLE

SCLEROSIS

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LDN Research Trust as a charity that is striving to bring LDN within the reach of all MS people.

There are 3 trustees, Linda Elsegood, Alex Parker, and Neil Lucas - all with MS and all work voluntarily.

The 2 doctors who advise the LDN Research Trust are Dr Tom Gilhooley and Dr Bob Lawrence

'The ultimate goal is to trial LDN for many diseases'. Linda has done an excellent job in telling people about LDN and putting people in touch with doctors who will prescribe LDN.

The cost of the trial is approx £50,000 of which the LDN trust has done an excellent job to date by raising £10,000.

This important trial requires the support of the MS community for full details go to..

www.ldnresearchtrust.org

Please forward any donation you may wish to make to the LDN research trust.

Dear All,

LDN advocated worldwide work to together for the benefit of all, and I have ways in which each of you can help, today.

Vicki Finlayson, to walk 53 miles from California to Sacramento for LDN.

Vicki Finlayson, a patient with multiple sclerosis (MS), used to have trouble walking from her living room to her kitchen. Now, with the help of one generic medication prescribed off-label, she is walking 53 miles from her home in Auburn California to Sacramento. Vicki is raising funds for research into the drug protocol that brought her MS into remission, low dose naltrexone (LDN). Besides its benefits in MS, LDN has been shown to improve many different autoimmune, oncological, and neurodegenerative conditions.

I have a message for you, from Vicki Finlayson in the USA:

Would it be possible for you to send this to all the people in your address book and encourage them to email the Governor, if we get attention from all over the world he might take this matter a little more seriously.

Click http://www.ldners.org/advocates.htm Scroll down to where it says email the Governor Click email this brings you to his email page, Fill in the contact info. Click submit and this brings you to his comment page, make your comment click submit and he has the emails.

I am leaving Wed, May 14th May and will be arriving at the capital on the 19th May around 2:00 pm. I am going to walk 10 miles a day; I can walk this in about 4.5 hours. It is 53 miles to the capital so I am going to take it easy each day and I already walk 5 miles a day with no problem so this should be a piece of cake.

We wish Vicki every success and ask if you could support her cause by emailing Governor Schwarzenegger as per Vicki’s request. Hopefully we can get everyone worldwide to send emails. Good Luck Vicki, we will be with thinking of you!!

 

LDN Petition:

Have you signed the LDN petition yet?

The petition is in support of the campaign to get Low Dose Naltrexone (LDN) into clinical trials as soon as possible.

At the moment there are very few Neurologists and GP's willing to prescribe LDN. We need it trialed urgently for the benefit of all those with Multiple Sclerosis.

The LDN Petition

Could we ask if you could get as many of your friends to take part in signing the LDN petition?

LDN Success Stories:

I am collecting LDN stories for various purposes:

I have a freelance Journalist in the UK trying to get the LDN story into the National media.

We are always looking for stories for our newsletter. If we have already used your story, could you send us an update?

Cris Kerr is compiling an eBook of LDN success stories for all conditions from around the world. This eBook will be available to download and print worldwide for free.

Althea is compiling a book of short stories from LDN users for different ailments. The book will be non-profit; any proceeds will go to LDN research or trials. The stories can be two to four paragraphs.

Stories can include when you got your diagnosis, how it affected you and your loved ones, what struggles you have gone through, what medicines or protocols you have tried, how you found LDN, if you had a difficult time getting a prescription and what you have experienced since starting LDN.

Some of the stories that we have received so far have brought in humour and some have brought tears. It is amazing what strength most people have gained from the many road blocks they have had to work around.

The book will include a chapter for doctors, pharmacists and researchers on how they found LDN, patients’ experiences and what they hope to see for the future.

All stories can be used anonymously or real name can be used. We can add a photo in our newsletter, it is entirely up to you; don’t worry if writing isn’t your thing as all stories will be edited for grammar, spelling etc without changing the meaning.

I await your emails and stories, which I will pass them on to the interested parties with your permission and they will contact you shortly.

LDN experience are inspirations to others wishing to know more about LDN and this can only be done with your help!

I would like to thank you all for taking the time to read this message and I thank you in advance for all your help and support. Together we CAN achieve so much!

Best Regards

Linda                                                                                               Continued next page

 

 

 

 

                                           

 

 

 

 

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