The Lyme Resource Centre is a charity with a mission to educate the public and healthcare professionals about Lyme disease and related tick-borne co-infections and work with others to research ways to combat all tick-borne illnesses.
We are dedicated to:
・ Educating the public
・ Educating healthcare professionals
・ Supporting patients
・ Working with medical, veterinary and countryside organisations to tackle the causes, diagnosis, treatment and care of Lyme disease and other tick-borne diseases, including matters affecting patients, their families and others.
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Babesia is endemic in North America Beginning in the northeast.
Thank you so much!! Very well explained!!
Persistent infections, environmental illnesses cause immune system problems and many symptoms.
God bless your efforts...but I love how complicated are humans.. Very easy robot approach: Step 1: where are the plants located? Step 2: where can we buy the plant or send humanoid to collect them?
Jack Lambert is best Dr in Ireland for these diseases well done jack great man
31 blood test in Ireland Notting showed up untill I meet Dr jack Lambert in matter hospital Dublin,
I have Long Cronic Lyme & co- infections. I just started LDN 3mg daily & have had 3 blood transfusions! I got bit the 2nd year of pandemic & after Dr-Dr-Dr. I had to find out on my own reading books from Amazon what I had little did I know HELL is the only way I can describe it!! Try reading with brain fog!!! Thanks ❤
This talk gives me so much hope. Thank you for hearing us, believing us and helping us.
Thank you for this presentation which does an outstanding job with integrating clinical practice knowledge of Bartonella and microbiology science - all in layman’s language. This global approach is much appreciated!
This man needs to run the hse not Stephen Donnelly who is a payed off mouth peice for drug companies
I have a nuerological heart problem caused by these nuisance diseases, but im not getting any kind of help within this conventional system. Lyme carditis is recognized but in the state I live this medical system does nothing. I know this comment won't be read because of these social media sites still committing censoring.
I totally understand what your going through.
I understand what you are going through too. It took me a couple years to get diagnosed, which is insane, and my state has no resources either. I have severe chronic Lyme now without the financial resources required to fight it. It's so hard to maintain hope 🥺
Great talk, I wish there was more info on the treatment.
35:13
41:50
Iv vit C and ozone for 30 days seemly knocks out lyme in the body but you have to starve the lyme and not feed it during treatment
I have psoriatic arthritis. It’s caused spondylitis in my spine. Years ago I was diagnosed with fibromyalgia. Then I was told I had psoriatic arthritis spondylitis, mutalins of the hands. My fatigue & pain is off the charts. No one until last week suggested I could have Lyme disease.. and that did not come from a rheumatologist or dermatologist or any of the specialists I have seen over the 20 years I have been sick. It was a good - fantastic nurse practitioner. Praise God i know and maybe healing to some level can come now. Please if you are a praying person please pray for me. I want to live and enjoy my life. I know the damage is done but there is so much I need / want to do. My youngest daughter is graduating with a doctorate in pharmacy next spring. I really want to be there to celebrate her accomplishments. I have a daughter who is a nurse also. And a very caring husband who has seen me through all of my illness. He’s my hero. He took off over 3 years to be home to help me. He’s gone back to work near by our home. He is insuring my youngest daughter has everything to finish her last year of internship in pharmacy school . Such a good step father to help her succeed. He also helped my oldest in her last year of nursing, her internships. We had just married in her last year of nursing school. See I must get better for him too. I have so much to live for. Thank you for your video ! And for anyone who can pray for me. God bless! Leslye
Thank God! I’m taking this for Babesia!
Is it working?
@@kumulsfan8090 yes.
Great info!!! Necessary for everyone! 🙏
This is the test my husband had showing borellia miyamotoi. Very expensive. And labs in US don’t do these. Had a dr from Belgium use RED laboratories to find it. What are your thoughts on phage therapy treatments?
What are your thoughts regarding phage therapy? From the US - pcr tests starting to come back for my husband so far he has Borrelia miyamotoi and he needs treatment and there is a center in Tennessee. Biologix. Just wondering your thoughts
Most needed research... Artemisinin IV as Garsus and tablet extracts Coartem are pharmaceutically derived (read concentrated) from artemisinin herbal plants known for over 25 years to be effective against various malaria strains and "discovered" in China also have implications for the effective treatment of babesia and bilharzia / schistomiasis... second only to malaria in terms of harm, destruction, and death especially in developing tropical and subtropical areas. Numbers in >200m annual deaths according to the World Health Organization in Geneva
I have the same, i have been bitten more then 60 times by ticks, and i am sick, but all tests where negative, but some pcr where positive, although not in the normal hospital. But every time i get doxicycline ill get way better then i was beffore. Now i am in such a state that i will buy a own Darkfiel Microscope to do research.
Thanks
If a Borrelia burgdorferi Total IgG/IgM Antibody with Reflex Test Value is 0.72 does that mean exposure to Lyme disease at some point? I know that indicates a negative result. I'm just curious if that result shows past exposure to the disease???
I hold a high record for writing you. I was 23 & woke up sick. On my dads side of family, he got sick a year and a half before me. Out of 6 kids-The 3 youngest passed prematurely! My aunt, the baby of the family, was only 49! She had problems similar to my dad & I. Other sister, 58yrs old, died MSA multiple system ATRAPY. The second youngest he was 62. My dad just turned 70, I'm 48. We were always full of spit & vinegar. Then, life put us in a cage. The mental torture COMING from physical pain. It's hard feeling worthy, when you're not able to clean. To have nice things. That hurts me. I went on disability 20's. I can't work overtime. That's my biggest trigger mentally. I want to feel worthy& that I'm good enough. Not having a clean house it knocks me down. I'm thrilled when I can run a sweeper. It's not enough. I've wondered if I'm just a burden many times. Being 90% bedridden for So LONG DAY AFTER DAY. When I have those "good" days, I fly outta this house like a 48yr old teenager! Able to see my kids & my grandbabies! I try posting some of my story where I can. You never know who needs to read this & helping them OR finding a person who can actually HELP us. I've had seizures up to 15 day. My bp dropping as low 54/34 & blackout. Cardio says dystolic dysfunction nothing to worry about. The one before said I was to young for heart issues I was 44. Getting the same answer from every specialty. Looking like I'm exaggerating all of this. I just want HELP. We can stop this! As today, we're still neglected 10/2022! I'm fighting & keeping hope. I keep screaming out. Anywhere & everywhere. I have a group page on fb I go live & you see with your own eyes how I morph into something totally different & then back to normal. PROOF! It's a disease where we're to feel shame. I'm a suicide survivor & the continued darks thoughts in my brain AND it's continually swelling W meningitis! Actually, this is acceptable, obviously! It continues to happen. I dug in my medical. There's abnormal from Feb 1998 to now. I'm 48. I have SO much to live for, my brain gets confused. I become overstimulated & my body is stuck.I have suicidal thoughts constantly & they're very scary. Alone! I have Myalgic Encephalomyelitis too & I have a family around the world who I love. We need understanding. You can help us. Help break through the stigmas of ME/CFS & Lyme. It's 100% abuse. Dr. Phil Will you help ME fight? Not just for me, but all the other #MillionsMissing, please? We need a hero Dr. P
Ivermectin horse paste, 1.87 is a pure form of ivermectin. It cure me of my Lyme disease and many many of its coinfections. I am 64 years old and have been sick since my teenage years with Lyme disease I am now cured. It is a long protocol on the ivermectin but very well worth it. You will experience flu/cold like symptoms as the parasites die off. I have been taking ivermectin for one year and two months. I will never stop taking it. I am healthy happy and full of energy ivermectin has been hidden from us as a cure for the Lyme disease. Spirochetes were bile Weaponized against, our immune system it is also discovered now that antibiotics feed those spirochetes
I know I’ve had 3 blood transfusions & a fake heart attack, fake COPD & I’m 70 & tired if I had more courage I would kill myself! Just started LDN 3 mg. And been on antibiotics for 2 years! Please Lord helpUS!!!💊
I keep this on my clipboard, addressed to Dr. Phil. I just paste it and pray the right person reads this. I'm desperate!! I really am. Dr Phil I've written many times. I'm screaming for help. I was only 23yrs old when I woke up sick. 4mths after my husband and I got married. I had a great job..I have 3 kids, 2 granddaughters and 1 on the way. My dads family out of six kids, 3 youngest have passed. One having MSA. My dad has been sick about a yr and half longer than me. All he did was wake up. We were all very outdoorsy, could barely keep us inside. Campaign fishing sports.. I'm now 47 dr. Phil..24yrs in Feb. My passion for life is so strong but my body so tired.. 90% bedridden, my dad 90%housebound. It's hars at times to keep going. You say you read the comments.. please, I absolutely believe it's lyme. I was diagnosed with myalgic encephalomyelitis starting with a staph inf. I'm uncovering so much in my medical records where they could have saved me. Now this past July, my brother, 51 my only sibling found out he has myelofibrosis a rare blood disorder secondary to phenylephrine. You say you use your show as a teaching tool. I have a group page I started in 2015..ppl all over the world just like me!! Behind 4 walls. My brother and I both have watched you since Oprah! Tracy Smith-Duncan!! I'm also a suicide survivor. I have many testimonies throughout my life. God has me here for a reason. I'm here to spread a message if I'm healed or not. If I can stop any one person from such a tortuous, life snatching disease. ..that's what is so important. My life may be to far gone, I don't know. I was just a baby myself waking up in this body that is not mine. I hope you read this! Sincerely, Daughter, sister, mom, wife, Memaw and friend 🙏🏽 My jaw started deteriorating at 24yrs old. Now, I have so much proof, they can't even deny anymore. If someone will just listen. PLEASE
I'm not homeless and got handle and quintana
That looks like exactly what happened to me now.
My God heal you completely! 🙏🏻 leslye
@@FourHuskyHomestead Me as well including atrophy and bell's palsey.
This video saved my life. I treated Lyme aggressively for years with multiple picc lines for abx. Found out Bart was the problem. I was deathly I’ll, and often said “Lyme was in my brain”
What u did for bart and what do u do know? Anything helped?
how did you treat bartonella then?
Oh and should add he has started the antibiotic Clarythromycin (slowly to prevent HERX reactions) and will soon add Minocycline
please help us, and thank you keep up the good work lymes awareness and treatment.
As an LD sufferer (bitten in 2007, undiagnosed for 2 years ) I would so like to speak to this GP.
Thank you for sharing your incredible knowledge and journey with this. I had micro changes to vessels in my brain which showed up in a cat scan. It was unremarkable and the scan was considered normal but now i have a deeper insight to this. My opinion is that Raynaud's is a red flag marker for Bart.
Omg! It is? I haven’t felt well for a long time and I have Raynaud’s!!
I was having sores on my lips and my genital part but after using a herbal medicine from Doctor Ani John on KZread right now I’m cured completely..
I did an ELISA test for Lyme and it the IGG and IGM came back saying "Not Detected". However the WESTERN BLOT IGG said not detected but the IGM said "Detected" for bands 39 & 41. My Doctor said I have a false positive result and that I don't have Lyme. From what I know in order to be diagnosed with Lyme Disease a patient must have a positive ELISA test and a positive WESTERN BLOT according to the CDC. If however the ELISA test is an old, out dated, non specific and low sensitive test, then does the WESTERN BLOT Lyme test become a better Gold Standard test?
I am Gay
Good for you
Me too. Nobody cares.
Trust in God!
What a wonderful podcast! Thank God for this doctor! I have a very frightening issue on my hands, and I’m scared and consumed with this! A year and a half ago, our son began living at my house, because he was living in a WDB, and had severe neurological and psychological problems. His mental decline is very apparent, and he’s had a plethora of neurological problems. However, after a year of trying to get his labs and blood work, to see an MD, who is a specialist in mold and stealth infections. A couple of weeks ago, we took him to get the final results,. We thought it was CIRS, because he had been living in a water damaged building, but he does have that plus, two types of Bartonella and Babesia, and she gave him three types of antibiotics to start 1 week apart; however, he felt worsebut it seemed as though he had a herx reaction. He went off the antibiotic and he got worse. He began having fevers and woke up soaked, severe head pressure, which has been going on for a few years, coldness, limbs that are numb, sleeps all day, has EXTREME anxiety and depression. He wakes up with horrible anxiety, has become so negative, has dark thoughts, and ruminates all day. He can’t think nor communicate well, and isn’t taking care of himself. His appetite is gone, except for sugary stuff. Some other things he doesn’t help himself with are that he smokes a pack of cigarettes a day, and he has a severe vulture posture. His neck hurts, and I’ve taken him to an upper cervical chiropractor, but he won’t go anymore. He hurts everywhere, and is psychotic and paranoid, which, at first, I chalked up to his mold toxicity from his house. He’s been staying at my house. His growth factor is sky high, and his blood work is all over the charts. It’s interesting, because tonight, I told him I was going to take him to an ophthalmologist because his vision is changing, and he can’t see well. I know they can diagnose other things besides the eyes. These symptoms have been going on for a few years, but he wasn’t living with me until his suicide attempt a year and a half ago. and since I had mold toxicity before, I thought that’s what this was. But, it’s both. I should mention, he has meningoencephalitis at age 7, and later, several severe TBIs. He feels like he’s going to die, and I’m scared he will. He is SO sick, his doctor told him to go to emergency, but I’m not sure if that’s the right thing. PLEASE direct me as to where to take him. We live in Rochester, MI., within driving distance to Detroit, U of M, and Cleveland Climic. I’m scared he is going to take his life or die. We need some help besides the local hospital! 🙏💫💕
My son is very similar as your son’s history and symptoms. He currently has a diagnosis of active cases Bartenella, Lyme and Mast Cell Activation Syndrome. He has had multiple TBI’s, chronic mold exposure, and reoccurring Epstein Barr infections. He had a very bad reaction to the Moderna Covid vaccine. His is positive for antibodies for every type of known mycotoxin. Agree that this is a very scary place to be and a lot of these symptoms are being deeply driven by the diabolical nature of neurobartonella We are finally starting to make some progress with a cocktail of medications that are very non-standard in terms of treatment, including Seroquel, Lamictal, Imantinib and Methylene Blue. Lots of binders. You are right that the local hospital is not going to be of any help except traumatizing your son further My son has been hospitalized several times, including 3 times at the Mayo Clinic, which was useless
I live in Canada, do you see patients over zoom? I am taking doxy and rifampin which I had to order from India. I am concerned now after listening to your channel that this might make my condition worse. No help here in Canada.
Does anyone know what to put on actual long term tick bites that have been confirmed as Lyme? What is the best topical treatment? Any links or info also appreciated please.
I was having sores on my lips and my genital part but after using a herbal medicine from Doctor Ani John on KZread right now I’m cured completely..
In terms of schizophrenia and bartonella, there is a new study using a more specific PCR test and 76% of schizophrenic patients tested positive for bartonella while only 7,6% of healthy controls. THus, Bartonellosis is the infection with the strongest association to schizophrenia as to date. However, the gut microbiome might also contribute to disease development. (and genetic susceptibility)
Psychiatry has a monopoly on Mental/Neurological Disturbances. They are swimming in money by only treating symptoms.
Chlorine dioxide penetrates and kills biofilms. Nice, mild, chemotherapy which damages very few human cells.
Brilliant, thank you so much!!!
I would be curious to know if Prof. Niels Hoiby has considered the work of Dr. Ed Calabrese and his revival of the notions of hormesis and biphasic response. I will look into Prof. Hoiby's work in greater depth because it seems to me that he is describing biphasic response without actually naming it as such.
Excellent. I found many of my questions answered before the end of the question period. But I would loved to have seen the use of Alginase discussed as a possible treatment, since there is some literature reference to others taking this approach (To be fair, the first reference I found was in Feb 21, while this talk was given about two years earlier.)
I recovered from Lyme disease. It was 2 years of torture.
Hiya, I'm glad you did this video. I should probably do one also to share a few tips I have learned through my 12 years of lymes disease. One I will share with you immediately is for joint pain, it is beef gelatin. It works extremely well and you'll be glad once you use it. Thank you kindly.
Very good presentation.
outrageous!!
Borrelia Miyamatoi 😩😢😢😢 that’s the strain I have and this illness it’s totally disabling. Hope one day I can feel like a normal human being again. Thanks for this video.
Does the rash appear where the bite occurred? Or does it appear anywhere else?