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ozone therapy
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Lyme Disease
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gfields
Veteran Member
Joined : Oct 2015
Posts : 1320
Posted 4/6/2017 11:06 PM (GMT 0)
Has anyone here tried ozone therapy? What's your experience?
Krimpet 🍔
Veteran Member
Joined : Apr 2016
Posts : 3275
Posted 4/6/2017 11:13 PM (GMT 0)
Gfields there a gazillion posts about
ozone therapy on the forum. Many very recent posts as well. Have you done a search?
magoo2
Veteran Member
Joined : Mar 2015
Posts : 1667
Posted 4/6/2017 11:55 PM (GMT 0)
I have been doing ten pass IV plus nose and ears-I have to say I feel better today than I have in years
jrpsf
Veteran Member
Joined : Aug 2014
Posts : 1762
Posted 4/7/2017 1:03 AM (GMT 0)
Agree with magoo. I feel it's very effective.
gfields
Veteran Member
Joined : Oct 2015
Posts : 1320
Posted 4/7/2017 1:12 AM (GMT 0)
No, I haven't searched. I can do that. I just saw a video about
it, and it seemed like people are having positive results. I was wondering if they are long term results or just temporary.
MA10
Veteran Member
Joined : Oct 2012
Posts : 693
Posted 4/7/2017 2:03 AM (GMT 0)
I've been doing IV ozone since January. I love it. It immediately helped brain fog. That's been my biggest symptom improvement.
bluelyme
Veteran Member
Joined : Nov 2015
Posts : 6219
Posted 4/7/2017 2:55 AM (GMT 0)
I believe it only hits the spirochete form ...and if you have a sod mutation it can be hard to process.. in europe they shoot o3 direct with a butterfly but here we tiptoe add to blood and heparin and sometimes saline ...i wonder if the blood thinning qualities and biofilme busting of the heparin help...i asked the local yokel here who just started doing 10 pass about
admin though my port ..he didnt know but for 600 a pop i think he could dig if the ozone degrades the catheder plastic? It holds up to contrast and h202 so idk..
anyways i did a few months of mah with ubv and all i got was tired may try again soon
gfields
Veteran Member
Joined : Oct 2015
Posts : 1320
Posted 4/7/2017 5:03 AM (GMT 0)
So you think the ozone is actually killing the spirochetes, or is it just masking symptoms?
magoo2
Veteran Member
Joined : Mar 2015
Posts : 1667
Posted 4/7/2017 11:24 AM (GMT 0)
There is a blog I read about
an ozone clinic-its on FB called Cyprus or Bust.
Gives some good insight into ozone
Purrrsiankitty
Veteran Member
Joined : Dec 2016
Posts : 1780
Posted 4/7/2017 12:47 PM (GMT 0)
My LLMD will have it soon. I will probably give it a shot.
I did read somewhere, I believe pharmacist Suzi, that people with babesia should not use it.
theskyking123
New Member
Joined : Aug 2017
Posts : 3
Posted 9/18/2017 6:52 PM (GMT 0)
Any update from folks using ozone?
MA10
Veteran Member
Joined : Oct 2012
Posts : 693
Posted 9/19/2017 1:10 AM (GMT 0)
I'm still going strong with it. I keep doing it because I still herx after every treatment. It doesn't make me feel better. It makes me feel worse. But somehow I validate that as a reason to keep it around.
jrpsf
Veteran Member
Joined : Aug 2014
Posts : 1762
Posted 9/19/2017 2:50 AM (GMT 0)
Just started back doing it today. Needed to treat Babesia for a while so my blood was thinner. It was too thick and would clot to fast to be able to do more than a pass.
I've also done IV peroxide and that helped. Anything that helps oxidize has been extremely helpful for me.
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