For those who have gone/are going to Poland
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- Family Elder
- Posts: 1125
- Joined: Wed Jul 29, 2009 2:00 pm
- Location: Slovakia, Europe
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Going to Poland
Oh it is so good to hear that people are still able to go to Poland even if they have to wait 10 months for the intervention.
Congrats.
Congrats.
Michele, warrior4MS, mother and champion for Ella, the MSer. The solution is out there we just have to ask the right questions.
That is great Guest. Something to look forward to. Maybe you will feel so good to swing over to Bavaria for Oktoberfest.Guest wrote:selkie
I’ve received an email from Dr. Simka today. He confirmed that I’m on the waiting list for October 2010.
This calls for a celebration.
:D
My name is not really Johnson. MSed up since 1993
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- Family Elder
- Posts: 1125
- Joined: Wed Jul 29, 2009 2:00 pm
- Location: Slovakia, Europe
- Contact:
Anything is possible. Even though I’m a light drinker, I sure appreciate a good quality beer.Johnson wrote:Maybe you will feel so good to swing over to Bavaria for Oktoberfest.
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colapesce
You read my mind.
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SandyK.
I’m so happy for you. There is light at the end of the tunnel after all. Welcome in the club.
SandyK,
That is very good news, and I am very glad for you. There is more light after these darkest of days.
Alica,
You can always hit the south of France for the Vendange. Red wine interferes with iron absorption, you know... (I was so pleased to learn that! And coffee too!) A nice bottle of Macon would do the trick for a celebration.
That is very good news, and I am very glad for you. There is more light after these darkest of days.
Alica,
You can always hit the south of France for the Vendange. Red wine interferes with iron absorption, you know... (I was so pleased to learn that! And coffee too!) A nice bottle of Macon would do the trick for a celebration.
My name is not really Johnson. MSed up since 1993
Jaguar, not sure if you have been trying St. Mary's in Montreal, but this may be a good lead for you. Read the entire page, there is a Dr there that is interested in CCSVI and apparently willing to look into it.
http://my-darn-ms.blogspot.com/2009/12/ ... pital.html
His name and phone number are in the link.
http://my-darn-ms.blogspot.com/2009/12/ ... pital.html
His name and phone number are in the link.
- greenandchic
- Family Member
- Posts: 45
- Joined: Sat Dec 12, 2009 3:00 pm
- Location: Portland, Oregon
- fiddler
- Family Elder
- Posts: 398
- Joined: Wed Dec 02, 2009 3:00 pm
- Location: Fredericton, Canada
- Contact:
St Mary's
Congratulations to everyone who has joined the club... guess we all have a lot more hope going into a new year.
Jaguar and others, regarding the information about St. Mary's hospital, there is more information in a later posting of mine: http://my-darn-ms.blogspot.com/2009/12/ ... aging.html. In summary, I found out that the CCSVI testing is going to be done in a private clinic, not at St. Mary's. I'm waiting for them to get the MRV going before I find out more so as to decide whether I want to risk the time and money going there to test for CCSVI. I can see one situation where what I could find out there might change my plans: if my veins are occluded by bone growth, it is possible that the people in Poland will not be able to help me.
...Ted
Jaguar and others, regarding the information about St. Mary's hospital, there is more information in a later posting of mine: http://my-darn-ms.blogspot.com/2009/12/ ... aging.html. In summary, I found out that the CCSVI testing is going to be done in a private clinic, not at St. Mary's. I'm waiting for them to get the MRV going before I find out more so as to decide whether I want to risk the time and money going there to test for CCSVI. I can see one situation where what I could find out there might change my plans: if my veins are occluded by bone growth, it is possible that the people in Poland will not be able to help me.
...Ted
Dx SPMS in 2004. Liberated 29/04/2010.
My blog: www.my-darn-ms.blogspot.com
My blog: www.my-darn-ms.blogspot.com