A possible BREAKTHROUGH in the treatment of Lyme Disease! This video is ten days post procedure.
Tag: als, babesia, bartonella, brain, ccsvi, cfs, chronic, disease, fatigue, fog, Health, klinghardt, Lyme, MS, Multiple, sclerosis, syndrome", treatment., ZamboniDottor T. Il divulgatore scientifico
DOGOOD HERE: Hang In There Brotha. God Bless You.
Very interesting. I wonder if the pressure from from our veins crosses over and effects the pressure in our arteries or the reverse? Are the systems open to each other? Or are they individually closed systems. If so, it is possible that a restriction in an artery is what leads to the later restriction in the veins in a given area? Thanks for the info.
I’m Keith Morey I was just talk to Dr. Dietrich Klinghardt about this and he said this worked for Autism. Give me a call and i maybe able to help you for free Email me at supergoodstuff@cox.net thank’s
Good to see u are doing so well bless u dear friend
Almost 10yr with MS and it sucks… But we got to stay strong my friend! Add me on FB if you have it… TOuber83@live.com or just search my name Tommy Ouber. Nice to meet you.
Is doxycycline the medication they give you once they diagnois you with Lyme?
@face2facechick
Yes, doxycycline is the standard antibiotic to treat lyme disease. If treated immediately (within 1 month) 2 months of doxy should completely eliminate the lyme
@face2facechick Thanks for the response! I think I’ve had Lyme for about 6 months now. Should I just go for IV treatment or see if the pills work?
Thane, I am so happy for you!….I could see a difference in your face before I even hit play. Thank you so much for sharing this info with all us lymies and the world. I will definitely look into it, as my poor brain feels like swiss cheese. Take good care! I look forward to watching your next vid!
Thane, I am so happy for you!….I could see a difference in your face before I even hit play. Thank you so much for sharing this info with all us lymies and the world. I will definitely look into it, as my poor brain feels like swiss cheese. Take good care! I look forward to watching your next vid!
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Interesting, is it possible that borrelia produces some chemicals that narrow veins ? hmmmm…….
Absolutely. There’s a group in Boston that has been studying the toxins produced by Borrelia for many years. Many pathogens output toxins. Research in ME/CFS found a toxin ciguatera (which is also a marine toxin from fish but in ME/CFS is an endogenously produced toxin and is a general auto-immune dysfunction in many illnesses) and we also have micro-circulatory and nitrosative dysfunction that affects peripheral circulation to such a degree that muscle metabolism is severely impaired.
Thane. You right on the money. Research in ME shows that all patients have diastolic cardiomyopathy. Combined with micro-circulatory dysfunction, it causes such problems with muscle metabolism that the “raggedy andy/ann fatigue is closer to a “bonk” (“hitting the wall”) when we run out of available glycogen (when your aerobic metabolism is so screwed up, the anaerobic has to take over.) This seems to cause the drop out in blood pressure.
The resulting blood flow problems in the brain are caused by these blood pressure drop outs and it has been shown in neurological research that transient ischemia in the brain results in excitotoxic brain damage and the hyperalgesia pain and the micro-seizure that results in the cognitive symptoms (when your brain is doing a “soft reset” every few seconds, attention and focus becomes problematic, memory, etc.) Multiple studies have confirmed circulation problems in the CNS with ME/CFS.
A small subset of FMS patients have excitotoxic damage from dietary excitotoxins (MSG and aspartame) due to a compromised blood brain barrier and this could almost be considered a chemical proof for excitotoxic damage. The spinal stenosis subset is another. There are a number of causes for excitotoxic damage incl. ischemia, infection, chemical damage, etc. so it would make sense that there are a number of routes for ME/.CFS and FMS to be caused.
All of these apply to Borrelia and most especially the direct infection since it has more ability to do this than the pathogens involved with ME/CFS. I actually suspect that my girlfriend (Dx with FMS) may have Borrelia from a trip to the UK. Unfortunately, since it would likely be afzelii or garinii, she can’t get tested. She deteriorated on the place coming back; not surprising since Borrelia is microaerophilic.
The main NMDA/glutamate antagonists in the CNS are endorphins and GABA and ME/CFS patients are low in central endorphins so when we do not have enough of these chemicals in the brain, excitotoxic damage is the result. This also explains why NMDA antagonists are the best palliative meds (incl. endorphins/opiates, GABA, cannabinoids, selective NMDA antagonists such as Dextromethorphan.) For some, opiates may literally be a form of “endorphin replacement therapy.”
In the article (interview with an EEG expert) about the micro-seizure in ME/CFS, he mentioned that it causes “alpha wave intrusion.” This is the same as the alpha/delta wave sleep studies. Sleep dysfunction, cognitive dysfunction, etc. are all from this micro-seizure. Unfortunately, even if you find an effective med, it’s not going to help the systemic features (cardiomyopathy and circulatory) and can only mediate the CNS dysfunction.
CCSVI was what made me realize that ischemia was a driving force in ME/CFS and combined with the heart and circulatory dysfunction research, it all started to fit together. After the initial illness, I didn’t start to go downhill again (after starting improvement in 3rd month) until I started having heart arrhythmia. No coincidence.
I also recently discovered that organophosphate poisoning causes excitotoxic brain damage and, surprisingly, the same kind of diastolic cardiomyopathy that occurs in ME/CFS and this is why they present similarly.
I am starting to think that the brain dysfunction in most ME/CFS is actually a completely secondary phenomenon to the heart and circulatory dysfunction. Explains why I have almost complete mediation of CNS symptoms with pain meds but no effect on systemic symptoms
I have been treated for CCSVI because I have MS, but I think I have Lyme disease go figure I think my doctors are wrong and have been for about 20 years I am in the midst of getting tested for Lyme disease. Most important I felt somewhat normal after angioplasty.
hey Thane–been looking into this out here in CA. These treatment centers seem to require that you have MS. What did you use as your diagnosis to get insurance to pay for this? Were the docs at that Atlanta clinic able to give you one to use after the imaging?
I have Lymes Disease and it Sucks!!!!!
This is very good info on CCSVI. To get more info, I suggest finding several of the larger CCSVI Facebook pages addresses and visiting them. Mine is “CCSVIUSA” on both YouTube and Facebook. I am not a doctor. The latest information is that stents work fine and are used for both arteries and veins, but they are used as last resort and after 2-3 angioplasties, only if they don’t work and stents are the last resort. Synergy Health in Costa Mesa, CA has treated Lyme patients with CCSVI.