Chronic Lyme Disease and CCSVI
In some cases, there is a development of alternate veins in an attempt to facilitate additional drainage. The research suggests that because these compensatory blood vessels do not have the same wall integrity as larger veins, they leak cellular waste into the adjacent tissue, resulting in an accumulation of toxins.
The discovery, and more importantly the surgical repair for CCSVI, has miraculous application to MS, but also to other diseases that has a vascular aspect that is a significant factor in the neurological component of the disease, such as neurological Lyme disease.
CCSVI and its treatment were pioneered by researcher, former vascular surgeon and professor Dr. Paulo Zamboni in Italy, whose wife suffered with MS. It is thanks to Dr. Zamboni’s tireless work that there are now hundreds of previously disabled MS victims who are now able to function and live their lives fully.
The success of this treatment has slowly made itself known to other diseases that could benefit from the same application. Due to the huge, but unknowable number of misdiagnosed MS patients who are actually suffering from Lyme disease, there is an exciting question about the possibility of the CCSVI treatment helping victims of neurological Lyme disease with some of the most disabling symptoms such as “Lyme Fog”, light sensitivity, sound sensitivity,difficulty remembering words, thoughts, speech, how to write, how to walk, emotional disturbances and unbalance, and/or as Thane Fredrickson calls it, “mental fatigue.”
Thane’s doctor considered CCSVI as a possibility in his condition and after appropriate tests verified his condition, Thane had surgery which significantly reduced the symptoms he suffered with his neurological “mental fatigue.”
Although Thane is the first to admit that he still battles the Lyme disease, those of us who struggle each day with Thane know that a large part of victory is being able to function like a normal person, and that means eliminating, or at the very least reducing, the debilitating symptoms of chronic neurological Lyme disease.
It will be exciting to see if his surgery continues to give him relief.
Watch as Thane tells his story of the discovery and ultimate treatment of CCSVI on YouTube here.
Similar Posts:
- The Dire Need For Doctors Who Heal
- Do You Have Neurological Lyme Disease?
- New Hope for Most Severe Chronic Cases of Lyme Disease! Part Three
- Social Security Disabilty for Lyme Disease
- Discovery of New Retrovirus XMRV Brings Hope to Millions of Sufferers.
- Dysautonomia and Lyme Disease
- Why Are My Ears Ringing? Its Driving Me Crazy!
- New Hope for Most Severe Chronic Cases of Lyme Disease! Part Two
- News From Dr. Brian Fallon at Columbia University’s Lyme Clinic
- WARNING: We Have Lyme Fog; Consult Healthy Friends Before Writing Big Checks



November 17th, 2010 at 3:49 pm
Hello thanks for yet another nice and good post. Where do you get your inspiration for all this
? – Tandarts
November 17th, 2010 at 7:36 pm
Another great blog, Jenna! Thank you!
November 19th, 2010 at 12:31 am
[...] Chronic Lyme Disease as well as CCSVI | Jenna's Lyme Blog [...]
November 19th, 2010 at 1:01 pm
[...] Chronic Lyme Disease as well as CCSVI | Jenna's Lyme Blog [...]
November 20th, 2010 at 4:11 am
[...] Chronic Lyme Disease as well as CCSVI | Jenna's Lyme Blog [...]
December 30th, 2010 at 3:38 am
Interesting article. Just came across your blog. I have dysautonomia and was recently diagnosed with CCSVI and underwent angioplasty in Nov 2010. Whilst it didn’t cure my dysautonomia I have certainly had similar experiences to Thane, with a reduction in brain fog and faigue. Also improvements in nausea and no migraines since the procedure. Very interesting to hear they are finding it in more disorders. I am the only dys patient in Australia to have the procedure but have recently heard from another woman in the US who was diagnosed with CCSVI and will be undergoing angioplasty.
October 14th, 2011 at 7:16 am
I’m now not sure the place you are getting your info, but good topic. I must spend a while studying more or figuring out more. Thanks for fantastic info I was searching for this information for my mission.
November 22nd, 2011 at 8:42 am
[...] Chronic Lyme Disease and CCSVI [...]
November 22nd, 2011 at 8:52 am
[...] Chronic Lyme Disease and CCSVI [...]
November 24th, 2011 at 9:32 am
[...] Chronic Lyme Disease and CCSVI [...]
November 25th, 2011 at 6:28 pm
I have chronic lyme with neuro symptoms. I had CCSVI in January, my jugular was 90% occluded, my symptoms are MUCH worse. I wouldn’t suggest it to anyone