Has anyone treated in Sydney had issues found in their Azygos? or any vein other than their Jugular?seeva wrote:also he has told me he will looked at all the veins including azygos vein.he does proper testing though and re balloons of and clear the stenosis. in my case my LJGV was very narrow and was balloned my azygos is fine.
CCSVI - Aussie Action!
- CureOrBust
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Re: RE CCSVI PROCEDURE IN SYDNEY
- CureOrBust
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- hwebb
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neuro referral?
If you have ever had a neuro referral to Prof T ...could you please PM me?
People who fell outside the trial (those who sought treatment before the idea of a trial was raised), now need a neuro referral to Prof T in order to receive follow up treatment.
My neuro at RMH has stated that the neuro dept at RMH has a policy to not provide referrals to Interventional Radiologists (evenn when already diagnosed with a vascular disease). Nice to know that pateint care is their first priority.
hwebb
People who fell outside the trial (those who sought treatment before the idea of a trial was raised), now need a neuro referral to Prof T in order to receive follow up treatment.
My neuro at RMH has stated that the neuro dept at RMH has a policy to not provide referrals to Interventional Radiologists (evenn when already diagnosed with a vascular disease). Nice to know that pateint care is their first priority.
hwebb
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If anyone is seeing Professor Pollard in the coming weeks, and would like to discuss CCSVI, bring the following list with you. http://www.thisisms.com/ftopicp-133768.html#133768 A year ago when I questioned him on CCSVI for the second time, he simply said that he was about to leave for ECTRIMS 2009, and if it meant anything in MS, it would be presented at ECTRIMS.
Has anyone discussed CCSVI with him recently? A year ago he wasn't a believer. I almost want to see him again just to know if he has changed his view at all.
Has anyone discussed CCSVI with him recently? A year ago he wasn't a believer. I almost want to see him again just to know if he has changed his view at all.
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diagnosis and management
CureorBust, the referral could say something along the lines:
"please accept this patient for treatment of their vascular disorder"
"please accept this patient for treatment of their vascular disorder"
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Re: diagnosis and management
That's what I was hoping to avoid. To sign off this statement, they would be accepting that I have a vascular disorder, when in the neuro's eye's I have MS, an immune disorder.hwebb wrote:the referral could say something along the lines:
"please accept this patient for treatment of their vascular disorder"
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get more accurate
well, you could request the referral say "my patient has a blocked vein preventing adequate brain drainage, please provide advice and management" or just "my patient does not have adequate brain drainage".
All true
All true
Re: diagnosis and management
the contentious bit is that you have both! Evidenced by Doippler and venogram, l presume. l'm most likely being overly cautious and l apologise for interfering, but PLEASE be very wary of saying that CCSVI 'causes' MS - you'll only put yr neuro's back up, and earn yourself the 'double-blind, placebo-controlled' spiel. As a matter of interest, why should u be the one responsible for supplying appropriate words anyway? lf he/she asks why the referral must come from them, simply state that it's an Ethics Comm requirement. why should we be the ones to go thru hoops? cheers, nicoCureOrBust wrote:That's what I was hoping to avoid. To sign off this statement, they would be accepting that I have a vascular disorder, when in the neuro's eye's I have MS, an immune disorder.hwebb wrote:the referral could say something along the lines:
"please accept this patient for treatment of their vascular disorder"
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The Alfred liberatos - call for united action
If you or your partner has received CCSVI treatment at The Alfred, and may like access to future treatment there, please post a message or PM me. I am in the process of taking action, with the aim of securing future treatment for us. I will require your email address to get further info (attachments etc) to you. Alternately, feel free to contact me on the CCSVI Australia FaceBook site.
thanks in advance, Helen
thanks in advance, Helen
Dear Friends,
The gloves are off.........
Kerri has drafted a letter to the Ethics Committee at the Alfred.
It is for all those who have had the procedure, but now not allowed another til we have a neuro's referral.
You don't have to be on facebook to access this, it is an open page.
We need ALL Alfred Liberatos to send the letter. We will only have weight in numbers.
If you have any problems, questions etc, ask away.
Jennifer
The gloves are off.........
Kerri has drafted a letter to the Ethics Committee at the Alfred.
It is for all those who have had the procedure, but now not allowed another til we have a neuro's referral.
You don't have to be on facebook to access this, it is an open page.
We need ALL Alfred Liberatos to send the letter. We will only have weight in numbers.
If you have any problems, questions etc, ask away.
Jennifer
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Hi, it's been a while since I posted but we haven't been idle.
We had a talk with our new neurologist, Dr Judith Frayne, who happens to also be on the ethics committee and is aware of Prof T's work.
She told us that her understanding of the outcome of the committee meeting was that no CCSVI related angioplasty was to be done AT ALL, neurologist referral or not. This was not her decision, and she made a point of telling me that she absented herself from the vote.
I am sorry to be the bearer of bad news, and I really hope I'm mistaken.
In response to this I have started a blog and have posted a long summary of the discussion that I had with Dr Frayne. It's too long to reproduce here but please take a look at what we discussed:
http://arubberchicken.tumblr.com/
The outcome completely sucks but it's just the first step in what I think will be quite a long process.
Science is both helping us and failing us at the same time.
We had a talk with our new neurologist, Dr Judith Frayne, who happens to also be on the ethics committee and is aware of Prof T's work.
She told us that her understanding of the outcome of the committee meeting was that no CCSVI related angioplasty was to be done AT ALL, neurologist referral or not. This was not her decision, and she made a point of telling me that she absented herself from the vote.
I am sorry to be the bearer of bad news, and I really hope I'm mistaken.
In response to this I have started a blog and have posted a long summary of the discussion that I had with Dr Frayne. It's too long to reproduce here but please take a look at what we discussed:
http://arubberchicken.tumblr.com/
The outcome completely sucks but it's just the first step in what I think will be quite a long process.
Science is both helping us and failing us at the same time.

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more info
Hi Taxi,
I have it in writing from The Alfred that if I am able to secure a neuro referral, I can continue my vascular treatment (as I've already been diagnosed by venogram, and have commenced a vascular maintenance plan with them).
I also have it in writing that The Alfred are not able to treat a new vascular problem I suffer, behind my knee. This is because I have MS. The letter strongly implies I will need a neuro referral for this too.
All in writing from The Alfred...not just Frayne's throwaway words that she drizzles out to patients behind closed doors.
I personally know of one person (an Alfred liberato...already liberated...just seeking follow up treatment) who has accessed angioplasty at The Alfred in recent weeks as was able to secure a neuro referral (from a semi-retired neuro who is not accepting new patients).
Either Frayne has crossed wires, or the Interventional Radiology team does. It's amazing that Frayne says she knows so much about what was decided in this meeting, if she made herself absent at the criticial time.
I'd really like her to get online and blog, or contribute to some of the public discussion - really stand by her opinions. Put them out there in black and white.
Anyway - thanks for the snapshot into how the members at The "Ethics Committee" operate. They need to get used to explaining themselves...they'll be feeling some heat shortly
BTW - love your blog, thanks for sending the link. I'll keep reading this in the future
H.
I have it in writing from The Alfred that if I am able to secure a neuro referral, I can continue my vascular treatment (as I've already been diagnosed by venogram, and have commenced a vascular maintenance plan with them).
I also have it in writing that The Alfred are not able to treat a new vascular problem I suffer, behind my knee. This is because I have MS. The letter strongly implies I will need a neuro referral for this too.
All in writing from The Alfred...not just Frayne's throwaway words that she drizzles out to patients behind closed doors.
I personally know of one person (an Alfred liberato...already liberated...just seeking follow up treatment) who has accessed angioplasty at The Alfred in recent weeks as was able to secure a neuro referral (from a semi-retired neuro who is not accepting new patients).
Either Frayne has crossed wires, or the Interventional Radiology team does. It's amazing that Frayne says she knows so much about what was decided in this meeting, if she made herself absent at the criticial time.
I'd really like her to get online and blog, or contribute to some of the public discussion - really stand by her opinions. Put them out there in black and white.
Anyway - thanks for the snapshot into how the members at The "Ethics Committee" operate. They need to get used to explaining themselves...they'll be feeling some heat shortly

BTW - love your blog, thanks for sending the link. I'll keep reading this in the future

H.