HELP ME!!!

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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annad
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Post by annad »

According to google translate annased24, says:

Would you like fries with that?
lol
Sorry couldn't resist.

No really, google says:

exactly ... and I spared no expense ....
I have my life at any price!
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silverbirch
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Post by silverbirch »

Annad

Thanks for translation - however I did laugh at annased24 Italian reply even prior to knowing what it really meant.

I need CCSVI procedure sooner that I had thought.....
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annased24
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Post by annased24 »

if all goes as I will go to a mega party but crisps!
:lol:
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AnnaP
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Post by AnnaP »

Hi Anna

I, too had an appointment for Poland for March 2011 with Dr. Simka.
I heard about Dr.Grozdinski (grozdinski@mail.bg) from Bulgaria. I tried my luck with him for an earlier appointment, sent him an email in Jan. and got an appointment for June 2010.
I think/know he is the real deal. I was skeptical about Bulgaria, luckily I have friends who live in Sofia Bulgaria, did research on him for me, Dr. G. comes highly recommened for this procedure and the procedure will be done in a very good state-of-the-art Japonaise Hospital(Takuda)

Good luck to him.
Anna
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darcie
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Post by darcie »

While we are all waiting for CCSVI treatment...

Anyone interested in an alternative method for keeping MS in remission,
I have developed mine over the past 25 plus years. Involves several key supplements, particular diet & regular exercise (stationary bike if you have one.) This plan has kept me in remission for 10yrs with some very good symptom improvements. At my lowest point I was bedridden for 4yrs & now I can walk with a cane & even do stairs.

My total drug cost for RRMS the way I do it is only about $20.00 per month. Nutrients would be substantially more. I have a testimonial from my physio-therapist & am thinking about getting a video online.

Details about what I have been doing will be found @ myMSaternative FIX.
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