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Follow-up from Grozdinski

Recently received a new email from the group in Bulgaria who are doing the treatment.

There isn’t terribly much new other then the inclusion of the location: Tokuda hospital, Sofia, Bulgaria

You have expressed an interest in liberation procedures, that our team held in Sofia – Bulgaria.

Until now we have studied over 40 patients with MS and is found in most CCSVI, which was treated with dilation or stent.
Each of our team physicians diagnosed and treated annually with thousands of cardiovascular disease and for us not a problem diagnosis and treatment of CCSVI.

If you are interested in undergoing treatment in Sofia in agreement with the above mentioned requirements please e-mail to me your request, including your names and address, so that we can provide you with the date for hospitalization and additional detailed information.

You have been included in the waiting list to undergo diagnostics and treatment at our Center for CCSVI in Tokuda hospital, Sofia, Bulgaria (More information can be obtained on the Internet – Tokuda hospital Sofia) In March 2010 you will be informed about the date for your hospitalization and further details. If it is possible to include you at an earlier date you will be duly notified.

Prof. Grozdinski

Chairman of the Bulgarian National Phlebology Society

Center for diagnosis and treatment of CCSVI

е-mail: Grozdinski@mail.bg

Previous posts:
http://liberation-treatment.com/treatment-bulgaria
http://liberation-treatment.com/letter-prof-grozdinski

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February 23rd, 2010
  • Nina karapetian
    my name isNina der Karapetian, I was diagnosed in 2005 with relapsing/remitting M.S but I think it has moved on to secodary or primary M.S. I live in england. My address is 9 Gloucester Terrace, Southsea, Portsmouth, Hampshire. I am very interested in having the liberation proceure with you, can you help?
  • debbie
    i requested a reference for a scan at woodbridge doctors referal only.i had to twist his arm because he doesn't know how? i told him its our only hope even if it relieves one sytom its good enough for me.its all we have
  • J Link
    Okay, okay, enough! Do we know why re-opening the veins would in fact, cause a lessening of the symptoms for MS. Can anybody point to or identify a success story, wherein somebody with MS underwent the CCSVI operation and is now no longer suffering from fatique, drop-foot, walking gait,dizziness, memory loss, spastiscity, etc, etc. Somebody help me out here. Do we have any hard proof?
  • angie from montreal
    too much proof out there - try facebook, you will be there fore days reading - good luck
  • Sibling of 4 with MS
    Google CTV or W-5. They have links to programs that have aired on television showing patients who have had the liberation procedure. The results are very exciting and proof that this needs to be available to all people with MS.
  • That's EXACTLY the reason why, Ashley. Because we now know MS isn't even a disease, it's blocked veins due to them being twisted, pinched,whatever. A 'condition'. That's why there's no blood test to detect it, no MS 'gene', no MS 'cell'. But the drug companies would lose billions if they accepted that the Liberation Treatment works. Which it does. Pure greed is why they want to block it.
  • joe
    Ashley you are right about that.
  • ashley
    I think the reason why were not getting help is cause the drug companies are making way to much money off people that somehow they are stopping us from getting the cure
  • Cayce
    Hello. I don't have MS. My Best Friend's Cousin-in-Law William Darnell was diagnosed with MS back in the 90s before his Wedding Night. My cousin Lynn Perkinson was diagnosed with MS when her 6 year old daughter Chloe was 6 weeks old. The Liberation Treatment sounds perfect for Lynn and William. Is it safe? Has anyone died during surgery in America? Lynn's taken a turn for the worst. She had to have some minor Surgery last week to put a Baclofen Pump in. Lynn's leg looks different. Lynn's getting horrible Headaches and she's so depressed that she said that she's ready to die. Lynn and William can't wait anymore. They need The Liberation Treatment now and it has to be available in North Carolina and South Carolina right now this year before it's too late. Please.
  • kevin
    I know from know the presenting fatores I've had RRMS for at least 34 years. I think some chace is better than nothing. everyone must hound their GP's to take this seriously, Good luck all of you guys
  • Dale Woolsey
    I was diagnosed with PPPMS in 1985, worked until 2005 & have been confined to wheelchair for mobility since July 2009 CCSVI & Liberation treatment are presently the best hope for me.
    Dale
  • Pedro Garcia
    I was diagnosed with MS in 1981. CCSVI sounds very promising. Like many others, Ill be following this very closely. MAY GOD BE WITH US ALL.
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