Please share Hansa Center experiences

Naomi- Everyone who comes there comes with their own illnesses and own experiences and so heals in different ways and different times.
It is the best healing center I have experienced.
I think my breathing flare up is a lyme/co infection flare up.
Hopefully the hansa medicines will take care of it.

Are you scheduled to go there? if so, when? once you do you can join the hansa patient fb page and share your experience. Most people are really glad they went there.

Thank you!  I hope I am in the category of "most people".  I am scheduled for Dec. 5 for 2 weeks.

Thanks.

Mavis

Anyone know about what it costs for the initial two week treatment?

Katebirch,

I don't think I replied to you. I am going to Hansa Dec. 5 for 2 weeks.

Naomi-- I am so excited for you to be going to Hansa! Please share your experience if you would like when you return.

Sadly I think I am having a babesia flare. No one can really confirm it for me for sure- unless I go back to hansa. If I took a blood test it would come up because I have had it in the past.
But it is the only thing that makes sense.
So in effect something is flaring in me- e but still I do not ever regret going to hansa. And if I get to a point where I cannot get rid of what is going on with me then I will choose to go back there. IT is the only place I have that much faith in, especially around tick borne things. But they are humans, and not gods. And sometimes people do have to go back. If it were less costly and closer to home, people would not think twice about having to go for repeated visits there But because it is so costly people want them to cure everything forever. IT is a hard thing to have to pay so much money. At any rate. I am so happy for you to be going there and I think you will find great healing there as so many others do.

Kate - I believe if you have the PCR or FISH test - that will only be positive if it's still active in your blood.

(not antibody testing)

But, lots of false negatives.

Thanks so much Kate. I am staying at a house that a former patient renovated for sensitive peope. It is 4-1/2 min. drive from Hansa.
I sure hope they can help with my sensitivities which I believe to be due to Leaky Gut Syndrome.
Wish I could move there for a year!
Naomi

Yes it is WW house.  So do you know if Hansa has helped folks with sensitivities?  This only started in Feb. when I got a virus.

Not sure if I asked this, but after your treatments at Hansa were you better in a few months?  Did you have fibromyalgia and neuropathy and stinging pain? 

I hope your breathing issue resolves soon. 

Best.

Naomi

Naomi can't put her email in a post, but she can enable her email option through 'My Profile' .

Then you can click on the envelope on the left below her screen name and email her.

Katebirch said...
thank you hopefully if she wants to do this she can figure out how!

Girlie means we do not want people posting their email address here on the comments. The board is public, it's a bad idea to post them where everyone who isn't a member can see them.

Our profiles on here are only available for other members to view, so enabling others to see your email address in your profile is much safer.

in a pretty crazy turn of events I am going back to the hansa center a week from today to try to address this breathing issues.

First time posting to this forum. Scouring all of the posts regarding Hansa Center. We are considering taking my daughter, who is now 17 1/2 there. She contracted Lyme when she was 4. By 9, was told she was mildly mentally retarded from the medical community. Long story short, she has neurological Lyme and has been affected cognitively. We did seven years antibiotics, PICC line, etc. Now on Cowden Protocol, as well as Buhner tinctures. We have made great strides. She has Lyme, babesia and bartonella. My husband has Lyme and Bartonella, supposedly accupuncturist says I have it, my 22 year old has Lyme that has attacked his heart. My mother suffers from Lyme. My youngest daughter just was bit in November deer hunting and ended up with "stretch marks" on her tush, which I now know is Bartonella. Just buried my brother-in-law, age 58 yesterday, who had Lyme disease since 9 years old. Need I say I HATE LYMES. I'm sure some look at me like I have horns coming out of my head when I state how many of our family has Lymes. We just placed an order for a sauna, which is NOT a luxury. Given the amount of people in my family needing it, we feel it is more of a necessity.

My main question is, does anyone who has visited the Hansa Center have experience with turnaround cognitively when affected by Lyme. Looking for some hope that we can reverse the damage done to her brain. There are so many clinics across the United States that treat Lyme. Just want to make sure we go the correct route, as it is ALOT of money. My husband and I are praying for wisdom from above!

Ok, thank you.