kzfaq.info/love/1PVLGWeT3a6Cto-kOD9IfQ Meeting you was a life changer Dr imenherbal on KZfaq for curing my daughter from lyme I'm more than grateful...

Look into Chorine Dioxide (CLO2) People with Lyme are saying it cures it within weeks. Good Luck

I’m really sorry, Momma. 😔I got diagnosed at the age of 43. It’s been a hard road for me. My Mom knew something was wrong when I was about 10. But I started feeling sick about the time I was @8 . She just has no idea. And I don’t honestly know how I’ve gotten through this. I really thought I was going crazy. But these buggers attack the brain and the whole body. So, it’s no wonder we deal with so many neurological issues and have so many symptoms. I know if I didn’t ask my rheumatologist to do the Lyme test, he would have never looked into it. If I didn’t get diagnosed when I did and take my herbal protocol, I probably would be dead. I want to thank you for your compassion, love, and care for your son. I’m sorry it has been a hard road. Please take care of yourself too. Caregivers are often forgotten and I just wanna let you know YOU matter too. 💚

One word: Bartonella

@@newfie_mom7300 sorry for your suffering. I'm trying to overcome Lyme and coinfections myself. Social depression and irritability/rage are my worst symptoms. Wave1 device from Fremedica seems to be helping. But the Herxheimer can be very difficult.

we’re not completely screwed. we’re screwed in the hands of the american healthcare system but the providers within it that acknowledge it’s flaws and look at lyme for what it is, are rare, but valuable and life changing. i just wish there was more accessible options to low income patients :/ were barely able to pay for mine

@@calli8795 I tried to tell my new doctor I struggle with a lot of continuing symptoms, my knees still get swollen, and my spine is on fire. I take an Lyme herbal protocol which is pricey. 😬My doc won’t acknowledge chronic Lyme; he simply says it’s PTLDS. I mentioned “How can that be when I have all the same symptoms before my treatments?” Honestly, I will keep this doc for routine stuff but I’m gonna be looking at getting an integrative/functional medicine doc who happens to also be an MD. I’m grateful I can pay for my supplements, my herbs, etc. I’m thinking how can I afford this doc? I’ve heard someone say “This is a rich man’s disease.” I understand now that I know what I’ve been dealing with since I got diagnosed finally in 2019! YEARS of going to doctors (including several specialists), iridologists, herbalists, chiropractors, etc. I was treating the symptoms instead of looking at the root cause. I got misdiagnosed with fibromyalgia 11 years ago. I had a neighbor, a random person on IG, and my daughter who was taking a microbiology class, tell me to look into Lyme. Unfortunately, I had to ask my doctor to run lyme tests. Positive ELISA and 5 bands on the WesternBlot. 1 month of IV treatments that did nothing. There’s a lot more research going, studies on with different medications like disulfiram for chronic Lyme, plus the trials on the new Lyme vax (not sure how I feel about that one yet. Waiting for Phase 3 of the trials to be complete). Sorry I rambled so much. I’m just frustrated and angry that I’ve looked back at my life 35 years later, thinking a doctor could have caught this early. I’m so sorry you are struggling so much too. I pray for all us Lymies that we can improve and feel better in the near future. Just hanging onto Hope.

Doctors don’t take any of this seriously. Unless there’s a way to make money off of it pharmaceuticals and doctors won’t get behind it.

My son’s doctor visited him in the hospital and told him it was all anxiety and to go home and relax! He completely dismissed anything we told him. We won’t be going back to regular doctors for this anymore!

@@Tinyteacher1111 The latest on Lyme disease is that insurance records find there are around 476k Americans being diagnosed with Lyme. But there is belief out there that there are many MORE! I do not believe doctors will listen until they as well as more of these important/key people at the CDC, NIH, elites, etc. get Lyme. Maybe they’ll finally listen. We are making progress as Lymies. There is better testing hopefully coming out as well as more funding for research. When did your son get diagnosed? I keep coming back to this post as a way to learn, encourage, and be aware of others who are suffering and any caretakers that are so tired but care about their loved ones.

they know everything they just don't care

How can I find the labs that identify them?

Did he do the Home Protocol? I just did a consult with them to learn about the whole package. All I need is the laser and they don't let you keep it. They want you to do herbals, buy a vibration plate, an oxygen concentrator, etc. I already did herbals for 1.5 years after being initially diagnosed. They just made issues worse. I already own those two devices. Then I made it very clear I was good on nutrition--Paleo for 10+ years and the Dr turns around and says he'll assign me a Nutritionist. I started reading about nutrition in 2013 and never stopped. It's like he didn't get the point I just said. So I'm just going to buy my own home portable laser device. I have been seeing practitioners that use the MLS laser and do acupuncture laser. I am getting results from those lasers. So I feel the laser is getting deep in my nerves and relieving some horrendous chronic nerve pain issues.

I suffer as well. I was diagnosed about 4 years ago and did antibiotic treatment for a year and a 1/2 . Prior to that, I was an athlete for years played many sports worked out I was always fit and active. I spend most days now living a more sedentary lifestyle. Thank God I work from home because i am able to care for myself better. II cannot do the things that I once did. I suffer terrible pain every day in my bones nerves, joints, muscles. I've been to just about every specialist and no one can help me. The pain is so bad most days I just wanna give up like you but I find a way to keep going. I have really good health insurance but chronic lyme is not covered and especially these holistic doctors. I've spent over 30,000 trying to heal. I feel your pain.

@@nancylicho3538 did you try cold laser, Hyperbaric oxygen or hyperthermia?

I too have Lyme 11 yrs and counting. I was in remission until togus hit last year. It has been a struggle coming back from that. But praise God I'm persevering. He is my strength without Him I don't know what I would do. 🙏🙏❤

Covid not togus

@@nannag5801 I have a question how many months was you miss diagnosed with Lyme disease. And if there's any tips that you can give me what helped you through your journey. Next month I'm going to buy organic cat's claw liquid supplement. There's a small study on the supplement with Lyme disease that kills the hard kind of lung disease the doormat kind. I do with a canesa my knees my shoulders and my neck every Bright lights bother me. Did you have a problem with your CBC blood like your white blood cells and platelets at all. Because my white blood cells and platelets are my little low because of this disease. I'm going to get a second opinion to see a blood doctor. If I had money I will go to the best lyme disease clinic. Plus there's other treatments that's not approved by the FDA but I heard it helped for some people that's suffering. When Lyme disease is misdiagnose for some time the Lyme disease bacteria can trick the immune the Lyme disease bacteria can trick the immune system but it depends on the person's immune system and all they react to the infection.. one thing that I saw her with a lot as my chronic issues. I know but I have to keep my faith strong in the Lord through My Savior Jesus Christ but I know he's going to work everything out for good even if it looks bad. There's days where I thank the Lord for my suffering because without my suffering I probably wouldn't have a relationship with the Lord. Because Paul the apostle says Not only that, but we rejoice in our sufferings, knowing that suffering produces endurance, and endurance produces character, and character produces hope, and hope does not put us to shame, because God's love has been poured into our hearts through the Holy Spirit who has been given to..✍️🇺🇸✝️✝️🙏

Can you send her Instagram

What is her business? I’m not far from that area

@@heatherk6287 she uses Cellcore Biosciences products as a side business to her Chiropratic practice. She sees wonderful results in many of the people that consults her. I believe there’s only one Chiropractoc office in downtown Kennett Square. Herself and her husband do their practice together in that clinic on the Main Street. I don’t know what that Main Street is called but it’s not very long so you can find it. I do believe she has a website too

@@heatherk6287 my sister and her husband are two chiropractor that have a clinic on the Main Street in Kennett Square. She has been practicing for over 20 yrs but discovered through seminars that a lot of patients had severe symptoms that would persist even with good chiropractic care. She was introduced to Cellcore biosciences products a little less than five years ago when she contracted lymes disease. It significantly helped her and also treats people with all sorts of parasitic problems. That is her side business but am not sure if she has a name for that business. There is I believe, one chiropractic clinic in downtown Kennett Square and it is where she is . Just ask for Dr. Nathalie Matte

@@heatherk6287 I checked with her….it’s called Total health care. She has a website

I think all of my symptoms from the past 3 years are late stage Lyme disease the more I read yours and everyone’s comments. same RA/fibro like symptoms in the knees, depression, anxiety, anger, ear ringing, fatigue, I mean the whole list. The time I got tested for Lyme it came back negative but that was in a hospital, definitely going to look into the test you mentioned so thank you. The symptoms are something almost inexplainable to someone that doesn’t feel it, physically and mentally, something I bet doctors go in the back and laugh at when you mention a natural healing method

kzfaq.info/love/1PVLGWeT3a6Cto-kOD9IfQ Meeting you was a life changer Dr imenherbal on KZfaq for curing my daughter from lyme I'm more than grateful...

stabbing pains are due to gases stuck in the intestines and pushing through anything it can. farts and burps are gone... Gases can't find exits.

@@NotXboxiie I had cellulitis in my wrist for three months, this led to my Lyme diagnosis. The stabbing pains from cellulitis remain… they come and go…. gas… ya think?

Do you have a strange kind of debilitating fatigue where you feel it in your nervous system?

Yeah, that sucks. Still I'd trade with you today. For I have an occasional less bad few hours. Day before yesterday I was doing a small task without the usual brain fog. It was done in no time at all! After I had done it, I had a sense of accomplishment and joy over a task well done. Usually such a minor task takes me weeks of working up to it and then is very hard to do. The contrast couldn't be bigger. I felt normal for a few hours. The first in a year or so. Got my hopes up! But came evening time, I felt worse, than I've felt for months. Hope all gone again. Was a walking outdoorsy person once. Now, I can manage a few hundred yards tops.

As I see it, if scientist like you give no hope nor solutions then it is up to the patients to look for alternatives. I don't have the disease but for me non sense is to accept such a diagnosis without fighting.

She gives truth maybe

Did I say "without fighting? Certainly not. But managing is all what you can do. With good management, you can have a quasi normal life. I have followed some patients for 40 years and recorded their "story". I know about those who claim they are cured, and then relapsed a few years later..for worse. There is A LOT of fluff on line about Lyme. A lot of opportunists who want to make their name or their face known, or make a lot of $ on the back of desperate people. @@galeriadesol948

Hi there, have you heard, that the Covid-19 infection (which was tampered with in a bio lab 4) causes the same chronic symptoms as Lyme? This Lyme for sure came from it's own bio lab 4 near that small town Lyme in Connecticut. KZfaq video "Lessons from Long Haul Lyme & Long Haul COVID | Johns Hopkins Rheumatology" Link: kzfaq.info/get/bejne/pJ12rcmnz8jLhWg.html Not a disease? That bio weapon makes you very ill though! How do you advice to manage it? I'm suffering from it myself. Badly.

There is biofilm. The issue I believe in is NOT to obsess about it. It's bad for the brain. Some people do brain retraining programs which help balance and calm the nervous system which is really much more important. Obsession is only letting the Lyme brain continue. Lyme sufferers tend to obsess and have OCD issues. Turn off the MSM news, meditate, do brain retraining exercises, completely readjust what you think about. Tarter in the teeth is a form of biofilm. Good to brush our teeth but you can't be obsessive about it. The body forms biofilm as a protective mechanism. The body doesn't malfunction.

Because MDs can't stray from the big pharma plantation.

@@rangerdoc1029 This is true! You can’t even say “Lyme” in a hospital! They put you in the psych ward! Lyme is now recognized by the CDC, and it says it’s in all 50 states, but this is new. They won’t accept it, and all these people are walking around with horrific symptoms and the hospitals won’t treat them. Check out my earlier statement about Lyme and why doctors walk away from it! It’s JUST like mold, breast implant illness, and any tick-borne infections! I hope things change (Kudos to Justin Bieber!)!!!! It’s all swept under the rug because doctors don’t learn about this in medical school.

@@rangerdoc1029 bingo! Try to tell this to people who cling to their indoctrination though 😅

Just visit a chiropractor near you that uses a laser. I've been seeing a chiropractor that uses the MLS laser and its helping! I also had laser acupuncture done and it's potent! I'm researching for a home use portable laser I can use myself. The laser gets deep into the nerves where the Lyme and company are hidden. I started having rashes over my ankles and lower legs after doing these laser treatments. I have nerve pain in my feet caused by Chronic Lyme. The laser treatments finally relieved nerve pain I had down my right leg for over a year. Nothing else worked. it was disabling. I couldn't walk down my hallway all that time.

How did they respond to you? Are you getting treated?

I am sure and convince that, the sickness and diseases Dr odija on KZfaq cannot cure doesn't exist. Thank you sir for having great doctor like you in our own time. Keep saving lives sir:::::::

Rife machines kill it

Manuka,coconut oil,papaya,turmeric+black pepper,grapefruit,garlic tincture

@@TheWordSpiritwhat the hell is that

Look into Buhner protocol (herbs) they have helped me a lot! I'm diagnosed with Borrelia, Babesia and Bartonella. Wishing you the best🙏

​@@KRAEMERP2010how did u get diagnosed

@@purplerainbow1995 At St. Lukes clinic in Gdansk Poland.

@@purplerainbow1995 Armin labs. In Germany can also help. Don’t know where you live..

@@KRAEMERP2010 new jersey

There are ticks in the U.K., actually in every country all over the world, maybe except of the upper Northern Hemispheres with general low temperatures. The U.K.: facebook.com/groups/LymeDiseaseUK

Lyme Disease is found on every continent I believe.

Wrong 😑 UK full of ticks …Lyme toooooo 🏴󠁧󠁢󠁳󠁣󠁴󠁿😎

There are ticks in the UK, I have a friend over there who has lyme.

What are you talking about??? I live in Scotland in the UK and there is plenty tick here. I went off of the walking path into the forest for around 10 minutes and found 5 ticks on my shoes, my daughter 3, the other day I found a tick attached to my legs for hours after being in a forest in Scotland. We have plenty ticks in the UK. And I Polish and first hear that Polish people treat Lyme with celery juice and I have Lyme since September 2009.

How do you know wich product to use, I'm having joint pain and muscle twitching. We have no lyme doctors in DFW area for help

@@duster71 thank you for your reply. I'm going to call them tomorrow and ask for advice. I'm currently on a keto diet but I do eat small items of processed food wich I need to cut out. The only thing that has helped me so far is using a infared sauna with a salt room and taking magnesuim glycinate.

Follow the Buhner protocol. Green Dragon Botanicals provides the correct herbs for this protocol

@@annmariekampf2066 I am half way through reading Buhners book,not an easy read but it's not suppose to be a novel

@@duster71 he has a book in a 3rd chapter about morgellons disease too. Medication is needed I c private d r in T O. Ontario

Please...

@@cbo9090 Who asked you? If you don't like what's written here, you don't have to read it.

@@christined9210 tell me, how am I to know if I don’t like what’s written unless I first read it?

@@cbo9090 lol

@@cbo9090 some people like the word of God. Just ignore if you don't believe!

Wow that’s amazing. I’ve been suffering with Lyme for a long time now and I’m currently trying to cure it. How could I get in contact with Dr.Odija?

Also if u don’t mind me asking, what herbs helped you the best?

​@MLee the OP is a scammer... I see similar posts on almost every health or disease video on YT.

​@@MLee45950spam

Who tried it and how did they get it?

@@user-id2pz9sq1q as far as i know, at least 20 people got it from FANDACHEM this company and tried it and get positive feedback.

Yep and they won’t give even if you tell them symptoms they don’t care

Also it’s the people that are in healthcare especially doctors are just literal demons. That why they won’t help because we are there entertainment

Call me crazy but it’s something about us they don’t like to wear they can’t kill us so they’ll either drive us mad or get us to do something stupid

Hey, how has sski been working for you these past months?

Do you take that for lyme or do you have Morgellons and Lyme?

@@MLee45950 it cured the worm cyst zits ! It totally cured thoes annoying big zits that i couldn't reach on my back. But as for the fibers i still have them. I noticed the fibers became mor black less collored but still have collor. Selenium of 200mg minimal is the most important co nutrient when taking sski

Saw your post, how did the sski treatment go?

try mms

@@rusmax13 what is MMS..?

@@rusmax13 Miracle Mineral Supplement, often referred to as Miracle Mineral Solution, Master Mineral Solution, MMS or the CD protocol, is a branded name for an aqueous solution of chlorine dioxide, an industrial bleaching agent, that has been falsely promoted as a cure for illnesses including HIV, cancer and the common cold.

@@rusmax13have u tried it?