Back again

[Guest guest]

In a message dated 99-07-05 21:33:55 EDT, you write:

<< just to let you know, that i know of 4 other people who have tested

positive for babesiosis recently that have been ill with lyme for several

years. accoding to my new dr., if you have an undiagnosed co-infection,

the lyme will never really get better until the co-infection has been

cleared up!!

>>

HELP! Please explain what babesiosis is? Are there separate symptoms? How

does one know if one has a co-infection? HELP!

New Bedford, MA

[Guest guest]

In a message dated 7/9/99 10:10:42 AM Eastern Daylight Time,

dakas@... writes:

<< As to your question about: what are the symptoms? They are similar to

Lyme Disease and if you also have Lyme Disease, the symptoms for

Babesiosis are not as predominant.

>>

Thanks Kathie. It will be something I'm going to discuss with my LLMD when I

see him again later this month.

, New Bedford, MA.

<A HREF= " http://members.tripod.com/LymeDizzez/ " >Lyme Disease and Me</A>

ICQ # 26791014

Need a new FREE E-mail Address: www.phlexmail.net

[Guest guest]

Hi :

There are a several other tick-borne diseases, and babesiosis is one of

them. This is a parasitic infection of the red blood cells (a cousin of

malaria). How do you know you have it? You have to be tested for it.

As to your question about: what are the symptoms? they are similar to

Lyme Disease and if you also have Lyme Disease, the symptoms for

Babesiosis are not as predominant.

If you would like more information, e-mail me at DAKAS@...

and I will be more than happy to send you more information!

kathie

[Guest guest]

Welcome back Caroline! So happy to hear from you. You sound like you are going to have your hands full with two little ones!!! Double trouble, but have tons of fun! They aren't little for long!

debby

[ ] Back again

Hi Debby Harper Tony etcYou may not remember me (aprt from anything else Iknow what my memory is like) - Caroline from NZ.Last posted at the end of Feb while I was inChristchurch and am now back home in Invercargill.It has taken me forever to get myself this new toy andget back on-line. I did go and use the computer inthe library but I can't think straight when I'm tryingto write in public - so just gave up on that. It is good to just scroll through and catch up withnew friends and old friends. Am looking forward tohaving daily access again.My twin neices (nearly 4) are coming to overnight atmy place today so I guess my time online will besomewhat restricted until they go -- but then I'mlooking forward to really catching up.Love to you all Caroline (NZ)__________________________________________________

[Guest guest]

Hi Caroline =)

welcome back,glad you have your new toy,only thing better than a kiwi is two

blessings. Amber

>From: caroline mayne <seajay192002@...>

>Reply-

>liver friends < >

>Subject: [ ] Back again

>Date: Mon, 22 Apr 2002 14:28:29 -0700 (PDT)

>

>Hi Debby Harper Tony etc

>You may not remember me (aprt from anything else I

>know what my memory is like) - Caroline from NZ.

>Last posted at the end of Feb while I was in

>Christchurch and am now back home in Invercargill.

>It has taken me forever to get myself this new toy and

>get back on-line. I did go and use the computer in

>the library but I can't think straight when I'm trying

>to write in public - so just gave up on that.

>It is good to just scroll through and catch up with

>new friends and old friends. Am looking forward to

>having daily access again.

>My twin neices (nearly 4) are coming to overnight at

>my place today so I guess my time online will be

>somewhat restricted until they go -- but then I'm

>looking forward to really catching up.

>Love to you all Caroline (NZ)

>

>__________________________________________________

>

[Guest guest]

HI CAROLINE,

I'M NEW HERE BUT WELCOME BACK.

[Guest guest]

Hi Caroline!

Nice to have you back as well. I know you have to be thrilled with

your computer at home. Enjoy it and I talk to you soon!

TONY

[Guest guest]

Hi Caroline!

Nice to have you back as well. I know you have to be thrilled with

your computer at home. Enjoy it and I talk to you soon!

TONY

[Guest guest]

Hi Elaine,

Great to have you back, but I'm sorry you've had such a rough time.

When you're ready, I'd love to hear more about what happened.

Thanks for asking about my mom. Her surgery is scheduled for May 13th.

I'm heading up on May 9th. She's having both the right hip and knee

replaced. She's also moving into a new house on June 1st, which means

I'll be coming back from the hospital each evening and and I will

be boxing up the contents of her apartment. She's wanted a house for a

long time, and needed something single story. I'm glad she found it,

but the timing could not be worse. My brother Jeff is going to have to

help out, no matter how busy he is. I don't want to end up in bed all

summer due to overdoing it during the month I'm in Atlanta with her.

The good news, I think, is that she'll only be about a block from Jeff.

Hopefully that will translate into her having more help once I head back

home.

Hope you're doing better!

Love and hugs,

Carol

[ ] Back again

My sincere apologies to those of you that so kindly answered my

messages and that I did not respond back. I assure you it was not out

of not caring. I do appreciate the kind and encouraging messages I

received.

Unfortunately I've had a very rough time and my trip to UCLA did not

go as planned. I will be sharing with all of you my experience in the

hope I can spare some of you what I went through. My recuperation was

also much slower than I'd anticipated.

Meanwhile I am back, I am trying to get caught up on reading my

email, and attempting to participate once again.

Heidi, how is " Tad " . Is your tummy getting bigger? We'd love to see a

picture (or did I miss something and you have posted a picture??).

Judi, hope your ankle heals quickly and completely. You've had more

than your share of illness and accident. Your grandchildren are

beautiful! You have a lovely family. Thanks for sharing the pictures.

Know you must love holding the babies and caring for them. It is

wonderful you are there to help out so much. Your daughter is

extremely fortunate. You and your family are living proof that no

matter how heavy our cross gets, the Lord is there to help us

through. God bless you all.

Carol, how is your mom? Isn't her surgery coming up soon? I'm sorry,

I'm not remembering the date.

Debs, how are you doing? I hope I haven't missed a post with your

update.

To everyone, i'm sorry I'm not remembering to ask individually about

each of you. It's not from lack of caring, it's from being in a " fog "

and the late hour. I know there are posts I want and need to respond

to, but will have to go back and re-read. Names are not my strong

point and I don't want to write the wrong message to the wrong person

and embarrass myself even more.

Elaine

[Guest guest]

Glad that you're back, Noreen.

I think they're supposed to be teaching compassion to med students now,

LOL. If they did in the past, very few who took that class did well.

Maybe a few CME courses are in order for those who didn't get it the

first time - and we'll do the grading!

I'm sorry that your mother and husband don't understand. It's so

frustrating to have to deal with that sort of constant burden.

I hope you can find an exercise program that works for you. Slow and

steady weight loss is the best. It's good that you're making progress. I

think that walking is a great, simple way to exercise, but I'm not sure

if your knee will cooperate.

[ ] Back again

> Hi, I've been off in lurking land for awhile. I read messages

everyday, but

> have been just watching, smiling, crying sometimes and glad to have

all of

> you.

>

> Welcome to the new people and glad to see Debs, Kathy, and others

back. I

> can't believe some of the jerk doctors there are out there. Makes me

want to

> scream.

> Don't they give any classes in compassion in med school?

>

> I made it through the holiday season quite well, joint pain was mild

enough,

> thank goodness, and the cortisone shot in my knee made me able to shop

and

> walk. Well, two months after the shot, and it's wearing off. My

rheumy says

> it's ok to have shots every few months as long as they work, but we

both

> know that eventually, I'll need a new knee. Years of weight stress, RA

and

> falling hard on icy driveways three times are taking their toll.

>

> I've lost a little weight. Rheumy says just keep it slow and that's

fine.

> For those of you who've heard me whine before, you know part of my

problems

> have to deal with a husband and mother who keep telling me I'm not

sick,

> just too fat. (the latest, my mother tells me I wouldn't be fatigued

if I

> wasn't fat. This despite the fact she lived with my Dad's RA for 30+

years

> and knew he needed a nap every day.)

>

> Now, I'm looking for some sort of exercise to keep me mobile. Has

anyone

> tried Tai Chi? I don't want anything that's hard on the joints, and

although

> I know that water aerobics would be best, I just cannot fit that into

my

> schedule. I also don't want to have to be on the floor too much,

because

> it's a royal pain getting up again.

>

> Thanks for letting me ramble, and it really is great to have this

place to

> come to, even on the days when I just want to listen.

>

> Noreen

[Guest guest]

Noreen....Reading your post I must confess to anger.....I know many

have family members that cant or wont try to understand, but it makes

me mad and sad to read how you are treated. I think I would look for

the most vivivly colored ear plugs I could find and everytime they

started insert them....I am sorry on top of everything else you must

also deal with this.....I havent tried Tai Chai, but I do water 3

days a week, and pilates stretching and it does make a difference.

There are times when I cant get there, but it does help and you

realize how much when you stop. I think Tess had a good suggestion,

as any movement routine will help.....Good luck and I hope you post

what you decide on and if it helps. My husband has that lovely phrase

of morbib obeisity.....hate that phrase....and I tell him it is the

person INSIDE we love.....so when they are concentrating on the

outside person, remember it is the inside person that is

loved......hoping you have better days... Kathi in OK

--- In , " Noreen Saukko " <nsaukko@r...>

wrote:

> Hi, I've been off in lurking land for awhile. I read messages

everyday, but

> have been just watching, smiling, crying sometimes and glad to have

all of

> you.

>

> Welcome to the new people and glad to see Debs, Kathy, and others

back. I

> can't believe some of the jerk doctors there are out there. Makes

me want to

> scream.

> Don't they give any classes in compassion in med school?

>

> I made it through the holiday season quite well, joint pain was

mild enough,

> thank goodness, and the cortisone shot in my knee made me able to

shop and

> walk. Well, two months after the shot, and it's wearing off. My

rheumy says

> it's ok to have shots every few months as long as they work, but we

both

> know that eventually, I'll need a new knee. Years of weight stress,

RA and

> falling hard on icy driveways three times are taking their toll.

>

> I've lost a little weight. Rheumy says just keep it slow and that's

fine.

> For those of you who've heard me whine before, you know part of my

problems

> have to deal with a husband and mother who keep telling me I'm not

sick,

> just too fat. (the latest, my mother tells me I wouldn't be

fatigued if I

> wasn't fat. This despite the fact she lived with my Dad's RA for

30+ years

> and knew he needed a nap every day.)

>

> Now, I'm looking for some sort of exercise to keep me mobile. Has

anyone

> tried Tai Chi? I don't want anything that's hard on the joints, and

although

> I know that water aerobics would be best, I just cannot fit that

into my

> schedule. I also don't want to have to be on the floor too much,

because

> it's a royal pain getting up again.

>

> Thanks for letting me ramble, and it really is great to have this

place to

> come to, even on the days when I just want to listen.

>

> Noreen

[Guest guest]

, Noreen and all, the Patient Partners programme covers in great detail

about compassion and it is comforting for me to see these young med students

listening to this message. During the class we also talk about function since a

doctor rarely mentions it to his patient and it is so important for the patient

to tell the doctor what limitations they have and how they cope day to day.

Hopefully, with this information the doctor can refer them to an OT or PT and

the Arthritis Society for additional help.

Noreen, I have had RA for 18 years and if anyone should know what it is all

about it should be my better half. However, when discussing my new scooter, he

said and I quote " Well if we put out all this money, I hope you use it, suppose

the next ortho fixes your ankle? " Some people, and unfortunately, it is usually

family members that just don't get it. We just have to keep trying to educate

them. Fortunately for Don, he stopped talking when he noticed I had THAT look on

my face, the same look I used on my boys when they were pushing my buttons

Hugs

June

Subject: Re: [ ] Back again

Glad that you're back, Noreen.

I think they're supposed to be teaching compassion to med students now,

LOL. If they did in the past, very few who took that class did well.

Maybe a few CME courses are in order for those who didn't get it the

first time - and we'll do the grading!

I'm sorry that your mother and husband don't understand. It's so

frustrating to have to deal with that sort of constant burden.

I hope you can find an exercise program that works for you. Slow and

steady weight loss is the best. It's good that you're making progress. I

think that walking is a great, simple way to exercise, but I'm not sure

if your knee will cooperate.

[ ] Back again

> Hi, I've been off in lurking land for awhile. I read messages

everyday, but

> have been just watching, smiling, crying sometimes and glad to have

all of

> you.

>

> Welcome to the new people and glad to see Debs, Kathy, and others

back. I

> can't believe some of the jerk doctors there are out there. Makes me

want to

> scream.

> Don't they give any classes in compassion in med school?

>

> I made it through the holiday season quite well, joint pain was mild

enough,

> thank goodness, and the cortisone shot in my knee made me able to shop

and

> walk. Well, two months after the shot, and it's wearing off. My

rheumy says

> it's ok to have shots every few months as long as they work, but we

both

> know that eventually, I'll need a new knee. Years of weight stress, RA

and

> falling hard on icy driveways three times are taking their toll.

>

> I've lost a little weight. Rheumy says just keep it slow and that's

fine.

> For those of you who've heard me whine before, you know part of my

problems

> have to deal with a husband and mother who keep telling me I'm not

sick,

> just too fat. (the latest, my mother tells me I wouldn't be fatigued

if I

> wasn't fat. This despite the fact she lived with my Dad's RA for 30+

years

> and knew he needed a nap every day.)

>

> Now, I'm looking for some sort of exercise to keep me mobile. Has

anyone

> tried Tai Chi? I don't want anything that's hard on the joints, and

although

> I know that water aerobics would be best, I just cannot fit that into

my

> schedule. I also don't want to have to be on the floor too much,

because

> it's a royal pain getting up again.

>

> Thanks for letting me ramble, and it really is great to have this

place to

> come to, even on the days when I just want to listen.

>

> Noreen

[Guest guest]

Thanks June. Glad to know my family isnt' the only blind one out there.

Noreen

[Guest guest]

There is hope then, June! I'm glad Patient Partners is teaching such

important aspects of patient care.

That's a hilarious story about you and Don. I know exactly what you mean

by THAT look, LOL.

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

Re: [ ] Back again

> , Noreen and all, the Patient Partners programme covers in great

detail about compassion and it is comforting for me to see these young

med students listening to this message. During the class we also talk

about function since a doctor rarely mentions it to his patient and it

is so important for the patient to tell the doctor what limitations they

have and how they cope day to day. Hopefully, with this information the

doctor can refer them to an OT or PT and the Arthritis Society for

additional help.

>

> Noreen, I have had RA for 18 years and if anyone should know what it

is all about it should be my better half. However, when discussing my

new scooter, he said and I quote " Well if we put out all this money, I

hope you use it, suppose the next ortho fixes your ankle? " Some people,

and unfortunately, it is usually family members that just don't get it.

We just have to keep trying to educate them. Fortunately for Don, he

stopped talking when he noticed I had THAT look on my face, the same

look I used on my boys when they were pushing my buttons

>

> Hugs

> June

[Guest guest]

Noreen,

Welcome back from lurkland. I've been visiting it myself lately. My house

is undergoing renovations and my computer has been getting shuffled.

It makes me angry when I hear people placing blame on being overweight. I

was skinny when I was DX'ed with RA. I was 5'6 " and only 104 lbs.

Congratulations on your weight loss. Try not to let the remarks get to you.

They just don't get it.

a

> Hi, I've been off in lurking land for awhile. I read messages everyday, but

> have been just watching, smiling, crying sometimes and glad to have all of

> you.

>

> Welcome to the new people and glad to see Debs, Kathy, and others back. I

> can't believe some of the jerk doctors there are out there. Makes me want to

> scream.

> Don't they give any classes in compassion in med school?

>

> I made it through the holiday season quite well, joint pain was mild enough,

> thank goodness, and the cortisone shot in my knee made me able to shop and

> walk. Well, two months after the shot, and it's wearing off. My rheumy says

> it's ok to have shots every few months as long as they work, but we both

> know that eventually, I'll need a new knee. Years of weight stress, RA and

> falling hard on icy driveways three times are taking their toll.

>

> I've lost a little weight. Rheumy says just keep it slow and that's fine.

> For those of you who've heard me whine before, you know part of my problems

> have to deal with a husband and mother who keep telling me I'm not sick,

> just too fat. (the latest, my mother tells me I wouldn't be fatigued if I

> wasn't fat. This despite the fact she lived with my Dad's RA for 30+ years

> and knew he needed a nap every day.)

>

> Now, I'm looking for some sort of exercise to keep me mobile. Has anyone

> tried Tai Chi? I don't want anything that's hard on the joints, and although

> I know that water aerobics would be best, I just cannot fit that into my

> schedule. I also don't want to have to be on the floor too much, because

> it's a royal pain getting up again.

>

> Thanks for letting me ramble, and it really is great to have this place to

> come to, even on the days when I just want to listen.

>

> Noreen

>

>

>

>

[Guest guest]

Hey Rhonda,

It's always good to realize that you atleast know what to do to make yourself

feel better. It's a tough battle, but you know how to fight it now, and you know

that there is a silver lining. You've done it once, you can do it again, this

time even better then before.

Good luck to you, not that you need it ;P

-B.B.

Back Again

Hello Everyone,

I don't know if there is anyone here that was around when I used to

post. I have been gone for a while and now I am back. For a while

last Fall and throughout the winter and spring, I did really well on

my Candida diet. I was almost symptom free. I lost a lot of excess

weight and I felt and looked really good.

Sadly, that isn't the case now. I have let the diet slide. I have

gained about 20 pounds. I have horrible sinus congestion, a constant

sore throat, pain in my ears and rawness inside my mouth. I am

cranky and lethargic. Plus, I seem to have no control over my

eating. No matter what I wake up telling myself ( " Today will be the

day that I turn a new leaf " ...) before too long, I am eating

mountains of sugary and starchy treats.

Since I started my Candida program last year, I have never returned

to eating dairy products or wheat. In fact, I have eliminated all

grains containing gluten after a vicious episode in March. After

eating only spouted grain and spelt for many months, I decided to

have a small piece of white birthday cake at a friend's party I

ended up in the Emergency with what the doctors suppose was a celiac

incident.

I guess, in short, I need the motivation to start my program again.

I was quite successful and after the initial die-off, I felt better

than I ever have in my life. During that time, I trained a ran my

first half-marathon.

I am hoping some words of support might help me start this process

again. I might go to the health food store today and start taking

Fungal Defense again. That seemed to help me before. If you can

share any thoughts or words of inspiration, I would appreciate it!

Rhonda

[Guest guest]

Hi Rhonda - and welcome back.

I've been hanging around this board for over a year now - that's after

battling Candida for 15 years (though at first, no one in my neck of the

woods had heard of it - I found a book overseas on Candida Albicans which

opened my eyes).

After many failures with staying on the program, last fall I decided to

" get serious " about eliminating the Candida and I went on the " diet " for

five months - and didn't cheat (even at Christmas). And then got a tooth

infection and got sick again.

This made me rethink the diet. Obviously it wasn't the whole answer.

Yes, the diet is good - no sugar, no white flour, yada, yada, does keep my

symptoms under control - but the fact is, it isn't a " cure " for what ails

you. And you have to stay on the regiman forever in order to feel well.

(As you have already found out).

I had to ask myself why the Candida was so persistent .

In the end, I had to agree with the burgeoning theory that the Candida

remains persistent for a reason - it's there to help us cope with toxic

overload.

So, bottom line, I think you have to take steps to get rid of the toxicity

by cleaning up your system - colon, kidneys, liver, lympth - the whole

magilla. And that's what I have been working on and I have to say that I am

seeing some real progress.

So, yes, you can do this again. But do it differently - think of doing some

cleanses. Was it g who advised the following? " Develop a plan; Make it

happen; Give yourself time; I CAN DO IT!! " And you can do it.

Here's to a new day and a new beginning for you. Chuck the cookies and haul

out the Stevia. YOU can do it!

Cheers - p

>

> ----- Original Message -----

> From: girlfromns

Hello Everyone,

>

> I am hoping some words of support might help me start this process

> again. I might go to the health food store today and start taking

> Fungal Defense again. That seemed to help me before. If you can

> share any thoughts or words of inspiration, I would appreciate it!

>

> Rhonda

>

>

>

>

>

>

>

>

>

[Guest guest]

Thanks for the kind words everyone. Penny, Asli...you are so correct. The diet

is not the ultimate answer for me. I am generally such a solution oriented

person, that in any other area of my life, I would be more focused on getting

the the root of the issue and solving the problem. Why I have convinced myself

that a difficult to maintain food regime is the answer I don't know....maybe the

lack of other viable solutions made it seem like the only way.

I will look into a few cleanses and do more research. I want to also review the

times when I felt best in recent years as well as the times when I felt the

worst and see what trends I can pick out. This time of year (mid August to end

October) seems to be the worst time of all for me, phycially and emotionally. I

need to really look at the big picture and stop beating myself up!

Its great to know there is somewhere to turn. Thanks for being there.

Rhonda

[Guest guest]

>

> I am finally back after two months of being off the list. I had bad

EMF > problems with the computer when I took Omnicef for a sinus

infection. I > couldn't use the computer without getting headaches and

feelings of not > being able to breathe while I was on the computer!

> I now have a sinus fungus. The Diflucan causes bad stomach-aches and

a > lot of double-beats for my heart. I am trying to up my probiotics.

I > have not experimented with the coconut oil or garlic yet. It feels

like > it is covering the top of my mouth and slowly sliding down my

throat. I > had a culture on it last week but no results yet. I am off

eggs, > bananas, and raw butter.

==>You need eggs and raw butter, because good foods will cause healing

reactions which are mistaken for allergic reactions. Diflucan is

extremely hard on the liver and your doctor should have tested you

before and every month while you are on it. IMO raw garlic, oil of

oregano, etc. are more effective than any drugs and won't harm the body.

==>Read the articles on Thrush and Sinus for help with that awful

feeling in your mouth.

==>I'm glad you're back Joyce!

Hugs, Bee

[Guest guest]

Hi Nithya,

I've been thinking of you lately, wondering how you've been and how school is

going (hopefully that doesn't sound too creepy! LOL!). It's nice to see you

back here again! Hopefully you will get back into the swing of things with

regards to the program.

I also had the feeling that my thyroid was 'off' because of my symptoms. I had

had several different doctors check it out, but nothing ever showed up. I think

the tests aren't necessarily sensitive enough to pick up everything. Bee's

program will certainly help with it. Here's an article about thyroid:

http://www.healingnaturallybybee.com/articles/treat19.php

Check out the Success Stories, too. There have been new additions since the

last time you were here about people who have been able to go off their thyroid

medications since their thyroid functioning improved after being on Bee's diet:

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

Take care,

>

> DEar Bee and everyone else in the group.

>

> Its been a while since I have posted a message in the forum. I have sort of

digressed from the diet since the end of last year because had a lot on my plate

and couldnot handle the die-off symptoms and I was also having trouble

financially. But now I realise that I have to bit the bullet and jump back on

the band-wagon beacuse Bee's diet is the road to recovery. I just have a few

questions that have been bothering me for a while and would greatly appreciate

any help with them.

>

<snip>

>

>

> Thanks in advance for your help and I hope everyones diet and eating plan is

working out!

>

> lots of love

> Nithya

>

[Guest guest]

>

> DEar Bee and everyone else in the group.

>

> Its been a while since I have posted a message in the forum. I have sort of

digressed from the diet since the end of last year because had a lot on my plate

and couldnot handle the die-off symptoms and I was also having trouble

financially. But now I realise that I have to bit the bullet and jump back on

the band-wagon beacuse Bee's diet is the road to recovery. I just have a few

questions that have been bothering me for a while and would greatly appreciate

any help with them.

+++Hi Nithya. It's good to hear from you again. You can get right back on the

band-wagon again, but ensure you do not makes changes to your diet too fast.

Also go easy with coconut oil, starting at a low amount and only gradually

increasing it so your die-off symptoms aren't so bad.

>

> 1.) Is it ok to use bamboo steamers when steaming veges? I have heard that

people, especially yeast sufferers, shouldn't because mold can grow on bamboo

steamers. If these arn't a viable option what can we use to steam veges? Are

stainless steal steamers ok?

+++Bamboo steamers are fine to use.

> Also with mold I have heard that we should not at all use tea bags beacsue of

possible mold contamination. Is this true?

+++No, I don't think tea bags are a problem for mold since you put them in hot

to boiling water anyway.

>

> 2.)Should we get stainless steel reverse osmosis filter rather then a plastic

one because of the dangerous chemicals that plastics can release into water?

+++I don't believe it is worth the expense and problems to use reverse osmosis

filters, unless your water is totally offensive. Reverse osmosis water is

totally devoid of minerals, so you have to add minerals to them. I think it is

better to " get those minerals " which are natural in tap water and can't possibly

be duplicated in mineral drops - so I recommend a charcoal filter like Brita

instead.

>

> 3.)I have heard that large magnetic fields (generated by alarm clocks Tvs etc)

are not good for immune depressed people, like people suffering from a yeast

infection. Is this true and do electric toothbrushes induce a large magnetic

field?

+++Yes, that is true, so you should do what you can to move electric appliances

away from your bed about 4 feet, i.e. lamp, clock radio, etc. But don't be

overly concerned since most people who are successfull on this program haven't

removed electromagnetic fields, yet they still get well because " proper

nutrients " are much more important.

+++However, you should not use an electric toothbrush.

<snip>

>

> 5.) Bee I know that you say we dont need to rotate foods whilst on your diet,

but is it ok to eat exactly the same foods everyday for the same meal(ie same

breakfast, lunch and dinner everyday of the week. I am asking this beacsue it is

just easier for me as a student to stick to and learn how to make one set of

staples everyday.

+++Yes, it is quite okay to eat the same foods every day, etc.!

>

> 6.) Also do you think that it would be a good idea to get a air dehumidifier,

air ioniser and air filter to get rid of toxins and chemicals?

+++They aren't necessary for most candida sufferers; some who get severe

reactions to environmental molds, dander, dust mites, etc. may need to. The

most important thing for health is " proper nutrients " - my diet plus all

supplements, so concentrate on those.

The best to you, Bee

[Guest guest]

Hello,

I have been a member of the support group but have not participated in a long

time....

Does anyone know of any genetics physicians (other than Emory Clinic) in the

Atlanta, Ga area?

I have heard they have done recent research on bpes and I am very interested if

anyone has any current info. My son, has bpes with developmental delays, speech

delays,ect...

Thanks,

Kim

[Guest guest]

Hi. I'm not from GA, I'm from MA. My son has BPES and also has developmental and speech delays as well as Hypotonia. I've heard from few that share this.

Good luck and I am waiting for some add'l results from our Genetics Physician and will share.

Sandy

From: kim_mcnatt <kim_mcnatt@...>blepharophimosis Sent: Tue, March 16, 2010 4:57:34 PMSubject: blepharophimosis Back again

Hello,I have been a member of the support group but have not participated in a long time....Does anyone know of any genetics physicians (other than Emory Clinic) in the Atlanta, Ga area?I have heard they have done recent research on bpes and I am very interested if anyone has any current info. My son, has bpes with developmental delays, speech delays,ect.. .Thanks,Kim

[Guest guest]

My son has BPES, developmental delays and hypotonia.  He was

recently diagnosed with a duplication on Chromosome 10.  The test was done at

Duke Children’s Hospital.  His physician is Dr. Marie Mc.

Maureen

From:

blepharophimosis [mailto:blepharophimosis ] On

Behalf Of sandy redgate

Sent: Tuesday, March 16, 2010 5:06 PM

blepharophimosis

Subject: Re: blepharophimosis Back again

Hi. I'm not from GA, I'm from MA. My son has BPES and also

has developmental and speech delays as well as Hypotonia. I've heard from few

that share this.

Good luck and I am waiting for some add'l results from our

Genetics Physician and will share.

Sandy

From: kim_mcnatt

<kim_mcnatt@...>

blepharophimosis

Sent: Tue, March 16, 2010 4:57:34 PM

Subject: blepharophimosis Back again

Hello,

I have been a member of the support group but have not participated in a long

time....

Does anyone know of any genetics physicians (other than Emory Clinic) in the

Atlanta, Ga area?

I have heard they have done recent research on bpes and I am very interested if

anyone has any current info. My son, has bpes with developmental delays, speech

delays,ect.. .

Thanks,

Kim

[Guest guest]

Hallo i am caterina and my daughter 18 months, has also BEPS and she is also speech delays. How old are your children?Will it be better in future? Has anybody experience with it?--- joseph pulliam <jcp@...> schrieb am Mi, 17.3.2010:

Von: joseph pulliam <jcp@...>Betreff: RE: blepharophimosis Back againAn: blepharophimosis Datum: Mittwoch, 17. März, 2010 01:36 Uhr

My son has BPES, developmental delays and hypotonia. He was recently diagnosed with a duplication on Chromosome 10. The test was done at Duke Children’s Hospital. His physician is Dr. Marie Mc.

Maureen

From: blepharophimosis [mailto:blepharophi mosis@group s.com] On Behalf Of sandy redgateSent: Tuesday, March 16, 2010 5:06 PMblepharophimosisSubject: Re: blepharophimosis Back again

Hi. I'm not from GA, I'm from MA. My son has BPES and also has developmental and speech delays as well as Hypotonia. I've heard from few that share this.

Good luck and I am waiting for some add'l results from our Genetics Physician and will share.

Sandy

From: kim_mcnatt <kim_mcnatt (DOT) com>blepharophimosisSent: Tue, March 16, 2010 4:57:34 PMSubject: blepharophimosis Back again

Hello,I have been a member of the support group but have not participated in a long time....Does anyone know of any genetics physicians (other than Emory Clinic) in the Atlanta, Ga area?I have heard they have done recent research on bpes and I am very interested if anyone has any current info. My son, has bpes with developmental delays, speech delays,ect.. .Thanks,Kim

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