Re: Digest Number 175

[Guest guest]

In a message dated 11/22/1999 11:29:26 PM Pacific Standard Time,

candidiasisonelist writes:

<< Maggi >>

Hi, it sounds like you haven't stayed on the Diflucan long enough to me, try

it for a few weeks rather than days..... >>

The only reason I didn't was because of the Hep C. Diflucan is bad for the

liver. I was too chicken to stay on it long. I believe I took it for 3

days. I tried this 2 times. Thanks!

Maggi

[Guest guest]

In a message dated 11/22/1999 11:29:26 PM Pacific Standard Time,

candidiasisonelist writes:

<< Look up vinegar on the net. I was told that it was bad for yeast, but I

was

at my wits end. I looked it up and it said that it killed yeast and fungus.

So I thought well it might work. >>

Thanks Myra. I actually have tried the vinegar. The only way I could drink

it was in Cranberry juice. It killed the taste. I took bath in it also but

it dried my skin out. I may try the feet soaking though. Sounds good to me.

maggi

[Guest guest]

In a message dated 11/22/1999 11:29:26 PM Pacific Standard Time,

candidiasisonelist writes:

<< << I was on a similar diet this summer (didn't help me so I switched to my

herbal product program) - but as for alcohol - anything that is fermented is

out - and that even includes non-alcoholic items that are fermented such as

cider or rootbeer!!!

However, vodka is distilled.. >>

Well, I don't touch the stuff. It can't be helpful. >>

I really can't drink wth Hep c so that's not a concern. When I do which is

very rare, it's a glass of red wine. I also love mushrooms. I'll quit

eating those for awhile. I didn't know that. But somethins is messing with

my system and I think it's candida. Maybe I'm wrong but I sure fit the

criteria. You know those Rolo chocolates. I ate one one day, nothing

happened. The another day I ate on and immediately began itching. That's

what I mean by very strange sensitivities to things. One night I made a

meatlof and mashed taters and veggies. I was itching like mad from it right

after I ate. I put Lipton oinion soup mix in it. Preservatives maybe? But

I've never had these problems. So I was thinking candida. It's the only

thing I could come up with. I guess I could be wrong.

Maggi

[Guest guest]

In a message dated 11/23/99 7:28:52 AM Pacific Standard Time,

M487@... writes:

<< The only reason I didn't was because of the Hep C. Diflucan is bad for

the

liver. I was too chicken to stay on it long. I believe I took it for 3

days. I tried this 2 times. Thanks!

Maggi >>

Ok, I understand....but I believe you need to be on it longer than that for

it to work

[Guest guest]

In a message dated 11/23/99 7:40:07 AM Pacific Standard Time,

M487@... writes:

<< put Lipton oinion soup mix in it. Preservatives maybe? But

I've never had these problems. So I was thinking candida. It's the only

thing I could come up with. I guess I could be wrong.

Maggi >>

Lipton Onion Soup Mix contains yeast

[Guest guest]

In a message dated 3/9/00 5:07:11 AM Central Standard Time,

onelist writes:

<<

I hope this isn't against the rules, but arcamax has frequent offers of

programs that would probably be helpful to you. They send the software free

for a s & h charge of $7.95 in US, a little more in Canada. I hve found

some

very good things there for my daughter who plans to home school and many

other interesting offers for me and for gifts. Address is: www.arcamax.com

Hope this helps.

Love and light, >>

;

Hi, I was looking at the software programs, which one are you talking about?

Which one did you get?

Thanks Much

Debi

[Guest guest]

Bev, the lye will heat up on its own, to about 200 or so degree. Youll need

to let that cool down.

Shaye

The Soap Shack

http://www.mysoapshack.com

************

Once the lye is all added, do I

need to heat it also in another stainless steel

container on the stove (or do it in the microwave in

glass), or does the reaction take it to 120 deg.

without additional heat?

[Guest guest]

> Could anyone give me any information on starting up a Jericho-type school

> program? Dr. Carbone gave us the name of a Randy Wells in Texas to

contact.

> Does anyone have her email address? We are very frustrated up here in

> Massachusetts as the public schools seem to have NO IDEA whatsoever of how

> to teach our children. Do you think we could get this type of program

> implemented within the public schools or would we need to do this

completely

> privately? If anyone has any information to share, please let me know.

I think many of us would like this information. Please post any advice to the

list. I would like to do this in Ohio also. Thankyou

[Guest guest]

In a message dated 5/16/00 10:41:19 PM Pacific Daylight Time,

egroups writes:

<< ........when you say ADHD are you talking about Attention

deficit/Hyperactive disorder? Risperdal won't help that. >>

Margaret:

Really??? Well, he didn't sleep all night and was an early riser....it seems

to be helping there....I also read here on the list that it helped some of

the kids with their grinding and growling noises and repetitive

behaviors......

And yes, I do mean Attention Deficit/Hyperactivity Disorder. Why would the

doc prescribe this then, when he knows has ADHD? How do you know it

won't work for that?

[Guest guest]

Donna,

What is floortime?

Lori

[Guest guest]

,

I have so much info. Their web site is: www.unc.edu/depts/teacch

Lori

[Guest guest]

IU stands for international units, and mcg stands for micrograms.

Normally, to convert these, 1,000,000 international units would be

100,000 micrograms, or 1/10 of the IU. This is not always true depending

on the material you are trying to compare.

[Guest guest]

Just a FYI,

Just ran my wife's 1 month end of therapy labs. She ia 1b, and had

to decrease her ribaviran to 600mg/day. But, while her labs were always

low, she was able to complete 49 weeks.

Do not have the viral load back yet, but, the rest of her blood

tests are returning to normal. Her liver function tests were always

normal while on therapy, but her " complete blood counts " were always

very low and she was anemic. Also, her thyroid panels which began to

rise have dropped back to almost full normal.

She still has some fatigue, and occasional muscle aches, but, they

are slowly going away also. So, like many, we sit, wait and hope that

her viral load remains undetectable. I am only sending this to offer

encouragement to many others. Marty

[Guest guest]

Marty we will keep her in our prayers

alley/

ICQ 12631861

alleypat@...

http://www.flash.net/~alleypat

[Guest guest]

Marty:

Congratulations and hope the viral load comes back normal and stays that

way. It was a long haul but maybe it will be worth it.

Suzy

From: " byteme " <byteme@...>

Reply-Hepatitis Cegroups

Hepatitis Cegroups

Subject: Re: Digest Number 175

Date: Mon, 05 Jun 2000 21:35:44 -0400

Just a FYI,

Just ran my wife's 1 month end of therapy labs. She ia 1b, and had

to decrease her ribaviran to 600mg/day. But, while her labs were always

low, she was able to complete 49 weeks.

Do not have the viral load back yet, but, the rest of her blood

tests are returning to normal. Her liver function tests were always

normal while on therapy, but her " complete blood counts " were always

very low and she was anemic. Also, her thyroid panels which began to

rise have dropped back to almost full normal.

She still has some fatigue, and occasional muscle aches, but, they

are slowly going away also. So, like many, we sit, wait and hope that

her viral load remains undetectable. I am only sending this to offer

encouragement to many others. Marty

________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com

[Guest guest]

Marty:

Congratulations and hope the viral load comes back normal and stays that

way. It was a long haul but maybe it will be worth it.

Suzy

From: " byteme " <byteme@...>

Reply-Hepatitis Cegroups

Hepatitis Cegroups

Subject: Re: Digest Number 175

Date: Mon, 05 Jun 2000 21:35:44 -0400

Just a FYI,

Just ran my wife's 1 month end of therapy labs. She ia 1b, and had

to decrease her ribaviran to 600mg/day. But, while her labs were always

low, she was able to complete 49 weeks.

Do not have the viral load back yet, but, the rest of her blood

tests are returning to normal. Her liver function tests were always

normal while on therapy, but her " complete blood counts " were always

very low and she was anemic. Also, her thyroid panels which began to

rise have dropped back to almost full normal.

She still has some fatigue, and occasional muscle aches, but, they

are slowly going away also. So, like many, we sit, wait and hope that

her viral load remains undetectable. I am only sending this to offer

encouragement to many others. Marty

________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com

[Guest guest]

Wayne, that is a very encouraging post. I also went through a

depression while using the electrification unit every day. It wasn't

real, real bad, but wasn't any fun either. It didn't last long, maybe a

couple of weeks, and I've been feeling terrific for a long time now.

Congratulations on your good results. pj

egroups wrote:

>

>

> There is 1 message in this issue.

>

> Topics in this digest:

>

> 1. Beck protocol progress

> From: ph Dunne <driftin3@...>

>

> ________________________________________________________________________

> ________________________________________________________________________

>

> Message: 1

> Date: Fri, 20 Oct 2000 14:32:49 -0400

> From: ph Dunne <driftin3@...>

> Subject: Beck protocol progress

>

> Hello List,

> I just found this group and am happy that there's a forum like this to

> discuss the Beck program. I use the silver pulser from Sota and I have a

> magnetic pulser. I started using these units about two months ago

> working my way up to 2 hours a day. I also make my own colloidal silver.

> I discontinued taking all vitamins while doing this so it wouldn't

> intefere with my progress. The only herx I got in the beginning was a

> migraine for a few days because I had to give up my coffee. After a few

> weeks I got an unusual reaction. I became very depressed and wanted to

> discontinue the treatment but I didn't. I made the right decision

> because it only lasted for a week or so but it was very difficult to stay

> on it at that time. I've been taking colloidal silver for a year for

> Lyme's and it's helped a little. It wasn't until now that I notice a

> remarkable difference. I am sleeping better, the joint and muscle pain

> is gone and the fatigue has disappeared (along with the depression). I

> will continue with this for a few more weeks and then use it for

> maintenance whenever I feel it's needed. I will post my progress

> whenever I get a chance.

> I think it would benefit someone in the future who is looking for

> information on this treatment to have information like this available to

> them - good and bad reactions. Anyone else?

> Wayne

>

> ________________________________________________________________

> YOU'RE PAYING TOO MUCH FOR THE INTERNET!

> Juno now offers FREE Internet Access!

> Try it today - there's no risk! For your FREE software, visit:

> http://dl.www.juno.com/get/tagj.

>

> ________________________________________________________________________

> ________________________________________________________________________

[Guest guest]

>Speaking of breakfast...Is anyone else out there into

>juicing?

>

>I've been juicing for a year and a half now (that is

>what got me started trying to be healthy) and I love

>it. I drink a juice mixture of carrots, parsley,

>apple, orange, zuccini, beet, tomato, boccoli,

>wheatgrass, (and whatever other veggies happen to be

>in the fridge) then I blend it all together with plain

>yogurt and banana for texture. I end up with about 12

>ounces.

Watch out for the fruit juices. Too much raises GI levels and also have

too many calories from all the sugars. For orange for example, the fruit is

better. Veggie juices are great tho. For a shortcut for us lazy people try

V-8 juice which I myself use regularly and often in cooking instead of

tomato sauce (more veggies in it).

[Guest guest]

,

What the heck is this? Looks like a scam

Janet

[Guest guest]

Yes, I guess.

I have instituted a policy of me approving everyone

who gets on the list. This person may have gotten in

as a member before (non-members cannot post to the

list).

I've deleted this person, but their e-mail may have

been hijacked.

Computer spammers are very creative.

Thanks for letting me know.

--- Sampleplea@... wrote:

> ,

> What the heck is this? Looks like a scam

> Janet

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

[Guest guest]

Why in the world would you " stop " therapy when given oxygen. If this

is for your study, you are indeed not using your own child!!! Do you

really believe you can fix the brain without normalizing the body

system as well. If we had all the time in the world to do one than

the other fine; however, this is our children's lives we are talking

about. Let's do what works, give the brain some oxygen, work the

neuromuscular system, and organize some brain cells. NO I AM NOT A

NEUROLOGIST, I AM A PARENT!!

I will continue to be the best advocate I can be for my child...and

remain open minded!

=====

Prayers of Healing,

Lynette LaScala-Kropf (Cody's Mom)

" Never doubt that a small group of committed people can change the world.

Indeed, it is the only thing that ever has. " ~ Margaret Mead

And we will...thanks for caring.

__________________________________________________

[Guest guest]

Lynette,

I trust your email was addressing Dr. ' note on the McGill study......

First, you are speaking to the choir, here! And, note that Dr. is

exceptionally dedicated to caring for CP/TBI children in the UK through the

100 or so HBOT centers that he manages.

Also, note that the McGill study was ORIGINALLY DESIGNED by Dr. Marois, et

al, to learn what effect HBOT has on kids like ours and to finalize that

issue in medical knowledge in order to get HBOT reimbursed. HOWEVER, the

Quebec government modified the research protocol (which they had the

authority to do so because they wrote the check). From there, the biased

intentions of that government has become very transparent and well known

(if not hideous and criminal).

With that said, it was not a bad research rational to implement the HBOT

study without the children having physical therapies AT THAT

TIME. Research knowledge must be foundational and be used to build

on. Today, we need more research to determine how to better discern and

classify injuries in order to optimize the returns from HBOT and PT's.

On a personal basis, we all agree on your statements! The underlying logic

for CP children is so overwhelming.... a neonate's brain in fully

underdeveloped in regards to patterns, pathways, and supporting

tissues. We cannot expect to " wake up " those neurons and that the child to

speak that day! His/her regenerated brain tissue has to " learn " and

" develop " just like they were a newborn. Today, we are just scratching the

surface on what learning is in the brain. However, brain injuries are so

complex, those ancillary physical therapies (as well as HBOT) have to be

individualized.

But, Dr. ' point (and part of my point) is that HBOT alone can remove

some impediments causing disabilities. This enables the patient to attain

higher returns from the PT with less time, effort and

frustration. Therefore, the key thing is to treat the injury first. (to

those who still disagree, when do you give PT's to a person with a broken

leg? Before the leg has healed, or after the healing treatment (cast)?)

This is not to say don't give physical therapies while giving HBOT - I

believe just the opposite. However, because all of us parents have to pay

for our children's medical care and therapies out of pocket, the biggest

bang for the buck is HBOT first. Then, the physical therapies has more

brain power to work with, and fewer disabilities.

Warm Regards,

Ed Nemeth

At 01:37 PM 5/20/2002 -0700, you wrote:

>Why in the world would you " stop " therapy when given oxygen. If this

>is for your study, you are indeed not using your own child!!! Do you

>really believe you can fix the brain without normalizing the body

>system as well. If we had all the time in the world to do one than

>the other fine; however, this is our children's lives we are talking

>about. Let's do what works, give the brain some oxygen, work the

>neuromuscular system, and organize some brain cells. NO I AM NOT A

>NEUROLOGIST, I AM A PARENT!!

>I will continue to be the best advocate I can be for my child...and

>remain open minded!

>

>=====

>Prayers of Healing,

>Lynette LaScala-Kropf (Cody's Mom)

>

>

> " Never doubt that a small group of committed people can change the

>world. Indeed, it is the only thing that ever has. " ~ Margaret Mead

>

>And we will...thanks for caring.

>

>__________________________________________________

>

[Guest guest]

Philip writes:

Dear

Thank you for your comments and the details of the 3 year old who has

improved so much with HDOT (High Dosage OXygen Treatment). However as you

have realised the most benefit will derive when HDOT is routinely used for

brain/spinal cord injuries. This requires a massive change in the mind set of

physicians.

Best wishes

Philip

Dear Philip

Since I've not had time to read the SCI results yet would you think that an

incomplete spinal cord injury where the patient has walked twice before may

possibly help get this patient up again after 16 years? Would the HDOT

treatments be of any benefit because the scar tissue compressed the original

injury but lack of health insurance stopped all the PT/OT that kept this

person up? The removal of the scar tissue compressing the spinal cord caused

the 2nd surgery. With intermittent therapies the patient seems to respond

positively. Is there a potential here for HDOT or is it to late? Thank you.

Kessler-

[Guest guest]

Jesus 'healed using cannabis'

Duncan in Los Angeles

Monday January 6, 2003

The Guardian

Jesus was almost certainly a cannabis user and an early proponent of the

medicinal properties of the drug, according to a study of scriptural texts

published this month. The study suggests that Jesus and his disciples used

the drug to carry out miraculous healings.

The anointing oil used by Jesus and his disciples contained an ingredient

called kaneh-bosem which has since been identified as cannabis extract,

according to an article by in the drugs magazine, High Times,

entitled Was Jesus a Stoner? The incense used by Jesus in ceremonies also

contained a cannabis extract, suggests Mr , who quotes scholars to

back his claims.

" There can be little doubt about a role for cannabis in Judaic religion, "

Carl Ruck, professor of classical mythology at Boston University said.

Referring to the existence of cannabis in anointing oils used in ceremonies,

he added: " Obviously the easy availability and long-established tradition of

cannabis in early Judaism... would inevitably have included it in the

[Christian] mixtures. "

Mr suggests those anointed with the oils used by Jesus were

" literally drenched in this potent mixture... Although most modern people

choose to smoke or eat pot, when its active ingredients are transferred into

an oil-based carrier, it can also be absorbed through the skin " .

Quoting the New Testament, Mr argues that Jesus anointed his

disciples with the oil and encouraged them to do the same with other

followers. This could have been responsible for healing eye and skin

diseases referred to in the Gospels.

" If cannabis was one of the main ingredients of the ancient anointing oil...

and receiving this oil is what made Jesus the Christ and his followers

Christians, then persecuting those who use cannabis could be considered

anti-Christ, " Mr concludes.

Special report

Drugs in Britain

Imagine

Peace Omi

_________________________________________________________________

STOP MORE SPAM with the new MSN 8 and get 2 months FREE*

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[Guest guest]

At 07:29 PM 1/16/03 -0600, you wrote:

>Jesus 'healed using cannabis'

>

>Duncan in Los Angeles

>Monday January 6, 2003

>The Guardian

I've seen this article and I have to say I find it fairly laughable. The

only mention of anointing oil in the NT are the paragraphs I quoted in the

email responding to the Religion and Scent questions -- and that clearly

names spikenard as the oil. (Furthermore, it wasn't part of Jesus' healing

practice -- it was a follower of Jesus named of Bethany who used the

oil on Jesus, to the consternation of Judas Iscariot, for one, btw). This

was not an everyday occurrence. Anyway, that oil is clearly named as

spikenard. The article also claims that cannabis oil was often used in

Jewish practice -- if so, why wouldn't its " healing " effects be known

rather than construed as miracles?

Anybody on this list want to speculate on whether or not spikenard

contained cannabis?

Janine