treatment centers

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Veteran Member

Date Joined May 2006
Total Posts : 1477
   Posted 2/10/2010 11:59 AM (GMT -7)   
How can we do a focused survey or thread on each of these places so everyone can see he options more in line .
and each place we get to only write about how it worked for us .
hep c , lyme
Dad has lyme

Post Edited (bucci) : 2/13/2010 11:25:24 AM (GMT-7)

Martha's Vineyard
Veteran Member

Date Joined Jul 2008
Total Posts : 1119
   Posted 2/11/2010 7:31 AM (GMT -7)   
Yes you are
Many people on this site have been healed by going to hansa in Kansas. And the funny thing is this. Most of the people who do get better. Do not come back to the site. Many other people on this site have gone to Envita and they too, have moved on. They are not on her complaining about being well.

And there is one women who did iv with tons of abx and she posted her one year of good health too.
So diff. things have worked for different people. That is for sure. It is up to people to see what they can or cannot do. It is just most important to let the new people know what their options are out there. And there are many.
There are a couple of people who are in this forum who live in AZ. And if someone asks for them, they may respond and help. They know the whole routine out there and DR.

There is nothing illegal about trying other treatments. And nothing wrong about posting whatever works for you.
Our system is not big on alternative medicine or berbs. There is no big money in not taking pills for everything. I guess.
But people all have a opinion on what has and what has not worked for them. And we have freedom of speach...still...don't we? Lol
Our family all got lyme in 2004. It has been a long battle. But all is well now with my children. Feb 8 TH of 2009 is when I left Envita. And I am celebrating a year of perfect health.

Martha's Vineyard
Veteran Member

Date Joined Jul 2008
Total Posts : 1119
   Posted 2/11/2010 9:58 PM (GMT -7)   
That is not true. They do not take medicare for the treatment of lyme disease.
It is against the law. 
I was there for almost 5 mos. And I know the protical and all of the people there very well. 
These people and Dr.s are all very dear to me and what they are doing is saving lifes.
The Enivta protical is alternative medicine and it is not covered by medicare or insurance. That is a fact.
Write to me directly so that we can discuss this one on one....
I am not pleased with the stuff that you are reporting. 

Post Edited By Moderator (1bitten2xshy) : 2/12/2010 6:03:48 AM (GMT-7)

Martha's Vineyard
Veteran Member

Date Joined Jul 2008
Total Posts : 1119
   Posted 2/11/2010 10:09 PM (GMT -7)   
I can talk about Envita's treatment all day long. And I can talk about the Dr.s that treated me there all day long. It is not a problem 
Envita's treatment is alterntaive medicine. And it is not the New Englands Journals of Medicine's suggested treatment. Or whatever.
And the insurance companies follow their guildlines if you will. And so does most of the rest of the world for that matter.
But, if one chooses to do alternative that is fine. It is going to have to come out of their own pocket.

The Dr.s that are not being mentioned on line and on post are Dr.s who are mostly LLMD's. A new term.
And they are trying to save lifes. Most have good intentions, I hope. But some are not following the NE Journal of med.'s rules for treatment. And if a Dr. chooses to do his own thing then he can have his liscense taken away.
So, to protect some of the Dr.s out there who are just doing something as bad as giving a man with lyme who got it yesterday. And who has a bulls eye and who is sick as hell, and who has a blood test saying that he is not sick....then the Dr. can get in trouble for giving the guy 30-60 days of amoxy with no blood test to prove that he has it.And plus they are treating beyond the two week limit.
BS...yes all of it. So....yes.
And there are also some DR.s out there who deserve to be hunted down. Because the are preying on the sick and in fact making huge amounts of money off of these people, and in fact doing them more harm.
So, everyone out there saying he or she is a LLMD is no different that all of these Dr.s that all want to do Botox. Money.

Post Edited By Moderator (1bitten2xshy) : 2/12/2010 5:54:30 AM (GMT-7)

Veteran Member

Date Joined Jun 2007
Total Posts : 849
   Posted 2/12/2010 6:05 AM (GMT -7)   
NE Journal of Medicine is NOT the guidlines any LLMD follows, whether they are pro or con for lyme treatment.

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