CCSVI in Bulgaria
Hi everyone,
Got back yesterday (June 13) from Bulgaria. I am LIBERATED!!! I have SPMS. I see a few changes: better bladder, fatigue gone and balance is better too, I will have to do physio for my drop foot to get my leg bending again.
You guys are in excellent hands.
Hi Burg, I'm glad I met you in person. It was fun to be with people who totally get it. See you on the blog! take care
Anna
Got back yesterday (June 13) from Bulgaria. I am LIBERATED!!! I have SPMS. I see a few changes: better bladder, fatigue gone and balance is better too, I will have to do physio for my drop foot to get my leg bending again.
You guys are in excellent hands.
Hi Burg, I'm glad I met you in person. It was fun to be with people who totally get it. See you on the blog! take care
Anna
Hi Anna...happy you guys are home and you're ok and improving..
It's one week since liberation...
Just for all of you with questions...I was the same...couldn't live without all the info I could get...so..hope I can help..
The last few days (3 or 4) I seem to be in a holding pattern. My walking seemed to be improving, but then, gotten worse. I'm just not sure anymore. I was able to cross my legs, so I was lifting my right leg,crossing my left, uncrossing and back on floor. I couln't do that for 5 years. so I did it...over and over. Now, it's become hard to do. My wife says that I was overdoing it. She's probably right...MS or not..They're always right! What keeps going through my mind is I restenosed. Reading about Sofia (one of my heroines..I follow all of your posts!!) and others, I thought that maybe,I restenosed. However..my bladder control, foot temperature and numbness are still improved, so...who knows.
Anyway...I am so elated that I did the procedure. There were people there that had immediate relief. Some that didn't. But...go for the gold. Look...it took me 10 years to get where I now am; its going to take time to get better.
I'm looking forward to all of you beating this, and getting well!!
It's one week since liberation...
Just for all of you with questions...I was the same...couldn't live without all the info I could get...so..hope I can help..
The last few days (3 or 4) I seem to be in a holding pattern. My walking seemed to be improving, but then, gotten worse. I'm just not sure anymore. I was able to cross my legs, so I was lifting my right leg,crossing my left, uncrossing and back on floor. I couln't do that for 5 years. so I did it...over and over. Now, it's become hard to do. My wife says that I was overdoing it. She's probably right...MS or not..They're always right! What keeps going through my mind is I restenosed. Reading about Sofia (one of my heroines..I follow all of your posts!!) and others, I thought that maybe,I restenosed. However..my bladder control, foot temperature and numbness are still improved, so...who knows.
Anyway...I am so elated that I did the procedure. There were people there that had immediate relief. Some that didn't. But...go for the gold. Look...it took me 10 years to get where I now am; its going to take time to get better.
I'm looking forward to all of you beating this, and getting well!!
I sure hope that all the people who have been LIBERATED dont forget to keep us all up to date on thier recovery and how they are doing with thier symtoms if they are continuing to go away or whatever. Ican only imagine they are all feeling so good they are all out whooopin it up!!But seriously it would be good to hear from some of the first ones that had it done to see how they are feeling.
Hi Anna, Imet you and your husband for a few minutes in the door way of my friends room in the hospital. I too have flown back home. Just have to say the first 2 day after the procedure I had so much energy and no ringing in my ear. Now I feel so tired, I never felt this tired before. Do you think they use steroids before,during or after the procedure to give us a bit of a lift.
Sofia/Bulgaria
Hiya,
I'm heading over to sofia on june 22 for the procedure. I'm staying in the greenville for 2 days and then I'm booked into the hospital. I hope to meet up with a few of you guys while I'm over there. I am traveling over from Dublin/Ireland.
I'm heading over to sofia on june 22 for the procedure. I'm staying in the greenville for 2 days and then I'm booked into the hospital. I hope to meet up with a few of you guys while I'm over there. I am traveling over from Dublin/Ireland.
Hello pan
I don't think they gave us steroids before, during og after procedure. I had my op on the 12th of May 2010. I know how I respond to steroids, and I am 100% sertain that nobody gave me any steroids.
I've had a setback, but the last month has been much better then any of the others for the last year.
I don't think they gave us steroids before, during og after procedure. I had my op on the 12th of May 2010. I know how I respond to steroids, and I am 100% sertain that nobody gave me any steroids.
I've had a setback, but the last month has been much better then any of the others for the last year.
<div>I have lived with ms for 8 years. The last year has been hell, I've gone from shite to even worse every single month, until my liberation in May. </div>
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Hope you get better from all the fatigue...
Hi Pan,pan wrote:Hi Anna, Imet you and your husband for a few minutes in the door way of my friends room in the hospital. I too have flown back home. Just have to say the first 2 day after the procedure I had so much energy and no ringing in my ear. Now I feel so tired, I never felt this tired before. Do you think they use steroids before,during or after the procedure to give us a bit of a lift.
Do you think the air travel had anything to do with you feeling tired? or is this the general MS "tired"?
Thanks for keeping us all in the loop as well...
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Setback...
Hi Sofia,sofia wrote:Hello pan
I've had a setback, but the last month has been much better then any of the others for the last year.
What type of setback are you experiencing? Please share if possible... and thanks!
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