CCSVI in Poland… fail

¸.•´ please SUBSCRIBE to my channel. thanks. mike `*.¸ A reflection on my visit to , , to have the . The trip was a disappointment, disappointed may be the wrong word, I feel ‘let down’ by the clinic and I would now be recommending alternative locations for the treatment such as Bulgaria, until the time comes that it is is available in every country. To sum up, yes I do have , but I did not have the treatment done.

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25 pensieri su “CCSVI in Poland… fail

  1. how are you now
    should i go for ccsvi?
    it’s so sad to having ms
    you are pessimistic about it is it?

  2. @mikeseesblueskies I agree with you, it’s a bit of a wrought. Actually the real travesty is that the very industries that promotes the lifestyle that causes arterial blockages, is subsidized by our hard earned money(tax), & yet the victims of their folly aren’t.

    Those who should be bearing the brunt of the expenses of, not only MS, but coronary heart disease, diabetes, osteoporosis, etc.. are the meat, dairy & fast food companies.

    Our tax dollars should subsidize, if anything, fruits & veg.

  3. Dr. Simka knew I had MS – but in fact he did NOT find clear evidence of CCSVI when he used his doppler; he had to check the results of my MRV to find enough evidence to proceed with the procedure. Wait? Maybe – but if the CCSVI theory is correct, all the time you’re waiting, your central nervous system is being damaged.

  4. Call CCSVI Clinic; (404)461-9560 to schedule your screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Yes, get screened within the US. No waiting….find out more at ccsviclinic.ca

  5. Good points you’re making here..

    I wanted to do the dopler and eventually undertake the liberation proceddure. So, when they doplered me, it was estimated 60-70 % narrowing of both vascular veins. Was told that 100 PERCENT !!! of the ms patients have it.

    First thing that crossed my mind was that the percentage I knew of was way less than that. The second was – by pressing my neck by the dopler itself couldn’t they narrow the veins? And after balooned, for how long the veins would stay widened?

  6. hey astrospliff. u think like me i feel. i really dont know which way is up with this whole ccsvi thing.. was outspoken promotor of it, but ive gone quiet on it recently…

  7. @npiltan
    hi sorry i only see your message now…
    well i guess the first step is to get scanned to see if you have it. so get scanned and then take it from there ;)

  8. @duncanthornton
    but of course, while you wait, damage is being done… IF damage IS being done

  9. @neocons1345
    hi. get me on facebook mike deegan.
    we will watch with interest how ccsvi plays out

  10. @chontos77
    medical tourism has the happy advantage for those practicing it of having a large price tag. if you have ms, the hospital should automatically scan for ccsvi, and if you have it,should be treated as a matter of course. period. . mike deegan on facebook

  11. @mikeseesblueskies yes they are getting on board. that release you talk about is the ONLY piece of paper worth anything so far re ccsvi

  12. @MrLeooreo
    i do agree when you say its not autoimmune. and for some, it will be vascular

  13. @collinchina
    hi. tell me when you come to dublin next time. mike deegan on facebook

  14. Thank you for sharing. I am thinking about this surgery since I’ve heard about it… And I am on the list in Poland. Sometime next year. It will cost me around 10 000 Can. dollars. My family and friends are planning fundraisers for me… I keep reading all the experiences and I know already that this is not a one time thing and… I won’t have another 10 000 to fly there again. And I have lots of doubts and lots of excitement and hope… all at the same time… You gave me more to think about.

  15. Hi ! As I’m English is not my mother langage it’s not easy for me to understand easily your story.
    Why are you disappointed ? Because of the price ? Or the liberation procedure ?
    Do you have good results with it ?
    thanks, Chrystèle, From France

  16. @catimini34
    yes disappointed because of unfair price. all others in waiting room were paying the ‘local’ price. was doubled for me..

  17. @mikeseesblueskies but Are you satisfied about the results of the liberation procedure ?

  18. We were the cash cows for the neuro’s and NOW? hmmm money…greed, the nature of the beast!! all the best my friend x

  19. Thanks so much Mike for sharing your experience. My husband has been diagnosed with MS within the last year and he’s found it very hard to deal with. It’s nice to hear such a positive approach to the condition. You’re like a breath of fresh air :0)

  20. Mike, you spat the dummy when you got there and they retold you the price.
    They’ve helped thousands and have given people back their lives!!
    Why didn’t you just get to the EHC in the UK? It makes me laugh that you’re selling your BS story and backing up a place who you’ve convinced to either give you $ or the procedure.
    What’ll they do when they realise that you’ve been a prick to many and YOUR face selling their brand will only turn people off? lol

  21. @sunshine071974 sweety, he’s not this nice – watch him on Facebook..but whatever you do, DON’T disagree with him!! lol
    He’s a tad too negative in all honesty – this happy (?), positive (?), ‘inspiring’ thing is BS!!
    Most of us have defriended or blocked him – he speaks of money being the problem? Well, he’s only in this to get his head on the news and be THE big male name of CCSVI – it’s pathetic.
    Just remember that you should speak2 a lot of people&get your info from more people too! :)

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