Відео

Igenex Lyme test received fda approval could help some get public treatment if broke. Keep up the fight Lyme warriors Hydromycin will be available just a matter of time I email the owner of flight path producer of hydro it looking good.

Thanks for this informative video. I’m getting my first SOT infusion tomorrow. I’m nervous. I was bitten when I was six years old and have had symptoms since then. But it didn’t get significantly bad until the last 10 years or so. I’m 44 now. I also have CIRS… And possible mold toxicity. So trying to get all of the things treated. What a wild ride this has been. I have periodic paralysis and my weakness has been getting worse over the years. To where I’m bedridden for months at a time. I’m planning on treating more while I’m going through the SOT treatments. I might as well get it all taken at the same time right? 😂

Cipro my Buttt ,it can destroy your tendons,it did mine

Excellent thank you

I just found this because I started taking methylene blue recently and today I got a very strange feeling in my legs. I have never experienced this feeling before, it scared me it felt like water under my skin

safe during pregnancy?

How can you possibly recommend Cipro, geeeze...

Can one SOT only address one organism?

I'm from Canada here and my drug plan coverage is pretty poor but they still cover compounded LDN thankfully. I honestly don't really feel too much difference on it. I have had Lyme for 4 years and difficulty finding effective treatment but I have to assume I would be worse without it so I continue to take it. My pharmacist said it is a great immune booster and anti inflammatory drug.

Cipro can be very damaging. Not worth the risk of permanent damage. Look it up.

The cheapest he found was $138? That is a lie lol

Ive been taking it for 3 days in the morning. First day 5 drops, 2nd 10, then 20. On the 3rd night before bed my neck and shoulder suddenly started aching. I fell asleep but woke up an hour later in really bad pain. I couldn't move my shoulder or neck and it didnt go away for hours. It felt like inflammation for sure. I woke up in the morning and it was gone completely. Bit worried about taking it now.

As a traumatic brain injury methylene blue has been a godsend do your own research PS under a penny for dose per day!

What about flair up

I'm curious if the symptoms of PANS are constant in your experience or if they come and go through the day. My daughter is currently switching between spending almost 1/3 of days repeating things (OCD), 1/3 of the day in a miserable crying meltdown, and the other third in a screaming rage. But in small windows between these we see her personality come back, the light come back into her eyes and the bubblyness come back into her voice, someone's even for a couple hrs at a tiny time. And then almost instantaneously she's back into one of the aforementioned modes. From your experience can PANS be like that or is it constantly the same every day every hr?

I first got limb pain, nausea and fatigue. My understanding is that this was a "Herx reaction" and is related to pathogens being wiped out in the blood stream then dumping toxins to be eliminated. I stick to a dropper full 2 to 3 days a week. I feel good and have no further issues.

cinnamon oil cinamon leaf oil 3x's per day 100 days cant miss a day or you start over

Yes I use blue as part of my preventative disease plan, works great on short term memory!

Very cool thank you

I have a 1% solution of MB and taking 30 drops in water twice a day with vitamin c do you think that’s enough to treat Lyme

Months ? 😂

It can raise blood pressure and tinnitus louder. Takes pain away feeling like 20 years younger 😅

Thank you for all the information Doc

Thank you for taking the time to share your clinical experience knowledge

Which brand?

Hogh dose vit c in drip for 25 to 30 days

You never mentioned diet its most important to starve of bacteria the diet is most important for 12 months

So this would be an alternative to taking opioids? Could it help to get off opioids after a decade of use to treat chronic pain from Lyme?

I don't get limb pain but I do get a headache within 5 minutes of taking 3-5 mg dosage orally. It doesnt' last long though.

NEVER TAKE CIPRO!!!! It has permanently damaged me.

I was diagnosed with late Chronic Lyme, after years of being sick. I finally found Dr. William Harvey. He started me on IV antibiotics, which alternated with something else, which I can’t remember. I followed this protocol for 6 months. It was a long road, but I hung in there, and it worked!!! I got my life back. It’s been 16 years, but I am healthy today! Dr. Harvey has since passed away. I would encourage anyone going through this, to do just as the Dr. says. He clearly understands the complexity of Lyme Disease. Great video! Should mine ever return I would go to this clinic! I also cut out carbs, and began exercising.

I experienced leg cramps, but simply backed down the dose. Now it is fine.

How about a time warp research like they did for this questionable covid vaccin. Why not because they won't make billions from it so it will take forever that's why

I am taking it 15drops a day for a week and my urine didn't turn blue I.dont know why

Herbs and carnivore diet really helps me😊

I have had symptoms for five years. I was previously tested and came up negative but JUST came up positive for Lyme. PTLDS fits what I am experiencing 100%.

the IDSA doesn't believe chronic lyme exists , I've been down that route with my doctor

Can this cause a herx reaction?

Very informative can I use peptides as well along with the protocol

Us there ny help for psychological and neurological in lyme

This stuff helped clear my brain fog (from diabetes) and I don’t know how but my knees stopped hurting 👍🏻

Thank you. As I go review my Vibrant test again, lol! The jury is still out for me. Lyme SOT this past September. Bartonella SOT this past December. Will test (with Vibrant) June 2024. Preying.

Iam experiencing body pain taking the liquid form

Do you have any more info on SOT - I have Lyme and interested in it

Thank you for your really informative and helpful videos/channel. I wish we lived closer to your office.

I'm very happy and congratulations for anyone who gets better from this insane life destroying disease, co infections, viruses and environmental illnesses. It costs money to get treated, which I don't have now. I wish the cost of treatments were much more affordable and some kind of insurance payed for some or if not all.

What about if you have the mthfr gene mutation is it harder to get results ?

I was recently diagnosed having antibodies for Lyme. I have Severe rashes, anaphylaxis due to allergies which become more severe after exposure, joint pain, sleep deprivation, brain fog, Cytokine storm, weird allergies, migraines, vertigo, mood disorders depression and anxiety, bell’s palsy, loss of muscle mass, weakness,exhaustion

So if I have muscle and joint pain already and interstitial cystitis, my gut reaction is that this would not be a good fit for me.. based on the side effects you listed. My doc recommended this for me.

All are antifungals right?