Journey for MS--off to Poland, **UPDATE** post #22

[quasar4legs]

Koala cuddles from 'down under' and I hope that all goes well during your journey.

Would also love to hear an update when you return.

 

[crazee4mickey]

We just returned from Poland 3 days ago and I was extremely shocked to see what an amazingly beautiful country it is and with such a tragic history.

I am posting to update more on hte MS liberation treatment as I literally witnessed miracles while we were there!

As for my brother, his MS was diagnosed 4.5 years ago and his symptoms are basically leg pain,fatigue. low heat tolerance, brain fog and bladder urgency. He had the treatment with angioplasty on one side.

Within 2 days after we were walking at least 5 miles a day in 34 C heat---this is the most he has walked since before he was diagnosed! No leg pain, fatigue and he didn't have the bladder urgency at all!

We met over 20 people who were there for the treatment and each and every one of them were seeing improvements in muscle strength, returning of feeling in areas which had been numb for years, brain fog, etc.!

I could go on and on about what this treatment has done for the people we met but my newest concern is why our governments are "dragging their heels" on a procedure which is routinely done for heart/stroke patients. Why should people suffering with MS be forced totravel thousands of miles to obtain a treatment which is not a cure but does better than life to any degree at all?

 

[cats mom]

Thanks for the update. I'm so glad the procedure resulted in improvements for your brother!

I've been surprised at the lack of progress in the USA and Canada too; although I don't think it helped that the word cure was thrown around a bit cavalierly early on.

Hopefully now that many of the most vocal proponents of CCSVI have changed their approach to it being just one piece of the MS puzzle, not the answer, it will help.

It's been my experience that neurologists don't like being told they're wrong, especially when it's patients doing the telling. If CCSVI does play a major role in MS, it certainly calls into question some long standing, generally accepted "truths" in their world.

Thanks again for updating us, and give my best to your brother.

 

[bumbershoot]

Congratulations!


The AMA is a powerful force, they like to keep "cures" under their wing, and fight tooth and nail to make sure that things that help people heal, but can't be done by them, don't happen. DH healed a brain tumor (not malignant, but growing so fast he was "given" 6 months by the diagnosing MDs if he didn't have THEIR treatment) with diet (even more strict than macrobiotic), juicing, enzymes, and hyperbaric chamber treatments. He paid it ALL out of pocket, and no one that he saw was allowed to officially know why he was there, as "cancer" can only be treated by oncologists, not anyone else. You'll noticed that there are more and more cancer care places that include the "alternative" therapies, along with pure eating, etc etc, and they have good cure/healing rates...but they don't allow you to just skip the western medicine. Gotta have it all, can't just go with the "alternatives" there.

Heck, the AMA continues to pay money to the chiropractic schools after losing a huge antitrust case where it was proven that the AMA as an entity was blackballing MDs who "allowed" their patients to see DCs... The AMA made DOs in America nothing more than MDs who *might* think about doing osseous manipulations.... They are powerful, and won't let things they don't understand into the realm of "cure" here in America. They just dno't like "healing" from within.


I have no idea what your brother had done (though I was rooting for him!), I'm just responding to your wondering why America doesn't allow the procedure....