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Wow, this is great. I'm so sad that so many people are so sick from Lyme. I have heard of a new test that doctors can have in their offices. The Sofia 2 Lyme f/a. You can get results within seconds! I imagine it would be very expensive but so worth it. I found out I have Lyme from getting Zytoscans. I could never figure out all my many health problems despite eating healthy and exercising. I need to find a blood test which is very accurate. I always read they are not. I would like to have it mainly because friends and family don't see to believe me. I know I have it. But it is very sad and hard to be on your own fighting Lyme when people you love may not even believe you. But I am working with a natural health professional and seen a functional health doctor. Super expensive. My dad passed from Alzheimer's and both of his sisters have it. I have the Alzheimer's gene. Two copies. So it is extremeley important for me to get the Lyme under control. I'm 59 so time is so important. This is such a good video and I hope this man John has made some headway in this area.

Is John thinking of PAYING for the doctors with his BILLIONS ?.....I WOULDN'T THINK SO 🤔....

Would love an update as to where John and family are at. Does anyone know of any Lyme literate experts in the nhs who understand the 10-15% (usually the more serious cases) of people who have negative igg and positive igm, that private blood tests can pick up and nhs can't. Especially one who will accept a positive blood test and a private doctor from England who has confirmed the Lyme disease and coinfections, then put be able to put on nhs medical notes. Any guidance appreciated 💚

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I've got it...I know it, I'm constantly exhausted, foggy, attacks of panic, blurred vision and just thought I was struggling after abuse and chronic exhaustion My cats sleep in my bed after playing outdoors...... I need testing.

Lyme disease is devastating. I have 2 family members who caught it about 20yrs ago and are now disabled.

Thank you for raising awareness. After 5 years of symptoms, I’m now referred to neurology for investigation. 🙏

Lyme disease from mosquitos, I think nano tech has played a part in this. John should also look up the lead poisoning scandal, which is huge

I've had multiple embedded ticks and just want to say you do not always have to have a bullseye rash or any rash at all, but most often it's a different appearing rash, depending I suppose upon the bacteria present within the tick?

Money cant buy good health what alot of shxt. The reason john has recovered is because he had money for treatment

So true what he's saying about the health system.

It's important to note that not everybody who has Lyme disease, gets a bullseye rash.

Looks so good! Cant wait to try with the kids - egg wraps so versatile and simple too :)

I’ve been bitten and it’s worrying how it’s affected me - I’ve received antibiotics and worried about my family - these ticks are tiny. Luckily I found the tick but I’m still worried - thank you for this video

TEST MUST BE CHANGED !!! test is rubbish ! tests are deliberatly rubbish , WHY u ask ? because its expensive to treat and people in high places are not being honest. Im watching my beautifull partner who has always been kind and careing DYING ! sent home from hospital with a feeding tube and a diagnosis of an eating disorder. Its a joke, hes not got an eating disorder, hes VERY sick from this lyme and co infections , he cant catch his breath, hes got migraines, hes in pain , has numb bits on body , he feels nausea constantly and throws up some days, hes dying , hes so thin , dangerous hot all the time , i love him so much but i cant do anything. Ive no money , why , unable to work as im sick too, also sickness benefits stopped for my hubby even though he is bed bound every day a bag of bones, so no saving for private tests, im sooooo upset, the doctors are not honest , no matter how sick you are you have anxiety or eating disorder or anything other than lyme and co infections. Test only picks up just bitten or infected people, a tiny % , many of us have this , DO NOT get Flue shots ! its destroys immune system even more than this evil lab created illness/s does, my hubby is sickest he had a flue shot. Me and my girl who are sick too but not as bad ( yet) did not have flue shots.

TESTING CENTER IN THE UK - YES!!!!! the UK desperately needs this

Thank you so much for bringing this terrible disease to the masses.

Hi everybody have a look at the website rovince.co.uk/ they supply tick proof clothing its affordable and durable. dont give this disease a chance. this clothing is your best protection against those nasty ticks

i was bit 6wks ago and developed the classic bulseye rash, which cannot be mistaken for anything else , but because the tests are so inaccurate my test came back negative for Lyme. I am now taking a small course of antibiotics but fear its not enough. If i hadn't asked for the medication the doctors weren't even going to treat me. Its a total joke. There has never been a single recorded case anywhere in the world where a person has tested negative for Lyme disease after being diagnosed with Parkinson's, or MS. There are a few more but i can't remember there names. These are all diseases that so far have no known cause. Well to me its obvious that lyme is a direct cause OMG i can't believe they haven't picked up on this already.

My mummy has cfs nothing has made her better she got worse after breast cancer so tired all the time

Terrible disease that has taken 7 years of my life with no doctor/s.

They should try Bemer Therapy...amazing!

Please donate to my friend who lives in the USA who cannot afford health care for her illness- www.gofundme.com/superheather

will never happen so sad for everyone that's suffering government doesn't give a crap health service on its last legs

thank you for future generations. I don't think it is going to happen in time for me. Australia is only just getting started. It has to get to the public health level before pensioners could even consider treatment. I wonder how your son is going. I had a psychiatric herx on an oral antibiotic combo but it could have been the bicillin IM injections. Dont't push it too far!

Casual call from the prime minister hhaha

Way to go, John Caudwell! Thank you for pointing out the medical drama surrounding Lyme Disease!!!

Thank you John Caudwell. Thanks for fighting for us.

The problem ist that the majority of all the doctors do NOT believe that it is true what John Caudwell says. They refuse treatment even if you are diagnosed with lyme disease. The tests are not reliable and the standard cure procedure is not effective BUT they do not care. They let us suffer.

Wonderful, Mr. Cauldwell! Absolutely the correct way to go about it, with the NHS... They MUST do the work. My thoughts are with your son and the rest of your family, I wish all of you the best. Thank you for giving a voice to Lyme Disease in the UK, here in the US I have all but given up hope for any true action to be taken, the problem is so enormous. Somehow, I feel as though your involvement is cause for hope... Respectfully, NKP

I am a 25 year old who was misdiagnosed bipolar and M.E. for 7 years, only just been diagnosed as having lymes disease. My life over this past 7 years has been hell, i have lost most my young 20s to this disease, and dont want to loose any more time. I am not very well off for cash so i imgaine as a british citizen the road ahead is going to be tough. Thank you for raising awareness John. It means a lot

The only comment I would say here is that many persons with Lyme that has become chronic patients will not test positive even to the two tiered testing. The immune system is depleted when borrelia takes up residence, and it weakens the bodies response, so that if you have chronic lyme the body may not be able to produce the antigens to show that they borrelia is there. Plus, there are 300 strains and we tests for one. I tested 5 times prior to finally showing a positive after supporting my immune system and body for 4 years. Testing should be imperative, but also a question are of symptoms and habits should be added to further pinpoint. The issue of lyme is much bigger then lyme itself and today's lyme and usually there alongside multiple co infections, which also may not show up accurately on testing..

www.webmd.com/a-to-z-guides/immunoglobulins thepowerhour.com/news/mycoplasma_testing.htm

www.lyme-symptoms.com/LymeCoinfectionChart.html = ( facebook.com/groups/448750418613708/ )

no IV antibiotics ever with Lyme meningitis encephalitis.

17 years I need another LLMD mine quit he has been treating for 30 years my MD won't treat me he keeps texting me with the fall to test and telling me I don't have it is but I've never felt better and they denied ivy treatment when needed it as I have neurological Lyme disease very bad an inadequate treatment I should have had idea long time ago

What he sais is so true also here in the Netherlands, almost all chronic Lyme patients have not the money to be helped. Most of the doctors here are not willing even to help because they are affraid for an unknown "something". So the patients (including me) are forced to accept the Lyme with all the terrible things that come with it :(

Thank you so much Mr. Caudwell! I was sick 14 years and was misdiagnosed bc of the horribly inaccurate CDC tests. Other tests are better, but we need much more investment in research for Lyme and other tick born disease testing so that so many hundreds of thousands in the UK and US alone are not missed every year. We need lobbying as the number one priority!! I agree 100%. But we need it to be very aggressive (CDC and NHS are extremely recalcitrant) and focus not just on more testing, but employing better tests and researching to develop better tests and treatments. This may take more than a few million in lobbying. Please hammer them! You could end so much suffering. I would also respectfully, but strenuously urge, no, *beg* you to spend heavily on research (after priority number one of lobbying to force NHS and CDC to do their jobs is planned and money started to be spent- no reason you can't do both :) )

A friend who has Lyme sent me this video - while I am very aware of the number of ways the illness affects her life, and the devastation of not being able to receive the treatment, support and even diagnosis she needs from the NHS, it is still heartbreaking to hear this story, and to read of others' experiences. "it's their responsibility, not mine" - this truth. yes, all well and good asking someone with millions to plough money into starting some sort of testing centre, but what he says throughout the interview - the need for a transformation of the health service, so they recognise Lyme, know what it is, and stop putting thousands of people through needless suffering - is what is going to make a lasting and sustainable change to those who suffer from Lyme, and those who may get the disease in the future.

Hi Sasha I agree that organic veg help, and I try to eat only organic produce. Sorry that colloidal silver hurt you, I use a spray which may be less dangerous. Homeopathy does help me a lot. Good luck, best wishes, Sue

Celiac may cause a low immune system and then it is easier to catch Lyme and harder to get rid of it until they get Celiac help. MS/ALS etc can be due to Celiac and some may also get Lyme eventually. United Kingdom is low sunlight/far from the equator...which lowers the immune system. No gluten/dairy/soy/sugar/GMO...vitamins/good oils/minerals...probiotic...LDN...detoxing may help Celiac/Lyme etc.

Thank you John Cauldwell. I had acute neurolyme from age 36-43. Caught 7 months in. I began a dramatic recovery in 2013 ... I'd be happy to help what finally got me out of Lyme Hell. I'm on FB. Look up Rebound and Reboot: Leaving Lyme Disease Behind.

Jim Edwards, I had just one week of antibiotics. Months after that I was using homeopathy daily and still got a negative result, i.e. no antibodies found. The only person I have met who had a positive test for antibodies was symptom free while his family were all very ill but with no antibodies . If you take antibiotics , sure , biofilms will form. If you take something else to break down the biofilms you will need several different antibiotics to kill the bugs which then emerge.

Well John I suspect you have more than enough money and hopefully common sense enough to tackle this issue with no government involvement to continue the same old BS that has been bought into by elements of the medical community.

My heart goes out to this family. Money can buy health, but the right approach is needed. The very best and most effective meothod of both healing and preventing this disease is with the correct functioning of the Natrual Control system. Since 2002 we have been working to correct the functioning. Now there is nothing more efficient than the inborn system of health. Please reply to find out more or visit www.nmt.md or my site www.nmtcanada.com

YES!!! Lobbying - the same is true in the US. We have got to get lobbying groups. I am grateful for your thoughtfulness in how to move forward.

Caudwell must be very careful in thinking that just "testing" folks will find those with Lyme disease; current tests, like he said are not very good. Positive test of Lyme doesn't mean you have the disease and a negative test doesn't mean you don't have it. It is a clinical diagnosis, taking into account all the symptoms/manifestations as well as the tests. If there were a simple answer, we would already have solved it. I went ~22 years undiagnosed and then spent better part of 6 years being treated, mostly antibiotics. Lyme disease doesn't necessarily kill you, but you wish, sometimes, that you had died. The symptoms are indeed horrendous for some people. Keep up the pressure on the medical community to do proper testing and find a better cure!! There are way too many folks suffering from this insidious disease.

you can fix a lot sir, you have billions, you can help a lot

You big millionaires please do something about this gross illness. Big Pharma doesn't care about people, they care about money.