Jump to content
RemedySpot.com

RE: Lyme that leads to Parkinson's

Rate this topic


Guest guest

Recommended Posts

How was he being treated for lyme? In the movie Under Our Skin one doctor

asserts he never met a parkinson or als patient that didn't have Lyme so

there is a big connection there.

Have you heard of Salt/C regimen btw? It something you can add to whatever

treatment you are currently using and it appears to help allot of people. My

wife is one of them.

You can get more information about it on the lymestrategies

list.

adams

> [ ] Lyme that leads to Parkinson's

>

> Does anyone have experience dealing with Lyme that leads to

> Parkinson's? Is

> there a doctor out there that treats patients with this problem

> specifically?

>

> My husband was being treated for Lyme then came down with

> Parkinson's or

> Parkinsonism. We are searchiong for the right treatment for

> him and the

> right doctor.

>

> Ann Prow

> annprow@...

>

>

>

Link to comment
Share on other sites

Ann....lowering his total body burden of pathogens and toxins, and working on

getting the Mercury/Lead out of his body will work....The Parkinson shake I have

had is now diminishing, as I work intensely on getting the Lead/Mercury out of

my body.....it is a slow process, BUT IT WORKS....

My getting rid of the Mercury/Lead will also help the Lyme....Lyme critters feed

off of heavy metals....

You can go to www.gordonresearch.com and type in these words in the search

box....You can't get into FACT, but I can however, I'm sure that the main search

box will give you a ton of reading....

Angel Huggzz

or Angel

www.lymecommunity.com

" stay tuned " for the exciting Lyme Conference here in June 2009....We have the

hotel, which is chemical free....

[ ] Lyme that leads to Parkinson's

Does anyone have experience dealing with Lyme that leads to Parkinson's? Is

there a doctor out there that treats patients with this problem

specifically?

My husband was being treated for Lyme then came down with Parkinson's or

Parkinsonism. We are searchiong for the right treatment for him and the

right doctor.

Ann Prow

annprow@...

Link to comment
Share on other sites

I'm glad Salt/C worked for your wife, . It put me in the

hospital, and it took over three months of strict bedrest for me to

even get back to where I was.

I'm just saying: it's something people need to be very, very careful

with. It turned out later I had a common-enough genetic anomaly (known

as an ACE deletion) that made it hit my body in a way that completely

disrupted my endocrine system.

A majority of people diagnosed with CFIDS have the ACE deletion, along

with other SNPs that also affect adrenal function And since nobody

really knows how many CFIDS patients really have undiagnosed Lyme, it

seems likely that these problems may be more common among us as well.

(I have a friend who is currently researching this very thing, in fact.)

The bottom line: Approach Salt/C very, very carefully. If your feet

and legs start swelling AT ALL, or your heart starts palpitating, get

off it immediately, and don't even think about going back. It's your

body telling you it's heading for deep, deep trouble.

Sara

On Sep 25, 2008, at 10:10 AM, wrote:

> Have you heard of Salt/C regimen btw? It something you can add to

> whatever

> treatment you are currently using and it appears to help allot of

> people. My

> wife is one of them.

>

> You can get more information about it on the lymestrategies

>

> list.

>

> adams

>

Link to comment
Share on other sites

Good to know! Thanks Sara!

> Re: [ ] Lyme that leads to Parkinson's

>

> I'm glad Salt/C worked for your wife, . It put me in the

> hospital, and it took over three months of strict bedrest for me to

> even get back to where I was.

>

> I'm just saying: it's something people need to be very, very careful

> with. It turned out later I had a common-enough genetic

> anomaly (known

> as an ACE deletion) that made it hit my body in a way that

> completely

> disrupted my endocrine system.

>

> A majority of people diagnosed with CFIDS have the ACE

> deletion, along

> with other SNPs that also affect adrenal function And since nobody

> really knows how many CFIDS patients really have undiagnosed

> Lyme, it

> seems likely that these problems may be more common among us

> as well.

> (I have a friend who is currently researching this very

> thing, in fact.)

>

> The bottom line: Approach Salt/C very, very carefully. If your feet

> and legs start swelling AT ALL, or your heart starts

> palpitating, get

> off it immediately, and don't even think about going back. It's your

> body telling you it's heading for deep, deep trouble.

>

> Sara

>

>

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...