Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
Hello,
I need to place a supplements order tomorrow and wanted some opinions....
I want to begin treating KPU, but I need to go gently as I have a lot happening in my body right now. Using The Core would be easier, but I don't think I am ready for high doses of zinc. So my thoughts are to start slowly with the zinc, but go ahead with the rest of the treatment Dr. K outlined in the paper Scott Forsgren's wrote. [ If you haven't read it, it's here: http://betterhealthguy.com/joomla/images/stories/PDF/kpu_klinghardt_explore_18-6.pdf]
It suggests zinc and manganese before breakfast. With breakfast Omega 6 oils and fish oil. Before bedtime B6, P5P, Magnesium, BioPure Microminerals and Biotin.
I think this sounds like a good plan, but I thought I'd ask for input.
Thank you much, Tammy
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
momlyme
Frequent Contributor (1K+ posts)
Member # 27775
posted
Tammy, that's what we are doing. If you PM me your email I will send my working KPU treatment for my son. You will just have to double the dosage for yourself.
I have him muscle test everything weekly to see if we should change dosage, add anything, subtract something. You will see I have crossed out several things and added others.
Have lots of binders on board and start small with the zinc and trace metals.
Try to get supplements without the magnesium stearate, calcium stearate, or stearic acid. I think there is another additive to avoid...
I'm not going to be up much longer, I will check PM's first thing in the morning to see if you need the list. We ordered most from vitacost...
He didn't muscle test well fro the zinc we got from vitacost so I bought the standard process zinc liver chelate at the ND's office.
Good luck... and I read your post about not sweating. Don't push it. My son doesn't sweat either and I think it has to do with the mercury toxicity. No proof yet.
Keep supplementing zinc and knock out that mercury. Do you have amalgams?
Careful, OK?
-------------------- May health be with you!
Toxic mold was suppressing our immune systems, causing extreme pain, brain fog and magnifying symptoms. Four days after moving out, the healing began. Posts: 2007 | From NY/VT Border | Registered: Aug 2010
| IP: Logged |
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
Thanks momlyme. Will PM you.
Anyone else have any thoughts to share?
Thanks.
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
momlyme
Frequent Contributor (1K+ posts)
Member # 27775
posted
Tammy, your mailbox is full. I hope you don't mind me posting here, I didn't want to lose what I had written to you. Clear your box, willya?
Have you tried oil pulling for clearing the mouth sores? I think I suggested this to you on the board, but I am not sure. Simple and fairly cheap... all you need is some cold filtered sunflower oil: http://www.oilpulling.com/oilpullingvideos.htm
Send my your email and I will send you that working hpu protocol.
It is in document form and won't cut and paste well into this kind of format.
-------------------- May health be with you!
Toxic mold was suppressing our immune systems, causing extreme pain, brain fog and magnifying symptoms. Four days after moving out, the healing began. Posts: 2007 | From NY/VT Border | Registered: Aug 2010
| IP: Logged |
ukcarry
Frequent Contributor (1K+ posts)
Member # 18147
posted
Tammy, my only doubt is whether you may be giving your body too much to cope with if you start on this so soon after beginning AI.
Perhaps you could consider starting when you are several rounds in to AI therapy so that your detox pathways are not overwhelmed.
sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141
posted
I think you have a good idea separating it out. If you just started a new protocol, like ukcarry said, it might be better to get used to that protocol first.
I use Depyrrol. I started KPU before Core came out and never switched over because Depyrrol was working well. It has less in it than Core does. Just something else to consider.
-------------------- sixgoofykids.blogspot.com Posts: 13449 | From Ohio | Registered: Feb 2007
| IP: Logged |
posted
Were all of you tested, or just treating on your own?
Posts: 847 | From upstateNY | Registered: Dec 2007
| IP: Logged |
sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141
posted
I was ART tested. I would have gotten the normal testing for it, but I didn't have anyone to do it for me. Since I don't have anyone overseeing me on the treatment, I never took the higher doses of zinc, only the dose that is in the Depyrrol, which is 30 mg elemental zinc, which is within the FDA "safe" limit.
-------------------- sixgoofykids.blogspot.com Posts: 13449 | From Ohio | Registered: Feb 2007
| IP: Logged |
posted
I asked b/c I have been asking my LD to be tested for well over a year. I have so many symptoms, and have not gotten any better yet. I just asked again this week, and he hasn't seem to change his mind.
He ticks me off b/c I don't see the big deal about getting tested. Have thought in the past of treating myself. Right now just started Byron White Drops, so can't do it right now. But it will be something I'll do in the future.
Posts: 847 | From upstateNY | Registered: Dec 2007
| IP: Logged |
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
momlyme - Cleaned out my inbox:)
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
I lost track of this thread...
ukcarry and six - thanks for your thoughts. I will tread lightly. I don't feel ready to jump right in to full doses yet (especially of zinc). But I think soon it will be a good idea to start with low doses to help with my deficiencies.
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
lightparfait
Frequent Contributor (1K+ posts)
Member # 22022
posted
Tammy,Dr. K is talking about this in NYC n Feb 12th at his lyme talk. If you live close you should attend and ask your questions directly! best wishes.
Posts: 1009 | From NJ | Registered: Aug 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