Help

[Guest guest]

Thanks a lot! Well I have made up my mind, I am going to get one of the Cathe DVDs. I love jumping so I am happy to hear she includes that in her workouts!!!!!!!!!! DiKassia <ldy_solana@...> wrote: i haven tried christi yet, and only did one amy bento so i can't really compare, but cathe is THE best i have done so far when it comes to advanced workouts. even if its low impact its still high intensity. constantly moving with interesting moves, some workouts are easier to catch

on then others choreography wise(i can do imax2 choreography no probs but rhythmic step always gets me in the thrid combo)and she likes to jump too LOL. kassia Ahhh...imagining that irresistible "new car" smell?Check out new cars at Autos.

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

new cars at Autos.

[Guest guest]

then you will love the imaxes and kick max. i think her new one drill max has lots of pylometric jumping. kassiaDi <dnew219@...> wrote: Thanks a lot! Well I have made up my mind, I am going to get one of the Cathe DVDs. I love jumping so I am happy to hear she includes that in her workouts!!!!!!!!!! Di

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

new cars at Autos.

[Guest guest]

Ruth,

I don't know about hot process and Dead Sea Minerals. I have used Dead Sea

Mud in my cold process soap. I take a portion of my soap mix and mix the clay

into that, then swirl it into the rest of the pot. Keep in mind that Dead Sea

Clay absorbs quite a bit of water, so don't discount your recipe.

As far as Dead Sea Clay goes, I would mix the clay with a portion of your soap

and do it the same way as with the mud. To start, I wouldn't use more than 1 Tbs

of clay per 1.5 lbs of soap.

Hope this helps.

Sincerely,

http://www.herbalnatures.com

" Ruth A. Kohl " <rkohl@...> wrote:

I didn't get a reply the first time so I'll ask again. Please could

someone tell me how to use Dead Sea Minerals in soap. I make HP soap, so

do I add the minerals after the cook, and how much? I hear about Salt

soap, what is it used for and how is it made. Just full of questions

tonight aren't I. :-)

Thank you

Ruth

[Guest guest]

Ruth

Some People say salt makes the soap harder,, but it can also make the soap

more of an irritant to the skin as well or cause contact dermatitis.

I would only use a very small amount added after the cook, if your doing HP or

liquid soap and mixed in well to dissolve the minerals. Say 1 ts per 1 lb of

soap batch.

Adding it to CP before trace will speed up the trace or can cause a falce

trace, so you would again want to add it after trace and mix in very well.

Because soap is a wash off product, the minerals will not have much of an

affect on the skin as would be the case in a lotion or cream or bath salts.

hth

Sherry

Sherry's Creations

Sherry Barker

http://www.herbalsoap-healingcreams.com/

[Guest guest]

In message <46490635.40506@...> you wrote:

> Hi All, I'm new to the list. I got advise a month ago re starting a

> scoby from commercial KT.

Hi Joan, I never started a Kombucha batch with commercial KT, because

there isn't any raw KT available here in the UK that I have discovered.

My guess is that it would always be quite difficult to brew from a

commercial starter, because the yeasts would be kept extremely low

in the commercial product in order to avoid undue pressure in the bottle

(secondary fermentation). That's my theory.

And that's why it takes such aaaages for any proper fermentation to happen

in your brew.

No 1 looks the more promising of the 2 brews and I should think, that given

several weeks, there might be a new culture forming on the top.

It's probably also a good idea to carefully taste your brews with a straw.

If they are gaining a good acidity, that would be a very encouraging

sign.

IMO, only time will tell, whether there were enough yeasts and bacteria

in the original commercial starter to form a viable brew for you.

Keep us posted! And All the best!

Blessings,

Margret:-)

--

+------------------ Minstrel@... --------------------+

<)))<>< http://www.therpc.f9.co.uk <)))<><

http://www.AnswersInGenesis.com

+----------------- http://www.Gotquestions.org ------------------+

The fear of the Lord is a fountain of life.

[Guest guest]

Thanks Margret, I have been looking at some of the photos from the list

members. My No 1 brew looks very like some of the very early scobys

although much thinner. Mine is almost transparent, it's so thin, and it

doesn't completely cover the tea, although it does cover almost the

entire area.. Anyhow I'm talking to it regularly. I'm hoping it will

work. Joan

Margret Pegg wrote:

> In message <46490635.40506@...> you wrote:

>

>

>> Hi All, I'm new to the list. I got advise a month ago re starting a

>> scoby from commercial KT.

>>

>

> Hi Joan, I never started a Kombucha batch with commercial KT, because

> there isn't any raw KT available here in the UK that I have discovered.

>

> My guess is that it would always be quite difficult to brew from a

> commercial starter, because the yeasts would be kept extremely low

> in the commercial product in order to avoid undue pressure in the bottle

> (secondary fermentation). That's my theory.

>

> And that's why it takes such aaaages for any proper fermentation to happen

> in your brew.

>

> No 1 looks the more promising of the 2 brews and I should think, that given

> several weeks, there might be a new culture forming on the top.

> It's probably also a good idea to carefully taste your brews with a straw.

> If they are gaining a good acidity, that would be a very encouraging

> sign.

>

> IMO, only time will tell, whether there were enough yeasts and bacteria

> in the original commercial starter to form a viable brew for you.

>

> Keep us posted! And All the best!

>

> Blessings,

>

> Margret:-)

>

[Guest guest]

In message <464AA46D.4040306@...> you wrote:

> Thanks Margret, I have been looking at some of the photos from the list

> members. My No 1 brew looks very like some of the very early scobys

> although much thinner. Mine is almost transparent, it's so thin, and it

> doesn't completely cover the tea, although it does cover almost the

> entire area.. Anyhow I'm talking to it regularly. I'm hoping it will

> work.

Joan, that sounds VERY hopeful to me!

I should go by the taste now. Remember, the scoby on top is not the

most important thing in a brew, it's the liquid you consume.

It, too, is the culture!

A bit of patience, and you'll get there! :-)

with blessings on you and your brew ...

Margret:-)

--

+------------------ Minstrel@... --------------------+

<)))<>< http://www.therpc.f9.co.uk <)))<><

http://www.AnswersInGenesis.com

+----------------- http://www.Gotquestions.org ------------------+

The way you know you've been given life, hope and a future is

when you begin giving those away to everyone else.

[Guest guest]

Hi Margret thanks for your help. I tasted No 1, really nice, just a

little sweet for my taste. No 2, terrible, like drinking vinegar.

Thanks again Joan

Margret Pegg wrote:

> In message <464AA46D.4040306@...> you wrote:

>

>

>> Thanks Margret, I have been looking at some of the photos from the list

>> members. My No 1 brew looks very like some of the very early scobys

>> although much thinner. Mine is almost transparent, it's so thin, and it

>> doesn't completely cover the tea, although it does cover almost the

>> entire area.. Anyhow I'm talking to it regularly. I'm hoping it will

>> work.

>>

> Joan, that sounds VERY hopeful to me!

> I should go by the taste now. Remember, the scoby on top is not the

> most important thing in a brew, it's the liquid you consume.

> It, too, is the culture!

> A bit of patience, and you'll get there! :-)

>

> with blessings on you and your brew ...

>

> Margret:-)

>

>

[Guest guest]

Hi,

I have posted several times and have been a bit afraid to ask my biggest question. I want an answer so bad that sometimes I don't ask the question as I am afraid there is no answer (I have heard it from so many "professionals). My daughter is 21 years old, since she was old enough to hold up her head she had rocked it back and for. It has caused her so much pain and ostrification, even more so than any of the other problems she has. I think because it is so blatant. She bobs constantly, worse when she is agitated. I have thought of a neck brace, but it I am afraid it will cause sensory issues. Has anyone ran into this problem and is ther anything we can do. We have done tons of behavior modification, discipline, rewards, visual cues, and of course she has to bear all of the nasty comments and looks that you would think would help end the problem. Any suggestions would be soooo helpful?

[Guest guest]

Faith

Man I know how it feels been having the same trouble with docs almost as you.

This is some things I do to help.

Take a warm to almost hot bath and soak tell I look like a raisin then go to

bed.

Take Ibuprofen dose not take it away but eases it some times just enof.

Try not stressing lots easier said then done

Take a walk if you can or do something you like to take our mind off it. (I put

on a movie and around here that means I will be falling asleep takes about 3 to

4 tries before I see it all LOL.

Do not cover with comfort food as later it seams to add stress at lest to me

when I step on a scale that is.)

Lay in the shade on some thing comfy and be warmed by the sun also this way you

should not burn if you do fall a sleep. Call both docs and ask them to talk to

each other but stress and I do mean stress how bad your hurting. Tell them every

thing your doing to try and get some relief. Tell them you know you need some

thing even before you have a dx. By the way some get fast dx's some do not mine

was over 6 months with no pain help to speak off.

Get a dx maybe faster got to a mayo center or some were other like Stanford on

the west coast all depends on were you live and what you can spend.

That¢s all I can think of now and well hope may be one helps you or at lest

some one

and the last one a great big ((((((((hug from us all here ))))))))))))

The redneck

Marty

________________________________________________________________________________\

____

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

[Guest guest]

Faith,

Why does your RD think that taking pain meds is a bad thing? I think

your GP needs to call your RD and talk. Nobody should have to live in

pain while you wait for docs to sort things out. I know, I had pain

for 6 years before anyone would give me any sort of pain meds, and

even then they were mild. It will drive you absolutely batty and make

you resort to trying to cover the pain in ways that aren't healthy.

Bottom line, you are in pain and someone needs to listen, diagnosis or

not. I'd stress to the rheumy this. I used to call mine crying all

the time. If he would not have been responsive, I would have fired

him and looked for another.

Let us know how you are doing.

Houston, Texas

[Guest guest]

Thanks Marty, you're great! I have been researching the Mayo Clinic. Is there

one better than another for Still's specifically? Faith

Marty wrote: Faith

Man I know how it feels been having the same trouble with docs almost as you.

This is some things I do to help.

Take a warm to almost hot bath and soak tell I look like a raisin then go to

bed.

Take Ibuprofen dose not take it away but eases it some times just enof.

Try not stressing lots easier said then done

Take a walk if you can or do something you like to take our mind off it. (I put

on a movie and around here that means I will be falling asleep takes about 3 to

4 tries before I see it all LOL.

Do not cover with comfort food as later it seams to add stress at lest to me

when I step on a scale that is.)

Lay in the shade on some thing comfy and be warmed by the sun also this way you

should not burn if you do fall a sleep. Call both docs and ask them to talk to

each other but stress and I do mean stress how bad your hurting. Tell them every

thing your doing to try and get some relief. Tell them you know you need some

thing even before you have a dx. By the way some get fast dx's some do not mine

was over 6 months with no pain help to speak off.

Get a dx maybe faster got to a mayo center or some were other like Stanford on

the west coast all depends on were you live and what you can spend.

That¢s all I can think of now and well hope may be one helps you or at lest some

one

and the last one a great big ((((((((hug from us all here ))))))))))))

The redneck

Marty

________________________________________________________________________________\

____

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

[Guest guest]

Faith

I do not know as I never looked into them . others here have gone to them so

lets ee what they say as nothing better then from the mouth that has been there

I say. I can say dr harris at stanford is well awsome and he dx me very fast

useing all the test i had alread had done I also sent and brought all my records

at the time so that helped also

hugs

the redneck

marty

________________________________________________________________________________\

____

Be a better Heartthrob. Get better relationship answers from someone who knows.

Yahoo! Answers - Check it out.

http://answers.yahoo.com/dir/?link=list & sid=396545433

[Guest guest]

I do get the pain meds from my GP so that's okay, I just don't really talk to

the RD about them because he would rather me take OTC stuff that doesn't help.

The RD wants me to real quick go to my GP when I'm feeling bad to get blood work

right then. Easier said than done because it doesn't usually last long or I'm

out somewhere and don't get a chance. Crazy. Faith

a_cone wrote: Faith,

Why does your RD think that taking pain meds is a bad thing? I think

your GP needs to call your RD and talk. Nobody should have to live in

pain while you wait for docs to sort things out. I know, I had pain

for 6 years before anyone would give me any sort of pain meds, and

even then they were mild. It will drive you absolutely batty and make

you resort to trying to cover the pain in ways that aren't healthy.

Bottom line, you are in pain and someone needs to listen, diagnosis or

not. I'd stress to the rheumy this. I used to call mine crying all

the time. If he would not have been responsive, I would have fired

him and looked for another.

Let us know how you are doing.

Houston, Texas

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

Luggage? GPS? Comic books?

Check out fitting gifts for grads at Yahoo! Search.

[Guest guest]

Faith-I don't know if you're thinking about the Mayo Clinic in Minnesota

or Arizona. I went to the one in AZ and was NOT impressed. They did the

usual-repeat all the tests that you've already had done by your rheumy and

a few more. Then, he told me he wasn't sure what I had so couldn't

recommend any treatment. But, I could come back in a few months and see if

anything had changed (gee, thanks a bunch!). If you're thinking of going

to AZ, I'll look up his name so you don't get him. He was nice enough and

thorough but of absolutely no help (and it's not cheap-costs above what my

insurance would pay). Let me know if you need his name. Best of luck-Ann

Heath lotr56@...

[Guest guest]

Hi Faith,

Duke University Medical Center has a great Rheumatology Department. They gave

me my diagnosis in one day. That was 10+ years ago though. Not sure about

now. I saw Dr Shanahan when I was there. Hope you feel better!

</HTML>

[Guest guest]

Faith honey,

Is there no RA closer to you or is this one just that good? As for

pain, I used to find ibuprofen helpful. Of course you must eat with

it.

Feel better. Take care and be well.

Ellen

[Guest guest]

Faith, from what I understand, Mayo and Cleveland Clinic are great for Still's.

I think you need to get a different RD if possible. If you can't, maybe you can

call him every day until he sees you. I sure hope you can get help soon.

Re: Help

Thanks Marty, you're great! I have been researching the Mayo Clinic. Is there

one better than another for Still's specifically? Faith

Marty wrote: Faith

Man I know how it feels been having the same trouble with docs almost as you.

This is some things I do to help.

Take a warm to almost hot bath and soak tell I look like a raisin then go to

bed.

Take Ibuprofen dose not take it away but eases it some times just enof.

Try not stressing lots easier said then done

Take a walk if you can or do something you like to take our mind off it. (I

put on a movie and around here that means I will be falling asleep takes about 3

to 4 tries before I see it all LOL.

Do not cover with comfort food as later it seams to add stress at lest to me

when I step on a scale that is.)

Lay in the shade on some thing comfy and be warmed by the sun also this way

you should not burn if you do fall a sleep. Call both docs and ask them to talk

to each other but stress and I do mean stress how bad your hurting. Tell them

every thing your doing to try and get some relief. Tell them you know you need

some thing even before you have a dx. By the way some get fast dx's some do not

mine was over 6 months with no pain help to speak off.

Get a dx maybe faster got to a mayo center or some were other like Stanford on

the west coast all depends on were you live and what you can spend.

That¢s all I can think of now and well hope may be one helps you or at lest

some one

and the last one a great big ((((((((hug from us all here ))))))))))))

The redneck

Marty

__________________________________________________________

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

[Guest guest]

Faith, one thing I did (and still do) is feed each of my Dr's every piece

of medical record I get from other Dr's, blood work, hospital records,

etc.... For me it was relatively quick (about 4 months of hell) but I've

found my Doctors seem to be a lot more in tune with what I say when I have

the information to back it up. Whenever I go anywhere, I ask for copies of

the records and then fax them to each & every one of my Dr's. I also keep a

pretty large book for myself so that whenever I wind up in the resort I get

past the " We don't know what the hell is wrong with you so we're not going

to treat you! " syndrome that I've come across a few too many times when I

could least afford to.

As far as Doc's that you don't feel " right " about, dump them, and quick!

My first RD always had a lot to say, such as " I don't know what to tell you "

" I don't know what to say " " I don't have an answer " and phrases alike this.

He also was of the mindset that I should take nothing for pain and let it

develop. I dumped him, did some research and found a pretty damn good one.

The only downside is that the first was virtually in my backyard and the one

I have now is 93.4 miles South of here!! The most expensive part of seeing

him is the God-Damn gas!!!! Aside form that, my life with my Dr's is great.

I can't offer advice on Mayo or Cleveland, but I have gone to " highly

touted " s Hopkins and wanted to punch the " SonofaB***** " right in the

face and break his head into tiny ******* pieces! I guess I offended his

intellect by not going there first and he treated me like a piece of shit.

Surprisingly I have had my best luck at a local hospital which is where I

got my diagnosis. I have also been to the Univ. of Penn., Jefferson Univ.

(headache Ctr, Great people! (just haven't found an answer for me yet and I

can't afford to go there for the time being) and a number of other places.

The best advice I can give is make sure your Dr's communicate with each

other and make sure you are comfortable with each of them. I think the

comfort part is most important as it leads to trust quicker than animosity.

Best of luck, Kirk.

>

> Hi Faith,

> Duke University Medical Center has a great Rheumatology Department. They

> gave

> me my diagnosis in one day. That was 10+ years ago though. Not sure about

> now. I saw Dr Shanahan when I was there. Hope you feel better!

> </HTML>

>

>

[Guest guest]

Faith, one thing I did (and still do) is feed each of my Dr's every piece

of medical record I get from other Dr's, blood work, hospital records,

etc.... For me it was relatively quick (about 4 months of hell) but I've

found my Doctors seem to be a lot more in tune with what I say when I have

the information to back it up. Whenever I go anywhere, I ask for copies of

the records and then fax them to each & every one of my Dr's. I also keep a

pretty large book for myself so that whenever I wind up in the resort I get

past the " We don't know what the hell is wrong with you so we're not going

to treat you! " syndrome that I've come across a few too many times when I

could least afford to.

As far as Doc's that you don't feel " right " about, dump them, and quick!

My first RD always had a lot to say, such as " I don't know what to tell you "

" I don't know what to say " " I don't have an answer " and phrases alike this.

He also was of the mindset that I should take nothing for pain and let it

develop. I dumped him, did some research and found a pretty damn good one.

The only downside is that the first was virtually in my backyard and the one

I have now is 93.4 miles South of here!! The most expensive part of seeing

him is the God-Damn gas!!!! Aside form that, my life with my Dr's is great.

I can't offer advice on Mayo or Cleveland, but I have gone to " highly

touted " s Hopkins and wanted to punch the " SonofaB***** " right in the

face and break his head into tiny ******* pieces! I guess I offended his

intellect by not going there first and he treated me like a piece of shit.

Surprisingly I have had my best luck at a local hospital which is where I

got my diagnosis. I have also been to the Univ. of Penn., Jefferson Univ.

(headache Ctr, Great people! (just haven't found an answer for me yet and I

can't afford to go there for the time being) and a number of other places.

The best advice I can give is make sure your Dr's communicate with each

other and make sure you are comfortable with each of them. I think the

comfort part is most important as it leads to trust quicker than animosity.

Best of luck, Kirk.

>

> Hi Faith,

> Duke University Medical Center has a great Rheumatology Department. They

> gave

> me my diagnosis in one day. That was 10+ years ago though. Not sure about

> now. I saw Dr Shanahan when I was there. Hope you feel better!

> </HTML>

>

>

[Guest guest]

I am in the middle of the boonies! All of the docs are 2-2 1/2 hours from me.

I don't mind the drive though, I'm just getting discouraged. from

Branson told me about her RD, I'm going to try them even though he is out of

network. Are you having a good day? Faith

Zovtic wrote: Faith honey,

Is there no RA closer to you or is this one just that good? As for

pain, I used to find ibuprofen helpful. Of course you must eat with

it.

Feel better. Take care and be well.

Ellen

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

Shape Yahoo! in your own image. Join our Network Research Panel today!

[Guest guest]

What???? Not old enough for psychotherapy? They have two and three

year olds that get psycho-therapy for parents that have died

tragically. My son is seeing a psychologist monthly. Does your

pediatrician suggest anyone? Ours suggested the one we go to and my

son looks forward to seeing him. I would look into the Rispidal. I

heard some moms post info that it made there son worse. I think it

got to the point where she was beaten up by her son when he went into

some pscyho rage. Sometimes meds can make things worse than better.

I know the feeling. We have the same problem with our son. It

always seems when he gets into trouble its with the same group of

boys. We tell him don't hang around them. Alot of kids at his

school some more than others have learned to push his buttons. We've

tried to talk to him about ignoring them and walking away, but it

doesn't always help.

At one point we were seriously thinking about homeschooling him or

sending him through a local homeschooling program cause of the very

same reason. The phone calls, oh the phone calls...don't get me

started. Anyway, three schools and hundreds of calls later we ended

up at a public school where the principal and school counselors

actually cared. I was starting to think the opposite until this

school. They got the " ball rolling " pull some strings at the

schoolboard and they started doing OT and interventions with him at

school the breakdowns, meltdowns etc. went from 15 average a day down

to 5. I found out then they are the only school I am aware of in my

surrounding area that actually has an Autism program. And my

understanding its one of the best.

Anyway, the problem is his lacking in social skills and

understanding his world around him like he should and he doesn't see

it like that. He sees it a different way. The problem is going

about seeing it how he sees it and channeling that into something

positive and it just purely observation and trial and error. To give

you an example, the Autistic counselor at my son's school when trying

to talk to him originally she said it took her two weeks before she

could come within 10 ft of him. I didn't or couldn't believe it.

Anyway, she figured out what his likes and dislikes were and

channeled that now they are great friends.

Getting to the example I meant to use. There is an autistic kid that

she had problems getting to stay still and pay attention during class

lessons and therapy sessions. He has a real nack for movies from

Casablancas to present day movies. He is literally the rain man of

movies. He can recall the movies' scripts line by line.

She said a thought occured to her that he almost seems to work like

a VCR. Welp, she thought it couldn't hurt. She drew, to the closest

of her ability, the exact replica of the front of a VCR. Complete

with stop, pause, rewind button etc. Well, the next day when he just

kept going and wouldn't pay attention she went to the replica drawing

and pressed the stop button. She said just like magic he stopped and

sat quietly for the rest of the lesson. She still uses that techinque

for him and it still works she says. He is not a real verbal child

except for his quoting movies and his hyperactiveness. The point is

these are exordinary children and it takes extrodinary ways to reach

them. If anything, it teaches you to stop and smell the roses. Some

of the most littiest things are important to them that you may not

even notice. That's the thing, can you notice them and how do you

work them into what you need to do to get him through the day. I'm

lucky his teachers and counselors have figured some ways to get him

through and were willing to work with him and us, his parents.

That's what you need. A good support system and group. Someone I

work with has a sister that literally packed up and moved to Florida

to place their child diagnosed with severe Autism, in an Autism

specialty school just so he could get what he needed. They spend

thousands of dollars a year, but he is doing so much better and has

improved and actually has a better outlook than he would've had if

they would've stayed around here.

Its exhausting I know. I don't know what I would've done without the

counselors and prinicpal at my son's school. You are headed in the

right direction just by posting this help topic. We are here for

you. Hope the info I gave you helps. By the way my son just turned

9 and his official diagnosis is ADHD presently.

The only med I we have ever been given to give him is Focalin XR

20mg. We take him off of it on weekends and have during the summer.

Last year he cleared his classroom three times that I'm aware of. I

can't recall why he cleared them, but something set him off and he

started tossing chairs. I've seen him at his almost worse. I know

how you feel. The way we got him to calm down was completely changed

the subject. He went from Dr. Hyde back to calm Mr. Jeckel. No

confrontations worked. Just changed the subject. Like weren't you

wanting to tell Mrs. so and so about that tv show you watched that

was talking about computers? and it was like I my original son

appeared out of no-where. ........I'll keep you in my prayers.

>

> I need help, my son is 9 1/2 Aspergers & ADHD he has had a

difficult school

> year socially. Academically his grades are great, but his so

called friends

> seem to bait him and he gets in trouble several times a week. He

is angry

> and rages several times a week and then will go to the depths of

disperse

> and talks about killing himself. He is on Concerta & Rispidal, we

tried

> Prozac a couple of years ago and it made him angrier. I don't know

how to

> help him. I have him in a social skills group weekly, he takes

judo, cub

> scouts, and music lessons. we have backed off the outside

activities

> because he was raging at his lessons. I can not find another

school setting

> that would work and the public school is no help. I think I might

home

> school him until he can acquire the skills to deal with people who

push his

> emotional buttons. He saw a therapist and she told us she could

not help

> until he was older for psychotherapy. any suggestions would be

welcome I

> just don't know what else to do

> Greta in MD

>

[Guest guest]

Have you tried Quantum Biofeedback therapies? I have

found them to be a blessing with my son who has

high-functioning AS and is also OCD.

Kernan

Quantum Biofeedback Therapist

www.quantumassociatesofutah.com

[Guest guest]

Dear ,

The only thing I can think is a whiplash collar.

And there is always prayer.

Francine

In a message dated 8/1/2007 2:11:34 A.M. Eastern Daylight Time, andee87@... writes:

HI

DON'T MEAN TO BE A BOTHER BUT I AM GOING TO ASK THE SAME QUESTION ABOUT A PROBLEM MY DAUGHTER HAS. I DIDN'T GET ANY FEEDBACK AND MAYBE NO ONE HAS EVER DEALT WITH THIS PROBLEM. I PERSONALLY DON'T KNOW OF ANYONE SO I MAY BE OUT OF LUCK. MY DAUGHTER IS A HIGH FUNCTIONING ASPERGERS, 21 YEARS OLD. SHE HAS A HEAD ROCKING PROBLEM THAT HAS/IS IMPACTING HER SOCIALLY QUITE DRAMATICALLY. I KNOW THEY MAKE THE BELTS THAT HELP WITH THE BODY. SHE HAS MASTERED HER BODY BUT CAN'T SEEM TO GET HER HEAD UNDER CONTROL. WE HAD DONE BEHAVIOR MODIFICATION WITH NO SUCCESS. PLEASE IF ANYONE KNOW ANYTHING!!!

THANKS,

ANDREA

Get a sneak peek of the all-new AOL.com.

[Guest guest]

,

Just wanted you to know there may be more

answers you will receive in a group called Gifted-NLD-AS I

suggest you ask there.

Hope this helps!

Deb’s

From: Autism and Aspergers Treatment [mailto:Autism and Aspergers Treatment ] On Behalf Of sunrose101@...

Sent: Wednesday, August 01, 2007

10:29 PM

Autism and Aspergers Treatment

Subject: Re:

re: help

Dear ,

The only thing I can think is a whiplash

collar.

And there is always prayer.

Francine

In a message dated 8/1/2007 2:11:34 A.M.

Eastern Daylight Time, andee87hotmail writes:

HI

DON'T MEAN TO BE A BOTHER BUT I AM GOING

TO ASK THE SAME QUESTION ABOUT A PROBLEM MY DAUGHTER HAS. I DIDN'T GET

ANY FEEDBACK AND MAYBE NO ONE HAS EVER DEALT WITH THIS PROBLEM. I

PERSONALLY DON'T KNOW OF ANYONE SO I MAY BE OUT OF LUCK. MY DAUGHTER IS A

HIGH FUNCTIONING ASPERGERS, 21 YEARS OLD. SHE HAS A HEAD ROCKING PROBLEM

THAT HAS/IS IMPACTING HER SOCIALLY QUITE DRAMATICALLY. I KNOW THEY MAKE

THE BELTS THAT HELP WITH THE BODY. SHE HAS MASTERED HER BODY BUT CAN'T

SEEM TO GET HER HEAD UNDER CONTROL. WE HAD DONE BEHAVIOR MODIFICATION

WITH NO SUCCESS. PLEASE IF ANYONE KNOW ANYTHING!!!

THANKS,

ANDREA

Get a sneak peek of the all-new AOL.com.

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