July 4th/ 2014
Continue to be Attack free I have tiring days and must be careful not to push
myself to much. But the treatment did give me a quality of life I have not had in a long time. I am thankful to continue living
a good life with my family and now grandkids. I was sliding down hill fast before treatment and the attacks were not fun to
deal with. I highly recommend anyone with MS to try this treatment. We still need a cure but we also need people to recognise
Liberation does help many of us.
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April
4th 2013 Update
Still attack free since CCSVI treatment. No body said this was a cure and I still have issues but nothing like
before. We are so close to finding a cure for MS if we could get everyone to work in the right direction. Blood flow is a
huge part of it and that is just a fact after the thousands of treated MSers like myself have proven. I am so thankful to
all who helped me and Dr. Zamboni.
In no way is the fight over all MSers should have availability to treatment and funds raised should go toward
serious research. As an MSer not having the attacks I had alone is a miracle.
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November 3rd 2012 ..... Update.
Tracey has been attack free since the Liberation treatment. Which will be I yr and ten months as of the 13th
of this Month. We went to Barrie three times since to make sure the blood flow was still fine and it is.
Nobody is saying CCSVI is a cure we most certainly are not. But I can say and we have hundreds of people to attest
to this. I say it is a God send... for such a simple fix the quality of life my wife lives post CCSVI is amazing. I was slowly
watching her fade away on us. Now she has hope for the future and even finnished a two yr college course in nutrition.
The Shame of it all is Canada still is not allowing MSers to have testing or treatment and that is a shame. Yes there are
a couple blind studdies but how does that help anyone. Angeoplasty has been a daily procedure used in Canada to clear blocked
blood flow since 1985. The fact that it helps MSers or anyone should be the issue. Emagine all the other things effected by
improper blood flow.
If you have MS and need to talk about this Tracey is more than willing to talk to anyone about before , during
or after CCSVI and her journey with MS. I am so thankful to all who helped us to help Tracey without every one of you we could
not have made it and who knows maybe my Tracey would just be another complications due to MS death. But no she is alive and
well and happy thanks to every one of you. We as a family are very greatful and we continue to fight for every person who
wants testing and treatment for CCSVI .
Don't let the media and neh sayers scare you from CCSVI its about blood flow and from my own research I have
not heard of anyone with full attacks since treatment. Renarrowing yes but that is another issue of blood flow that can be
fixed.
Thank you and keep fighting everybody........ Blessing from Tracey myself and our family.
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One Year Liberated- January 13th 2012.... A year has gone by and Tracey feels great. She has her quality of life
she dreamed of again. Over the last yr alot has changed at first many major things that were documented. But week by week
month by month more change has happened. As of today the only symptom still effecting Tracey is her one foot has the tingles
now and again. But concidering it was her whole leg and both feet before and the last yr bit by bit that went away to. So
she hopes that last little bit of tingles in her foot that is left will also go away. As her husband I can tell you all that
this treatment does work. My happy healthy wife is back yes she is 98% herself again. Lets not forget she could barely walk,
no longer drove, was in a constant fog as well as constant pain. And the attacks she had where hell for her to go through.
She now has a quality of life she deserves and we owe it all to Dr. Zamboni. You can't put a price on your health yet Canada
will still not recognise the good dr.s work. Many Canadians still go out of the country spending tens of thousands for treatment.
We are happy with Traceys results but we still shake our head at our government. No Canadian MS'er should have to suffer anymore
and until there is change we continue to fight the good fight.
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Update: Friday Nov.18th 2011 - Tracey just got results back from her second testing in Barrie. Ten months post
treatment and the results show she has good bloodflow and all is well. She is doing great to symptoms have returned at all.
Her muscles are back to normal and she has more energy than I ever remember her having in the past. CCSVI treatment does work
and has worked well for my wife Tracey. I highly recomend any MSer to get the treatment you can't put a price on the quality
of life you deserve to live with.
Canada is still not behind us MSers and there are very few places to get tested here too. Barrie is the only
one that follows the Zamboni protocals but the list can be long to get in. We will continue to fight for the rights of all
MSer's in Canada to have equal treatment and be able to be tested as well as treated for CCSVI at home in Canada.
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Update: 9 months since Traceys Liberation treatment. It took some time to build up the atrophied muscles. She
looks great and feels great absolute no comparison to the way she was the day before treatment.
There are still issues as far as how long or far she can push her body. But there are no attacks in nine months
which is amazing and her quality of life is so improved it can only be called an MS Miracle. Every day my wife has had a better
quality of life is proof enough that this works. She spent yrs suffering like many MSers and no governemnt should stop or
not allow MSers to be Liberated. The only issue we have seen with the research we have done that could be negative is
the stints. Current stints are not made for jugular viens. How hard would it be to make stints that do work? Thousands of
MSers have had the CCSVI treatment and all have a better quality of life in various degree's. Most we have known have such
a huge difference in quality of life like my wife Tracey. We keep fighting the good fight for all MSer's.
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Four months tomorrow May 13th that Tracey was Liberated. She is doing amazing the quality of life she has now
doesn't compare to what she was living before treatment. We are so thankful to all who helped us on our journey to Tracey's
Liberation.
Tracey's muscles are stronger from physio twice a week the last four months. Symptoms of MS are gone and no attacks
all miraculous to us. We recomend anyone with MS to look into testing and treatment for CCSVI . Just the quality of life alone
is so worth the journey.
Tracey just walked past me and said " I'm not where I want to be totally yet But I am way better than I was before"
smile.
Just for me to see her smiling and not in pain or suffering ........ thank you God.
So she will continue with physio and being healthy from here on out. Her sight is almost to the point she can
drive again otherwise she feels very good.
Again thank all of you so very much and we will keep you informed of her progress.
In other news our friend Domingo has had treatment and is doing better. AS well as Kim Nickles who I ran into
yesterday . He just returned from treatment in Florida last week and is so happy and full of energy.
The biggest news in MS circles is Montel Williams is going for testing and treatment for CCSVI . He has been
the most public figure in the MS fight and with the results so many MSers are getting even he is going forward now. Way to
go Montel............ Update Montel has since had treatment. With many noticable changes for hims just like many Liberated
MSer's. Rebuilding atrophied muscles and retro of damages from MS takes time. It's almost a yr for Tracey at the time of this
update and she continues to get better. DJ
