Guest guest Posted December 3, 2008 Report Share Posted December 3, 2008 My doc asked me to explain to him why people with MS and Lyme experience joint aches, stiffness, headaches more so than the average LDN user? I explained it in a nutshell but more details would be great- he told me to email it to him. He has been working with LDN for a while now. Is there some info on this I can fwd him? He really got happy when I told him about DLPA. Is there any archive of a doc specifically talking about this or DLPA? Thanks, Jodi Quote Link to comment Share on other sites More sharing options...
Recommended Posts
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.