posted
What is it?
Posts: 8981 | From Illinois | Registered: May 2006
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Cass A
Frequent Contributor (1K+ posts)
Member # 11134
posted
I have been taking it for several months now, on the advice of a friend of mine with neurologic issues, as I have neurologic problems from Lyme.
I haven't noticed anything spectacular.
I'm about to go off it to see if that makes a negative change.
Will report back with what happens......
Cass A
Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007
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I actually drafted a much longer post then had second thoughts about posting it publically, as explained in my original much longer drafted -but not posted-response.
Do people communicate at all by phone on this site, phone numbers provided through private posts, or is that against the rules or ill advised?
I have information to report but its complex and difficult to report on in a post.......
But my short answer is "the jury is still out".
Thank you as always,
still Winning
Posts: 55 | From Maryland | Registered: Aug 2014
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Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
posted
Quick search on Lymenet, came up with this;
posted
Bartenderbonnie, Thank you for your post, but there really wasn't much information on how people really fared on the product.
For me, I am still assessing.
Thank you again.
And you and everyone else should have a Happy New Year!
Posts: 55 | From Maryland | Registered: Aug 2014
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Cass A
Frequent Contributor (1K+ posts)
Member # 11134
posted
Well, here's my take on ASEA.
I took it on the advice of a friend who has Parkinson's Disease and felt it had really helped him.
I did the daily dose, not the super-dose, for four months and didn't notice much change.
So, I stopped it while I still had a week's supply in case there was a big drop in functioning. There wasn't.
My LLMD (who treats a lot of different types of conditions) in the San Fernando Valley stocks ASEA water and promotes it. However, he had never brought it up to me. With me, he's mainly focused on KILLING THE BUGS!! I asked him about it, and he was pretty neutral, said it had some overall benefit. He did not tell me to start it or promote it to me personally in any way.
I've been treating Lyme and co-infections specifically since 2005. This MD got me the biggest change for the better in 2013-2015.
From this, I would say that it's not something to spend your resources on----it's not cheap!!! His price came out to about $200 per month.
Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007
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