|
Post by itchin4answers on Jul 1, 2015 18:43:18 GMT -5
|
|
|
Post by itchin4answers on Jul 2, 2015 20:06:01 GMT -5
There were in total four segments to the Lyme story. This link provides all four stories, the last two being "Treatment" and "The Governments Response". www.nbnnews.com.au/category/feature-3/lyme-disease/These segments were on a local news station in New South Wales Australia. The Australian Government Department of Health link updatewww.health.gov.au/internet/main/publishing.nsf/Content/ohp-lyme-disease.htm Lyme DiseaseThe Australian Government is monitoring Lyme disease, in consultation with the states and territories, through the Communicable Diseases Network Australia. Page last updated: 01 July 2015 Update The Australian Government Department of Health welcomes the exciting and ground-breaking research publication from Professor Peter Irwin and his team from Murdoch University. This Australian Research Council funded work published in Parasites and Vectors (Inhibition of the endosymbiont "Candidatus Midichloria mitochondrii" during 16S rRNA gene profiling reveals potential pathogens in Ixodes ticks from Australia) has demonstrated for the first time a new blocking primer technique to quench inhibitory behaviour of the endosymbiont Candidatus Midichloria mitochondrii which occurs in large quantities in the tick microbiome and masks the presence of a potentially novel bacterium in the genus Candidatus Neoehrlichia. These findings reveal a new technique that can be used to detect bacterial DNA from ticks. While no Lyme disease associated bacteria were found in Australian ticks, the Murdoch team readily detected Lyme disease bacterial DNA in the ticks from Germany. In addition, in one Australian tick collected from a wild echidna, out of a sample of 196 ticks, the DNA from a Borrelia sp. associated with relapsing fever was detected. The department welcomes this work and will remain engaged with Prof. Irwin to consider the implications of this research for human health in Australia. The department anticipates research on ticks taken from humans will be published later in 2015. The Chief Medical Officer, Prof. Baggoley, had an opportunity to speak with Prof. Irwin on Wednesday 1 July. Prof. Irwin emphasised that it is not yet appropriate to link the bacteria he found in the ticks to them causing disease in humans. He said, however, it is reasonable to consider a possible link between bacteria and disease if the bacteria which are found have a close relationship to known pathogens. Nothing can be assumed without further research.
|
|
|
Post by Baraka Obam on Jul 3, 2015 11:28:08 GMT -5
I truly love at the end where he notes that the connection has to be to known pathogens, DOES HE KNOW EXACTLY HOW MANY DISEASE'S HAVE NO KNOWN CAUSE. What kind of search is this, we will look for anything that's known to harm, but after that, if its stealthy disease we are talking about its unlikely your see further study, which is usually the case, even if your covered with huge lesions, then your just crazy and digging holes in yourself, yup, no worries mate . We done figured it out your a loon. Certainly there is a way, take 500 ego maniac, scientists and doctors, and their familys put them in a glass enclosure with 1 million ticks with bacterial items not known to afflict mankind, wait 10 years and see how they are doing. Its ok with me, I have no objections, its worth sacrificing EGO MANIACS and their familys, although I suggest, we do not let any of their pets into the enclosure that would be cruelty to animals. OF course we will not let any of those German ticks on them, that would sully the results, we want the pure and uninfected of KNOWN pathogens that afflict people pure Australian ticks, the good kind. So say we all. There were in total four segments to the Lyme story. This link provides all four stories, the last two being "Treatment" and "The Governments Response". www.nbnnews.com.au/category/feature-3/lyme-disease/These segments were on a local news station in New South Wales Australia. The Australian Government Department of Health link updatewww.health.gov.au/internet/main/publishing.nsf/Content/ohp-lyme-disease.htm Lyme DiseaseThe Australian Government is monitoring Lyme disease, in consultation with the states and territories, through the Communicable Diseases Network Australia. Page last updated: 01 July 2015 Update The Australian Government Department of Health welcomes the exciting and ground-breaking research publication from Professor Peter Irwin and his team from Murdoch University. This Australian Research Council funded work published in Parasites and Vectors (Inhibition of the endosymbiont "Candidatus Midichloria mitochondrii" during 16S rRNA gene profiling reveals potential pathogens in Ixodes ticks from Australia) has demonstrated for the first time a new blocking primer technique to quench inhibitory behaviour of the endosymbiont Candidatus Midichloria mitochondrii which occurs in large quantities in the tick microbiome and masks the presence of a potentially novel bacterium in the genus Candidatus Neoehrlichia. These findings reveal a new technique that can be used to detect bacterial DNA from ticks. While no Lyme disease associated bacteria were found in Australian ticks, the Murdoch team readily detected Lyme disease bacterial DNA in the ticks from Germany. In addition, in one Australian tick collected from a wild echidna, out of a sample of 196 ticks, the DNA from a Borrelia sp. associated with relapsing fever was detected. The department welcomes this work and will remain engaged with Prof. Irwin to consider the implications of this research for human health in Australia. The department anticipates research on ticks taken from humans will be published later in 2015. The Chief Medical Officer, Prof. Baggoley, had an opportunity to speak with Prof. Irwin on Wednesday 1 July. Prof. Irwin emphasised that it is not yet appropriate to link the bacteria he found in the ticks to them causing disease in humans. He said, however, it is reasonable to consider a possible link between bacteria and disease if the bacteria which are found have a close relationship to known pathogens. Nothing can be assumed without further research.
|
|
|
Post by itchin4answers on Jul 4, 2015 0:02:51 GMT -5
More stupidly is the comment of "Nothing can be assumed without further research"....put the ticks down and start looking at the people. Everything is about "more research" that's all we ever hear, that's all they do.... build more research facilities to house more lazy people who are only comfortable with lies.
I feel the research holds no hope for us, where are the people mentioned. Take a look on the Government link where it says information for Clinicians...and see if you can make any sense of what they are saying. I do not hear anyone talking about examining a bunch of patients. This would uncover their entire scam. Without sounding like a loon myself the truth is the entire thing is a money making rort, I can not see it any other way. If we announce we have Lyme disease then what happens to all the other gazillion diseases with no known cause. It's a waste of time, it's an embarrassment and it is so completely wrong, how could this happen in the land of plenty? Our health system is like a third world country, even if you have private health insurance makes no difference, no one seems to know what they are doing...."Oh we believe you have bowel cancer, we won't know what surgery we will do until we open you up, yes you're 44yrs old very healthy and have no symptoms"...."trust us the tests must be right".. That is a true story. I am hearing this ALL too often.
Researching the ticks doesn't ease the situation for any of us, it only frustrates us all the more. Mosquitos, fleas and mites carry more than Borrellia and this information is readily available on the internet. Overseas travel of people and the import of goods, many things hitch a ride. I see things for what they are, though our government wants us to think that infectious disease stops at the border. Congenital Lyme disease and sexually transmitted Lyme disease doesn't even get a thought OR a mention. There is TOO much at stake financially...how COULD this happen in the lucky country?
|
|
|
Post by Baraka Obam on Jul 4, 2015 5:07:41 GMT -5
Want to talk about transfer of disease do not forget Thailand where many of you vacation, the men for the sex trade.
I do not know if you have been there yet but it is one of the CENTRAL countries used by troops in the 1970s as the sex party land, your troops and ours.
You can NOT walk down the street and not see a case of leprosy during the day in shopping areas, you will more than likely see 5 to ten, that is a fact, not just lesion cases but no hands, no arm, no feet, mutilated faces.
This disease is one of my focusses, it has all of our issues, the one item that people ASSUME says we do not have the germ, they think that everyone gets the worst case, they do not most people that are well fed with leprosy, you never know they have it. Most other cases start with lesions.
I saw a huge flock of Australians there, mostly men, young and old.
You know one very stunning item, one of a couple may get it, but not the other.
ONE OTHER THING, nobody will ever test for it, even though America has people from endemic areas all around the world coming here, especially the poor Mexicans.
They are known to foster this disease but nobody in America can be tested for it, I find that quite strange. I tried, it was a big fiasco.
|
|
|
Post by itchin4answers on Jul 19, 2015 16:58:37 GMT -5
Today Tonight - Cancer LymeAIR DATE: 16 July 2015 The Perth father forced to sell the family home, to save his two daughters. Both young women are desperately ill and doctors here can't help. www.youtube.com/watch?v=IaZ1eupzF_U&app=desktop
|
|
|
Post by itchin4answers on Sept 24, 2015 0:43:30 GMT -5
Phones4U billionaire John Caudwell 'devastated' after whole family diagnosed with Lyme disease Self-made billionaire John Caudwell speaks about the disease which has affected him, his ex-wife and three of his children The billionaire founder of Phones4U has revealed that his whole family have been struck down by the potentially deadly Lyme disease. Earlier this month John Caudwell told the Telegraph of his 20-year-old son Rufus’s long struggle with the disease, which started with “panic attacks, serious agoraphobia and a terror of sickness” before being correctly diagnosed in February. www.telegraph.co.uk/news/celebritynews/11881516/Phones4U-billionaire-John-Caudwell-devastated-after-whole-family-diagnosed-with-Lyme-disease.html
|
|
|
Post by itchin4answers on Oct 17, 2015 23:37:20 GMT -5
|
|
|
Post by itchin4answers on Oct 24, 2015 17:30:47 GMT -5
In the land of plenty, Australia, there is STILL nothing to offer those of us suffering this curse.
Yesterday wasn't such a great day. Woke with awful anxiety and my body hurt all over. Keeping in my mind to myself, I thought "well you're taking Sarsaparilla root, plant tannins this could be a herx"...though my denial is so great I never admit to a herx because no one (meaning a medical professional) is able to tell me of such.
Our plans for yesterday we're derailed, we're meant to meet for a play date though heard nothing. So by 5pm my boy and I felt sad, and he in tears we venture off to "Inflatable World" for my boy to get 30 minutes of play before the placed closed. I was aware then of this increasing pain in my lumbar spine. Long term spinal problem since I was 16 years. I have been wearing an orthotic shoe and spend a lot of time on my feet (for a person that body hurts) so inevitable given how I feel, stress etc, my pain back can increase.
We left the play centre at 6pm and the pain in my lower spine was then reaching 10 to 11. We got in the car to drive home, only a 5 minute trip. I burst into tears and said to my son that I felt so ill and the pain was terrible. I had the meat and vegies in the fridge ready to cook, but I said to my boy "I don't think I can cook, what about fish & chips". So I head straight to the chippy. I get out of the car and the pain was in my stomach and I was feeling sick. I placed the order at the chippy, feeling some what "out of it" a little dizzy and the sweats starting. We sit down waiting for the order and I got worse. Nausea, feeling like I wanted to vomit. The sweats worsened..."like a river coming off you"...was what my son later said.
There was a woman waiting for her order, she came over and asked my name. She said "you are not well, do you have a medical condition". By this stage I could hardly speak, I said "Lyme". She said to me she knew someone with Lyme disease. I was doubled over, trying not to vomit, my breathing was rapid trying to control the pain. My face became contorted and was pulling down, my arms lifted and were stiff. I could not focus my vision. I did not fall to the ground and have a seizure, what I experienced was something I had never experienced before.
Then the chippy staff came over and they were panicked, they asked if I wanted an ambulance, well I signalled I did because there was no way I was going to be able to get our order and walk out!
They called an ambulance and was asking me questions as to "is this your normal presentation"...of course "no"...I don't usually contort, sweat profoundly and have the inability to speak.
The ambos turn up and started checking vitals, and managed to get me on the stretcher, I could hardly lift my fragile frame. On the way in the ambulance the woman ambo was asking me to smile, which was pretty hard lol. She said "dropped on left side" referring to my face. My blood pressure had gone high, and it is normally very low. My hands and arms were still contorted above me and I was having difficulty speaking, the left side of my mouth wasn't working properly. Only twitching in my limbs, ever so slightly.
We get to the ER and asked if I'd been there before. Well yes I had last year after a dog bite, but I never got attended too. My partner (the man whom assaulted me) then said when we got to triage "she has psychological problems"...I butted in and said "I have Lyme". I got the nasty nurse who then tells me Lyme is not recognised in this country and what you have just experienced (the dog bite) has no bearing and what is happening to you now.
So they go off to find my file, which would have had the above written in it! I tried to give the nurse then doctor as clear a history as I could. Of course I'm asked by the ambulance "have you consumed any drugs". Well yes I said my cannabis which is medicinal and knowing very well this had not done this to me. The nurse explained that what happened with all the tingling in my arms, then feet was to do with lack of oxygen (I think) and something about the blood stream. It made sense to me, but was that really the reason? I don't know.
My son was holding our fish and chip order and I kept calling out to him. He wanted to phone someone, they're asking "do you have family, someone we can call". I'm saying "no". So my boy, grabs my phone and tries to call a couple of people. It's sad the way things are, people are either drunk or high and unable to operate a motor vehicle, or they just don't answer. This is the reality of the society we are living in.
The doctor came to see me, nice young man. Said he had compassion toward my suffering of Lyme because he had a family member who has been disabled for 3 years with Lyme disease. I had to tell them the stress I had been under and the assault. He quizzed me about drugs, saying some drug users develop infection in their spine. He was able to lift my legs, and locate the lower pain in my back. I said this pain in my back feels like nerves on fire. I'd explained that it flared up after washing windows and walls, and scrubbing floors. Then it settled, I went onto say I had seen my GP about it and she couldn't feel anything sinister.
I explained to the doctor that I had an IUD (Mirena) inserted on the 8th October without anaesthetic and the pain and sick feeling I experienced in the car and fish & chip shop was like the way I felt after the procedure, which was nothing short of barbaric.
The doctor didn't think it was the Mirena, even though he said they can attach themselves to the wall of the uterus. He said the episode he thought I'd had and I can not remember the name, but basically the stress I've been under exacerbated all of this. We spoke about what pain relief I had at home, I said Panadeine Forte but I hate it, and it messes with the bowels. They brought in another doctor and they got me to walk around and asked how I felt. I said my neck hurt, my head was a little dizzy and yes the back pain was probably a 6. I told the doctors I had lost an enormous amount of weight in one week.
It was decided that we go home, I take Panadol and one Valium, though I took 2 gel cap Ibuprofen. I had my Melatonin too, and was pretty much out like a light. To be woken before 7am by my lovely cat donging me on the head! she can be so grumpy if her bowl is empty and she needed to go to the toilet. Last thing I wanted to be woken early.
I still have the nagging back pain. Like I said to the doctors, this pain is like trying to target a tooth ache, you can't reach it. I've taken a Valium and Panadol. Yesterday, when I felt the pain starting in the afternoon I took a Voltaren with my lunch, that only eased it for a short time, and told the doctors this.
So we got a cab home from the hospital, hobbled out feeling totally embarrassed about the whole situation and will have to take a walk later to get my car from the Fish & Chip shop.
The psychological feelings of no answers, as they didn't take blood nor do scans, even after me describing the assault, not that I was implying or placing blame, it was very hard for me to tell them as I'm still in shock and scared. You feel like you're nothing more than a useless malingerer, which I'm not. But non of this helps the mind feel at ease, because I seriously thought I was having a stroke.
|
|
|
Post by itchin4answers on Oct 27, 2015 1:22:15 GMT -5
|
|
|
Post by itchin4answers on Jan 11, 2016 17:57:45 GMT -5
This segment aired on ABC TV Australia last night. The video is embedded in the news article. Lyme disease: Australians 'being treated worse than a dog riddled with mange', Senator John Madigan saysIndependent senator John Madigan has come out firing over the treatment of Australians suffering with Lyme disease. The existence of Lyme disease or diseases caused by the borreliosis bacteria in Australia has long been debated. As it stands, health authorities deny the existence of the tick-borne disease on Australia's shores and doctors have faced disciplinary action for treating it. "We've got doctors in this country that genuinely believe that these people are suffering from Lyme disease or Lyme-like symptoms," Senator Madigan told 7.30. "And you can't get any help, you can't get any respite, you can't get cured with the efforts [doctors] are using. "These are genuine Australians who are being treated worse than a dog riddled with mange." www.abc.net.au/news/2016-01-11/lyme-disease-treatment-in-australia-criticised-by-john-madigan/7080708
|
|
|
Post by itchin4answers on Feb 1, 2016 22:41:55 GMT -5
This is a segment on Lyme Disease, aired on Australian Television (I am guessing perhaps Adelaide morning show) from the 24th January, 2016.
Stories such as this to the lay person will say "the word is getting out"...NO it isn't. The public have a short memory, a 9 day wonder and when they interview a "pretty" doctor who puts more emphasise on "tick" removal and perhaps seeing a medical professional so you don't remove the tick wrong, I say it's sugar coated. Perhaps the medical professional would say "I don't see a tick"?
I did my submission for the Lyme disease association of Australia end of last year when the Lyme debate went to the Senate, they are now asking for more submissions. I refuse to do another submission and I know my son wouldn't do one because he refuses to talk about what Lyme disease does to him. My son says "I am not crazy"...that's sort of his catch phrase because he knows Lyme causes bizarre symptoms that can not be easily explained.
They are saying there is an increase in the ticks. Well dumb dumbs try 28 years ago when I was struck down with a mystery illness and knocked off my feet. I never went doctor shopping but when I did go to the doctors, or have a doctor visit my home it was because at the age of 20 and 21 years I was very sick and no one knew why. A virus or viral encephalitis but nothing was ever established.
This is the most disgusting shameful act in this country. We will never have Lyme disease recognised here, because the big wigs will just not allow it.
|
|
|
Post by itchin4answers on Mar 17, 2016 19:58:51 GMT -5
Lyme disease - the Australian epidemic Senator John Madigan giving a 15 minute speech, so well worth watching. I have to wonder why Parliament is empty.
Published on Mar 15, 2016
"Our medical system has a huge gap in it.
And we're behind the rest of the world by years.
This puts our citizens, friends and family at risk, and for some, causes them to suffer needlessly.
We have a treatable disease here, which has been overlooked by the bureaucracy.
Collectively, we can change this."
|
|
|
Post by itchin4answers on Apr 10, 2016 0:51:57 GMT -5
June is the month for the Senate Inquiry into Lyme Like Disease in Australia. Not so long ago I'd said I wasn't going to do a submission. I'd written something back in December for Lyme Australia, but that (I believe) was to just get an idea perhaps of how many people in Australia with this disease, what state we lived in etc. I was also wanting to "let the whole thing go"....after my son's birthday the other day I became so emotional, everything coming back to me. Reading about Patty Duke dying of Sepsis and that is how my son came into the world, with Sepsis because of no one listening or caring that my symptoms were not a delusion. I did my submission in a complete state of anxiety, I had not thought nor planned. I sat at the computer tense and focused as though it was my subconscious at work. I should have typed it into a word document then copied and pasted into the email but I typed straight into the email, and rather than pressing save to draft I pressed send by accident and hadn't finished! I was stressing about the time, my son needing his tea and wanting to get the submission sent. I didn't proof read, can you believe that, me the utter perfectionist of the Earth who always proof read. I keep beating myself up over this, and I keep telling myself this is the disease and I can't change it and stop worrying!! I did add two links into my submission on Morgellons which had my old Morgellons video embedded in it, because my own video mysteriously disappeared off the internet last year. I got an automated reply email to say the Senate had received my submission and that it had to be approved before being uploaded to the internet, apparently this could take a few days. If we are wanting anonymity we have to give a good reason why. I don't wish for that because we are all in this together. This link is where all the submissions are uploaded to. I haven't opened many, but from what I can gather it is not just about Lyme Like Disease, also chronic disease and many organisations are making submissions. Many of you may find some very interesting to read. www.aph.gov.au/Parliamentary_Business/Committees/House/Health/Chronic_Disease/Submissions?main_0_content_1_RadGrid1ChangePage=5_20
|
|
|
Post by itchin4answers on Apr 19, 2016 23:17:53 GMT -5
It's a "Lyme busting" day. The final hearing in Parliament in Canberra. I've travelled extensively and am still being denied health care. I see the GP the other day to end up blowing my top from her rudeness. I said I had pain and suffered fibromyalgia and wanted a chronic pain management plan. She said to me "says who"...meaning who said I had Fibromyalgia. I launched and said "not this again!!"....I was diagnosed 21 years ago. I had my medical file sent to this clinic and seriously it would pay for them to read my diagnoses. She harped at me that my Borrelia test through Australian Rickettsial Research Laboratory was negative. I said "I know!". I was most upset I said "you don't get it unless you had a chronic disease"...I was banging my fingers against my head saying "what you doctors are doing to us, you have no clue". I said a few things and defended my son on how rude she was saying my son didn't have Lyme even with positive serology. I told her I had my clinical diagnosis of Lyme in 2012. She said the diagnosis has to be backed up with pathology. I dug at her further saying "do you know how to read the bands on the results"...."do you know how hard it is to find the Borrelia bacteria". This is malpractice and contempt. That doctor was trying to say there really is nothing wrong with me. No repeat on my prescription and as I said to her on my way out, all return business you want, trainees - you're not a doctor you're a hypocrite. I came home and cried, told myself there was nothing wrong with me. My hands hurt and constantly go numb, my skin itches, my body hurts. I started a detox a week ago, and am having to cut it short. More symptoms this time round. The doctors in this country have totally done my head in and are still doing my head in. Feeling tired, fed up and frustrated beyond words. No word as yet from the Senate as to whether my Lyme Like Disease submission was accepted. Vital hearing in Canberra for people suffering Lyme disease "It's critical that these people across Australia have a voice and are listened to and their problems are addressed – just telling people they need to see a psychiatrist doesn't cut the mustard." Senator Madigan said he had an open mind on whether Lyme disease existed in Australia. "I've got more questions than I've got answers, there needs to be more work," he said. "I haven't made up my mind, but what I do know is these people are sick. "If it's not Lyme disease, what the hell is it? "What's to say we haven't got an indigenous illness in this country that has Lyme-like symptoms that manifests itself. "I'm not saying that's the case but there is something wrong and I sympathise with these people who are suffering, I don't know how you can just dismiss it or ignore it." Read more: www.smh.com.au/national/vital-hearing-in-canberra-for-people-suffering-lyme-disease-20160419-go9rml.html#ixzz46Kufiave Follow us: @smh on Twitter | sydneymorningherald on Facebook
|
|
|
Post by Baraka Obam on Apr 20, 2016 0:53:07 GMT -5
Do yourself a BIG favor, want to see many that are damaged the same way you are.
First just walk into a MILITARY HOSPITAL, then just inspect the people, find some with all your skin issues, look and see how many are walking with old people walkers.
Then find dermatology and sit in their waiting room or in the hall if they have a chair watch what comes in.
In your summer time go there and see, they are wearing long pants, maybe long shirts. You did not have as many men in the military during the Vietnam.
If you can strike up a conversation mention your dad and your mom went to Thailand for his leave and took you. That may open some doors, depending on how old you were in 1971.
Do this on a day you want to learn, they did not actually have to go to Vietnam but those that did are the first mass of infected to come home and will be in the worst shape.
|
|
|
Post by itchin4answers on Apr 21, 2016 22:41:05 GMT -5
I hear you Baraka and I sympathise greatly with the Veterans, however I did not sign up for the Military. My submission to Parliament for the Lyme Like Disease investigation to the Senate has been accepted. My submission is number 1020. The email said they removed my name and third parties, however they did leave in the links for the Morgellons videos! which is good. So my submission was uploaded the way I sent it, back to front lol with spelling mistakes. This is the link; www.aph.gov.au/Parliamentary_Business/Committees/Senate/Community_Affairs/Lyme-like_Illness/Submissions
|
|
|
Post by itchin4answers on Jul 5, 2016 23:13:30 GMT -5
Hello everyone, Unfortunately Senator John Madigan didn't win his seat in the senate. The Lyme controversy still continues and this Lyme story was aired last night on Australian Television. Do Australian ticks pose a greater health risk than we thought? For people suffering from Lyme-like disease, it’s a controversial mystery that science has so far been unable to resolve. For the first time, microbes inside native Aussie ticks are being probed, leading to new discoveries which may reveal the causes of unexplained illnesses in the future.www.abc.net.au/catalyst/stories/4494187.htm
|
|
|
Post by itchin4answers on Nov 6, 2016 2:44:43 GMT -5
The Lyme Senate enquiry in Australia recently reopened. The closing date I believe is the 30th November. There has been much media in the recent days. This particular one from this morning seems to be the all round winner. For me, possibly 28 years into this disease, a clinical diagnosis of Lyme and co infections in 2012, though in 2016 even that doesn't get me any special help, tests, nor treatment. My blood tests are glowingly normal and yet symptoms which have no explanation, other than that of my own, being a chronic long standing infection that is still yet to be acknowledged and treated. My son only a child is positive for Borrelia burgdorferi, where did he acquire this since he has never left Australia? He acquired it from me and since Borrelia burgdorferi is not recognised in Australia my son is denied treatment. Please follow link for video: au.tv.yahoo.com/sunrise/video/watch/33119104/does-lyme-disease-exist-in-australia/
|
|
|
Post by itchin4answers on Nov 20, 2016 5:28:12 GMT -5
Evidence of Lyme Disease in Australia was discovered in 1992
|
|