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>

> Ok Bee, I need your advice please. I have tried and tried, but I

> cannot drink a raw egg. I have trouble with cooked eggs! So a raw

> egg is just beyond me. I actually got the dry heaves from thinking

> about trying it this morning. I wrote a few weeks ago about my food

> aversions. I am definitely willing to give up my vegetarian lifestyle

> to do this, because I WANT to do this. But the egg drink, bone broths

> (EEWW I can't even eat chicken noodle soup) and organ meats is

> something I'm not capable of. I remember liver from my childhood. :(

> Anyway, can I still do this program if I do the supplements, coconut

> oil, avoidance of off limit foods and so on?

==>I had a friend years ago that had an aversion to meats, similar to

yours. However, she would eat eggs, and cheese. But cheese is a no-no

on the candida program.

You can still do the program but I cannot guarantee the results. If

you cannot stand eating meats and eggs you could try taking tons of

dessicated liver tablets, which would help.

The best, Bee

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" You can still do the program but I cannot guarantee the results. If

you cannot stand eating meats and eggs you could try taking tons of

dessicated liver tablets, which would help. "

Bee, I can make myself eat the meats and eggs, just not raw eggs and organs.

Cooked eggs are ok I assume? Just not as beneficial as the raw? Thanks so

much,

Bee <beeisbuzzing2003@...> wrote:

>

" You can still do the program but I cannot guarantee the results. If

you cannot stand eating meats and eggs you could try taking tons of

dessicated liver tablets, which would help. "

The best, Bee

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

You rock. That's why Blockbuster's offering you one month of Blockbuster Total

Access, No Cost.

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>

> " You can still do the program but I cannot guarantee the results. If

you cannot stand eating meats and eggs you could try taking tons of

dessicated liver tablets, which would help. "

>

> Bee, I can make myself eat the meats and eggs, just not raw eggs

and organs. Cooked eggs are ok I assume? Just not as beneficial as

the raw?

==>Hi . Sorry I misunderstood you. Cooked eggs are just as

nutritious as raw if the egg yolks are left runny, as in poached eggs.

You do not have to eat organs either. :)

Cheers, Bee

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cholesterol is a myth created by the pharmaceutical companies.

It doesn't take much research to discover the facts. Have as many eggs

as you like per day (maybe limit it to 2 dozen though...)

Here's some reading. Click on the facts to read a detailed analysis.

http://www.ravnskov.nu/cholesterol.htm

If you are not convinced just take a look at his credentials... quite

incredible really.

.

>

> How many eggs is it ok to eat each day? They say if you have high

> cholesterol (I do) to not eat eggs more than a couple times a week.

I've

> been hard boiling them and eating a couple a day.

>

>

>

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>

> How many eggs is it ok to eat each day? They say if you have high

> cholesterol (I do) to not eat eggs more than a couple times a

week. I've

> been hard boiling them and eating a couple a day.

>

>

>

,

Before going on Bee's program I ate a lot of eggs per week and had

very low cholesterol. As I started to add Coconut oil ( still before

the program) my cholesterol went up but still at 180. Now I gave

blood last month and it was 218. After blood tests for my annual

physical my HDL ( good cholestrol ) was 107 (over 40 is good) and my

LDL (bad cholestrol was 112 (under 130 is good). So all the fat and

lots of eggs (about 6 a day) is not hurting me. All my other blood

test levels were good after being on the program for 8 months.

Thank you Bee.

Gratefully, Ellen " -)

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>

> How many eggs is it ok to eat each day? They say if you have high

> cholesterol (I do) to not eat eggs more than a couple times a week.

I've

> been hard boiling them and eating a couple a day.

==>Hi . In addition to what other members write, see the

article " Low Cholesterol on 25 Eggs Per Day " ;

http://www.healingnaturallybybee.com/articles/eggs1.php

Bee

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Hi Ellen & ,

Cholesterol will go up while the body is detoxifying.

Bee

> ,

> Before going on Bee's program I ate a lot of eggs per week and had

> very low cholesterol. As I started to add Coconut oil ( still

before

> the program) my cholesterol went up but still at 180. Now I gave

> blood last month and it was 218. After blood tests for my annual

> physical my HDL ( good cholestrol ) was 107 (over 40 is good) and

my

> LDL (bad cholestrol was 112 (under 130 is good). So all the fat and

> lots of eggs (about 6 a day) is not hurting me. All my other blood

> test levels were good after being on the program for 8 months.

> Thank you Bee.

> Gratefully, Ellen " -)

>

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  • 1 year later...
Guest guest

have you used the cream.have you checked adrenal fatigue,sex hormones especially

progesterone.did you check thyroid.

>

> Hi all

>

> I have severe ulcerative colitis. I have been taking LDN now (only med) for 47

days. I have been keeping an LDN journal. I've had a very slight decrease in a

couple of my symptoms but nothing really helpful yet. I'm still housebound,

watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a

year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2

weeks. When I first started taking it I slept not bad but now I haven't had a

good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having

terrible pressure headaches where I can feel every pulse and heartbeat in my

head and ears - the pressure is terrible. Also have vomitted a couple of

mornings. Should I stop since it doesn't seem to be helping my UC and now I'm

not feeling well from the LDN or should I give it more time? If it doesn't start

to kick in soon I'm going to have to start back on Prednisone just to function

somewhat normally.

>

> Thankyou

> Deanna

>

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Hi Deanna,

If you’re taking the LDN capsules try the cream instead

that’s what I did and I have UC too, but mild they say and I don’t

believe it! I’m on 10mg of pred to get over this bad flare, but that’s

helping only a little. I put the cream on my inner wrist and night and rub it

in completely. Maybe you can do the cream and back down the dose a little. I’ve

started LDN the last week in January and by the mid of February I was on the

4.5mg dose, but switched to the cream. It’s only been a month and a week

for the 4.5 dose cream now, I’m still sticking with it. I don’t

have trouble sleeping it’s having to go to the bathroom in the middle of

the night that gets me. I was doing the antifungal diet and by my 7th

days I was in severe diarreah mode that I had to add back some bread and sugar,

it was terrible, I got a fissure from it and now my anus burns every single day

to a point where no meds help and I’m in tears. I just telling you b/c I

know how you feel. My pulse is felt in my rectum that’s how bad the

spasms are. I just completed a stool test by Doctors Data and hopefully in a

week they can shed some light on my situation.

Good luck and I’m praying for you.

From:

low dose naltrexone [mailto:low dose naltrexone ] On

Behalf Of Deanna

Sent: Wednesday, April 15, 2009 10:27 AM

low dose naltrexone

Subject: [low dose naltrexone] Having trouble

Hi all

I have severe ulcerative colitis. I have been taking LDN now (only med) for 47

days. I have been keeping an LDN journal. I've had a very slight decrease in a

couple of my symptoms but nothing really helpful yet. I'm still housebound,

watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a

year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about

2 weeks. When I first started taking it I slept not bad but now I haven't had a

good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm

having terrible pressure headaches where I can feel every pulse and heartbeat

in my head and ears - the pressure is terrible. Also have vomitted a couple of

mornings. Should I stop since it doesn't seem to be helping my UC and now I'm

not feeling well from the LDN or should I give it more time? If it doesn't

start to kick in soon I'm going to have to start back on Prednisone just to

function somewhat normally.

Thankyou

Deanna

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Guest guest

>

> Hi all

>

> I have severe ulcerative colitis. I have been taking LDN now (only med) for 47

days. I have been keeping an LDN journal. I've had a very slight decrease in a

couple of my symptoms but nothing really helpful yet. I'm still housebound,

watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a

year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2

weeks. When I first started taking it I slept not bad but now I haven't had a

good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having

terrible pressure headaches where I can feel every pulse and heartbeat in my

head and ears - the pressure is terrible. Also have vomitted a couple of

mornings. Should I stop since it doesn't seem to be helping my UC and now I'm

not feeling well from the LDN or should I give it more time? If it doesn't start

to kick in soon I'm going to have to start back on Prednisone just to function

somewhat normally.

>

> Thankyou

> Deanna

>============

Email Dr. Jaquelyn Mccandless for advice before stopping LDN. Do not rule out

the possibility of lyme disease. Lyme can cause chronic UC symptoms. You may

need to see a lyme literate doctor. First make sure candida yeast and molds or

other bacterias are not the culprits. Dr. McCandless can tell you of things you

can do to see if your situation improves and can give you her list of tests your

doctor can run to check for causing factors.

Dr McCandless

jmccandless@...

or

jmccandlessATprodigy.net put the @ sign in place ot the AT

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It " may " be the filler in the capsule causing some of the problem. I had the

same side effects (headache, nausea & vomiting) from the avicel filler. After I

switched to the acidolpholus filler, the eide effects were gone.

>

> Hi all

>

> I have severe ulcerative colitis. I have been taking LDN now (only med) for 47

days. I have been keeping an LDN journal. I've had a very slight decrease in a

couple of my symptoms but nothing really helpful yet. I'm still housebound,

watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a

year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2

weeks. When I first started taking it I slept not bad but now I haven't had a

good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having

terrible pressure headaches where I can feel every pulse and heartbeat in my

head and ears - the pressure is terrible. Also have vomitted a couple of

mornings. Should I stop since it doesn't seem to be helping my UC and now I'm

not feeling well from the LDN or should I give it more time? If it doesn't start

to kick in soon I'm going to have to start back on Prednisone just to function

somewhat normally.

>

> Thankyou

> Deanna

>

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Guest guest

Probably should try using LDN transdermal cream.

Art

---

>

> Hi all

>

> I have severe ulcerative colitis. I have been taking LDN now (only med) for 47

days. I have been keeping an LDN journal. I've had a very slight decrease in a

couple of my symptoms but nothing really helpful yet. I'm still housebound,

watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a

year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2

weeks. When I first started taking it I slept not bad but now I haven't had a

good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having

terrible pressure headaches where I can feel every pulse and heartbeat in my

head and ears - the pressure is terrible. Also have vomitted a couple of

mornings. Should I stop since it doesn't seem to be helping my UC and now I'm

not feeling well from the LDN or should I give it more time? If it doesn't start

to kick in soon I'm going to have to start back on Prednisone just to function

somewhat normally.

>

> Thankyou

> Deanna

>

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