Progress report

[Guest guest]

http://www.risingstarlc.com/schulze5.htm

Here is the order site for Dr Schulzé Products.

Christel

[Guest guest]

Were you able to purchase his products via the web or from a Health Food Store?

feathermist@... wrote:

Hi groupMy herbal Dr gave me the OK to use Dr. Schulze's formulas. I am sohappy because I am learning about herbs while fixing my problem.Thank you all. The things I've been using so far are helping a littlealso.Feather :)Subscription email: mailto:bowel cleanse-subscribeegroups

[Guest guest]

Hi, I was just gonna share this news with the group and saw your

message.

I went to the site that's linked on one of Dr. Shulze's pages, it

goes to a place in Florida called Southern Botanicals. I ordered from

there. I am so happy that I'm taking an active role in my recovery,

and learning too. I didn't know if any stores would have it, and

didn't know when I'd get the chance to check them out, and I want them

as soon as possible. When I remember, I'm gonna ask my Dr. about the

superfood, too.

Feather

-- In bowel cleanse@y..., Lane <Engle8@y...> wrote:

> Were you able to purchase his products via the web or from a

Health Food Store?

>

>

>

> feathermist@y... wrote:

> Hi group

>

> My herbal Dr gave me the OK to use Dr. Schulze's formulas. I am so

> happy because I am learning about herbs while fixing my problem.

> Thank you all. The things I've been using so far are helping a

little

> also.

>

> Feather

>

>

>

>

>

>

>

[Guest guest]

Great News , long may it continue!

Mx

[Guest guest]

Hi Mandy

Pep is short for Peptizyde, a high protease enzymes for gluten and casein

from

www.houstonni.com

HTH

Mandi in UK

> Can I ask what pep is? sorry I'm new to this.

> Mandy

>

>

[Guest guest]

Can I ask what pep is? sorry I'm new to this.

Mandy

[Guest guest]

This is good news - there you go, if at first blah blah!

Haven;t investigated it any further myself - up to my ears in annual review

and fighting for speech therapy

Catch you later

MAndi in Poole

[Guest guest]

Hi Ted,

Sounds like you're doing great. I'm just curious about one thing you said,

that you had to 'work out the best place to hold the handset' when you used

the phone. What is that about? Don't you just hold the phone to your ear

like a hearing person? Do you have to look for a 'sweet spot'?

I'm on the phone all day at work, and on my cell for pleasure, too. I have

a t-mic, and just use the phone like anybody else. I used to have to find a

sweet spot when i had aids.

Binns

----Original Message Follows----

From: " Ted F. " <ted.fletcher@...>

Reply-

Subject: Progress Report

Date: Fri, 12 May 2006 17:35:15 -0000

Not sure if I posted this:

After one week of using my C.I. my comprehension was already quite

good. I had my main programme on Pr1 and the same programme in the

Pr2 slot, but with noise suppression, which is excellent in the car

and the same programme again in slot 3 with the Beam feature. I have

only been in a noisy club once since switch-on and the beam feature

worked Ok, better than my two power hearing aids did, already. I had

a different programme in slot 4. After my first mapping on May 3rd, I

thought that I was worse off, but it must have been my brain getting

used to the new map, it took a couple of days and then it was OK.

I went for my second mapping this week and Jane ran some tests. With

my implant and my hearing aid, I scored 100% on the sentences and

about 90% on the single words. Previously with my 2 hearing aids I

had scored 60%. With the implant only, I scored 97% on the sentences,

I just got one word wrong and I scored about 70% on the single words.

Previously, with my left hearing aid only, (that was the ear that was

implanted), I scored 20%. So I am doing amazingly well considering

that its only been just over a fortnight since activation.

The hearing aid in the other ear IS beneficial to me, as it gives me

a better, more rounded sound. Jane also tested me with the phone, I

used the t-switch. She went into another room and buzzed the phone. I

didnt start off too well, because I had to work out the best place to

hold the handset, but once I found the right place, I heard most of

the sentences she asked me to repeat. But I didnt rush out to start

using the phone, theres plenty of time for that. I lack confidence on

the phone, because I havent been able to use it very successfully for

many years. But I will start to practise with it over the next few

weeks.

I'm sorry if my journey disheartens anyone, because of the way things

have happened for me so quickly, but they do tell us that we are all

different. I'm just one of the lucky ones that got some instant use

from their C.I.

Anything is possible.

Ted F.

[Guest guest]

>

> Hi Ted,

> Sounds like you're doing great. I'm just curious about one thing

> you said, that you had to 'work out the best place to hold the

> handset' when you used the phone. What is that about? Don't you

> just hold the phone to your ear like a hearing person? Do you have

> to look for a 'sweet spot'?

>

Hello

I am right handed and I had my left ear implanted and its natural for

me to pick up the phone with my left hand. I suppose I was trying to

locate the microphones on the C.I.

> I'm on the phone all day at work, and on my cell for pleasure,

> too. I have a t-mic, and just use the phone like anybody else. I

> used to have to find a sweet spot when i had aids.

It might be a stupid question, but I'll still ask it :-)

Why would I hold the phone to a deaf ear? The BTE processor is on top

of my ear, would the sound from the phone, carry to the mics?

Ted F.

>

> Binns

>

[Guest guest]

Ok, that's the difference in processors, then. This isn't bashing, it's

explaining. I have a t-mic. It hangs down over the ear, attached to the

top of the processor, and stops at the ear canal. (which, as you say, is

deaf, but that's not how it works) The mic captures the sound within the

bowl of the ear, and transports it to the processor and the implant. The

mic is attached to the processor. That's why I can use the phone normally.

----Original Message Follows----

From: " Ted F. " <ted.fletcher@...>

Reply-

Subject: Re: Progress Report

Date: Sat, 13 May 2006 02:57:06 -0000

>

> Hi Ted,

> Sounds like you're doing great. I'm just curious about one thing

> you said, that you had to 'work out the best place to hold the

> handset' when you used the phone. What is that about? Don't you

> just hold the phone to your ear like a hearing person? Do you have

> to look for a 'sweet spot'?

>

Hello

I am right handed and I had my left ear implanted and its natural for

me to pick up the phone with my left hand. I suppose I was trying to

locate the microphones on the C.I.

> I'm on the phone all day at work, and on my cell for pleasure,

> too. I have a t-mic, and just use the phone like anybody else. I

> used to have to find a sweet spot when i had aids.

It might be a stupid question, but I'll still ask it :-)

Why would I hold the phone to a deaf ear? The BTE processor is on top

of my ear, would the sound from the phone, carry to the mics?

Ted F.

>

> Binns

>

[Guest guest]

>

> Hi Ted,

> Sounds like you're doing great. I'm just curious about one thing

> you said, that you had to 'work out the best place to hold the

> handset' when you used the phone. What is that about? Don't you

> just hold the phone to your ear like a hearing person? Do you have

> to look for a 'sweet spot'?

I am right handed and its natural for me to pick up, or use the phone

with my left hand. I am also used to wearing BTE hearing aids, where

the microphones are up on top of the ears. I assumed that the C.I.

microphones are also up on top of my ears, so thats the area that I

try to find the right spot to hold the receiver/handset. It didnt

make any sense to me, to hold the phone to a deaf ear. If anyone can

give me any simple tips that work well when using the phone, please

fire away. This is still new territory for me. I never had much

success on the phones with hearing aids.

Ted F.

>

> I'm on the phone all day at work, and on my cell for pleasure,

> too. I have a t-mic, and just use the phone like anybody else. I

> used to have to find a sweet spot when i had aids.

>

> Binns

>

[Guest guest]

Bee,

I would be happy to send you my outstanding 4 month progress report. I will

put something together this week-end. I am eternally grateful to you, I have

tried every other program out there for the past five years and nothing has

gotten rid of this beast for me except your diet, thank-you.

I am curious, how did you know or determine you actually had candida in the

80's with no internet to do all the necessary research and without support

from the medical community as well? I can't imagine what you went through,

but you my friend are a pioneer, and I am sure glad to know you.

Given any more thought to going on tour?

Hugs back at ya

Shirley

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

>Wow, I'm so happy to hear it works too.

>May I put that in our Success Story folder? Would you put together

>info from your other post plus this one, and send it to me at

>beewilder@... ? Thanks a whole bunch.

>

>Hugs, Bee

[Guest guest]

>

> Bee,> I would be happy to send you my outstanding 4 month progress

report. I will put something together this week-end.

==>Thanks so much Shirley! I'll have more time on the weekend too.

> I am eternally grateful to you, I have tried every other program

out there for the past five years and nothing has gotten rid of this

beast for me except your diet, thank-you. I am curious, how did you

know or determine you actually had candida in the 80's with no

internet to do all the necessary research and without support

> from the medical community as well?

==>I was fortunate that my medical doctor in Toronto, Ontario (Dr.

Kathleen Kerr) read about Dr. Crook's discovery, and his

book The Yeast Connection, and she called me and said " I think there

is a solution to your problems. " I made an appointment and never

looked back. Dr. Kerr gave me many articles, and then when I moved

back to Edmonton, Alberta I started a Candida Support Group. I was

connected with the holistic practitioners in the City, i.e.

naturpaths, chiropractors, herbalists, etc. We met once a month and

had different speakers. I also had a telephone hotline in my

apartment. My name and number was listed with all of the health

food stores. We had a medical doctor in Edmonton too, Dr. Tris

Trethart - he was terrific! So I wrote my first article then, and

had many copies printed, giving them out to everyone, mailing them

to family and friends, etc. I still have an original copy of it.

>I can't imagine what you went through, but you my friend are a

pioneer, and I am sure glad to know you.

==>Thanks bunches and heaps. I'm glad to know you too Shirley.

> Given any more thought to going on tour?

==>Not lately. We are going to Wisconsin to see my parents June

17th-25th - he is 86 years old and ailing, so I want to deal with

that first before getting into too many commitments.

> Hugs back at ya

Tanks a lot. ((((Hugs to you too)))Be

[Guest guest]

Gima offices are closed for national holidays on 2nd June. Personally I will be

on holiday from 31st May to 04th June. Only from 31st May to 01st June please

address your inquiry to export@....

[Guest guest]

Dear Leo,

I feel for you but I think you are missing an important point. The

lethargy/depression/desire to give up and not fight is a symptom of mercury

poisening. Understand? You are fighting the effects of the mercury when you

suggest treatments. Go smaller. Start by trying to bring up their general

health with vitamins, diet, stuff like that. Little by little. Best of luck!

Leo <organicboy999@...> wrote: Hi friends.

I thought it was time for an update...some of you will remember me.

I have rapidely come out of the worst of the treatment and I am much

better. I still must complete another 6 months or so of the

treatment and I look forward to every round of chelation.

I worry though. Not for me because I am fine. It is my family ,

their mercury exposure and their incessant denial. Its ironic

because they wont pay any attention to what I say about mercury and

simply dont want to pay any attention, but I have my father on

selenium and it seems to me that I could get him on alot more stuff.

The question is what.

What i mean is what can you do for someone who is so mercury

polluted that they would rather live out their days without doing

what should be done (removal of fillings and chelation).There should

be a half way house for people who are just too far down the road to

go through the whole process of treatment.

I know this site is for kids and dont let me detract from that , but

it is also the epicentre of mercury treatment. No where else can one

find such a thing.

Anyway. In the meantime I guess it is up to me to scrape together as

much info as I can regarding the treatment of symptoms of mercury

and the altogether easing of the stresses caused by mercury without

going through the treatment. Of course I know that this will never

be a cure, but to alleviate the symptoms of the suffering and

possibly to have more " believers " would help us fundementally over

come this cover up and dare I say it, murder.

My heart reaches out to you all out there. If you are losing faith

then DO NOT. The Cutler protocol is bullet proof and works. I put my

life on it now.

=======================================================

[Guest guest]

Hey Leo,

So wonderful to hear from you!! It is great to get some good news!!

Don't worry about your family to much....usually those are the hardest to

convince! Just keep going the direction your going and let them see for

themselves!! Sometimes that says more then anything else.

Again, so good to hear from you!

Keep us posted,

God Bless,

Debbie

Leo <organicboy999@...> wrote: Hi friends.

I thought it was time for an update...some of you will remember me.

I have rapidely come out of the worst of the treatment and I am much

better. I still must complete another 6 months or so of the

treatment and I look forward to every round of chelation.

I worry though. Not for me because I am fine. It is my family ,

their mercury exposure and their incessant denial. Its ironic

because they wont pay any attention to what I say about mercury and

simply dont want to pay any attention, but I have my father on

selenium and it seems to me that I could get him on alot more stuff.

The question is what.

What i mean is what can you do for someone who is so mercury

polluted that they would rather live out their days without doing

what should be done (removal of fillings and chelation).There should

be a half way house for people who are just too far down the road to

go through the whole process of treatment.

I know this site is for kids and dont let me detract from that , but

it is also the epicentre of mercury treatment. No where else can one

find such a thing.

Anyway. In the meantime I guess it is up to me to scrape together as

much info as I can regarding the treatment of symptoms of mercury

and the altogether easing of the stresses caused by mercury without

going through the treatment. Of course I know that this will never

be a cure, but to alleviate the symptoms of the suffering and

possibly to have more " believers " would help us fundementally over

come this cover up and dare I say it, murder.

My heart reaches out to you all out there. If you are losing faith

then DO NOT. The Cutler protocol is bullet proof and works. I put my

life on it now.

=======================================================

[Guest guest]

>

> Hi Bee and group I haven't posted in a while...and have actually

not been reading a great deal here. Been out of town etc. While I

was in TX I visited my doctors and a full screen of lab tests were

performed on me. I had been having some irregular heartbeats,

shortness of breath, falling hair and a few other new symptoms since

my husband left to work out of state for a few months.

>

> To our surprise my tests were remarkable because everything had

> improved dramatically. No more need for thyroid medication. No

> anemia. No hormone irregularities. Cholesterol was great and the

> good cholesterol was very high..so much so that the doctor went

> out of her way to comment on it.

>

> We discussed this diet program and how eating good fats may have

> a lot to do with those results. The doctor was interested but not

un-> familiar with coconut oil and good fats.

>

> The symptoms that troubled me all summer have almost all disappeared

> now..except just now and then. Bee I thought you'd enjoy this news.

Marge, it's wonderful to hear from you with such terrific news!

Thank you so very much for letting us know. I am so very happy for

you my friend. Yippee! Hooray! ! May I please post this

message in our Success Stories Folder?

Luv & Hugs, Bee

P.S. Don't be a stranger Marge. We can use your help handling all of

our messages these days. Others need your support.

[Guest guest]

sherry, im following your lead. we all get alittle lazy with the food we eat and

im one for sure.congrats on the 7 pounds. since your post ive lost 3 pounds. and

i walked my dog yesterday! only a half mile but it had 2 hills! i just took my

time. abby enjoyed it and i did have some pain but the mental burst was sure

worth it. also ive been fixing veggies in a pan with alittle olive oil and sea

salt on low and the results are great. my husband thinks im doing something

gourmet! im cleaning out fridge and freezer. im going to take more walks.

there is also a program out now that uses the rules 35 grams of fiber per day

is equal to loosing 310 calories or walking 1 mile. and lots of water. and the

fiber helps detoxify your body. makes sense to me. i heard a quote awhile back "

if we ate it 100 years ago then it is ok to eat now " ......casey

" S. Zorzi " <szorzi_1999@...> wrote:

I'm determined to lose weight in an effort to help my liver (which has

fatty deposits) so that it can tolerate the miracle-meds I need to

treat my PA. See below for original post.

After 10 days of paying close attention to my diet, I've lost 7

pounds. I imagine this is mostly fluid and don't expect to see that

kind of loss anymore, but it's nice to feel a little lighter. I've

upped my portions of fruits/veggies to 10-12 per day. Surprisingly,

I've had no gas in spite of all the veggies I'm eating. No hunger

either since I'm eating so often.

I've discovered a couple of great new recipes, too! (I love to cook!)

regards,

sherry z

[Guest guest]

Way to go, Casey! Give mashed cauliflower a try in place of mashed

potatoes. I steamed the cauliflower until very tender while roasting a

whole head of garlic in the oven with olive oil drizzled over. Then

put the roasted pods in the food processor with the cauliflower, some

rosemary, sea salt and ground pepper. *Better* than garlic mashed

potatoes!

best regards,

sherry z

>

> sherry, im following your lead. we all get alittle lazy with the food

we eat and im one for sure.congrats on the 7 pounds. since your post

ive lost 3 pounds. and i walked my dog yesterday! only a half mile but

it had 2 hills! i just took my time. abby enjoyed it and i did have

some pain but the mental burst was sure worth it. also ive been fixing

veggies in a pan with alittle olive oil and sea salt on low and the

results are great. my husband thinks im doing something gourmet! im

cleaning out fridge and freezer. im going to take more walks. there is

also a program out now that uses the rules 35 grams of fiber per day

is equal to loosing 310 calories or walking 1 mile. and lots of water.

and the fiber helps detoxify your body. makes sense to me. i heard a

quote awhile back " if we ate it 100 years ago then it is ok to eat

now " ......casey

[Guest guest]

Fantastic news

Thanks for sharing with us

Aletha

[low dose naltrexone] Progress Report

>I wanted to give a progress report on my LDN use. I haven't posted before

>but have followed this site for several years. I was diagnosed with MS in

>July 2003 and started Copaxone. 1 1/2 years later I was getting very bad

>fast. I started LDN in Feb 2005. Within a month I was symptom free. I have

>had no episodes since. A month ago I had another MRI and it showed NO

>activity! I still work a full time job in a highly stressful field. For

>all of you thinking of giving LDN a try, you have nothing to loose and may

>gain freedom from this disease. Good luck to all.

>

>

>

>

>

>

[Guest guest]

NB - great testimony about LDN!! keep sharing; it helps all the newbies to hear this kind of news!!

marshiris@...

Get a sneak peek of the all-new AOL.com.

[Guest guest]

Hey man i feel ya i hope everything turns out well. You know on the

side not of this i have been planning on buying the sota zapper on

their site the $225 one, since i will probably be going out of town

sometime so i might as well have a handy dandy zapper to use instead

of taking an entire battery.

i am thinking of incorporating the mms into the Dc program or the bob

beck program we have here...

>

> I realize I haven't posted in a while, but after a full year off of

the meds, this is

> the first time I felt like I had anything to report, and I feel

pretty good about this.

> My CD4's had been steady around 85 until my last test on Tuesday

when they

> came in at a dismal 34. Can't tell you how disappointed I was, and

was really

> feeling lower than whale shit. Then the next day I got the viral

load test and

> was astounded to see it down almost 90%, 51,200 from 418,000 four

months

> ago. Haven't had the chance to go over this last test with the NP,

but I'm

> feeling pretty good about it. For the entire year really, I've been

doing Sota

> style blood purification for 2-4 hours four or five days a week.

Also, I have

> been drinking lots of ozonated water. Last summer, though, I did

about 5

> months of Ozone/rectal insufflation about 2 or 3 times a week. I

know this had

> to have an effect, as well as blood electrification. The only

conclusion I can

> draw at this point, at least for me, is that it was important not

to go back on the

> meds and just tough it out. It was very difficult at times when I

just wasn't

> getting the desired results, and the pressure from the NP was

enormous, but

> the key I believe was getting the old drugs out of my system, and

it's taken

> fully a year just to do that. I believe this is what's behind my

hair loss, but this

> time the hair is growing back as fast as it's falling out, the first

time I've ever

> seen that. CD4's of 34 is a dangerous level, I know this, but I'm

hopeful that

> this might be the artifact that Beck talked about when the numbers

go way

> down before going back up. Time alone will tell. I plan to continue

the protocol

> and include more Ozone rectal insufflation, and will keep everybody

posted

> as to my progress. Feeling a bit shaky lately, but still fully

functional.

>

> J

>

[Guest guest]

You might try adding coconut oil in there and see how that works.

http://www.coconut-connections.com/hivandaids.htm

V

> I realize I haven't posted in a while, but after a full year off of the meds,

this is

> the first time I felt like I had anything to report, and I feel pretty good

about this.

> My CD4's had been steady around 85 until my last test on Tuesday when they

> came in at a dismal 34. Can't tell you how disappointed I was, and was really

> feeling lower than whale shit. Then the next day I got the viral load test and

> was astounded to see it down almost 90%, 51,200 from 418,000 four months

>

[Guest guest]

...thanks a lot,I've posted it

good luck!

bG

>

> I realize I haven't posted in a while, but after a full year off of

the meds, this is

[Guest guest]

there's one vital thing in addition to know, whether you had any

opportunistic infections during this period?

If what you are doing with the electricity, etc is making up for the

lack of CD4 cells and you are in essence making your own immune

defense against opportunistic infections, then that is interesting

from an AIDS point of view. IF you were to stop the electricity and

got infections thereafter, it would show you are defending yourself

by outside means. I do not suggest anyone do that, since you seem to

be well, so stay that way, of course.

tests will only show those strains of HIV that can live in blood.

that's not much HIV compared to the rest in your body. many strains

cannot live in blood. They continue to destroy your CD4's from other

areas, even if the HIV in your blood goes very low count. the gut is

the largest reservoir of both HIV and CD4 cells. CD4 cells defend

from invasions via the gut. they are very busy down there. so HIV

clusters around them and kills them off.

so using blood electrification may reduce the strains in the blood,

while missing those in the gut which attack your CD4 cells there.

bG

>

> I realize I haven't posted in a while, but after a full year off of

the meds, this is

> the first time I felt like I had anything to report, and I feel

pretty good about this.

> My CD4's had been steady around 85 until my last test on Tuesday

when they

> came in at a dismal 34. Can't tell you how disappointed I was, and

was really

> feeling lower than whale shit. Then the next day I got the viral

load test and

> was astounded to see it down almost 90%, 51,200 from 418,000 four

months

> ago. Haven't had the chance to go over this last test with the NP,

but I'm

> feeling pretty good about it. For the entire year really, I've been

doing Sota

> style blood purification for 2-4 hours four or five days a week.

Also, I have

> been drinking lots of ozonated water. Last summer, though, I did

about 5

> months of Ozone/rectal insufflation about 2 or 3 times a week. I

know this had

> to have an effect, as well as blood electrification. The only

conclusion I can

> draw at this point, at least for me, is that it was important not

to go back on the

> meds and just tough it out. It was very difficult at times when I

just wasn't

> getting the desired results, and the pressure from the NP was

enormous, but

> the key I believe was getting the old drugs out of my system, and

it's taken

> fully a year just to do that. I believe this is what's behind my

hair loss, but this

> time the hair is growing back as fast as it's falling out, the

first time I've ever

> seen that. CD4's of 34 is a dangerous level, I know this, but I'm

hopeful that

> this might be the artifact that Beck talked about when the numbers

go way

> down before going back up. Time alone will tell. I plan to continue

the protocol

> and include more Ozone rectal insufflation, and will keep everybody

posted

> as to my progress. Feeling a bit shaky lately, but still fully

functional.

>

> J

>