LDN Conference

[Guest guest]

Since I can not make the conference does anybody know if it is going

to be taped or there is goign to be a synopsis on the web so those of

us who can not make it be informed?

[Guest guest]

I attended last year and was a speaker on the LDN advocates panel. I

can definitely recommend going if you want to meet other LDNers. It

was great to meet all the other LDN users/advocates, Dr Gluck and

the other organizers, and the researchers who came to share their

info. I recently checked with Dr Gironi, who attended from Italy,

and she is still in the process of getting her 60 person LDN / MS

trial approved, so it is still happening. Dr Tom Gilhooly is also

considering launching a symptomatic trial.

Susie Sedlock is doing a great job organizing an excellent program

for the second conference, with 4 new researchers presenting.

http://ldninfo.org/events.htm

If I don't make the second conference, I will definitely donate my

conference fee anyway to the US LDN Research Fund. So far we have

raised $4600 from LDN users who feel we can't wait to figure out how

it works, make it work better, and get LDN recognized as a viable

treatment for slowing MS progression and symptom relief. It's been

doing that for me now for 2 years - just got back from 3 weeks in

Kona, Hawaii with my husband to celebrate my recovery on LDN :-)

SammyJo

http://www.ldners.org

> is anyone going to the LDN conference? i would like to attend and

am just wondering who i'll meet from the group.