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>

> I can't find the cause of my positive etg. I have changed every

thing

> I consume and use but still test positive. I have had 4 positives

in

> a row over a month. It makes me think that I have gut

fermentation

> syndrome. I don't know what to do, please help

>

>

, I too have had 2 pos. etg tests. One for 1000 and one for

1200. I can't find any link to foods or beverages either. I'm

getting a bit desperate. I have been clean and SOBER for 4 yrs 2

mos. I have always been very careful of what I eat/drink. Because

of these tests I've been pulled from work and my transition status

in my diversion program has been revoked. What a nightmare.

Please let me know what you find out about the Auto-Brewery

Syndrome. I'm tempted to contact my MD for an evaluation.

Thnaks,

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Just wanna say to both and , that reading your posts makes my heart

race and

me sick to my stomach, as I relate to both of you..., the only thing I can

think of is

maybe you are inhaling something...? Have you made a VERY detailed list of

every single

thing you have eaten in the last month? And where you are and what you are

exposed to

at ALL times? (ie. cleaning solutions, someone waxing the floors or cleaning or

spraying air

freshner or whatever around you where you live or work, etc.) Do you keep track

of it on a

daily/ hourly basis? If not, start, REALLY detailed journaling/ notes...I can't

think of any

other way to begin to figure it out, cause there are SO many things that it

could be, and as

Lorie said it " would be nice to have a list " of stuff, but OH I'M SORRY, as I

have seen in the

literature that would be " too ECONOMICALLY and chronologically CUMBERSOME for

the

companies to publish such a list... " (I can't remember where I read that, but I

DID, a couple

months ago...)

, remembering how I felt for the few weeks when I was pulled from work r/t

my pos

level of 2400!!!, (which I cannot imagine what from, for obviously I did not

drink; and I

turned " 4 " last week) I don't know if I could get through it again it was SO

awful; Thank

God the DEC " cut me a deal " and after revoking it until I met with them,

" extended " my

transition for 6 more months, after I finally convinced them I did NOT drink

(with 5 letters,

a 8 page essay I wrote, etc, and backing from my shrink, etc.). Last week, I

had my second

+etg of 270, and I believe they are calling it " incidental " and I haven't heard

anything more

about it, but I am counting down the days now till my next DEC in Nov., and PRAY

something else doesn't happen AND that the SAMSHA report comes out and that we

can

ALL finally START to be able to breath again and have SOME PEACE...

Amy

> >

> > I can't find the cause of my positive etg. I have changed every

> thing

> > I consume and use but still test positive. I have had 4 positives

> in

> > a row over a month. It makes me think that I have gut

> fermentation

> > syndrome. I don't know what to do, please help

> >

> >

> , I too have had 2 pos. etg tests. One for 1000 and one for

> 1200. I can't find any link to foods or beverages either. I'm

> getting a bit desperate. I have been clean and SOBER for 4 yrs 2

> mos. I have always been very careful of what I eat/drink. Because

> of these tests I've been pulled from work and my transition status

> in my diversion program has been revoked. What a nightmare.

> Please let me know what you find out about the Auto-Brewery

> Syndrome. I'm tempted to contact my MD for an evaluation.

> Thnaks,

>

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> > >

> > > I can't find the cause of my positive etg. I have changed

every

> > thing

> > > I consume and use but still test positive. I have had 4

positives

> > in

> > > a row over a month. It makes me think that I have gut

> > fermentation

> > > syndrome. I don't know what to do, please help

> > >

> > >

> > , I too have had 2 pos. etg tests. One for 1000 and one for

> > 1200. I can't find any link to foods or beverages either. I'm

> > getting a bit desperate. I have been clean and SOBER for 4 yrs

2

> > mos. I have always been very careful of what I eat/drink.

Because

> > of these tests I've been pulled from work and my transition

status

> > in my diversion program has been revoked. What a nightmare.

> > Please let me know what you find out about the Auto-Brewery

> > Syndrome. I'm tempted to contact my MD for an evaluation.

> > Thnaks,

> >

>Does anyone happen to know how fast the etg level drops in the

body? I'm trying to find out all I can at this point to help my

cause. I went from 1200 on 9/16 to " negative " on 9/18. Just

curious if this sounds reasonable. Sounds kinda fast to

me. " Negative " for my program is <250 mcg.

Thanks,

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Hi ,

I am so sorry you are in this situation. I can definitely relate. The sad thing is, I don't think I can tell you what caused my positives (I had 5). They all happened last year. All I know is now I avoid anything with alcohol in it like the plague. My diet has been fairly bland, and I am careful of sprays, lotions, etc. I do not touch the hand sanitizers. I also stopped taking tylenol, which I think was a factor for me.

I am sorry I can't give you more info. My thoughts and prayers are with you.

Bonnie

(just turned 4 on 9/26......YEAH!!!)

From: Ethylglucuronide [mailto:Ethylglucuronide ] On Behalf Of jhartman32001Sent: Wednesday, September 27, 2006 1:44 PMEthylglucuronide Subject: hopeless

I can't find the cause of my positive etg. I have changed every thing I consume and use but still test positive. I have had 4 positives in a row over a month. It makes me think that I have gut fermentation syndrome. I don't know what to do, please help

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Are there any safe lotions and deoderants? Bonnie <bweinberger001@...> wrote: Hi , I am so sorry you are in this situation. I can definitely relate. The sad thing is, I don't think I can tell you what caused my positives (I had 5). They all happened last year. All I know is now I

avoid anything with alcohol in it like the plague. My diet has been fairly bland, and I am careful of sprays, lotions, etc. I do not touch the hand sanitizers. I also stopped taking tylenol, which I think was a factor for me. I am sorry I can't give you more info. My thoughts and prayers are with you. Bonnie (just turned 4 on 9/26......YEAH!!!) From: Ethylglucuronide [mailto:Ethylglucuronide ] On Behalf Of jhartman32001Sent:

Wednesday, September 27, 2006 1:44 PMEthylglucuronide Subject: hopeless I can't find the cause of my positive etg. I have changed every thing I consume and use but still test positive. I have had 4 positives in a row over a month. It makes me think that I have gut fermentation syndrome. I don't know what to do, please help

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I use Secret doedorant, and any lotion that is extra moisturizsing (i have to be careful, my skin is sensitive)

Bonnie

From: Ethylglucuronide [mailto:Ethylglucuronide ] On Behalf Of HartmanSent: Thursday, September 28, 2006 9:34 AMEthylglucuronide Subject: RE: hopeless

Are there any safe lotions and deoderants?

Bonnie <bweinberger001socal (DOT) rr.com> wrote:

Hi ,

I am so sorry you are in this situation. I can definitely relate. The sad thing is, I don't think I can tell you what caused my positives (I had 5). They all happened last year. All I know is now I avoid anything with alcohol in it like the plague. My diet has been fairly bland, and I am careful of sprays, lotions, etc. I do not touch the hand sanitizers. I also stopped taking tylenol, which I think was a factor for me.

I am sorry I can't give you more info. My thoughts and prayers are with you.

Bonnie

(just turned 4 on 9/26......YEAH!!!)

From: Ethylglucuronide [mailto:Ethylglucuronide ] On Behalf Wednesday, September 27, 2006 1:44 PMEthylglucuronide Subject: hopeless

I can't find the cause of my positive etg. I have changed every thing I consume and use but still test positive. I have had 4 positives in a row over a month. It makes me think that I have gut fermentation syndrome. I don't know what to do, please help

Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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  • 3 years later...

I feel hopeless tonite. I learned I had candida in June after suffering for

10years. However it has been such a battle for me. I keep modifying my diet as I

learn things. I try so hard. I fail at times. The holidays are hard. I just want

to eat what everyone else is. I dont want to have to think about all this. I am

tired of it. For the past 3 yrs they told me I was gluten and dairy sensitive. I

have had no gluten or dairy in 3 yrs. They were totally wrong. It was candida. I

want to have children some day. I know now is not the time. However I am in my

late 30s. That bothers me.Tomorrow doesnt always come for everyone. I lost my

first husband to cancer 6 years ago.

I have this because I got mono years ago and had strong antibotics. I had a

reaction then but it went away. I thought I was fine. I am mad at the drs. How

can they prescribe antibotics and never recommend probiotics. It makes no sense

to me.

I resigned from my job because I could not do it anymore being sick all the

time. I had a good job. Now I make a third of what I was. That has made me

miserable.

All of this is so unfair. I didnt deserve this. None of us did.

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Hey Keri:

You can heal on this diet and so can your children. Don't beat yourself up for

not knowing about the diet then, you know it now. Give them good food, cod

liver oil, good fats and Bee's supps and they'll BLOOM... just like you will.

And they'll need less time to get healthy. In fact, the changes you'll see in

them can be one of your motivators to stick with the diet!

Best,

Marissa

>

> I also wish I'd known all this before I'd produced my two children. I

> look back at the state my body was probably in when I conceived (years

> of the pill, stress, bad diet, antibiotics, general body abuse) and am

> painfully aware of why they have the issues they do now. I feel so

> guilty and angry at myself :( I we could turn back time eh?

>

> But I am grateful that I know now. Knowledge definately is power :)

>

> Thanks again!

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  • 2 years later...
Guest guest

Greetings,Is anyone using the BrainMaster 3.71 software and if so, does anyone know how to operate the games on the system? We have absolutely no idea if our child is actually receiving any type of training; we have been using videos - do they work? How do you find the points on the head? I would also like to know if there is anyone in the No.VA area that is doing this at home. Thank you for your time. From:

" " < > Sent: Tuesday, June 12, 2012 8:07 AM Subject: Digest Number 4132

BrainTrainer

BrainTrainer

Messages In This Digest (4 Messages)

1a.

Re: Basic Stuff

From: pvdtlc

2a.

Re: Article needed ASAP on paroxysmal dyskenisia following a TBI

From: Marcus Kurek

2b.

Re: Article needed ASAP on paroxysmal dyskenisia following a TBI

From: Elsie L. Ferguson Ph.D.

3a.

Re: severe sleep issue

From: Sharrie

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Messages

1a.

Re: Basic Stuff

Posted by: "pvdtlc"

pvdtlc@...

pe1746

Mon Jun 11, 2012 2:17 pm (PDT)

It's probably a symptom of the so-called "stubbornness syndrome".

Hopefully someone on the list can help you, but if that doesn't work out

you can always do as you suggested in your post--set up a time to work with

someone who has done hundreds of the installations. Let one or the other

of us know if you decide that might be a more efficient use of your time.

I've missed talking with you lately. Hope all is rolling along as you

planned.

Pete

--

Van Deusen

pvdtlcgmail (DOT) com

http://www.brain-trainer.com

USA 678 224 5895

BR 47 3346 6235

The Learning Curve, Inc.

On Sun, Jun 10, 2012 at 3:19 PM, neurorico <RVieillecs (DOT) com> wrote:

> **

>

>

> Dear Listmates,

> I'm going to get online with either Pete or Foxx soon because I have a lot

> of start up to do, but in the meantime I'm wondering if there is some very

> simple fix to the difficulty I am experiencing since it seems so consistent

> across three computers. I've followed the pocket neurobics directions to

> install bioexplorer and the installed drivers for the pockets connect to

> bioexplorer and show a connection, but when I push start, nothing happens.

> On three lap tops. I'm hoping it is some standard problem easily overlooked

> by a computer-phobe- semi-dunce.

> Please only attend to this if it is something simple.

> Thank you in advance,

> Vieille

>

>

>

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Messages in this topic (5)

2a.

Re: Article needed ASAP on paroxysmal dyskenisia following a TBI

Posted by: "Marcus Kurek"

marcus.cptr@...

marcus.cptr

Mon Jun 11, 2012 3:00 pm (PDT)

Hello Diane,

Levine, author of "Waking the Tiger" and Scaer, author of "The Body Bears the Burden" speak a great deal about myoclonic tremors secondary to traumatic events. In fact, Somatic Experiencing, a treatment model created by Levine, is based on accessing the myoclonic tremors and facilitating them to go to completion. This philosophy is the basis for a great deal of the somatic based trauma therapies.

Blessings,

Marcus

____________ _________ _________ __

From: "Diane Stoler, Ed.D." <dianedrdiane (DOT) com>

neuroguide@gro ups.com; ; brainmgroups (DOT) com

Sent: Sunday, June 10, 2012 4:25 PM

Subject: Article needed ASAP on paroxysmal dyskenisia following a TBI

I was contacted from an attorney who is looking for an article on

paroxysmal dyskensia following TBI. ASAP

Can you help? The opposition say the client is

faking.

The wrote lawyer wrote "I am helping a lawyer prepare a case and we

have to establish a causal connection btw a mild TBI and her movement

disorder which left her wheel chair bound. I have a TBI from an

assault and can no longer try cases. I help attorneys working on this

type of case whenever I can. "

I wrote back to her the following:

Yes. When the brain is dysregulated from injury, it can

effect the motor area. I have a constant tremor from my TBI that the

doctors...

She wrote back that they need articles to support this. If anyone

knows of them, please forward it. Appreciate

whatever help you can.

Thanks

Diane

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Messages in this topic (4)

2b.

Re: Article needed ASAP on paroxysmal dyskenisia following a TBI

Posted by: "Elsie L. Ferguson Ph.D."

pairofdocs@...

elsie_ferguson

Mon Jun 11, 2012 5:44 pm (PDT)

found the following on Google scholar:

Elsie Ferguson

Neurosurgery:

May 2002 - Volume 50 - Issue 5 - pp 927-940

Topic Review

Head Injury and Posttraumatic Movement Disorders

Krauss, Joachim K. M.D.; Jankovic, ph M.D.

Collapse Box <javascript: showHide( 'ej-article- box-text1' , 'img1')>

Abstract

WE REVIEW THE phenomenology, pathophysiology, pathological anatomy, and

therapy of posttraumatic movement disorders with special emphasis on

neurosurgical treatment options. We also explore possible links between

craniocerebral trauma and parkinsonism. The cause-effect relationship

between head injury and subsequent movement disorder is not fully

appreciated. This may be related partially to the delayed appearance of

the movement disorder. Movement disorders after severe head injury have

been reported in 13 to 66% of patients. Although movement disorders

after mild or moderate head injury are frequently transient and, in

general, do not result in additional disability, kinetic tremors and

dystonia may be a source of marked disability in survivors of severe

head injury. Functional stereotactic surgery provides long-term

symptomatic and functional benefits in the majority of patients.

Thalamic radiofrequency lesioning, although beneficial in some patients,

frequently is associated with side effects such as increased dysarthria

or gait disturbance, particularly in patients with kinetic tremor

secondary to diffuse axonal injury. Deep brain stimulation is used

increasingly as an option in such patients. It remains unclear whether

pallidal or thalamic targets are more beneficial for treatment of

posttraumatic dystonia. Trauma to the central nervous system is an

important causative factor in a variety of movement disorders. The

mediation of the effects of trauma and the pathophysiology of the

development of posttraumatic movement disorders require further study.

Functional stereotactic surgery should be considered in patients with

disabling movement disorders refractory to medical treatment.

Copyright © by the Congress of Neurological Surgeons

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Messages in this topic (4)

3a.

Re: severe sleep issue

Posted by: "Sharrie"

drsharrie@...

drsharrie

Mon Jun 11, 2012 5:06 pm (PDT)

I agree with you. I also use TMA's and 100% of the time when the NFB isn't working there is a metabolic imbalance! Not most of the time. All of the times. I offered to look at her asmnt and what she has done to make sure she is on target with training then talk metabolic concerns.

Sent from my iPad

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