I nominate Paul Auwaeter of the IDSA and the CDC as "MORON OF THE YEAR !" This guy wouldn't know a tick if it bit him in the ass. . .
Posts: 3217 | From Florida | Registered: Nov 2016
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posted
Phenomenal article, now people have a great article to give to their friends, family, and doctors that are in denial. I love the title!!!
Remember denieing chronic lyme disease, is denieing science.
Doctors and scientists are so blatantly pushing the science behind climate change, which I fully support, but where are they on chronic lyme disease, when the science is out... Especially when millions are suffering and thousands have died, oh my the ignorance and hypocrisy from the scientific community!
I lost a good portion of my 30s because of this disease and the greed, ignorance, and corruption over at the CDC. I sure hope someone serves time for this. I've already seen how they tried to throw corruption under the rug with Flint Water Crisis in my home town.
I've been using the antibiotics mentioned in the article and studies, having a lot of success with Stevia, the enzymes from Liverite Liver Aid, even using Special FX CBD oil from a local dispensary here in Michigan... The CBD oil I use actually has cinnamon in it too, remember what the article pointing to another article said about cinnamon bark. We already know through research that cannibnoids like CBD and THC are antibacterial, so this is a double whammy if you can find a CBD tincture with cinnamon in it. These 3 really been helping me with biofilms...... I want to try oregano oil next... But as I've found out, you must pair them up with strong antibiofilm antibiotics in order to get the full effect, like Tindamax and Flagyl.
I've been using Stevia with Doxy/Ceftin/Tindamax... I swear to God I can feel the brain fog, pins and needles, and weird tingling feeling of the biofilms expanding and contracting when using these antibiotics in my joints.
I've been treating for this disease for 6 years, I've never felt these expanding and contracting feelings I'm getting when I treat with these antibiotics and biofilm busters. I've tried nattokinase and serrapeptase, earlier in my treatment, but never felt what I've feeling now.
Dapsone has extremely helped me, but be careful with this drug, extremely toxic. The half life is a lot longer than what scientist and doctors say it is. I've changed my stance on this drug, it has helped me progress amazingly, but just be careful with it!!!
The borrelia bacteria is more resiellient than one could ever imagine, this has to be the most intelligent bacteria on this planet. It literally knows when to throw up it's self defense mechanisms(when you start taking antibiotics) and it knows when to come out of hiding when you stop.
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
posted
Right you are Charlie Fitzgerald.
I pulse flagyl on weekends and infuse oil of oregano throughout my house.
I'm not Italian but it sure smells like I am , ha ha. No disrespect intended to the politically correct.
Posts: 3217 | From Florida | Registered: Nov 2016
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I know some LLMDs recommend staying away from high carb foods and sugar because it feeds borrelia. But if you read the one article up above, even the one about Dr. S, she said that's how she figured out to try Xylitol and Stevia. These natural sweet sugars will bring down the natural defense mechanisms of the borrelia bacteria so it can feed, that's why I assume it's such a good biofilm buster.
I feel pins and needles in my joints when I take tindamax/ceftin/doxy with chocolate candies. Remember I've been treating for 6 years now, so the herxing when doing this could be super powerful for lyme patients in early treatment.
ILADs and these doctors are doing ground breaking work, I hope they come out with a solid treatment protocol soon!!!! I can concur all these natural biofilm busters do work with antibiotics... Even the antibiotics they mentioned have helped me progress.
Posts: 108 | From Germany | Registered: Jul 2017
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quote:Originally posted by Bartenderbonnie: Right you are Charlie Fitzgerald.
I pulse flagyl on weekends and infuse oil of oregano throughout my house.
I'm not Italian but it sure smells like I am , ha ha. No disrespect intended to the politically correct.
Great to hear!
Try Tindamax instead, Flagyl worked great for me in early stages, but I find Tindamax works better, just as Dr. S work has shown.
I want to try pyrazinamide, but my body is still recovering from Dapsone. Dapsone worked incredible, but it's half life is strong and it's extremely toxic.
I do take long breaks switching between antibiotics, like a full month, as well as take detox supplements. Good to detox with baking soda.
I sure hope all this helps lyme patients, the work they are doing is ground breaking. I hope it saves lives, I wish knew what I know now 4-5 years ago, it would of helped me progress so much faster.
Just so you know, I did make a good choice back years ago because I was staying up to date with Dr. H and what others were saying on the Lyme forums.
I was treating with Dr. Z and Dr. M in Michigan, neither of them used Flagyl. Once I understood that and Dr. L office freed up to take patients, I left both of them to use the best doc in Michigan who used Flagyl. It helped me progress rapidly, but Flagyl alone will not get you into in remission. I guess it all depends how long you've gone untreated, but you must pair flagyl up with other antbiotics, and other natural antibiofilm buster supplements.
Safe treating and hope this spreads hope for others. Remember knowledge is POWER!!!!!!!!!!!
I also must say, even though I've been critical over some of the alternative treatment on the Lyme forums, a lot of the people on Lyme Net are the reason I'm still standing today. There's a wealth of information on these forums as well as others that may save your life.... Knowledge is power....
Remember to support net neutrality and don't let anyone take it away from us, Internet has helped save my life!
Posts: 108 | From Germany | Registered: Jul 2017
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Before I found a LLMD in Michigan and started antibiotic treatment 6-7 years ago, I was craving sweats. Remind you I'm about 220, lean muscle and workout. I never had a sweet tooth, but when I was going down with head pressure, joint pain, food allergies etc... I was craving sweets...
Point I'm getting at is, this bacteria is so intelligent, I believe it can communicate with the human brain to help feed itself. It all makes sense why stevia, xylitol and even sugar with antibiotics will help kill this resilient bug.
Let that sink in for a few minutes... If you study science and watch documentaries like I do, you'll realize how every animal on this planet is a living breathing small ecosysm. When you get a foreign invader to mess your system up, that can seriously cause a lot of problems.
I remember watching some science channel once, where there was a bottom feeder fish in the ocean, the bacteria in its stomach lights up to allow it to feed on prey... That's communication between cells, pretty amazing. So bacteria communicates with our body, our brain, and it makes you, believe it or not!!! Pretty amazing stuff!
Just remember to take probiotics to replenish the good bacteria, I think we may learn in a few months that fecal transplants may be great for lyme patients in the some time future...
Posts: 108 | From Germany | Registered: Jul 2017
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Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
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Agree, Agree, Agree with everything charlie fitzgerald.
Another thing I do is take 1 TB spoon Silvercillin with my antibiotics. Research shows it increases effectiveness of meds.
Of coarse what works for one may not work for another. But atleast we have the power and knowledge to atleast try. We can all learn from each other and help each other.
STRENGTH IN NUMBERS LYME WARRIORS !!!!!!!
Posts: 3217 | From Florida | Registered: Nov 2016
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Brussels
Frequent Contributor (5K+ posts)
Member # 13480
posted
Fortunately, it's not only the bad bacteria that communicate, but the good bacteria too!
Look at the research on gut bacteria or microbiome to understand.
Then, there are our own cells that communicate!!! through low emission coherent photons.
Cancer cells lose the ability to communicate with others non cancer cells, that is why they go wrong and reproduce, having zero function to the host.
If you think Borrelia is intelligent, you gotta look into candida. It's even another level, of amazing pleomorphism!
when your brain can tune into these wonderful world of invisible (but REAL) communication, you start seeing less Borrelia and most pathogens as enemies, and more as 'talking partners'.
In my opinion, these pathogens are not 'evil' and 'resistant' like people think of them, but they are here, making our lives a hell to show us some metabolic problems, immune system failures.
Posts: 6200 | From Brussels | Registered: Oct 2007
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