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Hi Eliisa,

Welcome to the

group. I am 41, mom of 15 yr. old twin boys, wife to a wonderful man,

high school teacher and also am fighting the battle of the bulge. LOL!!

This is a great

group. I am sure you will find everyone friendly and supportive. I

live in MI. Where do you live?

Patrice

From:

[mailto:purple.fae@...]

Sent: Saturday, February 12, 2005

9:20 AM

' '

Subject: new

member

Hi all!

Just joined.

28, mom of 1, fighting the " battle of the bulge " ... looking forward

to cyber-meeting you all!

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Hi welcome to this group.

You'll find plenty of motivation and encouragement here! <purple.fae@...> wrote:

Hi all!

Just joined. 28, mom of 1, fighting the "battle of the bulge"... looking forward to cyber-meeting you all!

Ilja

Visit my website with fitness video reviews at www.videoworkouts.com

Support the website by doing your online shopping via the shopping mall, where you'll find the latest coupons and deals

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hi elisa!! welcome to the group! please post often!

:*carolyn.

--

No virus found in this outgoing message.

Checked by AVG Anti-Virus.

Version: 7.0.300 / Virus Database: 265.8.7 - Release Date: 2/10/2005

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Welcome Amy! I’m sorry that you’re

having such a terrible time in your life. It’s great that you are ready

to get healthy for those little boys since you’re all they really have.

Stay strong – you’ll find lots of support here. The key is to plan –

plan your menu – your exercise and your water. Check in often.

From: Amy Beth

Stafford [mailto:XOamybethXO@...]

Sent: Sunday, February 06, 2005

1:58 PM

100-plus

Subject: NEW MEMBER

Hello there! My name is Amy. I am 29 years

old, SAHM to 2 boys ages 2

and 8. I am begining my new lifestyle change

on wednesday Feb 9th. I

am looking fwd to it, although i am having a

hard time finding the

perfect group to help me along the way. Its

no fun doing it alone. I

am 5'10 " and weigh 335 pounds...i am

looking to lose 100 pounds

(Maybe more)!! My husband walked out on me

and my kids in

November...so i have decided that i am going

to make a change for ME

and be a better person. There will be no

chance for us getting back

together...this is the third time he left me

in almost 10 years of

marriage so i am giving up on him...as much

as i hate it. =*( Looking

fwd to meeting you all. Love, Amy xoxo

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try www.vaccinea.blogspot.com

--- Julius Carandang <julius_carandang@...>

wrote:

> Hello there! I'm new member on this site, can you

> send me more information about anthrax vaccine. tnx

> @ good day. julius

>

>

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

> Do you ?

> Search presents - Jib Jab's 'Second Term'

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

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Julius,

This is a public forum, where we all share information, stories, etc...

If you want information re: anthrax vaccine, you're going to have to do some

digging.

Some good sites are: www.milvacs.org; www.anthraxvaccine.org;

www.avip2001.net

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

Message: 3

Date: Sat, 19 Feb 2005 00:10:24 -0800 (PST)

From: Julius Carandang <julius_carandang@...>

Subject: new member

Hello there! I'm new member on this site, can you send me more information

about anthrax vaccine. tnx @ good day. julius

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Hi, Sharon,

Welcome to you and Kearsten, pretty name. My son Charlie 5 1/2 has always

slept fairly well. But a sleep study showed moderate obstructive sleep

apnea. And neck x-rays to rule out subglottic stenosis did that but also

showed huge adenoids to go along with his huge tonsils. So he's scheduled

for a T & A at CHOP--sorry if that's too much alphabet soup, that's a

tonsillectomy and adenoidectomy at Children's Hospital of Philadelphia.

Anyway, you might want to read Dr. Leshin's essay on obstructive sleep

apnea. Here's a link, http://www.ds-health.com/apnea.htm

Regards,

Bob, Charlie's dad

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Hi, Sharon,

Welcome to you and Kearsten, pretty name. My son Charlie 5 1/2 has always

slept fairly well. But a sleep study showed moderate obstructive sleep

apnea. And neck x-rays to rule out subglottic stenosis did that but also

showed huge adenoids to go along with his huge tonsils. So he's scheduled

for a T & A at CHOP--sorry if that's too much alphabet soup, that's a

tonsillectomy and adenoidectomy at Children's Hospital of Philadelphia.

Anyway, you might want to read Dr. Leshin's essay on obstructive sleep

apnea. Here's a link, http://www.ds-health.com/apnea.htm

Regards,

Bob, Charlie's dad

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Sharon

Welcome to the list from another Sharon! I have a 13 year old daughter with DS,

, and , 9.

had her tonsils out when she was 20 months old. She also has a small

airway, and because of a fistula she had when she was born that was corrected

surgically, anyone the intubates her has to be careful about how far the tube is

advanced. We had the anesthesiologist that put to sleep for her

tonsillectomy call the pediatric surgeon that repaired her fistula to get all of

the pertinent information. did very well.

It does sound like her sleeping problems might be associated with the sinuses,

tubes etc. I would definitely get a second opinion.

We are glad you are here, you will finds lots of great people, and great info.

Sharon

Mom to , (13, DS) and , (9)

South Carolina

new member

Hi! Im a new member to this group. My name is Sharon Higgins and I

have a 3 year old daughter with Down Syndrome. Her name is Kearsten.

I was hoping someone good give me some advice or just hear your

stories about a couple of issues that I am having with Kearsten.

The first thing is she sleeps terribly. Every night she has to come

to our room to sleep with us. I take her back to her bed but she

always returns. Kearsten does not talk yet so it is hard to

communicate with her with these issues. Her other issue is that she

is on her 3rd set of tubes in her ears. She is always very congested

and can hardly breathe. I think this might relate to her sleep

disorder. She just had a cat scan on her sinuses and we are looking

at getting her a second opionion by another ENT Doctor. She is at

High risk for surgery because she has really small airways. They want

to take her adnoids out. This is all very scary to me.

I would appreciate any help if anyone has some.

Thank you

Sharon Higgins

Click reply to all for messages to go to the list. Just hit reply for

messages to go to the sender of the message.

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Sharon

Welcome to the list from another Sharon! I have a 13 year old daughter with DS,

, and , 9.

had her tonsils out when she was 20 months old. She also has a small

airway, and because of a fistula she had when she was born that was corrected

surgically, anyone the intubates her has to be careful about how far the tube is

advanced. We had the anesthesiologist that put to sleep for her

tonsillectomy call the pediatric surgeon that repaired her fistula to get all of

the pertinent information. did very well.

It does sound like her sleeping problems might be associated with the sinuses,

tubes etc. I would definitely get a second opinion.

We are glad you are here, you will finds lots of great people, and great info.

Sharon

Mom to , (13, DS) and , (9)

South Carolina

new member

Hi! Im a new member to this group. My name is Sharon Higgins and I

have a 3 year old daughter with Down Syndrome. Her name is Kearsten.

I was hoping someone good give me some advice or just hear your

stories about a couple of issues that I am having with Kearsten.

The first thing is she sleeps terribly. Every night she has to come

to our room to sleep with us. I take her back to her bed but she

always returns. Kearsten does not talk yet so it is hard to

communicate with her with these issues. Her other issue is that she

is on her 3rd set of tubes in her ears. She is always very congested

and can hardly breathe. I think this might relate to her sleep

disorder. She just had a cat scan on her sinuses and we are looking

at getting her a second opionion by another ENT Doctor. She is at

High risk for surgery because she has really small airways. They want

to take her adnoids out. This is all very scary to me.

I would appreciate any help if anyone has some.

Thank you

Sharon Higgins

Click reply to all for messages to go to the list. Just hit reply for

messages to go to the sender of the message.

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One of my biggest questions is...............Are there any state or federal laws

about vaccinating? Can a school deny your child because they aren't vaccinated?

Do I need to get a religious exemption, and if so, how?

crazeladyshopper <crazeladyshopper@...> wrote:

Hi ne and welcome. Congrats on making the best decision for

your little one. You are correct in the assumption of the damage

vaccines do to the body :-(

You will find there are many knowledgeable people on this list that

will be able to guide you in your decision.

I do not know of any physicians in that area but maybe someone else

on the list does.

My husband is not whole heartedly with me on the non-vaccine issues

but he has seen the damage it did to our son. He is sort of sitting

on the fence I guess you could say.

Yes, get all the documents together that you can. There are so many

studies out there now about vaccine damage.

Just Google search vaccine damage or vaccine dangers and you will be

shocked at how much is out there.

Congrats on the little one on the way as well :-)

Sherry

> Hi, My name is ne Sevigny-. I live in lin

Tennessee (30 miles south of Nashville). I am 22 years old. Just got

married in December and am expecting a baby girl July 4th. I first

became interested in homeopathy and not vaccinating, a couple years

ago, with my dogs (great danes). I took/take it very seriously. My

great dane that I have now, is unvaccinated and eats a completly raw

food diet. Well, now that I am pregnant, these instincts have kicked

in again and it leads me to questions about vaccinating my precious

baby. I've heard of and seen the damage it does to our animals. I

can only imagine what it does to US. Of course, everyone around me

thinks i'm crazy, that I'm considering not vaccinating my

baby....one of them being my husband. So I figured I would go out

and try to gather as much information as possible, to back up my

reasonings. I am also in search of a alternative/homeopathic

doctor/pediatrician, in the area, so that I have professional advice

as well. I

> am glad to have joined the group and I hope I will get all I need

from it.

> Thank you.

> ne

>

>

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

> Do you ?

> Small Business - Try our new resources site!

>

>

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Guest guest

Hi Danah and welcome to our LL sisterhood...YAYA! I think Bonnie gave you a

great explanation on holding your breaths. It does become easier, but there

are times for me anyway, that I can't hold for very long. Then times when I

have no problem. I'm a big believer in the visual healing with the breaths

too. Hope you keep posting, we love new people to join in and learn from

each other!!

Blessings,

Kiki

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Hi Danah, Welcome! Welcome! I think if you hold your breath to what is

comfortable for you, you have it right. The main thing is to do it and do it

often! You won't be sorry, you will feel so great and have wonderful energy.

Just

know that you have done something great for yourself, a true gift to you. :-)

Have fun and WELCOME!!! Connie :-)

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Danah,

I hold my breath for as long as is comfortable -- and I've noticed that the

duration has increased with time. At first, it was hard for me to complete an

exercise, now it's relatively simple.

I also have noticed that my breathing in general has improved -- I breathe more

correctly even when not doing the LL breathing -- deeper breaths, less shallow

breaths -- this has got to be a good thing! And I no longer get " winded " when

climbing stairs, and I can actually jog a bit.....

Rashelle has (somewhere, the first video?) some suggestions for getting

increased oxygen to various joints -- I remember a seated exercise that is

particularly good on your knee joints -- someone else will need to direct you to

this..... I think she has you visualize just where you want the oxygen to go, I

use this if I feel a headache starting, I just take a couple of LL breaths and

" think " the healing power to go to my head -- works every time!

Good luck!

Bonnie

new member

Hi everyone,

I'm new to this group and I have a question about the lifelift

breathing. How long do you hold your breath while doing a stretch for

maximum fat burning? I have the basic tape only and it doesn't say how

long to hold the breath. I hold my breath for between 7-14 seconds

depending on the exercise, because that's all I can do. Is this enough

time or should I try to hold it longer or less? I need to lose about

60-70 pounds and I have severe arthritis and tendonitis in my joints

so I'm hoping this breathing exercise can help!

Thanks!

Danah

P.S. Enjoyed reading all of your inspirational posts!!!

What can changing the way you breathe do for you? Everything!

See why tens of thousands agree, Life Lift is the best! http://www.oxygenzoo.com

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Jenni, you're so right, that when it gets quiet here we miss each other.

Kinda why I think we all do the 'tests', just to make sure we're still

connected and not missing anything! I would have been very upset and worried

yesterday when I found LL wasn't listed as one of my groups, 'cept that I had

been

getting messages.

Love you,

Kiki

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Hi Danah!

Welcome to our group! You will simply love it here...everyone is so

encouraging. It gets quiet on the weekend sometimes and I think we all miss our

buddies!

with love,

Jenni

Proud Air Force Mom!

May God guide and protect our troops!

new member

Hi everyone,

I'm new to this group and I have a question about the lifelift

breathing. How long do you hold your breath while doing a stretch for

maximum fat burning? I have the basic tape only and it doesn't say how

long to hold the breath. I hold my breath for between 7-14 seconds

depending on the exercise, because that's all I can do. Is this enough

time or should I try to hold it longer or less? I need to lose about

60-70 pounds and I have severe arthritis and tendonitis in my joints

so I'm hoping this breathing exercise can help!

Thanks!

Danah

P.S. Enjoyed reading all of your inspirational posts!!!

What can changing the way you breathe do for you? Everything!

See why tens of thousands agree, Life Lift is the best!

http://www.oxygenzoo.com

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I would have been too Kiki. I can do without my other groups okay, but NOT this

one!

love you back!

Jenni

Proud Air Force Mom!

May God guide and protect our troops!

Re: new member

Jenni, you're so right, that when it gets quiet here we miss each other.

Kinda why I think we all do the 'tests', just to make sure we're still

connected and not missing anything! I would have been very upset and worried

yesterday when I found LL wasn't listed as one of my groups, 'cept that I had

been

getting messages.

Love you,

Kiki

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Guest guest

Welcome JSPRINGERHOU! The thumping will be adjusted out. Your unit can be set to not feel the pacing. That happened to me as well when my unit was implanted - the Docs couldn't believe I could feel it - but they duplicated it and that is what I was feeling, so they adjusted the pacing. I have had mine almost 6 years now - ready for the second replacement.

The days get better and there will be days in your future that you will not even think of the ICD!

Stay posted, you will find lots of friends and zapper family here and all your questions will be answered.

~guin

New member

I had my ICD implant on 4/1/2005 (April Fool's Day)and I am still getting used to the idea of an object in my chest. The incision is still a little touchy and the thumping in my chest is a little aggravating.I have to go back to the Dr to have the device adjusted.If I consider the alternative...it ain't too bad.Please visit the Zapper homepage athttp://www.ZapLife.org

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Thanks for the info.

My next venture to the hospital is this Friday and a good old

fashioned roto rooter job.

Two surgeries in one month. What did I do to deserve this :<) I

guess it is one way to forget about the ICD.

> Welcome JSPRINGERHOU! The thumping will be adjusted out. Your

unit can be set to not feel the pacing. That happened to me as well

when my unit was implanted - the Docs couldn't believe I could feel

it - but they duplicated it and that is what I was feeling, so they

adjusted the pacing. I have had mine almost 6 years now - ready for

the second replacement.

> The days get better and there will be days in your future that you

will not even think of the ICD!

> Stay posted, you will find lots of friends and zapper family here

and all your questions will be answered.

> ~guin

> New member

>

>

>

>

> I had my ICD implant on 4/1/2005 (April Fool's Day)and I am

still

> getting used to the idea of an object in my chest. The incision

is

> still a little touchy and the thumping in my chest is a little

> aggravating.

> I have to go back to the Dr to have the device adjusted.

> If I consider the alternative...it ain't too bad.

>

>

>

>

>

>

>

>

> Please visit the Zapper homepage at

> http://www.ZapLife.org

>

>

>

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

-----------

>

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Guest guest

Well count your blessings.... I wasn't going to tell you this, but things can be worse - my ICD was recalled 5 mos after implant!!! Thank God Medtronic keeps great records!

Good luck to you and we will keep you in our thought on Friday.

Keep us posted.

~guin

New member> > > > > I had my ICD implant on 4/1/2005 (April Fool's Day)and I am still > getting used to the idea of an object in my chest. The incision is > still a little touchy and the thumping in my chest is a little > aggravating.> I have to go back to the Dr to have the device adjusted.> If I consider the alternative...it ain't too bad.> > > > > > > > > Please visit the Zapper homepage at> http://www.ZapLife.org > > > > ------------------------------------------------------------------------------>

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What do you mean by roto rooter?

Deb

From: [mailto: ] On Behalf Of jspringerhou

Sent: Monday, April 25, 2005 2:36

PM

Subject: Re: New member

Thanks for the info.

My next venture to the hospital is this Friday and

a good old

fashioned roto rooter job.

Two surgeries in one month. What did I do to

deserve this :<) I

guess it is one way to forget about the ICD.

> Welcome JSPRINGERHOU! The thumping will

be adjusted out. Your

unit can be set to not feel the pacing. That

happened to me as well

when my unit was implanted - the Docs couldn't

believe I could feel

it - but they duplicated it and that is what I was

feeling, so they

adjusted the pacing. I have had mine almost

6 years now - ready for

the second replacement.

> The days get better and there will be days in

your future that you

will not even think of the ICD!

> Stay posted, you will find lots of friends

and zapper family here

and all your questions will be answered.

> ~guin

> New member

>

>

>

>

> I had my ICD implant on 4/1/2005

(April Fool's Day)and I am

still

> getting used to the idea of an

object in my chest. The incision

is

> still a little touchy and the

thumping in my chest is a little

> aggravating.

> I have to go back to the Dr to

have the device adjusted.

> If I consider the

alternative...it ain't too bad.

>

>

>

>

>

>

>

>

> Please visit the Zapper homepage

at

> http://www.ZapLife.org

>

>

>

>

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

-----------

>

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Guest guest

sounds like an angioplasty.

On Apr 25, 2005, at 9:39 PM, debra j cruz wrote:

>

>  

> What do you mean by roto rooter?

> Deb

>

> From: [mailto: ] On

> Behalf Of jspringerhou

> Sent: Monday, April 25, 2005 2:36 PM

>

> Subject: Re: New member

>  

>

>

> Thanks for the info.

> My next venture to the hospital is this Friday and a good old

> fashioned roto rooter job. 

>

> Two surgeries in one month.  What did I do to deserve this :<)  I

> guess it is one way to forget about the ICD.

>

> > Welcome JSPRINGERHOU!  The thumping will be adjusted out.  Your

> unit can be set to not feel the pacing.  That happened to me as well

> when my unit was implanted - the Docs couldn't believe I could feel

> it - but they duplicated it and that is what I was feeling, so they

> adjusted the pacing.  I have had mine almost 6 years now - ready for

> the second replacement.

> > The days get better and there will be days in your future that you

> will not even think of the ICD!

> > Stay posted, you will find lots of friends and zapper family here

> and all your questions will be answered.

> > ~guin

> >   New member

> >

> >

> >

> >

> >   I had my ICD implant on 4/1/2005 (April Fool's Day)and I am

> still

> >   getting used to the idea of an object in my chest.  The incision

> is

> >   still a little touchy and the thumping in my chest is a little

> >   aggravating.

> >   I have to go back to the Dr to have the device adjusted.

> >   If I consider the alternative...it ain't too bad.

> >

> >

> >

> >

> >

> >

> >

> >

> >   Please visit the Zapper homepage at

> >   http://www.ZapLife.org

> >

> >

> >

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

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

> >  

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Guest guest

TURP (removal of part of the prostate)

New member

>

>

>

>

> I had my ICD

implant on 4/1/2005 (April Fool's Day)and I am

still

> getting used

to the idea of an object in my chest. The incision

is

> still a

little touchy and the thumping in my chest is a little

> aggravating.

> I have to go

back to the Dr to have the device adjusted.

> If I

consider the alternative...it ain't too bad.

>

>

>

>

>

>

>

>

> Please visit

the Zapper homepage at

> http://www.ZapLife.org

>

>

>

>

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

-----------

>

Groups Links

>

>

a.. To visit your group on the web, go to:

> /

>

>

b..

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Welcome ,

I've been on this group for years but only just came out public a couple a

days ago. I mostly lurk but want to change that. I have a 5 year old

daughter that has never been vax'd. I also stress from time to time, which

is why I'm here. LOL In our case also my daughter has always been the

healthy one and rarely even has a cold, even when everyone else in the house

is sick she will not catch it.

Melyssa

> Hi, my name is and I am a new member. I have a 22 month old

> son, never vaccinated. I live in California in the Bay Area. My

> doctor seems to be ok with the fact that I do not plan to vaccinate

> him. Of course, I stress out over my decision and read a lot of

> different views on vaccinations but so far he is healthier than any of

> his vaccinated friends. Of course this could just be the luck of the

> draw but he is the only one with out a chronic runny nose, earaches,

> asthma and seizures.

> I have been enjoying all the different posting these past few days. I

> really appreciate all the different views.

> Have a great day.

> From,

>

>

>

>

>

>

>

>

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Hi. Two of my three have been at least partially if not fully

vaccinated. My third, the non-vaccinated one, has very good health in

comparison to her siblings and friends.

different views on vaccinations but so far he is healthier than any of

> his vaccinated friends. Of course this could just be the luck of the

> draw but he is the only one with out a chronic runny nose, earaches,

> asthma and seizures.

> From,

>

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