The first open o.p. on the JIV- the reduction of diameter

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

Postby Rici » Tue Mar 29, 2011 12:09 pm

Hi

I repeat once again at the request of the forum participants:

I did not have surgery azygos. Only jugularis.

Regards
Rici
User avatar
Rici
Family Elder
 
Posts: 296
Joined: Thu Nov 12, 2009 4:00 pm
Location: Poland Bialystok

Advertisement

Postby David1949 » Tue Mar 29, 2011 1:32 pm

Rici
Your case is an interesting one. It suggests that when veins are too big it causes problems too. I'm not a doctor but it seems to me that perhaps the blood passes through the brain too fast and is not retained long enough for oxygen and nutrients to pass through the capillaries and into the brain tissue. Is that possible? I wonder if this issue might affect others who have had their veins opened by venoplasty.

Good luck with your recovery. I wish you the best. Thank you for being another pioneer in this research.
David1949
Family Elder
 
Posts: 640
Joined: Mon Aug 23, 2010 3:00 pm

Postby Cece » Tue Mar 29, 2011 4:08 pm

HappyPoet wrote:Btw, how's your MS doing, Lyon? I hope you're feeling okay these days. I know you were an early participant in the BNAC trial -- did you ever get the CD of your imaging? If yes, you should post some of your images.

HappyPoet, you are mistaken? Lyon has said that his wife is the one with MS.

Rici, much healing and hope to you.
Cece
Family Elder
 
Posts: 9018
Joined: Mon Jan 04, 2010 4:00 pm

Postby Lyon » Tue Mar 29, 2011 6:28 pm

..
Last edited by Lyon on Fri Jun 24, 2011 6:29 pm, edited 1 time in total.
Lyon
Family Elder
 
Posts: 6063
Joined: Wed May 03, 2006 3:00 pm

Postby HappyPoet » Wed Mar 30, 2011 6:36 am

Hi Rici,

I believe it would be unfair to you for the discussion of Lyon being the one who has MS, not his wife, to continue on your thread -- if Lyon and Cece would like, they can start their own thread titled, "Does Lyon have MS?" (I would LOVE to participate!)

Wishing you continued happy healing, Rici.
User avatar
HappyPoet
Family Elder
 
Posts: 1401
Joined: Thu Jul 09, 2009 3:00 pm

Postby Rici » Thu Mar 31, 2011 1:35 am

frodo wrote:
Rici wrote:The scar will go down and there will be almost not sign. In the hospital where the surgery is done i.e. Medicover http://www.medicover.com/plpl/ - starting from the next week, there will be English speaking call center operator. At the same moment the prices are lower by several thousands in comparison to Euromedic. With no doubts it is much better solution also with the location - 20 minutes journey from the international airport.
Regards
Rici


Hi Rici. Some time ago I was speaking with a doctor named Dr Maciej Jaworski, from Medicover Poland. Finally I decided not to go there, but I am thinking it over. Was Dr. Jaworski the surgeon? Do they treat CCSVI in a regular basis?

Hi
http://www.medicover.com/plen/hospital/ ... ackage.htm
Regards
Rici
User avatar
Rici
Family Elder
 
Posts: 296
Joined: Thu Nov 12, 2009 4:00 pm
Location: Poland Bialystok

Postby Rici » Fri Apr 22, 2011 3:54 am

Hi
One month after the open JVI operation
I wrote already about the medical conditions and I will not write it again. In each case you can compare a CCSVI treatment and the reduction of the vein with a smooth ride with a Mercedes class S with a dangerous Formula 1 ride. What is most important: I start to feel much better even without cold applications! Today I woke up and did not feel concrete in the legs, or the feeling in the legs to be “heavily bandaged”. I do not feel the weight on my shoulders. I can lift the legs more sitting on a chair. I do not need half an hour to come to myself after waking up, and my body does not have so many strong spastic motions anymore. It is cliear that my TURBO M.S. is just behind me. Also with the urination it is much better, only once every night and normally in the morning. Not as I went back after my first CCSVI treatment in Katowice on December 22nd 2009, when I had to go three times during the last 200 km on my journey home (within 2 hours): and our known doctor S. sent me to other control tests to check if I do not have “an urinary inflammation”. This was just then a clear worsening of my situation just after 24 h after the damage to my vein valves and after the enlargement of my veins. Now my legs do not “jump” anymore, even when I took 4x25 mg Baclofen and 50 ml Mylostan it did not help much and I took it badly. Today I took only 50mg Baclofen and it was more than enough! During the night yesterday evening I went to the first floor to train on the cyclette! It is true then what Dr. Maciej Jaworski said after the operation in MEDICOVER HOSPITAL: about 4 weeks is the waiting time until the hematom inside the vein disappears. My jugularis has now a diameter of 12 mm, but on the site of the hematom it had a diameter of 4 mm and it affected the blood flow. There was a too high occlusion. I have the same feelings now as I had immediately after December 22nd 2009, when my vein valves were damaged and my vein was enlarged too much. Immediately after the operation then and now I can read SMS without glasses! Now immediately after my last operation I needed cold applications to feel better, now I feel better even without applications. My friends tell my that my voice tone is much stronger now than right after the last vein reduction operation. I will test one more time to sleep with the cold application and to see if I can get rid of this in the future. I can write using all fingers on the laptop and not only two shaking fingers of each hand. I do not shiver anymore. I do not have back pain when awakening. The left side of my face does feel better now and the fingertips are feeling much better. I will keep you all informed about my conditions, but I do see now already clear signals that the first operation in the world to reduce the diameter of the jugularis brings very good effects. It is a clear path for others in my condition to follow. This is basic physics: the hydraulic law. It was not possible inside the vein to create a suction movement in order to “pull” the blood from the brain because of the enlarged diameter of the vein. This is a warning and a request for all doctors: do not enlarge the veins too much and do not destroy the vein valves. The theory that mankind since coming down from the trees does not need the vein valves is simply wrong. This is a relation about the vein valves after CCSVI treatments: : http://tnij.org/lh7n and http://tnij.org/lh7o (especially what is underlined). Please learn also from the web page of Dr. Schelling: http://www.ms-info.net/evo/msmanu/984.htm. This special person dedicated his whole life to this theory. You can not boycott him telling that “Dr. Schelling exaggerates”. He does not exaggerate, we are the result of an evolution and we cannot change this fact. We can only follow the pathology. No doctor is cleverer than the evolution. The reduction of the diameter to 12 mm enables enough suction to drain the blood from the brain and to clear the space for new fresh blood to the brain. Everything must be according to norm. Our body is build in a perfect way and there is no much room for improvisation.

Best regards and best holidays to everybody
Rici
http://tnij.org/lici
User avatar
Rici
Family Elder
 
Posts: 296
Joined: Thu Nov 12, 2009 4:00 pm
Location: Poland Bialystok

Postby bluesky63 » Fri Apr 22, 2011 5:31 am

Yes, it was my computer being weird. It is haunted.

Any time someone gets relief it is a wonderful thing. It is clear that everything is easier, and the happiness shines through. You are lucky that there are physicians willing to try being pioneers. Best wishes for the most positive outcome possible. :-)
Last edited by bluesky63 on Sat Apr 23, 2011 3:10 am, edited 1 time in total.
User avatar
bluesky63
Family Elder
 
Posts: 441
Joined: Mon Apr 18, 2005 3:00 pm

Postby Reytan » Fri Apr 22, 2011 1:43 pm

bluesky63 wrote:So why, when I clicked on that link, did my computer warn me about malware??????


I just opened the link without any warnings from my Norton Internet Security. If I may suggest please update your antivirus software and perform a full computer scan.
Reytan
Family Member
 
Posts: 35
Joined: Wed Jan 13, 2010 4:00 pm

Postby Rokkit » Fri Apr 22, 2011 8:08 pm

Congratulations, Rici, it's been a long and difficult journey.
Rokkit
Family Elder
 
Posts: 669
Joined: Tue May 19, 2009 3:00 pm

Postby Cece » Fri Apr 22, 2011 8:45 pm

Thank you for the detailed list of improvements, I wish you well!
Cece
Family Elder
 
Posts: 9018
Joined: Mon Jan 04, 2010 4:00 pm

Postby Rici » Fri Apr 29, 2011 5:09 pm

Cece wrote:Thank you for the detailed list of improvements, I wish you well!

Hi
Thank you Cece
attached the actual pictures of the wound after the operation:
http://www.ccsvi-ms.pl/foto/scar1.jpg , http://www.ccsvi-ms.pl/foto/scar2.jpg
Regards
Rici
User avatar
Rici
Family Elder
 
Posts: 296
Joined: Thu Nov 12, 2009 4:00 pm
Location: Poland Bialystok

Previous

Return to Chronic Cerebrospinal Venous Insufficiency (CCSVI)

 


  • Related topics
    Replies
    Views
    Last post

Who is online

Users browsing this forum: No registered users


Contact us | Terms of Service