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In a message dated 3/1/2006 1:08:38 PM Eastern Standard Time,

beachbodytan2002@... writes:

He can't hear the sounds of the letters of a word to try to spell

them. He is doing very well with math, science, social studies.

Thanks for reading. - Rose

You should look at Dyslexia. You teach people with dyslexia in particular

ways because they do not hear the individual sounds, cannot break words apart

or put them together, cannot read fluently, etc. He may not need all that

reading tutoring if you have a specific program being used such as orton

gillingham. Just " general reading help " may not be good enough. More of the

same

that isn't working isn't a good solution.

Roxanna ô¿ô

Don't take life too seriously; No one gets out alive.

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Dyslexia should be diagnosed by a reading specialist, not an OT.

Orton-Gillingham is an approach used to teach children with dyslexia. Pete

, a

very well known special education lawyer, starts out his boot camps with the

story of how he had SEVERE dyslexia as a child and was lucky enough to have

parents who were ahead of their time. He was tutuored by one of the original

founders of the Orton-Gillingham approach and he grew up to be a lawyer. :)

_What is the Orton-Gillingham Approach?_

(http://www.ortonacademy.org/approach.html)

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Yes, Roxanna! that is exactly what I've been telling the school. instead they

give me more strategies to do with him. " It's not working " !!!! They gave him an

O.T. eval and she said its not dyslexia & when she asked him to copy something

she said he did o.k. (I'm not satisfied with that). Is there an outside place

I can take him to to test him for dyslexia?. I'm waiting for Faxton to call us

back. should I ask the speech therapist to test him for dyslexia? if its that,

at least we would have another way of teaching him. Who should I ask to test

him for dyslexia? please don't say the school. Should I also take him for a

hearing test? if yes, what kind? He can hear. is there a special hearing test

that he can take? What is Orton Gillingham? I do know that more of the same

thing is not going to work. It hasn't worked yet. he can't read fluently but

learned to memorize a story by looking at the pictures which can fool the

teacher into thinking he can read. but, give

him a new book, he reads like a pre-k. any advise I will try! I'm going to

look into " orton gillingham " I've never heard of this but I will find out

anything I can & try it. thank you - Rose

kneeleee@... wrote:

In a message dated 3/1/2006 1:08:38 PM Eastern Standard Time,

beachbodytan2002@... writes:

He can't hear the sounds of the letters of a word to try to spell

them. He is doing very well with math, science, social studies.

Thanks for reading. - Rose

You should look at Dyslexia. You teach people with dyslexia in particular

ways because they do not hear the individual sounds, cannot break words apart

or put them together, cannot read fluently, etc. He may not need all that

reading tutoring if you have a specific program being used such as orton

gillingham. Just " general reading help " may not be good enough. More of the

same

that isn't working isn't a good solution.

Roxanna ô¿ô

Don't take life too seriously; No one gets out alive.

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>

> I'm going to look into " orton gillingham " I've never heard of

this but I will find out anything I can & try it. thank you - Rose

>

Hi Rose

Orton Gillingham is a multi-modal structured method of teaching

reading. It focuses on teaching the sound/symbol correspondences in a

very systematic fashion and has been proven to be very successful

with individuals who have difficulty learning to read. Your schoold

district ought to be able to help you with getting this kind of help

for your son. The LD resource teacher can do the kind of testing that

would highlight this kind of problem - there are many standardized

tests of reading achievement that would document a reading difficulty.

Hope this was of some help.

Trish

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This was very helpful. Thank you

drexel459 <trish459@...> wrote:

>

> I'm going to look into " orton gillingham " I've never heard of

this but I will find out anything I can & try it. thank you - Rose

>

Hi Rose

Orton Gillingham is a multi-modal structured method of teaching

reading. It focuses on teaching the sound/symbol correspondences in a

very systematic fashion and has been proven to be very successful

with individuals who have difficulty learning to read. Your schoold

district ought to be able to help you with getting this kind of help

for your son. The LD resource teacher can do the kind of testing that

would highlight this kind of problem - there are many standardized

tests of reading achievement that would document a reading difficulty.

Hope this was of some help.

Trish

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Guest guest

Awesome information!. He is finally in a reading resource program at school. I

knew I had to do something because everything I'm already doing is not working.

so, Faxton Hospital got back to me. listened to my concerns about my son and

said I need to have him come in for a Central authorial processing testing with

a hearing test.

that is part 1.

next: while this is being done I will also get a reading specialist to

evaluate him to test him for dyslexia, and I will mention about

Orton-Gillingham.

thanks to the support of everyone in this group. I can explain my concerns

about my son and Know what to ask for and give - mention " Orton-Gillingham. "

WOW!!! it does help when a person knows what to ask for because they(the school)

sure do offer.

Big thanks and hugs to you all!! I now feel by the time school is over my son

will be able to read, write & spell. ( I will post it when he does).. - Rose

ppanda65@... wrote:

Dyslexia should be diagnosed by a reading specialist, not an OT.

Orton-Gillingham is an approach used to teach children with dyslexia. Pete

, a

very well known special education lawyer, starts out his boot camps with the

story of how he had SEVERE dyslexia as a child and was lucky enough to have

parents who were ahead of their time. He was tutuored by one of the original

founders of the Orton-Gillingham approach and he grew up to be a lawyer. :)

_What is the Orton-Gillingham Approach?_

(http://www.ortonacademy.org/approach.html)

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  • 1 month later...
Guest guest

Hello

Willow my daughter also had bad eczema. We just used the aveeno

products on her. We made the oatmeal stuff into a paste and put it

on her little noggin. Learned that trick from and it worked

great.

Your ped can write you an Rx for the band, you do NOT have to see a

specialist if you want to save yourself some time.

Sandy Willow's Mom (6-2-2003)

Torticollis resolved (02-2004)

Cranio Germany Grad (02-2004)

www.geocities.com/samipa74/Willow_Lanette.html

www.palmerfamily.armedforcesfamilies.com

www.drmy.net/spalmer

>

> When you babies got their bands, were they really

> uncomfortable and what were any skin reactions they

> had. Logan already has severe eczema so I'm wondering

> if he had to get one, how he would react to it, on the

> plus side I guess he couldn't scratch his head anymore

> :)

> P.S. I emailed my ped about the referral to the neuro

>

> -Oregon

> mom to alyssa former 30 weeker now 7

> kaelyn full term now 5 and

> Logan 33 weeker now 7 months(may need banding)

>

> __________________________________________________

>

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Guest guest

Logan has state paid insurance so I'm not sure if I

can go straight for the band. I don't mind the

referral. My ped is pretty quick about getting things

done so hopefully it will be quick. thanks for all the

help. I'll let you know what she says.

heather-oregon

mom to alyssa former 30 weeker now 7

kaelyn full term now 5 and

logan 33 weeker now 7 1/2 months (may need banding)

--- Sandy <samipa74@...> wrote:

> Hello

> Willow my daughter also had bad eczema. We just

> used the aveeno

> products on her. We made the oatmeal stuff into a

> paste and put it

> on her little noggin. Learned that trick from

> and it worked

> great.

> Your ped can write you an Rx for the band, you do

> NOT have to see a

> specialist if you want to save yourself some time.

> Sandy Willow's Mom (6-2-2003)

> Torticollis resolved (02-2004)

> Cranio Germany Grad (02-2004)

> www.geocities.com/samipa74/Willow_Lanette.html

> www.palmerfamily.armedforcesfamilies.com

> www.drmy.net/spalmer

>

>

>

> >

> > When you babies got their bands, were they really

> > uncomfortable and what were any skin reactions

> they

> > had. Logan already has severe eczema so I'm

> wondering

> > if he had to get one, how he would react to it, on

> the

> > plus side I guess he couldn't scratch his head

> anymore

> > :)

> > P.S. I emailed my ped about the referral to the

> neuro

> >

> > -Oregon

> > mom to alyssa former 30 weeker now 7

> > kaelyn full term now 5 and

> > Logan 33 weeker now 7 months(may need banding)

> >

> > __________________________________________________

> >

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Guest guest

Fortunatley my son didn't have any skin reactions with his docband.

He had redmarks from his starbands due to fit issues. I think I

have read that some babies eczema gets better after banding and some

have some flareups.

Haylee

mom to andre doc band grad

>

> When you babies got their bands, were they really

> uncomfortable and what were any skin reactions they

> had. Logan already has severe eczema so I'm wondering

> if he had to get one, how he would react to it, on the

> plus side I guess he couldn't scratch his head anymore

> :)

> P.S. I emailed my ped about the referral to the neuro

>

> -Oregon

> mom to alyssa former 30 weeker now 7

> kaelyn full term now 5 and

> Logan 33 weeker now 7 months(may need banding)

>

> __________________________________________________

>

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  • 3 months later...
Guest guest

,

You could very well run into trouble increasing the Minocin while at the

same time reducing the prednisone.

If you are still incurring a lot of inflammation, then you need to consider

staying on the higher dosage of prednisone until it subsides.

If you increase the Minocin, do it slowly, and if in doing so an increase in

symptoms occurs, you might want to back down to a lower dose until they

subside, then try again.

Remission is when symptoms are gone and lab values have returned to normal

and remained stable over a period of time determined by your physician.

Ethel

rheumatic Another question

> To group: I have a couple of more questions. I am weaning off of the

> prednisone while increasing the Minocin. Is this okay? I am increasing

> to 200mg Minocin and I am decreasing my prednisone from 9mg to 8mg and

> hoping to decrease 1mg every 2weeks. My other question is...What

> constitutes remission? Where do my stats need to be before I am

> technically in remission? Do I go by my sed rate and my RA factor? And

> is normal 0 and 20?

>

>

>

> Thank you,

>

>

>

>

>

>

>

>

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Guest guest

Ethel,

Thank you for responding so quickly, this information helps me a lot. I

do not hardly have any inflammation at all but if it gets worse with the

increase of Minocin, I will increase the prednisone back to 9mg.

________________________________

From: rheumatic [mailto:rheumatic ] On

Behalf Of Ethel Snooks

Sent: Wednesday, August 02, 2006 11:01 AM

rheumatic

Subject: Re: rheumatic Another question

,

You could very well run into trouble increasing the Minocin while at the

same time reducing the prednisone.

If you are still incurring a lot of inflammation, then you need to

consider

staying on the higher dosage of prednisone until it subsides.

If you increase the Minocin, do it slowly, and if in doing so an

increase in

symptoms occurs, you might want to back down to a lower dose until they

subside, then try again.

Remission is when symptoms are gone and lab values have returned to

normal

and remained stable over a period of time determined by your physician.

Ethel

rheumatic Another question

> To group: I have a couple of more questions. I am weaning off of the

> prednisone while increasing the Minocin. Is this okay? I am increasing

> to 200mg Minocin and I am decreasing my prednisone from 9mg to 8mg and

> hoping to decrease 1mg every 2weeks. My other question is...What

> constitutes remission? Where do my stats need to be before I am

> technically in remission? Do I go by my sed rate and my RA factor? And

> is normal 0 and 20?

>

>

>

> Thank you,

>

>

>

>

>

>

>

>

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  • 3 weeks later...

50/50 i think a biopsy is the same just like TX.that's why i feel that we all choose based on our own feelings and beliefsTim Parsons knoxville,tn 37931 865-588-2465 x107 work www.knoxville1.com

How low will we go? Check out Messenger’s low PC-to-Phone call rates.

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  • 2 weeks later...

Carol – I slept flat on my back for

about 8 months and didn’t move from that spot! I was scared to move –

Just recently I’m able to sleep on my right side. The doctor didn’t

specify how to sleep at all – the drugs made me quite sleepy so I lied

pretty still all night.

Lorrie

From: [mailto: ] On Behalf Of Carol

Sent: Sunday, September 03, 2006

6:16 PM

Subject: [ ]

Another Question

The other question I just remembered is: What was the

most comfortable

sleeping position after revision--side or back? And did your doctor

recommend or discourage one or the other?

I have been sleeping on my sides since my surgery 32 years ago with a

pillow between my legs, and rarely sleep on my back. Just because the

back sleeping is too uncomfortable.

Carol V (CA)

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Hi Carol V,

I think different surgeons recommend different sleeping positions

based on the work that is done. I was told all through the hospital

stay, to lie on my back only. Occasionally, they would prop me at a

30 degree angle. This went on after I got home for about 3 months. I

was told at that point anything goes, what ever is comfortable. The

surgeon promoted belly sleeping to stretch gluts but I only last

about 2 minutes. I know others are told their sides and sleep like

that in the hospital so I suppose it depends on the work done and

the surgeon.

>

> Carol - I slept flat on my back for about 8 months and didn't move

from that

> spot! I was scared to move - Just recently I'm able to sleep on

my right

> side. The doctor didn't specify how to sleep at all - the drugs

made me

> quite sleepy so I lied pretty still all night.

>

>

>

> Lorrie

>

>

>

> _____

>

> From:

> [mailto: ] On Behalf Of Carol

> Sent: Sunday, September 03, 2006 6:16 PM

>

> Subject: [ ] Another Question

>

>

>

> The other question I just remembered is: What was the most

comfortable

> sleeping position after revision--side or back? And did your

doctor

> recommend or discourage one or the other?

>

> I have been sleeping on my sides since my surgery 32 years ago

with a

> pillow between my legs, and rarely sleep on my back. Just because

the

> back sleeping is too uncomfortable.

>

> Carol V (CA)

>

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  • 2 weeks later...

Jo wrote:

>

> sorry, i forgot, i was wondering if druing die off when a large

number of toxins are being released if this could have an effect on the

> strength of the immune system? and if it was therefore better to take

> things very gradually

==>Yes, it is better to take things very gradually so you function okay

instead of your body being overwhelmed by too many candida toxins being

released at one time. And yes, toxins are affecting the strength of

the immune system that is why the diet and supplements are so

important. I had to be on the diet for 6 mos. before I could take

antifungals and even then I was horribly sick (I wasn't working and I

was single so I pushed through it, but my mother had to take care of

me).

> also i am studying nutrition with cnm, and i would like to learn

about candidiasis in depth, could u recommend any sources?

==>The main sources I use are two books Copyright 1986:

1) Back to Health: Yeast Control, by Dennis W. Remington, M.D. and

Barbara W. Higa, R.D., Publisher: Vitality House International Inc.,

Provo, Utah, 1986, ISBN 0-912547-03-0.

2) The Yeast Syndrome, by Parks Trowbridge, M.D. and Morton

, D.P.M., Publisher: Bantam Books, 1986, ISBN 0-553-26269-0.

Bee

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  • 2 months later...

I had to give blood before my hip replacement.

I had to give three units and the Dr. forgot to tell me until

a month before

surgery so we had to forget/ignore the usual rules about giving blood. After the

third unit I

was a little green

around the edges for a while but I’m glad I gave because I needed all

three units. I’m not

a true “bleeder”

but I do bleed more that most people during surgery. I tried to tell my back

surgeon about

this but he didn’t

listen very well. He will the next time!

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Lindy, I couldn't. Because of my veins, they can't get more than a fourth of a pint at any one time. I considered having a compatible family member donate, but my doctor said he didn't think it was necessary because blood transfusions from the blood bank are very low risk now with improved and more stringent screening than ever before. Regards, Donnalindy <everyothername.istaken@...> wrote: who asks more questions than moi? lol has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? hugs,~ linDUHlou ~RTHR/1/22/2007

Need a quick answer? Get one in minutes from people who know. Ask your question on

Answers.

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I gave a pint of blood before my surgery - they wanted me to give 2

pints, but I have very small veins and the Red Cross nurse couldn't

find but one vein large enough. As it turned out, I did need two

pints after surgery...

Judy

-- In Joint Replacement , " lindy "

<everyothername.istaken@...> wrote:

>

> who asks more questions than moi? lol

> has anyone here given their own blood prior to the surgery in case

you need blood after? or is anyone with a surgery coming up, thinking

of doing this?

> hugs,

> ~ linDUHlou ~

> RTHR/1/22/2007

>

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has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? >>>> I did for my first & second... third doc said no cuz I was anemic. You can speak 2 your doctor about donations or call the red-cross in your area~ they'll advise you as to the step by step process. Just make sure if your interested in doing so... that you give yourself enough time~ AND CHECK YOUR MEDS if your taking them... some you have to stop taking prior to donating.

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>>>has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? >>>> I did for my first & second... third doc said no cuz I was anemic. You can speak 2 your doctor about donations or call the red-cross in your area~ they'll advise you as to the step by step process. Just make sure if your interested in doing so... that you give yourself enough time~ AND CHECK YOUR MEDS if your taking them... some you have to stop taking prior to donating.

I've always given 3 units (short units - my veins can't do normal size ones) before each of my replacement and revision surgeries (4 total surgeries). I've used every drop of those too! Felt much better each time afterwards. I'm one of those that runs anemic. My last donation was 6 yrs ago, drawn at our local Hospital and shipped across the State to the Hospital that was doing my surgery. The Hospital doing the surgery made me verify it was my signature on the blood packets, all 3 of them prior to getting wheeled into the operating room.

I just wanted to suggest, if you are donating your own blood to use -- don't forget to verify what your Insurance will cover in regards to the donation, who they prefer to draw it etc. Not all Insurance carriers (at least in my experience) cover this the same and may have their own rules/regulations to follow.

tanya

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Now that is great advice Sassy, and one I hadn't heard before - but is

pretty obvious now it has been said.

I donated my own blood and no one mentioned that to me. I wasn't on

anything that had to be stopped, but I wonder if the blood bank would have

stopped me if I had, and would they be aware?

Valuable information on this group. Well done everyone.

Aussie Margaret

RTHR 1990 revised 2004

Re: another question

(on the subject of storing your own blood)

AND CHECK YOUR MEDS if

| your taking them... some you have to stop taking prior to donating.

|

Send instant messages to your online friends http://au.messenger.

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Hi,

I gave two pints before my double TKR and boy am I happy I did. As it

turns out, I needed to get both back on day #3 post Op. If I hadn't

given my own blood I would have needed someone else's. Since it was

my own I had no quams about getting both units. If you have a choice

give the blood just in case. If not you I'm sure someone else will

get good use out of it.

Best Regards,

Alan B.

>

> who asks more questions than moi? lol

> has anyone here given their own blood prior to the surgery in case

you need blood after? or is anyone with a surgery coming up, thinking

of doing this?

> hugs,

> ~ linDUHlou ~

> RTHR/1/22/2007

>

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in one of the books about joint replacement i just read it stated that giving one's own blood doesn't necessarily guarantee that if you need blood you'll get your own . . . that stinks. does anyone know if B Rh Negative is considered rare?

hugs,~ linDUHlou ~RTHR/1/22/2007

Hi,I gave two pints before my double TKR and boy am I happy I did. As itturns out, I needed to get both back on day #3 post Op. If I hadn'tgiven my own blood I would have needed someone else's. Since it wasmy own I had no quams about getting both units. If you have a choicegive the blood just in case. If not you I'm sure someone else willget good use out of it.

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I didn't donate my own blood prior to my surgery in August, but my primary

physician

advised me to do it for my other hip which will be done in January. He said

" there is no

blood better than your own " .

Arianne

>

> has anyone here given their own blood prior to the surgery in case you need

> blood after? or is anyone with a surgery coming up, thinking of doing this?

> >>>> I did for my first & second... third doc said no cuz I was anemic. You

> can speak 2 your doctor about donations or call the red-cross in your area~

> they'll advise you as to the step by step process. Just make sure if your

> interested in doing so... that you give yourself enough time~ AND CHECK YOUR

MEDS if

> your taking them... some you have to stop taking prior to donating.

>

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