Going to Envita!

New Topic Post Reply Printable Version
27 posts in this thread.
Viewing Page :
 1  2 
[ << Previous Thread | Next Thread >> ]

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 8/26/2009 2:16 PM (GMT -7)   
Its for sure now. I got my first appointment yesterday and got my testing
and bloodwork done.
I am going to get a port in next week and then start treatment.

Wish Me luck.!

Post Edited (KeepHope) : 9/1/2009 12:30:41 PM (GMT-6)


nefferdun
Veteran Member


Date Joined Feb 2008
Total Posts : 900
   Posted 8/26/2009 5:09 PM (GMT -7)   
I don't know anyone else. I wish you the best of luck. Keep us posted about how you are doing. I hope you come home well and that you can manage your finances to get by until then.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 8/26/2009 5:19 PM (GMT -7)   
I know of a couple people who went...about 3 from this site..but not for me to say.
I spoke on the phone with the man who took his wife.
It was a heart breaking story what he had to do. But not for me to share. He has tried many things to save his sick wife. I think that she has alzthemiers. But I am not a Dr. I think that he was a wondeful and caring husband. But again...not my place to talk about my personel conversations with he and his wife.

It is also not for me to say who else I met at the clinic. Many, but it is for them to share not me. It is a private matter.
Most people sort of get on with thier lives when they get better. That is their right.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 8/26/2009 5:22 PM (GMT -7)   
I am so proud of you girl....I am so sick of you being sick already....hehehe
I enjoy chatting with you..and I know that they will take good care of you there.
I pray that you get the same wonderful results that I got there.
Hey..and don't go and run off when you get all better...lol
I know you better than that, you are a sweetie.
Hurry up and get better so that we can go and trick and treat together...lol

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 8/26/2009 8:20 PM (GMT -7)   
OH Yea.. Of course I will not go anywhere.. I can not imagine after everything
just leaving and not staying around to keep talking and learning and growing.
I know this is a journey and this is a short part of that journey.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 8/27/2009 2:46 AM (GMT -7)   
Good for you!

sickof lyme
Regular Member


Date Joined Aug 2008
Total Posts : 110
   Posted 8/27/2009 7:56 AM (GMT -7)   
Good luck Keephope ,Im sure you will be feeling better in no time at all! When I
told everyone on here I was going,I got some private e-mails telling me they went and did not get better at all,then I asked Envita for anyone that has gotten better from this protocol and the only name they had was Marthasvineyard,soooo I cancelled the day before my appt,and my mom had already bought her plane ticket and did not get a refund! I just chickened out,mostly becuase it is sooo much money and I have a son in school ,I just couldnt take the risk of spending that kind of money and not feel better! But I still think they do help people ,I just wish they would have some testimonies! Please let us know what happens ,there is ALOT of people interested in going! And I still am thinking about if we get a buyer on some land we have for sale! Its a shame people dont come back after getting better!

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/1/2009 11:35 AM (GMT -7)   
I already can see why people who want to or have been to Envita do not come here or any other forums to talk about this subject. IT seems to be the BIG BAD Subject and people want to jump down its throat! I guess its the cost that gets people so upset but I am not sure. Who Knows.

I was going to post about my progress or how it went but I decided I will not be doing it openly. I am sick and tired of the negative people..

Not on this forum, but did you guys know that other forums watch this one and cut and paste and watch over what you say and take your words over to their forum and then pick it apart and make fun of you and ridicule you.!!! Its horrible.

And it seems by those who claim to know better and know it all and more than the rest of us in this world and even God Himself it seems.

If they would just give their opinions or post science to read that would be great. But no, it all has to be personal. They seem to like to be horrible to others..

IM OUT!

Post Edited (KeepHope) : 9/5/2009 12:36:39 PM (GMT-6)


RottenDog
Veteran Member


Date Joined Apr 2009
Total Posts : 1013
   Posted 9/1/2009 11:49 AM (GMT -7)   
i'm sorry you whent thro this on another forum. and if its so ugly there why bother?

i havent seen it in HW so much so i have never gone to another site as i have made friends here and i learn what i need right here.

and i for 1 would love to hear all about your treatment. as i also know what works for one does not mean it will work for me. but its all part of the ugly disease too.

i pray this all works for you, and that your better very soon :)
   RD
 
still looking for answers.
 
Remember that advice is free, its your choice what you do with it.  :)


KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/1/2009 2:04 PM (GMT -7)   
I agree RD. I started here and never had a problem . Some friends had me try a couple other spots and I said Hey> why not? This is one spot (and I found one other) I enjoy and are stress free. I do not like knowing though that whatever I post is copied over and picked apart. I mean it just I guess is a hot topic. Some of the support forums like .ning ones are more private and you can get close to people without it being so public.

So I will be letting people know whats up but maybe I will start a personal blog or do it somewhere I can really feel I can be open and honest and type freely without the mess. I know there is healthy debating but in some arenas it is not healthy at all. I still do appreciate and like to hear about experiences of others and I learn so much from it. I want to give that back to the community from me..

So you will hear from me in some form... not sure what yet...

THANKS For the SUPPORT

And Your so right.. We each can respond so differently and DO respond so differently to different things. No one answer is for a the group and if it was that easy we would not be talking about all the options so much. It is such a tough road.

I wish all the best to each and every one of you..

Post Edited (KeepHope) : 9/5/2009 12:47:33 PM (GMT-6)


3whiteroses
Regular Member


Date Joined Jun 2009
Total Posts : 184
   Posted 9/1/2009 3:48 PM (GMT -7)   
KeepHope

The important thing is you are on the road to recovery. We all have to choose our paths and go in the direction that is best for us. I guess I'm confused that other support groups would ridicule someone else for being a part of a different group. No matter where we post, we are all in this together. Lyme disease is ugly and all people who suffer need to stick together.

I wish you all the best in your recovery! And yes keep positive thinking...I believe it is an important part of the healing process.

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/1/2009 4:03 PM (GMT -7)   
THANSK for the POSTIIVE thoughts and Notes and Ideas!.

RottenDog
Veteran Member


Date Joined Apr 2009
Total Posts : 1013
   Posted 9/2/2009 12:20 AM (GMT -7)   
Hope,

see the more folks who get well and let the others know what worked for them, the more hope it gives to me and others. as i am not in a place where i can go to anyone for my treatment right now.

but 1 day i will be able to get help i pray, and if others post of treatments that work for them i will have a step up in knowing what i need to do when the time is right. i will have more options open to me is how i see it.

i can not in no way understand anyone with lyme belittle anyone for the form of treatment they use. as in reality there is no set rule as what works to kill this hideous disease. it had no rules that it goes by. yes in my thinking it plays dirty with our bodies.

i feel that you should never say anything to someone you wouldnt want said to you also, and i find so much peace in here with ya'll.
i learn things everyday too. isnt this what its all about? i think so.

maybe 1 day they will come up with a set rule for Dx and treatment for lyme. and i pray it is in our life time.

the blog thing maybe a good thing too, but i pray you post here so i can know how your doing. who knows i may win the lotto and then i can go too hehe.
   RD
 
still looking for answers.
 
Remember that advice is free, its your choice what you do with it.  :)


CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 9/2/2009 5:09 AM (GMT -7)   
keephope,

I am sorry you had to see ignorant and low life people do that. It is disgusting, especially doing that to people that are ill. I've read some posts on another forum from someone who left here. That person is lying about a few things that happened here. It doesn't bother me though and I say that you should just ignore it too. People like that are not happy with their own lives and they feel they have to belittle or berate others to make that person feel lower than they feel.

I truly hope you do come back and post your outcome...good or bad. I was a little upset myself about the cost. I wish I could afford it because to me, it makes sense to pump the immune system up, then the body is allowed to fight off this disease on it's on.

I hope everything works out for you. I know we are all tired of being sick all the time. So, if this is what you want to do, then you go for it. Don't worry about anyone else because in the end, it's your life, not theirs.

Good luck hun.
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum

Post Edited (CajunGrl) : 9/5/2009 7:27:57 AM (GMT-6)


KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/4/2009 11:35 PM (GMT -7)   
So... for those who are reading this who take this post as a way to put down the clinic and process....

I ask.. Since you think you know what is so WRONG.

Why dont you provide to everyone what is so RIGHT and how everyone can GET WELL>

Because .. I look around and here are many suffering people....

I will safely assume. YOU do not know what is right.... WHATSOEVER

So try to build some things or people up instead of tear them down. You might find that it works much better that way and will accomplish so much more.

Its like a whining child........ IT does not work!

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 9/5/2009 6:29 AM (GMT -7)   
Amen!
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum


2long4this
Regular Member


Date Joined Apr 2008
Total Posts : 37
   Posted 9/5/2009 8:05 AM (GMT -7)   
Keep Hope,
You have to do what is right FOR YOU.

Who cares what other people think. You don't have to answer to them.

They're not living your life, and it really doesn't sound like they're living their own either if they
have so much time to pick apart what you say and do.

I wish you all the best and I hope this is your answer!

TOguy
Regular Member


Date Joined Jan 2007
Total Posts : 193
   Posted 9/8/2009 7:41 AM (GMT -7)   
Keephope do what you think is right for you, what may work for you, might not work on others , I am curious about Envita and I would like to hear about your thearapy at Enivita,I think they have helped many people and there approach makes sense, there is no silver bullet out there so we got to find what works for each one of us , we should all share our experiences and help each other, after all everyone seems to get better on different approaches, so that being said we have to find what works for each one of us, and the immune system is a big part along with detoxing properly, good luck on your road to recovery and keep us updated :)


 
 
     Respectfully,JB

Post Edited (TOguy) : 9/8/2009 3:35:37 PM (GMT-6)


CaveCeekmama
New Member


Date Joined Sep 2009
Total Posts : 3
   Posted 9/8/2009 11:19 AM (GMT -7)   
Keephope, how is Envita doing for you?

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/10/2009 9:08 PM (GMT -7)   
Hello. !!
I am having a nice Rough week..! In a Great way. !!
I am impressed and very happy with how it is going. It is hard to explain in words but its like nothing I have ever felt.
Even though its is hard ... its the kind of hard I wanted.!

In 3 short days, and they are ramping up on some treatments, I already feel like things are getting hit !
Not much time to do anything but treatment... sleep.. bath... detox... eat something... and get back there..

Thanks for the kind words and support. I will drop by when I can.!!

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 9/10/2009 9:11 PM (GMT -7)   
keephope,

That is great! I'm so happy for you! Please keep coming back and letting us know how things are going. Good luck!!!
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum


CaveCeekmama
New Member


Date Joined Sep 2009
Total Posts : 3
   Posted 9/11/2009 8:11 AM (GMT -7)   
Keephope,
Thanks for keeping us updated! I am glad things are going so well for you.
From what your post, am I correct in stating that Envita modifies your treatment as you respond, as you go along...is flexible and does not stick with a rigid pre-determined treatment plan?
The reason why I am so interested is that I am considering treatment at Envita myself and want to make sure it is the right way to go because it is a lot of money and my insurance will not cover it.
Thanks so much!

KeepHope
Regular Member


Date Joined Oct 2008
Total Posts : 222
   Posted 9/11/2009 2:35 PM (GMT -7)   
hi Cave. They do have an ovearll protocol they use but they will evaluate your case and pick and choose or change according to your case. That is my understanding and how it went and is going for me.
I assume by your name your in AZ ?
So far I have insurance will cover some items but everyone has different insurance and depends on the insurance too. Some people can get help with insurance to cover Labs, Doc Appts, Antibiotic scripts, Port procedure and such.
I can try to help you with any other questions if you would like. Its been a long week.. I am not even used to be up that many hours a day so I am tired that is for sure.....Its a lot of changes and new things to be thrown at a body in one week.....
Going to sleep..!!! : )

nefferdun
Veteran Member


Date Joined Feb 2008
Total Posts : 900
   Posted 9/12/2009 6:55 AM (GMT -7)   
I am glad you feel you are already making progress and I hope this is the ticket for you to get well. Please continue to keep us posted.
As far as other people go that make fun of individuals - you are not talking to them - you are talking to us. We hear you and are grateful to you (and everyone) for sharing what works no matter how bizzare it may seem. My recovery is completely dependent upon this forum. I have no doctor.

runkiteer
New Member


Date Joined May 2012
Total Posts : 2
   Posted 5/4/2012 8:24 PM (GMT -7)   
If anyone has any experience with envita medical clinic and wish to share good or bad please contact me. I will provide you with some very interesting information and I would love to add your feedback to my research. much thanks.

Post Edited By Moderator (achievinggrace) : 5/5/2012 5:22:08 AM (GMT-6)

New Topic Post Reply Printable Version
27 posts in this thread.
Viewing Page :
 1  2 
Forum Information
Currently it is Monday, December 11, 2017 6:11 PM (GMT -7)
There are a total of 2,904,182 posts in 318,729 threads.
View Active Threads


Who's Online
This forum has 158125 registered members. Please welcome our newest member, PolarisBug.
389 Guest(s), 13 Registered Member(s) are currently online.  Details
MDNative, mattamx, MamaLama, Corvette Joe, countess18, Girlie, Sherrine, Herophilus, Mergirl, jrpsf, LivingThroughLyme, three 5's and a jack, Tall Allen