Hello

[Guest guest]

Good for you for giving it another go. And yeah, the nutrition is

probably 80% of the program. " you are what you eat " How's this

challenge been, what are your results?

Dianne

>

> Hello,

> I've been checking out this site for about three weeks and

found it to be

> helpful, inspiring and very informative

> I am on my 7th week of c2w7d2 and just wanted (well really

challenge 1 since

> back in '99' I didn't follow the most

> important aspect of the program -nutrition) to throw my vibes in.

I am in

> Phoenix, Az and I don't want to tease anybody

> but the weather is most excellent! here (he he ). well I really

don't have

> much to say but just wanted to say hello

> stay strong in mind, body, and soul.

>

> boogiesdad2002

[Guest guest]

Hi , and welcome to the group! I don't wanna come right back

atcha with the weather thing, but I'm in CA and it's ~70 degrees and

sunny here today. Ahhhhh, life is good!

Glad to have you as part of the group!

Jen B.

C6W11D2

>

> Hello,

> I've been checking out this site for about three weeks and found it

to be

> helpful, inspiring and very informative

> I am on my 7th week of c2w7d2 and just wanted (well really

challenge 1 since

> back in '99' I didn't follow the most

> important aspect of the program -nutrition) to throw my vibes in. I

am in

> Phoenix, Az and I don't want to tease anybody

> but the weather is most excellent! here (he he ). well I really

don't have

> much to say but just wanted to say hello

> stay strong in mind, body, and soul.

>

> boogiesdad2002

[Guest guest]

Ann, welcome to the group. Please feel free to vent and talk away here

(Lord know I do!).

I'm so glad that your brother will finally come to see what it is you are

dealing with on a daily basis and pray that he will offer you more help than

just a pat on the back.

Courage

Hello

>Hi, First off I would like to say hello to everyone here. My name is

>Ann and I signed up for this group a couple weeks ago. I've been

>reading your posts, but I'm not one to say much. It took me along

>time even to look for a LBD caretaker group on-line. I'm not one to

>look for support for myself.

>A couple years ago my mom had had an incident where she thought she

>had picked up a friend of hers in the morning, later that afternoon

>she stopped at a business and told them her friend was dead in the

>car. The police were called and me. They checked out her car, her

>house and went to her friends house, friend was still alive and

>waiting for my mom to pick her up. That's how it all started.

>She had a ton of tests done to her, but she came out fine on most of

>them. BTW she was 80 at the time.

>It was about 6 months after that, odd behaviors and confusion were

>more noticable and her Dr. wanted her to be retested and mentioned

>LBD and since Christmas this year she's gotten real bad.

>I was finally able to get my brother, that lives 1500 miles away, to

>come home for Easter to see what I have to deal with. She was in the

>hospital Jan. 4th, I had to take her in, she felt bad about calling

>me, she had an ulser rupture and lost alot of blood. She was there

>for a week and then went to a NH for 2 weeks to get strenght back.

>Then she went home. I have a home aide that comes in twice a week for

>her showers. I stop over every morning to give mom her pills before I

>go to work. I stop over after work and call her at night. I took her

>car back in Jan.

>This is getting long, sorry. But brother finally showed up and we

>have her on a list to get her into a home that specializes in

>demensias and some days I'm ready to look into a room for myself.

>I've been e-mailing and we've talked on the phone since Jan. But now

>he can see it for himself. I have to be calm around her, but I end

>up taking out on my hubby and my friends. They understand, but that's

>not fair to them.

>Well, when I'm in the mood to vent, I guess I vent and babble on.

>But Thanks for taking time out to read.

>Ann

>

>

>

>

>

>Welcome to LBDcaregivers.

>

>

>

[Guest guest]

Dear Ann,

You've definitely found the right place. This group *defines*

compassion. There's so much good, practical information and support,

here, I can't find the words to describe it.

You sound tapped out. No wonder! You've been through a terrible

ordeal. Promise us something, if you will: don't hesitate to vent

here. That's one of the very best things about this group. You can do

it, without fear of judgment, and odds are, you'll see many supportive

replies.

I'm glad you found this group, Ann. None of us want to be here, but

the thought of coping all alone is unthinkable, to all of us.

You'll have several more visible welcomes, before long, and untold

silent ones.

Being alone with LBD is over for you, now, if you so choose,

Love, Deborah

> Hi, First off I would like to say hello to everyone here. My name is

> Ann and I signed up for this group a couple weeks ago. I've been

> reading your posts, but I'm not one to say much. It took me along

> time even to look for a LBD caretaker group on-line. I'm not one to

> look for support for myself.

> A couple years ago my mom had had an incident where she thought she

> had picked up a friend of hers in the morning, later that afternoon

> she stopped at a business and told them her friend was dead in the

> car. The police were called and me. They checked out her car, her

> house and went to her friends house, friend was still alive and

> waiting for my mom to pick her up. That's how it all started.

> She had a ton of tests done to her, but she came out fine on most of

> them. BTW she was 80 at the time.

> It was about 6 months after that, odd behaviors and confusion were

> more noticable and her Dr. wanted her to be retested and mentioned

> LBD and since Christmas this year she's gotten real bad.

> I was finally able to get my brother, that lives 1500 miles away, to

> come home for Easter to see what I have to deal with. She was in the

> hospital Jan. 4th, I had to take her in, she felt bad about calling

> me, she had an ulser rupture and lost alot of blood. She was there

> for a week and then went to a NH for 2 weeks to get strenght back.

> Then she went home. I have a home aide that comes in twice a week for

> her showers. I stop over every morning to give mom her pills before I

> go to work. I stop over after work and call her at night. I took her

> car back in Jan.

> This is getting long, sorry. But brother finally showed up and we

> have her on a list to get her into a home that specializes in

> demensias and some days I'm ready to look into a room for myself.

> I've been e-mailing and we've talked on the phone since Jan. But now

> he can see it for himself. I have to be calm around her, but I end

> up taking out on my hubby and my friends. They understand, but that's

> not fair to them.

> Well, when I'm in the mood to vent, I guess I vent and babble on.

> But Thanks for taking time out to read.

> Ann

[Guest guest]

Welcome Ann,

So sorry you have to deal with this. I think it is difficult for a lot of

people to admit that their parent has a problem. We never want anything to

happen to our parents.

cathyM

>

>Reply-To: LBDcaregivers

>To: LBDcaregivers

>Subject: Hello

>Date: Wed, 07 Apr 2004 22:05:52 -0000

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>

>Hi, First off I would like to say hello to everyone here. My name is

>Ann and I signed up for this group a couple weeks ago. I've been

>reading your posts, but I'm not one to say much. It took me along

>time even to look for a LBD caretaker group on-line. I'm not one to

>look for support for myself.

>A couple years ago my mom had had an incident where she thought she

>had picked up a friend of hers in the morning, later that afternoon

>she stopped at a business and told them her friend was dead in the

>car. The police were called and me. They checked out her car, her

>house and went to her friends house, friend was still alive and

>waiting for my mom to pick her up. That's how it all started.

>She had a ton of tests done to her, but she came out fine on most of

>them. BTW she was 80 at the time.

>It was about 6 months after that, odd behaviors and confusion were

>more noticable and her Dr. wanted her to be retested and mentioned

>LBD and since Christmas this year she's gotten real bad.

>I was finally able to get my brother, that lives 1500 miles away, to

>come home for Easter to see what I have to deal with. She was in the

>hospital Jan. 4th, I had to take her in, she felt bad about calling

>me, she had an ulser rupture and lost alot of blood. She was there

>for a week and then went to a NH for 2 weeks to get strenght back.

>Then she went home. I have a home aide that comes in twice a week for

>her showers. I stop over every morning to give mom her pills before I

>go to work. I stop over after work and call her at night. I took her

>car back in Jan.

>This is getting long, sorry. But brother finally showed up and we

>have her on a list to get her into a home that specializes in

>demensias and some days I'm ready to look into a room for myself.

>I've been e-mailing and we've talked on the phone since Jan. But now

>he can see it for himself. I have to be calm around her, but I end

>up taking out on my hubby and my friends. They understand, but that's

>not fair to them.

>Well, when I'm in the mood to vent, I guess I vent and babble on.

>But Thanks for taking time out to read.

>Ann

>

>

_________________________________________________________________

Watch LIVE baseball games on your computer with MLB.TV, included with MSN

Premium!

http://join.msn.com/?page=features/mlb & pgmarket=en-us/go/onm00200439ave/direct/0\

1/

[Guest guest]

Welcome to the group! We are known for " babbling on " so don't worry, you

will fit in just fine. You aren't left handed too, are you? Never mind...

Sorry you had to find us, but glad that you did.

Kath

Hello

> Hi, First off I would like to say hello to everyone here. My name is

> Ann and I signed up for this group a couple weeks ago. I've been

> reading your posts, but I'm not one to say much. It took me along

> time even to look for a LBD caretaker group on-line. I'm not one to

> look for support for myself.

> A couple years ago my mom had had an incident where she thought she

> had picked up a friend of hers in the morning, later that afternoon

> she stopped at a business and told them her friend was dead in the

> car. The police were called and me. They checked out her car, her

> house and went to her friends house, friend was still alive and

> waiting for my mom to pick her up. That's how it all started.

> She had a ton of tests done to her, but she came out fine on most of

> them. BTW she was 80 at the time.

> It was about 6 months after that, odd behaviors and confusion were

> more noticable and her Dr. wanted her to be retested and mentioned

> LBD and since Christmas this year she's gotten real bad.

> I was finally able to get my brother, that lives 1500 miles away, to

> come home for Easter to see what I have to deal with. She was in the

> hospital Jan. 4th, I had to take her in, she felt bad about calling

> me, she had an ulser rupture and lost alot of blood. She was there

> for a week and then went to a NH for 2 weeks to get strenght back.

> Then she went home. I have a home aide that comes in twice a week for

> her showers. I stop over every morning to give mom her pills before I

> go to work. I stop over after work and call her at night. I took her

> car back in Jan.

> This is getting long, sorry. But brother finally showed up and we

> have her on a list to get her into a home that specializes in

> demensias and some days I'm ready to look into a room for myself.

> I've been e-mailing and we've talked on the phone since Jan. But now

> he can see it for himself. I have to be calm around her, but I end

> up taking out on my hubby and my friends. They understand, but that's

> not fair to them.

> Well, when I'm in the mood to vent, I guess I vent and babble on.

> But Thanks for taking time out to read.

> Ann

>

>

>

>

>

> Welcome to LBDcaregivers.

>

>

>

[Guest guest]

Hi Robin!

Welcome to this wonderful group. My name is and I'm one of the

co-moderators of the group. Its been very quiet here lately. Sometimes

everyone is very talkative, sometimes we're very quiet.

I will look for some affirmations for you. I KNOW they work - I've come a long

way in the past 3 years, and affirmations have been a tremendous help to me.

We have a wonderful treasury of affirmations and articles in the archives. Feel

free to browse thru there. I think you'll find a lot of help there.

Blessings,

---- sereniti4mi wrote:

=============

I am new to the group. I am 43 have MS. I left my husband about 7

months ago almost 8 he said he couldn't take the fact that I had the

disease with all of the issues. A few months ago I lost my job to

the MS also. I have relapsing remitting which is the mildest form.

I have been up and down with my emotions but figure its due to the

fact of everything that has happened in the last 8 months its a

lot. I do have a good support system of people but sometimes its

not easy. Unfortunately when I was laid off I lost my insurance

also. I am trying to get SSI but If I don't I plan on getting a

lower impact stress job if there is one out there that exists. I

was wondering if you have any suggestions or affirmations to help me

keep positive. I have put a complaint against the company that laid

me off because once I told them that was it four days later I no

longer had a job.

Anything would be appreciated. I know that I need to build my self

esteem back up. I have done affirmations before and I want to get

myself back into doing them again. Also I don't have insurance and

once I do I plan on going into counseling.

Thanks,

Robin

[Guest guest]

Welcome to affirmations to de-stress! We are very happy to have you here. I

just got back from my son's wedding, but hopefully will be back on later this

week! Be sure to check out the older messages that are on the affirmations group

site under archives or " Messages " in the left hand column. That is always what

we recommend, especially on those days when not too many members post messages.

Take Care,

Hugs, PJ group leader

prcheney76 wrote:

Hi, I am new to the group. I am usually stressed out by thursday or

friday. I am trying to relax and was hoping to get some tips on

handling stress.

thanks

PR

http://groups.yahoo.com/group/The-Complaint-Station

http://health.groups.yahoo.com/group/AffirmationstoDe-Stress

A positive thinking, positive affirmations support group, that discusses ways to

cope with the stresses of daily life. Come aboard! PJ and Gang

[Guest guest]

Well, I grew up a few blocks from a very productive oil refinery,

spent nearly 20 years near one, in fact. That would explain why my

mother, father, 2 sisters, 1 brother and me all have hypothyroidism

(3 confirmed Hashis) -- but my two girls were not raised in the same

town and they both have Hashimoto's. My grandmother had two thyroid

surgeries for Graves and she sure didn't grow up where I did. My

aunt and cousin (Oklahoma folks) -- hypo. With all of that going on,

I really thought genetics was the culprit.

(just my 2 cents)

>

> Thyroid disorders often run in families, but in most cases there is

no specific genetic link. Exposure to common environmental toxins as

well as exposure to the same bacteria, viruses, fungi and associated

antibodies might be the link in many families, especially when the

disorders extend to the pets and other unrelated household members.

Then you have the stress factor.

>

> It all comes down to the causes of hypothyroidism. How many of

you with Hashimoto's thyroiditis know what caused you to acquire this

disease? My doc's wife reports becoming hypothyroid after a major

infection (mono or maybe chicken pox? I forget what kind.) and a

period of great stress in her life. There may have been other factors

as well. Their natural daughter and their adopted daughter also

became hypothyroid during that same time frame. Then there was the

cat. . . .

>

[Guest guest]

I do not know about the safety of iodine for thyca patients. I am seeing my doc in Lubbock on May 2, and I will ask him about that. Finding a doc to Rx Armour is not too hard. Getting one who will treat adrenal fatigue is very difficult. Karma wrote: Hi, I had made a post to the Thyroid_Cancer_Texas group asking about adoctor on the Armour doctor's list. After that post I received ane-mail from this group with an invitation to join. Thanks so much forthe invitation. I didn't even know about this group.The doctor I was asking about is Mc Mullen, MD

InternalMedicine on Northloop in Austin. I was wondering if anyone uses himor knows anything about him. Any other suggestions for aknowledgeable thyroid/adrenal doc in Austin?A little history about me. I started having pretty severe hyposymptoms around December 2005 but I didn't go to the doctor. I waslooking at all the symptoms individually not as a group. I was justgetting ready to make a doctor's appointment for symptoms when July 2,2006 I found a nodule in my neck. Yep, papillary cancer. I hadsurgery to remove the thyroid on August 8th at MD in Houston.The cancer had not spread out of the nodule. In fact, when I wentback for RAI, I had absolutely no uptake and did not have to have theablation. So, for cancer, I am okay. Of course, I was put on 125 mg of synthroid. But now, I still do notfeel better. I still feel achey, puffy, gaining weight like crazy,tender feet, charlie horses, etc.

So now, I am slowly trying to explore other possibilities of help. Iam researching Armour, Iodine and adrenals. Unfortunately, betweenbeing tired and having to have a life with work, husband and child, itseems my research is progressing at a snails pace.Thanks again for the invitation.K

Ahhh...imagining that irresistible "new car" smell? Check out

new cars at Yahoo! Autos.

[Guest guest]

Thanks for offering to check with your doctor. Much appreciated.

> Hi,

>

> I had made a post to the Thyroid_Cancer_Texas group asking about a

> doctor on the Armour doctor's list. After that post I received an

> e-mail from this group with an invitation to join. Thanks so much for

> the invitation. I didn't even know about this group.

>

> The doctor I was asking about is Mc Mullen, MD Internal

> Medicine on Northloop in Austin. I was wondering if anyone uses him

> or knows anything about him. Any other suggestions for a

> knowledgeable thyroid/adrenal doc in Austin?

>

> A little history about me. I started having pretty severe hypo

> symptoms around December 2005 but I didn't go to the doctor. I was

> looking at all the symptoms individually not as a group. I was just

> getting ready to make a doctor's appointment for symptoms when July 2,

> 2006 I found a nodule in my neck. Yep, papillary cancer. I had

> surgery to remove the thyroid on August 8th at MD in Houston.

> The cancer had not spread out of the nodule. In fact, when I went

> back for RAI, I had absolutely no uptake and did not have to have the

> ablation. So, for cancer, I am okay.

>

> Of course, I was put on 125 mg of synthroid. But now, I still do not

> feel better. I still feel achey, puffy, gaining weight like crazy,

> tender feet, charlie horses, etc.

>

> So now, I am slowly trying to explore other possibilities of help. I

> am researching Armour, Iodine and adrenals. Unfortunately, between

> being tired and having to have a life with work, husband and child, it

> seems my research is progressing at a snails pace.

>

> Thanks again for the invitation.

>

> K

>

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

> Ahhh...imagining that irresistible " new car " smell?

> Check outnew cars at Yahoo! Autos.

>

[Guest guest]

Actually, I was going to ask that very question for myself. I have uterine fibroids. Dr. Derry mentions shrinking a uterine fibroid with iodine in his book Breast Cancer and Iodine.Karma wrote: Thanks for offering to check with your doctor. Much appreciated.>> I do not know about the safety of iodine for thyca patients. I amseeing my doc in Lubbock on May 2, and I will ask him about that.> > Finding a

doc to Rx Armour is not too hard. Getting one who willtreat adrenal fatigue is very difficult.

Ahhh...imagining that irresistible "new car" smell? Check out

new cars at Yahoo! Autos.

[Guest guest]

My sister has lobular carcinoma in situ breast cancer. We are

interested in the iodine for her too.

> >

> > I do not know about the safety of iodine for thyca patients. I am

> seeing my doc in Lubbock on May 2, and I will ask him about that.

> >

> > Finding a doc to Rx Armour is not too hard. Getting one who will

> treat adrenal fatigue is very difficult.

>

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

> Ahhh...imagining that irresistible " new car " smell?

> Check outnew cars at Yahoo! Autos.

>

[Guest guest]

What about the progesterone to estrogen ratios, Jan? From everything I've read over the yrs, it's that lack of progesterone, or the imbalance thereof, that makes these things. I had uterine fibroids way back when, that could not be shrunk with the dangerous synthetic crap (progestins), thus, not knowing any better, had a hyst. Little did I know about the fact that the lack of this could cause that. However, had I know that then, I would have had to fight tooth and nail to get natural progesterone. At that time, I doubt if one doc could be found that would even know what the heck we were talking about, just take the uterus out and be done with it. Trouble is, the trouble just begins with a hyst, even though it may be the only thing we can do at the time. I know he's got you on what, biest, but I don't remember whether he's got you on progesterone, for some reason.

Re: Re: Hello

Actually, I was going to ask that very question for myself.

I have uterine fibroids. Dr. Derry mentions shrinking a uterine fibroid with iodine in his book Breast Cancer and Iodine.

[Guest guest]

I am on a low dose of progesterone. 50 mg. We had reduced the dose from 75 mg. I don't especially like progesterone. . . . . . I will see "The Doc" on May 2 with lots of questions. I just want to find a non-surgical solution. wrote: What about the progesterone to estrogen ratios, Jan? From everything I've read over the yrs, it's that lack of progesterone, or the imbalance

thereof, that makes these things. I had uterine fibroids way back when, that could not be shrunk with the dangerous synthetic crap (progestins), thus, not knowing any better, had a hyst. Little did I know about the fact that the lack of this could cause that. However, had I know that then, I would have had to fight tooth and nail to get natural progesterone. At that time, I doubt if one doc could be found that would even know what the heck we were talking about, just take the uterus out and be done with it. Trouble is, the trouble just begins with a hyst, even though it may be the only thing we can do at the time. I know he's got you on what, biest, but I don't remember whether he's got you on progesterone, for some reason. Re: Re: Hello Actually, I was going to ask that very

question for myself. I have uterine fibroids. Dr. Derry mentions shrinking a uterine fibroid with iodine in his book Breast Cancer and Iodine.

Ahhh...imagining that irresistible "new car" smell? Check out

new cars at Yahoo! Autos.

[Guest guest]

What kind of symptoms are you experiencing with your uterine

fibroids, Jan? Have you thought about/discussed progesterone cream

with Dr. R? Have you read Lee's books about the benefits of

progesterone cream? I think there is a definite connection between

hypothyroid and uterine fibroids.

>

> I am on a low dose of progesterone. 50 mg. We had reduced the dose

from 75 mg. I don't especially like progesterone. . . . . .

>

> I will see " The Doc " on May 2 with lots of questions.

> I just want to find a non-surgical solution.

>

>

>

> Actually, I was going to ask that very question for myself.

>

> I have uterine fibroids. Dr. Derry mentions shrinking a

uterine fibroid with iodine in his book Breast Cancer and Iodine.

>

>

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

> Ahhh...imagining that irresistible " new car " smell?

> Check outnew cars at Yahoo! Autos.

>

[Guest guest]

We do not know for sure, but the fibroids are the only remaining likely cause of my edema. I have no other symptoms. I am on progesterone, but we may talk about increasing my dose and/or moving part of it from the capsule to a cream. My GYN says that progesterone can cause edema, however. rose_nancy8 wrote: What kind of symptoms are you experiencing with your uterine fibroids, Jan? Have you thought about/discussed progesterone cream with Dr. R? Have you read Lee's books about the benefits of progesterone cream? I think there is a definite connection between

hypothyroid and uterine fibroids.>> I am on a low dose of progesterone. 50 mg. We had reduced the dose from 75 mg. I don't especially like progesterone. . . . . . > > I will see "The Doc" on May 2 with lots of questions. > I just want to find a non-surgical solution.> > > > Actually, I was going to ask that very question for myself. > > I have uterine fibroids. Dr. Derry mentions shrinking a uterine fibroid with iodine in his book Breast Cancer and Iodine.

Ahhh...imagining that irresistible "new car" smell? Check out

new cars at Yahoo! Autos.

[Guest guest]

Yep, that's what I meant. I just didn't know then what all that was about. The progesterone cream in the "standard" 40 mgs dose is way too much for me, I've found out. More like 21 to 25 mgs on the skin. Otherwise, it makes me soooo sleepy.

Re: Re: Hello

I am on a low dose of progesterone. 50 mg. We had reduced the dose from 75 mg. I don't especially like progesterone. . . . . .

I will see "The Doc" on May 2 with lots of questions.

I just want to find a non-surgical solution.

[Guest guest]

And HUGS back to you, Nachi! You add SO much to our group with

everything your share! Bless you!

Jace

nachi2006@... wrote:

>

> Dear PJ & Dear All,

>

> I was reading messages, replies from all of you..and I felt something

> in my

> heart..

>

> What You all have shared from your life..means a lot..while reading..I

> think

> we all fill in gaps for each other..at some moments...I love this

> experience..

>

> I want to HUG All of You.

>

> {{{{{{{{{{{{{{Hugs}}}}}}}}}}}}}

>

> Blessings n Love,

>

> Nachi

>

>

[Guest guest]

Ooooh! That one is quite powerful! I've never heard it before, but I'm

keeping a copy of this! Thanks so much! PJ

Sheila Moffatt wrote: Courage is Fear that

has said its prayers.

Sheila Moffatt

sheilaemoffatt@...

sheilaemoffatt@...

evonnalynn@...

Yahoo Messenger: sheilaemoffatt

Owner:

www.scctecinc.com

sheilaemoffatt@...

http://groups.yahoo.com/group/sheilascreativeconcepts/

Bread cast on the waters comes back to you.

The good deed you do today may benefit you or someone you love at the

least expected time.

If you never see the deed again at least you will have made the world a

better place -

6:27 NIV

He rescues and he saves; he performs signs and wonders in the heavens and on the

earth. He has rescued from the power of the lions.”

[Guest guest]

Hi Norma,

You found a nice place to land....I'm glad you joined. I am new to this group

too, and only after a short time, I have found that many people here email

helpful techniques, practices and good solid advice to help get through

stressful times in daily life. Hopefully you will find out some things here to

help you through your trails in life.

All the best...Kenny

Norma wrote:

Thanks for allowing me to join you here. I am Norma and am 40 years

old. I

am facing several health issues and my husband whom I love dearly is on a

mental health unit after having a complete breakdown, so of course, things

are very stressful for me at the moment. I would like to ask your help. Also

I am here for you all also.

Take care.

Norma

[Guest guest]

Thank you so much for replying. I am glad that you all are here and I will

do my part to be an encouragement. I have found some very helpful things

already.

Norma

-- Re: Hello

Hi Norma,

You found a nice place to land....I'm glad you joined. I am new to this

group too, and only after a short time, I have found that many people here

email helpful techniques, practices and good solid advice to help get

through stressful times in daily life. Hopefully you will find out some

things here to help you through your trails in life.

All the best...Kenny

Norma wrote:

Thanks for allowing me to join you here. I am Norma and am 40 years old. I

am facing several health issues and my husband whom I love dearly is on a

mental health unit after having a complete breakdown, so of course, things

are very stressful for me at the moment. I would like to ask your help. Also

I am here for you all also.

Take care.

Norma

[Guest guest]

Hi Kat and welcome to the group!

Hugs!

Vickie

marie6lee wrote:

Hello, my name is Kat. I have FMS/CFS and reated disorders. I am 40

and

have had it since I was 16. Just signed up to this group and wanted to

say hi and wish everyne a happy season whaever you each celebrate. I am

sure I will post ore about me later bt just wanted to say hi for now.

[Guest guest]

Hi Kat and welcome to the group!

Hugs!

Vickie

marie6lee wrote:

Hello, my name is Kat. I have FMS/CFS and reated disorders. I am 40

and

have had it since I was 16. Just signed up to this group and wanted to

say hi and wish everyne a happy season whaever you each celebrate. I am

sure I will post ore about me later bt just wanted to say hi for now.

[Guest guest]

Hi Kat, and welcome, my 14yr old son has been housebound over 2yrs with ME (sad

isn't it) it's a terrible illness, and leaves people very isolated.

Try and have as nice a christmas as possible

Take Care

Antoinette x