randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
i saw somebody who had a piece of paper divided in daily squares and it told you what to take and how many drops of each per day.
it listed the stuff you needed at the bottom and how many bottles per month.
does anybody have a copy or know about this piece of paper?
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- I just posted these at your other thread. Not sure, but what you seek may be here. It's always good to start with the official website and pages by the author himself.
Protocol for Borrelia and Lyme Co-Infections & Most Chronic Conditions
Scroll down: COWDEN SUPPORT PROGRAM
Protocol for Borrelia and Lyme Co-Infections & Most Chronic Conditions
The Cowden Support Program (CSP) is a 6-month protocol developed by Wm. Lee Cowden, MD initially for the treatment of Borrelia and Lyme Co-Infections.
Since the protocol helps to resolve the majority of the root causes of most patient�s symptoms it can also be used to treat most chronic health conditions.
The Cowden Support Program utilizes 14 different Nutramedix products including 6 Microbial Defense herbals (3 pairs of herbals) that are taken rotationally over at least 6 months. . . . -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
do you have to order from nutramedix? do they have a protocol where you can order a kit and everything is included?
ain't too good at trying to figure out which and how much and so on right now. just a little distracted.
i need a package deal where it says here take these bottles and so many drops etc.
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- It might be best to work with a LL ND. I know there is a good one near you as others have posted that.
You need an experienced ILADS LL expert to determine treatment variables. I think it would be nearly impossible to figure out what is needed otherwise.
You might contact your area lyme support groups for the name of the LL ND near you. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
if anybody knows of one, i sure would appreciate it.
there is a woman who does this in colleyville at the sunshine vitamin shoppe but don't know much about that.
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Contact the support groups.
I know a guy (forget who) posted here that he sent you a PM quite a while back with a LL ND who is very LL - you might look in your mailbox for that. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
surprise
Frequent Contributor (1K+ posts)
Member # 34987
posted
Randibear-
I called nutrimedix, and asked them to email the pages you are referring to-
It is a day by day, month by month calendar, and lists what can be mixed with what, and an area for you to check off as you go.
It is on their website, but I couldn't get it to pull up fully for me there.
I am not on the full protocol- but I am taking Samento and Pinella right now,
and have their burbur and parsley for detox.
I am considering the full 6 month condensed protocol for my daughter- haven't decided yet.
It is only 4 doses a day, since you can combine certain things together.
-------------------- Lyme positive PCR blood, and positive Bartonella henselae Igenex, 2011. low positive Fry biofilm test, 2012. Update 7/16- After extensive treatments, doing okay! Posts: 2518 | From USA | Registered: Nov 2011
| IP: Logged |
randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
well i ordered the one month package and we'll see how it goes.
i've got to cheap it down with all his family problems right now.
sounds like this is something i can do that i haven't tried already. seems i know somebody who did this but can't remember who and they had good results. wish i could remember...
i know of a llmd near here but unfortunately didn't have any luck. may go see that woman in colleyville or try a support group. there is one group that i have tried repeatedly to contact but no results. the group leader is supposed to live around here someplace.
i tried to print that sheet also but my computer is apparently not compatible with the printer i have. maybe i can get onto my husband's computer next time he has it up and try.
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Do not go see just any ND, you need someone who is ILADS educated. Seriously.
Ask them directly - I think they are right there in Dallas but not sure if they actually treat patients or not:
He says "here in Dallas . . ." -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- You have enough links to find someone, I hope.
I still think a RIFE might be a better idea - but if Cowden interests you, be sure to get a good cross section of posts about that from previous threads. There have been many.
If you connect with an ILADS LL ND near you, they would have a much better knowledge base and flexibility to work with various protocols. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
annxyzz
Frequent Contributor (1K+ posts)
Member # 20404
posted
PM jarjar he is in texas and I think he knows of one in DFW area .
-------------------- annxyzz Posts: 1178 | From East Texas | Registered: May 2009
| 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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic