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> Unfortunately therapy here

> is very expensive ($150/half hour)

Ouch! If he isn't getting much out of it I would try someone

different. It is not so much the diagnosis as it is the results.

He now just saw a SLP who seems to think

> that he has articulation/phonology disorder and not verbal

apraxia.

> This is because he is speaking in 3-5 word sentences consistently

but

> has very poor articulation.

What ideas does she have for therapy? My son too is talking but his

artic is not great either. He still loses consonants in longer

utterances.

He also is still talking in the 3rd

> person, and we try to have him repeat back with " I " or " me " which

he always does. I was wondering what is the progression with verbal

> apraxia? Does it follow a general pattern? Does that question

make sense?

He still is young and being that he talked late may explain that. I

would keep an eye on it and continue to work on it.

> He has some characteristics of verbal apraxia like little babbling

> when young, but he has never lost any sounds or words, doesn't

grope to talk, and imitates.

Same here approximations have always been consistent. The only time

we " lose " sounds is with the multisyllables and longer utterances.

He doesn't have oral apraxia as he can blow

> bubbles, candles, pucker for kisses, etc...

So as you can tell I am one VERY CONFUSED mommy. Four SLP's and not

one straight answer. I live in Minden, NV (near Lake Tahoe) and it

seems that good specialists are very hard to find. I am wondering if

> I should take him to someone who specializes in apraxia and

> artic/phonology disorders in California for a proper diagnosis?

> Would the approach to therapy be any different? His current ST

> treats him as if he has verbal apraxia, when he does see her.

Only you know if it seems helpful. If he is miserable and it is

always a battle, I would consider someone else.

Will a diagnosis make a difference in terms of insurance or school?

Then I would pursue it more. Are there any other issues, sensory,

receptive, processing, fine motor then I would pursue a medical

opinion.

> Any thoughts or advice would be greatly appreciated. Thanks in

> advance!!!

Wish I could have helped more.

denise

>

> Angie and Seth

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Kaufman specializes in apraxia and she is in Detroit Michigan. You

can send her a video for a price and she will write a report and diagnose.

She has her own clinic and is the creator of the Kauffman cards.

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  • 4 years later...

Hey .

Unfortunately the symptoms of many diseases mimick those of Stills

and the medication used to treat those symptoms also alleviate some

of the symptoms of Stills. Like most here in this group, I have gone

through a myriad of diagnoses before Stills. Included in this list

is Multiple Sclerosis, Undifferentiated Connective Tissue Disease,

Mixed Connective Tissue Disease, Bechet's Disease, Lupus and so on

and so on... The main medicines to treat any of theses diseases and

Stills disease are NSAID's, DMARD's and TNF's. These are the " front

line " of defense in managing most of these diseases ( and including

yours, I'll bet! ).

You are your only advocate. Research, research, research. If you

don't like your doctors, fire them and find others. If you don't

like your medicines, tell your doctor to change them. The search for

a doctor who will treat not only your disease, but you as a person is

a long voyage. Your search is only beginning. Do not lose faith and

have patience. Be tough with your doctors and those managing your

health. They work for you. Hang in there, you are not alone.

Joe

>

> Hi All,

>

> I was posting here about 2 months ago. Several doctors were giving

> me the possible diagnosis of Still's Disease. I was in the

hospital

> several times this summer. My diagnosis went from bacterial

> infection to Rheumatic Fever to virus to Still's and many more. At

> least 3 doctors down here think Still's is a possibility.

According

> to the University of Miami, " it's not a textbook case, however. "

> Hmmm...it seems they have only seen it in a textbook...

>

> Anyway, I have since has a positive Lyme test and I went to see a

> specialist in this area. He feels definitively that I have Lyme

> Disease. So, I am being treated for that currently.

>

> My doctors down here just do not think it is Lyme. It seems

> Rheumatologists see things differently.

>

> So, many of my symptoms have disappeared since I have started

> treatment. However, I still wonder...

>

> How will I know if it is Still's and it is just temporarily

going

> away?

>

> It's just so difficult. I have doctors who DEFINITELY disagree on

> the diagnosis as well as the treatment.

>

> Any insight?

>

>

>

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Hey .

Unfortunately the symptoms of many diseases mimick those of Stills

and the medication used to treat those symptoms also alleviate some

of the symptoms of Stills. Like most here in this group, I have gone

through a myriad of diagnoses before Stills. Included in this list

is Multiple Sclerosis, Undifferentiated Connective Tissue Disease,

Mixed Connective Tissue Disease, Bechet's Disease, Lupus and so on

and so on... The main medicines to treat any of theses diseases and

Stills disease are NSAID's, DMARD's and TNF's. These are the " front

line " of defense in managing most of these diseases ( and including

yours, I'll bet! ).

You are your only advocate. Research, research, research. If you

don't like your doctors, fire them and find others. If you don't

like your medicines, tell your doctor to change them. The search for

a doctor who will treat not only your disease, but you as a person is

a long voyage. Your search is only beginning. Do not lose faith and

have patience. Be tough with your doctors and those managing your

health. They work for you. Hang in there, you are not alone.

Joe

>

> Hi All,

>

> I was posting here about 2 months ago. Several doctors were giving

> me the possible diagnosis of Still's Disease. I was in the

hospital

> several times this summer. My diagnosis went from bacterial

> infection to Rheumatic Fever to virus to Still's and many more. At

> least 3 doctors down here think Still's is a possibility.

According

> to the University of Miami, " it's not a textbook case, however. "

> Hmmm...it seems they have only seen it in a textbook...

>

> Anyway, I have since has a positive Lyme test and I went to see a

> specialist in this area. He feels definitively that I have Lyme

> Disease. So, I am being treated for that currently.

>

> My doctors down here just do not think it is Lyme. It seems

> Rheumatologists see things differently.

>

> So, many of my symptoms have disappeared since I have started

> treatment. However, I still wonder...

>

> How will I know if it is Still's and it is just temporarily

going

> away?

>

> It's just so difficult. I have doctors who DEFINITELY disagree on

> the diagnosis as well as the treatment.

>

> Any insight?

>

>

>

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It is very tricky and it is easy to say do not worry. What ever stay with us

and let us know how you are.

Ask the rheumy who said it was not Lyme Why he says that.

Did you have spiking fevers?? Weird sore throat? Rash?( Stills stuff)

It seems like it is wise to try the antibiotics since cure is a good word if

it is Lyme.

Otherwise, many of these diseases are treated the same...mild level

treatment, serious level treatment etc...so as long as a good doctor monitors

you,

you seek other opinions and rest I think you are doing everything. I hope it

goes away for ever and ever. But I hope you stay here just to be our friend!!

Hang in there!...Remember not everyone is a textbook case.

Hugs

Liz NJ

************************************** See what's new at http://www.aol.com

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It is very tricky and it is easy to say do not worry. What ever stay with us

and let us know how you are.

Ask the rheumy who said it was not Lyme Why he says that.

Did you have spiking fevers?? Weird sore throat? Rash?( Stills stuff)

It seems like it is wise to try the antibiotics since cure is a good word if

it is Lyme.

Otherwise, many of these diseases are treated the same...mild level

treatment, serious level treatment etc...so as long as a good doctor monitors

you,

you seek other opinions and rest I think you are doing everything. I hope it

goes away for ever and ever. But I hope you stay here just to be our friend!!

Hang in there!...Remember not everyone is a textbook case.

Hugs

Liz NJ

************************************** See what's new at http://www.aol.com

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:

I am very new to this disease, diagnosed last December, but it does

seem that there are very few " textbook " cases anyway. I know the say

they diagnosed mine was by excluding all those other diseases like

Rheumatic fever, lymphoma, leukemia, lymes, etc. Since there is not

one test that says " yes, this is Still's " , we end up just having to

trust and see if the medications recommended provide any relief. I

hear that you don't always know until a " flare-up " happens. It was

the Rheumatologist in my case that made my diagnosis, although he has

only seen three cases now in 40 years of practice.

Keep the faith and be persistent.

---

In Stillsdisease , " edandcyn1969 "

wrote:

>

> Hi All,

>

> I was posting here about 2 months ago. Several doctors were giving

> me the possible diagnosis of Still's Disease. I was in the hospital

> several times this summer.

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:

I am very new to this disease, diagnosed last December, but it does

seem that there are very few " textbook " cases anyway. I know the say

they diagnosed mine was by excluding all those other diseases like

Rheumatic fever, lymphoma, leukemia, lymes, etc. Since there is not

one test that says " yes, this is Still's " , we end up just having to

trust and see if the medications recommended provide any relief. I

hear that you don't always know until a " flare-up " happens. It was

the Rheumatologist in my case that made my diagnosis, although he has

only seen three cases now in 40 years of practice.

Keep the faith and be persistent.

---

In Stillsdisease , " edandcyn1969 "

wrote:

>

> Hi All,

>

> I was posting here about 2 months ago. Several doctors were giving

> me the possible diagnosis of Still's Disease. I was in the hospital

> several times this summer.

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,

?? I have to agree that there is no one textbook case of still's. It would make

it alot easier to diagnose and we would not have to be put through all the

painful tests and misdiagnoses. I am finding out the hard way what autoimmune

diseases can do to an already weak immune system.Please keep your spirits up, I

know that is easier said then done. I am finding that my friends and family

support has helped alot.

Danni

________________________________________________________________________

Email and AIM finally together. You've gotta check out free AOL Mail! -

http://mail.aol.com

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,

?? I have to agree that there is no one textbook case of still's. It would make

it alot easier to diagnose and we would not have to be put through all the

painful tests and misdiagnoses. I am finding out the hard way what autoimmune

diseases can do to an already weak immune system.Please keep your spirits up, I

know that is easier said then done. I am finding that my friends and family

support has helped alot.

Danni

________________________________________________________________________

Email and AIM finally together. You've gotta check out free AOL Mail! -

http://mail.aol.com

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HI ,

Don't really have a lot of answers for you. Just wanted to say that I too had

a positive Lyme test. I also was diagnosed with many different things from

bacterial infection to Parvo virus. I think Still's is just what we wind up with

when everything else is ruled out. As for a textbook case, I don't think one

exists. Feel better soon.

</HTML>

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HI ,

Don't really have a lot of answers for you. Just wanted to say that I too had

a positive Lyme test. I also was diagnosed with many different things from

bacterial infection to Parvo virus. I think Still's is just what we wind up with

when everything else is ruled out. As for a textbook case, I don't think one

exists. Feel better soon.

</HTML>

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