Jump to content
RemedySpot.com

general

Rate this topic


Guest guest

Recommended Posts

  • 2 months later...
Guest guest

Cliff writes:

> I have known of quite a number of folks over the last eight or nine years

> who have died because they refused to do anything the doctors did not tell

> them to do or who believe that if anything is suggested other than what

the

> doctors recommend it cannot be of any real value.

Cliff,

This is a natural phenomenon that you shouldn't worry about. It is

called " the thinning of the herd. " Eventually, through attrition, natural

medicine will be the only medicine for chronic disease.

Link to comment
Share on other sites

Guest guest

On Wed, 9 Aug 2000, Cliff Beckwith wrote:

> HI,

>

> Yesterday I had a telephone call that seems to me significant. It is

> a way that I hear of the " unacceptable anecdotes " that I have

> mentioned from time to time.

Testimonies and accurate Case Histories are the best way to find Cell

Medicines that cure. That's how I cured myself--by taking what worked for

others. The term " unacceptable anecdotes " is used to confuse and steer

people away from real disease cures.

The " acceptable scientific method " is often used to provide room for

deception and lies. I was surfing the web last night, and found a site

which tells how a doctor started the " fat scare " in the United States.

He is part of the Drug Cartel. He reported false data at a conference in

the 1980s, linking heart disease to cholesterol. Since this " doctor was

in charge of the conference, he wouldn't let other doctors state their

objections, and didn't let their written views get into the final written

report.

[About heart disease--There is another " sticky " substance which encircles

the cholesterol which is the " bad guy " , not the cholesterol.]

http://www.drrath.com

[About cholesterol--60% of your brain is cholesterol, isn't it? Babies

fed mom's milk is about 8% IQ smarter--most Baby's milk formulas don't

have Essential Fatty Acids.]

> The phone call was from a lady who has Lymphositic [?] Leukemia and

> she had been using Flaxseed Oil. The doctors are watching her white

> counts and do not feel there is any need for " treatment " at present.

> She was concerned about a rise in the white count. Earlier the white

> count had gone down. It seems to be fluctuating.

Did you tell her to stop putting toxins into her body? Or tell her to

cleanse her body of toxins and parasites? Or about taking more Immune

Supports and other Cell Medicines? And how about some of Dr. Krebs'

Cancer Vitamin [b17]?

> Then the significant part to me.

>

> Her husband had cancer in the esophagus. He is a veteran and was

> being checked through a VA hospital. I do not know the treatment

> regimen.

>

> However, he heard of the use of Flaxseed Oil and began using it. I

> believe at four tablespoons a day.

>

> Now the cancer is gone. He continues to use the Flax Oil. He told

> the doctor what he is doing. The doctor told him that he didn't know

> about things like that but whatever he was doing, keep doing it.

One job of FlaxSeed Oil-Cottage Cheese is to make healthy cell membranes.

If you have a very sick membrane, " food " cannot go into the cell, and

" wastes " cannot get out of the cell, and the cell cannot do it's job.

The Immune Soldiers also use their Cell Membranes to fight and kill germs

and parasites. So the Immune Soldiers cannot kill cancer cells if they

have sick membranes. [ A membrane is like the rubber of a balloon. ]

> This was not the major story as far as she was concerned. She only

> mentioned that as the reason that she had begun using it for her

> situation. These were just matter of fact statements.

>

> Over the years I have discovered that when one gets well or improves

> someone who knows them and also has cancer does not need clinical

> double blind studies to get started.

Read what I said above about Testimonies versus Drug Cartel's deception

and lies.

> I have known of quite a number of folks over the last eight or nine

> years who have died because they refused to do anything the doctors

> did not tell them to do or who believe that if anything is suggested

> other than what the doctors recommend it cannot be of any real value.

The Drug Cartels found that people don't question " authority. " So they

use " authority " to lead people astray. Read the Conspiracy email which

tells how they have gained control of the Authority Base in this country.

> I would think that if doctors were really interested in getting people

> well there would at least be some that would be curious enough to

> seriously double check Dr. Budwig's work with the Flax Oil PLUS the

> protein which researchers are omitting in their experimental work.

There are doctors who are interested in getting people well. But they can

lose their license, go to jail, or even be murdered if they suggest

anything but what the Drug Cartels tells them to do. A Harvard doctor who

graduated top in his class had his Cell Medicines confiscated. The FDA

broke into his office with BIG GUNS....

> Cliff

>

>

Link to comment
Share on other sites

  • 1 year later...
Guest guest

Yeah no worries, We've just come from offshore Poland, currently pootling

around the mouth of Den Helder in Holland. Let me know when you'll be out. I'm

here untill the 5th April, then home for a month and back out at the end of

April beginning of may. Drop me a line offline later on.

Take care now.

.

pg reynolds <pg.r@...> wrote: to Otoole

I see from one of your emails that you are in the North sea somewhere

maybe we can have a chat on the air some time when I come out for my

next tour of duty. Iam just getting ready to go to Poland to pick a new

offshore support vessel up for the north sea.please call me Pete by the way .

regards

Link to comment
Share on other sites

  • 10 months later...
  • 2 years later...

Cliff - Alice did say if repeated MRI's were anticipated that the CI could be

implanted sans the magnet. That way scar tissue and repeated minor surgeries

would not be necessary. I don't see where or how she misrepresented anything.

- hope things go well at the surgeon's today. Please let us know. I

had my ci surgery on Sept. 9 and am still feeling some residual dizziness and

nausea. I hope the bump is nothing more than common surgical swelling and

recedes soon. By the way - I am in the town area of PA and had my first

surgery done at HUP. Where are you located?

- thinking of you and not having to go through the entire weekend

worrying! Hope all goes well and recovery is uneventful.

Alice - good luck in your upcoming surgery!

:o) Jackie

Implanted - right ear - Oct.2002 - Nucleus 24/3G

Reimplanted - right ear - Jan.2005 - Nucleus 24C/3G

Implanted - left ear - Sept.2005 - Nucleus-Freedom

Link to comment
Share on other sites

  • 1 month later...

Mike - I am thrilled for you that your audi was able to make you the new

Freedom setting of " MILM " . May I offer you the prayer I use concerning my

mother-in-law? I heard it originally in the movie " Fiddler on the Roof " and

I've adopted it as my own. " May G-d bless you and keep you---FAR away from ME! "

Eva and others who use clips to keep the CI on the head - thanks for the

tip, but, my hair is extremely thin and most barretts, clips and even bobby

pins, slip right out. I agree that if a clip stays in it's a good solution.

- I know the earmold is a good solution, too, but yuck! LOL If I

can figure out just how to make the attachment, however, I may just try that.

Glad your cold is going away.

- does Dr. Maggie make house calls out of state? I will pay

airfare and provide her with a nice room at the " Flash Hilton Hotel " LOL Also,

G-d bless the movie theater guy who accomodated you and your friend so

graciously. He is definately deserving of an award - or a hug and a kiss for

his

warmth and understanding.

:o) Jackie

Implanted - right ear - Oct.2002 - Nucleus 24/3G

Reimplanted - right ear - Jan.2005 - Nucleus 24C/3G

Implanted - left ear - Sept.2005 - Nucleus-Freedom

Link to comment
Share on other sites

Jackie,

LOL! I don't blame you! I stopped wearing an earmol a week after my CI was

activated because it was too annoying. It's amazing how I could wear an

earmold for 20 years without giving it second thought, but after 7

*wonderful* days without it, I suddenly realize what I've been missing. LOL!

Implanted: 12/22/04 Activated: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 20 years

Severe-profound hearing loss 10 years

Link to comment
Share on other sites

Good morning ,

You will really appreciate the difference when you are approved for a

second CI and you never have to wear another earmold. NO MORE SORE EARS.

Larry

Re: Re: General

> Jackie,

>

> LOL! I don't blame you! I stopped wearing an earmol a week after my CI was

> activated because it was too annoying. It's amazing how I could wear an

> earmold for 20 years without giving it second thought, but after 7

> *wonderful* days without it, I suddenly realize what I've been missing.

> LOL!

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

>

>

>

>

>

>

Link to comment
Share on other sites

The liberated ear........

At first my ear said it's too dang cold without that earmold. Funny

how I noticed the slightest draft coming in my ear after 44 years of

wearing an earmold day in and out.

Freedom 9/21/05 HOOKED!!

>

> Jackie,

>

> LOL! I don't blame you! I stopped wearing an earmol a week after my

CI was

> activated because it was too annoying. It's amazing how I could wear an

> earmold for 20 years without giving it second thought, but after 7

> *wonderful* days without it, I suddenly realize what I've been

missing. LOL!

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

>

Link to comment
Share on other sites

Hi Larry,

I'm anxiously awaiting the day I can go bilateral! <smile> When I spoke to

my audi this morning, she said we should receive some news from Medicaid in

January. Keep your fingers crossed that I'm approved! smile>

I'm glad you're doing so well with your bilaterals! I'm sure having two CIs

has made a significant difference in your life. Keep up the great work and

do keep us posted on your CI moments!

Implanted: 12/22/04 Activated: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 20 years

Severe-profound hearing loss 10 years

Link to comment
Share on other sites

hi ,

Congratulation! (smile) Since your audiologist and surgeon concur with

you being bilateral, how can you fail? It took me a long time, but I'm glad

I didn't give up.

I now listen to music with headphones. Of course, I have to use the

telecoils. It sounds very clean and as good as when I had normal hearing.

The finale of the overture of 1812 is fantastic! Would you believe, I have a

CD with a Russian chorus? One of my favorite compositions, and a good one

for beginners is the Serenade In G by Mozart. It's beauty will almost make

you cry with happiness.

I heard Handel's Messiah with two CI's last night. It was a Christmas

treat.

Well, I guess I will stop rambling.

btw, to hear good Christmas musiic, as well as great Christian messages

including an interactive Womens' Bible class, go to:

www.cjoyinternetradio.com

Sincerely,

Larry

Re: Re: General

> Hi Larry,

>

> I'm anxiously awaiting the day I can go bilateral! <smile> When I spoke to

> my audi this morning, she said we should receive some news from Medicaid

> in

> January. Keep your fingers crossed that I'm approved! smile>

>

> I'm glad you're doing so well with your bilaterals! I'm sure having two

> CIs

> has made a significant difference in your life. Keep up the great work

> and

> do keep us posted on your CI moments!

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

>

>

>

>

>

>

Link to comment
Share on other sites

Larry,

Reading your post makes me even more excited about the possibility of

receiving bilaterals. Although my surgeon and audi have recommended

bilaterals, I want to keep my expectations low so that if we run into any

problems, I won't be disappointed.

It must be a *wonderful* experience to hear music with two CIs! I know how

amazing it is to hear music with one -- I can't imagine how much better it

sounds with two. <smile> You mentioned Handel's " Messiah. " The last time I

heard the " Messiah " was when I was in our high school's A Cappella choir and

we performed it during one of our Christmas concerts.

Thanks so much for the music link! If you have any others to share, please

feel free to e-mail me privately.

P.S. How does music sound to you through the Freedom? Does it sound close to

what you remember before you lost your hearing? It took 6 months before I

could *really* appreciate music. From that time on, my

experience has continued to get even better to the point where 95% of what I

hear sounds like I remember with hearing aids. Sometimes it's easy to forget

how awful music sounded when I first received my CI. Classical music sounded

like cats and dogs fighting. LOL!

Now everything I hear from jazz to country music sounds so much better than

it ever did with hearing aids. Listening to music went from being a

one-dimensional experience with hearing aids to a 3 dimensional experience

with my CI.

As I continued losing my hearing I remember thinking, " God, please don't let

me lose my music. " Obviously my prayers have been answered and I couldn't be

more thankful.

Implanted: 12/22/04 Activated: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 20 years

Severe-profound hearing loss 10 years

Link to comment
Share on other sites

hi ,

Since I have had my Freedom activated only two month's, I am still in

the early stages of getting used to it. I would compare it to a baby just

learning to hear. This is why I will get Audio rehabilitation therapy with

my Freedom.

The Freedom still doesn't sound quite as good as the 3G, but the two

seem to compliment each other. I know they will make a better sound team as

time goes on.

I have noticed I can understand and respond to my mother and sister

while sitting in the back of the car going down the freeway since I have my

second implant. I know you must get tired of me bragging, but this is

wonderful! Sometimes I feel guilty for feeling so happy while my darling

Sharon is wheelchair bound at Monette Manor nursing home.

My sister said she will take a picture of me with my bilateral CI's. How

can I put them on the Forum Digest, or CIhear? How do you make a blog?

Sincerely,

Larry

Re: Re: General

> Larry,

>

> Reading your post makes me even more excited about the possibility of

> receiving bilaterals. Although my surgeon and audi have recommended

> bilaterals, I want to keep my expectations low so that if we run into any

> problems, I won't be disappointed.

>

> It must be a *wonderful* experience to hear music with two CIs! I know how

> amazing it is to hear music with one -- I can't imagine how much better it

> sounds with two. <smile> You mentioned Handel's " Messiah. " The last time I

> heard the " Messiah " was when I was in our high school's A Cappella choir

> and

> we performed it during one of our Christmas concerts.

>

> Thanks so much for the music link! If you have any others to share, please

> feel free to e-mail me privately.

>

> P.S. How does music sound to you through the Freedom? Does it sound close

> to

> what you remember before you lost your hearing? It took 6 months before I

> could *really* appreciate music. From that time on, my

> experience has continued to get even better to the point where 95% of what

> I

> hear sounds like I remember with hearing aids. Sometimes it's easy to

> forget

> how awful music sounded when I first received my CI. Classical music

> sounded

> like cats and dogs fighting. LOL!

> Now everything I hear from jazz to country music sounds so much better

> than

> it ever did with hearing aids. Listening to music went from being a

> one-dimensional experience with hearing aids to a 3 dimensional experience

> with my CI.

>

> As I continued losing my hearing I remember thinking, " God, please don't

> let

> me lose my music. " Obviously my prayers have been answered and I couldn't

> be

> more thankful.

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

>

>

>

>

>

>

>

Link to comment
Share on other sites

Larry,

No need to apologize for bragging about your CIs! Anyone who has a CI knows

what kind of a wonderful gift they've been given and it's only normal that

we share our excitement with others. <smile> I'm so happy for the success

you're experiencing with your second CI! I'm also glad that you're able to

enjoy music in stereo sound.

I was brought to tears last night after watching a chamber choir with

orchestra, pipe organ and bells. It was amazing being able to hear all of

their voices in harmony as well as the instrumental accompament. Too bad I

didn't record it -- it was unlike anything I've heard before.

It has been such a joy being able to hear and enjoy Christmas music once

again! Thanks so much for the radio links you sent me. <smile> Ever since

getting my CI, I'm starting to enjoy classical music and jazz more than I

ever have before -- probably because all of the instruments sounded like

" mush " with hearing aids. <smile>

Thanks for the tip about the 3G wire earhook. I asked a neighbor to help me

put it back on, so hopefully it will stay put until I see my audi next month

for my one year evaluation. Yikes! Has it really been that long?? My, oh my!

How time flies when you're having fun listening! <smile>

All the best to you and Sharon for a very Merry Christmas and a healthy and

prosperous New Year!

Implanted: 12/22/04 Activated: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 20 years

Severe-profound hearing loss 10 years

Link to comment
Share on other sites

Hi ,

I am so glad you like classical music. I know what you mean about music

sounding like mush with hearing aids. Music also affects me and causes me

to get emotional because I am filled with such joy it is almost

overwhelming. A good example is music by Ferrante and Teicher, and Leroy

. I also love music by Chopin.

I had a new Cristmas ornament for the door yesterday, my CI. The magnet

grabbed a Christmas decoration as I was going out the door. My mom took it

down after laughing about it.

Two more websites you may enjoy are: www.wfpl.org it is spoken

word. www.wfuv.org is folk and eclectic radio. It is located in

Jersey city, New Jersey.

I guess I will say so long for now. ttyl Larry

Re: Re: General

> Larry,

>

> No need to apologize for bragging about your CIs! Anyone who has a CI

> knows

> what kind of a wonderful gift they've been given and it's only normal that

> we share our excitement with others. <smile> I'm so happy for the success

> you're experiencing with your second CI! I'm also glad that you're able to

> enjoy music in stereo sound.

>

> I was brought to tears last night after watching a chamber choir with

> orchestra, pipe organ and bells. It was amazing being able to hear all of

> their voices in harmony as well as the instrumental accompament. Too bad I

> didn't record it -- it was unlike anything I've heard before.

>

> It has been such a joy being able to hear and enjoy Christmas music once

> again! Thanks so much for the radio links you sent me. <smile> Ever since

> getting my CI, I'm starting to enjoy classical music and jazz more than I

> ever have before -- probably because all of the instruments sounded like

> " mush " with hearing aids. <smile>

>

> Thanks for the tip about the 3G wire earhook. I asked a neighbor to help

> me

> put it back on, so hopefully it will stay put until I see my audi next

> month

> for my one year evaluation. Yikes! Has it really been that long?? My, oh

> my!

> How time flies when you're having fun listening! <smile>

>

> All the best to you and Sharon for a very Merry Christmas and a healthy

> and

> prosperous New Year!

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

>

>

>

>

>

>

>

Link to comment
Share on other sites

  • 3 years later...
Guest guest

Davina, I would recommend that you fine a surgeon that has a lot of experince

with this disease and then get as much knowledge as you can about the disease. 

This is a great place to start.  Another place to look is www.achalasia.us

in Georgia

 <FONT face= " comic sans ms " color=#ff0000 size=5> in Georgia </FONT><IMG

src= " http://us.i1.yimg.com/us.yimg.com/i/mesg/tsmileys2/04.gif " >

________________________________

From: dwright2404 <dwright2404@...>

achalasia

Sent: Sunday, March 1, 2009 4:53:27 PM

Subject: general

Hi i just wondered if i could aska general question it looks as though

my mum is going to be diagnosed with Achalasia and i just wondered what

the way forward is re treatment what are the most successful route and

with her age is there better ways of treating than others.

Many thanks

Davina

Link to comment
Share on other sites

  • 1 year later...

i had a metametrix test last year which showed no candida but a parasite and h

pylori. i worked with a nutritionist www.health-truth.com on diet and rotation

of herbs for 1 year and for leaky gut. also i had a retest recently and all the

herbs i took had decreased my good bacteria and i had got a worm. i have done

candida diet for 8 years just to keep it at bay and well. i do take probiotics

daily or cultured probiotic veggies is this ok.

should i continue on the candida diet anyway but i struggle with eating lots

protein, i tried dr robert youngs alkalising programme which made me feel

depressed just eating veg and no protein.

i also take liver support herbs like milk thistle and artichoke and biotics beta

tcp for bile flow. is this ok.

Link to comment
Share on other sites

if i have no candida should i still do the programme. also how much water can

u drink after u have taken hcl 40n mins after will it still work if u drink as

for me it feels like it sits and doesnt dissolve. is 6 litres water too much

a day. is it not ok to take pancretin as i have an elastase pancreqtic

disorder.

also do u recommend oil of oregano or not

thanks

angela

From: Ed

Sent: Sunday, January 09, 2011 5:53 AM

Subject: [ ] Re: general

>

> i had a metametrix test last year which showed no candida but a parasite and h

pylori. i worked with a nutritionist www.health-truth.com on diet and rotation

of herbs for 1 year and for leaky gut. also i had a retest recently and all the

herbs i took had decreased my good bacteria and i had got a worm. i have done

candida diet for 8 years just to keep it at bay and well. i do take probiotics

daily or cultured probiotic veggies is this ok.

>

> should i continue on the candida diet anyway but i struggle with eating lots

protein, i tried dr robert youngs alkalising programme which made me feel

depressed just eating veg and no protein.

>

> i also take liver support herbs like milk thistle and artichoke and biotics

beta tcp for bile flow. is this ok.

>

@@ Hi ,

As I stated, read and review the articles I've suggested. You do not need to

take anything you have mentioned. The diet plus the recommended supplements will

provide all the nutrients and everything it needs to heal.

Probiotics are removed from Bee's Candida Program because the body is smart

enough to create any probiotics required, when, and if, needed, just like it

balances out all nutrients if given " proper nutrients " (diet plus supplements).

Also probiotics taken by mouth couldn't reach the large intestines where they

are " supposedly " needed, since probiotics can only be implanted in the large

intestines with an enema.

Your Friend in Health,

Ed

group moderator

Link to comment
Share on other sites

>

> if i have no candida should i still do the programme. also how much water

can u drink after u have taken hcl 40n mins after will it still work if u drink

as for me it feels like it sits and doesnt dissolve. is 6 litres water too

much a day. is it not ok to take pancretin as i have an elastase pancreqtic

disorder.

>

> also do u recommend oil of oregano or not

+++Hi ,

Yes, you still need to do this program even if you do not have candida, since it

IS an overall healing program.

You can have enough water with the HCl to swallow it. If you need more water

you can have it, but don't go overboard.

Don't worry about how much water you have for now, since there's so many things

going on that can make you more thirsty than is normal, and you're low on

minerals, good fats, etc., etc.

Elastase is a type of protein enzyme but there are others, including HCl in the

stomach. Like I wrote before stomach acid (HCl) is most important so your

pancreas will work better. Stomach acid neutralizes any type of pancreatic

enzyme you take so it is a waste of money.

Read the stomach acid article first, and then ask questions.

Thanks a bunch, Bee

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...