Our Battle Ongoing: Lyme Disease in Australia | Full Documentary
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- čas přidán 24. 05. 2017
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Our Battle Ongoing takes a look into the lives of Australians across the nation currently suffering from Lyme disease or a Lyme-like illness. Every individual has their own unique story as symptoms differ from person to person, but they are all united in a common cause of seeing recognition come to those suffering now and for the generations to come. With little to no help currently available, some have to take drastic measures in order to receive treatment. Our Battle Ongoing brings to light the tragedy of living with an invisible illness in Australia.
Directed by Andy Smith
www.ourbattleongoing.com
The suffering is immense. The ignorant response to illness from medical doctors is brutal. Hope god heals all those suffering somehow as the world is full of greed and power to help those in need
It's killing me in the US and they don't care. Homeless and in ago y in mycar and fighting alone
Maybe my house can be turned into a real house of God.
And here we are 5 years later, and patients are being told the same thing, even here in the US. It's absolutely disgusting and inhumane the way Lyme disease patients are treated. Whoever those are in power that are responsible for the mishandling of so much suffering, deserves stiff punishment. I don't mean jail, fines, or death. No, they deserve to feel the torturous effects of Lyme themselves, without any additional help that would be available to the general population. That would be the most appropriate punishment.
Or maybe hell.
Or both
Agree
It’s odd how the symptoms of Lyme disease are so close to Fibromyalgia, lupus and other autoimmune conditions. When you have been suffering so long and it becomes your daily life no one believes that any one person could tolerate the pain….but we do. We suffer so much. I’m in a flare up and for days I can’t walk or move my legs, rashes, hair falls out, the exhaustion feels like you’re dying….i throw up a lot…and no one understands…or “Why would you need pain meds?” …Let me hit you with a 2x4 in all your joints for a month every couple months for years…..then ask me WHY?!!
It’s not odd if it was designed as a debilitating bio weapon.
I'm still undiagnosed after 9 years of suffering, my husband left me, my life has broken into pieces.... Can't walk normally, can't sit, it's walking dead.
This is so so misunderstood by the society worldwide and ignored by the medical profession, often labelled as fibromyalgia!!!!
Sending much Love to All Warriors!!!
Calling LIGHT IN!
THE TIME IS NOW!
💜☀️💚
A new study, a year ago, shows Stevia (the whole leaf) can kill the pathogen causing Lyme disease.
Or not labeled at all in my case they keep telling me there's nothing wrong. Was given one test for caropultunnel Wich came out negative of course cuz I believe they will text for things they know it isn't just to alienate patients from trying to get a diagnosis especially if they are on state funded medical insurance. Discrimination at it's best
I hope you get better
I contacted Lyme in 2004, 17+ ongoing years later I've over 100 symptoms, in fact in a current flare up / herx. From my hips down, sending the tremor up my spine. Came on abruptly as they all do just a bit ago. America doesn't care much for us Lyme people. Thank you so much for creating this documentary. 💚
I’m so sorry. I’m a fellow Lyme sufferer. It took 30 years to get a diagnosis. Did you ever find a practitioner to treat you?
@Dana no one seems to be able to help me. When diagnosed in 2004 they immediately put me on doxy but I had a severe allergic reaction to it and was never taken back for other medications or treatments. A few years later the doctor lost his license and practice....records were sent home and my mother who was a hoarder and narcissistic blindly threw away my only documents proving it. So for years I've looked for help but without a positive test they all refuse. And holistic doctors who only focus on lyme and coinfections can't help do to how deep in my brain it's gotten and how badly sensitive and allergic I am to alot of remedies they'd put me on....so they just tell me to keep doing whatever it is I'm doing and good luck type of thing. I'm approaching 19 years this July.
@@LadyRedBird I’m so sorry. That must be beyond maddening. Have you tried contacting the lab that processed the test? I had to do that for one of my kids’ tests. The diagnostician we saw closed her practice after a bad case of Covid that resulted in Long Haul. The records were mailed to us, but one of the tests was missing. I called the lab and they couldn’t release the info, but they put me in contact with the records department at the hospital that they were affiliated with, and they sent me the info.
I’m also not under treatment. My case has become very complex and all of my drs, including a CDC doctor who called my immunologist when the lab accidentally sent him all of my test results , have all told me that I need to go to Mayo. Mayo refused my case. I’m about to start calling out East, but that’s a long drive for me.
Did you see that the CDC is finally recognizing that Chronic Lyme is a valid diagnosis? Their position change came after a study was published in May or June. The researchers found a persistent marker in the spinal fluid of those who still had symptoms years after the initial infection. Maybe that would be a way around not having medical records?
It's not too late 💚💚💚
@@LadyRedBird What part of the world are you living in?
I hope I can help you.
Have you tried any of the private or non private Lyme Disease support groups?
Facebook has a lot.
You can get answers there too.
It's truly an illness of crime.
Lyme crime.
What happened to you is unconscionable.
Horrible.
Me too.
Although I was lucky to find a correct Lyme provider after searching for 2 years with Lyme, Babesia and Rocky Mountain Spotted Fever in my body.
I was confirmed positve on the 3rd day of tick attachment.
Although refused antibiotics.
That actually broke the law.
Stupid CDC law , if you have a Classic Bullseye Rash 🎯 (Mine was huge)
That's how I was confirmed positve.
- not all barely anyone has seen their Rash.
Or have different looking ones.
It still didn't help me.
That CDC law.
My rash faded in 10 days.
It was bigger than a dvd 📀 with 4 rings around a perfect circle.
I saw the tick.
It detached and rolled down my back.
Please know they have made headway with Lyme Disease treatments.
It went to my Brain after a tooth extraction.
I started iv Ceftriaxone pulsed every 3rd day.
In the 1st 3 weeks I started waking up again.
Every one could notice.
I remember feeling a sense of confidence, that I didn't know was missing.
Love & blessings to you and a recovery.
You can always call this office, they take out of town patients.
Phone call appointments.
Sfpmg.com
✨️💚✨️🙏🏻💚✨️
Many of these practitioners ignoring Borelia and chronic co infections should be brought to book for crimes against humanity!!!
G-d is watching
@@BJ-bc7sl People know the truth!
NOT REALLY..ONCE A TICK BITES YOU AND DELIVERS ALL THESE DISEASES THAT ARE COVERED IN BIOFILM..THERES NOTHING DOCTORS CAN DO FOR YOU..ONLY YOU CAN EITHER CURE YOURSELF OR MAKE THINGS BETTER
We need more research on chronic lyme disease
Agreed. Thanks for the comment. 👍
There is lots if you look.
Look into the medical medium books.
Pandemic weaponized lyme biowarfare. Read lab 257 and bitten
There’s a lot, but people, including doctors, don’t want to know about it, because it requires too much work!
That was a brilliant & insightful documentary, thank you to everybody who helped in the making it’s truly & warmly appreciated, thank you
I've had just been diagnosed with Lyme and nobody believed I was sick. People in my neighborhood started taunting me because they think I'm a dole blunger. Even my doctors listed Hypochondria as one of my symptoms.
I hope you are feeling better. Sending love, hugs, and healing.
I have had Lyme the first time 1998 here in Southern IN I am woman of faith. I prayed daily The treatment was doxycycline for 14 days Doctor said "you are cured". Far from it!! I spent the next year using herbal supplements . Cleansing liver is big deal ! ALFALFA FOR PAIN IT DOES HELP I was able to work here on farm. Able to lift 5 gallon buckets again full of water!! There is hope!! Research herbs!! GOD bless you 😊
Doctors are the cruelest POS - I don't think I have Lyme, but I'm in similar predicament - handing over lots of $$ that keeps them happy, but no help for me. Read Julie Mellae's book Australian Lyme Crimes - an eye opener.
I can’t hardly watch this as I’ve been through it myself. I’ll just leave this inspiring message here-if not soon after a bite with antibiotics and natural meds, people usually get in into remission within about 5-6yrs. Hold on. You WILL get better.
I got Lyme disease in 1986. It took 27 years to get diagnosed. I have late stage Lyme. It destroyed my jaw joint and mandible. I had a total jaw joint replacement and partial mandible replacement. My mouth was wired shut for 3 and a half months. It was a 9 hour surgery with 2 surgeon's. I've had 3 major jaw surgeries. I live in constant pain.
Same 30 year to get a diagnosis 🙏❤️
Would you be willing to chat for a partial blog post? I'm gathering stories of those with lymes and would like to help advocate your voice and story.
I have had Long Covid M E for four years now and no real support just daily rheumatic fever, joint pains neuralgia, tremors, blurry vision, light sensitivity, brain fog, periodic breathlessness, acid indigestion and fatigue. And now the government wants to stop vulnerable peoples benefits. Life on the street with this will likely kill me. I cannot work. I cannot sustain it. The fatigue kicks in with pain.
Wow, what a great documentary! I will say even here in the United States if you can't fine a Lyme "literate" doctor all the patients here also go through many many Drs, and misdiagnosis, unnecessary testing etc...Its such a shame that so many Drs are in denial all the while the ungodly suffering these patients go through! seriously who would make these symptoms up? who wants to live a miserable lonely painful existence?? especially when most of the attention they "supposedly " seek turns out to be negative and disbelief by doctors who took an oath to "do no harm" and how do they explain all the physical symptoms that are impossible to deny?? I'm ashamed of the medical field constantly blowing this REAL disease off! my heart goes out to all the sufferers and I pray everyday they find good, solid treatment and begin to heal and get some type of quality of life back....I truly believe there is power in knowledge and as hard and frustrating as it is please please please never give up....More research and testing needs to be poured into this chronic disease...so again thank you for bringing this to the forefront, together we will all make a difference and hopefully make future medicine appropriate for these sufferers....Amd lastly I believe if every Dr got very sick (preferably with an "invisible chronic illness" very early In their career and were scared with the lack of knowledge and utter denial it would breed way better doctors!!! Bravo on a documentary well done BRAVO!!! never give up those that believe and want go help are out there! God bless and God speed to an amazing recover ❤❤❤
Dariako333@gmail.com send this please to me. Wellwritten comment
Stephanie Dunn , God bless you! 🙏
It's really a shame we have to wish invisible illness on doctors. I agree, but it's still a shame. It means the majority of those in the medical field lack empathy. Maybe things would be different if empathy was a requirement for getting in to medical school.
I have M.E. myalgic encephalitis for 35 years, NHS in uk useless, fobbed off many times, yet mostly housebound, 3 hours bedrest every afternoon, no medical treatment, it's a nightmare. Years of my own research and buying supplements to try, 2nd and 3rd opinions. I do what I can when I can. Hope there will be real effective treatments for all people with Lyme and autoimmune disease xx
I live in Minnesota in the US. I got Lyme disease in the early 80’s before most Doctors had heard of it. My diagnosis was in 2013 when I was 46. I’m now 51 and it’s chronic incurable Lyme disease.
So sorry to hear. Thank you for sharing your story.
Chronic lymes can be curable if you find the right Doctor.
It's curable. You just haven't heard about liposomal herbal formulas from Europe.
@@RK1FX can you tell me the source? Would be very thankful. I am in my early 30s with lyme since mid /end 20s.. biggest relapse since corona lockdown :(
My son lost 14 years of his life to this disease! Permanent heart damage and so much more. The gaslighting has been horrific! Heartless people only make the immense suffering worse! When the money runs out, you are left to die without treatment! The co-infections and related parasitic infections are pathogenic and destroy organs. Most heartbreaking journey ever!! I began suffering years later after a major spine surgery and still battling. The cardiac damage that we both have has no cure. Praying for new laws and more support. The gaslighting inflicts unspeakable damage. Family and friends need to take the time to learn so that they can at least offer emotional support. Feeling alone, attacked, and labeled only impedes healing! The body's immune system can't work properly while left in fight or flight mode! We are living in fear constantly due to economic abuse because the court system refuses to even believe this despite lab testing, physician letters, and other tests that can't possibly be fabricated! After 6 opinions all having the same exact conclusions, one would think it's rather obvious! Praying for all sufferers!
Never give up!! Love and blessings to all!
I just wish that Everybody could see this, especially medical staff and services. So well done.
+Gedda Burnell thanks Gedda. 😀
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New reply on "its simple, I have connected the dots to this social engineering project gone bad, I have applied sacred geometry, people are targeted, implanted with nanotechnology/MEMES sensors/ micro electrode arrays and have now been in communication with software, the 1st part is the malicious use of the technologies of the cochlear implant with its microprocessors and computer software that can manipulate sound through frequencies, "targeted individuals" /homeless hear man made voices through software, "spiritual awakenings" get into trouble , go to a jail/prison/drug courts and rehabs and finally see a "specialist"/"expert witness" and one in a profession that deals with the system. Now political agenda can be pushed and voted on to keep the money flowing and the research coming in. Its all a design and its all coerced. There is more much more like disease and electronic harassment and tracking .. hit me back if you want to hear more ,, im on twitter and Facebook"
@@maxmaxwell1791 Hmm well I hesitated. According to the symptoms I have tracked in my life and those of Lyme, Bartonella, babesia, and who knows exactly what else I have had this issue for at least 60 yrs, since age 2. I am deteriorating as of 08. The last 3 yrs due to being stressed and homeless I'm getting worse. I believe the"powers that be", are THE culprits... period. MK? Sure, 5G on the horizon, pestilence, famine... it's ALL Biblical. We are being made ready for the_New World...to become zombies to worship the beast. I can tell you THIS.... ONLY the Holy Spirit of Jesus will be able to protect a person from being completely turned into a mindless follower of the beast. I believe these newer generations utilize each other with their nano technology. They are weapons to weaken us. What fun these evil conspirators are having. But I know the end of the story. The man riding the white horse out of heaven will destroy ALL these devices and wipe ALL tears away. I continue to trust HIM in the midst of this. You can too.
Excellent work getting all this put together. Much needed for educational purposes but also for others to know they aren’t alone in the struggle. Thank you
Thank you for the kind words
The Australian medical system here has a lot to answer for when it comes to Lyme disease & other chronic invisible conditions that our government doesn't recognise.
In France not any better!
They know exactly what the disease is , it’s ignored intentionally
Lots of people with chronic illnesses, especially rarer or under diagnosed ones that have many, many wildly variable symptoms are told they are crazy. People with Multiple Sclerosis were treated the same years ago too. I takes a long time for Dr's to accept new diseases at the best of times. Same
Money is involved here, crooked people who want to be known for finding a cure and until then the fear to treat by practitioners is eminent. You want to prove morbidity and mortality stats and without treatment.
Thank you to Andy and Cassie for their hard work on this project.
The Australian medical community has a long way to go.
+VegemiteQueen1 thank you 😀.
A young scientist came down the south coast a couple years ago and collected some ticks. She found 14 unknown bacterium and just as many unknown viruses on our ticks.
Wow
They were deliberately infected as bioweapons. Ticks were used in wars
My Grandaughter had been very poorly for over a year. She’s eight, she’s just been diagnosed as having Lyme. A 17 year old in next village has committed suicide last week, because he could no
Longer live With the symptoms. Thanks for this tough to watch but insightful documentary.
My son was able to get rid of his Lyme through light therapy, (ontario, Canada)one of the worst cases they have ever seen, it took about a year, but now it is out of his system, the problem now is the long term effects from it, nerve damage and inflammation. Although he is feeling much much better, he has to stay on top of the inflammation, detoxing, diet, etc.
What's light therapy? I'm in Sask with it
@@user-xf3cu4le5z BIE clinic read their reviews!!
Thank you for your documentary.
This issue needs to be taken seriously in Australia.
God bless all of you people with tick-borne diseases - and all the researchers, film makers, doctors and specialists bringing this story to the light.
Thank you for a great doco. This is a national disgrace. Australia had perhaps the best response in the world to HIV/ AIDS in the 80s/90s. What has happened to our medical system since then (other than privatisation) that makes the doctor's response to Lyme (the new HIV/ AIDS on a bigger scale) the worst in the world? Australians also (including new Australians) have become too materialistic and greedy over the past 20 years and lost their care for each other, leading to the current psycho-spiritual-environmental-health crisis.
When I was in medical school the first year students were surveyed as to their top 3 reasons for wanting to be a doctor, they said 1) money 2) prestige 3) because my parents did it. Anything altruistic were down the bottom of the list (numbers 15-20). Of course it did not help that Sydney Uni took 80% of its students from full fee paying rich asian families (only 15 students were from Australia). So this is what it looks like now. I dropped out due to these attitudes (among other attitudes like all disabled babies should be aborted) and in recent years chose to work overseas.
PS - I speak from experience when I say don't bother with infectious diseases doctors in Australia, they are the worst, particularly those of the northern Sydney area. However, one would think they should be leading the way.
Sadly in Australia you are meant to insist your GP on personally paying for your Lyme/Encephalitis disease test to be flown overseas to America to get a second opinion .As was designed to reduce avoid having to tax pay for the medical treatment. Dating back to the 1950's inspiration was said to have been taken from the American system at the time.
What happened you ask? Socialized medicine.
I had heard that all doctors treating lyme in Australia were being run out of the country. I SO hate this for everyone suffering. I've been fighting 10 yrs now and can so relate. Question: For everyone in Australia, do you feel like more LLMD's are coming out to treat it.. or are they keeping a low profile? Are your doctors being threatened? Do you have medical insurance that will cover your treatment? Do you have any alternative, holistic doctors that are helping you? Would love to hear if you are dealing with the same issues we are here? Too many people are sick here to ignore anymore.. it's slowly changing here, but still too slow! God bless you guys and praying God heals us all quickly and that we get more LLMD's treating us and that all of our medical communities wake up!!
I would say that I’m flabbergasted over it, but now over the past few years I’m not surprised:/
My husband and I both struggled with Lyme as well and doctors told us for over 6 years that we were nuts. So the lack of compassion and knowledge surrounding Lyme is global. The only thing I can say now is thank God they told use we were nuts because that only motivated us even further to find an answer on our own which is what eventually got us well again without any medical intervention at all! Even today if there was a treatment available for Lyme's patients through main stream medicine, I can honestly say we wouldn't even take it because we have absolutely no faith in conventional medicine anymore. I believe that that industry (Big Pharma) needs to slowly wither away and allow for newer technologies like electromedicine to take the spot light but we all know that won't happen because sick people make them a lot of money! Quantum physicists and doctor's who are willing to abandon old theories of medicine is where we need to focus our attention.
Thank you for sharing your story.
YES!!!
What helps please
I definitely think there is an issue within the medical community with medically unexplained symptoms in general. I understand doctors want to be able to provide solutions for people and can get frustrated when people are presenting with very real symptoms but they’re not able to see what’s going on. This does not automatically mean that it’s psychiatric just because we can’t easily see or understand the physiological problem. Regardless of whether disease is present or not, if people are experiencing symptoms help and support is required, not dismissal
poor woman, i cant imagine how painful it is!!!!
The suffering shown here is awful!!
My friend became ill in the US. It wasn’t until she returned to Australia that she finally got diagnosed and treated for Lyme disease.
I had a very serious case of Ross River Fever. It took me years to get back to normal and even now I get polyarthritis if I even catch a cold.
It’s time doctors listened to their patients
This is an absolute excellent film that should be required viewing of all medical personnel. What was not mentioned was the biowarfare weaponised infections concerning OPS (outer surface protein) manipulation by injecting viral genetic material making the microbes more virulent.
End times .... ?... how one can be so evil. I barely remember my early years but I was a very woke child shining. Now with this disease and foreign Material in my body - who am I ? I hope though the Lord and my genes will win. I wish healing for everyone.
So evil to create such warfare
@Project Archivist morgellons too
Yep
@@Tails_of_Life I n the end I followed Stephen H Buhner's protocols, at least what I could afford and I have to say that made all the difference. Still struggling with fatigue though...but it knocked a lot of it down so I could function more. By the way Mr Buhner just passed away this past December notification only published by the Lyme group. A true hero.
My poor friend suffers from this as well. So sad.
and i thought the medical ignorance, indifference or denial of Lyme Disease was bad here in Canada, id say we are a close second as the worst place in the world to have it, this is a very good presentation... i just finished watching it and find it to be the best ive yet seen..seems it is like Canada
+Lymersteve thanks steve. It is hard. Things might be changing soon in Aus. We will see.
Come to america especially east south part. Its like lyme is bigfoot or flat earth theroy.
When your doctor thinks they know it all. When you can’t afford to see specialists or get medicines. On days you look fine, but you can’t stay awake or stay out of the toilet. When you can’t get any financial help because the government says you’re not sick. When your family can’t bail you out and try to understand your pain, but they really don’t. Etc, etc, etc.
Ooh myy..🥺.. what to miss here... all in this doku show a great amount of inflammation.. visually! Why do the medical see and do... NOTHING.. just about that..?!?.. MINDBLOWN🤯. Thanks for done such great doku❣️, its my maybe.. sixth..time watching it💚🇸🇪
I live in Texas, and I have had Lymes since I was 7, and I still haven’t been to a doctor that believes me.
So sorry to hear. Thank you for sharing and keep fighting the good fight.
Pls see a intergrative Socorro
In Dallas
I have a new version called morgellons which has many of the same symptoms along with hair and threads coming out of my body and parasites under my skin, my family & bf think I’m crazy so I won’t even attempt to see a dr. They already think morgellons is bs but I know I went from A healthy 30-year-old woman to being 60 pounds lighter in less than six weeks not being able to lift to even cut hair which is my profession and I can barely walk. I have a huge lesions on my back and they put pressure on my spine with lots of fluid and junk in them. When the fibers were tested that were coming out of other patients that have similar illness they did find that it is a strain of the same thing as Lyme disease.
@@TiffanysBunnyGangYour not crazy, this is so so so sad & real!
I don't mean to offend, but have they never run a blood test to see if you have the borellia (?spelling) sprockets? That should be definitive.
Regardless, sending love, hug, and complete healing!
Thank you to the producers of this film - we're indebted.
Thank you
Lyme disease is real , I never knew such pain existed in all the world!
I’m so sorry. I’ve been there. Stay strong!
My friend Jana has battled Lyme for 21 years. She lost her home to mold, spent their life savings trying to get well and she pretty much lost her husband as a result. She now had Non-Hodgins Lymphoma and is dying because even though this is a curable cancer, she does not have the strength left to fight it.
The universal antidote
It's a documentary
Omg this brings me to tears… I also suffer greatly from Lyme disease and this is exactly… this is what I’d look like and sound like, e x a c t l y
WHERE YOU GET IT..WHEN?
fir the second gentleman: he said he went to the nurse when he discoverred the tip and was told tick born diseases dont exist. I am shocked by it. Bulgarian here, I have a friend that was bitten by a tick, was put immediately on antbiotics ( if I rememebr well the treatement), as preventive measure. I was always aware that the protocol woulb be imeddiate preventive treatement , if not, the risks are too high
I would like to start on my blog advocating more lymes patient voices. I think we need to start making more noise for ourselves.
Thank you for spreading awareness on this disease. It takes patience, self-compassion, and an experimental, open minded attitude, but there is a light at the end of the tunnel. I never thought that I would recover and I am actually better. The medical community has a long way to go. I highly recommend meditation and/or yoga, as well as whatever medicines you take.
+A Boston thanks for the kind words. It's always a pleasure to hear from someone who has beat this thing. 😀
Unfortunately you have variables - types of infections, past medical history, how and where Borrelia go, behaviour in you, affordability of treatment, your genetics, your social support, and home and spiritual environment. This is a costly cluster of infections.
Thanks Andy for this wonderful and touching documentary. Shared
+Kate Allardice thank you Kate. It means a lot to us. 😀
Im from Poland and im sick its terrible how we feel and how we walk throutgh rest of our life. All of us feel like a zombie
Thank you all & bless you all for making this documentary.. I’m in USA & I don’t know how many years I went thinking I just had Fibromyalgia . There are 2 “quarreling” Lyme organizations with 2 completely different ways of treating Lymes which is NOT covered by insurance as the CDC says chronic Lyme doesn’t exist! Sure the insurance companies are in on it too! Have @ least 2 co-infections. I send you all virtual healing thoughts❤
thank-you so very much andy and cassie for this fantastic documentary so appreciated by all here I am sure to all sufferers god bless you all an I wishh all the best have suffered 13 years of hell but slightly better with some herbs
Shameful! I had it and suffered as a child and now at 68, I have a live Babesia infection in MI. It is brutal!!!
Thers a pill you can take for like a week. To get rid of them.
Whats it called ?
I am so sad for these people . I have had Lyme . Found a good Dr. That worked hard to get me well . Took many herbal tinctures and essential oils . The Lyme had gone to my brain, had a hard time thinking . Took a few years to get better . Finally I realized that Cats Claw was in a number of my tinctures .so I ordered cats claw and started taking two to three capsules three times a day and the Dr. Wondered what I was doing cause the markers for Lyme was less .
Something is wrong when people suffer like this and nothing is being done . Is this a type of bio-warfare?
Yes. From what I understand, DDT wasn’t working fast enough, or well enough, as a chemical weapon in the 1970’s Vietnam.
Losing the war was a huge embarrassment to the US, so somebody came up with the idea of weaponized ticks. The research scientists are known ( check out a CZcams channel called The Why Files ).
I have noticed when I start to have a attack
I head outside...I call it a change of scenery. going to a cooler room or outside helps me.
sorry for your pain.
While watching this video my whole body started itching! I am so scared
Facial paralysis is called Bells Palsy.
It, I learned from experience is caused by a tick bite. I live in BC, Canada. I saw a acupuncturist who really work on my face and body to get rid of the paralysis which took about 3 weeks. At that time I didn't know about lyme disease. I was so relieved that my face returned to normal. Thank Goodness.
It's not from a tick Bella Palsy it's a nerve thing
It does affect the nerve. Mine was the 7th nerve behind my ear. Google "tick bite,Lymes disease and Bells Palsy" for more information. Just trying to make people aware. Have a wonderful day.
You can get Bell’s palsy as a side effect of a vaccine. Google Bell’s palsy c19
This disease has taken my once beautiful, happy life..to that of utter suffering.
lyme is no joke. I am from Connecticut USA where Lyme originated and my sons dad got Lyme, it’s actually not even one microorganism anymore. It comes with five tickborne illnesses together. Hardly any doctors really know about it even when they take blood test there’s only like two labs that really know what they’re doing and even when they check your thyroid. They’re not checking the availability of the thyroid hormones. Your stomach is out of whack. You can’t eat you have brain fog you’re anxious. You just don’t feel right and you get gaslighted. As a nurse it’s very frustrating to even try to help. He has purchased millions of vitamins and naturopathic medicine and tried acupuncture and massage and cleaning out your blood in vitamin intravenous and light therapy and he therapy and you name it
Doxy and Avelon together, wait three weeks , Teralysel and Flagyl together wait three weeks Cyclimysin and purmysin together , are just some of the anti biotics that should be used together to treat intracellular spirachetal infections!
Medical doctors are not the only health professionals to behave this way.
As a psychotherapist for 32 years, patients came to me after unsucessful treatment elsewhere. They reported that their previous therapist terminated treatment, declaring, "You are not ready for care, not motivated to improve."
Translation: I failed to help you improve, but its your fault.....go away.
I had ONE condition for my services: The person cooperate in the process, keep appointments, and provide honest feedback.....so that treatment can be modified to be effective. IN less than 5 cases I was unsuccessful. I told the patient that I was unable to help them, but I was referring them to someone that could.
One patient said, "So, I am too sick to be helped?"
My response, "No, untrue, I am not good enough to help you, but I know someone who is."
Sickening disease . My wife has this and it has torn us apart .
Her meltdowns are insane !
Please share more.....I think my partner is hella sick of my meltdowns
@@gabriellemitchell3745SHARE YOUR STORY..I CAN CURE YOU IF YOU FOLLOW MY APPROACH
Top marks to all involved = thank you
+Carol Beechey cheers.
In South Africa presure from the public forced the health department into doing the right thing when it came to ivermectin for covid treatment, the same thing must be done when it comes to lyme disease!
We have a tick problem here in nova Scotia Canada. I've been bitten over a year ago. The spots and rash still has not healed. Hope the best for you guys.
Australia (and many Australians) have sold out to BigPharma and corporations in recent decades (and the CIA/ USA).... lock, stock and barrel. When I was a med student in the early 90's I could see it coming, hence I dropped out. At least back then, we had perhaps the best western medical system and research in the world. The top 3 reasons for med students choosing medicine when I was at Sydney Uni (by official survey) were 1) money 2) prestige 3) 'because my parents did it'. Also 80 of 100 students were rich asian students who had bought their way in (anyone tell the aussie students who missed out?). Any altruistic reasons were way down the bottom of the list, so this is the system we how have, and in fact many Aussies have voted for it somewhat.... (I am a Lymie too). Materialism wins, and that's without going into CDC corruption, Plum Island, USA bioweapons released on civilians, human caused climate catastrophe..... so here comes the karma.
You are correct. Infact a Med Student only has to use their brain to get through Med School and will never have to utilize it ever again. Why? Because of our Medicare System, they Bulk Bill and get paid whether they solve the problem or not. If it was in any other Trade where only the easy stuff was seen to and anything that came with complications ignored then there would be an National Uproar but among Doctors and the Medical Fraternity somehow its acceptable
The whole world has sold out!!!
@@charlesfeatherstone6196 are These perhaps really end times?! What has become out of the world?
Very well said
They have used Aid organizations to monopolize the whole world, buying vacines in bulk to take control of pharmacuetical companies!!
It’s like I’m watching my journey the last 10 years… anyone dealing with Lyme also chronically please comment back 💜
It's bad, but the 'One Minute Cure' works, just go very slow, healing takes months
I too have been through this for the past 7/8 years. The pain and suffering was terrible. Paralysing attacks, seizures , unable to walk and everything else it entails, ie brain fog, left facial paralysis, pain and throbbing behind eyes, severe nausea and vomiting, diarrhoea, sensitivity to light and heat. Pain in right arm.
Any many other symptoms to numerous to remember.
I have chronic lyme disease gor 13 years. Pains coming back big time was better for 5 years back now... live in France got diagnosed in germany. Went on strong meds for 6 months then got hepatitis and liver failure from the meds. Its a horrible disease we feel very lonely and ignored by many people including médical. Do not give up my green warriors. Xxx
At our clinic we treat lyme disease.After 1 month of the treatments there is no infection found in the blood.We have lots of patients from Australia as well.
+Med Institute cheers for the comment. Good luck with your clinic.
Med Institute The bacteria goes deep into the body when antibiotics are used and are not detected in the blood. This is too short a treatment for a bacteria that reproduces so slowly, very much like TB. The docs wouldn’t consider such a short treatment for TB but with Lyme they proclaim a cure. Please check out Dr Alan MacDonalds results on you tube. This bacteria and co infections is hard to cure.
Dear Kathleen Gustafson,
The virus + bacteria can be killed after 1 month of treatment. However, physiological and neurological rehabiliation of the patient mght need 6 months to 4 years, depending on the intensity of the damage in the organism.
For further information do not hesitate to contact our intitute.
Thank you for your comment.
Who are you how can i contact you
Yes but do the SYMPTOMS disappear?? Who cares about blood work! Those pathogens go in hiding. They’re smart
My province put out a video about a man who passed away from it, because it attacked his heart. I also know of a woman who had a son who got it when they were in Australia, and it completely disabled the child. By disabled I mean non verbal and wheelchair bound, for life! But yea, sure, it’s not real and it’s just people attention seeking! 🙄 Give me a friggen break! I’ve only been looking into this a bit because I pulled an attached deer tick off me a few days ago and so I figured I should probably read up about this (yes, I saved the tick). I can very clearly see this disease is very real. I’m deeply disturbed by all the reports about the attitude of soo many of the medical “professionals” about this clearly very real disease!
My brother has suffered chronic Lymes disease for 10 years now...
So sorry to hear. Thank you for sharing.
Question , Could you treat with a bacteriostatic (Cell opener) and bacteriocydel anti biotic used together in a 7 day a month pulse theraphy?
The girl with the head pain.made me cry. I had a weird autoimmune reaction at 16 years old. How she described the vice grip and the worst pain of her life. If reminded me of that thing. I really did have inflammation then. High sed rate. But in my case, steroids cured me and my pain. I had a virus and then my immune system decided to attack me too. And it wouldn't turn off. But they turned it off and I went back to normal. For a while.
But I believe her even if I don't know much about Lyme. Or know the pathology or the science behind it. I don't understand what makes it so controversial. The conspiracy theories. Then you know the government really had his stuff and conspiracy theories have been true. But then you're down the rabbit.hole. really does feel like the world has gone crazy. Really.
I've had head pain that was so bad I could feel my bones in my skull. I would NOT have been able to talk for a video. I don't know how she did that.
I know the feeling!! Have had Lyme,Rocky Mountain spotted fever and every co infection and virus for the past 37 yrs and its living hell!! Most days I look forward to dying so it’s over! I’ve been told bye all the best Lyme drs in the United States and they can’t believe I’m still alive and all wanted copies of all my labs and everything medical I’ve ever had done for taking to Lyme disease gatherings for drs do show all the drs how sick I am and still alive!!! Scary to hear the best drs in the United States say that stuff about me!!!!! Makes me think my last day will come soon
So sorry to hear. Keep fighting.
Andy Smith and the worst part of it all is...people treat you like you’re acting like you’re sick and nothing really is wrong ! My sister in law is a dr and she thinks Lyme disease is not real Because that’s what she’s been told by the medical community and if she treats a person for Lyme she’ll lose her medical license. It’s real and it takes your life one way or another
@@crazykuup9271that’s odd because Avril Lavigne ( the Canadian singer ) had Lyme. It took years to get a diagnosis, but she went to a specialist doctor, dedicated to Lyme disease.
OMW, not even a minute in and the doctor's go-to diagnosis 'it's in your head' pops up! Honestly how can drs be so ignorant on a worldwide basis? Same here in South Africa.
It's so very sad.
Guys - please try Zapper! It really works. I had all of those symptoms in the video and this zapper machine helps tremendously. I have lyme and co. for a few years and it's been terrible. But now I have my life back! Not 100% still, but this machine is amazing. It should be used for several hours daily, it kills all parasites and bacteria, but you must be really consistent and eat healthy. Cat's claw is also amazing. Sending you much love!!
Hey Jane but Bob beck pappers target's blood viruses my unstaning is boralia stays in blood on 1st few days.
Would magnet pluser not be better?
@@jasontierney123 I haven’t heard about that. Not sure what it is.. zapper kills parasites and bacteria so it is a good choice.
Which zapper do you use?
JANE U LOST UR MIND😂
Hi from Germany!!! Really??? I am nearly dying caused by Lyme... Can you please tell me more???
Prayers.i suffer from chronic pain.Doctors are refusing to treat people because of junkies out there abusing system.I wish I dint have pain.I wish I could contribute more.I ignore negative comments.My family n I know the truth n so does my Lord.
Thank you for your comment. Please keep fighting.
Pls see a intergrative dr
I pray god grants u health and strength
Got bitten by tick lyme disease in 1995 the year spring before yellowstone reintroduced the grey wolf USA. Got MisDiagnosed with epilepsy 1998 in Australia .Does the illness need to be diagnosed and managed as Lyme disease? to be able to live life to it's fullest managing to live with it! vs Epilepsy ? As the pain symptoms still linger multiple decades 28years later
Reply
In South Africa we have exactly the same scenario with the health department not recognising Lyme disease! Here many people have actually tested positive for Borrelia! Anti Biotics are the key, multiple regimans that get rotated in a pulse theraphy. Low iron levels high feratin levels are tell tale signs in blood tests!
True, I found a doctor in Cape Town who has worked hard to help us with the disease, understands exactly what is needed to fight it. After 20yrs of misdiagnoses and suffering, she found what was wrong.
@@ilvaafrica2159 so happy for you is it dr m.t
Also fibromyalgia and Lupus SLE in Australia they don’t understand the illness and at first they told me It’s all in my head until a blood test for lupus I hate the medical diagnostic area
Lyme?.. got the same diagnosis as You.. but its Lyme..🥺💚
Exactly, Lyme is behind the AI diseases
Yeah, clinical presentations in Australia seem a bit different from what I've seen in the u.s.
Lyme hurts God bless you all!!
When my son was about 7 months old I noticed a tick had burrowed in the top of his head. I directly took him to the hospital where the doctor gave him a shot of antibiotics. He was good after that. People need to be informed about ticks since it seems a quick dose of antibiotics will safe you a lifetime of pain.
Feel so sad for the young man on the respirator
The blood was sent to Germany for testing ? this is really quite hard to believe ? Not being able to test blood in Australia for Lyme disease ? are we a third world country ?
It is not countries that run our health care systems, it is the business people somehow tied up with making money off a cure.
yes we are
moora mcmillan Germany is the most medically advanced in terms of Lyme disease. They have the best Lyme disease clinic in the world. They can find Lyme Disease in blood that has been cleared for Lyme Disease.
We have to send our bloods to Germany too. It costs a fortune. It's madness. I just got mine back and tested positive for Lyme....my journey begins.
Same goes for Finland. Doctors would not give the order to take the test. I resorted to private sector, they send my blood to Estonia-> test positive. Public sector, lets retest this because we don't trust it -> negative and now nothing. Headaches, dizziness, pain in joints my back is killing me, insomnia, insanely poor memory almost dementia level, panic attacks from nowhere triggered by nothing emotional infact I can hardly feel anything other but this sickness. To doctors I'm just mentally ill but not in any particular way so no diagnose no nothing if anything. Suffered more than 10 years already. Rich people here go to Germany get treated, unfotunately I'm poor.
Simply put I'm feeling like I have 24/7 influenza but I just look like I haven't slept last nigh. I've had bulzzeye rash twice. First time age of 6 bullzeye rash spread over my whole leg before treated with 2-weeks of amoxicillin. Then again bulzzeye rash age 12, treated month after appearing with 2-weeks of amoxicillin. Age of 14 weird symptoms started accumulatng by age of 18 I was feeling really sick but yet looking healthy and even my parents were like what the heck I'm complaining nothings wrong.
Now age 28 I'm starting to look like I have cancer or something, first gray hairs... You be the judge whats wrong, doctors won't even consider lyme.
Those lines on that kid were typical bartenella symptoms !
Boy i believe i might have been infected... I was bite a couple months ago & haven't felt well since , heavvy brain fog & zero energy. I am not ( yet ) where these folks are but yeah. Pray they get well
Patient: I am in so much pain for so long.
Doctor: I am really smart. I dont have a clue what's wrong with you. I've determined that you are neurotic and need a psychiatrist.
My diagnosis of the doctor: Hubis, pride, denial and cruelty.
No one I know has Lymes. If a friend or family member were treated in this manner, my only reaction would be murderous rage.
I dont expect a doctor to know everything.
I do expect honesty, compassion and the dedication to investigate the cause of my suffering, or the humility to refer me to someone who can help me.
1:04:00 absolutely heartbreaking. This should NEVER happen to a patient with symptoms. Whomever wrote that letter needs to go back to school.
My life. No help. Need help.
Doctors are very difficult to navigate. I find It is easier not to get help than to try and try and try and try....I think AI will help us with this. I wish I had more faith in the medical system.
Pancure invermetin !! Fenbendazole
What's with the music?
I was treated in franklin Tennessee with phage teropy it realy worked for me
Are there any Facebook groups for people in Australia in regards to getting access to testing?
Wondering the same. Did U find any good pages Joseph?
My husband had a tick bite that looked like it was turning very strange! I used iodine on it and it made it worse. I then tried Colloidal silver, combined with sodium chlorite and hydrochloric acid. It all went away.
trying to survive this late stage hell damaged all through so much pain
my Dr doing his best keep me stable as he can til I can get back overseas where more treatment and support available for later stages
my life is hell but I try smile as I'm still here and fought hard to be here but I have so much pain
imagine waking everyday so stiff you can barely move inside brain spine burn like acid your brain vibrating against your skull jaw locked shoulder severe pain so weak at times able to get out for only shortest time son an old lady mobility scooter and this is hard
and this is good to what I was
I can't have my daughter as much as I want
now her symptoms coming back
ama should be held accountable for this denial and to continue to slander and put restrictions on few drs brave enough to help us
shame
it's not their fault we got so sick and damaged they should be applauded
ahpra is a wasted organisation targeting the wrong people.
Natalie Young , soo sorry to hear 😢. My Lyme test came back negative but Epstein Bar IGG was 300-400 but have a lot of the Lyme symptoms . I have some extreme brain symptoms too and have a hard time coping and functioning. Thank you for sharing your sty
That was incredibly made. And heartbreaking. I am hoping to understand a part. How did the two buys and Ithink the mom also get it in the family where the dad was having rage Lyme episodes. Is it at times possibly contagious? Strep bacteria is spread so isn’t it plausible? And if it is in respiratory droplets. Help!
Lyme can be passed through saliva and sexual secretions, as well as in utero. My whole step family has it.
Lyme is transmissible in human sperm.
I read that It was once thought that it was not possible to be passed through sperm but that was found to be incorrect.
“Having to rediscover who I am”
“I could be having this fun fabulous life why would I be doing this for attention” both of those that hit home SO HARD.
I still struggle with multiple problem even though I managed to get free of this horrific disease. I too traveled. Saying it “can’t be in Australia’ is disgusting. People travel. It’s like saying you can’t get covid because it was only in china ….
I would love to know what that lady (Karen) treatment was ... the one who use to sleep 22 hours ... that is my average sleep time for most of 2021 !
EDIT
OMG ! Loud sound and bright light triggers some neurological symptoms abit like her ! I wanna to get in touch with her so, Karen, if you see this message, plz email me 🤗💚
Me gustaría que estuviera en español.
So horrible. Wondering, would you consider fasting and cutting down on processed sugars ti a bare minimum? So many doctors having success reversing other diseases. Sending love and healing energy. Prayers.