Fibromyalgia

[Guest guest]

As I was saying guys - I think most of the General Practitioner's are only there now to send us to a specialist. But, they are the ones that get to insinuate that we are fat and need more exercise. If it's not right on the open page of your file, they will not remember that they themselves sent us to see an arthritic specialize and he sent back this prognosis. Oh, I love it even better when my own GP is away on holidays and the up and coming young doctor tells you, you must exercise. I always want to say back to them - now go back and read my file and you'll probably find out why I can't.Gloria

I like her alright I just have to ignore her on some things like this. I know I exercise enough. I work my tail off. My husband and I share the same doc. That is why I am not wanting to change at this pt. She is not my hep doc thank God. She is good at getting me into specialists I need though. She does listen to me too. So not changing docs for now. Just grumping. grrrr. Thanks Cinder

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From: Gloria <gadamscan (DOT) ca>Subject: Re: [ ] Fibromyalgia Date: Tuesday, May 18, 2010, 10:43 PM

Don't I ever love that kiss off from the Dr's. Go exercise more and that will help your Fibro. But Dr., I can not walk further than 1/2 a block most days, so where is the exercise in that???Or, even better - I had one young Dr. even describe how to lift cans of soup to help with my huge belly and chest.. Oh how I would like to see him now to show him that it had nothing to do with lack of exercise and everything to do with an extremely enlarged, inflamed liver.Gloria

Hi all and God Bless those on their way to DC, safe travels! I did not finish tx, I did not develope fibro till post tx, I was only on tx for 9wks, I think the HepC brings it on! I suffer as many of you do, only my doc's won't give me anything for pain, I tried the lyrica and it made my feet legs swell up like an elephant,I was allergic to cymbalta. I do take klonopin which helps me sleep. I SUFFER alot and it sucks! but hey! I am alive, I take ibprofen alot, I just don't know what else to do. We just had rain and boy oh boy was I a hurtin.All my primary dr says is exercise.... .every time I see her. I guess just gotta push through the pain and endure. but sometimes it gets pretty hard to keep going..I am so excited about the new combos becoming available and pray many reach svr, I can't do interferon period so it counts me out! Hopefully soo something that stands alone without standard tx will come along! My prayers are with and for all of us

Heppers around the world.I am gonna go lay down now for awhile, just one of those days. Don, u r an inspiration, thankyou for all your hard work and knowledge!

[Guest guest]

yep you would be right on that. I am lucky I have any more energy or muscle left to exercise anything by the time I get off work. There are times after work I get home I am sitting in my car crying because it hurts too bad to get out of my car. I started taking my night meds with me and taking them an hour before I get off work so they are working before I get home. That way I can avoid that pain. I sat there last week one morning about 20 min waiting for a stupid tramadol to kick in so I could walk to the door. I felt like crawling. This job takes it all out of me. My husband has no idea how hard it is on me. I know he knows I hurt. I fought for drugs for the pain but I guess there isn't anything I can get that will help without being another chemo or something that messes with my liver too much. So will muttle through somehow. I told the doc I would be taking

more than the recomended dose of tramadol then. So she had better order a bigger doseage. Don't know if she did. I have to work while I can. When I can't work any more my husband is going to go get another job and will be working two jobs. So I won't have any help through tx. It was not have money to cover the bills and have help or not pay bills and have help and lose everything. So life is hard. Well better get around. Love you all thanks for listening. Love Cinder

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From: Gloria <gadamscan (DOT) ca>Subject: Re: [ ] Fibromyalgia Date: Tuesday, May 18, 2010, 10:43 PM

Don't I ever love that kiss off from the Dr's. Go exercise more and that will help your Fibro. But Dr., I can not walk further than 1/2 a block most days, so where is the exercise in that???Or, even better - I had one young Dr. even describe how to lift cans of soup to help with my huge belly and chest.. Oh how I would like to see him now to show him that it had nothing to do with lack of exercise and everything to do with an extremely enlarged, inflamed liver.Gloria

Hi all and God Bless those on their way to DC, safe travels! I did not finish tx, I did not develope fibro till post tx, I was only on tx for 9wks, I think the HepC brings it on! I suffer as many of you do, only my doc's won't give me anything for pain, I tried the lyrica and it made my feet legs swell up like an elephant,I was allergic to cymbalta. I do take klonopin which helps me sleep. I SUFFER alot and it sucks! but hey! I am alive, I take ibprofen alot, I just don't know what else to do. We just had rain and boy oh boy was I a hurtin.All my primary dr says is exercise.... .every time I see her. I guess just gotta push through the pain and endure. but sometimes it gets pretty hard to keep going..I am so excited about the new combos becoming available and pray many reach svr, I can't do interferon period so it counts me out! Hopefully soo something that stands alone without standard tx will come along! My prayers are with and for all of us

Heppers around the world.I am gonna go lay down now for awhile, just one of those days. Don, u r an inspiration, thankyou for all your hard work and knowledge!

[Guest guest]

, have you looked at Dr Lowe's web site? Read the

information there about fibromyalgia and the use of T3. CFS, ME and FM are

often 'dustbin' diagnoses that doctors will give their patients who are on

thyroid hormone replacement, who have normal blood results, yet who still

complain of symptoms, along, of course, with that other old chestnut " you

are suffering from a functional somatoform disorder " a phrase made famous

by the long-gone President of the British Thyroid Association.

For some reason, doctors are not taught about the effects of

specific thyroid hormones in the cells, or that a lack of the active thyroid

causes many problems such as constant pain. I suffered with this when I was on

levothyroxine only. I was so incapacitated with the severe pain in my back,

shoulder and under both feet I was on the point of becoming wheelchair bound. I

started natural thyroid extract as recommended by a private doctor. The T3

worked like magic. 7 years later, I still have no pain and am still taking NDT.

Mind you, this is not always the answer for everybody.

http://www.drlowe.com/geninfo/explain.htm

Luv - Sheila

Hi,

can anyone

offer an tips on how to deal with my fibromyalgia. I am at an all time low....

I am in constant pain (all joints and muscles) can't sleep and can't function

normally. I am trying hard to recover with yoga and core exercises but I'm

getting worse.

I don't

understand how I can be like this with my thyroid status up to par.... unless

this is a whole different avenue of auto immune disease that I am now walking

down.

If anyone has

any tips on how to deal with fibromyalgia, I would be very greatful to hear

them.

many thanks,

julia

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18:34:00

[Guest guest]

You may want to check out the use of LDN (low dose Naltrexone) for FM. I believe

there is a group for this.

Trials have been done and may still be in progress in the U.S. and good things

are happening for those on the trial in terms of improvement.

You can online v cheaply.

Mo

>

> can anyone offer an tips on how to deal with my fibromyalgia. I am at an all

> time low.... I am in constant pain (all joints and muscles) can't sleep and

> can't function normally. I am trying hard to recover with yoga and core

> exercises but I'm getting worse.

>

> I don't understand how I can be like this with my thyroid status up to par....

> unless this is a whole different avenue of auto immune disease that I am now

> walking down.

> If anyone has any tips on how to deal with fibromyalgia, I would be very

> greatful to hear them.

>

> many thanks,

>

> julia

>

[Guest guest]

Hi ,

You have my deepest sympathies.It is an absolutely miserable condition and with the lack of sleep on top of it...well it drives one to utter depair.Can I ask what meds you are taking for your thyroid and what your latest results are?

I was told I had Fibromyalgia years ago and it certainly felt like it at the time. 2005 was my worst year.I was on thyroxine alone and hurt everywhere.I couldn't get sleep 5 nights out of 7 and had to get my daughter off to school and function.It was impossible...

Anyway,I just couldn't live like that so I consulted a private doctor who prescribed me Hydrocortisone and the improvement was phenomenal.My neck which I had been unable to turn was freed up and the stiffness and aching eliminated.I had more energy and my mood improved although sadly I still couldn't really tolerate my thyroid meds so I'm still plagued by Hypo symptoms.

I have a few suggestions for you and I really hope they will help.

1.)Follow an anti- inflammatory diet.Avoid gluten.Try cherry juice every morning.

2.)Try a trial of H/C (please discuss with your doctor)

3.)Try T3 (please discuss with doctor)

4.)Supplement with high dose Fish oils,vitamin D and Magnesium and Malic acid.

5.)Try pilates and gentle walks instead of Yoga(Yoga made my symptoms worse too surprisingly)

6.)Try Epsom salt bath(500g of Epsom salts and 500g of Bicarbonate of Soda)Run bath as hot as you can tolerate and pour in salts.Dry brush towards heart before soaking in bath till water feels cool.Towel dry and rub sesame oil onto soles of feet and put warm socks on.Get into bed and rest till morning.

7.)Never overdo things.It will only cause a flare-up!

8.)For sleep I tried two remedies recommended by a renowned nutritionist and and fellow insomniac.These are Seditol and Sleep Well .The former has good clinical studies behind it and really helped me.Please look them up.Anything else just didn't work for me.Valerian,Hops,Chamomile etc did nothing.

9.)If all else fails a trial of amitriptyline can be helpful for muscle relaxation and sleep,although it can leave one drowsy the next day.I still use it periodically.

,I cannot promise that trying the above will alleviate all your Fibromyalgia symptoms but I honestly believe they will help you alot.They may just make life that more bearable.Good luck!

Peary

>> > > > Hi,> > can anyone offer an tips on how to deal with my fibromyalgia. I am at an all > time low.... I am in constant pain (all joints and muscles) can't sleep and > can't function normally. I am trying hard to recover with yoga and core > exercises but I'm getting worse.> > I don't understand how I can be like this with my thyroid status up to par.... > unless this is a whole different avenue of auto immune disease that I am now > walking down.> If anyone has any tips on how to deal with fibromyalgia, I would be very > greatful to hear them.> > many thanks,> > julia>

[Guest guest]

You can go to our FILES section and check out the FOLDER

entitled Low Dose Naltrexone (LDN) and read through the information there.

Luv - Sheila

You may want to check out the use of LDN (low dose Naltrexone) for FM. I

believe there is a group for this.

Trials have been done and may still be in progress in the U.S. and good things

are happening for those on the trial in terms of improvement.

You can online v cheaply.

Mo

>

[Guest guest]

Hi Peary,

It's interesting that Hydrocortisone worked for you. My GP wanted to diagnose

CFS/FMS and prescribe antidepressants. I asked him for evidence that

antidepressants alone had been successful because I had found sources which

stated that cortisol treatment was a viable option. I'm really interested to

know how your doctor decided on this course of treatment.

Also how does the anti-inflammatory diet help?

Lesney x

> Anyway,I just couldn't live like that so I consulted a private doctor who

prescribed me Hydrocortisone and the improvement was phenomenal.

Follow an anti- inflammatory diet.Avoid gluten.Try cherry juice every morning.

[Guest guest]

Hi , Have you seen http://www.drlowe.com ? Have you tried T3 alone? I find that too much T4 causes joint pain. thyroid treatment From: juliamoonrock@...Date: Sun, 5 Sep 2010 07:49:49 +0000Subject: fibromyalgia

Hi,

can anyone offer an tips on how to deal with my fibromyalgia. I am at an all time low.... I am in constant pain (all joints and muscles) can't sleep and can't function normally. I am trying hard to recover with yoga and core exercises but I'm getting worse.

many thanks,

julia

[Guest guest]

Hi,

Is the HC in tablet form?

I am going to try and ask my GP for this next time as I have had a stiff neck

with loads of neck and shoulder pain and general feelings of pain - like flu

symptoms pain in the bones/joints etc - on and off but more recently often.

Also some nights where I don't sleep well at all - waking a lot and restless not

getting a good position etc.

Stacey

--

> > Anyway,I just couldn't live like that so I consulted a private doctor who

prescribed me Hydrocortisone and the improvement was phenomenal.

>

> Follow an anti- inflammatory diet.Avoid gluten.Try cherry juice every morning.

>

[Guest guest]

Hi ,

I'm sorry to hear that you are feeling so upset at this point. We all know how

tough it is. Many of us have been where you are now and have made it to a

better point through the use of Bee's program. It's been a life saver for me.

I, too, had fibromyalgia and chronic fatigue, so I know just how debilitating it

can be. My sister had it much worse than me. Three years ago she was pretty

much bed ridden, walked with a cane and could barely feed herself. She's been

following Bee's diet for the past two years and can now hold down two part-time

jobs, takes care of two autistic teens and has recently taken up running! I

know it sounds too good to be true, but it is. Bee's program is really the only

thing that has helped.

Don't be too concerned if you can't afford all organic foods. Many of us here

either can't afford or don't have access to organic food and are still making

great progress in our healing. One thing I try not to compromise on is eggs.

I think it's important to get eggs from chickens who can get outside, but just

do the best you can with the budget you have to work with.

To begin with, you might not want to do so much walking. 3-5km is a long way

and right now you need to save your energy for healing. Perhaps just a 20minute

walk is enough to get your blood flowing, but not enough to wear you out. Bee

doesn't recommend any strenuous exercise since it's takes up the energy your

body needs for healing. For now, getting as much rest as you feel you need is

important.

With regards to your supplements. You should take the recommended dosages just

as Bee has written them, even if you are experiencing loose stools. Loose

stools is not necessarily a bad thing. It is one way of getting rid of toxins

from the body, so you don't want to stop that process. I've been having loose

stools pretty much since the time I started Bee's program over two years ago.

While many might see this as a bad thing, I don't see it that way at all. In

fact, I feel so much better afterward. So, while it may not seem all that

pleasant, I encourage you to allow this process to take place so that you can

get rid of those toxins.

It's a shame your wife isn't interested in doing Bee's program with you.

Perhaps if you could get her to read Bee's website, she might recognize many of

her symptoms and to see that she, too, can get healthy again. My husband and my

son are also following this program with me. It's nice because it is something

we can do as a family and we can recognize healing symptoms in one another. As

a couple, it is another important thing we can share. We can also make our

house a sort of 'safe haven' free from all the no-no foods. This is really

helpful, especially when those cravings arise. The way I look at it is: If it's

not in your house, you can't eat it! Perhaps once she sees how well you are

doing, she'll become more interested.

For more encouragement, take a look at the Success Stories on Bee's website.

http://www.healingnaturallybybee.com/success/index.php

All the best,

(a group moderator)

>

> Hi all,

> I am sorry for the lengthy email but I feel so terrible and lonely in all this

suffering. I am getting weaker and weaker in this fight. I must say the last few

months have been very hard for me and I lost almost everything I had in my life.

>

<snip>

>

> Diet and Supplements issues:

> I am getting ready for Bee's diet; I got the supplements and started on the

diet but can't afford organic food yet, hopefully next month. In my first days

on Bee's supplements I got some good response and I started walking more.

Currently I can walk for up to 3-5km and end up with muscle pain which usually

go away on the next day. I noticed that tendons are the worst and once overused

it takes weeks/months to recover from the pain. I can't drive a car as they

affect the tendons more. I noticed my leg muscles got stronger after stopping

buckwheat (as suggested by Bee). Bee was right that I was full of toxins. I have

a pretty big problem with the supplements intake. I tried taking magnesium and

calcium but it looks like my body has enough of both from the diet. I tried many

combinations but I have either running stool = too much magnesium or twitching

eye and constipation, which I think means too much calcium. I stopped both

supplements and all the symptoms are gone. I will appreciate some feedback. In

addition, vit c when taken alone or magnesium gives me running stool too! If I

take both magnesium and vit C I get even worse.

>

> God bless you all,

>

>

>

[Guest guest]

Hi ,

I am sorry too to hear that you are not where you would like to be right now,

and even though some days may seem impossible and long know that everyone here

is all here to listen & lend support.

I am sure that almost everyone here has said that they have had enough smome

days, but the will and strength from within keeps us pushing back. Damn will and

strength

Take it one day at a time.

Nance

>

>

> >

> > Hi all,

> > I am sorry for the lengthy email but I feel so terrible and lonely in all

this suffering. I am getting weaker and weaker in this fight. I must say the

last few months have been very hard for me and I lost almost everything I had in

my life.

> >

> <snip>

> >

> > Diet and Supplements issues:

> > I am getting ready for Bee's diet; I got the supplements and started on the

diet but can't afford organic food yet, hopefully next month. In my first days

on Bee's supplements I got some good response and I started walking more.

Currently I can walk for up to 3-5km and end up with muscle pain which usually

go away on the next day. I noticed that tendons are the worst and once overused

it takes weeks/months to recover from the pain. I can't drive a car as they

affect the tendons more. I noticed my leg muscles got stronger after stopping

buckwheat (as suggested by Bee). Bee was right that I was full of toxins. I have

a pretty big problem with the supplements intake. I tried taking magnesium and

calcium but it looks like my body has enough of both from the diet. I tried many

combinations but I have either running stool = too much magnesium or twitching

eye and constipation, which I think means too much calcium. I stopped both

supplements and all the symptoms are gone. I will appreciate some feedback. In

addition, vit c when taken alone or magnesium gives me running stool too! If I

take both magnesium and vit C I get even worse.

> >

> > God bless you all,

> >

> >

> >

>

[Guest guest]

Hi ,

I can hear you are feeling very alone.

There will be lots of healing reactions in your journey. These

can be scary because there is a belief that if something is hurting etc then

that means we are getting sicker. But if you are sticking to Bee's diet this is

not the case, it is a healing reaction.

I think the coconut oil is a very vital ingredient to gets the fats up to the

right fat, protein, carb ratios. I can eat so much more now. It used to make be

gag and feel sick. Fats are great! I love them they are so healing!

The more healing that happens through this diet the more sense it makes as the

brain starts to function better and better. It doesn't function well when we are

sick.

I don't buy much that is organic either. Except free range eggs.

I have been on Bee's diet 5 months and am getting better and better.

You are worth the effort you make to heal.

Cassie

>

> Hi all,

> I am sorry for the lengthy email but I feel so terrible and lonely in all this

suffering. I am getting weaker and weaker in this fight. I must say the last few

months have been very hard for me and I lost almost everything I had in my life.

>

> Recently, due to my symptoms getting worse I lost my job and income, lost

apartment, barely able to pay the bills. I was unable to walk more than 300m a

day, still can't sit to long due to stiff muscles in my back pulling my neck and

shoulders, cant use my hands to type too long as I pull the rhomboid muscles (I

think). My wife also suffers from a bad digestion (gallbladder at 6%) and

chronic fatigue. I try to get her on the diet but it is so hard for her to

follow. It is much easier for me as I educated myself about Candida for a few

years now. I know I will lose her within the next 5 years unless we do something

about it. She is now the only person working (barely), I cannot work anymore. I

feel as if my body shrunk, muscles got shorter etc. Initially there were a few

symptoms where my tendons would hurt from overuse and do not recover for days

mostly in my wrists tendons. Then I got worse and worse, I thought it was

overuse but even 8 weeks of rest would do nothing. I got stiff in shoulders,

rhomboid and trapezes muscles as if no nutrients were delivered to those areas

to heal, I feel as if my entire body was no longer flexible, elastic. Recently

my legs started hurting, I initially did a bit of bicycle at the gym and noticed

that I had better blood flow and healing of the tendons would happen quicker.

>

> Diagnosis:

> That was when I realized it was no longer a simple muscle overuse. I was told

by muscular specialist and neurologist that I had fibromyalgia/mayofascial

syndrome = no cure. I was told my tendons are not getting enough collagen and

keep the muscle contracted. Thanks for nothing�I said. I mentioned Candida but

they did not agree, on the other hand they told me in was due to chemical

imbalance. That made me think of my diet again. I lived with Candida (I know

based on symptoms dandruff, eczema) for over 15 years but it never affected me

so badly until the last dose of antibiotics 5 years ago. After that I developed

dry mouth symptoms and allergic reactions to everything even water. It took me a

while to find that I could eat meat and buckwheat and drink a lot of tea as

liquid. After reading Bees notes I calculated my diet nutrients and was

deficient in almost all areas, mostly magnesium and calcium. I also did the IgA

which came up positive for fungal infection in my mouth. I was on a very high

carbs (buckwheat) and high protein (pork and lamb) diet for 3 years. No veggies

due to intolerance and burning in my mouth. Did gastroscopy and colonoscopy and

nothing. Tried Lamisil tablets but ended up with an outbreak of huge eczema on

my face. I stopped taking it die to side effects. My face was were the toxins

started coming out. I did feel great for a few days, I was back to normal and my

tongue was clear and plenty of saliva in my mouth. But I knew Lamisil tablets

could kill me and that was not the solution. I stopped after a week. When I

mentioned that to the gastrologist who gave me the tablets he could not explain

and said they do not really know how the tablets work yet�!!!???

>

> Currently:

> Now I can clearly see how the little signs were showing me how weak I was

getting. Tendons, muscle weakness, eczema, constantly acidic both urine and

saliva and dry body. My face was so dry and eczema was slowly taking over, hands

cold, dandruff, oily skin and hair etc.

> I know Bee does not recognise that making your body alkaline with supplements

will fix the problem. I do agree 100%, I know my body will get alkaline only

through proper diet. However I must say that by drinking a very little amount of

baking soda 1.25mg with 1 lime juice and water twice a day I managed to stop my

oily skin, eczema, oily hair, oily back and back acne, within a few days. I hope

it is okay with the diet and will not destroy the entire program. I have really

suffered for 15 years from eczema and oily face etc, unable to shave properly

due to dry, irritated skin. In the last few years my penis got also very dry and

eczema would start getting there, after that simple drink it is all gone now.

>

> Diet and Supplements issues:

> I am getting ready for Bee's diet; I got the supplements and started on the

diet but can't afford organic food yet, hopefully next month. In my first days

on Bee's supplements I got some good response and I started walking more.

Currently I can walk for up to 3-5km and end up with muscle pain which usually

go away on the next day. I noticed that tendons are the worst and once overused

it takes weeks/months to recover from the pain. I can't drive a car as they

affect the tendons more. I noticed my leg muscles got stronger after stopping

buckwheat (as suggested by Bee). Bee was right that I was full of toxins. I have

a pretty big problem with the supplements intake. I tried taking magnesium and

calcium but it looks like my body has enough of both from the diet. I tried many

combinations but I have either running stool = too much magnesium or twitching

eye and constipation, which I think means too much calcium. I stopped both

supplements and all the symptoms are gone. I will appreciate some feedback. In

addition, vit c when taken alone or magnesium gives me running stool too! If I

take both magnesium and vit C I get even worse.

>

> God bless you all,

>

>

>

[Guest guest]

Hi Cassie,

Thank you for your reply. I really need it. For the last few days I noticed real

change, my legs got so much stronger. I feel like everyday bit by bit I move

forward, sometimes is just too hard.

Thanks for email,time for my delicious breakfast,

Good luck to you all,,

Rob

> >

> > Hi all,

> > I am sorry for the lengthy email but I feel so terrible and lonely in all

this suffering. I am getting weaker and weaker in this fight. I must say the

last few months have been very hard for me and I lost almost everything I had in

my life.

> >

> > Recently, due to my symptoms getting worse I lost my job and income, lost

apartment, barely able to pay the bills. I was unable to walk more than 300m a

day, still can't sit to long due to stiff muscles in my back pulling my neck and

shoulders, cant use my hands to type too long as I pull the rhomboid muscles (I

think). My wife also suffers from a bad digestion (gallbladder at 6%) and

chronic fatigue. I try to get her on the diet but it is so hard for her to

follow. It is much easier for me as I educated myself about Candida for a few

years now. I know I will lose her within the next 5 years unless we do something

about it. She is now the only person working (barely), I cannot work anymore. I

feel as if my body shrunk, muscles got shorter etc. Initially there were a few

symptoms where my tendons would hurt from overuse and do not recover for days

mostly in my wrists tendons. Then I got worse and worse, I thought it was

overuse but even 8 weeks of rest would do nothing. I got stiff in shoulders,

rhomboid and trapezes muscles as if no nutrients were delivered to those areas

to heal, I feel as if my entire body was no longer flexible, elastic. Recently

my legs started hurting, I initially did a bit of bicycle at the gym and noticed

that I had better blood flow and healing of the tendons would happen quicker.

> >

> > Diagnosis:

> > That was when I realized it was no longer a simple muscle overuse. I was

told by muscular specialist and neurologist that I had fibromyalgia/mayofascial

syndrome = no cure. I was told my tendons are not getting enough collagen and

keep the muscle contracted. Thanks for nothing�I said. I mentioned Candida but

they did not agree, on the other hand they told me in was due to chemical

imbalance. That made me think of my diet again. I lived with Candida (I know

based on symptoms dandruff, eczema) for over 15 years but it never affected me

so badly until the last dose of antibiotics 5 years ago. After that I developed

dry mouth symptoms and allergic reactions to everything even water. It took me a

while to find that I could eat meat and buckwheat and drink a lot of tea as

liquid. After reading Bees notes I calculated my diet nutrients and was

deficient in almost all areas, mostly magnesium and calcium. I also did the IgA

which came up positive for fungal infection in my mouth. I was on a very high

carbs (buckwheat) and high protein (pork and lamb) diet for 3 years. No veggies

due to intolerance and burning in my mouth. Did gastroscopy and colonoscopy and

nothing. Tried Lamisil tablets but ended up with an outbreak of huge eczema on

my face. I stopped taking it die to side effects. My face was were the toxins

started coming out. I did feel great for a few days, I was back to normal and my

tongue was clear and plenty of saliva in my mouth. But I knew Lamisil tablets

could kill me and that was not the solution. I stopped after a week. When I

mentioned that to the gastrologist who gave me the tablets he could not explain

and said they do not really know how the tablets work yet�!!!???

> >

> > Currently:

> > Now I can clearly see how the little signs were showing me how weak I was

getting. Tendons, muscle weakness, eczema, constantly acidic both urine and

saliva and dry body. My face was so dry and eczema was slowly taking over, hands

cold, dandruff, oily skin and hair etc.

> > I know Bee does not recognise that making your body alkaline with

supplements will fix the problem. I do agree 100%, I know my body will get

alkaline only through proper diet. However I must say that by drinking a very

little amount of baking soda 1.25mg with 1 lime juice and water twice a day I

managed to stop my oily skin, eczema, oily hair, oily back and back acne, within

a few days. I hope it is okay with the diet and will not destroy the entire

program. I have really suffered for 15 years from eczema and oily face etc,

unable to shave properly due to dry, irritated skin. In the last few years my

penis got also very dry and eczema would start getting there, after that simple

drink it is all gone now.

> >

> > Diet and Supplements issues:

> > I am getting ready for Bee's diet; I got the supplements and started on the

diet but can't afford organic food yet, hopefully next month. In my first days

on Bee's supplements I got some good response and I started walking more.

Currently I can walk for up to 3-5km and end up with muscle pain which usually

go away on the next day. I noticed that tendons are the worst and once overused

it takes weeks/months to recover from the pain. I can't drive a car as they

affect the tendons more. I noticed my leg muscles got stronger after stopping

buckwheat (as suggested by Bee). Bee was right that I was full of toxins. I have

a pretty big problem with the supplements intake. I tried taking magnesium and

calcium but it looks like my body has enough of both from the diet. I tried many

combinations but I have either running stool = too much magnesium or twitching

eye and constipation, which I think means too much calcium. I stopped both

supplements and all the symptoms are gone. I will appreciate some feedback. In

addition, vit c when taken alone or magnesium gives me running stool too! If I

take both magnesium and vit C I get even worse.

> >

> > God bless you all,

> >

> >

> >

>

[Guest guest]

My therapist told me the same thing. Many of his patients have had a traumatic

event around the age of 5 and have either fibro, RA or lupus.

I was molested by a friend of my dad and no one knew and I carried this all my

life. By the age of 45, I developed RA, then fibro. Now there is a type of

therapy called release something (not sure, searching) and it is specifically

for those of us who had those traumas. Hope others can get the help they need

before they become sick. It is so sad to suffer for something that someone do to

you....

Pain free days to all

in Ca

[Guest guest]

Hi ,

Have similar symptoms re. tendons,muscles etc. Was wondering how you are going

on the diet and if you have seen any improvement?

Lavinia

>

<snip>

>

> That was when I realized it was no longer a simple muscle overuse. I was told

by muscular specialist and neurologist that I had fibromyalgia/mayofascial

syndrome = no cure. I was told my tendons are not getting enough collagen and

keep the muscle contracted. Thanks for nothing…I said. I mentioned Candida but

they did not agree, on the other hand they told me in was due to chemical

imbalance. That made me think of my diet again. I lived with Candida (I know

based on symptoms dandruff, eczema) for over 15 years but it never affected me

so badly until the last dose of antibiotics 5 years ago.