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Hi Sylvia,I too am new to the group and to the Masgutova method. We have found it is helping our son in just a few weeks. He has cerebral palsy. My daughter has epilepsy and we had great success with an osteopath. She went seizure free for 40 days last year after only 3 visits which is amazing considering she was having several daily for as long as I can remember.I am finally realizing that moms like us MUST take proper care of ourselves in order to care for our kids. I know it's easier said than done but I find that even sitting in a lawnchair for 15 minutes in the sun with my barefeet on the grass helps me to connect with Mother Nature and feel so much better. As the other have mentioned, breathing is crucial. Try to be conscious of your breath when you're stressed out. Take deep

cleansing breaths and before you know it, you'll be doing it more often without even realizing it.All the best,From: SEO <silviaeortiz@...>" " < >Sent: Tue, May 11, 2010 2:51:30 PMSubject: Re: Intro

Thank you I will definetly look into that and I am trying to make a habit or routine of locking myself away from the world even if it's 15 minutes THANK YOU I am excited to be hereSent from my iPhoneOn May 11, 2010, at 11:13 AM, "Annette Musso" <annettemusso@ comcast.net> wrote:

Hi Silvia,lf Wow! Well, all I can say is that you've chosen the right group

to join. I don't think you'll find a more supportive, caring, loving group of

parents, therapists and doctors that those here in this group. Do you

know much about the Masgutova Method? Having had the opportunity to attend 2

family conferences and spend time with many of those who chat on this site, I can

tell you with all honesty, that there is no better place to receive nurturing

advice and support! If you can find a therapist who specializes in the

Masgutova Method and begin this work on your kids, you will also experience the

benefits! I look forward to my son's PT session as much for myself each week

as for him! This work empowers those who have chosen to do "whatever it

takes" to help their kids…to be able to help them feel better is the best

therapy there could be for me! I feel like I'm an active participant in my

son's quest to overcome the challenges of autism. Best wishes to you and your family. Take deep breaths and get a

massage once in a while!!!!! Take people up on offers of respite when

offered and schedule in some time for yourself each day…even if it's just 15

minutes!! Take care! annette

From:

childrenwithchallen gesgroups (DOT) com

[mailto:childrenwit hchallenges] On Behalf Of SEO

Sent: Thursday, May 06, 2010 5:40 AM

childrenwithchallen gesgroups (DOT) com

Subject: Re: [childrenwithchalle nges] Intro

Thank you for the warm welcome and advice, the weather was

beatiful but I had company to enjoy the walk maybe today :)

Sent from my iPhone

On May 5, 2010, at 10:25 AM, " Palasti" <lisapalsympatico (DOT) ca> wrote:

Hi Silvia, Welcome to

the group. You must be going through a lot of stress with your kids. I know I have

2 with special needs as well and it’s a constant battle to help them waged with

the balance needed to refuel and reenergize myself so that I can be there for

my kids. Remember we (parents) are no good to anyone else if we are not

good to ourselves first so it’s like that old saying when you fly “put your

oxygen mask on firstâ€. You need to take care of yourself and give

yourself permission to do so – so that you can take care of your dear

kids. I hope you have nice weather were you are today and you can spend

20 minutes going for a walk or whatever makes you feel good. Warm

wishes,

From:

childrenwithchallen gesgroups (DOT) com [mailto:childrenwit hchallenges]

On Behalf Of SEO

Sent: May 5, 2010 9:44 AM

CHILDRENWITHCHALLEN GESGROUPS (DOT) COM

Subject: [childrenwithchalle nges] Intro

Good morning my name is Silvia I have four children a fifteen year old girl,

a thirteen year old boy who suffers from learning disability, ADHD and bipolar

disorder and twins girls age 8 who suffer from asthma, learning disability,

seizure, hypothyroidism, dyslexia and are having issues with their stomach,

intestines and kidneys. I was suggested to join a support and community group

to help me learn more about my childrens illnesses as well as be where others

understand what I am actually going through. I am frustrated, overwhelmed and

drained of every energy I have and I am in need of a lot support and I am

hoping to find great friends as well as lot of tips and info to cope with it

all.

Sent from my iPhone

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hi sandra,

my microcephaly son also tried osteopath but we did not see visible progress a year ago. so we stopped. recently, we adjusted his seizure medicines, unfortunately it caused a relapsed in seizures and hit him harder. read about osteopath having helped to reduce your child's seizures? does your child lie still during osteopath session?

Hi Silvia,

Welcome to the group. You must be going through a lot of stress with your kids. I know I have 2 with special needs as well and it’s a constant battle to help them waged with the balance needed to refuel and reenergize myself so that I can be there for my kids. Remember we (parents) are no good to anyone else if we are not good to ourselves first so it’s like that old saying when you fly “put your oxygen mask on firstâ€. You need to take care of yourself and give yourself permission to do so – so that you can take care of your dear kids. I hope you have nice weather were you are today and you can spend 20 minutes going for a walk or whatever makes you feel good.

Warm wishes,

From: childrenwithchallen gesgroups (DOT) com [mailto:childrenwit hchallenges] On Behalf Of SEOSent: May 5, 2010 9:44 AMCHILDRENWITHCHALLEN GESGROUPS (DOT) COMSubject: [childrenwithchalle nges] Intro

Good morning my name is Silvia I have four children a fifteen year old girl, a thirteen year old boy who suffers from learning disability, ADHD and bipolar disorder and twins girls age 8 who suffer from asthma, learning disability, seizure, hypothyroidism, dyslexia and are having issues with their stomach, intestines and kidneys. I was suggested to join a support and community group to help me learn more about my childrens illnesses as well as be where others understand what I am actually going through. I am frustrated, overwhelmed and drained of every energy I have and I am in need of a lot support and I am hoping to find great friends as well as lot of tips and info to cope with it all.Sent from my iPhone

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hi Silvia

its important to recharge ourselves whenever we can. i was advised to occassionally let go a little in order to continue with the marathon of helping my microcephaly son. hope u'll have a chance to

best wishes :-)

Hi Silvia,

Welcome to the group. You must be going through a lot of stress with your kids. I know I have 2 with special needs as well and it’s a constant battle to help them waged with the balance needed to refuel and reenergize myself so that I can be there for my kids. Remember we (parents) are no good to anyone else if we are not good to ourselves first so it’s like that old saying when you fly “put your oxygen mask on firstâ€. You need to take care of yourself and give yourself permission to do so – so that you can take care of your dear kids. I hope you have nice weather were you are today and you can spend 20 minutes going for a walk or whatever makes you feel good.

Warm wishes,

From: childrenwithchallen gesgroups (DOT) com [mailto:childrenwit hchallenges] On Behalf Of SEOSent: May 5, 2010 9:44 AMCHILDRENWITHCHALLEN GESGROUPS (DOT) COMSubject: [childrenwithchalle nges] Intro

Good morning my name is Silvia I have four children a fifteen year old girl, a thirteen year old boy who suffers from learning disability, ADHD and bipolar disorder and twins girls age 8 who suffer from asthma, learning disability, seizure, hypothyroidism, dyslexia and are having issues with their stomach, intestines and kidneys. I was suggested to join a support and community group to help me learn more about my childrens illnesses as well as be where others understand what I am actually going through. I am frustrated, overwhelmed and drained of every energy I have and I am in need of a lot support and I am hoping to find great friends as well as lot of tips and info to cope with it all.Sent from my iPhone

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Hi Sylvia,Yes, my daughter lies still during the sessions because I take her at the end of the school day so she's tired and I also bring relaxing music to play. She's out like a light in no time.What medication did you just put your son on? We have dropped the dose of my daughters medication (epival) because it seemed to be causing more seizures and they have actually improved. In fact, we just did blood work and it showed the level of the drug was too high which definitely can cause more seizures in some cases.Thanks,From: Tan Cheryl <peckbuay@...> Sent: Wed, May 12, 2010 6:49:36 PMSubject: Re: Intro

hi sandra,

my microcephaly son also tried osteopath but we did not see visible progress a year ago. so we stopped. recently, we adjusted his seizure medicines, unfortunately it caused a relapsed in seizures and hit him harder. read about osteopath having helped to reduce your child's seizures? does your child lie still during osteopath session?

Hi Silvia,

Welcome to the group. You must be going through a lot of stress with your kids. I know I have 2 with special needs as well and it’s a constant battle to help them waged with the balance needed to refuel and reenergize myself so that I can be there for my kids. Remember we (parents) are no good to anyone else if we are not good to ourselves first so it’s like that old saying when you fly “put your oxygen mask on firstâ€. You need to take care of yourself and give yourself permission to do so – so that you can take care of your dear kids. I hope you have nice weather were you are today and you can spend 20 minutes going for a walk or whatever makes you feel good. Warm wishes,

From: childrenwithchallen gesgroups (DOT) com [mailto:childrenwit hchallenges] On Behalf Of SEO

Sent: May 5, 2010 9:44 AM

CHILDRENWITHCHALLEN GESGROUPS (DOT) COM

Subject: [childrenwithchalle nges] Intro

Good morning my name is Silvia I have four children a fifteen year old girl, a thirteen year old boy who suffers from learning disability, ADHD and bipolar disorder and twins girls age 8 who suffer from asthma, learning disability, seizure, hypothyroidism, dyslexia and are having issues with their stomach, intestines and kidneys. I was suggested to join a support and community group to help me learn more about my childrens illnesses as well as be where others understand what I am actually going through. I am frustrated, overwhelmed and drained of every energy I have and I am in need of a lot support and I am hoping to find great friends as well as lot of tips and info to cope with it all.

Sent from my iPhone

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Congrats on the switch.

Sounds like you're doing good.

Just speak up with any questions or idea requests and you will usually get

plenty of info responses.

K

On Sat, Jun 5, 2010 at 11:23 AM, jjsarmentolmt <jjsarmentolmt@...>wrote:

>

>

> Hey everyone!

> I'm Jen, on Cape Cod. After hearing how awesome an O+ friend of mine feels

> when she eats right for her blood type over the last few years, we finally

> did a test for me and the results: O+! We had it figured out when she would

> describe how she felt after eating certain foods - and it was similar to my

> own issues. I'm a comfort food eater & food addict, so eliminating chocolate

> and dairy is a challenge I'm working on. The switch off coffee has been made

> - I now consume a cup of yerba mate instead, with honey instead of coffee

> with sugar and cream. I've been gluten free for 6 months, and for sure will

> never go back. I look forward to learning more from all of you!

> Regards,

> Jen

>

>

>

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You can still eat chocolate, just not milk chocolate. Some dark

chocolate is good for you! Gluten free is close, but make sure to read

the ingredients. No potato or corn starch, either. Rice pasta is a good

sub, even spelt occasionally. Lots of meat and greens, some fruit. Now

if I could just get the exercise part... <sigh> Good luck!

E Long

O+ Gatherer in Austin, TX

Posted by: " jjsarmentolmt " jjsarmentolmt@...

<mailto:jjsarmentolmt@...?Subject=%20Re%3AIntro>

jjsarmentolmt <jjsarmentolmt>

Sun Jun 6, 2010 2:49 am (PDT)

Hey everyone!

I'm Jen, on Cape Cod. After hearing how awesome an O+ friend of mine

feels when she eats right for her blood type over the last few years, we

finally did a test for me and the results: O+! We had it figured out

when she would describe how she felt after eating certain foods - and it

was similar to my own issues. I'm a comfort food eater & food addict, so

eliminating chocolate and dairy is a challenge I'm working on. The

switch off coffee has been made - I now consume a cup of yerba mate

instead, with honey instead of coffee with sugar and cream. I've been

gluten free for 6 months, and for sure will never go back. I look

forward to learning more from all of you!

Regards,

Jen

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Hi Jen, I just joined this group, too, and have been trying to modify my food

intake for type Os.  So far I've done pretty well but find the hardest thing

is to eliminate mayonnaise.  I take a lunch to work and it's so hard to change

from sandwiches to something else.  I did find Veganaise which seems to have

okay ingredients.  The vinegar is apple cider vinegar so, at least, that's a

better alternative.  I've also been cheating by using Hellmann's canola oil

mayo when the Veganaise was not available. 

Instead of wheat bread, I've been using brown rice cakes and put my tunal or

chicken salad on top.  I've tried the Ezekial bread and spelt bread and they're

good but cause some mucous for me so I try not to eat them very often.

Anyway, nice to meet you! 

Crafts: www.garlinjake.blogspot.com

Poetry: http://lindaspoetry.blogspot.com

Reading: http://lindasreadingblog.blogspot.com

Photos: http://lindas365project.blogspot.com/

________________________________

From: elp <elongp@...>

Sent: Wed, June 9, 2010 10:18:03 PM

Subject: Re:Intro

 

You can still eat chocolate, just not milk chocolate. Some dark

chocolate is good for you! Gluten free is close, but make sure to read

the ingredients. No potato or corn starch, either. Rice pasta is a good

sub, even spelt occasionally. Lots of meat and greens, some fruit. Now

if I could just get the exercise part... <sigh> Good luck!

E Long

O+ Gatherer in Austin, TX

Posted by: " jjsarmentolmt " jjsarmentolmt@...

<mailto:jjsarmentolmt@...?Subject=%20Re%3AIntro>

jjsarmentolmt <jjsarmentolmt>

Sun Jun 6, 2010 2:49 am (PDT)

Hey everyone!

I'm Jen, on Cape Cod. After hearing how awesome an O+ friend of mine

feels when she eats right for her blood type over the last few years, we

finally did a test for me and the results: O+! We had it figured out

when she would describe how she felt after eating certain foods - and it

was similar to my own issues. I'm a comfort food eater & food addict, so

eliminating chocolate and dairy is a challenge I'm working on. The

switch off coffee has been made - I now consume a cup of yerba mate

instead, with honey instead of coffee with sugar and cream. I've been

gluten free for 6 months, and for sure will never go back. I look

forward to learning more from all of you!

Regards,

Jen

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Olive oil and lemon or apple cider vinegar, some mustard. Then maybe a

touch of real mayo to blend together. Keeps any avoids to a bare minimum

and you get good stuff.

On Thu, Jun 10, 2010 at 8:22 AM, s <garlinjake@...> wrote:

>

>

> Hi Jen, I just joined this group, too, and have been trying to modify my

> food intake for type Os. So far I've done pretty well but find the hardest

> thing is to eliminate mayonnaise. I take a lunch to work and it's so hard

> to change from sandwiches to something else. I did find Veganaise which

> seems to have okay ingredients. The vinegar is apple cider vinegar so, at

> least, that's a better alternative. I've also been cheating by using

> Hellmann's canola oil mayo when the Veganaise was not available.

>

> Instead of wheat bread, I've been using brown rice cakes and put my tunal

> or chicken salad on top. I've tried the Ezekial bread and spelt bread and

> they're good but cause some mucous for me so I try not to eat them very

> often.

>

> Anyway, nice to meet you!

> Crafts: www.garlinjake.blogspot.com

> Poetry: http://lindaspoetry.blogspot.com

> Reading: http://lindasreadingblog.blogspot.com

> Photos: http://lindas365project.blogspot.com/

>

> ________________________________

> From: elp <elongp@... <elongp%40gmail.com>>

> <%40>

> Sent: Wed, June 9, 2010 10:18:03 PM

> Subject: Re:Intro

>

>

>

> You can still eat chocolate, just not milk chocolate. Some dark

> chocolate is good for you! Gluten free is close, but make sure to read

> the ingredients. No potato or corn starch, either. Rice pasta is a good

> sub, even spelt occasionally. Lots of meat and greens, some fruit. Now

> if I could just get the exercise part... <sigh> Good luck!

>

> E Long

> O+ Gatherer in Austin, TX

>

> Posted by: " jjsarmentolmt " jjsarmentolmt@...<jjsarmentolmt%40>

> <mailto:jjsarmentolmt@...

<jjsarmentolmt%40>?Subject=%20Re%3AIntro>

>

> jjsarmentolmt <jjsarmentolmt>

>

> Sun Jun 6, 2010 2:49 am (PDT)

>

> Hey everyone!

> I'm Jen, on Cape Cod. After hearing how awesome an O+ friend of mine

> feels when she eats right for her blood type over the last few years, we

> finally did a test for me and the results: O+! We had it figured out

> when she would describe how she felt after eating certain foods - and it

> was similar to my own issues. I'm a comfort food eater & food addict, so

> eliminating chocolate and dairy is a challenge I'm working on. The

> switch off coffee has been made - I now consume a cup of yerba mate

> instead, with honey instead of coffee with sugar and cream. I've been

> gluten free for 6 months, and for sure will never go back. I look

> forward to learning more from all of you!

> Regards,

> Jen

>

>

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That sounds like it would work for me.  I love all these new ideas!  Thanks!

 

Crafts: www.garlinjake.blogspot.com

Poetry: http://lindaspoetry.blogspot.com

Reading: http://lindasreadingblog.blogspot.com

Photos: http://lindas365project.blogspot.com/

________________________________

From: s <responsiblywell@...>

Sent: Mon, June 14, 2010 2:02:50 PM

Subject: Re: Re:Intro

Olive oil and lemon or apple cider vinegar, some mustard.  Then maybe a

touch of real mayo to blend together.  Keeps any avoids to a bare minimum

and you get good stuff.

On Thu, Jun 10, 2010 at 8:22 AM, s <garlinjake@...> wrote:

>

>

> Hi Jen, I just joined this group, too, and have been trying to modify my

> food intake for type Os.  So far I've done pretty well but find the hardest

> thing is to eliminate mayonnaise.  I take a lunch to work and it's so hard

> to change from sandwiches to something else.  I did find Veganaise which

> seems to have okay ingredients.  The vinegar is apple cider vinegar so, at

> least, that's a better alternative.  I've also been cheating by using

> Hellmann's canola oil mayo when the Veganaise was not available.

>

> Instead of wheat bread, I've been using brown rice cakes and put my tunal

> or chicken salad on top.  I've tried the Ezekial bread and spelt bread and

> they're good but cause some mucous for me so I try not to eat them very

> often.

>

> Anyway, nice to meet you!

> Crafts: www.garlinjake.blogspot.com

> Poetry: http://lindaspoetry.blogspot.com

> Reading: http://lindasreadingblog.blogspot.com

> Photos: http://lindas365project.blogspot.com/

>

> ________________________________

> From: elp <elongp@... <elongp%40gmail.com>>

> <%40>

> Sent: Wed, June 9, 2010 10:18:03 PM

> Subject: Re:Intro

>

>

>

> You can still eat chocolate, just not milk chocolate. Some dark

> chocolate is good for you! Gluten free is close, but make sure to read

> the ingredients. No potato or corn starch, either. Rice pasta is a good

> sub, even spelt occasionally. Lots of meat and greens, some fruit. Now

> if I could just get the exercise part... <sigh> Good luck!

>

> E Long

> O+ Gatherer in Austin, TX

>

> Posted by: " jjsarmentolmt " jjsarmentolmt@...<jjsarmentolmt%40>

> <mailto:jjsarmentolmt@...

<jjsarmentolmt%40>?Subject=%20Re%3AIntro>

>

> jjsarmentolmt <jjsarmentolmt>

>

> Sun Jun 6, 2010 2:49 am (PDT)

>

> Hey everyone!

> I'm Jen, on Cape Cod. After hearing how awesome an O+ friend of mine

> feels when she eats right for her blood type over the last few years, we

> finally did a test for me and the results: O+! We had it figured out

> when she would describe how she felt after eating certain foods - and it

> was similar to my own issues. I'm a comfort food eater & food addict, so

> eliminating chocolate and dairy is a challenge I'm working on. The

> switch off coffee has been made - I now consume a cup of yerba mate

> instead, with honey instead of coffee with sugar and cream. I've been

> gluten free for 6 months, and for sure will never go back. I look

> forward to learning more from all of you!

> Regards,

> Jen

>

>

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Hi ! Welcome! Good luck with Weight Watchers, have heard its a good program.

Liliann

From: Ilniski <rilniski@...>100-plus Sent: Sat, July 31, 2010 7:31:52 PMSubject: intro

HI everyone. I'm rebecca. I need to lose about 100 pounds or maybe alittle more. I'm in the 200's and am short. I work as a spanish instructorat the school for the blind, and am totally blind myself. I use a seeingeye dog, his name is nuncio an he's a black lab. I'm considering going backto weight watchers when I come back from my family reunion. Some of myweaknesses are chocolate, and cheese. I also drink more of the diet sodasand crystal lite than I probably should because I feel I need flavor in mywater. Any help, support, tips, would be appreciated. I'm single and findit hard to cook for one. Anyway so far I've gotten in to the fiber oneproducts. The next time I buy yogurt I'm going to get the greek yogurt andwhen I want to buy potatoes I am going to get the red. Anyway I lookforward to this list and getting and giving support. Ilniski and Nunciofacebook:

http://facebook.com/rebeccai5twitter: www.twitter.com/clady2009skype: rebeccai5

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Lana have you tired liquid lye mixed with flower of sulfur or jasons sulfur

shampoo? Also bathing with MMS would help. If adding sulfur to liquid lye use

olive oil to mix, I also put peppermint leaves in my olive oil and let fuse for

weeks.

http://www.internatural-alternative-health.com/ingr/ingr182081.cfm

http://www.vitacost.com/-Dandruff-Relief-Dandruff-Shampoo

>

> Hello Angie...Sorry to hear all this about your family and the birdmites,

Ihave

> had this for 2 years+..Tried many things to get rid of them but no soluition

> fully works for me yet...epsom salts and baking soda helps the itching and

calms

> them for a little while..I find these too all through my house ..I did have

the

> samples took to the extension office here and they are some type of

> birdmite...the ones in my scalp are driving me insane have tried everything to

> get them out but no go..I think they carry parasites of some sort too, because

I

> have seen these fiberlike things come from my skin since these things have

been

> here...we have fumigated, used foggers, sug sprays , diatamatious earth

> powder,probably didn't spell that right, vinegar, clorox, lysol, 2 showers a

> day, super cleaning things and still have them,especially in my scalp, they

> think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find

something

> to get rid of them...Will be praying for you and your family...Lana

>

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Also when bathing I use no towel or wash rag, soak all hair brushes combs. I

have a gallon ice tea plastic container filled with ammonia then close with lid.

> >

> > Hello Angie...Sorry to hear all this about your family and the birdmites,

Ihave

> > had this for 2 years+..Tried many things to get rid of them but no soluition

> > fully works for me yet...epsom salts and baking soda helps the itching and

calms

> > them for a little while..I find these too all through my house ..I did have

the

> > samples took to the extension office here and they are some type of

> > birdmite...the ones in my scalp are driving me insane have tried everything

to

> > get them out but no go..I think they carry parasites of some sort too,

because I

> > have seen these fiberlike things come from my skin since these things have

been

> > here...we have fumigated, used foggers, sug sprays , diatamatious earth

> > powder,probably didn't spell that right, vinegar, clorox, lysol, 2 showers a

> > day, super cleaning things and still have them,especially in my scalp, they

> > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find

something

> > to get rid of them...Will be praying for you and your family...Lana

> >

>

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Marie - here I am with my 20 questions again... On the site that you sent me

for MMS - do you order the liquid or the powder? How do I tell the difference

between MMS and MMS2 - what is the difference? I have some moldy places in our

house (found one around our shower) How do you treat it with MMS2? Or what is

the best way to treat it do you think? Our Golden has this so very bad. The

mites seem to get immune to whatever treatment we have her on after awhile...

Her ears are bothering her again and I was wondering what you would do for that?

I have them in my ears and so does one of my sons...kind of at a loss as to what

would work well.

Have you ever felt a sensation like little bubbles popping on your skin? Very

like a crawlie but not... I have been getting that all over my back and wondered

if it was the bug.

How do you mix sulfur into your lye lotion? lol I just poured some in...

Thank you so much Marie.

> > >

> > > Hello Angie...Sorry to hear all this about your family and the birdmites,

Ihave

> > > had this for 2 years+..Tried many things to get rid of them but no

soluition

> > > fully works for me yet...epsom salts and baking soda helps the itching and

calms

> > > them for a little while..I find these too all through my house ..I did

have the

> > > samples took to the extension office here and they are some type of

> > > birdmite...the ones in my scalp are driving me insane have tried

everything to

> > > get them out but no go..I think they carry parasites of some sort too,

because I

> > > have seen these fiberlike things come from my skin since these things have

been

> > > here...we have fumigated, used foggers, sug sprays , diatamatious earth

> > > powder,probably didn't spell that right, vinegar, clorox, lysol, 2 showers

a

> > > day, super cleaning things and still have them,especially in my scalp,

they

> > > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find

something

> > > to get rid of them...Will be praying for you and your family...Lana

> > >

> >

>

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Guidelines for MMS1 MMS2Methods of Using MMS1 and MMS2 Compared: Comparisons MMS1 MMS2 Is an Activator Required? Yes: Unfiltered Vinegar or citric acid Water Does It Purify Water? Yes Yes Ingest Through Stomach? Yes Yes Spray on Skin? Yes Not tested Can be Inhaled to Sinuses Yes (Cautions) Never Can be Inhaled to lungs? Yes (Cautions) Never Use as a Douche? Yes Not Tested Use as an Enema? Yes Not Tested Tub Bath Benefits? Yes Probably Yes Mouth, Teeth, Gum? Yes Never Useful as a Deodorizer, Fumigator? Yes No Can be dripped Intravenously? Yes Probably not Removes Heavy Metals? Yes Not Tested> > > >> > > > Hello Angie...Sorry to hear all this about your family and the birdmites, Ihave > > > > had this for 2 years+..Tried many things to get rid of them but no soluition > > > > fully works for me yet...epsom salts and baking soda helps the itching and calms > > > > them for a little while..I find these too all through my house ..I did have the > > > > samples took to the extension office here and they are some type of > > > > birdmite...the ones in my scalp are driving me insane have tried everything to > > > > get them out but no go..I think they carry parasites of some sort too, because I > > > > have seen these fiberlike things come from my skin since these things have been > > > > here...we have fumigated, used foggers, sug sprays , diatamatious earth > > > > powder,probably didn't spell that right, vinegar, clorox, lysol, 2 showers a > > > > day, super cleaning things and still have them,especially in my scalp, they > > > > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find something > > > > to get rid of them...Will be praying for you and your family...Lana> > > >> > >> >>

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Please read this site throughly.

http://jimhumble.biz/

MMS1 is your treatment for mold NOT MMS2. Activate 10 drops MMS1 on saucer leave

room no pets children or humans in room for an hour. Then open room and air,

then reenter. Order the liquid and activator.

For animals ears use cedarcide if unable to buy and short for money use bag

balm. I buy the horse and stable from cedarcide makes 25 gallons of application

for mites. You can also soak the animals with this I use a squirt bottle and rub

into coat well. If dealing with mange or for that matter just to be safe use

latex gloves. Cover bedding with diatomaceous earth .

http://wolfcreekranch1.tripod.com/defaq.html

http://www.cedarcidestore.com/catalog/item/3571008/3185649.htm

For your ears and sons 2 alternatives, first rubbing alcohol and white vinegar

half and half. The second alternative is listed below.

http://www.kornax.com/Merchant2/MSM_Drops.htm

Spray your back with mms1 spray every whisp or crawl. Yes these creature grow

immune to a lot. Chemicals the worst for immunity's. Use these outside only

preferably. Cyonara, bifen. Cover yard with granules of either. Actually I found

a excellent granule by sevin at tractor supply that list springtails. Inside try

orange guard, fels naptha for linoleum floors shower ect. Remeber to treat

drains! I use my homemade enzyme now, before vinegar, bleach. For enzyme I use

grapefruit peel and brown sugar peppermint leaves.

http://www.soapsgonebuy.com/

http://www.o3enzyme.com/enzymeproduction.htm

For mixing the flower of sulfur with liquid lye use olive oil to fuse. In other

words mix sulfur with oil the blend or whip with mixer into soap. I also let my

olive oil fuse with peppermint leaves in a small canning jar, not necessary just

added hint.

> > > >

> > > > Hello Angie...Sorry to hear all this about your family and the

birdmites, Ihave

> > > > had this for 2 years+..Tried many things to get rid of them but no

soluition

> > > > fully works for me yet...epsom salts and baking soda helps the itching

and calms

> > > > them for a little while..I find these too all through my house ..I did

have the

> > > > samples took to the extension office here and they are some type of

> > > > birdmite...the ones in my scalp are driving me insane have tried

everything to

> > > > get them out but no go..I think they carry parasites of some sort too,

because I

> > > > have seen these fiberlike things come from my skin since these things

have been

> > > > here...we have fumigated, used foggers, sug sprays , diatamatious earth

> > > > powder,probably didn't spell that right, vinegar, clorox, lysol, 2

showers a

> > > > day, super cleaning things and still have them,especially in my scalp,

they

> > > > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find

something

> > > > to get rid of them...Will be praying for you and your family...Lana

> > > >

> > >

> >

>

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Forgot this little tid bit for " Golden " which I amuse is a retriever? Didn't

think one of the children were named golden?:) Bless at Wolf Creek Ranch

she has helped, and taught me much about herbal healing. For pets this is

invaluable info.

http://www.poos4u.com/Remedies.htm

http://www.ehow.com/how_5254433_kill-ear-mites-dogs-cats.html

> > > > >

> > > > > Hello Angie...Sorry to hear all this about your family and the

birdmites, Ihave

> > > > > had this for 2 years+..Tried many things to get rid of them but no

soluition

> > > > > fully works for me yet...epsom salts and baking soda helps the itching

and calms

> > > > > them for a little while..I find these too all through my house ..I did

have the

> > > > > samples took to the extension office here and they are some type of

> > > > > birdmite...the ones in my scalp are driving me insane have tried

everything to

> > > > > get them out but no go..I think they carry parasites of some sort too,

because I

> > > > > have seen these fiberlike things come from my skin since these things

have been

> > > > > here...we have fumigated, used foggers, sug sprays , diatamatious

earth

> > > > > powder,probably didn't spell that right, vinegar, clorox, lysol, 2

showers a

> > > > > day, super cleaning things and still have them,especially in my scalp,

they

> > > > > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can find

something

> > > > > to get rid of them...Will be praying for you and your family...Lana

> > > > >

> > > >

> > >

> >

>

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lol yes she is a golden retriever. I raise, and train Golden Retrievers. One of

them, Lily, was spayed in January. She developed a nasty secondary infection

which seemed to erupt from the inside. The vet said it was staph and it looked

like it was on the stomach wall and had erupted out (very ugly - would barely

respond to treatment). She then killed a rat and would carry it around, hiding

it from us for weeks. I was handling her everyday treating her staph infection.

I broke out with " hives " in Feb. she broke out with the worst case of " mange " I

have ever seen in March. The mites she has are tenacious. We are giving her 1

1/2 cc of iver everyday... and she started looking good for the first time in

months although her stomach was still rough. She had dug her ears up and even

those have started to heal. She got two bald spots on her hind quarters last

week - so we started spraying her with a cattle dip (Prolate) and that has

stopped getting worse, and her stomach seems to be slowly re-growing hair, but

they have moved to her ears... I have never seen anything like this before. The

rest of the dogs are starting to get something. It doesn't look like hers, but

is presenting more like a sarcoptes mange...but iver isn't helping either.

I will try the cedarcide and DE treatment and maybe alternate the MSM ear

treatment with bag balm...can't hurt. These mites seem to figure out how to get

around whatever you are treating with - mixing things up seems to be a good

idea.

Thank you Marie.

> > > > > >

> > > > > > Hello Angie...Sorry to hear all this about your family and the

birdmites, Ihave

> > > > > > had this for 2 years+..Tried many things to get rid of them but no

soluition

> > > > > > fully works for me yet...epsom salts and baking soda helps the

itching and calms

> > > > > > them for a little while..I find these too all through my house ..I

did have the

> > > > > > samples took to the extension office here and they are some type of

> > > > > > birdmite...the ones in my scalp are driving me insane have tried

everything to

> > > > > > get them out but no go..I think they carry parasites of some sort

too, because I

> > > > > > have seen these fiberlike things come from my skin since these

things have been

> > > > > > here...we have fumigated, used foggers, sug sprays , diatamatious

earth

> > > > > > powder,probably didn't spell that right, vinegar, clorox, lysol, 2

showers a

> > > > > > day, super cleaning things and still have them,especially in my

scalp, they

> > > > > > think I am a freaking Bird UGGGHHHH!!!. Hopefully some day we can

find something

> > > > > > to get rid of them...Will be praying for you and your family...Lana

> > > > > >

> > > > >

> > > >

> > >

> >

>

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Hi, Pam!

"Too much" PULP! "Total juice" with carrots is a far cry from fresh carrot juice. You're not only not concentrating the essence of the carrots but you're adding a different dimension to the mouthfeel as well, plus you have to dilute it with water to make it drinkable. I realize that this is a semi-heated topic but for me, juice is juice--if I want a "total" result, I make a smoothie. Others disagree--that's okay. Be aware, though, that blending carrots with water and sweetening the result isn't going to give you anything that resembles carrot juice. And BTW, if you do continue juicing, try using Fuji apple and some fresh ginger with the carrots, omitting the lemon.

I posted a recipe a little over a week ago for sweet potato soup with star anise and ginger that's out of this world! Give it a try--I think you'll like it. And since you like ice cream, check the archives for 's "recipe" (yuk, yuk) for pumpkin ice cream.

Intro

Hello!

Im new here! Just got my long awaited Vita Mix a week ago from QVC. I LOVE IT! I have to have 'ice cream' every night!!

I have started reading the messages when the group started. I decided it will take me a long time to catch up to date, so I may as well introduce myself now.

Tried a green smoothie this am. hmmmm, and to think I just bought some greens for the week. I wasnt carried away with it. It stinkith! Im not much on measuring, I just throw it in, but Im thinking for the GREEN smoothie , following directions might be in order!

I have made sweet potato soup. First time I wasnt carried away with it, too much stuff. Second time I sauted the onions and celery, and one carrot first, it was much better!

I think I like it better to keep the cooked stuff together, and the raw to itself. They dont mix well in my stomach.

I used to juice carrot, green apple and lemon every morning. I love it. But I dont really like carrot in the Vita Mix. Too much something.

But I sure do love my healthy 'ice cream'!!

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Jane,

Welcome to the forum.

You can order 5% Lugol's very cheaply, (from within or outside of

Canada) in small or large quantities, from Health-in-Sync in

Ontario. Email Kerrie at

info@...

_,_._,___

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Hi Jaye,

Welcome to the forum!

Although Xenex Labs are a supplier to compounding pharmacies, they do sell to

the public. That's where I bought my Lugol's. They are cheap ($38 / 500ml),

cheerful and do not have a limit on how much they will sell you (I bought a box

of 12 since we were moving overseas and they didn't even blink). They will also

ship domestically and internationally.

http://www.xenexlabs.com/catalogue.php?cid=1 & pid=484

Their retail store is located in Coquitlam, BC, just off of the #1 Highway.

Alternatively you can buy 25ml bottles of Lugol's from Finlandia Pharmacy in

Vancouver (they will also ship it to you).

Ziggy

>

> Hi folks

>

> I " m Jaye and I've been lurking for a few days. I have migrated from the LDN

groups.

>

> I have fibromyalgia (FM) (not so much pain, but severe brain fog and

insomnia), Chronic Fatigue Syndrome (CFS), Osteoarthritis (OA) and possibly

Sjogren's.

>

> I'm 47, have 5 children, and have just started actively 'attacking' these

conditions that have disabled me.

>

> I am currently taking 150mg Wellbutrin daily, and 4.5mg naltrexone, and 7.5mg

zopiclone at bedtime.

>

> For supplements I take a good multivite (includes some potassium iodide), 2g

Omega-3, 300mg Magnesium Citrate (when my throat is not sore and I can get the

tab down!), 1000mg Vit D3, @2g Vit. C.

>

> I know very little about iodine, but am becoming increasingly convinced I have

an underactive thyroid (TSH tested repeatedly , but you know...). I've managed

to lose 50 lbs since my hips were replaced 2 years ago, but I have the dry skin,

hair drops, fatigue...I've even been told (not recently) that my thyroid gland

is 'prominent'. Easily seen, but it apparently feels normal.

>

> Given that I am in Canada, can I get Lugol's? I saw in the archives that

someone suggested Xenex Labs in Vancouver, but I could see no indication that

they sell to the general public. My main pharmacy cannot get it. I haven't

done much footwork yet, but I haven't found much on line either. I did call an

aquarium store! I would prefer to order from within Canada.

>

> Where do I even start?

>

> Thanks for any help you can give.

>

> Jaye

>

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Thank you !

I have fired off an email!

Jaye

>

> Jane,

>

> Welcome to the forum.

>

> You can order 5% Lugol's very cheaply, (from within or outside of

> Canada) in small or large quantities, from Health-in-Sync in Ontario.

> Email Kerrie at

>

> info@...

>

>

>

>

>

> > _,_._,___

>

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Just reading your symptoms. Out of interest have you every been prescribed and

take any antibiotic of the quinolone group. ie Levaquin?

The symptoms are very similar to Quinolone toxicity ...

Jane

>

> Hi group. Thought I should introduce myself. A few of you know me from

> NTH and I see Gracia from the other thyroid group is here (please

> don't mentiont testosterone LOL).

>

> My problems began at birth and progessively got worse over the years.

> I will be 58 in June. I've tried MANY MANY things over the years

> including 6 grains of Armour, expensive supplements and hormones and

> NOTHING has worked. Well the first time I tried HC for adrenal fatigue

> it helped for a few weeks. then quit working after I crashed for 3

> weeks (history of a below normal temp dropping as low as 96 and

> leaving me flue like and fatigued. I won't go into all the details

> unless someone really wants them. I've currently come full circle in

> my search and I'm working on eleminating my candida using a product

> called Three lac and watching my diet. I'm also currently taking 1

> grain Thyroid S every other day. Testing and symptoms w/o meds show

> the need (at least to the alternative doctors) but it never does me

> any good. I even have delayed reflexes. When I go completely off I

> start to gain weight again (the ONLY good thing it did) so I'm staying

> on a little till I get completely well, then I will test probably

> through Health Check to see where my levels are. Iodine is something I

> haven't tried but was reading about it on NTH and decided maybe I

> should check it out. After all, I've tried everything else (long

> story). I have Brownsteins book comming and I'm slowing reading the

> posts here.

>

> I'm also on 50 mg of DHEA (since I couldn't get a script for

> Testosterone and I have a number of low symptoms)

> Some of my symptoms are: LOW to NO energy, muscle problems, chronic

> sinuitus with swelling and puffy eyes and facial/head pressure that is

> unbelievable (I am a litteral barometer), IBS, gluten intolerance

> (according to Entero Labs), osteoporosis, tinitus, ADD, memory

> problems, sinus/allergy (I'm currently back to allergy shots), NO sex

> drive and an inability to you know what (have these two symptoms for

> years) and probably some others. I also had my amalgams out 3 years

> ago or so (11 of them). Just getting them out did NOTHING. I did some

> ALA, and chlorella and noting happened either good or bad. I have

> since given up on that. I'm interested in the thread about iodine and

> detoxing heavy metals. The hair test from Doctors Data Lab showed a

> mercury problem (after the removal) and I couldn't decipher the rest

> of the test. I just read also that Iodine is good for candida killing.

>

> Look forward to learning and getting to know everyone. Carol B

>

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Hi Jaye,

I have fibro with fatigue being my primary symptom too. The best help I've

received has been changing my diet to gluten-, caisen-, soy- chemical-free whole

foods, eliminating toxic substances in my life...including working on some toxic

relationships and reducing stress, addressing adrenal insufficiency and low

thyroid function and now using iodine to detox. Coconut oil is also a good one

if your body can metabolize fats. Mine cannot because of liver issues. But

getting gluten out of my life resolved so many issues. I have Linn here on this

forum to thank for that.

It sounds like you're taking your health into your own able hands and that's

great. I hope you'll go slow and give yourself time to implement one change at

a time. It's less overwhelming that way. I started with diet and then moved

toward detoxing our home. And you know what? I'm STILL detoxing our home! LOL

You might call a local compounding pharmacy to learn which doctors are best for

your particular situation. My local compounding pharmacy referred me to an MD

who is also a doctor of Chinese medicine. She's very open-minded and great

about teaching me new things...spends a lot of time with me and now with my

hubby too.

Dr. Lowe in Boulder, Colorado is a chiropractor who has done extensive

research with other MDs and scientists on fibro and metabolic processes. I'm

just beginning to work with him. He consults over the phone and will help you

either self-treat or work with a local physician if you can find one you'd like

to work with. Here is his web site: http://www.drlowe.com/

Fibro for me first started showing up during the hormonal imbalances of pre- and

now post-menopause. Did you know guys can go through a hormonal change in life

too? It's called andropause and our doc said lots of what's been ailing my

hubby's 49-year-old body is probably due to imbalances that hit most men when

they least expect it. There are no warning signs of hormone changes for you

fellas as there are for us gals.

I also have problems detoxing and metabolizing things. For example, even though

I take a generous amount of magnesium daily, I'm low in mag according to

testing. So I bought some magnesium gel and taking Epsom Salts baths and will

test again to see if I've been able to increase my mag levels. You might be off

in one thing or another and did you know you can order your own tests? I have

used Life Extension in the past and also Direct Labs. And you can learn what

any abbreviations on lab tests mean if you go here:

http://www.labtestsonline.org/understanding/index.html

I'm sorry this is so long, but I am excited for you and have babbled on too

much. Please think about getting in touch with a compounding pharmacy in your

neck of the woods and checking out some saliva testing for adrenals, thyroid and

sex hormones. That's a really great place to start.

Be well,

>

> Hi folks

>

> I " m Jaye and I've been lurking for a few days. I have migrated from the LDN

groups.

>

> I have fibromyalgia (FM) (not so much pain, but severe brain fog and

insomnia), Chronic Fatigue Syndrome (CFS), Osteoarthritis (OA) and possibly

Sjogren's.

>

> I'm 47, have 5 children, and have just started actively 'attacking' these

conditions that have disabled me.

>

> I am currently taking 150mg Wellbutrin daily, and 4.5mg naltrexone, and 7.5mg

zopiclone at bedtime.

>

> For supplements I take a good multivite (includes some potassium iodide), 2g

Omega-3, 300mg Magnesium Citrate (when my throat is not sore and I can get the

tab down!), 1000mg Vit D3, @2g Vit. C.

>

> I know very little about iodine, but am becoming increasingly convinced I have

an underactive thyroid (TSH tested repeatedly , but you know...). I've managed

to lose 50 lbs since my hips were replaced 2 years ago, but I have the dry skin,

hair drops, fatigue...I've even been told (not recently) that my thyroid gland

is 'prominent'. Easily seen, but it apparently feels normal.

>

> Given that I am in Canada, can I get Lugol's? I saw in the archives that

someone suggested Xenex Labs in Vancouver, but I could see no indication that

they sell to the general public. My main pharmacy cannot get it. I haven't

done much footwork yet, but I haven't found much on line either. I did call an

aquarium store! I would prefer to order from within Canada.

>

> Where do I even start?

>

> Thanks for any help you can give.

>

> Jaye

>

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Nice to have you, Wanda--I have a 5000, too. :)

Your husband's diet of choice sounds like a lot of stuff I enjoy, too! However, I'm lucky enough to actually enjoy healthful food, too, so I don't get into trouble. Maybe smaller smoothies? I can't imagine they'd be more bloat-producing than southern-fried anything.

BTW, I was one of those who was really disturbed when Smucker's closed town the White Lily plant. Horrible that local food products disappear when huge corporations buy them. :((

Intro

After being accepted into this wonderful group several weeks ago, I feel a little guilty for not introducing myself sooner. I wanted to be current with the email before commenting, and now I've accomplished that. I am enjoying this group so much and read every email so I won't miss anything. Everybody seems to get along so well, and it's wonderful, Lea Ann, that you allow us to talk about any topic.

I have owned a Vita-Mix Super 5000 for a few years but hadn't been using it as much lately. My husband is not interested in eating healthy, but I plan to keep on trying. He liked the smoothies I made but says not to make any more for him because they cause him to "feel bloated." I have to cook what he likes, and it's hard not to eat what he eats. His likes good old Southern cooking with fried this or fried that, mashed potatoes with gravy, cat-head biscuits, banana pudding or homemade ice cream with chocolate syrup, etc. Well…you get the picture. I need some moral support and motivation, which this group is providing. Thanks so much.

My name is Wanda, and I live in East Tennessee. I have been making and enjoying kombucha tea for almost three years. I have an Excaliber dehydrator, nine-tray I think. I loom knit, and we have a vegetable garden. We planted our potatoes and onions just a few days before the heavy rains came earlier this week. The water washed most of four rows of potatoes out of the ground, but we have them recovered now so I`m not complaining.

Thanks again, everybody. Have a fun day!

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