OK but I can see this is a no win-win situation. It would be easier if you just post my email or move my post off the other thread to here. I really thought I was talking about
same think as Willy.? But I am not the best at staying on the issue. So here goes....
Okay, Heather's Dad, yes I get it that you are not advertising and making any money off of your sharing and I LOVE LOVE LOVE hearing about
your MAJOR break through with your daughter.
I appreciate all the cures I have heard of going on everywhere.
I have heard from people who had no success at Hansa but do not want to sound negative on the site so they don't post. ( ????)
I do know that Envita has it's own rewards program going on for referrals.
I also know that they HELP people but every case is individual and some people are not going to have the same experience that other's had and the same goes for Hansa. These are both cash money places.
I feel the people on antibiotic treatment may be getting psychically rail-roaded off their own treatment and doubting it because they hear of the miracle people from Hansa that ddin't go through the torture of the antibiotic treatment.
I also know that people do get well with good LLMD's on antibiotics. We just don't hear much about
it here.
I see how many hundreds of people are reading our posts that don't post in themselves. There are a lot of people in trouble out there. We have a huge responsibility with what and how we share on lyme. This is way more than just us guys chatting here.
LLMD's have their own websites now .
No one is hiding in the closet about
treating anymore if they feel they know what they are doing and have the courage and conviction to find the answers and treat people to completion.
I'm sorry to hear that an LLMD got bashed on the forum. Do you know I never knew there was "an owner" of this forum ? I thought this was like a public health type thing. not that it was owned by the government but I am so dumbed down that it never occurred to me that there was an owner here who could get sued.
I'm thinking know this is a brilliant web site and seeing all the sponsor's.. Is that Verizon I see on the right of the screeen? wow! I am really in the clouds. I never realized this was like a business. anyone who was smart enought to put this together I am sure is incorporated and protected "personally" and is committed to
doing what ever it takes to support the people who are clicking in here everyday. This is the USA. we do everything to make money and that's how lawyers make all their money. It's all part of it.
Isn't this why we have moderators ??? To keep people from bashing. The EDITING process ???
I think this forum could support the people on antibiotic treatment better if we could get off this "we have to protect out LLMD's" thing and share more about
who is getting the good results with which LLMD's.
Here is the thing that is really tricky. We can say we had sucess with someoone like Hansa and not get sued but can we say we didn't and spent thousands of $$? can we? i don't know.
I'm all talked out and this tread is all over the place already and I am the only one who posted so far. !!!
lots of love to all of you
bucci
I feel we are making the LLMD's look like they are these doctors are hiding and it kind of adds to the war that we are fighting here in the first place which is the acknowledgement that this is a disease or really plague that is real and not made up. We are trying more than anything to end that whole debate. It is one of the big reasons why the government get's to still hide on the whole issue.
Post Edited (bucci) : 12/29/2010 3:39:41 AM (GMT-7)