3 weeks since Liberated feeling GREAT but a couple of ?'s

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

3 weeks since Liberated feeling GREAT but a couple of ?'s

Postby BecSayz » Thu Jul 28, 2011 10:29 am

The last three weeks have been surreal! :D Here are a few things that I have noticed since my Liberation Treatment:
· My balance has improved
· The vertigo is gone
· My speech is clearer and can recall words better
· My drop foot has gotten better
· My right leg is working a lot better – I do not have to lift it as much.
· My physiotherapist says there isn’t as much tone in my foot
· My toes still curl under but it isn’t as painful
· My body still gets overwhelmed in the heat but is 100% better then it was especially considering the humidity
· I haven’t been napping nearly as much
· My body is working better overall; I can get into the shower as long as I do it without thinking about the process – I guess my brain isn’t sending the messages properly yet. Involuntary movement is still a lot than voluntary.

I have two questions:
1.I want to get into shape – I have a recumbent bike. I was on it for 5 mins, burned 50 cal and my heart rate was max 159. After I got off the bike I got a really bad headache. Is this because of the procedure? What can I do to prevent that from happening? I am planning on doing 5 mins a day until it becomes a bit easier.
2. At night my right foot has been driving my husband crazy. I asked my physiotherapist to help me explain it. My foot goes into Dorsi flexion it beats like it’s in Clonuses. It is completely involuntary and I sleep through it. In the morning my muscles feel like they have been working out all night. I am also kicking my husband a lot!

Overall this has been an awesome experience! I really never thought this much would happen! None of this is placebo either because I was VERY cautious at the beginning on believing what was going on.
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Postby PointsNorth » Thu Jul 28, 2011 11:22 am

Hi Bec,

Welcome to our forum! Nice to hear of your improvements! :)

I hear from doctors/physios that pool excercises are worth trying. I haven't gotten around to it :oops: so it's simply another case of "do as I say, not as I do".

Not able to do as much on the bike as I used to but I still enjoy the weights 2-3 times/wk for 30 min.

Maybe the kicking of your husband is unrelated to your MS ? :wink:

Please post on our Tracking thread.

Best, PN
Albany 2010. Brooklyn 2011
Hayes inspired Calcitriol+D3 2013-2014
Coimbra Protocol 2014-16
DrG B12 Transdermal Spray 2014-16
Progesterone 2015-16
Low-Dose Immunotherapy 2015-16
My Current Regimen http://www.thisisms.com/forum/regimens-f22/topic25634.html
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Postby Cece » Thu Jul 28, 2011 1:05 pm

BecSayz, that's quite a list, congrats!!

You might ask a doctor about the exercise headache. All I can think of is to go at a lower intensity.

For the foot, what about changing which sides of the bed you each sleep on, so the right foot wouldn't be near him to kick him?
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