Is CCSVI a condition/symptom

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Is CCSVI a condition/symptom

Postby fee001 » Tue Aug 09, 2011 1:38 pm

HI!

I see it as CCSVI is a symptom of something yeah, procedures to correct this anomily i.e. stents etc do not necessarily solve the problem permenantly or rectify all ms symptoms i.e. being wheelchair bound.

Am I right so far.

What I am trying to establish in plain simple terms is, why could a misaligned Atlas not be the cause.

The reason why I say in plain simple terms is, I want to cut to the chase yeah, I get confused by too much info. I just do bottom line (call me simple)

Nobody is expecting to walk again are they, just to improve blood circulation yeah

Fiona
Last edited by fee001 on Wed Aug 10, 2011 12:41 am, edited 1 time in total.
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Postby Cece » Tue Aug 09, 2011 2:14 pm

I had badly malformed valves at the base of my jugulars.

I could have a misaligned atlas too. I've heard enough here that I am thinking of getting tested sometime in the not too rushed future.

But if I turn out to have a misaligned atlas, that would be in addition to those malformed jugular valves.
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Postby fee001 » Tue Aug 09, 2011 2:28 pm

Cese,

I didnt realise before Atlas adjustment that I had a blood flow problem, it was only when I noticed the viens in my hands increased that I knew.

You see I have inherrited my Dad veiny hands and I only rembered that I had when they returned in their full glory.

Each time I look at them I smile and think of me Dad.

I just worry that the whole issue of CCSVI is distracting people from perhaps alternative solutions. The Atlas if misaligned alters blood pressure. theres got to be something in it.

Fiona
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Postby fee001 » Wed Aug 10, 2011 12:53 am

Cese,

Just another point yeah, my gums had bled for years over 9,I was told by a dentist that I had gum disease, but dont ask me why, prob gut reaction, I knew that I hadnt, so I came to the conclusion that it must have been a reaction to the drug amitryptiline (cant spell it) Which did seem a little odd because pre diagnosis I had taken the same drug for years in a much higher dosage as an anti-depressant and had no probs then. post diagnosis I take it to aide sleep.

Anyway, horrible horrible bleeding gums, but as soon as my Atlas was adjusted after 1st or 2nd session bleeding just suddenly again unexpectedly stopped. Because of both these factors I've told you about I honestly believe there is an Atlas link to CCSVI.

Thanx
Fiona (you can have your ears back now)
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Postby civickiller » Wed Aug 10, 2011 2:03 am

Cece I want to warn u as my Upper Cervical Care Dr. told me and the UCC Dr you might see hopefully tells u, you might see a relapse of every MS attack you had at once. Im not sure if that would be less whatever improvements u felt with ccsvi. they call it retracing since now nerves are firing that havent fired in years,its a shock to you nerves. Idk how much people go through retracing but it might happen and most recover in a few weeks. thats is the only downside that may happen with UCC that i know

Ive been doing UCC since 12/10 4 month of once a week visits now im at till i notice my alignment going out so far i went 2-4 weeks but everyones different some shorter some longer

please come visit the ccsvi and ccvbp thread and ask Dr. Flanagan any questions u or anyone has
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Postby civickiller » Wed Aug 10, 2011 2:41 am

Some of the benefits ive felt, LOST my heat intolerance, lost my lower back pain, no shocking with neck flexing, no migraines, none stop headache gone, but each returned as my atlas pulled out of alignment

I am a believer in if every single person always kept their atlas in alignment for life since birth, we would see a major reduction in neurological diseases
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