Hansa and CCSVI and OMD, oh my!

Hi all,

I had started posting Hansa updates on another thread. I was referred by Hansa to Las Vegas for a CCSVI procedure and from Las Vegas to Phoenix to a biological dentist!

So I posted a new thread! :)

CCSVI means chronic cerebro-spinal venous intervention. My jugular veins were not working properly at the valves due to the lyme infection. It causes problems there. I just (today in fact!) had the procedure to correct it here in Las Vegas. It was pretty cool. Kind of scary, but great docs and nurses and really not a hard procedure. They put a camera through the veins..via a catheter in the groin. Local anaethetic. Look at the veins, then put a balloon through if neccessary. Both my jugular veins needed it.

I felt my head clear during the procedure! Pressure went away. I have had almost constant pressure, throbbing in the head for a long time. gets worse and better.

Now this evening, I have had pressure coming and going and doc says it is normal for a few days.

My veins has been backflowing into the brain and the blood flow was poor. The doc said they are flowing good now!

OMD: this is a device or maybe it stand for a condition. Anyway, my jaw and tongue are not aligned properly..probably always were like this. Causing, again, vein pressure..but on different veins, low oxygen to the head, hyper-stimulation of adrenals. Because you don't get enough oxygen at night...body is in fight or flight mode. You wake up snoring, etc. The nervous system is always on edge.

So...after the MRI assessment for the CCSVI..the doc referred me to a biological dentist in Phoenix. I flew there in one day and got fitted for these plastic retainer-like things. One for night and one for day.

I will get them in a couple of weeks. That should correct the last vein problem, and oxygen and help with fatigue tremendously! woohoo!

THEN...after the dentist fitting...I go back to Hansa for three days. To see where my body is after all this and what it will need for lyme.

So far, so good. I as so impressed with these doctors. The neurologist here who runs this clinic has worked with lyme patients for years.

I feel I am finally getting to some root issues. I will keep updating as this progesses.

Anyone else have either CCSVI or the dental devices??

Wow Nan! Sounds like you've really learned some interesting stuff about your body! Thank you so much for sharing your journey with us. It's so important that we can get as much information as possible about all of these things! Please let us know how your trip back at Hansa works out and let us know how you are feeling then. Best to you!

Any updates??