6 months post CCSVI treatment shout out

Just me finally getting around to a post treatment video – I forgot to mention a couple of other benefits I found post treatment and will try and get another video up here with those.

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7 pensieri su “6 months post CCSVI treatment shout out

  1. Thanks Sarah, I’d been wondering how you were going. Interesting about what you say about the azygos. You are right – I had a doppler last week (showed restenosis btw) but the sonographer did say that the venogram is still the most accurate measure. I agree with what you say, if you under-promise yourself it is better to be surprised than disappointed. Yes – may the research give us more answers to our more questions. Yay to having no relapses – that is fantastic. Happy Chrissy :o )

  2. No relapses and though I did 2 vids I forgot to mention at least one lasting benefit!!! Dang it all LOL. Before we went for my treatment I had to call on my hubby now and again to lift me out of the tub – NOT ONCE SINCE! Also I can take warmer and longer baths AHHHHH

    There’s a lot we don’t understand yet, but I don’t think there can be any denial that better blood flow is good!

    Cheers and I wish ya a very merry Christmas =o)

  3. Also I’m mad as hell that there are doctors who treat this as garbage when if you look up other vascular illnesses voila – a list of MS symptoms right before your eyes!

    Do they think they are making those things up? DO they think that these people having their symptoms improve with vascular treatment is a joke?…

    Anywhoozles I’ve done my post vids for now *pats self on back* hehe

  4. Glad to hear about your improvements, and I hope that you continue improving. Sounds like you have access to good vascular treatment. :)

  5. Good video, I agree with your quiet attitude of not getting over excited & expecting too much so soon.
    Keep well.

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