The following symptoms of mulitple sclerosis I no longer experience: double, blurry vision, balance disturbance, fatigue, brain fog, activity intolerance, and spasticity. Once I stopped experiencing spasticity, my legs felt loose and limber. It is difficult to go from stiff legs to relaxed legs!! The following symptoms of mulitple sclerosis have been dramatically decreased: Urinary urgency/retention, headaches behind the eyes, inability to concentrate, sleep disturbance, intention tremor, leg weakness. I feel as though my MS has been cured by this procedure. I have the slightest remnants of things that made life more difficult on a daily basis. I understand now that I had less permanent damage to my brain (despite I had a doctor tell me the damage to my cerebellum appears “catastrophic”.) than I once believed. This procedure has cleared inflammation apparently. I also want to convey to the reader that my results are probably not typical. I feel that my reaction to the procedure physiologically is a “best case scenario”. I hope that everyone with MS will get the chance to have the procedure to find out the nature of their MS. Many who thought they could not be helped will, I feel this in my bones. There will also be disappointment from some who see very little. My experience has changed my mind about stents. I now support the use of stenting with severe blockage. It is my belief that many blockages that restenose will eventually need a stent. I also have developed my CCSVI …
Tag: ccsvi, cerebrospinal, chronic, insufficiency, MS, mulitiple, sclerosis, venous
@lennonleekeith
Been a Beatles fan from a boy, although I was born 5 years after they broke up.
Here lately, Radiohead is my weapon of choice.
To be honest with myself, the Beatles were probably the best of all time; however, I relate personally with Radiohead more. They resonate with me on a spiritual level.
Your username is perplexing.. I get the John Lennon and possibly the Keith Richards reference. I do not know if Lee is the frontman for RUSH or Alvin Lee from 10 Years After?
TELL ME
@Alexknobsob
You cannot argue with Amanda’s results.
@Kanny989
YUM YUM
CYBERKISSES!!!!!!!
Thank YOU for your kind words.
Take care,
Mark
@WithCourage2008
My insurance covered it.
It is very expensive. (There is NO WAY I could afford it without insurance. $2,000 is the cost).
The results are phenomenal in my case.
Blessings,
Mark
@52lcr
I will do a 30 day follow up very soon
Tell your hubby that I said, “YOu are very much welcome”
@irishbear76 Crossed lines?
@Alexknobsob
Always do.
Cannot please everyone. And that is F–KED UP!!!
See Thom Yorke’s Black Swan for inspiration.
So great to see you doing so well!
Love watching your videos Mark, your progress is so similar to mine. Also, a musician here too
Drummer.
Stay well,
San
@irishbear76 WOW! You got ur insurance to cover it?? How did you convince them to do it?
@WithCourage2008
NO convincing.
A lady named Maribeth took care of all the insurance nonsense.
I am glad she worked so hard for me.
Mark
@SanSandySandra
Great to have someone else who has shared in an experience with you.
I hope you continue to do well.
blessings and health to you,
Mark
@CTYankeeMS
I thank you.
We are so happy for you …… Pray it goes as well for my wife. Waiting on the call and fundraising still…… all the best DJ
DUDE! I would say, you have no idea how awesome your vid is, but you do. So here’s wha sup, I have MS, it sucks, and I would love out of this thing.
Creator and Hope, Nice.
You have a new sub & friend. Out!
@irishbear76 Great 4 u! That gives me a lot of inspiration!!
What an amazing story. I am so glad and happy for you. Where did you go to get this done? I really want to try this but trying to find a reputable doctor has been overwhelming.
I just found your videos and I am interested in learning about CCSVI. As I am a conspiracy theorist with MS, perhaps you could count me twice!
@WithCourage2008
The person responsible for scheduling took care of the insurance.
Once I had reflux from the Doppler, they really couldn’t say, NO.
@nyc0053
Hve you made any progress?
Peace be with you.
@irishbear76 Thanks for the information, Mark!! Good luck to you!
@irishbear76 No where near dude. Just eating super right, staying relatively active, and keeping as stress free as possible ya. MS is NARLY! I’ve loss the use of both legs at different times, 1 eye for a while, my hands are sought of numb (messed up my piano progress) major bummer. Hey, whatever’s next, can’t say I’m looking forward it ya. Thanks for the Peace. Keep rocking! Seriously, one day this will all be over. Cheers
got surgery yesterday…VERY LIL RESULTS JUST SEEING A VIEN THAT WASN’T FULL, PLUMP UP…thats it dude!
I THINK THERE IS A SIGNIFICANT POTENTIAL FOR SYMPTOM IMPROVEMENT FOR THOSE FOUND TO HAVE CCSVI AND TREATED.
THIS ISSUE IS THE APPLICATION. STANDARD ANGIOPLASTY I THINK WOULD BE FINE TO SEE IF THERE IS AN IMPROVEMENT IN SYMPTOMS. BUT IS NOT DESIGNED TO BE A PERMANENT SOLUTION. PROCEDURE COULD BE DONE AGAIN BUT IT BECOMES MORE COMPLICATED.
THEY NEED TO DEVELOP A STENT SPECIFICALLY FOR THE JUGULAR. I THINK THIS HAS THE POTENTIAL TO OFFER A PERMANENT SOLUTION. DEVELOPING THE TECHNIQUE
& TECHNOLOGY MAY TAKE SEVERAL YRS OR MORE. SO IN THE MEANTIME ANGIOPLASTLY OFFERS A CONFIRMATION AND “HOLIDAY” FOR A MORE PERMANENT POTENTIAL SOLUTION IN THE FUTURE.
BUREAUCRACY UNFORTUNATELY SLOWS DOWN THE PROCESS, SO MUCH EFFORT IS PUT INTO THE POLITICS OF DEFINITION AND VERY LITTLE COLLECTIVE EFFORT INTO DEVELOPING THE TECHNIQUE THAT IS STILL IN ITS INFANCY. FRUSTRATING, OBJECTORS ARE LOOKING TO FAULT IT INSTEAD OF RECOGNISING THE BREAKTHROUGH AND TAKING IT FORWARD.