Jump to content
RemedySpot.com

LDN Trials

Rate this topic


Guest guest

Recommended Posts

I have been taking LDN since last August and have had a significant

improvement in my MS. I know that this message board wants to get

the story out, but it does seem to be hitting a wall with the

neurologists.

We need to get a clinical trial done, NOW.

To start the ball rolling we will need to have some idea as to the

cost of doing a trial, and who could do the trial. This needs to be

found out first. Once we have this information we can then get the

funding.

If anyone has information on either of these two items I would

appreciate it.

If we can use this group to find out this information, we can then

go onto the next stage of funding.

All comments welcome,

Joyce

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...