RE: Fw: MS Friends Announcement - MS Challenge

[Guest guest]

For the education of Lynn and any other members of the ~1400 LDN listserv, please don't just hit REPLY here. The 1400 folks on our LDN listserv don't need to know your contact info. The folks who do want it are the 'Managers of MS Friends' organization over in London, although I question why they are asking for it? If you want to send it though, I suggest you compose an email to contact@..., Subj: Contact info (or whatever) and type your name, location & email address info in the body of your email.

Best regards, Rae Bower

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of LynnSent: Friday, July 22, 2005 4:26 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Fw: MS Friends Announcement - MS Challange

Lynn Shaw

bilzy@...

Florida, USA

MS Friends Announcement - MS Challange

Announcement from Managers of MS Friends

Reply

Our MS Challenge

Are you able to help with our challenge?

Dr Tom Gilhooly, has a target for us. We know there are at least 2 ½ million people in the world with MS; he would like to see at least 50,000 people on our database within the next 2 years. We feel this number is only achievable with everyone's help. It doesn't matter if people are taking LDN or not, to be eligible you only have to be among the elite with MS.

As a charity the more people we have behind us, the more power we have.

How can you help?

All we need are names of people with MS, their email addresses and country they live in.

Could you send this email to everyone you know with MS and get them to pass it on to people they know. We should have the message being sent around the world in hours.

We would also like to add people you know with MS, that don't have an email address. Could you ask their permission to send us their names?

I've attached a LDN Flyer on the message board; it can be printed on both sides of a sheet of A4. You can then half the paper giving 2 flyers. What we would like is for people to take copies to MS therapy centres, ask your MS nurse if you could leave some at your hospital (we have 4 MS nurses very interested already), and ask your local MS Society if you can hand them out to members that are interested. Plus any other places where you have gatherings of people with MS.

Always ask permission first before handing out the flyers, the last thing we want is to upset anyone.

To date we have 1,700 people on our database, I will keep you updated monthly as this number grows.

Thank you all for your help and support.

www.ldnresearchtrust.org

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