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Well, you're in luck. There are automated systems available you can

purchase that allow you to control things around your house by computer,

and, i suppose, by portable remote control. They cost quite a bit of money

obviously, due to all the wiring and other things the electricians and

custom installers would have to do.

I don't know about any mounts for camcorders specifically designed for a

wheelchair but well, you could always duct tape a camcorder to one of your

wheelchair arms, LOL.

On 8/5/06, loki200673 <loki200673@...> wrote:

>

> My cousin had a highschool project to make a movie. This got me

> thinkng, " boy, that sounds like fun. " Now, I have SMA II, and very

> little movement, but I'd like to try this. Does anybody have any info

> on camcorders, mounts to put it on my wheelchair, or adaptive

> equipment that could help me out?

> I'm also interested in technology to help me around the house.

> Especially things that make it easier to operate tv, vcr, dvd, lights,

> etc.

>

> Mike

> loki200673@... <loki200673%40>

>

>

>

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Hey Larry,

I have 2 handy pages on the HDI I keep on file from Yeoman's book on

outcomes assessment. Send your fax # and I'll send it over. He mentions no

criteria for judging the emotional/functional score but does give references

to establish ranges of impact on the overall score.

W. Snell, D.C.

Hawthorne Wellness Center

3942 SE Hawthorne Blvd.

Portland, OR 97214

Ph. 503-235-5484

Fax 503-235-3956

drpsnell.chiroweb.com

>From: " Larry Oliver, DC " <dro@...>

> " Chiro ListServe " < >

>Subject: (unknown)

>Date: Fri, 11 Aug 2006 11:56:02 -0700

>

>Your wisdom is needed: We came across a Headache Disability Index

>questionnaire. When scored it gives a percent of emotional and percent of

>functional, the two equaling 100%. It is not clear to me how to interpret

>those percentages. Does a functional score greater than 50% mean it is

>more

>of a functional problem? I appreciate your knowledge. Thanks.

>

>BTW if found it at www.clinicalhealthservices.com

><http://www.clinicalhealthservices.com/> . It can be scored on-line with a

>nice printed report.

>

>Larry L. Oliver, DC

>408 NW 7th

>Corvallis, OR 97330

>dro@...

>541-757-9933

>

>The information contained in this electronic message may contain protected

>health information which is confidential under applicable law and is

>intended only for the use of the individual or entity named above. If the

>recipient of the message is not the intended recipient, you are hereby

>notified that any dissemination, copying or disclosure of this

>communication

>is strictly prohibited. If you have received the communication in error,

>please notify Heresco Chiropractic & Associates, 408 NW 7th St, Corvallis,

>OR 97330, 541-757-9933 and purge the communication immediately without

>making any copy or distribution

>

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  • 4 weeks later...

I just wanted to add that my son does have a one on one aide and he is in 1st

grade- I wouldn't have it any other way. He gets his space but he also has the

help right there when he needs it. I personally would rather her assist than

another child who may or may not have a cold. I think with some of the kids,

limiting the exposure to more germs is important- at least with my son I feel

that it is. It has also helped him transition into school- he is used to having

me near and he didn't want to go to school until I told him there would be

someone helping him when he needed it. He was homebound for Kindergarten.

Hopefully, the need of her being so close can dissipate and Brett can rely more

on friends. His school has been phenomenal with all of our requests and gone the

extra mile in every way possible- I feel very lucky!

Kristal

Mom to Brett- SMA II- 6-1/2 years old

Visit Brett's website at: http://www.our-sma-angels.com/brett/index.htm

Learn more about SMA:

www.fsma.org

www.smasupport.com

(unknown)

Thanks to all who gave info on my earlier post. I will get busy with

calling and letters. This isnt a problem that has just started. I

have fought with this school since PreK. I do know that If we were in

a different county we wouldnt be having these problems. But we arent

looking to move, and its the county and the schools responsiblility to

accomodate to Zack and the other children. The buddy system gets old.

He has tons of friends, but most ten year old children dont get the

responsibility thing like they should. So even with them helping, the

class is still waiting on him. Zack does speak his mind to us and

tells us what he thinks and wants. He is so very much main streamed in

every way possible. And there have been times where the friend was

with him opening doors for him, but take off and decide they are done

so thats leaves him where? I have looked at this from all different

ways. Im not asking for someone to sit on top of him, just be there

when he needs them. Its just our school system here. Didnt have this

problem with the school when we moved away for a short time. Once

again thanks a bunch and anything helps.

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Bekka's soap sounds wonderful how can one get the receipe?

Carol

(unknown)

This was suppose to be the infamous soap cake that Bekka makes.....but I

tweaked her original recipe and add a couple of different oils and used my

log mold. If you haven't tried Bekka's soap cake recipe you are really

missing out on a rich creamy soap.

The half n half with the addition of silk gives this soap it's rich creamy

texture.........awesome!!!

This soap is actually colored with pink oxide.

http://www.flickr.com/photos/51707978@N00/

__________________________________________________________

Search from any web page with powerful protection. Get the FREE Windows Live

Toolbar Today! http://get.live.com/toolbar/overview

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Wow, I'm really shocked by how many SMA kids have one-on-one assistance at

school. This is actually common practice now? I'm only 22, it hasn't been long

at ALL since I graduated, and I definitely never had nor wanted that kind of

help as a kid. I had an aid to help me in the bathroom at a scheduled time, but

that was all. The other kids would help me open doors and get books out of my

backpack. I don't think I needed much help beyond that. And I never had an

assigned buddy system, it was always just whoever was around at the time. My

friends, the people I sat by, whatever. The kids never minded helping, usually

they thought it was fun. And I learned how to ask for things politely and show

appropriate appreciation. I wouldn't have had it any other way. I was such a

painfully shy child; asking peers for help and explaining my needs helped me to

develop some badly needed assertiveness. Besides, I eventually was able to leave

home and go to college, where there definitely isn't anybody following me around

all day at my beck and call. I'm glad I learned early on to rely on myself and

the kindness of whoever happens to be around.

If this is the trend for SMA kids now, I have to wonder where the funding and

staffing are coming from. I've just started my student teaching in the special

ed department of a local high school, and all I ever hear about is all the cuts

they've made to save money. The resource rooms don't have any para eds, the self

contained unit is full so kids get placed inappropriately, the secretaries who

used to handle paperwork are gone, the classes don't have textbooks, the

teachers have way more students in their classes than state law allows... I just

hear nonstop stories about kids and teachers that aren't having their needs met

because of fundingcuts, it surprises me that there are so many stories of SMA

kids with the opposite experience.

Just interesting is all. :)

e

Re: (unknown)

I just wanted to add that my son does have a one on one aide and he is in

1st grade- I wouldn't have it any other way. He gets his space but he also has

the help right there when he needs it. I personally would rather her assist than

another child who may or may not have a cold. I think with some of the kids,

limiting the exposure to more germs is important- at least with my son I feel

that it is. It has also helped him transition into school- he is used to having

me near and he didn't want to go to school until I told him there would be

someone helping him when he needed it. He was homebound for Kindergarten.

Hopefully, the need of her being so close can dissipate and Brett can rely more

on friends. His school has been phenomenal with all of our requests and gone the

extra mile in every way possible- I feel very lucky!

Kristal

Mom to Brett- SMA II- 6-1/2 years old

Visit Brett's website at: http://www.our-sma-angels.com/brett/index.htm

Learn more about SMA:

www.fsma.org

www.smasupport.com

(unknown)

Thanks to all who gave info on my earlier post. I will get busy with

calling and letters. This isnt a problem that has just started. I

have fought with this school since PreK. I do know that If we were in

a different county we wouldnt be having these problems. But we arent

looking to move, and its the county and the schools responsiblility to

accomodate to Zack and the other children. The buddy system gets old.

He has tons of friends, but most ten year old children dont get the

responsibility thing like they should. So even with them helping, the

class is still waiting on him. Zack does speak his mind to us and

tells us what he thinks and wants. He is so very much main streamed in

every way possible. And there have been times where the friend was

with him opening doors for him, but take off and decide they are done

so thats leaves him where? I have looked at this from all different

ways. Im not asking for someone to sit on top of him, just be there

when he needs them. Its just our school system here. Didnt have this

problem with the school when we moved away for a short time. Once

again thanks a bunch and anything helps.

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In a message dated 9/9/2006 12:05:11 A.M. Eastern Standard Time,

herdqueen13@... writes:

Hi, my name is Susie.I'm new to soapmaking and would enjoy picking your

brains! LOL I would like to start making and selling soaps for a little extra

income. Any help would be most appreciated

~~~~~~~~~~~~~~~~~~~~~~~

Hi and welcome, Susie. Please take my comments in the helpful light I mean

them in.

Good soapmakers invariably make soap for quite awhile before selling it

because there is so much to learn about making good soap. So, go ahead and

begin

making soap with an eye toward selling in the future, but if you want to

make money now, you might look for something else. In addition, start learning

about what it would take for you to start a business. It's not as easy as it

looks!

Beth

_www.soapandgarden.com_ (http://www.soapandgarden.com/)

www.saponifier.com

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yes it took my son who is 12 from 1 and a half til 9 yrs old to get the dianosis of pdd i had to fight at the school and take him from one dr to another trying to get it figured out what makes it worse is i still get people asking are you sure this is the right diagnosis it drives me nuts ,my 10 yr old his diagnosis keeops changing becus he makes more eye contact and can talk to drs they think maybe he isnt pdd but yet the teachers( autistic support) in the classes he is in say he shows the classis symptoms of the pdd autistic child it is very nerve racking he was dignosed at the a yr after his brother so he was 8 we battled trying to find out since he was 4.stick to it and if you dont feel it is accurate or there is something more dont be afraid to voice your objections and change drs . good luck to u dawn greenwood-osullivan <hex_1970@...> wrote: Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting

worse as he gets older especially with his anger and obsessive behaviour. All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine Hosted by Sparkle Tags vickie

Messenger with Voice. Make PC-to-Phone Calls to the US (and 30+ countries) for 2¢/min or less.

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Hi and welcome to the group:

I am new here as well. My 4-year old daughter is on the spectrum. We did not have any trouble getting a dx on paper, in fact just the opposite was true for us. has had since she was little a feeding disorder and that is what prompted the docs to look deeper into all her behaviors and dx her as being on the spectrum. We weren't even looking for a dx except for someone to help us help her to eat nutritious food. They asked if they could test her for autism and I agreed thinking nothing would come of it, but then they said she has many of the signs. After talking to the doc about it, I guess she always did display signs and I always knew she was wired differently than my other kids. I hope that you can get your written dx soon and get the help your little one needs. Good luck and again, welcome to the group.

TERIMommy to 5, 10 HH, le, 8 HH, Brittany, 5 HH; , 4 HH, Autistic, feeding disorder; , forever 18 months, 13 days HLHS (Modified Norwood with Sano shunt; coarctation; Glenn & tricuspid valve repair, g-tube; became an Angel 6-22-06--I love you baby girl--Always & Forever))carepage name: Girlhttp://www.carepages.com/Login?seed=844556http://www.babiesonline.com/babies/p/peanutbutter5/http://knightfamily-adventures.blogspot.com/

(unknown)

Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting worse as he gets older especially with his anger and obsessive behaviour.

All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine

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Dawn

check out this group HomeschoolingAspies it is for home schooling Aspie kids and you may get lots of advice, I home school my DS currently and did last year for 5th grade and this year 6th grade. there is also a book I recommend you check out "Homeschooling the child with Asperger Syndrome" by Lise Pyles the isbn# 1-84310-761-9 from JKP.com

I would also recommend you find a social skills group ASAP to help him identify the bulling and to give him the skills to deal with it and lots of other things a good social skills therapy is worth its weight in gold :-) I love my sons therapist and she has helped him grow so much and handle things that I did not think were possible. 4 is young but if you state where you are maybe someone can recommend a good developmental pediatrician to help you work out a diagnosis. for insurance purposes and to get any state help its necessary.

email me off list if you want

Greta

-----Original Message-----From: Autism and Aspergers Treatment [mailto:Autism and Aspergers Treatment ]On Behalf Of dawn greenwood-osullivanSent: Friday, September 08, 2006 3:30 AMAutism and Aspergers Treatment Subject: (unknown)

Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting worse as he gets older especially with his anger and obsessive behaviour.

All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine

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Hi Felicia, How long did it take for the cimetidine to start working for Blake?

just curious how different it is from child to child. Thanks, Gretchen,

13 (waiting for test results....????)

Felicia Olson <co_olson@...> wrote: Hello All,

I have not posted in a while, I do read all the posts and I am sorry to hear of

all the families that are struggling with the fevers and other symptoms. I would

love to hear more on the conference since we were unable to attend. My son Blake

3, has been on Cimetidine for nearly a year now and fever free, knock on wood!!

God Bless to All,

Felicia

Blake 3,

Caitlin, 10

Alec, 1

, CO

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

Get your email and more, right on the new .com

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wrote:

> somethng's not right with

> the way this stuff's posting

If by that you mean in email the menu on the right sometimes covers up

part of the text, I agree. I hate that menu. I don't use it but I have

to fight it to edit the messages when I reply.

notan

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Hi Sharon and others!

Sharon's post reminded me of something my daughter's speech therapist

told me years ago. The therapist has a beautiful voice and she sings

songs to the kids all of the time to help them with their speech. She

was so happy, at first, when a mom of a little boy with DS called and

said that he started singing one of the songs at Wal-Mart while they

were out shopping. Then the mom said, " PLEASE! Don't ever sing that

song to my son again! " Apparently he was singing the song (quite

loudly), " Where is Thumbkin? " very loudly, and was pronouncing the " th "

as an " f " . Pretty funny!

Terri

Sharon wrote:

>

> Okay, I have been laughing about this one. I can just see her doing it.

>

> When was 18 months, was 5. I was cooking dinner,

> kept trying to get my attention saying " poo poo " . Finally I

> turned around, and had poop all up her back and front, oozing

> out her diaper to the floor, and of course, smeared on the floor where

> she had stepping in it. In my kitchen. I remember just sliding to the

> floor, shaking my head and I said " Oh sh** " . (Now I honestly

> don't curse, I am fairly strict about that, but this was one of those

> times.) then sat down, shaking her head, and clear as a bell

> said " Oh sh** " . I thought, oh great, the speech therapy is

> working, can't understand half of the other stuff she says, but she

> got that one out loud and clear.

> Isn't it fun?!?!?!?

>

> Sharon H.

> Mom to , (15, DS) and , (11)

> South Carolina

>

> " Be kinder than necessary, for everyone you meet is fighting some kind

> of battle. "

>

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You'll need to take the PCAT, get admitted into Pharmacy School, and

make it through the 4 year program.

Della :)

On 9/18/06, ronald aguilar <ronrhon27@...> wrote:

> I you're curently a pharmacy tech, and you wanted to continue your education

as a pharmacist what do i need to take and how long?

>

> thanks,

> ronald

>

>

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Hi Della,

Isn't it 6 years now? I thought all the pharmacy schools discarded the

traditional BS degree in favor of the PharmD?

Or are you assuming he finished his first 2 years?

Thanks,

--

Life should not be a journey to the grave with the intention of arriving safely

in an attractive and well-preserved body, but rather to skid in sideways,

champagne in one hand, strawberries in the other, body thoroughly used up,

totally worn out and screaming " WOO HOO - what a ride! "

-------------- Original message --------------

From: Della <dhengel@...>

You'll need to take the PCAT, get admitted into Pharmacy School, and

make it through the 4 year program.

Della :)

On 9/18/06, ronald aguilar <ronrhon27@...> wrote:

> I you're curently a pharmacy tech, and you wanted to continue your education

as a pharmacist what do i need to take and how long?

>

> thanks,

> ronald

>

>

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Hi and welcome...I had implants almost 3 years..saline. I just had them removed last Tuesday after being sick and not knowing why for over 2 years....read on ...it's your implants...no Ps will tell you but read here and go to www.explantation.com and read the stories there you'll know you are not alone. Good Luck. Where do you live ? karen

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Hi Maritza,

Where are you?

It sounds like you are having typical problems from implants.

What can we do to help you?

Lynda

At 05:09 PM 9/18/2006, you wrote:

>Hi, my name is maritza perez,

>i just went into this web site becouse for the

>past month i've been very ill, i had my

>surgery about 1year ago and i have been

>notecing my left implant has been deflating

>alot, i read the web site about the

>complacations of leaking implants, to my

>surpriced i now know that it was not my

>imagination as to why i have been so, so ill my

>back has been hurting me a great deal specialy

>the middle uppper back it goes all the way up to

>the back of my neck, been having a flu like

>symptoms having a dry cough that does not go

>away, head aches, muscle ache and last but not

>least my right leg has been hurting me all the

>way to my ankle and the buttom of my foot. been

>going to my physician which tells my it's just a

>muscle spasm to the er thinking it was my hurt

>because my left arm gets numb am also i have

>been itchy every where, now my head has been

>itchy like crazy and no one knows what is wrong

>with me, please help am going crazy.

>

>__________________________________________________

>

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>

> >Hi, my name is maritza perez,

> >i just went into this web site becouse for the

> >past month i've been very ill, i had my

> >surgery about 1year ago and i have been

> >notecing my left implant has been deflating

> >alot, i read the web site about the

> >complacations of leaking implants, to my

> >surpriced i now know that it was not my

> >imagination as to why i have been so, so ill my

> >back has been hurting me a great deal specialy

> >the middle uppper back it goes all the way up to

> >the back of my neck, been having a flu like

> >symptoms having a dry cough that does not go

> >away, head aches, muscle ache and last but not

> >least my right leg has been hurting me all the

> >way to my ankle and the buttom of my foot. been

> >going to my physician which tells my it's just a

> >muscle spasm to the er thinking it was my hurt

> >because my left arm gets numb am also i have

> >been itchy every where, now my head has been

> >itchy like crazy and no one knows what is wrong

> >with me, please help am going crazy.

> >

> >__________________________________________________

> >

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My dear Maritza, No, you are not going crazy, the symptoms you are suffering from are identicle to alot of other women who have come here looking for answeres. This includes myself. I came here last December looking for reasons for all my physical symptoms. I was so sick, and was told by a couple of doctors that it was all in my head. I was explanted in February. I have seen some improvement in my health, however, I still struggle with Chronic Fatigue and Fibromayalgia. We have many knowledgable women here who can help you understand what is going on inside your body. Keep coming and posting, we are here to care for you. Have a good night, maritza perez <maritza_perez9@...> wrote: Hi, my name is maritza perez, i just went into this web site becouse for the past month i've been very ill, i had my surgery about 1year ago and i have been notecing my left implant has been deflating alot, i read the web site about the complacations of leaking implants, to my surpriced i now know that it was not my imagination as to why i have been so, so ill my back has been hurting me a great deal specialy the middle uppper back it goes all the way up to the back of my neck, been having a flu like symptoms having a dry cough that does not go away, head aches, muscle ache and last but not least my right leg has been hurting me all

the way to my ankle and the buttom of my foot. been going to my physician which tells my it's just a muscle spasm to the er thinking it was my hurt because my left arm gets numb am also i have been itchy every where, now my head has been itchy like crazy and no one knows what is wrong with me, please help am going crazy. __________________________________________________

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Hi ,

Your letter just made me think of something. Have you been checked for

Epstein Barr Virus? If not, you might want to have a blood test for it. If

you are positive, anti-viral supplements can help you beat your chronic

fatigue and fibro symptoms. My son and I are both EBV positive.

Kenda

> No, you are not going crazy, the symptoms you are suffering from are

> identicle to alot of other women who have come here looking for answeres.

> This includes myself. I came here last December looking for reasons for all

> my physical symptoms. I was so sick, and was told by a couple of doctors that

> it was all in my head. I was explanted in February. I have seen some

> improvement in my health, however, I still struggle with Chronic Fatigue and

> Fibromayalgia. We have many knowledgable women here who can help you

> understand what is going on inside your body. Keep coming and posting, we are

> here to care for you.

>

> Have a good night,

>

>

>

> maritza perez <maritza_perez9@...> wrote:

> Hi, my name is maritza perez,

> i just went into this web site becouse for the past month i've been very

> ill, i had my surgery about 1year ago and i have been notecing my left

> implant has been deflating alot, i read the web site about the complacations

> of leaking implants, to my surpriced i now know that it was not my imagination

> as to why i have been so, so ill my back has been hurting me a great deal

> specialy the middle uppper back it goes all the way up to the back of my neck,

> been having a flu like symptoms having a dry cough that does not go away, head

> aches, muscle ache and last but not least my right leg has been hurting me all

> the way to my ankle and the buttom of my foot. been going to my physician

> which tells my it's just a muscle spasm to the er thinking it was my hurt

> because my left arm gets numb am also i have been itchy every where, now my

> head has been itchy like crazy and no one knows what is wrong with me, please

> help am going crazy.

> __________________________________________________

>

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Mammograms can rupture implants. Possibly there

was something growing inside your implant that

leaked into your body and is making you ill. You

need to have the implants and the scar tissue

that formed around them removed, we call it en bloc removal.

The doctors you are seeing will not help you with the implant problem.

Lynda

At 05:40 PM 9/18/2006, you wrote:

>

> >

> > >Hi, my name is maritza perez,

> > >i just went into this web site becouse for the

> > >past month i've been very ill, i had my

> > >surgery about 1year ago and i have been

> > >notecing my left implant has been deflating

> > >alot, i read the web site about the

> > >complacations of leaking implants, to my

> > >surpriced i now know that it was not my

> > >imagination as to why i have been so, so ill my

> > >back has been hurting me a great deal specialy

> > >the middle uppper back it goes all the way up to

> > >the back of my neck, been having a flu like

> > >symptoms having a dry cough that does not go

> > >away, head aches, muscle ache and last but not

> > >least my right leg has been hurting me all the

> > >way to my ankle and the buttom of my foot. been

> > >going to my physician which tells my it's just a

> > >muscle spasm to the er thinking it was my hurt

> > >because my left arm gets numb am also i have

> > >been itchy every where, now my head has been

> > >itchy like crazy and no one knows what is wrong

> > >with me, please help am going crazy.

> > >

> > >__________________________________________________

> > >

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Kenda, I don't know if I have been checked or not. I have had so many blood tests and I can't remember the names of any of them, I just know the results all say "normal or negative." I guess I will ask my GP when I see him next. Thanks, Kenda Skaggs <skaggs@...> wrote: Hi ,Your letter just made me think of something. Have you been checked forEpstein Barr Virus? If not, you

might want to have a blood test for it. Ifyou are positive, anti-viral supplements can help you beat your chronicfatigue and fibro symptoms. My son and I are both EBV positive.Kenda> No, you are not going crazy, the symptoms you are suffering from are> identicle to alot of other women who have come here looking for answeres.> This includes myself. I came here last December looking for reasons for all> my physical symptoms. I was so sick, and was told by a couple of doctors that> it was all in my head. I was explanted in February. I have seen some> improvement in my health, however, I still struggle with Chronic Fatigue and> Fibromayalgia. We have many knowledgable women here who can help you> understand what is going on inside your body. Keep coming and posting, we are> here to care for you.> > Have a good night,> > > > maritza perez <maritza_perez9 > wrote:> Hi, my name is maritza perez,> i just went into this web site becouse for the past month i've been very> ill, i had my surgery about 1year ago and i have been notecing my left> implant has been deflating alot, i read the web site about the complacations> of leaking implants, to my surpriced i now know that it was not my imagination> as to why i have been so, so ill my back has been hurting me a great deal> specialy the middle uppper back it goes all the way up to the back of my neck,> been having a flu like symptoms having a dry cough that does not go away, head> aches, muscle ache and last but not least my right leg has been hurting me all> the way to my ankle and the buttom of my foot. been going to my physician> which tells my it's just a muscle spasm to the er thinking it was my hurt> because my left

arm gets numb am also i have been itchy every where, now my> head has been itchy like crazy and no one knows what is wrong with me, please> help am going crazy.> __________________________________________________>

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Maritza, I think it's your implants. You've got one that's ruptured!

You need some good advice, which you can get here, about your options

for getting rid of those things. Your symptoms don't sound like breast

cancer. You're going to be OK. Keep writing, and pay attention to what

info you get here on the list. We've all been through something like

what you're going through.

Hugs,

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