All is quiet in the Land of Stanford

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

All is quiet in the Land of Stanford

Postby ndwannabe » Wed Jan 06, 2010 8:45 am

So, I left the voice-mail on one of the phones I found for Dr Dake’s office on Monday.

Yesterday I found another phone # on the Internet and left a voice mail there

Also sent an e-mail to the Dr. Dakes’ e-mail address (yesterday as well)
I have not heard anything back.

I know I am probably being impatient, but for those of you who went through Dr Dake, how long did it take you to get to talk to a live person, even the receptionist?
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Postby cheerleader » Wed Jan 06, 2010 8:58 am

Mark just posted this info two days ago....
for new visitors to the site, welcome....but please just search the term (like Stanford) you're looking for, and all the pertinent posts will come up.



Click on this link for information of Stanford:
http://www.thisisms.com/ftopict-9589.html

cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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Postby ndwannabe » Wed Jan 06, 2010 9:33 am

Thank you for your reply.

I understand this and I did the due searching.

I got the contact information from the posts, I got the testimonies from the posts, however my simple question was - how long did it take for people to get a response?
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Postby SandyK » Wed Jan 06, 2010 5:02 pm

I received a response within a day, but since it has changed at Stanford to trial mode calls aren't being returned.
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Postby ndwannabe » Mon Mar 22, 2010 9:16 pm

Belated "thank you" to you Sandi.

Yes, I got the same response - "Trial only" :?
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