Round 2 post

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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Post by zap » Thu Sep 17, 2009 12:46 pm

Hell yeah! That's more like it. :D

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Post by mrhodes40 » Thu Sep 17, 2009 12:48 pm

Lew wow I am so glad for you!! YEAH!! this is going to be different it sounds like that is good news and what a confirmation, last time you felt some better but not as good as hoped....but there was this extra issue wth the valve; how really COOL that you can tell already that has made a difference. Yeah!! I am really happy for you
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you... This is my regimen thread Read my book published by McFarland Health topics

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Post by bestadmom » Thu Sep 17, 2009 3:02 pm

I am sooo happy for you, Lew. You sound terriffic.


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Post by Arcee » Thu Sep 17, 2009 3:16 pm

Lew, just repeating what I said yesterday: I am so psyched for you! Chowing down food, looking good, moving around - -all sounds great. Welcome to HD :D
diagnosed RR in spring '04
1 stent placed in left jugular vein 7/15/09
on and off Copaxone
allergric to interferons and Tysabri

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Post by CNClear » Thu Sep 17, 2009 7:47 pm

Lew...Ditto what everyone has said!! I felt like I breathed a sigh of relief after holding my breath for a few days! I am soo happy for you...I'm trying not to cry...but I am saying thank you prayers!!! (And Lisa (From HS) said to tell you that her whole family is thinking of you!! We are all SO EXCITED for you!!!!

(aka CNClear)
(still waiting to hear back from Alex...fingers crossed)

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Post by prof8 » Thu Sep 17, 2009 8:52 pm

Hi Lew, congrats on the success (and for Dr. Dake too)! I've been following your blog and am very happy for you. It sounds like you have hope back which is wonderful! Take care of yourself.

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Post by whyRwehere » Fri Sep 18, 2009 12:34 am

I am relieved and happy to hear that. Hope Sawdog gets improvement like you. And my husband, too, someday. Amen.

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