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RE: Digest Number 1088

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Hi,

I'm using NaturesSunshine products and PureHerbs products b/c that's what my

naturopath is familiar with. I'm not sure of what everything does, but I'll

list what I'm taking.

Noni Juice - digestion

D.W. (PureHerbs) - digestion

Intestinal Sooth and Build (NaturesSunshine)- intestinal healing/digestion

Whole Leaf Aloe Vera - not sure, think for sugar assimilation

KID-W (PureHerbs) - kidneys

HYG-W (PureHerbs) - regulate blood sugar

L-Glutamine - for sugar cravings

Also, I know that Licorice Root/Licorice tea is good for cravings as it

strengthens the adrenals. Depending on how these things go, I'll try that

later, if necessary. Also, I started the ER4YT diet (albeit very

reluctantly) and since I'm an A, that means a predominantly vegetarian diet.

And I will say that since I cut out meat (though I still eat fish) I have

felt a lot better. My stomach has flattened out and the cravings have gone

down a lot. , I will ask about the menstrual problems; I have the same

thing. I hope this helps.

Hugs

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,

You mentioned you have menstural problems. Do you get your period? I

havne't gotten mine since 1999.

>From: " Poag " <kamepo@...>

>Reply-candidiasis

>candidiasis

>Subject: Re: Digest Number 1088

>Date: Fri, 11 Jan 2002 18:19:30 -0500

>

>Hi,

>I'm using NaturesSunshine products and PureHerbs products b/c that's what

>my

>naturopath is familiar with. I'm not sure of what everything does, but

>I'll

>list what I'm taking.

>

>Noni Juice - digestion

>D.W. (PureHerbs) - digestion

>Intestinal Sooth and Build (NaturesSunshine)- intestinal healing/digestion

>Whole Leaf Aloe Vera - not sure, think for sugar assimilation

>KID-W (PureHerbs) - kidneys

>HYG-W (PureHerbs) - regulate blood sugar

>L-Glutamine - for sugar cravings

>

>Also, I know that Licorice Root/Licorice tea is good for cravings as it

>strengthens the adrenals. Depending on how these things go, I'll try that

>later, if necessary. Also, I started the ER4YT diet (albeit very

>reluctantly) and since I'm an A, that means a predominantly vegetarian

>diet.

> And I will say that since I cut out meat (though I still eat fish) I

>have

>felt a lot better. My stomach has flattened out and the cravings have gone

>down a lot. , I will ask about the menstrual problems; I have the

>same

>thing. I hope this helps.

>Hugs

>

>

>

>

>

>_________________________________________________________________

>MSN Photos is the easiest way to share and print your photos:

>http://photos.msn.com/support/worldwide.aspx

>

_________________________________________________________________

MSN Photos is the easiest way to share and print your photos:

http://photos.msn.com/support/worldwide.aspx

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  • 5 months later...
  • 2 months later...
  • 3 months later...

I recently had taken my daughter to an allergist because she gets sick a lot

I was trying to find out if she has allergies or what. She keeps a cold in

the winter so at the visit he set up blood work for some allergies ,but also

checking other things like titers,and IGA,IGG,IGM few other ones I can not

remember my ? is has anyone went threw this,and what will these tests show if

anything? I think maybe he thinks she has a immune def or something whats the

chances of that? le

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> Your daughter sounds alot like mine. We were on allergy medication year round

and sometimes she was still sick even on that. What made all the difference in

the world was when I put her on the gf/cf diet. We did do the 90 panel screen

first (IGE, IGG) but those tests didn't come back for a few weeks. About 2 weeks

into the diet I tried to pull her off of her meds, and started supplementing her

with necessary vitamins and minerals she was low in (you can test for that too),

I didn't just did some research and tweeked them to meet her needs. It's been 3

months now and she hasn't needed any medications and she hasn't been sick enough

to warrant even one dr visit!!! I would suggest the food allergy panel it may

answer alot of your questions, once you've taken these things out of her diet

and possibly even doing a roation diet, you may find that if you watch what she

eats and how often she eats it, may make all the difference in the world. Don't

know if you are gf/cf, but the difference it made in my daughter was amazing.

Karyn

> From: dannilynn700231@...

> Date: 2002/12/13 Fri PM 06:47:44 EST

> Autism_in_Girls

> Subject: Re: Digest Number 1088

>

>

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I agree! As soon as we went on the diet (specifically eliminating

caesin/dairy), went from about a cold a month to one short one for

the whole winter!

<klmitch@...>

Autism_in_Girls

12/13/02 10:56 PM cc: (bcc: Joy

Insinna/Content/Element K)

Please respond to Subject: Re: Re:

Digest Number 1088

Autism_in_Girls

> Your daughter sounds alot like mine. We were on allergy medication year

round and sometimes she was still sick even on that. What made all the

difference in the world was when I put her on the gf/cf diet. We did do the

90 panel screen first (IGE, IGG) but those tests didn't come back for a few

weeks. About 2 weeks into the diet I tried to pull her off of her meds, and

started supplementing her with necessary vitamins and minerals she was low

in (you can test for that too), I didn't just did some research and tweeked

them to meet her needs. It's been 3 months now and she hasn't needed any

medications and she hasn't been sick enough to warrant even one dr visit!!!

I would suggest the food allergy panel it may answer alot of your

questions, once you've taken these things out of her diet and possibly even

doing a roation diet, you may find that if you watch what she eats and how

often she eats it, may make all the difference in the world. Don't know if

you are gf/cf, but the difference it made in my daughter was amazing.

Karyn

> From: dannilynn700231@...

> Date: 2002/12/13 Fri PM 06:47:44 EST

> Autism_in_Girls

> Subject: Re: Digest Number 1088

>

>

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> 's too - she tested +4 in all dairy!!!! Have you checked out the phenols

and stuff like that as well? I found that even after going gf/cf she had issues

that were underlying those as well..

KAryn

> From: joy_insinna@...

> Date: 2002/12/16 Mon AM 11:46:12 EST

> Autism_in_Girls

> Subject: Re: Re: Digest Number 1088

>

>

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  • 3 weeks later...

And I would love the recipes as well.

You can send them to me personally at sknapinsky@... if that works

better for you.

Thank you and I look forward to making and trying them all.

Sophia

Message: 5

Date: Tue, 31 Dec 2002 22:47:02 -0000

From: " carmapaden <paden@...> " <paden@...>

Subject: Re: breakfast ideas

Meg, I'm interested! I missed this thread when it came around the

first time, but if you're able I would love to have these recipes.

I'm pregnant too, and easy, already-prepared breakfasts are a MUST!

I find myself wishing I kept cold cereal in the house, just to have

something easy to feed my kids (and myself).

Thanks,

Carma

> We always keep breakfast raw. It usually consists of a dish made

with

> sprouted grains, soaked & dried nuts & seeds, dried fruit (usually

figs

> & dates) and a small amount of fat (raw dairy or coconut oil).

Carrot

> cake or cranberry cake with cream cheese frosting, banana cake,

> apple-cinnamon cereal, crunchy granola, chocolate-mint cookies,

> chocolate fudge brownies, carob-chip cookies, " chocolate " pudding

> cereal, banana mousse with whipped cream and lemon fluff are our

> favorite breakfast choices. We often have a glass of raw milk or

some

> fresh fruit with them. I feel so good after these meals, they're

> delicious and they really keep us until lunch.. we eat between 7-8

a.m.

> and we're often not hungry until 1 pm. I'd be happy to send you, or

> anyone interested, my recipes.

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  • 10 months later...
  • 1 year later...
Guest guest

,

Another thing to consider when trying to find peak

alpha in a young child is this. The assessment is

finding the tent pole within the range of 8-12, which

it identifies as peak alpha. For some kids, though,

peak alpha might not be within that 8-12 range.

I'm training a 7-year-old, for example, and his alpha

is 6.5-8.5. (On his assessment, 8.5 showed as his peak

alpha.)

In this case, you have to do the

yes-closed/eyes-opened thingie with an electrode at P4

and watch the bars go up and down.

Pete & , please correct anything that I've said

that isn't right.

Thanks,

Jane

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  • 10 months later...
Guest guest

In a message dated 3/18/2006 10:49:27 A.M. Central Standard Time,

writes:

Message: 9

Date: Sat, 18 Mar 2006 13:15:13 -0000

From: " chefsuz2 " <thenaturalkitchen@...>

Subject: Re: patch under the breast, healing reaction?

hi marge

so glad you've joined us!

thank you Suz...and to every one who welcomed me. It's warming. :-)

to me it sure sounds like your body is expelling some extra yeast, as

it would in a vaginal infection.

but of course, please keep an eye on it, and keep us posted.

one form of redness on the breast that i know to be concerened about

is on or around the nipples, and upper chest area, resembling (and

sometimes diagnosed as) dermatitis, which can be a form of

inflammatory breast cancer.

I am confident the rapid onset indicates yeast, but I have to tell you I had

to think about it a minute when I found it..was very unnerving.

this is not to alarm you in any way, the location of your red patch,

the moistness and the odor you describe tends to indicate yeast.

you will find lots of information and support here!

Thanks again. I am pretty bummed this morning. My chiro who is following

the yeast apparently has few clues other than hit it with Oregamax (didn't

even know about the oil). He is absolutely remarkable as a chiro, gets me

better results than anyone before and has never " cracked " or " jerked " anything

on

me. But I am going to have to sort this out with little help from him or my

GP. The GP is the one who treated me for a couple of years with Minocycline,

for which I am thankful for being rid of the inflammation from mycotoxins

from the L-tryptophan. But all he is able to do for me re Candida is write

prescriptions for Nystatin IF I get him the right information. I emailed Bee's

article on nystatin powder to him this morning

Marge

happy healing ~ suz :)

Blessings,

Marge

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In a message dated 3/18/2006 10:49:27 A.M. Central Standard Time,

writes:

Message: 15

Date: Sat, 18 Mar 2006 14:00:54 -0000

From: " Bee Wilder " <beeisbuzzing2003@...>

Subject: toxins eliminated through the skin

>

> I am wondering if I may be having a healing reaction too.

>

> As I was undressing tonight my hand felt a slick wetness

> under a breast. I had not had pain. So I was surprised to

> find a large red patch. I thought it could have been perspiration

> but I had not been hot and the other breast was not wet or red.

>

> Immediately I noticed a foul odor to the moisture and I recognized

> it as an odor I get when I have a yeast infection in the bladder or

> vagina.

>

> I do not recall ever having such a red patch. I have occassionally

> been red the from a soap allergy but this is different.

==>Hi Marge. During natural healing many symptoms like you describe

do come and go. Even symptoms you've never had before will appear.

The body detoxifies through any orifice (opening of the body),

including the skin, and it also tends to externalize healing to the

skin in order to protect vital inner organs.

>>>>>>>>so you don't think it was a rapid onset from having something sweet?

It would have had to have occured in less than an hour. But rather it is

the healing process? I realize you will be speculating but I would appreciate

your best guess.

==>The odor is caused by toxins being eliminated. I wouldn't be too

concerned about it. Take an epsom salt bath to encourage detoxifying

through the skin, submerging your breasts. You can also soak a hand

towel in the epsom salt water during your bath and apply them to your

breast, especially underneath. After your bath rub coconut oil well

into that area of both breasts and all over them as well. Do this at

least once a day.

>>>>>>I can handle that. My husband is going out for Epsom salts now. And

I have the coconut oil. Should I apply a gauze or something under the

breast to absorb any moisture that collects there?

Bee

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  • 5 years later...
Guest guest

Not being anywhere near a Core Specialist I can only speak a little to you about my experience. At first when I started MNRI I expected to see consistent improvement and felt discouraged when it was two steps forward and one step back. Now I understand better that integrating is much more of a process than an event. On the days he is stressed or wanting to hurry my son will revert back to some behaviors. We have been doing this for a few months shy of 2 yrs. So now when he regresses it is not to

the same degree that it was during the first year. I have learned to watch the level of his reflex integration and I can tell his level of stress, fatigue or excitement. If he is coming down with a sickness or didn't sleep well (or stayed up late reading) he will struggle more. So we step up the reflexes or Tactile as I can or I just give him a little more grace. So your child doing the toe walking sometimes and sometimes not doesn't sound out of the norm from my experience. It sounds like progress...But definitely work with a Core Specialist if you can or take more classes. California has a lot going on. Hi Everyone,My name is Hela and I have been in the group for more than a year reading daily posts , I have been doing reflex from August of last year with laser and have started MNRI this year and have seen Dr Masgatuva for my daughter assessment in April and been doing my home program reguraly , my daughter is 7 with Autism, her communication is still delayed and she has some of the main reflex non integrated.my questions to all are the following:1- My daughter has been toewalking for years, none of the diet nor the supplement or the OT or Handle had helped her, our MNRI home program include the Foot TG 5 days a week, I have been doing it daily twice a day

and she it seems that she is getting of her toe better specially when she is outside but in the house when she is bearfooted she is toewalking again and when she is detoxing usually it is very severe.I am trying to get feedback from other parents and consultant on this, what other reflex are important other than the FTG, I do undestand that the foot TG we are trying to relax the muscle but how about the main reason why the child is toewalking, I beleive it is a protection from stimulus or a fear , is there visual and Auditory reflexes that have a role to help with the toewalking.everyone opinion is very important to me and would love to hear from other parents and core specialist.Her Automatic gait reflex is in normal range,all the other reflex in the home program are getting very nicely improving, only

the toe walking is what make me wonder what else I am missing.There is a course that Dr Masgatuva is teaching in Belgium in November that address the visual and Auditory reflex, it mention the FTG also, so I am trying to see if there is a connection , you guys core specialist might know the answer????my second question is there a core specialist in Southern California that we can work with ...the majority of the specialist are located in N. California and I have traveled to NC but would like to find out if there is support here in Southern California.Thank you so much for the feedback is greatly appreciated!!!Sincerely,HelaMessages in this topic (1)------------------------------------------------------------------------

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Guest guest

Hela~You might consider an intensive (1 or multiple days) with a core specialist you bring to your area.  Yes, the V/A protocol is informative as it provides cranial symmetry and systemic calm.All best,Janet

Core SpecialistFacial Reflexes  and Tactile Integration InstructorOn Tue, Aug 9, 2011 at 8:34 AM, Kayte <k_sisler@...> wrote:

 

Not being anywhere near a Core Specialist I can only speak a little to you about my experience.  At first when I started MNRI I expected to see consistent improvement and felt discouraged when it was two steps forward and one step back.  Now I understand better that integrating is much more of a process than an event.  On the days he is stressed or wanting to hurry my son will revert back to some behaviors.  We have been doing this for a few months shy of 2 yrs.  So now when he regresses it is not to

the same degree that it was during the first year.  I have learned to watch the level of his reflex integration and I can tell his level of stress, fatigue or excitement.  If he is coming down with a sickness or didn't sleep well (or stayed up late reading) he will struggle more.  So we step up the reflexes or Tactile as I can or I just give  him a little more grace.  So your child doing the toe walking sometimes and sometimes not doesn't sound out of the norm from my experience.  It sounds like progress...

But definitely work with a Core Specialist if you can or take more classes.  California has a lot going on. 

Hi Everyone,My name is Hela and I have been in the group for more than a year reading daily posts , I have been doing reflex from August of last year with laser and have started MNRI this year and have seen Dr Masgatuva for my daughter assessment in April and been doing my home program reguraly , my daughter is 7 with Autism, her communication is still delayed and she has some of the main reflex non integrated.

my questions to all are the following:1- My daughter has been toewalking for years, none of the diet nor the supplement or the OT or Handle had helped her, our MNRI home program include the Foot TG 5 days a week, I have been doing it daily twice a day

and she it seems that she is getting of her toe better specially when she is outside but in the house when she is bearfooted she is toewalking again and when she is detoxing usually it is very severe.I am trying to get feedback from other parents and consultant on this, what other reflex are important other than the FTG, I do undestand that the foot TG we are trying to relax the muscle but how about the main reason why the child is toewalking, I beleive it is a protection from stimulus or a fear , is there visual and Auditory reflexes that have a role to help with the toewalking.

everyone opinion is very important to me and would love to hear from other parents and core specialist.Her Automatic gait reflex is in normal range,all the other reflex in the home program are getting very nicely improving, only

the toe walking is what make me wonder what else I am missing.There is a course that Dr Masgatuva is teaching in Belgium in November that address the visual and Auditory reflex, it mention the FTG also, so I am trying to see if there is a connection , you guys core specialist might know the answer????

my second question is there a core specialist in Southern California that we can work with ...the majority of the specialist are located in N. California and I have traveled to NC but would like to find out if there is support here in Southern California.

Thank you so much for the feedback is greatly appreciated!!!Sincerely,HelaMessages in this topic (1)

------------------------------------------------------------------------

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My thought is to pay more attention to Fear Paralysis tapping protocol. If freeze is hyperactive, it can keep a lot of reflexes from developing, especially fight / flight tendon reflexes.

On Tue, Aug 9, 2011 at 6:13 AM, Janet Mc <janetomcdonald@...> wrote:

 

Hela~You might consider an intensive (1 or multiple days) with a core specialist you bring to your area.  Yes, the V/A protocol is informative as it provides cranial symmetry and systemic calm.All best,

Janet

Core SpecialistFacial Reflexes  and Tactile Integration InstructorOn Tue, Aug 9, 2011 at 8:34 AM, Kayte <k_sisler@...> wrote:

 

Not being anywhere near a Core Specialist I can only speak a little to you about my experience.  At first when I started MNRI I expected to see consistent improvement and felt discouraged when it was two steps forward and one step back.  Now I understand better that integrating is much more of a process than an event.  On the days he is stressed or wanting to hurry my son will revert back to some behaviors.  We have been doing this for a few months shy of 2 yrs.  So now when he regresses it is not to

the same degree that it was during the first year.  I have learned to watch the level of his reflex integration and I can tell his level of stress, fatigue or excitement.  If he is coming down with a sickness or didn't sleep well (or stayed up late reading) he will struggle more.  So we step up the reflexes or Tactile as I can or I just give  him a little more grace.  So your child doing the toe walking sometimes and sometimes not doesn't sound out of the norm from my experience.  It sounds like progress...

But definitely work with a Core Specialist if you can or take more classes.  California has a lot going on. 

Hi Everyone,My name is Hela and I have been in the group for more than a year reading daily posts , I have been doing reflex from August of last year with laser and have started MNRI this year and have seen Dr Masgatuva for my daughter assessment in April and been doing my home program reguraly , my daughter is 7 with Autism, her communication is still delayed and she has some of the main reflex non integrated.

my questions to all are the following:1- My daughter has been toewalking for years, none of the diet nor the supplement or the OT or Handle had helped her, our MNRI home program include the Foot TG 5 days a week, I have been doing it daily twice a day

and she it seems that she is getting of her toe better specially when she is outside but in the house when she is bearfooted she is toewalking again and when she is detoxing usually it is very severe.I am trying to get feedback from other parents and consultant on this, what other reflex are important other than the FTG, I do undestand that the foot TG we are trying to relax the muscle but how about the main reason why the child is toewalking, I beleive it is a protection from stimulus or a fear , is there visual and Auditory reflexes that have a role to help with the toewalking.

everyone opinion is very important to me and would love to hear from other parents and core specialist.Her Automatic gait reflex is in normal range,all the other reflex in the home program are getting very nicely improving, only

the toe walking is what make me wonder what else I am missing.There is a course that Dr Masgatuva is teaching in Belgium in November that address the visual and Auditory reflex, it mention the FTG also, so I am trying to see if there is a connection , you guys core specialist might know the answer????

my second question is there a core specialist in Southern California that we can work with ...the majority of the specialist are located in N. California and I have traveled to NC but would like to find out if there is support here in Southern California.

Thank you so much for the feedback is greatly appreciated!!!Sincerely,HelaMessages in this topic (1)

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