posted
www.geneticssummit.com - starts today - they'll be covering material that's relevant to us in this summit.
Posts: 13119 | From San Francisco | Registered: May 2006
| IP: Logged |
Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
Thanks for always taking time to remind us of these programs.
You are a good, although a bit goofy (or is that "creative") member and we appreciate it.
posted
Thx! I'll go for good, creative, goofy and more adjectives...
This is one heck of an interesting program. I suggest folks look at the speaker list each day and see if something sounds of interest to you.
Posts: 13119 | From San Francisco | Registered: May 2006
| IP: Logged |
map1131
Frequent Contributor (5K+ posts)
Member # 2022
posted
One speaker today talked about Lyme disease. He was talking about folks that have these genetics issues and Lyme can't always handle the supps/vits recommended.
I've tried over and over again to use manganese, NAC, B2 and B5 etc....which apparently I need for my genetic issues. I just can't do them.
It's like going back in Lyme bad times. I really need to find a good Functional medicine doc to help me. Of course that means travel out of state and more $$$$.
Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6485 | From Louisville, Ky | Registered: Jan 2002
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/