HealingWell
Search Close Search
☰

ADP Oil of Oregano - started Monday

Support Forums
>
Lyme Disease
✚ New Topic ✚ Reply
1 2
❬ ❬ Previous Thread |Next Thread ❭ ❭
Posted 4/7/2016 12:28 AM (GMT 0)
I also started taking the ADP brand on the advice of my LLMD and I haven't noticed any difference yet. I continued to dramatically up the dosage and still nothing. However, I may have been overlooking some of the subtle changes experienced by others, so I'll definately give it another go...

Then again, it could also be the fact that I'm Italian and I already use high amounts of oregano and garlic in everything! :-)
Posted 4/7/2016 12:35 AM (GMT 0)
Thanks for the suggestions, bluelyme! I didn't realize royal jelly could help.....I've been taking Lion's Mane for at least 4 months now.

I take 600mg 2x daily Magnesium Malate powder and that dosed was determined by my bowel tolerance per Carolyn Dean ND's advise in "The Magnesium Article"....she did mention her personal need to add Mg oil. Maybe I should look into that.

The Oil of Oregano was an experiment for me and something good is definitely happening because my symptoms have lessened in their frequency and intensity (and that's on only one dose per day since Monday!! I just added a 2nd dose this evening). Whether the good stuff continues remains to be seen ;)

I was herxing in my head/face/sinuses so I'm thinking some sort of fungus since I have no GI symptoms whatsoever. Today I could barely feel anything symptom-wise in my head, etc. except for a couple of episodes of numbness near the left corner of my mouth. That's why I added the extra dose tonight...and my left cheek is now slightly numb. The stuff is doing something lol

If I decide to go for an expanded parasite protocol, I'll probably go with Hulda Clark's which I know have the first two other herbs you mentioned....not sure about quisalis.

Oh, Bart....yes, I've heard the fascilations are Bart as well. I'd been telling my LLMD from almost the beginning that I thought I had Bart. He didn't think so and kept telling me doxy hits it. I know better but I still got to 90% on abx. Herxing on Cowden's Bart herbs pretty much confirmed things for me and Buhner's herbs are the only ones that have resulted in improvements. I might just need to give everything more time - I've only been at full doses of the Bart (and Babs) herbs since December of last year. Buhner writes of 8-12 month treatment time.

How are you doing these days?
Posted 4/7/2016 11:07 AM (GMT 0)
OH MY cd - you sure have alot of nerve issues! have you ever taken SL vitamin B12 or pC body bio? I had a ton of nerve issues too, and these two things help heal the nerves faster. recommended by my Dr!!

pc body bio is very expensive, but i think it worked! something to look into if you haven't already.
Posted 4/7/2016 12:10 PM (GMT 0)
Yes, Chapelle - nerve issues have ruled my life with these infections.....I started with them and it looks like I'm ending with them.

I've been taking SL methylated vitamin B12 for years and I added a methyl B complex when I went on abx and continue to take both.

I take a bunch of EFA's (Marine Omega, Krill Oil, Flaxseed Oil and recently added Borage Oil). I took a peek at PC body bio and see it's derived from soy which I usually avoid.

Tell me, please....what type of nerve issues did you have and how long did you take PC Body Bio before they improved?
✚ New Topic ✚ Reply
12