A recent study was done in a psychiatric hospital, and they tested all the patients for tick-borne infections. It brings out rage and mania, and my son has just recently found out he’s had it since he was 7! 90% of the patients tested positive for a tick-borne infection! I feel so sorry for the people who never have been diagnosed and have no idea why they are like they are! No one wants to hear the word Lyme! It’s like saying “bomb” in an airport! They tell you there’s nothing wrong and it’s anxiety! My poor son went through his entire life with one of these infections and the only reason we found out about it was because I took him to a specialist to be tested for mold toxicity. This had emerged from the lowered immune system from the mold. He has horrific headaches, neurological disorders, hallucinations, sweats, etc. I’m just thankful we found this out now at his age of 36. It explains his life! Now, he has to get well, and it’s going to be a long road ahead for both of us. I’m a retired teacher and babysitting him has been my life for the past two years.
ru-vid.com/show-UC1PVLGWeT3a6Cto-kOD9IfQ Meeting you was a life changer Dr imenherbal on RU-vid for curing my daughter from lyme I'm more than grateful...
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. 💚
@@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.
So a spokesman from the CDC said we should talk to our healthcare provider about the risks of doing alternative treatments? How is that gonna help when doctors don’t believe that Lyme can become chronic. We’re screwed. Any Lyme patient knows that.
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.
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.
The CDC and Medical Industrial Complex will not acknowledge alternative therapies. I’m very happy this woman found help. A friend of my sister’s killed herself because of the pain she was suffering from Lyme disease.
Lyme disease is one of the major causes of fibromyalgia! There are only a couple labs in the country that identify Lyme through the genetics of the organism. Now I am taking binders, and my symptoms are slowly going away… This is after 25 years!
I suffer with chronic lyme disease 6 years ago I'm still suffering today I had to get three bone marrow biopsies done finding out that I have feel less cells in my bone marrow currently at 20 to 25% and it should be at 70% for my age my blood doctor tested me for syphilis HIV leukemia lymphoma everything came back negative except I had high levels of bar virus that most people have in the United. I suffer with chronic got issues I lost a lot of weight my knees ache my shoulders and my neck I have mildly low white blood cells and platelets but they are stable low. I don't have no infection in my bone marrow but I know it's Lyme disease that lessen my cells. Bright lights bother me I deal with chronic fatigue depression anxiety and I'm only 35 years old. I only can do so much of the income that I'm on for SSI doctors looked at me as a patient not a human being. The CDC denied me once and I had all the symptoms of blood work and testing I have no idea what to do I just want to give up on some days and be with the Lord through My Savior Jesus Christ. I got copy of my medical records from Dean clinic now I'm getting all my medical records from UW clinic and I'm going to get a new doctor and discuss why I'm still sick and sit down with infectious disease doctor give me some answers because it's not right.
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.
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. 🙏🙏❤
@@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..✍️🇺🇸✝️✝️🙏
My son did this treatment in Canada, it works....it took almost a year to clear it from his system, although he feels so much better, he is still dealing with the long term damage from the lyme disease, including inflammation, and nerve pain.
My sister has a chiropractic practice in Kennett Square PENSYLVANIA and has a detox business on the side. She is helping people get rid of parasites and Lymes symptoms. Many of her patients are more than pleased with the results of her treatments.
@@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
Hope for her it sticks. I seemed to be cured once too. But it came back and now I'm partly disabled. Brain fog all the time, which makes me confused of what to do. Any simple problem throws me off my ideas for the day. Before I got Lyme, I was a focused trouble shooter. It's left me a shadow of a shadow of myself. No way to live. Most horrid.
Hey, I just found out that my fibromyalgia that I’ve had for 24 years, has actually been a whole bunch of tickborne diseases! I wonder how many other people with fibromyalgia have tick problems? Regular testing -Did not find it! I was diagnosed negative twice. You have to use the Vivant test for the antibodies. And genetics. Vivint lab.
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
ru-vid.com/show-UC1PVLGWeT3a6Cto-kOD9IfQ Meeting you was a life changer Dr imenherbal on RU-vid for curing my daughter from lyme I'm more than grateful...
I’m 60, strong and fit , for my self, outdoorsy. When I have a flare up… I have a hard time moving my arms turning my head my neck hurts, my skin burns, my ears ring. I have shooting and stabbing pains in different parts of my body and terrible muscle spasms. Could last and evening, could last a day or two, just like that it fades days for a week or two. Those are the times I think I can go back to work and be normal then bam, it comes back😢
@@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?
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.
"It takes 9 months to break the biofilm all over the body" As a Lyme researcher, it pains me to hear such non sense. Managing Lyme is much more complicated, unfortunately. It is incurable, as it is not a disease, but a multi-pronged bioweapon. Managing is all what you can do.
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.
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. RU-vid video "Lessons from Long Haul Lyme & Long Haul COVID | Johns Hopkins Rheumatology" Link: ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-n7FzfvjbgU4.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.
Chronic lyme sufferers are at the mercy of zll snakeoil salesmen because they rarely get help from their GP. As . GPS are cdc approved so the test kits can't pick up Chronic lyme symptoms as 5hey are 3xpensive and hit and miss. Chronic lyme is very good at faking symptoms of something else.
@@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.
I was tested for Lyme and Syphilis. Oth came back negative. But I honest to god believe i have syphilis from 2009, and am desperate for a doctor to give me a lumbar puncture to test for it. Anyone have an idea how i can get this done?
I am sure and convince that, the sickness and diseases Dr odija on RU-vid cannot cure doesn't exist. Thank you sir for having great doctor like you in our own time. Keep saving lives sir:::::::
Thank our profit driven health care system. We go to the gas station for a gallon of gas but if you only got a 1/4 of a gallon you would be outraged, well welcome to the spirochete world.
I must appreciate Dr odija on RU-vid for helping me in getting rid of Norovirus, Your product for healing stomach bug is really the best keep saving lives
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
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.
@@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.
Living with the stigma of HSV 1 and 2 and not been able to have a healthy relationship was messing up my life until I got some super herbs from Dr odija, I haven't had symptoms for some while now and planning to get another test done. Am grateful and advise you help yourself also!!!!
@@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
I suffer with chronic lyme disease 6 years ago I'm still suffering today I had to get three bone marrow biopsies done finding out that I have feel less cells in my bone marrow currently at 20 to 25% and it should be at 70% for my age my blood doctor tested me for syphilis HIV leukemia lymphoma everything came back negative except I had high levels of bar virus that most people have in the United. I suffer with chronic got issues I lost a lot of weight my knees ache my shoulders and my neck I have mildly low white blood cells and platelets but they are stable low. I don't have no infection in my bone marrow but I know it's Lyme disease that lessen my cells. Bright lights bother me I deal with chronic fatigue depression anxiety and I'm only 35 years old. I only can do so much of the income that I'm on for SSI doctors looked at me as a patient not a human being. The CDC denied me once and I had all the symptoms of blood work and testing I have no idea what to do I just want to give up on some days and be with the Lord through My Savior Jesus Christ. I got copy of my medical records from Dean clinic now I'm getting all my medical records from UW clinic and I'm going to get a new doctor and discuss why I'm still sick and sit down with infectious disease doctor give me some answers because it's not right.
@@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.
