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hi t...interact away....glad you liked the book and seemed to have

learned a lot. Some of us have been following the diet for 2 to 3

years now. We will be happy to help you any way we can.

OKC

anybody outthere that is O type looking for input, red the book in 3

hours totally enthralled. wish to interact.

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Hi

Welcome to the group.

I follow the plan to help me with my fight against ME.

Should be eating meat but am a vegetarian and doing very well.

I also take 2 Olive leaf capsules per day.

Best wishes

Elize

Johannesburg

South Africa

>>> t1@... 04/07/00 03:12AM >>>

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which book did you read?

sparrow

new user

> anybody outthere that is O type looking for input, red the book in 3

> hours totally enthralled. wish to interact.

>

>

> --------------------------------------------------------------------------

------

>

>

>

> --------------------------------------------------------------------------

------

>

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hi my son is allergic to animal protien, he breaks out in a horrible

rash and can't breath, poops liquid, and is general very bitchy if he

get some. relatives always used to try to test if he really was by

slipping some in his food. they thought we were just saying that as we

are all vegan.

he is fine and is taller and stronger than all his peers.

re jn

> Hi

>

> Welcome to the group.

>

> I follow the plan to help me with my fight against ME.

>

> Should be eating meat but am a vegetarian and doing very well.

>

> I also take 2 Olive leaf capsules per day.

>

> Best wishes

>

> Elize

>

> Johannesburg

> South Africa

>>

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Nice to hear from you!! Waste no time implementing Dr. D'Adamo's

recommendations!! They work!!

Kathleen

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Dear Kathleen

ME = Myalgic Enchephalomyelitis - or also called cronic fatigue syndrome CFS

Greetings

Elize

>>> kmschafer101@... 04/08/00 03:54AM >>>

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hello

i am irene and live in sweden. i have been on diet for 3 month now and lost

weight but not anymoore. i am working fulltime and have to take food with me

every day. i usally eat rostbeef and romanasallad or fish and sallad. here we

dont have all the things like they have in usalike spelt meal or

essen/ezekielbread. i make my one and use ricemeal instead. i really hope you

like this diet and look forward to hear from you.

bye

irene nielsen

new user

hi

My name is samantha and have just joined the group.

I have been on the diet for about 3 months. The first month and a

half were easy but things are getting hard. Like many others i have

a busy work life and find the only foods available are wheat based.

I also miss ice cream and sweet foods in general.

I'm assuming others have been through this and would therefore

appreciate some advice and guidance.

I would also like to know if anyone in the UK has come across essene

bread because nobody i know has!?

Thanks

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Hi ,

Welcome to the group. If you can keep to the diet you might find the

craving for sweet foods will disappear as your tastes change.

I too have never seen essene bread here in the UK... but a quick search on

the internet found this web site http://www.cantost.com/uk2shop-8.htm don't

know anything about it but might be worth looking at...

LnL,

Steve - Cheltenham, UK

-- new user

hi

My name is samantha and have just joined the group.

I have been on the diet for about 3 months. The first month and a

half were easy but things are getting hard. Like many others i have

a busy work life and find the only foods available are wheat based.

I also miss ice cream and sweet foods in general.

I'm assuming others have been through this and would therefore

appreciate some advice and guidance.

I would also like to know if anyone in the UK has come across essene

bread because nobody i know has!?

Thanks

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Thanks for the website.

Have you tried the breads, which would you recommend?

Have you done the secretor test?

> Hi ,

>

> Welcome to the group. If you can keep to the diet you might

find the

> craving for sweet foods will disappear as your tastes change.

>

> I too have never seen essene bread here in the UK... but a quick

search on

> the internet found this web site http://www.cantost.com/uk2shop-

8.htm don't

> know anything about it but might be worth looking at...

>

> LnL,

> Steve - Cheltenham, UK

>

> -- new user

> hi

> My name is samantha and have just joined the group.

> I have been on the diet for about 3 months. The first month and a

> half were easy but things are getting hard. Like many others i have

> a busy work life and find the only foods available are wheat based.

> I also miss ice cream and sweet foods in general.

> I'm assuming others have been through this and would therefore

> appreciate some advice and guidance.

> I would also like to know if anyone in the UK has come across

essene

> bread because nobody i know has!?

> Thanks

>

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Your Welcome :-)

No and no... :-)

As I said I just did a quick internet search and found that website but know

nothing about the products they sell... sorry

LnL,

Steve - Cheltenham, UK

-- Re: new user

Thanks for the website.

Have you tried the breads, which would you recommend?

Have you done the secretor test?

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Hej Irene,Just to say that ezekiel bread is readily available in Denmark,made by

Aurion Bageri.I´m sure it could travel from Denmark to Sweden,Regards,.

new user

>

>

> hi

>

> My name is samantha and have just joined the group.

>

> I have been on the diet for about 3 months. The first month and a

> half were easy but things are getting hard. Like many others i have

> a busy work life and find the only foods available are wheat based.

> I also miss ice cream and sweet foods in general.

>

> I'm assuming others have been through this and would therefore

> appreciate some advice and guidance.

>

> I would also like to know if anyone in the UK has come across essene

> bread because nobody i know has!?

>

> Thanks

>

>

>

>

>

>

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Guest guest

>Hi a,

Welcom to .. it's a great placeto gather information and get

support.

Your family sounds similar to ours..My mother had the Nucleus

implanted 11 years ago and while she does well, 2 of my sisters and I

have all been implanted since Oct. 2001. the changes in the

technology are amazing. We have so many more options and speech

strategies available to us than mom did.

I went from 5% hearing to 96% sentence recognition after my implant.

Where are you from?

Whatever questions you may have, please feel free to ask them.

Just curious, what kind of implant do your other family members have?

Looking forward to hearing more from you and with your family

history, I think you will do wonderfully with an implant.

Regards,

Silly in MI

volunteer advocate

hereditary progressive nerve deafness

N24C and 3G bte

Hi! I just found this group today on About.com I am 23 years old

> and have been wearing hearing aids for about 11 years now. I am

> interested in the Implant because I have had two members of my

> family have the surgery. One was really recent so we're still

> waiting to see how that went. The other member had the surgery

> several years ago. He was pretty much deaf beforehand but now can

> hear about as well as a normal hearing person can. I am interested

> in finding out more about the procedure and talking to others who

> have had it done to see if it really does work. TTYL.

>

> a

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Hi Sillygirl

I am from Kentucky and I'm not really sure exactly what kind of

implants the other family members had, I'll have to find out. Thanks

for replying so soon. I don't really have any questions right now

that I can think of, maybe later I will once I find out more. I'm

so glad to find a group of other people who are also hard of hearing

and know what it's like to go through the things we go through!

Talk to you later.

a

> >Hi a,

> Welcom to .. it's a great placeto gather information and get

> support.

>

> Your family sounds similar to ours..My mother had the Nucleus

> implanted 11 years ago and while she does well, 2 of my sisters

and I

> have all been implanted since Oct. 2001. the changes in the

> technology are amazing. We have so many more options and speech

> strategies available to us than mom did.

>

> I went from 5% hearing to 96% sentence recognition after my

implant.

>

> Where are you from?

>

> Whatever questions you may have, please feel free to ask them.

>

> Just curious, what kind of implant do your other family members

have?

>

> Looking forward to hearing more from you and with your family

> history, I think you will do wonderfully with an implant.

>

> Regards,

>

> Silly in MI

> volunteer advocate

> hereditary progressive nerve deafness

> N24C and 3G bte

>

>

>

> Hi! I just found this group today on About.com I am 23 years

old

> > and have been wearing hearing aids for about 11 years now. I am

> > interested in the Implant because I have had two members of my

> > family have the surgery. One was really recent so we're still

> > waiting to see how that went. The other member had the surgery

> > several years ago. He was pretty much deaf beforehand but now

can

> > hear about as well as a normal hearing person can. I am

interested

> > in finding out more about the procedure and talking to others

who

> > have had it done to see if it really does work. TTYL.

> >

> > a

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Shawa,

Just read your post and I was SHOCKLY! Because you are from

Kentucky, then I AM FROM KENTUCKY TOO! Thank God, I found a twin in

my home state. LOL. I have implanted at University of Kentucky Clinic

in Lexington. I live in Harlan County... I do have Nucleus 22 ESPrit

22 BTE and long time ago in 1994, I have been implanted in 1994 when

I was 4 years old, I have implanted a Nucleus 22 cochlear implant and

recieve a Spectra body-worn processor. On Feb. 18th, 2003, I have

upgrade to ESPrit 22 BTE and it is wonderful, and yes, FREEDOM! Thank

God, No long wires.. Believe it or not, when I was down to pick

something up from the floor, my BWP always got out of my tee-shirt

pocket and the long wire was disconnected from the headset (had

microphone) and it hurts my right ear! When I have BTE, it is

comformable, and also, it helps me making alot of new friends

starting to communicate with me at school. Yes I am 13 years old,

atrending public school with a interpreter (ASL and SEE cerficated

and licnesed, lives in Harlan too). Really soon, I will recieve a new

ESPrit 3G for Nucleus 22 wearers because I am on the waiting list to

get it, just trade ESPrit 22 to 3G just for $750 dollars.

> > >Hi a,

> > Welcom to .. it's a great placeto gather information and

get

> > support.

> >

> > Your family sounds similar to ours..My mother had the Nucleus

> > implanted 11 years ago and while she does well, 2 of my sisters

> and I

> > have all been implanted since Oct. 2001. the changes in the

> > technology are amazing. We have so many more options and speech

> > strategies available to us than mom did.

> >

> > I went from 5% hearing to 96% sentence recognition after my

> implant.

> >

> > Where are you from?

> >

> > Whatever questions you may have, please feel free to ask them.

> >

> > Just curious, what kind of implant do your other family members

> have?

> >

> > Looking forward to hearing more from you and with your family

> > history, I think you will do wonderfully with an implant.

> >

> > Regards,

> >

> > Silly in MI

> > volunteer advocate

> > hereditary progressive nerve deafness

> > N24C and 3G bte

> >

> >

> >

> > Hi! I just found this group today on About.com I am 23 years

> old

> > > and have been wearing hearing aids for about 11 years now. I

am

> > > interested in the Implant because I have had two members of my

> > > family have the surgery. One was really recent so we're still

> > > waiting to see how that went. The other member had the surgery

> > > several years ago. He was pretty much deaf beforehand but now

> can

> > > hear about as well as a normal hearing person can. I am

> interested

> > > in finding out more about the procedure and talking to others

> who

> > > have had it done to see if it really does work. TTYL.

> > >

> > > a

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Hi a

Believe me the CI does work!!I was profoundly deaf in both ears before I

received my implant..I received wonderful hearing after Hearing impaired almost

all my life and then deaf for 10 years.It has given me the life that I had

always wanted ..I can now talk and laugh with my Grandkids and life has been

made so much easier for my husband and family.My sister also has the implant and

hers really works too!!LOL!!Any questions just ask

Love Dora

New User

Hi! I just found this group today on About.com I am 23 years old

and have been wearing hearing aids for about 11 years now. I am

interested in the Implant because I have had two members of my

family have the surgery. One was really recent so we're still

waiting to see how that went. The other member had the surgery

several years ago. He was pretty much deaf beforehand but now can

hear about as well as a normal hearing person can. I am interested

in finding out more about the procedure and talking to others who

have had it done to see if it really does work. TTYL.

a

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Hi a,

How nice to see you here on CI Hear. I'm glad you

joined us to learn about our group and we are here to

provide answers that you may be looking for. It's

interesting that you already have family members who

have gone before you. Feel free to introduce them to

this list as they are welcome too.

There is no doubt that this procedure works. Tell us

a little more about yourself and your hearing history.

Have you been to a CI Center for evaluation?

We'll look forward to hearing more from you very soon.

Alice

N24 11/99

N24C 04/03

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Hi Alice

Im glad I found this group also! : ) I can't introduce the other

family members because they don't have internet access. I have not

been to a CI Center for evaluation yet. I would like to try to look

into the procedure more someday, but right now isn't a good time. I

will tell more about it later when I have more time... right now I

gotta get ready for work! :) TTYL

a

> Hi a,

>

> How nice to see you here on CI Hear. I'm glad you

> joined us to learn about our group and we are here to

> provide answers that you may be looking for. It's

> interesting that you already have family members who

> have gone before you. Feel free to introduce them to

> this list as they are welcome too.

>

> There is no doubt that this procedure works. Tell us

> a little more about yourself and your hearing history.

> Have you been to a CI Center for evaluation?

>

> We'll look forward to hearing more from you very soon.

>

> Alice

> N24 11/99

> N24C 04/03

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> Hello everyone. I just started taking Lexapro, 10 mg 3 days ago

for

> treatment of recurrent depression and anxiety. I took Celexa for

2

> years several years ago and had great results. I was prescribed

> paxil CR last year by my general practice Dr. and I just couldn't

> handle all the side effects. I'm very hopeful that I get similar

> results to Celexa with the Lexapro.

>

> So far the only side effect I've noticed is a kind of metallic

taste

> in my mouth and food seems to have a more pronounced flavor. I've

> read posts on this board about increased teeth grinding at night.

> I'm concerned about this as I am a bad teeth grinder already. I

> actually have an appointment to have a night guard made for me

next

> month so hopefully that will counter any increased grinding.

>

> Like everyone here, I just hope that taking lexapro will help me

to

> feel better. I've finally accepted that fighting depression alone

is

> not a viable solution. I swear if I heard a therapist telling me

to

> define my boundaries or to locate my inner healing light one more

> time I would scream :). Well, that's about it for me. I'm glad I

> found this group and plan on checking in regularly. Good luck to

us

> all!

Mike,

Curious as to why you didn't go back to the Celexa?

Pik

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Hi Pik. That's the same question my new pdoc asked. At the time I was

prescribed the Paxil CR I had just recently begun experiencing panic attacks.

I wasn't having them when I first took Celexa. The doctor at the time said she

thought the paxil cr would be better for the anxiety and panic attacks. To be

honest, it seems like alot of the Drs. will prescribe whatever is being pushed

on them most by the pharm. sales reps at the time.

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Celexa actually isn't approved for panic attacks. Although the

chemical make up reacts better for the serotonin surge during a

panic attack. As a anxiety/panic disorder sufferer I was also on

Paxil, for almost 3 yrs. It worked wonderfully for the panic

attacks. In fact, I haven't had one since starting paxil and that

was over 4 yrs ago. Paxil is more of a " governer " where panic

attacks are concerned. It takes control of them and helps to teach

you how to control them, if you let it. Celexa and Lexapro has work

well on the anxiety part for me. But the biggest plus of all is the

lack of side effects. Paxil is high on the side effects for me.

Celexa didn't quite work right and Lex has been PERFECT, once

finding the right dose that is.

> Hi Pik. That's the same question my new pdoc asked. At the time

I was

> prescribed the Paxil CR I had just recently begun experiencing

panic attacks.

> I wasn't having them when I first took Celexa. The doctor at the

time said she

> thought the paxil cr would be better for the anxiety and panic

attacks. To be

> honest, it seems like alot of the Drs. will prescribe whatever is

being pushed

> on them most by the pharm. sales reps at the time.

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>

Hi,

I have been on Lexapro for a few weeks and have not noticed any

itching.

I wear a sunscreen faithfully, and was wondering if you do?

You really should wear one if you don't, as sometimes certain meds

cause a photosensitivity.

I would also check with your doctor.

Let me know how you do.

Longell

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I would definitely ask your doctor about it. I bet that it does have

to do with the Lex. I know when I first went on, I had something

like that (it was not so much itching as a " crawling feeling " in my

skin) luckily, it went away and was not terrible while it was there.

Call the doc and hang in there. If Lex is the right drug for you,

it's a miracle.

> Hi everyone,

>

> I just joined the list and scanned the archives to see if I could

> find any one having what may be a side effect to Lexapro. I'm

> starting my third week on 10mg of Lexapro. The only side effects I

> have noticed so far are some differences in bowel movements, which

> really aren't a bother, but I'm also itching over most of my body.

> It's mainly on my upper half - arms, back, chest, breasts, but also

> my legs. I can't figure out if this is due to the Lexapro or

> something else. I'm getting bruises because I'm scratching so

hard.

> I've tried using anti-itch creams and powders to keep me cool from

> the heat, but I still itch all the time. I don't have a rash, or

> history of skin problems, and nothing has changed in terms of soaps

I

> use. If anyone else has noticed this, please let me know.

>

> Thanks.

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So far, after 2 1/2 weeks, I haven't had any other problems. But I'm

itching like crazy. I have no rash, no bumps, no hives, or

anything. And I don't suffer from allergies. Just itching. I've

tried non-itch sprays, creams, powders, etc. Tonight I'm going to

try Benydrel to see if that helps.

Thanks for the input. If it doesn't go away, then I'll have to try

something else.

> > Hi everyone,

> >

> > I just joined the list and scanned the archives to see if I could

> > find any one having what may be a side effect to Lexapro. I'm

> > starting my third week on 10mg of Lexapro. The only side effects

I

> > have noticed so far are some differences in bowel movements,

which

> > really aren't a bother, but I'm also itching over most of my

body.

> > It's mainly on my upper half - arms, back, chest, breasts, but

also

> > my legs. I can't figure out if this is due to the Lexapro or

> > something else. I'm getting bruises because I'm scratching so

> hard.

> > I've tried using anti-itch creams and powders to keep me cool

from

> > the heat, but I still itch all the time. I don't have a rash, or

> > history of skin problems, and nothing has changed in terms of

soaps

> I

> > use. If anyone else has noticed this, please let me know.

> >

> > Thanks.

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My first two weeks or so on lex seemed to be an improvement, but

then I experienced a mood " slump " . My doc said this was common, and

usually, the mood goes back up. It has gone back up for me. The

slump only lasted about a week (and coincided with my usual PMS

time, interestingly enough).

I hope you bounce back from the slump as well. I know it's

discouraging; hang in there.

Patty

In Lexapro , " ronner23 " <rraph29@h...> wrote:

>

> Just started last week 10 mg. I've been on every possible drug

for

> anxiety/depression. I'm still on Zoloft 300mg but we were gonna

> taper it if this worked. I felt great for a few days and now a

week

> into it, I can't get out of bed. Anyone else feel like this? Any

> input would be greatly appreciated.

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