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This will be interesting cause I just wore that thing overnight. Im waiting for results

Im gonna wait, even though I have felt my m.s. progressing its just been fatigue and nothing else yet. I think if I was having major issues I would go ahead with it. Thanks to everyone here....Brian

Im gonna wait a little longer i think, my MRV was from the head up and showed 1 cranial vein pinched. that was enough evidence for him to proceed. Just a tough situation, dont want to wait till its to late.

It is in Fresno Ca. and yes insurance is gonna pay. I talked to a localIR here who is gonna do it for me. Just getting cold feet, I think im gonna wait.

My appt for venogram ccsvi is at the end of the month. Im getting cold feet regarding restenosis. why get the surgery if you are more than likely going to restenose after a year? FYI im not really disabled yet soo im having trouble convincing my wife. Ugh Brian

I need help with this,
Has anyone with an HMO succesfully gone out of network and had insurance cover the cost? This is the position I am in

Calm down and relax.....im 35 now and have had it since my early 20's. I am working full time and have had the exact fear that you are talking about. You are young and have your whole life ahead of you, just take it one day at a time. You will learn to adjust as things happen and you will adapt. Ada...

Well it seems that the Tysabri is not slowing down this damn disease, Ive only had 2 infusions but i am progressing. I have to talk with neuro next week to discuss further treatments. should i stick this out on tysabri or look into something different? Oh I have had 2 mris in the last few months wit...

Well had #2 last week and I feel like I am finally stabilizing! knock on wood....LOL I still have some cog fog but not like a few weeks ago, i think that is just be the MS and nothing more. I hope this only gets better...

well I have a mri scheduled for wed. and this should give us some info. Im tired of the cog fog, but this weekend i felt a little better maybe cause im getting used to it. this disease is strange and i will go with my gut feeling to give it at least 3 doses, but my neuro may say no more. all i know ...

Had my first dose 2 weeks ago and I am feeling out of my skin looking in, its horrible and my neuro thinks its stress related since it started a few days ago. we did a blood test and everything was normal, so what now is something that should pass its awfull!

gees these are the same symptoms I am having, actually i am awaiting a call from my neuro. on the results of a blood test i took yesterday. I am having SEVERE brain fog in which it is interfering big time. Just had my first infusion 2 wks ago.

I need some imput from you all regarding this study. Would you do it or not? Im really considering taking the next step in the review process just kinda having second thoughts...

jimmylegs I think i am going to get the zinc tested..it definately cant hurt right?lol

It just seems that most people that have m.s. eye probs have double vision or some vision loss. I have not had that (yet)lol and hopefully i wont, my main issue now is the ability to look someone in the eye and have a conversation with them. If they are talking to fast i cant keep up and i need them...