Cost of Envita Treatment

I believe if you do a search, there are several posts by Martha's Vineyard discussing the costs.

The first person I spoke to at Envita quoted me approximately $18,000. The second person quoted $2,500-$3,800 per week. If money was not an issue, I'd be on the next plane to AZ. lol They don't accept insurance, as most llmd's don't, but I was told depending on coverage some costs are usually covered. I'm assuming expenses like having the port inserted, certain meds, etc. would be covered the same way it is when someone is being treated by a llmd in private practice.

I went back in Oct of 08. I did not pay for my treatment. And the treatment has not remained the same.
Plus everyone has different co -infections and not one thing works for all.
But I think that it is ab out 3,500 a week now.
but that is a ball park.
When I went I told them that I only had lyme.
But later they found bart too.
So.....
Again.....I was out of my mind when I got there.
I saw others with lyme who were so much better off than me, and even able to work and drive. I could not do much at all.
Some people seem to be under the impression that I am rich. Let me just tell you that I lost my job 5 years ago...my homes and my kids and my mind.
And when I got out of Envita I cannot tell you how much stuff I had to deal with. Coming out of a coma...my phone was off and had been off for two years....
My yard men had not been paid in over a year...my plates on my car were over two years expired...
And my mortages was was behind.
I did not have any support from parents or family while getting my treatment. My kids were very effected and one dropped out of school.
My dog toto died in dec. who also sufferd from lyme..so boo hoo....it has not been easy for me either.
And moreover I could not lean on three of my best friends because two of them had brain cancer and died during my treatment and my best friend in the whole world who died last may...well he was worse of that me and I was giving him money so he could get teh med.s he needed of his pain...
So....I am no victum I am a surviver....lol...or so my therapist tells me....:>)

Oh please give them Lyme, give them pain in their neck and shoulders, give them swollen painfull knees, give them confusion such that they cannot remember family members names, tell them nothing is wrong with them, tell them NOTHING is wrong.

Thanks Everyone ! After four years on ABX and horrible relapse trying to explore every option !

Is it really true then that there has only been one person we know of that
has gone there with a good story..

How many people do you think have gone there that have Lyme?

I wonder? I think I will give them a call..

Keep hope. Look at my previous post on this post for the info I got! You can e-mail me if you like! And

Dowa, There is no cure for Lyme from any source but if you can get your immune system to take over it may be worth it for some!