IVUS treatment in Medicover

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

IVUS treatment in Medicover

Postby Rici » Thu Jun 07, 2012 12:23 pm

I greet everybody!

I would like to inform all patients what is important after my IVUS treatment in Medicover according to the instructions of Dr. Schelling. The stent which was implanted 19.X.2009 was completely blocking the vein.
A better status after the IVUS treatment http://ccsvi-ms.pl/flebo/014.avi on 31.V.2012 is noticeable from hour to hour: .
Since the beginning of the year my health status was rapidly worsening due to the infection of my urinary tract (a side-effect from Fingolimod/Gilenya, and probably the beginning of a myeloma cancer). I could only lie on a bed over a anti-bedsores mattress. I was completely dependent on the help of the hospital personnel. This status lasted until .. today! I could not raise myself alone from the bed, and I could not sit on the bed without the help of the nurses. I do not even speak about putting myself on a lying position on the bed: I could not do it by myself. Now on 3 VI.2012 at around 9 PM I could raise myself alone without any help to a sitting position (a nurse was nearby for any case but she did not help), I put even my hands on the knees without putting them on the side for keeping my equilibrium. I could also put myself back alone to a lying position (only with raising one leg I needed the help of the nurse). Today afternoon I could not do it by myself. Only yesterday only for this activity two nurses were necessary.
This is not a untrue and lying placebo effect, which neurologists claim that the disease has some better and some worse days. No! This is the effect of oxygenating the brain, the effect of the nutrition of my brain with fresh oxigenated blood, which the authorities over this disease – read: the neurologists – deny to the point of letting people die.
I will see what will happen next. This very simple activity gives a lot to be happy about. I will inform you constantly. I have a lot to catch up with and also the battle with this new tumor caused by Fingolimod! I a week time I will perform a new blood analysis to check the albumine levels one month after discovering the tumor. I do not have more renal pains, no back pains lying on the side and I do not sweat during the night.
Best regards
Rici
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Rici
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Re: IVUS treatment in Medicover

Postby Rici » Fri Jun 08, 2012 7:08 am

Hi
The outflow of blood before and after surgery : http://ccsvi-ms.pl/flebo/018.gif , http://ccsvi-ms.pl/flebo/014.gif
Regads
Rici
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Rici
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Posts: 296
Joined: Thu Nov 12, 2009 3:00 pm
Location: Poland Bialystok


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