Under Our Skin

[@nagged74]

11 years on and still nothing has changed with helping Lyme patients,the health organisations need to listen. I am going through the same problems now.

[@powaqqatsi8]

MMS and Jim Humble

[@LuminaryLeadershipCo]

Go see Dr. Nemeh in Cleveland OH. He has cured this disease in others I know personally.

[@Bigshoots11]

Public health institutions are corrupt follow the money

[@duster71]

You need to learn about the herbal solution to this problem.

[@LuminaryLeadershipCo]

@@duster71 where do you learn that?

[@Kellycreator]

2024 in U.K. and still suffering after nobody believed I was ill until my whole body shut down and paralysed from chest down to my toes. Tested for everything, Lyme serology came back negative three times. Thankfully a neurologist recommended IV treatment straight into my heart. He saved me as by that time my spinal fluid was 95% infected. I was very close to dying. I’ve been left with so many problems and have to take meds to prevent my body seizing up. I’m 48 and after being an active archer, horse rider, hiker, yoga and now I spend all day in bed just so I can walk my dog once a day. It tires me out so much I can sleep for twelve hours, many of those hours are disturbed as my body hurts and wakes me constantly. I have numb feet, hands, shooting pains. I have weeks of feeling forgetful, brain fog. I forget how to spell words. I’m adding my story to an 11 year old video. I’m so saddened that nothing much has changed and I know there are many more people like me in my home county. We have lots of deer and it’s a tick hotspot. Norfolk U.K.

[@powaqqatsi8]

Look up MMS and Jim Humble to get rid of biofilm and then kill the bacteria.

[@deniseprohaska6962]

unite with others, I know it sounds impossible but all over the world the only way to be heard anymore is to be very loud, shame the medical money that prevents healing, We all have to unite and make ourselves heard. I pray you get some relief.

[@phideauxiii]

my father is a physician specializing in treatment of chronic Lyme... a disease the entire medical community, except for a handful of brave physicians, has shit on for reasons of money and power. for those suffering... i feel you. you aren't faking, arent lying, don't have Fibromyalgia, you don't have arthritis... Chronic Lyme will be defined one day, and it will be done. Until then, keep fighting!

[@vaccinefraud5570]

The doctors have probably been sent National Security Letters threatening them if they reveal the origin of the weapon.

[@joshwhitney7463]

SOT therapy and peptide therapy is something that I see doctors using in the U.S inplace of antibiotics. There theory is to strengthen the immune system to beat the lymes. Interesting stuff.

[@DariaRock1]

@@joshwhitney7463 but antibiotics are working... ? It is a bacteria...these infections are bacteria...

[@joshwhitney7463]

@@DariaRock1 You can take all the antibiotics in the world if you have no immune system they will not work. HIV is an infection aswell why do you think indefinite antivirals dknt cure the disease ? No immune system.

[@DariaRock1]

@@joshwhitney7463 I have made a special blood test and I only have slight IGA deficiency... I am battling lyme and coinfections for years sadly and I desperately want out of this hell. Without the disease I would have been a doctor already but I only managed to get a BA in philosophy. I was also a translator once (also studied Russian) and singer (Berklee Summer School). The antibiotic combination which helped me most was tinidazole and azithromycine but my doctor stopped treating and I have had a major relapse. I am crying almost every day. I am still a young woman. 31. Unmarried, no children. Ukrainian/Austrian. Many talents previously. Good genes, made a lot of sports once...now my muscles are giving up, etc... Why do I deserve this suffering? Where I live no one wants to recognize chronic lyme. I live in Vienna, Austria...capital of classical music and culture....who can help me ?

[@johnberens2898]

Amazing doc!!!!! It infuriates me to know my ALS could have stopped years ago if Drs listened to my tick/rash story. Now I begin my journey of healing I pray 🙏

[@annsweetwater8110]

And I pray for you too.

[@hove131]

Hopefully you can heal now that you know it's Lyme.

[@AmySharpton]

Lifting you in prayer this morning, and sending thoughts of love and healing.

[@barbarabfree2]

Look into Dr. Cass Ingram. The Lyme Disease Cure. When reading note the prevention treatment for those in your life. I had the tick, the rash, and went undiagnosed for 40 yrs. I'm alive bc of fish antibiotics. I KNEW I had a systemic infection and a neighbor suggested them. There are better ways of course. Dr Cass Ingram gives us an alternative.

[@LJolie-jz8go]

My heart goes out to you

[@sarahlynn7894]

Here I am, watching this in 2022. It’s been 15 years that my life has been taken from me and I was just diagnosed with Lyme only 3 months ago. This documentary has been the story of my life! I’m still searching for doctors to help me and am so confused. I’m absolutely terrified for my future and I’m wondering how am I going to afford treatment if insurance companies won’t cover this? It’s such a devastatingly lonely disease, but so grateful to have found this documentary.

[@whatsmname7271]

Hi Sara I hope you are ok.

[@tinanolen7675]

I am in tears watching this . This too was my life , my family turned on me I was all alone and dying I thought. Why I just seeing this too. I was diagnosed in 2014. I have to give All Glory to God for me surviving all that this illness three at me. Thank you Lord for this journey that I've been on and thank you for opening my eyes to what's about to come. I pray for everyone dealing with Lyme. I had lost my insurance , no money to see one of two Lyme disease Drs in the south , cost 400 $ first visit. Well I did homeopathic things but mostly Alot of prayer, quit eating Gluten, no white sugar. Coffee and lemon juice enemas periodically Mainly changed appetite, cut out all pharmaceuticals, smoked alot of marijuana,. I've been better for few years but I'm feeling like the bacteria that have been laying dormant are waking up. I kind of slipped on my diet and feel it coming back. Hope this maybe help someone else

[@LuminaryLeadershipCo]

Go see Dr. Nemeh in Cleveland OH. He has cured this disease in others I know personally.

[@johnpaul5037]

Watching in 2021 and not much has changed, there is so many of us out here suffering.

[@Kaiveran]

The fact that post-acute infection syndromes are being documented and treated _right now_ for COVID - complete with evidence of immune malfunction and lingering pathogens - and yet "Long Lyme" sufferers _still_ have to bear this atrocity is appalling. Love and solidarity.

[@reds542]

💚💚💚💚

[@dondewitt8964]

Why would they find an answer for a disease that creates 425 illnesses when the medical field big Pharma and all them are making buchu dollars off of us! We are their paycheck so they need a sick!

[@surfingisfun001]

I was actually wondering, are there any updates as of 2022? Took me 15 years to get the proper diagnosis. Just started treatment. Is there a better blood test yet? Has anything changed from what is in this movie?

[@Woolykins_Clubhouse]

@@surfingisfun001 nope, unfortunately nothing has changed really.

[@MelToll]

My heart goes out to Dr. Allan MacDonald, he might have forgotten his wonderful work but the World will be always grateful for his dedication and discovery. Good bless him.

[@yaakovantokol9702]

Did he pass?

[@blackdudemedia]

I think The Dr is alive. Claritin cures Lyme and all other spirochete based diseases.

[@l.c.345]

@@yaakovantokol9702 I don't think so - see my last response to my former response that I posted yesterday 11-15-22.

[@vickipetsy1851]

He got his memory back. Doctors don't know what happened. He redid his research with a more powerful microscope and all tested positive for Lyme in brain tissues.

[@JacquelineMcIntoshNo1]

@@yaakovantokol9702 I think he's still alive. I saw that he had submitted a paper to, I think, the NIH, just a year or two ago. They've begun doing new research on Lyme since 2017.

[@inthemagic1]

Anyone who says Lyme is fake can switch bodies with me for 10 minutes. They would be screaming for help.

[@wkjeom]

rachel howe You have that right!!!

[@nikbilotti9977]

Haha very true! I'd love the deniers to feel my pain with Lyme

[@phylr3983]

@@nikbilotti9977 Me too. Lyme disease is so scary and painful. I never know where the pain is going to stab me next. I was FINALLY diagnosed by an infectious disease doctor in NY (doctors are protected in NY). Started doxy and heart pain, palpitations, pressure slowly subsided. I am able to walk again, sometimes with a cane. I am still dealing with other pain and arthritis, poor short term memory is BAD. Very scary disease. I feel for all you out there suffering through this. I hope a big fat tick crawls up Wormser's ass in his sleep and bites his tiny nymph sized brain.

[@nikbilotti9977]

Phyl R wow im surprised an infectious disease doctor even suggested Lyme.. thats not common haha! But yeah anti-biotics wont do so much to cure lyme, it takes a lot more, sadly :(

[@phylr3983]

@@nikbilotti9977 i went ARMED, not with a firearm, but with a file filled with lab reports and bloodwork I have had. I also had a google earth image in there too showing that I live and walk my dog in a lyme endemic area, next to fields and woods (though we know you can get lyme in the city!) I was prepared with payment to strongly suggest she do igenex lab tests. But my file and my presentation was enough for her to believe she quite possibly had a very sick woman with lyme disease crying in front of her. Yeah, you are not the only person to be surprised. She told me she had personal experience with lyme.

[@Vizzini_KungFu]

This should infuriate everyone. All those people sitting on those boards, insurance companies, the government should be triad for malpractice, child endangerment, manslaughter etc.

[@IsaacLHarrison]

Watched this to understand what my mate is going through. So heartbreaking this is why I don't trust medical boards, insurance companies and big pharma.

[@heidi22209]

Its not in their head... thank u for taking the time to understand and be an advocate for US.

[@Eugene17420]

as someone with debilitating chronic lymes I can tell you your friend appreciated that more than anything in the world. it is so unknown and nobody really gets how severe it is so when a friend goes out of their way to do research and you do not have to try and explain what you are feeling it means the world.

[@rd-lw4td]

@@heidi22209 I'm from CT. Friends and family have long-term effects. I always believed them. I'm lucky I never got it. I always had ticks on me from going in the woods. I got treated for Lyme disease right away. It's taken seriously there.

[@bigshoots1181]

free market healthcare is the solution

[@katesun2957]

@ShipperS7 You really find out who your friends are, when you aren't "fun" anymore.

[@anthonyflannery222]

After 1.5 years of being posted, this video has 75,226 views as of right now. It should be 175,000,000 views. Everyone should watch this. Most people have no idea what is going on with this. This could happen to anyone...anywhere. This could happen to you while you are mowing your yard. Truly astonishing. The fact that the medical community is influenced by those who are tied to insurance companies and pharmaceutical companies, is nothing less than criminal.

[@pattyneill4358]

i have been sending it to the lawyers of the doctors who stood firm during the pandemic & asking them to please look closely at this situation , include us , in their class action lawsuits for crimes againsat humanity against the ones directly involved . i hope that they do

[@rangerdoc1029]

9 years later.... Only 314k views.

[@thosefjbeyese5315]

@@rangerdoc1029 So sad as they chem us daily with the poison

[@dexked]

No one gives a fuck. Poor people die rich people can afford the treatment. Why would they change anything? Insurance companies and doctors are making money hand over fist by sending us to endless drs appointments endless referrals and never a solution.

[@funnyvid7634]

It is already happening they just don't know

[@maddyK17]

How does this documentary NOT have more views?!

[@labasrytas2876]

i assume, its same as HIV (aids) - only those who has it is interested...

[@lindaallen8481]

Thank you to all who participated in this documentary. My children both have Lyme. My daughter was the first to become ill...that was at the age of 10. She will be 13 in 2 weeks. She has battled this debilitating disease for over 2 years! We were told it was all in her head many times. It wasn't until our 16th doctor that we found help. He listened! He respected her! He believes in her! She also has Bartonella and other co-infections, Hashimoto's disease and other aliments. I noticed the Bart marks on my son, along with his horrible fatigue and struggles in school. Soon discovered he has Lyme, Bartonella and other infections as well. It is simply imperative that we all bring light to this illness!! To see your children struggle and not have anyone believe something is wrong is devastating. For those out there without help as yet, DO NOT GIVE UP!!! Stay positive...there is help! We must stick together. Speaking of Plum Island below...Read the book "Lab 257' as well as..."Why Can't I Get Better" Solving the Mystery of Lyme and Chronic Disease".

[@vaccinefraud5570]

If you have pets just be aware that they can be reservoirs to give it back to any family member regardless of their healing status.

[@pompilo7256]

К

[@pompilo7256]

Приветшт

[@Tara-._.-]

Hi Linda. It has been seven years- how are your darling children doing now? How has their care been in the medical community? I’m praying you all made it through the COVID-19 Pandemic 😷 safely so far. 🙏🏼 for great health for you all in the coming year! 🙂🌻

[@trinitytwo14992]

I am sorry to hear you children are Ill, I have had Lyme for 9 years. or more) One thing that saved me, Hatha Yoga, consentrating on Cleansing techniques.

[@allisonbarrett3517]

This is very hard to watch for anyone, but especially a Lyme Disease sufferer like myself. I am just getting started in the treatment process. This documentary taught me so much and made me realize how serious of a disease it is as well as how controversial. I am so incredibly grateful that this was produced, Lyme will completely change all aspects of your life and ruin it but I am so glad that people are working towards better treatment and awareness.

[@VBLN]

I pray for you 🙏

[@kellyanneree3252]

See the unknown cat.

[@ellorajones4961]

Hey there. Are you feeling aby better? I'm starting treatment soon.

[@sweetjulz2044]

Lyme litterally took all I had and all I was !! Never felt this destroy physically, psychology, emotionally, intellectly/cognitively and financially ! It is a living hell ! 2 yrs in treatment, although not being on the death row anymore, but I still sleep most of the time from 20/22 hrs to 36 hrs straight skipping treatment and pills !!! What about that constant pain ... even at 5/10 when it is 24/7 can get debilating ! The brain fog and lack of energy are my biggest battle right now ! 💚🤍

[@amandam6449]

@@sweetjulz2044 me toooo it’s awful 😞

[@amyvincent6080]

I had contracted Lyme disease about 20 Years ago and when I went to my doctor he tested me for it. The test came back negative and I told him I knew I had it and wanted him to prescribe the antibiotic for me. He was not willing to prescribe them until I told him what made me think it was Lyme. I advised him my dog kept falling over 2 months prior to me getting sick. We took the dog to the vet and she was diagnosed with Lyme. I advised my doctor that I too was having a severe problem walking and that he will prescribe the antibiotic. He did and after the first week on the antibiotic I became increasingly better. If it was not for my dog and her diagnosis, God only knows what would’ve happened to me.

[@JacquelineMcIntoshNo1]

I recently learned from a video by Alan B. MacDonald; the pathologist who studied Lyme beginning in the early 80's; that it can cause MS, which I was just diagnosed with, 2 years after having Lyme Meningitis and 1 month of strong antibiotics I still tested positive; he said it's curable with Ivermectin, for one. They first learned in farm animals.

[@amyvincent6080]

@@JacquelineMcIntoshNo1 I think I read about it but, I never delved into the research behind the connection. It’s not surprising though given the symptoms associated with Lyme and MS. They’re almost the same. However MS is not curable and therefore, perhaps Lyme is also not curable. Truth be told, my body has never felt the same. Some people may have such a mild case they do not require any treatment but, they still have MS.

[@JacquelineMcIntoshNo1]

@@amyvincent6080 I'm with you and I completely understand, my body hasn't been the same since the Lyme Meningitis. And, I'm sure as is with you, things got worse, then the MS diagnosis came. The only difference was a new lesion that caused vertigo. Allopathic doctors only treat disease, they never find the cause, I've lost faith in all of them. I lived my life with Lupus until I was in my early 50's and began Keto/IF which heals the body with weight loss as a side effect; and the Lupus did go away, it was the best I'd ever felt. Alan MacDonald has proven that Post Treated Lyme Disease Syndrome; as the NIH now calls it; and MS caused by the Lyme Borrelia Spirochete, are curable when treated as a parasite with antibiotics. His video explains it in detail. 'Alan Macdonald: Multiple Sclerosis is a parasitosis'; It's on youtube. They've kept this from us for over 50 years, I'm not beat yet. The best of luck to you. Happy Easter.

[@amyvincent6080]

@@JacquelineMcIntoshNo1 thank you. I’ll check it out. Best of luck to you also.

[@fitnesstraining4u977]

@@JacquelineMcIntoshNo1 I would highly recommend looking into the benefits of fasting for all these issues. ❤

[@25patberk]

I've had Chronic lyme for 27 years now. It breaks my heart to see so many people sick like me but at the same time makes me happy to know im not alone in this battle. I pray to we can end lyme disease once and for all in the future 🙏

[@pattyneill4358]

i was diagnosed in 1989 , 33 years , ive only began to feel better , more like a human instead of some big blob of misery , just the past year or 2 , so grateful , i remember times when opportunity was there to tell my story & speak up about lyme , i remember being too tired ., brain fog , i always said if i ever got to feeling better . I will; not stop talkjing & sharing until lyme disease gets the recognition it deserves & its victims are receiving rthe care & respect and medical attention that they need . IThe victims who are too weak & tired to even help themselves need & deserve to be heard / healed . I Hope my voice can help do them justice , until they are stronger

[@trudysimmonds7691]

If you haven't gotten help yet go to dirt road discussions he cured himself of lime and is trying to help others

[@LuminaryLeadershipCo]

Go see Dr. Nemeh in Cleveland OH. He has cured this disease in others I know personally.

[@duster71]

Use must use herbs from Green Dragon Botanicals,Logos Nutritionals, NutraMedix,educte yourself,and use Bentonite Clay daily to cleanse you body of toxins,heavy metals and the dead spirochetes dead bodies,you diet ishugly important,no dairy,no potatoes or potatoes,no sugar , alcohol,and only whole foods.

[@lymeresearch1414]

Never give up, i am suffering with this crap aswell, and it is the worst disease on planet earth!

[@addexiopremium2165]

I love your video on lyme, it is great!

[@lymeresearch1414]

Thanks

[@gatesofhades534]

Tried Aajonus Vonderplanitz's raw primal diet?

[@ionaworld7034]

10 years. Keep fighting my lyme friends xxxx

[@JacquelineMcIntoshNo1]

Thank you. I never knew I had it until I was in the hospital with lyme meningitis in 8/19. Thank you so much for your information.

[@jenlea9095]

2024 and still no recognition of this in Australia. I contracted it in Connecticut in 1988 and was taken to ER in NYC to be given Tylenol for the extreme pain and leg numbness that lasted 8 mths. Only years later I saw a doco and realized what had happened to me. Multi-system issues that persisted once found a bacteria in my bowel that was only seen in Syphilis or Lyme. I was sent to an infectious disease hospital and was told " We see this in 10% of patients, it's common" and you can't have Lyme, you just need a holiday" I stood up and left, my GP warned me it would be controversial !! Still here dealing with it all these years later. Follow the money - not the science !!

[@benporter964]

Just working it out I sure I have it busselton western Australia 😮

[@moonjudas]

May I ask what bacteria?? - feeling lost in the US lol

[@WhatDoYouConsume]

Its been five years since I contracted lyme disease, how the disease realy affected me was it earased my identity. In the first year after being diagnosed and treated with doxyclonine I was basically drooling on my self, most of the time I couldnt recall my own. Ownly in recent times i have been able to recall and rember my past before lyme disease. This documentary is the only that helps me feel not alone and shows too me how lucky i am to walk away from lyme with only the symptons i have.

[@shiarafigoni1464]

I have this same story

[@LuminaryLeadershipCo]

Go see Dr. Nemeh in Cleveland OH. He has cured this disease in others I know personally.

[@liberal7133]

I have lyme disease and i am very ill, but i am not as diseased as politics and the healthcare system. Its no different here in Norway, a doctor who treated people with the amounts of antibiotics they needed lost his license here also. So the center got shutdown and i and many other patients were denied the treatment we need. I wouldnt be here today without herbs and plant medicine, but my body and brain have taken alot of damage because of how long i went without treatment.

[@DariaRock1]

:( I am so sorry. What herbs are helping you , can I ask you?

[@ediprobertcuthbert]

I have been diagnosed on March 3,2020. with Chronic Lyme Disease and I have had it for 10 years and it's been hell.

[@heidimelrose]

As I started watching this documentary I got physically sick. My son has been suffering for over a year with similar symptoms and was just diagnosed last week with Lyme disease. It infiltrates a person's life so thoroughly....the constant intense physical pain coupled with the random attacks on body and mind. He just started treatment this week and his symptoms have become more acute and more debilitating. We need more public exposure on this horrible disease, more research and a cure fast!!

[@trudysimmonds7691]

If you haven't gotten help yet go to dirt road discussions he cured himself of lime and is trying to help other people do the same

[@LuminaryLeadershipCo]

Go see Dr. Nemeh in Cleveland OH. He has cured this disease in others I know personally.

[@bubblesbubbles3415]

Yes. Iver 🐎 paste has me feeling a lot better !

[@PoisonApple-pd6ih]

This movie has become my validation that it is real and it is happening. I have Lyme disease. I am 19, and it's estimated I caught it at 7-8. My siblings abandoned me recently, because they didn't believe me. I feel like my body is falling apart around me and the people who are supposed to love me and be there for me have all left. I'm scared because I had a life ahead of me, taken by a tick.

[@powaqqatsi8]

Do not let fear take a hold of you.🙏 You are not alone and your life is not over. Don't use the western allopathic medical system to heal, because they are a business that wants to keep you sick. Do a search on MMS and Jim Humble, and check out the testimonies on those with Lymes. Learn about biofilm's role in spreading Lymes as well as other bacterias, viruses, fungus, etc. You need to dissolve the biofilm. Check out monolaurin. The information is out there. Here is to your health journey. Ask and the door shall open.

[@laurenm.2166]

My doctor - "Aww poor baby, arthritis at such a young age.... Anything else? Okay have a great day bye." I was really depressed at that point and couldn't even explain to her in words how I was feeling, I just cried. We have a cottage and I used to take naps on rocks and in trees. Never even knew to protect myself from ticks. I am sure I had/have Lyme disease. I still have major back pain and arthritis in my hands & knees, very stiff neck & jaw pain, pain in wrists, always tired, cry easily, can't concentrate, smelling the same burnt smell when nothing is burning, ringing ears, diarrhea, bladder infections, nights sweating sometimes until my sheets are completely soaked, extreme stuttering once in a while, vertigo, tennis elbow, heart palps, bruxism, no sex drive, weight loss, GERD, sensitivity to light, all of which I've told the doctors. This brain fog is off and on and I had gone to the doctor a bunch of times for swollen lymph nodes. Another doctor said "Well that's normal you can get swollen lymph nodes from just touching your face!" Very rude! The fact that I never had a rash? I live in Northern Ontario and we get tonnes of insect bites. How are you I had Strep Throat 3 times in a row and I'm sure that's an amazing coincidence that has helped me get better. Getting Strep Throat & not knowing or being informed about changing my toothbrush was a blessing in disguise. Doctors just laugh in your face if you tell them what you think you have. It's a disgrace! I hate doctors, they have god complexes.

[@wkjeom]

Lauren M. I really understand what you have been through, not that it does you any good. I hope and pray you can get the help you need. There are so many of us.

[@AndiHembroff]

Lauren M. I’m here with ya, sister. Suffering with most of the same. Here’s hoping you are finding relief 5 years after writing this.

[@MisterInsomaniac]

Eat raw meat

[@vaccinefraud5570]

Tell me more about the burnt smell. I've never heard of that before.

[@wind10miko]

I am not even an outdoors person due to being scared of getting ticks but have attempted to go for short hikes over the years and haven't found a tick on me but I have all the symptoms that you have and nothing abnormal found in any medical tests or blood results.

[@psychedelicpython]

It took doctors 46 years to do a test for Lyme disease, and only because I practically demanded it. The other day I got a call from the regional health district, infectious disease office, telling me the test was positive for Lyme. Over the years, a lot of doctors have ignored my symptoms. I'm 61 years old now and a mess with physical problems. Severe pain in my muscles and bones, along with severe headaches and memory problems, are just some of the things I deal with on a daily basis. The pain clinic I go to doesn't even give the proper dose of medicine to help me. I had no idea so many other people are in the same situation as I am. My heart goes out to them.

[@katinahockney9387]

I too have insufficient pain relief

[@Brentj2254]

Ok I’m sick as hell have been for 3 years gasping for air every minute bed ridden completely treated so poorly this brings tears to my eyes

[@_einodmilvado]

♥️🙏sending strength. I've been biten have many bites and waiting to see what to do. 9 days ago it started. Praying you all heal and are free. I'm so sorry

[@reneerosser329]

As someone who has Lyme...I bawled and bawled.Why does nobody believe us?What a sin for those Drs ro have to go through.Thank you to all of you and support💔❤

[@josephdockemeyer6782]

I believe it's about money. Also, somewhere somebody fucked up in a big way and now they're trying to sweep it under the rug. The medical profession is inherently resistant to thinking outside the box. They won't change their belief system until the CDC (insurance companies & Big Pharma) give them permission. Back in the nineteenth century, Dr. Joseph Lister (Listerine disinfectant) discovered the cause of childbed fever. He asserted that the mortality of new mothers could be greatly reduced by simply washing hands between vaginal exams. He also observed doctors and students going directly from cadaver dissection to performing vaginal exams without proper hand washing. He was chased out of the medical community for pointing out this fact. Lister proved his theories by preventing the bacterial infection that was the cause of childbed fever. He saved lives. However, he so offended the other doctors by pointing out their mistakes, that they ran him out of the medical profession. They also REFUSED to wash their hands. How dare Lister criticize??? I wish I was kidding... This was in the days when surgeons went from surgery to surgery in their filthy, blood crusted surgical coat without changing. Because it increased patient's confidence to see the bloody battle encrusted coat of the experienced, great surgeon. It showed he had much experience... Stearalization? What's that?!?!

[@TheBlue2be]

We will never be believed as long as there are fortunes to be made,. when and if these are solved thet will make new ones. There is more money to be made in lies than in TRUTH!!! Good and Bad work together for the greater good and that is LIFE, whereas Money and Power without a Conscience or Consequences for profit is PURE EVIL, and the TOP INDUSTRIES, they are corporations and they reach around the WORLD, THEY ARE THE BEAST!!!!!!! Think about it, Pain, suffering, illness, poverty, control, and the destruction of human rights and natural resources makes for a great corporate business model and this model when fully played out can only lead to the dominion over all of man kind. Study the lobbyist groups and who they represent you will find the heads of the beast. THEY CAN'T POINT OR BLAME THE OTHER BECAUSE ALL THERE HANDS ARE IN EACH OTHER'S POCKETS.... The only way to kill this giant beast is to starve it, and we are the ground on which it stands.

[@jesusheals2]

There is a spiritual component to Lyme. Nazi's (Hitler and the SS were Satanic Warlocks) used ticks to spread disease from an infected to non-infected person. Our Govt. saved the "scientists" at Nuremberg because their" research was too valuable". If you study Deliverance Ministry/Exorcism you find out what a Malefice is. It is a mockery of Holy Communion, getting a person to ingest or be injected with a cursed substance (Poison/Pharmakeia Rite). All of us with 'Lyme' have been infected with a cursed illness so besides non-treatment we get Accused. The name Jesus used for Lucifer at times was Satan=Accuser of the brethren in Hebrew. All of us are Accused of not being that sick or not being sick at all-including by our own families and MD's. And now this same evil scheme is playing out with C-19 worldwide...

[@TheBlue2be]

@@jesusheals2 The mighty US Corporations took the examples of Dr. Josef Mengele's experiments and have continued with the backing of our own government. Control and $$$$$$$$$ are the fuel, it will not stop until we the people stand and demand TRUTH or until they have total dominion.

[@funk4everc]

I believe you. I feel helpless.

[@blueallison]

Thank you for making this. I've been fighting a myriad of symptoms for about 3 years now, and I'm so tired of doctors telling me I'm crazy and it's all in my head. There aren't enough words to express my gratitude.

[@vaccinefraud5570]

The absolutely criminally insane aspect of it based on MacDonald's work is that it IS in most people's heads if the filarial worms bring the borellia into the spine and brain.

[@MM-db1ri]

I've just cried my way through this. Thank you for this. My resolve to find a doctor who may help is back.

[@debbiecraftjones7973]

Starting this journey with my adult son. HOW and WHERE do we find doctors? And then how do we pay for them??? This video is 9 yrs old and we are no further. Even with this law suit, Look up RICO for LYME. Numerous health bills attempting to be passed for insurance coverage.

[@Ifyoublvintmhputyerhndsntheair]

Apitherapy for Lyme Disease. Research it.

[@heidi22209]

♡♡♡♡. Thank u mom. My mom drove me to my dr. Appointments, as they passed me around. She knew I had it as a child in the 80's. Keep u head up. It's not in his or your imagination.

[@Studio27Talent]

Where do you live M M?

[@Studio27Talent]

Where do you live?

[@mandy4cookielee]

I just been diagnosed a month ago and my Doctor still hasn't spoke to me about even tho my symptoms are kinda serious. I'm having memory loss my coordination is off I'm losing the strength in my my hands ,my pain is ridiculous and to say I'm tired just can't define it enough I'm exhausted all the time. It's such a lonely and helpless feeling. I'm the one that asked my Doctor to test me due to my symptoms and he was reluctant and said he guess but he just thought it was arthritis and said the test is in the same scope of testing..Thank God I finally listened to my instinct although it's taken years to hear it..

[@etdmike]

I will assume you are not seeing a LLMD? You will need to find a LLMD for "appropriate" testing of all tick-borne diseases and proper treatment. Any other doctor will simply prolong the recovery process. If you have any questions or need help finding a LLMD in your area, please feel free to email me. I have over 3 decades of experience with all tick-borne diseases. My email address is in the "About" section of my KZbin profile.

[@michelekisly2535]

@@etdmike good for you

[@barbarasmith4560]

My doctor did a basic blood test it was negative. Unfortunately it's a lie.

[@janesmith510]

the sad story of lyme is no one is cared for even as people see their friends and family members suffer from loss of life and die from the disease no one cares . its the biggest coverup in the medical community its hopeless and obviously unjust . hugs and love to all lyme victims

[@Ifyoublvintmhputyerhndsntheair]

Some people have found that Apitherapy helped cure their Lyme disease.

[@avontiffany]

Thank you as a sufferer this means so much!

[@simoncowell2694]

How many poor people have taken there own life because of this awful disease

[@paulo1149]

Death panels, indeed. Insurance companies are driving treatment regimens, and no deviation will be tolerated. Very powerful film. Thank you so much. God bless all the brave people who have suffered from this disease, and the good doctors who dare to treat them.

[@sandyweltman4358]

I am halfway through watching this, and already I can see how this touches on everything that is wrong with our healthcare system, and why I have zero trust in conventional medicine physicians.

[@josephdockemeyer6782]

Same.

[@lashawnrenee1596]

Are you getting the vaxcine👀 (misspelled on purpose)

[@sandyweltman4358]

@@lashawnrenee1596 absolutely not. I had the virus almost a year ago, self treated at home, and will rely on my naturally aquired immunity. I am an RN, so I may be forced to find other employment, but if thats what it takes to protect my freedom of choice then so be it.

[@arachnidadvocate2073]

Agree but with just one caveat; Modern conventional medicine is amazing when it comes to life and/or limb threatening emergency type trauma (car accidents etc). For all else such as chronic illness, prevention of disease, minor aches, pains & ailments- I will stick w using the vast array of medicines & treatments our beautiful planet provides in abundance freely & which we humans have evolved over countless millennia to benefit from through a miraculous symbiotic relationship intended (ie designed) to be mutually nourishing. Humans are not a plague nor some type of evil parasite on this earth; we have only temporarily lost our way & forgotten our purpose. We are entering an age of alignment which is why so many are feeling a profound energetic shift as more & more of us are actively seeking out the truth about ourselves, each other, our co-inhabitants & our shared environments.. Anyway, my point was only that the earth gives us what we need for physical health (arguably mental health as well). I've had a lifelong a respect & even love for science, but many in these spaces have now become so corrupted, to the point of causing more harm, pain, & misery than the good health, well being & healing toward which they once strived. Again.. a major shift is occurring and I have a feeling that we will soon find the right path(s?) again & will begin to thrive in harmony once again as we are meant to. I have hope.. still working on the faith part tho lol. Sending my prayers, love, & healing strength out to anyone/everyone reading this who may be in need.. 💨🌦️🌱🍄💚💐🕊️🍃🌈🌊🌻

[@tinanolen7675]

@@arachnidadvocate2073 my thoughts exactly.

[@TheJaxbeach]

After 8 years, my nearly 26 year old son had been told that Kansas "doesn't have" Lyme Disease. After severe migraines and vomiting, he went to the doctor today. Our Dr. is a specialist in Lyme. He said that the Lyme is back in full force. My heart is breaking. Even Mayo said he didn't have Lyme. It wasn't until we shipped his blood to Igenex in CA 8 years ago and $600.00, our local hospitals have turned him away eleven times over the years. This is a terrible disease and as a mom, I feel totally helpless. God bless all of you who either have it or have a family member that does.

[@wkjeom]

Terri B I am so sorry, heartbroken for you. A child should not have to go through this.

[@Anita3kidsS.]

As a disabled nurse ( from diseases that are "all in my head") as well as ones that aren't *says sarcastically* I've been bitten by two ticks that I'm aware of...they're may be more ? I was tested 15-20 yrs ago approximately & guess what...Both came back negative.Big Surprise. I have grown to despise medicine & all that it stands for. Nowadays ( besides Big Pharma) Medicine is all about the Almighty Dollar...it's no longer about caring for the patient, what's BEST for the patient...it's about how much money can this patient bring in? Is it advantageous for us to treat them? What insurance do they have? IT IS A BUSINESS through & through .

[@rd-lw4td]

@@Anita3kidsS. shit, that sucks. It was probably a false negative. I got treatment for it even though I tested negative, but that was in CT and the area I lived in took it very seriously in the late 80s when this happened. I have family and friends who have chronic Lyme disease. :( Sorry you've got this awful disease.

[@trudysimmonds7691]

If you haven't found help yet go to dirt road discussions he cured himself of Lyme disease and is trying to help others

[@trudysimmonds7691]

@@Anita3kidsS. if you haven't found help yet go to dirt road discussions he cured himself of Lyme disease and is trying to help others

[@Arthuriantimes]

I contracted Lyme in 2015 and I wouldn't wish it on my worst enemy. I couldn't walk, couldn't lift my arm, couldn't sleep and I was in severe pain 24 hours a day. Lyme is horrendous. After a few weeks in hospital the doctor's told me that they couldn't do anything. What saved me was Buhner's protocol. I read his book and then followed his protocol to the letter. I also devoured books on body chemistry and how the immune system works. When I told the doctors I was going to try and heal myself using herbs and a special diet they just laughed. Yeah well what else was I supposed to do? It was a very slow process because first you have to reboot your immune system and second you have to fight the bacteria of which actually hides from your immune system - known as 'pathogenic bacteria'. What is different about the Lyme bacteria to other bacteria is that they eat the magnesium in your body whereas most bacteria eat iron. Without magnesium your muscles just can't work. Most antibiotics are made to protect the iron in your body but not the magnesium - that is why normal antibiotics fail against Lyme (if you wait too long). Using Buhner's protocol I gradually began to improve. I won't lie, it was the fight of my life and took about one year to fully recover. Only when all the bacteria was gone could I then begin to build up my muscles again. Today I play golf and am an 8 handicap. Anyone who has Lyme - don't give up - your body can kill it. It takes a special diet, special herbs and sheer will power. If I ever contracted it again however, I don't think I could go through it a second time and would probably just end my life. That's how vicious it is. If any one wants to actually hear my full Lyme story I made a video about it and posted it on my youtube space. It contains what actually happened, how I defeated it and how it changed me forever. Take care, give care and be careful out there..

[@wadeanding726]

I was diagnosed in April 20 20, three weeks after the Covid pandemic was declared. It was good timing because I started treatments immediately, which made me miserable, but everything was shut down, so I couldn’t do anything anyways. What you just shared was very helpful. I’ve been very deficient. I magnesium and knew that before I thought I had limes. And I’m still taking magnesium supplements. Unfortunately there’s no link to your comment section. How can I find it?

[@Arthuriantimes]

@@wadeanding726 You are very lucky to start treatment immediately as it will have reduced your suffering enourmously. Buy magnesium oil or gel and rub it directly into the muscle. Magnesiym supplements lose most the magnesium in the digestive system. With oil or gel you get 100% of the magnesium direct into the muscle. Take care my good fellow. If want to hear my story just go to youtube@Arthuriantimes

[@carahurley1]

Thank you for making this documentary. Its so devastating..I also have Lyme two years and no end in sight. I hope one day we will get an apology

[@carolfox9620]

I'm stunned by how well this film was put together. Bravo, really. Excellent work.

[@-gh8bf]

watching 2023 * thank you for Raising Awarness on this devastating Lyme disease ,😌

[@ceciliaamirati4470]

God bless Dr. Jones for his honesty, compassion and bravery....Hope he is aware of how much of a true blue hero he is! A real life warrior for truth and healing.

[@EileenSharp]

I'm really glad my Lyme Disease experience wasn't like this. Very sad for those who are struggling with it.

[@michellelovesanimals2237]

How are you today? Has it ever came back or still in remission? Hope u are well. I am scared for myself, i have it now💔

[@yogijaya2897]

It's BAD. Not MJ bad.

[@25patberk]

It absolutely breaks my heart to see children being so effected by this disease. They have their whole life ahead of them and should never have to worry about something like this. We as lyme disease patients owe it to them to continue this fight so that this doesn't continue to hurt innocent children.

[@KINGofkingsYaweh]

My son is 10 and we just found out. I'm beyond devastated. I don't know how I'm going to watch him suffer. I'm in such a panic

[@trudysimmonds7691]

@@KINGofkingsYaweh if you haven't gotten help yet go to dirt road discussions he cured himself of lime and is trying to help other people

[@thenaturalhorsetrainer]

I got Lyme disease as a kid and I'm 18 now. I got it estimated 10 years ago, even other kids knew something was wrong with me so they stayed away from me. Doctor after doctor, medication after medication, therapist after therapist. Damage from all of it. Not just the Lyme. Teachers would tell me to stop being lazy, family would call me a brat. I don't want other kids to have to go through that mess.

[@laurenm.2166]

Thank you to the doctors who ARE trying to help.

[@tshirtsofwildlife9022]

Thanks for posting & I would like to thank everyone who posted their comments.

[@LaurensMaas]

sounds like the erlichia bacteria damages the adrenal hormone pathway ` especially the Pregnenolone pathway as all tissues rely on the adrenal hormones. Low adrenal hormones = lowered immunity, memory decreases, nerves start misfiring, the guts start malfunction with the consequential cardio-vascular effects from malabasorption. I bet alot of Lymes dis patients have burnt out adrenals. Tick bacterial worms drill down into the tissues and produce toxins, these are massive stressors. Toxic stress depletes the adrenals. My wife caught Lymes from a deer park in Richmond 2002. We caught it early as she told me within days that she had pulled a tick out of her thigh after a walk. She had the cardiac, neurological and dermatological signs and symptoms. She took the antibiotics for a couple of weeks, but she was pregnant at the time with our 2nd child so we were cautious with antibiotics and pregnancy, so we intergrated our approach ~ we did functional medicine, analysed her blood deficiencies , changed her diet, rebooted her adrenals and used emf zapping to stun any remnants of the bacteria for several months. She would have periodic flare=ups when she got really stressed , her skin is the first to flare, so we retested her adrenals and supported with more yams hormones and supps / emf zapping. She's been healthy since 2006. She made a full recovery : ) Best Laurens

[@wkjeom]

Laurens Maas So glad she recovered. Is the baby OK?

[@joanneclark8256]

Glad to hear she's doing better. My question to? You. Is what do you mean by EMF zapping question? Mark and what is she using for adrenals? I do believe that I'm low and not as well.What are the supplements and vitamins are you willing to share any information please thank you

[@zissler1]

How do you do emf zapping?

[@markjohnson9455]

I feel for those who are affected and appreciate those who stayed with them because the patient is not the only one who is affected but so does the caretaker because of the emotional stress they encounter.

[@josephdockemeyer6782]

I only have one person who stands by me. My significant other... I'm not even "allowed" to mention my health to other family members.

[@josephdockemeyer6782]

@M W Yes. It's very sad. My wife believes me 100%. My siblings have turned their backs.

[@hollylittlejohn5035]

I know exactly how that feels... Because no one believes me. I've said over a hundred times in the last 6 years that I feel like I'm 20 something going on 80. I suffer day in and day out. I was made to feel like a giant burden by my then husband & now ex-husband, when I was already so hard on myself as is. I was left struggling with all these horrible symptoms alone while trying to raise my 5 young kids and I get so upset, feeling like I can't even be the mother that they deserve because there is no cure, there is no fix for lyme. My family doesn't listen, care, or help and it just sucks going through all of this alone.

[@Eugene17420]

@@josephdockemeyer6782 breaks my heart. I believe you man as I know the struggle. I am so sorry they invalidate you

[@katesun2957]

@@josephdockemeyer6782 Yes, this year I finally put my "family" behind me. Family does not call you a constant complainer and tell you to go to either a mental hospital or a nursing home. Of course, they're all "true Christians". My children and friends are my family.

[@analovesflowers]

Omg I seen myself in so many of these ppl, I live in Indiana where there is no where to get help. I believe I'm in the last stage. I have fluid around my heart, I'm bed ridden, I believe I am knocking on deaths door. I'm blind, pain, seizure's, can barley walk. If anyone knows a Dr around me pls leave a message. Ty fighting every day Lyme disease

[@mnewlond]

[@trinidadbreeze]

read my post

[@brianmontero8566]

Try oregano oil or tea. I havent been diagnosed but i feel i have it. I can Relate with most of this people. It's so awful how i feel that i just wanna go crazy.

[@analovesflowers]

TY for advice

[@trinidadbreeze]

annmarie mendoza you should read up on carnivora.com

[@JacquelineMcIntoshNo1]

I was in the hospital with Lyme Meningitis for a week in 8/2019. My neighbor was diagnosed with it a few months before me. We are in Upstate New York and it's a serious epidemic, but the Infections Disease Assoc. in Central New York treats it as though it's nothing. When I had my blood test again after 4 weeks with a PICC for antibiotics, the lyme was still there. I asked the women who was drawing my blood if they are getting a lot of people testing positive; she said that it was almost all they were getting in 2019. There was a line of people going out the door. Lyme has made my life horrible. As far as I'm concerned, the CDC has been complicit with allowing this disease to get so out of hand. How dare them blame this on us. It has nothing to do with Climate change. They have finally admitted that they've been creating bioweapons using bugs for decades now.

[@vaccinefraud5570]

The CDC is uniformed military with a Surgeon General. They're in on it.

[@vaccinefraud5570]

​@@phukcguugel5811 That's precisely my point. ALL modern medicine is uniformed military. Lysander Spooner said that unless someone swears an oath specifically to you then it was just words to the wind. There are dozens of meaningless 'hippocratic oaths' that students may or may not make, but not a single person entering these military bases called hospitals or clinics demand that these soldiers swear to protect them. It is all an international scam.

[@vaccinefraud5570]

​@frostek Unfortunately I did not get a notification of your insultive lunacy a month ago or I would have gone all werewolf on your jugular. "Crazed" as in: stating UNDENIABLE FACTS: the CDC is Uniformed Military. Even a Karen can look that up. "Fear-mongering" as in: there are some loons who swear an oath to the Constitution to protect it against ALL ENEMIES FOREIGN AND DOMESTIC. The CDC running fraud and murder scams would fit that bill since WAR IS A CRIME. In fact, those that aid and abet crimes are co-conspirators, so now you are own Notice despite being an avatar with no content. Tell your C.O. that you are unfit for duty since you don't have the skills to contend with the big boys, you crazed fear-whoring loon.

[@michelekisly2535]

Right....disabling American citizens

[@philspurling6414]

Agree, this has zero to do with the climate. The climate was indoors, so to speak.

[@christinebowker2864]

The chair at MAYO of endocrinolgy, actually asked "what can I do for you?" Then before I even left the hospital, I saw on patient portal that he diagnosed me with " "chronic fatigue syndrome". I have never felt so alone, scared and p**sed. I felt my demise and the many doctors had no clue what was wrong with me until I started having seizures. A neurologist in Iowa City tested me and found a diagnosis. Unfortunately so late for me. I even made a book for the doctors chronologically documenting everything that was happening to me.

[@heidi22209]

And back u go to a different doctor... to start the process over. But u now have a diagnosis. So you can never dispute it on paper. The dr. Said so. Now ur screwd. I feel for u deeply. Seriously... who is abusing prescription antibiotics??? Its a really great high man! No it messes up ur guts but it can cure chronic Lyme. We are grown ass people. Yet we can't get treated.

[@katesun2957]

I would love to have Mayo Clinics and advent health cares all removed. They treat people like mice. I think that's all we are to them, science specimens. They're criminals, all of them.

[@yogijaya2897]

We don't want to have this.

[@moonzappa911]

27 years and counting. During those years several co-infections are countless. God help us all.

[@Misfit.Sanctuary]

41 years here. Healing is possible 💕 I was born with it and have gone through hell. I’m finally feeling a little better one day at a time. Keep hope alive.

[@julymorning09]

For me it's been 37 years and counting, and just noticed today notated on my medical records "opiate dependent" Not one word about the destruction and pain Lyme disease has done to my body, eating away at every bit of connective tissue I have. Destroying my nervous and vascular systems. Every joint in my body is bone on bone. Sure I'm dependent on my narcotic pain medication. But not in the way 'they' mean. I've not had to increase my dosage, I've even made myself take less than prescribed to avoid dependence and addition. But without it the inflammations in my body from the Lyme bacteria would prevent me from being able to move. I know, because I suffered for 19 years before getting my first perscription. And believe me, I've had plenty of years of this to test out everything else they'd prescribed, to no avail.

[@SinisterDev85]

Same... I'd like to say "it's a living nightmare," but that would imply that I'm "living". This isn't living, this is surviving! Been sick since I was 10 years old. 36 now. These diseases robbed me of my childhood and so very much. Im still far from living a healthy life. When will we see Global awareness? When will we see justice be served and a cure created? Or at very least respectably accurate testing and effective treatments and prevention methods for Chronic Lyme and other chronic tickborne infections?! Tick borne disease is the modern day equivalent of the AIDS crisis. Tickborne disease is the Pandemic that isn't being talked about publicly. So sorry for all your suffering everyone... I can truly empathize.

[@sheilaloya8900]

@@julymorning09 it's traumatizing isn't it? I was diagnosed with morgellons disease, which some think is a type of Lyme, others think it's all in our heads. I'm still not convinced that I don't have Lyme. I never had the fibers that morgellons sufferers speak of But I got treated very similarly. I first thought it was a parasite infection, due to many of the symptoms being similar. After a few negative stool tests and a standard Lyme panel, negative, they gave me this diagnosis and recommended I see a psychiatrist. I have every symptom listed in this documentary, plus sores all over my body. I saw in my patient notes "possible methamphetamine use?" 🙄 They tested me for drugs at ever visit and all came clear. I begged for a dermatologist and infectious disease referral for months and months. Finally I got to the dermatologist and after reading my referral, she already had her mind made up. She accused me of picking at myself, causing the sores, and then sort of implied threatened me with "I see here you were told to see a neuropsychologist and haven't been yet. You seem like a very smart, rational person... I suggest you let this go." 😱😱😱 It was crushing to hear that. Nobody cares. At least if I had a Lyme diagnosis I'd have SOMETHING. But I know exactly how you feel.

[@rd-lw4td]

@@julymorning09 there will be an opiate dependence physiologically by taking them long term. However, I don't see that as abuse in your case. Pain like that is what opiates are for.

[@urdrwho7897]

Over the years I have had so many, many ticks. I've had rashes from tick bites but I can't remember a "classic" bulls eye but really I guess we can ask, what is a "classic" bulls eye? I've had round rings but I thought it was from me itching. Fifteen years ago (or more) my family physician put me on Doxy after a tick bite (14 days) and I remember him saying, you never want to get Lyme disease. That same doctor came down with it, lost his practice and is in a wheel chair. I had one doctor send me for a blood test, it came back negative (big surprise eh??) and that doctor told me it was in my head. In 2009 when I walked I had terrible pain in my feet, it felt like I was walking over sharp pebbles in bare feet. I was very, very tired. I went to the doctor and explained to her that I think (because of all the ticks and rashes) there is a possibility that I may have Lyme. Apparently the ticks like me and over the summer it is not unusual for me to have 3 to 5 tick encounters. She said that she treats on symptoms, not blood test and sees so many patients with a Lyme like illness. She ordered 30 days of Doxy. The pain was gone, the tired feeling disappeared and I was fine until this summer. In June 2014 I had three different tick encounters. One created big rash, another created a large red round area that I again attributed to itching. July 25, 2014 my feet started to hurt again and the tired was back. I called the doctors office, it is a new doctor because the doctor from 2009 left the practice. Later in the day the doctors office called me back and said I don't even have to come in to see the doctor, he is prescribing 10 days of Doxy. Ten days? Well some antibiotics is better than none. It did help but then 2 weeks later the pain returned. Wow has the price of Doxy gone up since 2009. I bet it went up 400%. Now I don't work in the yard as much and if I do go out I put on anything I have with DEET in it. So I am sitting here trying to get to see another doc because clearly the doc that prescribes 10 days of Doxy isn't what I would call Lyme literate. On a straight line up the road, within a half mile from me there are 4 people being treated for Lyme and one dog. I started to research the history of Lyme and it has been around forever but there are some big differences in the disease today. Here is a link to something that is very interesting and my answer the question, "why didn't we hear about this debilitating Lyme when we were kids in the 50's?" The reason my be that it is now a much worse, a much stronger bug. "We can thank Erich Traub for that...may he burn burn burn. Posts: 3815 | From British Columbia, Canada | Registered: Jun 2013 | IP: Logged | Report this post to a Moderator w0tm LymeNet Contributor Member # 13104 Icon 1 posted 08-21-2014 01:10 PM Profile for w0tm Send New Private Message Edit/Delete Post Reply With Quote I have researched this extensively so I believe this is as accurate as you will find. If not, anyone reading this please add to what I'm writing. Lyme as basic bacteria has been around for millions of years. As have a thousand plus other exotic diseases. 1. during WW2 Nazis sent many scientists into jungles looking for lost diseases they could "weaponize". They found some including Lyme. 2. Lyme itself was weak and wore off like a common cold. 3. the Nazis began to "harden" Lyme but then WW2 ended. 4. Americans brought hundreds of Nazi germ warfare scientists to America in a move called "Operation Paperclip" (Google it). 5. after WW1 most countries including America signed a treaty NOT to engage in germ warfare work or development. Everyone then ignored the treaty. 6. written in great detail in the 2004 book titled Lab 257 is proof that the USA was the WORST offender! America developed more killer germs and viruses than anyone else! I am reading the book again. It is an amazing book! 7. You can buy the book used very cheap via alibris dot com. I paid $4. 8. Yes, Erich Traub was the key German scientist brought to America to head up the new operation located on Plum Island off the coast of Connecticut. from the book Lab 257 it is obvious BAD germs got loose. Including hardened ticks carrying weaponized Lyme disease impossible to get rid of. 9. Beyond belief but Americans "tested" the ticks by dropping them on Lyme, CT in 1975 to see if anyone would get sick. 10. They thought they had a fast cure. They did not. The ticks made MANY people sick and it has spread since then now spreading faster than any other disease. 11. So the original Lyme of millions of years ago is almost harmless. The ticks from Plum Island are killers. 12. Read Lab 257 and your outlook on government will completely change. Even Americans placed no value on human life. That continues today in other things we see government doing. 13. IMO "governments" are gone. The world is now "run" by an "international group of criminals who have no regard for life". 14. So Lyme is not new but the "killer hardened Lyme disease" is new. It was turned loose in 1975 dropped on Lyme, CT. 15. As I say, the book Lab 257 will inform you of 95% of everything. Since the USA government helped spread it and they weaponized it they are now trying to cover their tracks. BUT it is spreading so fast that covering it up is beginning to become impossible. Posts: 119 But it was made Stronger and Worse at Plum Island Bio Weapons lab where the first Reported release was in 1975 it infected a huge amount of people in Lyme CT. almost instantly - Lyme CT. is the town Lyme disease is named after Plum Island Lab is 8 miles from Lyme CT. When I first heard about Plum Island Bio weapons lab I Did Not believe it But now I am Personally 100% Sure that this is where the Really Bad Lyme came from. Recently there has been more info come out about Plum Island and the spread of Lyme from the lab- Why do I believe that there is a possibility that the above is true? Because the government has done such things before. Remember the Tuskegee syphilis experiment? Then there is this -- "In 1966, the U.S. Army dispensed Bacillus subtilis variant niger throughout the New York City subway system. 1977 Senate hearings on Health and Scientific Research confirmed that 239 populated areas had been contaminated with biological agents between 1949 and 1969, including San Francisco, Washington, D.C., Key West, Panama City, Minneapolis, and St. Louis." Our friends or fiends are probably still busy in their labs trying to create the next weaponized bio-agent. God help us. My wife gets upset because she thinks I am not aggressive enough about this but I get so tired of fighting with the docs. In the movie the one woman describes twitching, that is a good term. Some days the twitches are more apparent. I think stress causes more twitching. The pain, the twitching, the tiredness, the forgetfulness is not in my head. Well I am over 60 so maybe forgetfulness is a part of getting older but you can tell me something and 15 seconds later I don't remember. The computer to-do and calendar is a big friend these days. I'm in sales and I can tell you that this has not been good for my sales. It is as though I've come down with a case of ADHD. Staying on task, keeping a marketing strategy going is almost impossible. I think back to what I once was and think, "what happened to my energy and focus because I am not the sales person I once was."

[@csk062353]

Strange that I had no problems registering a thumbs up on other comments, but am unable to do so on yours. Hence, this reply instead. Maybe it's because you edited your comment?

[@wkjeom]

URDRWHO I am so sorry you are so sick. A very good post for anyone who wants to know what it is like to be a Lyme patient. I do hope you can find that one-in-a-million doctor who will help you. I wish you the best. God bless!!!

[@vaccinefraud5570]

Trivia: Typhoid Mary was incarcerated at Plum Island for a short time.

[@elizabethtowers3321]

I've been thru the insults of "it's all in your head" etc. for other health issues so watching this made me feel better. I am not alone in being blown off. I had one Dr. blow me off over difficulty breathing etc., years later it was diagnosed as a major heart attack that killed off part of my heart ( years ago), but no worries, it's all in my head or asthma or delusions etc.. Thank you for making this documentary because it's helped me. There are some very careless Dr.s out there.

[@rogerdeacon5878]

Hi all you beautiful people..this video broker my heart tears are in my eyes. I was bitten by a tick in Germany walking a dog. Within two weeks had the bright red ring around a painful bite. My doctor immediately gave antibiotics but within 4 weeks I had severe shingles on the left side of my face ears neck and pack. I had very bad pain and fatigue and was bedridden for 3 months. I took oral bit c and lysine also put but c plus tea tree oil on skin plus slow Vera gel.I had no scars was better but over years had severe chronic neuralgia. Years later in New Zealand a doctor I found administered intravenous vitamin c..ascorbic acid...I had treatment for 5 months my neuralgia pain was completely cured. I also take heaps of vitamin d..plus magnesium zinc cooperation and amino acids..and oral vitamin c...hope this helps sending you all love and light and praying for you all to be well again God bless you all

[@lenscapingmaine]

This is Such an important video ! If you haven't watched it please do, it tears to my eyes... Everyone in the Medical field should see this ! It is a must see and very moving.

[@bubblesbubbles3415]

It wouldn't help. They are controlled by the elites so that Big Pharma and such can make BIG bucks off of sickly people.

[@fitnesstraining4u977]

I really wish documentaries like this, could also showcase those that recovered or on remission and how much work it took and what kind of work it took. I feel like they are pointing out the problem, but not offering or showing any solutions.

[@jenniferhahn2851]

They recently came out with part two of this following up with some of the people on this video. I agree, a more detailed story of treatment, actions, and outcomes would be very helpful

[@chantelmogollon820]

I wouldn’t wish this on my worst enemy. Got diagnosed earlier this year after suffering for over a year just finished my first round of antibiotics and am waiting for my test results

[@muleyscousin6258]

Everyone who hikes the Appalachian Trail or the Pacific Coast Trail or the Continental Divide Trail!should watch this.

[@melissaerwin2002]

Exactly where I contracted it from. 😕

[@JacquelineMcIntoshNo1]

This video was removed for quite some time; really glad that it's back.

[@rzone9546]

I live in the woods. When I first moved here we had every tick you can imagine. I bought some guinnea fowls and chickens, 2 years later no ticks anywhere. Get some guinnea fowls amd teach them to stick around your property

[@yogijaya2897]

Possums eat ticks as well...... Bless

[@rzone9546]

@@yogijaya2897 where can I buy a gaggle of possums?

[@twistedgoatfpv6542]

My wife differs from Lyme. 10 years living the same as these people in the documentary. I watch it every couple years just to remind myself that we are not the only ones, there are others out there going through the same thing. Feel so alone.

[@powaqqatsi8]

Do a search on MMS and Jim Humble and lymes testimonies.

[@pattyneill4358]

thank you so much for your dedication , i was diagnosed late stage in 1989. its taken almost 25 years . im not well , but a great improvement . . Praying for all that continue to suffer , i cried watching this , seeing your pain , i could feel your pain now , i have felt your pain in the past . 💔🙏

[@ralphalexander7324]

"Lyme disease diagnostics are designed to fail" (Source: Truthcures)

[@dddddd2100]

I have had many symptoms of Lyme Disease but have never been tested for it. I started taking Turmeric Curcumin and have gotten a lot better. I'm not sure if I have Lyme or something else. I had so many different symptoms that even my wife thought I was faking it. I told her and other family members that I know my own body and I know these symptoms exist and that something is wrong with me.

[@josephdockemeyer6782]

I have siblings who work in the medical profession. I'm not even "allowed" to discuss my health with any of them. Almost eighteen years of this illness... One even said "oh, I thought you'd gone ahead and gotten better because you never complain about it anymore"... No, after getting screamed at for mentioning the Mayo clinic, I just quit mentioning my constant severe pain and fatigue.

[@pamelamorris3148]

You need a new wife then because this is not a disease people can even fake.

[@katesun2957]

@@josephdockemeyer6782 I feel so bad for you. Last year I broke my neck, on top of everything else, and the only thing my dad had to say was, I'm glad you aren't complaining about it. Nothing from anyone else, besides, glad you aren't paralyzed.

[@lisasternenkind6467]

My father had Neuroboreliosis. The first really severe symptoms occurred in 1978/79. He got his diagnosis in 1984 and he died in the year of 2000. From 1984 to 2000, my father was closely examined by several specialized doctors from all over the world. They saw him every few months in Vienna. The leading doctors were from the US, from Harvard. It makes me sooo angry that now, in the year of 2024, this devastating disease is still not being taken seriously. . My father got his disease from some insect in Asia, as he was in diplomatic service for 20 years - 5 years in India and 15 years in Pakistan. Shortly before he retired in 1979, he got his first really severe symptoms. Throughout his retirement, he was so ill. The short times he was a tiny bit better, were so seldom and just lasted a few days. 😢😭

[@wyndella7212]

I was diagnosed with ms was given tons of steroids and a few years later I have now been diagnosed with Norwegian scabies I have all signs of morgellons. I have been kind of my own Dr and have been treating myself with farm store products for animals essential oils food herbs etc. I specifically remember pulling a tick off of me I looked for rash with bulls eye and never seen anything. All my symptoms started after the tick but I never thought of Lyme. I was unable to walk brain fog shaking fatigue etc. I was able by the grace of God be able to walk again and feel some what normal again. Then the skin problems started my family has decided this is in my head. I don't think I have MS or Scabies. I had a stroke a year ago and have been doing tons of research. I believe I have some sort of Lyme or something from the tick. How would I go about finding a Dr im in Fl. I am tired of being my own doctor. I'm taking ivermectin and have had noticed an improvement. I'm on a strict diet no gmo's local grown food little meat and liquid vitamins and minerals. I'm also taking binders bentonite clay charcoal essential oils. My grandmother who is American Indian has been helping me pull our heavy metals. I am able to function but I'm not cured by no means. I believe this is disease was created in a lab by government as population control. May God punish the people who have created this and are holding back the cure. The bio film is extremely hard to break down. I am only 40 yrs old and until all this I was in perfect health great job happy home life happy social life and it was changed.

[@etdmike]

You need to find a LLMD for "appropriate" testing and proper treatment. Any other doctor will simply prolong the recovery process. If you have any questions or need help finding a LLMD in your area, please feel free to email me. My email address is in the "About" section of my KZbin profile.

[@JacquelineMcIntoshNo1]

It's not in your head, I'd say you have the parasites from Lyme in your spinal fluid; also in other areas of your body, but it's easier to find in the spinal fluid. I'm having many of the same issued you are, not the stroke, yet. I just learned that it has to be treated as a parasite. I had Lyme Meningitis in 3/2019, was just diagnosed with M.S. four months ago when the constant vertigo on my left side began, Jan. 1st, still have it. But I found Alan B. MacDonald's video about MS being a Parasitosis; he's proven it. I just found a Neurologist who's agreed to have a spinal tap to check the fluid in my spine. MacDonald is the Pathologist who's been researching Lyme since the early 80's. If they won't come clean with the fact that they are still there then I'll take MacDonald's advice and find a doc who will treat me with the meds; one is what you mentioned; he's suggested in his video. Once I'm well enough to function I'm getting back on the keto/IF way of eating. He heals the body, weight loss is a side effect. It healed many issues I had before I became so ill with lyme, for me I know it'll work again. Best of luck to you.

[@alisonhunter4506]

You might want to consider albenzadole. With the ivermectin, it seems to break the cycle. You will know if it's working. Sounds like you have been at this a while. Check it out. Albenzadole.

[@AlischiaRunyon]

I also believe it has to do with morgellons and high metals including strontium.

[@sarahMuahahaha]

I have morgellons/lyme. My first tick bite was over 20 years ago and that's when the hell started. I'm also in florida

[@pattyneill4358]

i see the lady in the green shirt , thats right after the beginning of this video & seeing her trying to walk , brought back so many memories . this disease , unless youve experienced it , its virtually impossible for the average person to comprehend the hell

[@michaelbailey1578]

One of the worst, most painful part of Lyme Disease is when you realize that your doctor thinks you are faking it or just nuts. One doctor was convinced it would all be better if would only quit smoking. He stood before the door as I was leaving and demanded I swear an oath, then and there, to quit smoking which I, of course, refused to do, the silly fool.

[@lelamoore7178]

the doctors who treat us are heros.

[@krscott7]

Suspending doctors from giving correct good treatment to patients and hurting patients by doing this it will come back on you one day there will be justice. You playing God keeping treatment from patients is evil. People will hold you accountable. Allow doctors to give treatment that is working, please stop hurting US!!!

[@GabrielU1tr4k1ll]

What is the treatment?

[@bubblesbubbles3415]

Eternity will come to ALL of us and if they don't repent then Hell for eternity.

[@carolinemerald77]

Caroline Lato 1 second ago Have just finished reading Kris Newby's book 'BITTEN - The Secret History of Lyme Disease and Biological Weapons' published in 2019.------- 'Under Our Skin' -- is an enlightening and informative documentary, made before Kris Newby learned about bio-warfare research carried out by Dr. Willy Burgdorfer and others, which included weaponizing insects by loading them with disease carrying viruses - ticks were specifically used . . . ....

[@wowzow]

...Except that lyme existed for eons before the USÀ was even in existence. Look up otzi, the 5000 + year old oldest (known) victim of lyme. Also, the US bioengineering lyme, has been debunked over and over and over. Ie. ( theconversation.com/no-lyme-disease-is-not-an-escaped-military-bioweapon-despite-what-conspiracy-theorists-say-120879 ) But, hey if you get your news from Facebook, it must be true, right? Or if an author writes it, it must be true too. :(

[@antoinettealbarado2693]

Ticks were injected with spirochetes by the government. That is true!!

[@josephdockemeyer6782]

@@wowzow Otzi didn't have Lyme; he had syphilis. Lyme is weaponised syphilis. Trust me on this...

[@jenn2597]

But this doesn’t explain why the cases of Lyme have sky rocketed in the past 10 years! Bioweapons are always a bacteria or virus found in nature. They are then taught how to be stronger, be more resilient to treatments, be more infectious - they create a super bug. Look at what’s happened with the Corona virus we call Covid-19. It was taught, through breeding, to cross over from an animal to animal virus, to a animal to human virus, and then to a corona virus that could be transmitted from human to human!

[@Supsup7777]

I see a doctor in St. Louis who treats Lyme. He doesn’t take insurance. And sadly that is the route you have to go to get actual treatment. Doctors who are willing to break ties with the insurance companies are the ones you want.

[@gingerbug2010]

Who is your doctor? I live in Missouri and need a doctor that treats Lyme.

[@ShaynaPulley]

What a disaster, this needs to change now. I am so devastated about Alan's condition, I hope his research makes all of the difference in how Lyme is researched and treated from now on.

[@lynncrf]

Luckily Alan has recovered and is active in the Lyme community again. )

[@ShaynaPulley]

That's fantastic, I've never heard of anyone recovering from Alzheimer's like that. Did he continue his work portrayed in the film, lynncrf ?

[@lynncrf]

Shayna Pulley Yes, he is still working in the Lyme area. You can google his name to see his latest research. :) He had a type of dementia that wasn't actually Alzheimer's. So recovery was possible for him.

[@aprilwilliams906]

lynncrf Yes I am hoping that after the spirochetes are out of my brain and the swelling is gone it will be back to normal. I also got lost from my daughters house a 10 minute drive from me. Just lost, I called for help, I was 2 blocks from my house.

[@wkjeom]

april williams I am so sorry. You have my sympathies.

[@l.c.345]

Interesting and informative film especially for those who want to learn about Lyme disease and the political controversy surrounding it which prevents those with it from getting proper treatment. This film is 12 or 14 years old and I heard that Dr McDonald has since lost all his research due to Lyme disease, what a shame 😭 Thank God Dr. Jones is at least 90 years old and is still treating children with Lyme😇 - he will be forever blessed🙏 for the thousands of children he has helped! Wish we had more doctors like him. I've seen this film twice before with closed captioning so I could pretty much follow what was being presented. I have been afflicted with multiple bites for decades and I'm in the end stages, just had to go to the ER last week for a lyme related emergency, but of course it was written off as something else by most of those who treated me, but one was aware. It is imperative that traditional doctors are informed of the truth of this devastating disease!

[@reds542]

💚💚💚

[@l.c.345]

I apologize for saying that Dr McDonald has passed😱, don't ask me where I got that information but I have had 20-30 embedded engorged ticks and many co-infections which have obviously affected my brain, so please forgive me for such a horrific mistake 🙏 Now upon rereading this comment, I see that Dr. Jones has passed, may he rest in peace, I'm sure he will be blessed from all the service he provided to approximately the 15,000 children he treated in lifetime.

[@kathleens.mcgowan4636]

Excellent information that needs to be shared with everyone! Thank you to all those who made this film possible. My heartfelt prayers for all those who suffer from this disease, (a disease that no one is immune to), and prayers for their loved ones as they travel this difficult journey with them.

[@luciangabrielpopescu]

Seeing these people I'm feeling like I'm well. In my case I've left it untreated for 7 years after I had the bulls eye rash (by that time, Lyme was unknown in Romania), ignoring many insidious warning signs to the point that I got a bacterial form of "multiple sclerosis". I'm feeling better after antibiotics, but progress is slow as can be seen in the movie.

[@joycehaines2055]

Thanks for sharing years been struggling for im glad i found your video in 24' we've struggling for years.

[@makeupbyrowyn]

thank you for bringing awareness.

[@janicegoodwin8559]

I have many friends with Lyme, it’s sickening that money and power are more important than human suffering! I believe there’s a cure for many illnesses but big pharma will interfere because they’ll lose their fortune. Everywhere you look there are new pharmacies on every street corner! It’s disgusting! I wish relief for all sufferers. 😔

[@katesun2957]

New pharmacies that will help you for a year, and then their pharmacy gets taken away.

[@wkjeom]

So difficult to understand, now 61, thumbs down people who want the destruction of other people. These are really no different than any serial killer. Can't wrap my brain around the cruelty.

[@rosesprog1722]

What a crazy place, nothing seems to make sense in the US anymore.

[@bornfree7788]

I live in Queensland Australia and got bite from tick that left a red rash on my chest which was very irritating. I was worried about Lyme and asked doctor to remove the head of it that I had broken off when removing it. He just smiled and told me that it’s not necessary and left it in. I became very ill with many strange symptoms. Because of falling over a few times a day and losing most off my strength I thought I had ALS but the two neurologists I saw just made lite of it all and believed I may be over sensitive. 7 years later I’m still falling over and have illnesses that are almost unexplainable in nature that change after weeks or months to something else. Was it the tick? I may never know. Australia doesn’t have Lime disease, so they tell us.

[@jamaldeandredavion5223]

Dude this is 100% the tick go and try and find more help man

[@katiebrookzorena3643]

YOU NEED TO CONTACT ILADS and find a Lyme Literate MD!

[@katiebrookzorena3643]

www.ilads.org/patient-care/provider-search/

[@simonenash6718]

Yes I was told 2ce ,no such thing in Tasmania and Victoria..I have had lyme for 10 years,before I found Judy,Lyme literate Practitioner...after years of certain diets supplements,diagnosis, Im definately a lot better after 2 months...to be continued....p.m me if you want details.

[@tuckerkoch7027]

It's crazy how long ago this is now. They still don't know.

[@shiarafigoni1464]

Oh, they know

[@mmackify]

Great informative video on Lyme Disease ~ March 2014 I was told / informed from my Feb 2014 lyme blood test that I have most likely had this for 10, 20 or 30 years. . . Yet, another gift from Virginia ~ Chronic Lyme Disease . . . SADLY, AND FOR U WHO WATCH THIS VIDEO ~ U WILL NO LONGER TAKE WALKS IN THE WOODS OR CAMP EVERY AGAIN!!!! BEACHES ARE SAFE THOUGH! :)

[@joanneclark8256]

Cistus incandescent tea

[@adrianaortega2005]

Esta enfermedad me a robado mi vida , lo que me gustaba hacer , el compartir con mi hijos . Mi esposo a gastado tanto dinero y la mejoría es poca , no camino desde ya casi tres años , necesito reemplazó de rodilla en ambas. Lo que me mantiene con fuerzas de seguir adelante son mis hijos, el tesoro más grande que tengo

[@jennyjohnson5428]

💚💙💜💔

[@christinebowker2864]

This story is my life, thank you for doing this story

[@stacyjudd1668]

Same girl!!

[@jenafir]

Most Common Lyme Disease/Coinfections Associated Auto Immune System Diseases (Lyme disease and coinfections bacteria/viruses present in all) These all have Peer Reviewed and Published Medical Research proving the connection (The secondary list is below) 1. Atrial Fibrillation 2. ALS - Amyotrophic lateral sclerosis - Lou Gehrig’s Disease 3. Alzheimer’s disease 4. Arthritis 5. Autism 6. Bell's palsy (Bell's palsy is defined as an idiopathic unilateral facial nerve paralysis) 7. Cardiac Disease 8. Cardiomegaly 9. Cardiomyopathy 10. Carditis 11. Carpal tunnel syndrome 12. Chronic encephalomyelitis 13. CFS - Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis; Systemic Exertion Intolerance Disease 14. Chronic muscle weakness 15. CRPS - Complex regional pain syndrome 16. Dementia 17. Demyelinating disorders 18. Dermatomyositis 19. Depression 20. Eczema 21. Encephalitis 22. Encephalomyelitis 23. Encephalopathy 24. Endometriosis 25. Epstein-Barr Virus 26. Erythema chronicum migrans 27. Fever 28. Fibromyalgia 29. Gastrointestinal Disorders 30. Graves’ disease 31. Guillain-Barre syndrome 32. Hashimoto's thyroiditis 33. Headaches (severe) 34. Hearing loss 35. Heart block 36. Hypothyroidism 37. Irritable Bowel Syndrome 38. Isolated acute myocarditis 39. Isolated lymphadenopathy 40. Isolated neuritis of the sciatic nerve 41. Isolated oculomotor nerve paralysis 42. Lyme Disease Co-infections (main): Borrelia Burgdorferi, Bartonella, Babesia Microti, Anaplasma Phagocytophila, Ehrlichiosis (HE, HME), Rickettsia 43. Lupus - Systemic Lupus Erythematosus 44. Ménière's Disease 45. Mental, Depression, Psychological problems 46. Memory loss 47. Migraine headaches 48. Mitochondria Disease 49. MND (Motor Neuron Disease) 50. Morgellons 51. Multiple Sclerosis (MS) 52. Multiple System Atrophy 53. Myasthenia gravis 54. Myositis (Muscle tissue inflammation) 55. Narcolepsy 56. Ocular problems 57. Parkinson’s disease 58. Parvovirus 59. POTS; Postural orthostatic tachycardia syndrome, also postural tachycardia syndrome 60. Psoriasis 61. Psoriatic Arthritis 62. Raynaud's syndrome 63. Rheumatic Fever 64. Rheumatoid Arthritis 65. Rocky Mountain Spotted Fever 66. Sarcoidosis 67. Scleroderma 68. Seizures and Neurological disorders 69. Sjögren’s Syndrome 70. Skin and Dermatological manifestations 71. Systemic Scleroderma 72. Thyroiditis 73. Tinnitus 74. Tourettes Syndrome 75. Transverse Myelitis 76. Vertigo 77. West Nile Virus Less Common Lyme Disease/Coinfections Associated Auto Immune System Diseases (Lyme disease and coinfections bacteria/viruses present in all) These all have Peer Reviewed and Published Medical Research proving the connection 1. Abdominal wall weakness 2. Acrodermatitis chronica atrophicans (ACA) 3. Acute Acral Ischemia 4. Acute conduction disorders 5. Acute coronary syndrome 6. Acute exogenous psychosis 7. Acute febrile illness 8. Acute hemiparesis 9. Acute ischaemic pontine stroke 10. Acute meningitis 11. Acute myelo-meningo-radiculitis 12. Acute myelitis 13. Acute myopericarditis 14. Acute pediatric monoarticular arthritis 15. Acute peripheral facial palsy 16. Acute perimyocarditis 17. Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) 18. Acute pyogenic arthritis 19. Acute reversible diffuse conduction system disease 20. Acute septic arthritis 21. Acute severe encephalitis 22. Acute transitory auriculoventricular block 23. Acute transverse myelitis 24. Acute urinary retention 25. Acquired Immune Deficiency Syndrome (AIDS) 26. ADD/ ADHD 27. Algodystrophy 28. Allergic conditions 29. Allergic conjunctivitis 30. Alopecia 31. Amyotrophy 32. Anamnesis 33. Anetoderma 34. Aneurysm (some) 35. Anorexia nervosa 36. Anterior optic neuropathy 37. Antepartum fever 38. Anxiety 39. APS (antiphospholipid antibody syndrome) 40. Arrhythmia 41. Arthralgia 42. Asymmetrical hearing loss 43. Ataxia Telangiectasia & Cerebellar 44. Ataxic sensory neuropathy 45. Atraumatic spontaneous hemarthrosis 46. Atrioventricular block 47. Back pain without radiculitis 48. Bannwarth’s Syndrome 49. Behcet's disease 50. Bell’s Palsy 51. Benign cutaneous lymphocytoma 52. Benign lymphocytic infiltration (Jessner-Kanof) 53. Bilateral acute confluent disseminated choroiditis 54. Bilateral carpal tunnel syndrome 55. Bilateral facial nerve palsy 56. Bilateral follicular conjunctivitis 57. Bilateral keratitis 58. Bilateral papilloedema 59. Bilateral retrobulbar optic neuritis 60. Biphasic meningoencephalitis 61. Bipolar Disorder 62. Blau Syndrome (extenuating symptoms) 63. Brain Tumor 64. Brainstem tumor 65. Brown recluse spider bite 66. Brown-Sequard syndrome 67. CAID - Childhood Auto Inflammatory Disease 68. Cardiac abnormalities (mitral valve prolapse; myocarditis; tachycardia; palpitations; dysrhythmia) 69. Catatonic syndrome 70. Cauda equina syndrome 71. Central vestibular syndrome 72. Cerebellar ataxia 73. Cerebellitis 74. Cerebral atrophy 75. Cerebro-vascular disease 76. Cervical facet syndrome 77. Cheilitis granulomatosa 78. Chiasmal optic neuritis 79. Chorea 80. Choriocapillaritis 81. Cerebellar Ataxia Syndrome 82. Cancers (some) are infected with Borrelia burgdorferi 83. Celiac disease 84. Chronic inflammatory demyelinating polyneuropathy 85. Chronic recurrent multifocal osteomyelitis 86. Chronic urticaria 87. Cerebellar ataxia 88. Cogan’s syndrome 89. Collagenosis 90. Complete flaccid paraplegia 91. Concomitant neuroretinitis 92. Conduction disorder 93. Conus medullaris syndrome 94. Coronary aneurysm 95. Cortical blindness 96. Coxitis 97. Cranial Neuritis 98. Cranial polyneuritis 99. Craniopharyngioma 100. Crohn’s Disease 101. Cutaneous B-cell lymphoma 102. Cutaneous marginal-zone B-cell lymphoma 103. Cutaneous marginal zone lymphoma (SALT) 104. CVID - Common variable immunodeficiency 105. Dermatomyositis 106. Diaphragmatic paralysis 107. Diffuse fasciitis 108. Dilated cardiomyopathy 109. Diplopia 110. Discopathy 111. Disseminated choroiditis 112. Dorsal epiduritis 113. EDS - Ehlers-Danlos Syndrome (affects) 114. Endogenous paranoid-hallucinatory syndrome 115. Eosinophilia 116. Eosinophilic fasciitis (Shulman syndrome) 117. Epidermolysis Bullosa (Recessive Dystrophic) (related to Scleroderma) 118. Epilepsy 119. Epileptic crises 120. Episcleritis 121. Eosinophilic Granulomatosis with Polyangiitis (EGPA; formerly Churg-Strauss Syndrome) 122. Exanthema (local and generalized) 123. Extrapyramidal disorders 124. Facial diplegia 125. Fascicular tachycardia 126. Fatal adult respiratory distress syndrome 127. Fetal death 128. Fibrositis 129. Focal nodular myositis 130. Frontotemporal atrophy 131. Generalised motor neuron disease 132. Geniculate neuralgia 133. Giant cell arteritis 134. Gonarthritis 135. Granuloma annulare 136. HLA-B27 negative sacroiliitis 137. Hallucinations (Painful) 138. Hemiparesis 139. Hemophagocytic syndrome 140. Hepatic disorders 141. Hepatitis 142. Herniated discs 143. Holmes-Adie syndrome 144. Horner's syndrome 145. Human necrotizing splenitis 146. Hydrocephalus 147. Hyperacusis 148. Hyperbilirubinemia 149. Idiopathic atrophoderma of Pasini and Pierini (IAPP) 150. Idiopathic facial paralysis 151. Infarction pain 152. Impaired Brainstem response 153. Infantile sclero-atrophic lichen 154. Infectious Mononucleosis 155. Infiltrating lymphadenosis benigna cutis 156. Inflammatory cerebrospinal fluid syndrome 157. Inflammatory choroidal neovascular membrane (CNVM) 158. Influenza 159. Internuclear ophthalmoplegia 160. Interstitial cystitis 161. Interstitial granulomatous dermatitis 162. Intracerebral haemorrhage 163. Intracranial aneurysm 164. Intracranial hypertension 165. Intracranial mass lesions 166. Intrauterine growth retardation 167. Iritis 168. Isolated posterior cord syndrome 169. Jaundice 170. Juvenile Rheumatoid Arthritis 171. Keratitis 172. Keratoconus 173. Kleine-Levin Syndrome 174. Leber's hereditary optic neuropathy 175. Left sided sudden hemiparesis 176. Leptospirosis 177. Leukemic meningeosis

[@elizabethaman1947]

I Want to live again!

[@debraderr6359]

Every medical professional and individuals should view this film. This is the future of our world 🌎.

[@phillipallen8288]

unsheepled...reading the book about it now. Truly unbelievable.

[@ManikMekanik]

Took me about 40 years to get diagnosed, after many many Dr's, Psychiatrists finally found a Dr that tests for Lyme in 2017 ....been fighting this disease & co-infections for the last 6 years.

[@powaqqatsi8]

Search MMS and Jim Humble.

[@xAmosX]

Someone didn't want his discoveries to become widespread truths. That's what I believe.

[@aandistudiophotographyvide2986]

It sounds like it was made in a lab in 1970

[@silentvalentina]

Before that

[@yogijaya2897]

It is named after this man

[@carolwest3886]

I have trouble typing these days....🤭 If not for the Grace of the Savior Jesus Christ I may have taken my life years ago...Receiving help from a qualified doctor with an effective protocol for Lyme and MD would be an answer to my prayers! I Am grateful for this documentary as it gives me a platform for a voice to be heard!

[@mmv0401]

Thank you for posting and having this here!! So needed to get out there.

[@tarahawk6244]

Wow....what a fantastic film! I was first "enlightened" to the Lyme Disease issue reading Michael Specter's article in the New Yorker (2013). The unfortunate medical politics re: this disease is, in a way, a microcosm of what is wrong in US heath care: cronyism, biased/interested research & arrogance/insulting attitude from many physician. This will not change until we have an integrated heath care SYSTEM.......not the "business" in place now.

[@annakona4022]

It’s now 2022. Still praying for change.

[@laureanolucero3481]

god, I can't stand even listening to the first sentences in this documentary, it makes me feel so bad... I wished the people in power would be, wel... more HUMAN

[@pam883r]

This should be require viewing. I know several people diagnosed w/Lyme's, but several other with Lou Gerigs or Parkinson's or MS. What I don't understand is the resistance to treatment for long term Lyme's and the persecution of these physicians. Let's get this info out to people- lots out there suffering in silence.

[@CharlieBoy360]

It's clear there is an agenda where they don't want this cured.

[@katesun2957]

They're lab rats.

[@bubblesbubbles3415]

It's on purpose lol Big moneyyyy in sickly people

[@danakinsey5814]

Kinda sad morgellons disease wasn’t mentioned here. It’s real and the stigma is worse than Lyme itself.

[@QuantumHealingwithTenaKaren]

Treat for fungus. Fungus creates the nest for the nanotech and other pathogens.

[@chadhart146]

YES! I just finally found out that I have morgellons... I've lived with this crap for years now and the entire time I have been treated as if I am clinically insane. I am in the middle of losing my wife my business my home, everything basically. I am going from a $500k+ business and owning a large horse farm living the dream. Now I only have 2 more weeks to get any and all of my personal belongings out because my now ex wife doesn't want me anymore. I'm going to move into a semi trailer with my stuff packed wall to wall ceiling to floor. I'm having to leave so much behind. But I can't get it all in the trailer. I have a 8 foot cube in the front of it to live. I don't have a place to take it to park it to live in it. Hell I don't have a truck to haul it. I'm totally hopeless. Defeated. Lost. And Alone... And to just make sure i will never get through this alive, my body feels like it's trying to eat me alive. I can't anymore

[@chadhart146]

Very sad

[@joanneclark8256]

Ivermectin? Dirt roads discussions on telemessage ... what are ya doing to get well ?

[@joanneclark8256]

How are you ? Your wife cany just do that? You paid for it why you going ?

[@SN-ty2rg]

BETWEEN ME HAVING POST-LYME DISEASE, DAILY ALL OVER BODY PAIN, PRE-MENOPAUSAL TO NOW MENOPAUSAL, EXTREME WEIGHT GAIN, EXTREME FATIGUE & NOW DEPRESSION, GMO'S, WIFI & CELL TOWERS, TININITUS, I FEEL LIKE I'M IN A LOSING BATTLE WITH EVER GETTING MY HEALTH & LIFE BACK IN CONTROL.

[@whatsmname7271]

I'm sorry

[@Mojosfire]

My 23 kd, and 41 kd came up positive, after having years of horrible symptoms, just be told we don't see anything wrong. This also being told I have abnormal brisk reflexes, tremors, uncontrollable muscles movements, abnormal gait, still nothing wrong?!? I was bitten by a black legged tick several years ago, when I discovered it was on the back of my head. I had flu like symptoms, I was dizzy and had bad headache. But was told Lyme does not exist in Florida. So there you go, according to who I have seen so far there's nothing wrong with me. Pfft, wish they could experience all the pains, and suffering I'm going through, and see if they still say this!

[@phylr3983]

If you still read this, there is a highly rated doc in California who posted the revised western blot on his blog and according to his experience and education those 2 bands along with your experience would render you a clinical diagnosis.

[@Mojosfire]

@@phylr3983 thank you! That is good to know, as I've gotten much worse now with problems. My white blood cell count is always high. My co infections test showed ranges for Babesia, and Erlichia. Sorry may be spelled wrong. A regular physician already said to me, he thought I might have Mycholplasma, I didn't know what that was, till I read it can come from an infected tick. He said this because I'm constantly having infections. I'm interested to know about this doctor in California.

[@LilithGearrachaille]

a nicely-crafted documentary, but misses one MASSIVE POINT: your "Lyme Disease" is known as "boreliosis" in Northern Europe (Poland, Germany, the Czech Rep. and other countries) and has been extensively researched. Come summer, every TV station is reminding the viewers to take extra precautions when venturing into the forests and checking for ticks upon arriving at home. Sure, there are still aspects of the disease that remain, as of yet, unfathomed, but that does not change the fact that EVERY RESPECTING MD IN EUROPE KNOWS WHAT BORELIOSIS IS, including a vast majority of TV watchers. The good old grandiosity of the US fails her yet again - don't assume you're at the cutting edge of all medical/technological developments. Learn foreign languages and do some research. (sic!)

[@lucius215]

My blood was sent to the US for testing, and im from The Netherlands.

[@echastee]

Do you honestly think people who are chronically ill are Gunn be able to learn new languages just to learn enough to be their own doctor?

[@premabanshari7481]

Not really true. MDs know fresh borreliosis, and in my EU-country health insurance from government pays four weeks of antibiotics (doxycyline). But if you don't recognize the infection in time (not everybody gets a bull-eye rash!), there hardly is belief in persistant infection, or typical co-infections of lyme disease like bartonella etc. One can be lucky if MDs believe, there may be a post-lyme disease, meaning that the immunesystem keeps attacking ("autoimmune"), though they pretend there is no infection there any more, thinking maybe it's a reaction just to toxins not yet excreted.

[@Humanaut.]

I'm a German and what you say does not apply. I had to go to over 10 doctors just to get a diagnosis. The diagnosis i did get (including extensive lab testing) i only got because I went to a private doctor and paid 1000€ (700 of which for testing). I went with to other doctors with a total of 7 things positive (borellia co-infection). They did not accept may paperwork and held on to "if you still have symptoms after antibiotics you don't have Lyme and it's psychosomatic". You obviously are not very informed and used your surface level knowledge to try and make a point - but you missed the mark. Yes - doctors know what Lyme is, but they don't know how to properly diagnose it reliably/accurately and they also don't know how to treat it.

[@maecarpenter6735]

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