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Joined: Oct 16, 2009 Posts: 840 Location: St. Louis, Missouri
Posted: Fri Feb 05, 2010 1:38 pm Post subject:
MaggieMae,
Dr Mehta looks like a wonderful doctor. I am so glad that Kacey found him !!! Maybe I should start a new list and have an "Original Pioneers" and "New Pioneers" list !!! I need to put my thinking cap on here because Dr James Laredo at Georgetown University should be added also.
Posted: Sat Feb 06, 2010 2:57 pm Post subject: Finding a right doctor
Hi all MS sufferers,
I am from Romania but living in Dubai. My diagnosis for MS is not yet fully confirmed, but the disease seems to be installing slowly but surely, as I am just having my second optical neuritis attack. I've seen the article about doctor Zamboni and I would really like to reach him or any other doctor that works with him or considered experienced enough to identify the venous insuficiency and perform the procedure. Also, I would like to be able to make an appointment as soon as possible. Please contact me at lazalexandra@yahoo.com. Thank you everyone. all your comments are really helpfull
Joined: Oct 27, 2009 Posts: 52 Location: Melbourne - Australia
Posted: Wed Feb 17, 2010 3:55 am Post subject:
For Folks who live in the UK or who can travel there...
In another thread another member (Edser) has posted email details for another Interventional Radiologist who is interested in CCSVI and is offering diagnostics and if appropriate baloon angioplasty interventionsin the United Kingdom - Birmingham.
Joined: Oct 27, 2009 Posts: 52 Location: Melbourne - Australia
Posted: Tue Mar 02, 2010 6:58 pm Post subject:
Folks in Melbourne - Australia
For Imaging/Diagnosis via Color Doppler Ultrasound of Internal Jugular and Vertebral veins only (extra-cranial) using Menegatti protocol, (cost AUD300.00 - no medicare refund at this stage) ask GP for a referral to:
Melbourne Radiology Clinic
3-6/100 Victoria parade
east melbourne
Phone 9667-1667
sonographer: Dr Julie Gregg. http://www.melbourneradiology.com.au/diagnostic-imaging/ultrasound.html N.B.An MRV assessment will be available in mid to late march 2010 at this clinic. No details as yet
In the event of the detection of impaired blood flow or other abnormal findings in the above 45min-1hour ultrasound scan:-
For Endovascular Investigation and possible treatment via Venogram and Percutaneous Transluminal Angioplasty (ballooning only) ask GP for a referral to:
Professor Ken Thomson
Director of Radiology - The Alfred Hospital
55 Commercial Road
Prahran
Phone 9076 2536
For info on costs etc please refer to the following pages:
http://www.alfredhealth.org.au/radiology/ http://www.alfredradiology.org.au/Content.aspx?Page=5
Posted: Wed Mar 03, 2010 4:12 am Post subject: ccsvi trials in buffalo
HI,
can anyone tell me if they took part in the ast trail that was done in buffalo?? How did they get on? is a good, reliable clinic? did your results come back positive for ccsvi? do they keep in touch with you after? how much did you pay?
Alot of questions, i know, but i got a phone al last day saying i was excepted for next trial? I am from ireland, a log way to go i know, so hope i'll get somethingfrom it??
Anyone else out there get excepted??
john
From: Brian Putman [mailto:brianputman125@hotmail.com]
Sent: Thursday, March 04, 2010 8:21 PM
To: ms@ameds.pl
Subject: CCSVI examinations and treatment
Dear AMEDS,
I am a UK citizen who has had MS for eight years. I am interested in your CCSVI examination and surgery, if needed. I would like to book a date for a comprehensive medical examination, and the subsequent surgery.
HELLO TO ANYONE WHO CAN ASSIST- I think I can speak for most MS sufferers around the globe that the CCSVI scan gives us something to look forward to ... just having the test. But it doesn't seem so straight forward to get the test in the first place.
Today alone we tried to call the Paris hospital over 8 times, and no one answered the phone. We are trying to get the Doppler as soon as we can as I am in a wheelchair, can't walk and now my hand and arm are getting worse and I fear I won't be able to get myself into my chair on my own soon. I am losing my faith - and need someone to help me find a way to get this all important appointment which I understand may help me. Is there something I'm missing? A special number? Do I need to go through my very dismissive neuro or GP? What ever advise someone can offer I would be so grateful. I am based in London.
Dear Brian,
Thank You for Your interest in AMEDS.
....
I look forward to hearing from you.
Brian Putman
It starts out as the same form letter I received a few weeks ago but yours contains much more detail. Mine was about 1/5 as long as yours. I haven't heard back from them in a few weeks.
My 'feelers' are out in India, Poland, Frankfurt & 2 in New York. One of them is going to come thru by this summer.
Remember; "The squeaky wheel gets the grease" - keep squeaking people !!!!
Posted: Sat Mar 06, 2010 10:39 pm Post subject: RE DR. ZIVADINOV'S SYDNEY VISIT
HI members the recent visit ofDR. ZIVADINOV' toSYDNEY on the 2nd of MARCH WHO is the neurologist has done the researches of CTEVD/CCSVI STUDIES AT BAFFALO NEURROIMAGING ANALYSIS CENTER. was arranged to give precentations on UB RESERRCH WORKS to MOST OF THE SYDNEY neurologists including my neuro.I have had a meeting with my neuro. very next day. 3rd of march My neruo told me that he and his friends DRS. were very disappointed on the infomation they were told by DR.ZIVADINOV' from his UB studies none of them supporting DR.ZAMBONI'S THORIES OR his LIBRATION PROCEDURE treatment can hep to treat CCSVI ON M.S His staement was complely oppasite to his first results press release which is in UB REPORTER dated march 4th. Which say that promising results in M.S study.But when he came to SYDNEY gave different picture on DR.ZAMBONI'S WORKS AND HIS treatment.Now my neruo say that he and his frinds neurologitsts were not supporting DR.ZI. And his treatment for CCSVI ON M.S I had my doppler examnination by DR.PAUL THIBULT at his newcastle clinic on the 24th march and he found i have very bad venous stenosis on my right internel jugular vain.his next step is he is arranging to go to a experienced interventional radiologist at St VINCENT'S hospital to have my venography first subsequntly for a possible LIBRATION PROCEDURE in the same day.But my neuro now after the meeting with DR.ZIVADINOV SAYS that any MRV OR DOPPLER examinations will not give clear picture.SO DR. ZAMBONI'S treatment do not work. asked me to not to go for any examination or any opration.If i want he can send me to RPA hospital's interventional radiologist his name is DR. PARKER;lwho is my neruro's friend for a venography first then after six month time he wants me to go for oprations if i want.So my wife not willing to send me for any opration now. ALL US BACK WERE WE STARTED.
REGARDS
SEEVA :roll:
Posted: Sun Mar 07, 2010 4:57 am Post subject: CCSVI
Seeva,
CCSVI has been established as a medical condition which is seperate to MS. All these arguments and controversies are about the connection between MS and CCSVI.
If your reports show that you have CCSVI, as suugested by Dr Theabault go and see an intervantional radiologist. Do not talk about MS. Just say you have CCSVI and ask him to fix the problem. He may even do it under Medicare.
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