Jenna’s Lyme Video Blog
Video blog about chronic and/or neuro-Lyme
18 Responses to “Lyme Disease in Europe”
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July 11th, 2008 at 12:24 am
Anne
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.
July 11th, 2008 at 3:47 pm
Franny
“melikerns” idea to openeyepictures
The movie has brought much needed awareness, however, why don’t you post a list of petitions,a list of political representatives that we can contact. Put the links on your page; this will make it easier for those who barely have the energy to move. Please
July 13th, 2008 at 10:29 pm
Cameron
I read a book years ago, called “Sugar Blues” by William Dufty. An absolute read. He states that during the Bubonic Plague, the rich who could afford sugars, were dropping like flies, the poor country folk who could not, faired well.
July 14th, 2008 at 12:48 pm
Christopher
Google…..”Low Dose Naltrexone Homepage.” And also here on You tube…”Controlling Lyme Disease,” and see the LDN videos by “TropicalDawg” here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind…”Including Fruit!”
July 14th, 2008 at 7:35 pm
Sherry
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
July 15th, 2008 at 4:02 pm
Samantha
I was also diagnosed wit Lyme Disease and still haven’d found a cure…
July 16th, 2008 at 12:56 am
Joan
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.
July 17th, 2008 at 7:31 pm
Vichelle
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.
July 19th, 2008 at 7:29 pm
Anne
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.
July 20th, 2008 at 10:26 pm
Dan
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.
July 22nd, 2008 at 2:32 pm
Susy
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.
July 25th, 2008 at 12:37 pm
Marilynne
“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.
July 25th, 2008 at 3:30 pm
Susanna
Has anyone considered? that the heavy spraying of Chemtrails, may have contributed to our susceptability to Lyme Disease?
July 26th, 2008 at 10:24 pm
Michelle
I had extreme symptoms, many emergency room visits and ambulance rides. I thought I was going to surely die. Please all, eat healthy, no sugar. Keep it simple. I am hopeful and considering MMS? I use visualization as well and prayer. I was unable to withstand any drugs after a week fearing a heart attack. My heart is now much better and I am no longer afraid. Diet first defense. NO FRUIT OR SUGAR or packaged foods. Be well all. Love…:)
July 28th, 2008 at 5:35 am
Tom
I am hoping to make this Lyme dormant it not kill it. I am juicing veggies. “NO SUGAR OF ANY KIND, INCLUDING FRUIT! I eat just vegetables, some free range chicken and wild Salmon. Take Ionic Silver 100, Lomotium, Coconut oil and a clove of pressed garlic daily. Drink only water beyond veggie juice. I was bedridden for five months and unable to care for mylsef or drive. I no live at home again. Not well, but many symptoms have subsided.
July 29th, 2008 at 2:49 am
Mary
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..
July 30th, 2008 at 10:49 pm
Violette
Thank you. Gunnar Torbohm, Germany
August 2nd, 2008 at 5:32 am
Scott
Wrote an informative Lyme brochure with the help of 2 Lyme specialists. Will email to anyone.
Elaine in VA