News from Rici, a polish patient being operated
News from Rici, a polish patient being operated
Rici is a polish patient being operated several days ago in Katovice. He is 54 years old and has EDSS 6.
Rici reports every day about his improvements in health in our german forum so here is a short summary I made as Rici only speaks polish and german:
Day 1
"I can stand heat. Can bend my fingers without any physical exercises. Fingers aren't as stiff as before and the feeling is different. Tinitus is better and speaking is better, too. No pain in my head and back without any physical exercises. No more "double vision". The vein was blocked totally so they had to go thru the vein in my neck. After an hour everything was complete and I felt an instant relief. Spasms are remaining but not as strong."
Day 2
"Just arrived at home. Better feeling in my hands not so much numbness. After having woken up I instantly was able to close my fingers to a fist. Spasms improved. Had to use less Baclofen during the night. Only had to go the bathroom once this night. Before I had to go every 2 hours. I managed to reach home (5 hours drive) without going to the bathroom. Tired now and going to bed."
Day 3
"This night I also had to go only once to the bathroom. Instead of 75 or even more units of Baclofen against the spasms I only needed 35. Before I had to do "bicycle" with my legs every night to avoid uncontrolled movements of my legs. Some years ago I even demolished a bed in the hospital with my leg movements. I was able to stand close to the radiator without feeling uncomfortable. I believe it's not wrong to claim that I HAD MS. Only the consequences of the former wrong treatment are remaining. Such a great relief only after 3 days!"
Day 4
"Already my problems with keeping the balance have started to vanish! Unbelievable!"
(will be followed)
Rici reports every day about his improvements in health in our german forum so here is a short summary I made as Rici only speaks polish and german:
Day 1
"I can stand heat. Can bend my fingers without any physical exercises. Fingers aren't as stiff as before and the feeling is different. Tinitus is better and speaking is better, too. No pain in my head and back without any physical exercises. No more "double vision". The vein was blocked totally so they had to go thru the vein in my neck. After an hour everything was complete and I felt an instant relief. Spasms are remaining but not as strong."
Day 2
"Just arrived at home. Better feeling in my hands not so much numbness. After having woken up I instantly was able to close my fingers to a fist. Spasms improved. Had to use less Baclofen during the night. Only had to go the bathroom once this night. Before I had to go every 2 hours. I managed to reach home (5 hours drive) without going to the bathroom. Tired now and going to bed."
Day 3
"This night I also had to go only once to the bathroom. Instead of 75 or even more units of Baclofen against the spasms I only needed 35. Before I had to do "bicycle" with my legs every night to avoid uncontrolled movements of my legs. Some years ago I even demolished a bed in the hospital with my leg movements. I was able to stand close to the radiator without feeling uncomfortable. I believe it's not wrong to claim that I HAD MS. Only the consequences of the former wrong treatment are remaining. Such a great relief only after 3 days!"
Day 4
"Already my problems with keeping the balance have started to vanish! Unbelievable!"
(will be followed)
Last edited by Ana on Tue Nov 03, 2009 8:49 am, edited 3 times in total.
LOLaddict for stories like this

Wonderful Rici!! Thanks Ana!
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
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Rici and also Dr. Simka told me, there were no side effects after Clexane - those under skin injections of Heparine. I can even take my LDN with it.
I can not find the post, but somebody here was explaining why you in the USA take Coumandine.
Of course, I prefer Clexane - I do not have to see more Slovak doctors to check my INR - this is already big reason for me. The side effects you mention is also big issue.
So why do you have suffer?
Erika
I can not find the post, but somebody here was explaining why you in the USA take Coumandine.
Of course, I prefer Clexane - I do not have to see more Slovak doctors to check my INR - this is already big reason for me. The side effects you mention is also big issue.
So why do you have suffer?
Erika
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
Coumadin is cheap in the US, low molecular weight heparin is expensive for us. In my case $3500 and the company not covering it. I would have preferred it.
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
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- Family Elder
- Posts: 1125
- Joined: Wed Jul 29, 2009 2:00 pm
- Location: Slovakia, Europe
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Yes, I remember something like this. It is not expensive here.mrhodes40 wrote:Coumadin is cheap in the US, low molecular weight heparin is expensive for us. In my case $3500 and the company not covering it. I would have preferred it.
I do not understand more things in this world. I do not even ask why is it so.
I remember you with this problem.
Well, come to see me to Slovakia to get Clexane

This world is crazy anyway.


Erika
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
Erica - be aware that you need to go off the LDN while on pain killers after the operation. Check the list of pain meds that are contraindicative with LDN
SharonCautionary warnings:
Because LDN blocks opioid receptors throughout the body for three or four hours, people using medicine that is an opioid agonist, i.e. narcotic medication — such as Ultram (tramadol), morphine, Percocet, Duragesic patch or codeine-containing medication — should not take LDN until such medicine is completely out of one's system. Patients who have become dependant on daily use of narcotic-containing pain medication may require 10 days to 2 weeks of slowly weaning off of such drugs entirely (while first substituting full doses of non-narcotic pain medications) before being able to begin LDN safely.
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- Location: Slovakia, Europe
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Oh, thank you! I am going to check it right now.Sharon wrote:Erica - be aware that you need to go off the LDN while on pain killers after the operation. Check the list of pain meds that are contraindicative with LDN
Sharon
I know I must stop LDN 72 hours before the procedure.
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse