Lyme Disease in Europe

[Elizabeth1234ism]

At least I've gotten to see this in a Microscope that my friend in Edmonton brought over for me to see my blood. So sorry that my family didn't want to share that with me either .

[KarinOll]

Look up this video on youtube and you will know what to do (copy and paste): “HemoPyrrol-Lactam-uria (HPU), Lyme disease and autism presented by Dietritch Klinghardt, MD”! It is a phenomenal lecture given by Dr. Klinghardt!

[holobody]

see YT - MMS Cure For Lyme Disease

[freedomchaser2402]

i got bitten by a tick last year and developed erythra migrans (bullseye rash) not knowing what it was, i ignored it until i saw a picture of it a few weeks later. my doctor gave me a blood test and it came back negative. though their test is not 100% accurate. is there anything else that couldve caused the erythra migrans? as im looking for another explanation. the idea that im getting, if id went to the docs while i had the rash i wouldve been diagnosed with lymes disease

[anthonypetertravis]

@freedomchaser2402 . You now surely have disseminated Lyme disease. You need antibiotics at once. Ceftriaxone or penicillin G.given intravenously at hospital or intramuscular by doctor or nurse. Also at the same time oral metronidazole, doxycyline, clarithromycin, tigecyline. You may have up to 360 different conditions so you will have to work with your doctor. Worst is that you start getting paralysis somewhere, the brain starts being destroyed and you die in weeks. You need abx for months.

[hitcan79]

I have seen a dog with a Tick on it, at first I wasn't sure what it was, it looked like a wart or something on the dog's ear, I had to look really close but when I did I seen the two tiny hind legs of the tick just barely sticking out of the dog's skin, I noticed them move ever so slightly, I decided to pull it but it was really stuck in there, I grabbed a set of vice grips, and yanked it out of the dogs ear, there was a hole left by it, I then took the vice grips and killed the tick.

[FoodOrFail]

Prescription antibiotics are not the answer. They lower the body's ph, making bacteria, fungus and SPIROCHETES proliferate. Better: Alkalize (raise ph), SULPHUR, eggs, onions, garlic, antiparasiticals (wormwood, black walknut hull, clove), salt (good natural organic, not processed), Salt/C formulations. Take it from a daughter whose mother was misdiagnosed as having 'Lupus' until the day she DIED.

[anthonypetertravis]

Yes, it is truly devastating. Check out my other videos about how to treat yourself to keep the disease at bay.

[WatchMeGoDown]

I am only 26 and have lost everything to this horrible, horrible disease.

[anthonypetertravis]

I am sorry you suffer so much. You certainly should get a Lyme test even though it would probably be negative after such a long time. Morgellons looks similar to Lyme bacteria but 100 x as large. The only hypothesis I can think of is that Lyme bacteria are known to form clusters like the Morgellon clusters. Lyme bacteria also communicate. They might invade the blood or, more likely, the lymphatic system to form long chains that appear like threads. Take photos.

[TheRedline333]

really imformative video! do you have any thoughts in regards to the morgellons lyme disease connection? i have morgellons disease and while i suffered tick paralysis when i was younger i have not been tested for lyme. i read that forty percent of those with morgellons also have lyme. take care

[anthonypetertravis]

Thanks for your appreciation.

[silentobservor]

What a horrible disease

[whiskerchild]

This is very informative. Thank you.

[HPEJuggalo93]

the pictures of the bites made me itch 

[Catherine8raw]

Since getting lymes I got a grinding knee, creaking joints, it has upset me greatly, when origionally I was running happily thru a tick infested area and had lost lots of weight and felt like I got my life back. I have found on diagnose me dot com horsetail grass for lymes disease and memory loss. Now silica is in all the places lymes attacks, i.e. eye, cartilage, connective tissues, heart, what if silica is depleted or kills spirochetes like Pasteur mentioned something about removing disease.

[anthonypetertravis]

Pleased to hear you are fine Daniel. The rash does go away anyway. What antibiotics did you have? How long after seeing the rash did you start antibiotics? Was it a Czech doctor that treated you? Peter

[danielsaun1]

Take Lyme in Europe seriously. I got Lyme in Easter Czech Republic. Found tick in my groin area and 2 weeks later bulls eye mark. 2 weeks of strong antibiotics and rash is gone and I have been fine. There are some alternative treatments which people have used MMS-Chlorine Dioxide, Colloidal Silver, and Blood Electrification via Zapper that claim to have given them positive results. I can't confirm their effectiveness but maybe worth a try to some that are suffering.

[fhattest]

when,how and where did lyme disease become so widespread

[HealthAndCures]

Find out Exactly How To Cure Lyme Disease From Home here: ZIfk6cBZN_E

[anthonypetertravis]

Unfortunately what you say is true of the type of Lyme found in North America, borrelia burgdorferi s.s. There is often a multiude of symptoms, initially terrible fatigue, pain in joints that my lead to arthritis even for children. You should always ask for a Lyme test fast. The US medical community does not treat Lyme after three weeks while European doctors will treat chronic Lyme. You are therefore stuck with it if you miss it in US.

Borrelia afzelius in Europe often creates skin conditions.

[cronelesbo]

This is good, but many people never see or have these rashes or bites or

any of these skin things so it's important for people to know that so they

won't be expecting these physical signs. Are these skin things particular to

European Lyme?

[marijuni71]

@cronelesbo

The skin conditions are NOT only in Europe. Altho more common in Europe esp. in the Balkans and Norway & Sweden..Borrelia Burgdorferi has in Europe found in skin biopies with patients with acrodermatiits chronica atrophicans, and many other skin conditions. Yes Travis is right about esp on feet can easily be mistaken for fungal infection. I have the ACA on lower legs plus my husband had on his feet exactly like that cover photo-mistaken for a fungal. IT IS NOT ONLY IN EUROPE.

[marijuni71]

@marijuni71 Additional reply in ref to the skin conditions. The best thing that helps it is hyperbaric with antibiotic as one also can get ulcerations from the ACA. iT IS NOT ONLY FROM B. AVZELI, PLUS HOW DO WE KNOW ALSO AVZELI ISN'T IN US ALSO. SEARCH PUB MED. BBURGDORFERI ALSO CAUSES THESE SKIN ITEM, BUT AS COMMON IN US. I GUESS POSSIBLY ONES GENETIC WEAKNESS. IF INTERESTED I CAN SEND YOU PHOTOS OF IT ON MY LOWER LEGS. HORRIBLE.

[cronelesbo]

This is good, but many people never see or have these rashes or bites or

any of these skin things so it's important for people to know that so they

won't be expecting these physical signs.

[Catherine8raw]

I feel much much better on fatty meat and vegetables, but my lump near my ear lobe did not go down but increased! (suspect my immune cells were stimulated by the diet). Alot of lymes symptoms decreased staying of all sugars. BUTover the last 3 days I have been chewing teasal root... a bit scary because I did not know what to expect but it is working. My lump is decreasing in size more so than it has in 16 months. I took this root after weeks on lapacho (removed fungus etc..).

[lymemj]

Thank you very much for posting your videos, they help a lot specially to the ones living in the US where everyone seems to be hiding the illness. There is many people extremely sick here specially because Doctors don't treat against parasites plus the antibiotic treatment approved is really short. We are dying here!

[anthonypetertravis]

You need to look on the internet for sites that describe microscope use in more detail than I can give here. Many manufacturers have such sites. Forty years ago every doctor had a microscope on his desk so there are some books which are still relevant on microscopy that you might find in charity shops or libraries.

[Catherine8raw]

@anthonypetertravis what symptoms do you get with lymes after all this time? You seem like your ok mentally, how about numbness? Are you on regular antibiotics to keep you going? you blood seems overloaded with bacteria. I have found adding lard from beef/lamb is really getting rid of all pain/numbness, also I am on several herbs, but nothing beats fat, it has given me amazing results.

[Catherine8raw]

check out the dark field scopes

[Catherine8raw]

I have brought a microscope with a very strong like, it is almost cooking my blood. I brought it to look for spirochetes in my blood. Dr. says I am IgG and IgM negative for Bb but my symptoms are present. Please can you help advise me, how I can produce a slide with my blood and make my whole session of searching a success. You have done a brilliant job at finding yours, and I have little experience in this. Thanks and best wishes.

[anthonypetertravis]

ARTEMISININ has been a treatment for malaria, but is now creating resistant strains. It may help against Lyme disease. However, there is no research yet to support this conclusion. Lyme disease is named after the town Old Lyme in CT and is strictly speaking not referred to as lymes disease. Peter

[Catherine8raw]

What sort of microscope would I need to be able to see the bacteria? How much would it cost for such a microscope. I suspect I am in the second stage of it, I got bitten 12 months ago.

[anthonypetertravis]

@Catherine8raw A microscope with a halogen light source, a table for slides, a condensor to focus the halogen light onto the slide, a x100 objective lens that has an iris, and an eyepiece lens. The microscope less the x100 lens costs about $200 2nd hand on Ebay. The iris lens costs less. You can buy darkfield condensors, but they can be created by cutting out a circle of black paper so that you get a black centre below the condensor. Phase contrast microscope x 3 in price.

[Catherine8raw]

Is there anything that may look similar? Also, if I have lymes will it show bacteria in every blood sample I make? How do I become successful at finding lymes? You may it look/sound simple, in reality do you search through lots of blood, or is it everywhere in your system? Also why do we do a lymes antibody test that has 50-60 false positives, when we can look thru a microscope? Will what you mentioned anable me to get 2400 magnification like you mentioned you had?

Thanks very much : )

[anthonypetertravis]

@Catherine8raw Syphilis looks the same. If you haven't had abx then Lyme bacteria will be in your blood. Not in every drop, but most. You keep looking. Blood circulates and the bacteria with it. Microscopy takes time, while antibody tests are automated, but I agree: it's illogical. 70 yrs ago every doctor had a microscope on his desk. Then came penicillin. They thought there were no more bacteria to see. Microscopes thrown away. 1982 Lyme pops up. X100 lens x 10 objective x 3 camera = x3000.

[Catherine8raw]

What are the circular ones, in the pink/purple region. I have been reading that it is common that patients with lymes disease have serum magnesium deficiency and by increasing this, it can stimulate the immune system and defeat it , usually along with antibiotics. What has helped you?

[anthonypetertravis]

@Catherine8raw The five or six round ones with a diam about a tenth of the width of the view are red blood cells. The small dark dots could be borrelia spirochetes viewed from the top of their length so that you only see a dot instead of a spiral, though this cannot be proved merely by looking. They may also be fragments of borrelia spirochetes called L, though this too cannot be proved by looking. I know nothing of serum magnesium deficiency with Lyme.

[Catherine8raw]

Have you not had your serum magnesium tested?  Has antibiotics failed to get rid of lymes? What do you suggest for sufferers?

[Catherine8raw]

Saturated fats via coconut/lard have antimicrobial properties, ad if the cells is made up of 50% saturated fats this may decrease/stop lymes disease. Look into it.

[anthonypetertravis]

@Catherine8raw Thanks you for your interest in the video. Microbes may be bacteria, fungi,archea and protists, microscopic plants and animals. Unfortunatley there is no research to support the hypothesis that saturatured fat has any effect on the bacteria borrelia s.l., the bacteria which causes Lyme disease.

[MadriverP]

Thank you for this information. I have seen Lyme do great harm to a dear friend who battles on courageously. I am in Europe and my 83 year old husband has toe nails like in the picture. I deeply appreciate your attempts to educate the public in this way. Thank you so very much.

Ann Mayo

[thetorrebermeja]

Interesting information and presentation!

[Ilovedownloads]

Excellent Video.

[PeterTravis41]

Lyme disease itself is not a reportable disease in any European country. One must therefore study limited research projects in various countries where the incidence of a strain of Lyme diseases in humans in an area is determined by PCR. In some countries such as Italy it is clear that b. garinii is the most common, while in Scandinavia b. afzelius is the most common. Another approach is to collect ticks and check the strain.

[jeisinga]

awsome very good information ..didnt now that the borrelai garinni was the most commen borrelia bacteria in europe.

Are sure about that because all the major labs check for burgdorferi

[vivalaleta]

My son was diagnosed - in absence of real evidence 6 years ago when he was 8. He had a swelling of his scalp, terrible headaches that made him faint and Bell's Palsey. I was told by the time his body produced enough antibodies that would show the Lyme disease marker his symptoms would likely be gone. He's been well since.

[pur3ly]

is this rare to get ?

[anthonypetertravis]

In endemic areas such as in Southern Sweden the incidence, which is the number of persons who are treated for Lyme disease per year, is 500per 100,000 inhabitants. This means that in a lifetime you have about a 50:50 chance of being infected.

Many do not know about the disease and some do not notice that they have been bitten so that the actual number getting infected is greater than 500 per 100 000 per year. Perhaps about 1000 per 100,000 are infected each year.

Then there are pre-1982 cases.

[neelubird]

@pur3ly - Nope, it's worldwide and becoming increasingly common. Mainstream conventional Drs will have people believe that it is rare and easy to treat but those who are actually infected know better.

[txsherrie]

Wow. How informative-thanks. I am from US, so I wonder what symtoms overlap. Have had Lyme 35 yrs, Rocephin 2 yrs ago, inadequate, taking Doxy 5 mos, 8 to go. Have the spider veins in my face like shown-didn't think of Lyme! My feet peel, too like cig paper, though never as serious as shown. Knew it wasn't fungal: rarely wear enclosed shoes, but again, never considered Lyme. Probs w/temp stop of parestalsis in esophagus, too. Lyme? Horrible disease.

[PeterTravis41]

@txsherrie It's a vicious disease. Half of the bacteria is identical with the syphilis bacteria.

[Catherine8raw]

When you got the spider veins, what stage after bitten did you get them?

I get feels like a hair is moving on my skin, inside my skin, like a craling feeling in the vein or capillary, I also am developing itchy skin, high adrenalin at times and I have had it for about 13 months. Did you feel crawling sensations? Did you feel the spider veins being made, or do they just appear? Also, after all these years, do you know of any food/things that worsen lymes? Do you keep neeing different drugs

[datzfast]

why did not the scientist in this video not make a acridine orange stain and show up the blood on florescence microscopy

for the untrained eye? but 5 stars for the photographs of the skin conditions. i need to see some photos of negroid skin

[anthonypetertravis]

Please you liked the photos. I looked for photos of non-white skin but sadly only found one from USA. A flourescence microscope costs 1000s while a microscope cost 100s. Staining is an advanced technique, but better pics of course.

[usergroupX]

i got bit about 3 months ago, and removed the tick within 5 seconds of it biting me. my doctor tested me and also told me that it takes 24 hours for the bacteria to travel from the abdomen of the tick into its mandibles. that reassured me.

[anthonypetertravis]

The bacteria passes from the blood in the tick's stomach to the tick's saliva duct. As your doctor said this takes some hours.

The tick then injects saliva into the victim: this stops blood clotting and also means that you do not feel the mouth of the tick. The saliva also has a component that protects borrelia bacteria from the victim's immune system.

The bacteria follow with the saliva into the victim.

[luminescentfeeling]

Is these testing available in the UK? The NHS don't want to know.

Excellent video, well done.

[anthonypetertravis]

This type of microscopic test is available privately, but the UK state medical service does not provide such a test unfortunately.

[coltenandscott]

Is that beneficial with lymes disease borrelia afzeli? I have been treated with sporonox it did not get rid of it.

Thanksanthony petertravis

[anthonypetertravis]

Borrelia afzelii is thought to be associated with acrodermatitis chronica atrophicans, ACA. Griseofulvin is a penicillin which penetrates skin and nail. It was in common use in the 1960s when doctors assumed all toe and nail infections were fungal. Griseofulvin then fell out of use as meds that cured fungal infections became more available. Sporonox is an anti-fungal agent. it would have no effect on ACA or any Lyme infection which is in no way fungal.

P

[synapse131]

I think my girlfriend may have gotten afzellii on a trip to the UK. She wasn't feeling well during the trip (had several instances of falls that were blamed on her ankle at the time and was generally not feeling well) but could walk onto the plane. When it landed in the US, she had to be taken off in a wheelchair. She has feet that look just like that, has been Dx'd with Fibromyalgia, and has a number of small petechial hemorrhages. Seems consistent with a microaerophilic pathogen.

[anthonypetertravis]

Hi. Where were you in the UK? In what situation do you think your gf was bitten? How long ago was this? As you use the term 'petechial', which is the Latin for 'spotty', I assume you have seen a doctor and got at least a description of her condition. The next few weeks will be crucial for her so I hope she gets treated at once and in a suitable manner. Peter.

[synapse131]

She spent a fair amount of time outside, on the coast (exactly where I do not know but she mentioned being in Wales so i would assume on the west coast) and laid on the ground, in grass one evening for several hours. If she had an EM, she didn't particularly notice but did say that she gets bitten by flies, mosquitos, and spiders a lot and probably wouldn't have noticed. The petechial hemorrhages look like tiny blood blisters under the skin. She doesn't look like she has full on ACA though.

[synapse131]

This was about 10 years ago. About 2 months after we started to have sex (after waiting to get HIV tests) I started having prostate/bladder problems with unknown bacteria and then developed a skin infection on my ankle. One month of Doxy and 4 more month-long runs of Cipro over the past 2 years hasn't helped. My skin in the affected areas has been rough and thick; "scleroderma-like" in manifestation with red areas left after ABX Tx.

[synapse131]

I already have what is most likely post viral ME that I may have gotten from a cat in Alaska (where I lived at the time; so borreliosis was unlikely but could also have gotten Q fever or Borna-which are endemic to Alaska wildlife. Had a pos. monospot so EBV likely a factor and tested for and treated mycoplasma incognitus previously .) Borrelia seems a likely culprit for this series of events (her "fibromyalgia" illness and my subsequent infection and worsening.) Thoughts?

[synapse131]

P.S., her doctor wouldn't consider Lyme if it bit him in his ass. He knows nothing about Fibromyalgia, ME, CFS, Lyme, or anything generally useful. I'm trying to find her a better doctor.

[thepowerofozone]

@synapse131 i had lyme for 20 years. try ozone, vit c drips, frequency treatments. check out heather's story on my channel. she got rid of it too.

[matte5299]

@synapse131 She had Lyme....The only Lab close to being worthy of testing for Lyme is IGENEX. Anyways find an LLMD immediately!!!!!!!! and get her treated.

[poppymoone]

I have JUST been diagnosed with lymes after 23 years of trying to get an answer. I was told it could NOT be passed to my children. Now it seems that is wrong. I will be asking for them to be tested too.

[suzlwilliams]

This is awesome. Could you please show this to the medical school in the US? They don't learn ANYTHING about Lymes there. I inherited Lymes from my mother, could you cover that too? You are brilliant. Thanks.

[TheAngelwhisperer]

Wow! I learned a lot from that one. Thanks! I'm in the US but have some of those symptoms.

[nnetandrei]

Search the internet neuro - lyme bee venom.

[nnetandrei]

Very well explained mister.

[supporttruth]

this is a video which does not waste time ,bang on the money !5 stars for you sir .i hope you have recovered or are recovering !

[lukeandlea]

Thank you for posting, sir.

[ecftube]

Hey guys....PLEASE register at the Oprah Winfrey website and let her know how much you would like to see her do a show on Lyme disease. Dr. Oz thinks the "UNDER OUR SKIN" documentary is wonderful but a show about Lyme won't be done unless she sees lots of interest. Request that LLMDS and patients be the guests so that we can be heard. Also, Daryl Hall would make a great guest. OPRAH needs to hear about YOUR experience with Lyme disease. WE ARE ALL IN THIS TOGETHER !

God Bless,

Elaine

[syl22k]

I got something like this in the good ole USA in 1974. I had Bell's palsy then, and then recovered. It wasn't until 1990 that I came down with Chronic Lyme disease with neurological problems and the feet shown here. I also had groin pain and acid reflux that felt like a burning in my upper middle chest. Contrary to this film, however, my feet have improved greatly over the many years that I've been medicated.

[neelubird]

Does anyone have any idea as to what proportion of Bells Pallsy cases can be attributed to Lyme Disease? My cousin had Bells Pallsy in 2002 and although he recovered but he's since been prone to getting other illnesses so not exactly a picture of health either. He now has heptatis C and IBS so has to eat a careful diet and is managing it okay but I worry as to whether the IBS and Bells Pallsy might be attributable to Lyme at all? Any ideas anyone?

[suzlwilliams]

It doesn't hurt to test him for Lymes. As long as it's done properly with antibiotics first and using IGENEX lab in CA. Don't let anyone fool ya that they can do it other ways.

[coltenandscott]

I have lyme disease and was on IV antibiotics for along time along with lots of other more natural treatments. I have nail involvement and the skin peals on feet etc. It seems better but may nails peal and lift and I wonder if you know how to fix and cure the nails?

Thanks

[anthonypetertravis]

Many have experienced that griseofulvin helps the nails. They take between 0.5 and I gram per day for several weeks. Unfortuntately you will probably have to take griseofulvin for several months after that to prevent the infection from returning.

P

[dogsrs]

I was finally diagnosed with Lyme after it invaded my CNS and PNS. I been on IV antibiotics sine may 2008 and continue to hope for a magic bullet of a cure. Thus far in Iowa we have no lyme literate docs. It's the blind leading the blind I use my computer to educate myself on everything I can about Lyme. For right now it's my only hope.

Dogsrs

[MLDInfo2000]

I was also diagnosed wit Lyme Disease and still haven'd found a cure...

[KOMBUCHABABY]

Wow! I was diagnose with Lyme in 2005. The rashes shown on the patients legs look just like what I get on my back and legs. None of the doctors know what it is. I put a paste of doxycycline and vaseline on the outbreaks and they improved by 90%. Still working on them. Thank you for this clip. Why can't we get help with this disease? It is so terrible. Thank you so much for this clip. It is clear and informative. I will send this to my doctor.

[maciejwrotek]

yes, it can be borrelia as well. I too have Lyme Disease and microscope and seen these forms, but many people who do not have lyme, see these forms in their blood too. But on the secon thought aspergillus it can't be i think, too small.

[maciejwrotek]

there is no way saying these are borrelia, can be fungus aspergillus or streptococcus. Only genetic analysis can say what it is. Nonetheless, these are definitely pathogens, not apoptotic bodies.

[PeterTravis41]

The bacterium seen running from the top of the filmed picture to the centre can but be Borrelia burgdorferi sensu latu. The families of bacterium you mention are entirely different.

[Catherine8raw]

@maciejwrotek Why do you say it could be aspergillus, it would not turn or be a thread shape like Borrelia, surely? IS there any vids on you tube you have seen that looks like borrelia?

[neelubird]

Excellent vid (albeit gross lol).I got bitten by a tick in Pakistan in 1995 but wasn't diagnosed with Lyme Disease till August 2008 after I researched and paid for private testing myself.I've had a gradual onset illness and back when it wasn't so bad in 2000, my toenails first started looking odd but I was given terbinafine for it and left to get on with it.The toenails have since turned orange, 1 toe is touch sensitive and I can't walk properly anymore.I have to pay 4 treatment privately too.

[Azorka82]

"PLEASE DON'T FEED THE TICKS": I was a long distance hiker but contracted Lyme disease. ER doc diagnosed 2002 (tick bite/EM rash). Positive serology. ER doc confirmed diagnosis 2007. Wikipedia Lyme page emphasizes 'no chronic Lyme' yet describes disseminated Borrelia/late stage Lyme (?!).

See my personal profile here for more about IDSA conflict of interest, etc.

[Prethenie]

Has anyone considered? that the heavy spraying of Chemtrails, may have contributed to our susceptability to Lyme Disease?

[leesbet]

thankyou its an education viewing & listening to your clip. I hope you post more clips on lyme.. Its an evil disease.. left undiagnosed its a killer.. It sadly will devastate & destroy many lives unless awareness is raised & new research & treatments pioneered. 5stars..

[huhnibuhnii]

Thank you. Gunnar Torbohm, Germany

[ecftube]

Wrote an informative Lyme brochure with the help of 2 Lyme specialists. Will email to anyone.

Elaine in VA