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In a message dated 2/25/2003 1:21:48 PM Pacific Standard Time,

exercise4u2@... writes:

> My

> question is this how many times per week do you each workout to the

> tae-bo tapes? Also how long before you started seeing weightloss and

> your endurance built up?

>

Welcome April :o)!!!!!!!

It's up to you and your schedule. Start out with 3-4 times a week and then

you can work your way up. I usually do it 6 times a week, but when I'm

slacking about 5.

Everyone is different, so there's no perfect guideline. Some folks see it

immediately, others it takes several months. It depends on what you're

eating, your body composition and how often you're working out. I started

seeing results pretty much immediately. I started WW a month later and that

helped get my eating in control. I don't remember how long it took me to get

to get the endurance up.

Sandie, Tae and Bo :o)!!!!!!!!!

" One day at a time, no guilt and move on " Dotti

Today is " Monday "

Breaking Free in 2K3

Week of 2/23 Goals

Wednesday Abs Challenge

128 oz. Water

Weights

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You might check Nolo Press, they have a lot of do it yourself legal document

kits, and they are based in CA, so should have a CA LLC kit.

j

denise gali wrote:

Hi everyone,

Does anyone have any information on what procedures or steps a home base

handmade beauty business which is a sole proprietorship now needs to take in

order to become a LLC base business.

Also, how to make this transition as easy and uncomplicated as possible. I live

in Southern California.

Thanks much,

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

We have the perfect Group for you. Check out the handy changes to Yahoo! Groups.

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Hi

You can email me personally at Kristy@... This email goes to the support

group.

Kristy

Blay wrote:

Is this email going to the president of MDS?

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Where at in Washington are you ? We live in Washougal, near Vancouver.

Marriah, (Gideons mommy)

/09, wrote:

Subject: (unknown)

To: MosaicDS

Date: Monday, March 9, 2009, 10:49 AM

I haven't been following the egroup very well lately, but I do have 2 cents to

add concerning early intervention so I figured I'd take some time to share my

experiences with you.

My son was diagnosed at age 2 and was put into the preschool program they had in

Utah, which was great. We were only there for a couple months though and

unexpectedly moved back up to Washington. Here they have a " birth to three "

program that I can't say enough good things about. The other kids in there had

different delays and issues (for lack of a better word) - Aidan was the only one

with DS. You'll have to check on the specifics of the programs in your area, but

this one started in a large motor room (ball pit, slide, climbing toy, riding

toys, etc.), then onto free play (smaller manipulatives, imaginary play,

puzzles, etc.), snack (where they focused on eating/texture issues, help with

feeding, etc.) and ended with circle time (they had to learn to sit still and

take turns in the cirle, doing songs, more large motor, etc.). I thought the

program was great. They had separate speech time twice a week with an SLP so he

got that in a private setting.

She had some really great tips on things to help him get that headstart that we

needed and things to watch for. When he turned three he went to a " developmental

preschool " (through a local elementary school here) where they had peer models,

along with the kids with delays. The peer models pay a tuition, which helps the

school and are on track in their development, which helps the kids have positive

models. Anyway, things there were set up like they would be in elementary

school, with an IEP, evaluations through the school district, etc. Like I said,

that's how they do it here - I don't know if it's different in other states.

Even though there were other kids in the program with delays, Aidan got the help

he needed (especially the social interaction) so I thought it was great. The

program was set up similar to how it works in school so there are evaluations,

parent-teacher conferences and IEPs. Since he was on an IEP, he gets

re-evaluated every 3 years

(is that right ?) so if something isn't necessary anymore they

discontinue and if there are added challenges they address those. So as far as

your question of whether having a diagnosis means they're stuck in special ed,

with this program that's not the case. Aidan is in 1st grade now and mostly

needs help with speech (although there have been other minor things in his IEP

like social interaction and math) so he's in a mainstream classroom with an IEP

teacher who comes in and helps with IEP goals. And, for speech he's pulled out

once a week during a time that will disrupt his progress the least.

Anyway, obviously I could go on and on. Our school district is really great and

does really well so I have nothing but praise for Early Intervention. Looking

back, if I hadn't done it I would have wondered what help I could have gotten

for him so that would be my motivation more than anything. Plus, having him

constantly going to school from a very early age has helped with each transition

that much more. Each start of a new year, he's already used to a school setting

so he's ready to focus on learning, rather than wasting time getting his stamina

and mind used to sitting in school all day. Think about what a headstart that

can be! I can't speak for every program out there though so I would loook into

what specifics they offer and how the program is structured. Good luck!!

IMDSA Newsletter Editor

Mom to Aidan (6) MDS, a (5), Addie (3), Evan (almost 1)

stephanieimdsa (DOT) org

* Do you want to have access to our quarterly newsletter, MOSAIC WORLD? First

you need to become a member of IMDSA. To find out more go to www.imdsa.org. Our

next newsletter comes out in May so hurry and sign up today! Don't miss another

issue!

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Marriah,

We live in Kent/Covington, about 20 minutes north of Tacoma (give or take).

>

>

> Subject: (unknown)

> To: MosaicDS

> Date: Monday, March 9, 2009, 10:49 AM

>

>

>

>

>

>

>

> I haven't been following the egroup very well lately, but I do have 2 cents to

add concerning early intervention so I figured I'd take some time to share my

experiences with you.

> My son was diagnosed at age 2 and was put into the preschool program they had

in Utah, which was great. We were only there for a couple months though and

unexpectedly moved back up to Washington. Here they have a " birth to three "

program that I can't say enough good things about. The other kids in there had

different delays and issues (for lack of a better word) - Aidan was the only one

with DS. You'll have to check on the specifics of the programs in your area, but

this one started in a large motor room (ball pit, slide, climbing toy, riding

toys, etc.), then onto free play (smaller manipulatives, imaginary play,

puzzles, etc.), snack (where they focused on eating/texture issues, help with

feeding, etc.) and ended with circle time (they had to learn to sit still and

take turns in the cirle, doing songs, more large motor, etc.). I thought the

program was great. They had separate speech time twice a week with an SLP so he

got that in a private setting.

> She had some really great tips on things to help him get that headstart that

we needed and things to watch for. When he turned three he went to a

" developmental preschool " (through a local elementary school here) where they

had peer models, along with the kids with delays. The peer models pay a tuition,

which helps the school and are on track in their development, which helps the

kids have positive models. Anyway, things there were set up like they would be

in elementary school, with an IEP, evaluations through the school district, etc.

Like I said, that's how they do it here - I don't know if it's different in

other states. Even though there were other kids in the program with delays,

Aidan got the help he needed (especially the social interaction) so I thought it

was great. The program was set up similar to how it works in school so there are

evaluations, parent-teacher conferences and IEPs. Since he was on an IEP, he

gets re-evaluated every 3 years

> (is that right ?) so if something isn't necessary anymore they

discontinue and if there are added challenges they address those. So as far as

your question of whether having a diagnosis means they're stuck in special ed,

with this program that's not the case. Aidan is in 1st grade now and mostly

needs help with speech (although there have been other minor things in his IEP

like social interaction and math) so he's in a mainstream classroom with an IEP

teacher who comes in and helps with IEP goals. And, for speech he's pulled out

once a week during a time that will disrupt his progress the least.

> Anyway, obviously I could go on and on. Our school district is really great

and does really well so I have nothing but praise for Early Intervention.

Looking back, if I hadn't done it I would have wondered what help I could have

gotten for him so that would be my motivation more than anything. Plus, having

him constantly going to school from a very early age has helped with each

transition that much more. Each start of a new year, he's already used to a

school setting so he's ready to focus on learning, rather than wasting time

getting his stamina and mind used to sitting in school all day. Think about what

a headstart that can be! I can't speak for every program out there though so I

would loook into what specifics they offer and how the program is structured.

Good luck!!

>

>

> IMDSA Newsletter Editor

> Mom to Aidan (6) MDS, a (5), Addie (3), Evan (almost 1)

> stephanieimdsa (DOT) org

>

> * Do you want to have access to our quarterly newsletter, MOSAIC WORLD? First

you need to become a member of IMDSA. To find out more go to www.imdsa.org. Our

next newsletter comes out in May so hurry and sign up today! Don't miss another

issue!

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

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Great, thanx for letting me know. Thats about 200 miles from here. If you are

ever in this area (vancouver near portland OR) write me!

Marriah

Subject: Re: (unknown)

To: MosaicDS

Date: Tuesday, March 10, 2009, 6:20 PM

Marriah,

We live in Kent/Covington, about 20 minutes north of Tacoma (give or take).

>

> From: <stephanie@. ..>

> Subject: (unknown)

> To: MosaicDS@yahoogroup s.com

> Date: Monday, March 9, 2009, 10:49 AM

>

>

>

>

>

>

>

> I haven't been following the egroup very well lately, but I do have 2 cents to

add concerning early intervention so I figured I'd take some time to share my

experiences with you.

> My son was diagnosed at age 2 and was put into the preschool program they had

in Utah, which was great. We were only there for a couple months though and

unexpectedly moved back up to Washington. Here they have a " birth to three "

program that I can't say enough good things about. The other kids in there had

different delays and issues (for lack of a better word) - Aidan was the only one

with DS. You'll have to check on the specifics of the programs in your area, but

this one started in a large motor room (ball pit, slide, climbing toy, riding

toys, etc.), then onto free play (smaller manipulatives, imaginary play,

puzzles, etc.), snack (where they focused on eating/texture issues, help with

feeding, etc.) and ended with circle time (they had to learn to sit still and

take turns in the cirle, doing songs, more large motor, etc.). I thought the

program was great. They had separate speech time twice a week with an SLP so he

got that in a private setting.

> She had some really great tips on things to help him get that headstart that

we needed and things to watch for. When he turned three he went to a

" developmental preschool " (through a local elementary school here) where they

had peer models, along with the kids with delays. The peer models pay a tuition,

which helps the school and are on track in their development, which helps the

kids have positive models. Anyway, things there were set up like they would be

in elementary school, with an IEP, evaluations through the school district, etc.

Like I said, that's how they do it here - I don't know if it's different in

other states. Even though there were other kids in the program with delays,

Aidan got the help he needed (especially the social interaction) so I thought it

was great. The program was set up similar to how it works in school so there are

evaluations, parent-teacher conferences and IEPs. Since he was on an IEP, he

gets re-evaluated every 3 years

> (is that right ?) so if something isn't necessary anymore they

discontinue and if there are added challenges they address those. So as far as

your question of whether having a diagnosis means they're stuck in special ed,

with this program that's not the case. Aidan is in 1st grade now and mostly

needs help with speech (although there have been other minor things in his IEP

like social interaction and math) so he's in a mainstream classroom with an IEP

teacher who comes in and helps with IEP goals. And, for speech he's pulled out

once a week during a time that will disrupt his progress the least.

> Anyway, obviously I could go on and on. Our school district is really great

and does really well so I have nothing but praise for Early Intervention.

Looking back, if I hadn't done it I would have wondered what help I could have

gotten for him so that would be my motivation more than anything. Plus, having

him constantly going to school from a very early age has helped with each

transition that much more. Each start of a new year, he's already used to a

school setting so he's ready to focus on learning, rather than wasting time

getting his stamina and mind used to sitting in school all day. Think about what

a headstart that can be! I can't speak for every program out there though so I

would loook into what specifics they offer and how the program is structured.

Good luck!!

>

>

> IMDSA Newsletter Editor

> Mom to Aidan (6) MDS, a (5), Addie (3), Evan (almost 1)

> stephanieimdsa (DOT) org

>

> * Do you want to have access to our quarterly newsletter, MOSAIC WORLD? First

you need to become a member of IMDSA. To find out more go to www.imdsa.org. Our

next newsletter comes out in May so hurry and sign up today! Don't miss another

issue!

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

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That is one of the responses I received about Miralax vs MOM from a doctor. But I am going to be asking a GI next month specifically about MOM, Kids Calm, Miralax, and many of the other solutions suggested here.

I will be prepping the doctor before our visit, so I expect a thorough and complete response. I will share that response with the group.

From: miralax [mailto:miralax ] On Behalf Of BarnettSent: Wednesday, September 16, 2009 5:41 PMTo: encopresissupport ; miralax Subject: (unknown)

My grandson was put on MOM and Mineral Oil and we were happy that he was doing better ( still occasional smear, but no accidents like he has had in the past). But in researching the Mineral Oil, I'm thinking the bowel problems would be better than possible effects from the mineral oil. Site after site purported that it is not recommended for long term use, can interfere with absorption of vitamins and calcium, and may collect in tissues and cause inflammation of the liver, spleen, and clog the lymph system! I told my daughter to quit giving it. We'll go back to the olive oil but it doesn't seem that it was helping as well as the mineral oil . Perhaps we weren't giving enough. I'm starting to think that Miralax is the lesser of 2 evils!__________________________________________________

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We used an entire bottle of MOM after the ER suggested it when

we went in and found out my daughter was ‘compacted’ even though

she was having daily bm’s….NOTHING happened with the MOM-I

mean-nothing….not a single thing other than my daughter hated drinking

the chalky stuff. We have used Natural Calm/Kids Calm. We did have some results

with this but I have not continued on it consistently. Is there concern about

staying on magnesium? We are not using Miralax. We used one small dosage and my

daughter went into a fit of rage right after-I went looking online for side

effects from taking Miralax because she was wigging out which was what led us

here.

I am trying to find a way to heal her gut now….it seems

like it is never ending!

-

Snip >That is one of the responses I received about Miralax vs MOM from a

doctor. But I am going to be asking a GI next month specifically about

MOM, Kids Calm, Miralax, and many of the other solutions suggested here.

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Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Welcome Home Diane

Remind me - where is home for you??

Gloria

________________________________

Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Welcome Home Diane

Remind me - where is home for you??

Gloria

________________________________

Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Guest guest

Welcome Home Diane

Remind me - where is home for you??

Gloria

________________________________

Hi Dave,

Diane here. I am doing fantastic!!!! For the first time in nearly 4 years,

I am writing from my own home tonight!!!! Praise the Lord!!!! I just

returned home tonight. We had moved out in August, 2006 to live with my MIL

and take care of her. Then, my husband got very ill and died and I am just

now getting back to where I felt competent to make a decision about where to

live. I have to tell you, coming home is the best decision I have made

since Terry died!!!! I am sooooooo happy to be home!!!!

Hope you are doing as well as you can. God bless!

Many hugs............

Diane

>

>

> How's everyone? Hope you are doing good.

> Dave

>

>

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Oh my goodness , that is fabulous news. I hope for you that it lasts too. It's kindof hard I noticed, to get a good balance between watery you-know-what or nicely formed but loose bowels. I still don't have it good. I guess it takes time to figure it out.

Meanwhile though, at least we are feeling better!!!

Shauna

Subject: (unknown)To: Lyme_and_Rife Date: Saturday, July 24, 2010, 10:08 AM

Hi Shauna, Thank you so much for the charchol/mag comboI tried it yesterday .. and woke up today feeling sooo much better I have been sick for so long .. no good days constant fatigue , brain fog , mailaise , headaches (for a year) and today my head is clear and not fatigued just a bit tired I just took my 2nd dose .. and will continue to do so 3 times a day Im going to get the chlorrella too I just hope this continues and wasnt just a fluke ..lol ;)"Until one has loved an animal, part of their soul remains unawakened."

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Thank you for posting this!

I had the thought to go out to buy oregano oil this morning, and this confirms it.

I wonder - does anyone know if it's possible to make you own? 

I live in Korea, and am not sure what's available there.  I'm in Canada now, so I will pick up a few things to take back with me.

Thanks,

Elana Rodgers

 

hi, Jodie

I am often reading people's postings and i guess feel lucky: i probably had Lymes all my life (tic bite at age 9) and it only came through at the time when i was massively stressed out.

I think when conventional does not work with ease - go Unconventional.

What helped me a great deal was advice of a famous nutritionist in Chinese medicine: i took one drop of essential oil of Oregano internally (in the morning! not at night)+ 15 drops of lobelia  which is said to help immune system to find Lyme , chopped garlic with morning and lunch meals (not at night).. I am much better.

Recently went to see an N.D. who used to be the partner of Dr K and they developed his current muscle testing methods together .. she said.. and she is the second N.D. i  recently spoke to: Lyme is opportunistic.. it is all about Terrain TTerrainTerrain.. 

Rekwig remedies eliminated a breast lump i had within a week..... anyway just some thought..

Oil of oregano helped my mind to be clearer.

best wwises Olga

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Thank you for posting this!

I had the thought to go out to buy oregano oil this morning, and this confirms it.

I wonder - does anyone know if it's possible to make you own? 

I live in Korea, and am not sure what's available there.  I'm in Canada now, so I will pick up a few things to take back with me.

Thanks,

Elana Rodgers

 

hi, Jodie

I am often reading people's postings and i guess feel lucky: i probably had Lymes all my life (tic bite at age 9) and it only came through at the time when i was massively stressed out.

I think when conventional does not work with ease - go Unconventional.

What helped me a great deal was advice of a famous nutritionist in Chinese medicine: i took one drop of essential oil of Oregano internally (in the morning! not at night)+ 15 drops of lobelia  which is said to help immune system to find Lyme , chopped garlic with morning and lunch meals (not at night).. I am much better.

Recently went to see an N.D. who used to be the partner of Dr K and they developed his current muscle testing methods together .. she said.. and she is the second N.D. i  recently spoke to: Lyme is opportunistic.. it is all about Terrain TTerrainTerrain.. 

Rekwig remedies eliminated a breast lump i had within a week..... anyway just some thought..

Oil of oregano helped my mind to be clearer.

best wwises Olga

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Guest guest

Thank you for posting this!

I had the thought to go out to buy oregano oil this morning, and this confirms it.

I wonder - does anyone know if it's possible to make you own? 

I live in Korea, and am not sure what's available there.  I'm in Canada now, so I will pick up a few things to take back with me.

Thanks,

Elana Rodgers

 

hi, Jodie

I am often reading people's postings and i guess feel lucky: i probably had Lymes all my life (tic bite at age 9) and it only came through at the time when i was massively stressed out.

I think when conventional does not work with ease - go Unconventional.

What helped me a great deal was advice of a famous nutritionist in Chinese medicine: i took one drop of essential oil of Oregano internally (in the morning! not at night)+ 15 drops of lobelia  which is said to help immune system to find Lyme , chopped garlic with morning and lunch meals (not at night).. I am much better.

Recently went to see an N.D. who used to be the partner of Dr K and they developed his current muscle testing methods together .. she said.. and she is the second N.D. i  recently spoke to: Lyme is opportunistic.. it is all about Terrain TTerrainTerrain.. 

Rekwig remedies eliminated a breast lump i had within a week..... anyway just some thought..

Oil of oregano helped my mind to be clearer.

best wwises Olga

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I don't make my own, it's not that expensive. I take 1 about 2 days out of 3 -

am mixing up the herbs. I was told it was an antibacterial - a bug killer - so

rotate what I do for killing and always support detox.

Same with rifing - only about once a week.

>

> >

> >

> > hi, Jodie

> >

> > I am often reading people's postings and i guess feel lucky: i probably had

> > Lymes all my life (tic bite at age 9) and it only came through at the time

> > when i was massively stressed out.

> >

> > I think when conventional does not work with ease - go Unconventional.

> >

> > What helped me a great deal was advice of a famous nutritionist in Chinese

> > medicine: i took one drop of essential oil of Oregano internally (in the

> > morning! not at night)+ 15 drops of lobelia which is said to help immune

> > system to find Lyme , chopped garlic with morning and lunch meals (not at

> > night).. I am much better.

> >

> > Recently went to see an N.D. who used to be the partner of Dr K and they

> > developed his current muscle testing methods together .. she said.. and she

> > is the second N.D. i recently spoke to: Lyme is opportunistic.. it is all

> > about Terrain TTerrainTerrain..

> > Rekwig remedies eliminated a breast lump i had within a week..... anyway

> > just some thought..

> > Oil of oregano helped my mind to be clearer.

> > best wwises Olga

> >

> >

> >

> >

>

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Thanks .It's not the cost I'm worried about - it's the availability.  I live in Korea.  But, I went to a great health food store and got a couple bottles to take back with me next week.Merry Christmas!

 

I don't make my own, it's not that expensive. I take 1 about 2 days out of 3 - am mixing up the herbs. I was told it was an antibacterial - a bug killer - so rotate what I do for killing and always support detox.

Same with rifing - only about once a week.

>

> >

> >

> > hi, Jodie

> >

> > I am often reading people's postings and i guess feel lucky: i probably had

> > Lymes all my life (tic bite at age 9) and it only came through at the time

> > when i was massively stressed out.

> >

> > I think when conventional does not work with ease - go Unconventional.

> >

> > What helped me a great deal was advice of a famous nutritionist in Chinese

> > medicine: i took one drop of essential oil of Oregano internally (in the

> > morning! not at night)+ 15 drops of lobelia which is said to help immune

> > system to find Lyme , chopped garlic with morning and lunch meals (not at

> > night).. I am much better.

> >

> > Recently went to see an N.D. who used to be the partner of Dr K and they

> > developed his current muscle testing methods together .. she said.. and she

> > is the second N.D. i recently spoke to: Lyme is opportunistic.. it is all

> > about Terrain TTerrainTerrain..

> > Rekwig remedies eliminated a breast lump i had within a week..... anyway

> > just some thought..

> > Oil of oregano helped my mind to be clearer.

> > best wwises Olga

> >

> >

> >

> >

>

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Guest guest

Thanks .It's not the cost I'm worried about - it's the availability.  I live in Korea.  But, I went to a great health food store and got a couple bottles to take back with me next week.Merry Christmas!

 

I don't make my own, it's not that expensive. I take 1 about 2 days out of 3 - am mixing up the herbs. I was told it was an antibacterial - a bug killer - so rotate what I do for killing and always support detox.

Same with rifing - only about once a week.

>

> >

> >

> > hi, Jodie

> >

> > I am often reading people's postings and i guess feel lucky: i probably had

> > Lymes all my life (tic bite at age 9) and it only came through at the time

> > when i was massively stressed out.

> >

> > I think when conventional does not work with ease - go Unconventional.

> >

> > What helped me a great deal was advice of a famous nutritionist in Chinese

> > medicine: i took one drop of essential oil of Oregano internally (in the

> > morning! not at night)+ 15 drops of lobelia which is said to help immune

> > system to find Lyme , chopped garlic with morning and lunch meals (not at

> > night).. I am much better.

> >

> > Recently went to see an N.D. who used to be the partner of Dr K and they

> > developed his current muscle testing methods together .. she said.. and she

> > is the second N.D. i recently spoke to: Lyme is opportunistic.. it is all

> > about Terrain TTerrainTerrain..

> > Rekwig remedies eliminated a breast lump i had within a week..... anyway

> > just some thought..

> > Oil of oregano helped my mind to be clearer.

> > best wwises Olga

> >

> >

> >

> >

>

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Guest guest

Thanks .It's not the cost I'm worried about - it's the availability.  I live in Korea.  But, I went to a great health food store and got a couple bottles to take back with me next week.Merry Christmas!

 

I don't make my own, it's not that expensive. I take 1 about 2 days out of 3 - am mixing up the herbs. I was told it was an antibacterial - a bug killer - so rotate what I do for killing and always support detox.

Same with rifing - only about once a week.

>

> >

> >

> > hi, Jodie

> >

> > I am often reading people's postings and i guess feel lucky: i probably had

> > Lymes all my life (tic bite at age 9) and it only came through at the time

> > when i was massively stressed out.

> >

> > I think when conventional does not work with ease - go Unconventional.

> >

> > What helped me a great deal was advice of a famous nutritionist in Chinese

> > medicine: i took one drop of essential oil of Oregano internally (in the

> > morning! not at night)+ 15 drops of lobelia which is said to help immune

> > system to find Lyme , chopped garlic with morning and lunch meals (not at

> > night).. I am much better.

> >

> > Recently went to see an N.D. who used to be the partner of Dr K and they

> > developed his current muscle testing methods together .. she said.. and she

> > is the second N.D. i recently spoke to: Lyme is opportunistic.. it is all

> > about Terrain TTerrainTerrain..

> > Rekwig remedies eliminated a breast lump i had within a week..... anyway

> > just some thought..

> > Oil of oregano helped my mind to be clearer.

> > best wwises Olga

> >

> >

> >

> >

>

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