Re: Dr. Chez, in ILL............

[Guest guest]

Donna,

We see Chez's associate DrArshad. One thing I can tell you is they NEVER

run on time. We've waitedup to 90 minutes before. So be prepared with lots

of stuff for your sweetie. E me privately for specifics. (ie: he is really

into prescribing meds).

kweav@...

Dr. Chez, in ILL............

>Hi the subject tells it all, I would love to hear from anyone who has seen

this Dr. and what you think?

>Thanks

>you can email me private if you want.

>markswis@...

>Donna/Indiana

>Mom to 4 sons, Carl 18 (ADD)

>Hayden (DSI,Speech Delay, Seizure Disorder, Possible PDD-NOS), (DSI),

Trevor(NT) 33 months

>Scrapbook Addict

>To view my scrapbook and family go to:

>http://albums.photopoint.com/j/AlbumIndex?u=200373&a=2424512

> " The mother of a disabled child will never take for granted a " spoken

word " . She will never consider a " step " ordinary. When her child says

" momma " for the first time, she will be present at a miracle and know it "

Erma Bombeck

>

>

>

>

>

[Guest guest]

Donna,

We see Chez's associate DrArshad. One thing I can tell you is they NEVER

run on time. We've waitedup to 90 minutes before. So be prepared with lots

of stuff for your sweetie. E me privately for specifics. (ie: he is really

into prescribing meds).

kweav@...

Dr. Chez, in ILL............

>Hi the subject tells it all, I would love to hear from anyone who has seen

this Dr. and what you think?

>Thanks

>you can email me private if you want.

>markswis@...

>Donna/Indiana

>Mom to 4 sons, Carl 18 (ADD)

>Hayden (DSI,Speech Delay, Seizure Disorder, Possible PDD-NOS), (DSI),

Trevor(NT) 33 months

>Scrapbook Addict

>To view my scrapbook and family go to:

>http://albums.photopoint.com/j/AlbumIndex?u=200373&a=2424512

> " The mother of a disabled child will never take for granted a " spoken

word " . She will never consider a " step " ordinary. When her child says

" momma " for the first time, she will be present at a miracle and know it "

Erma Bombeck

>

>

>

>

>

[Guest guest]

I had to pull some strings to even get to see him a few years ago for my

daughter, as he was so busy. People I spoke to said I'd either love him or

hate him. I felt both ways. I loved the fact that he was willing to try

" theoretical " interventions within what I truly felt were very responsible

perameters of medical practice. (My daughter has a chronic, co-morbid,

potentially life threatening condition) What I hated about him was that he

was all too willing to take all the credit for her improvemments and none of

the responsibility for negative side effects arising from his treatment. I

finally found I couldn't work with this and we stopped seeing him.

Dr. Chez, in ILL............

> Hi the subject tells it all, I would love to hear from anyone who has seen

this Dr. and what you think?

> Thanks

> you can email me private if you want.

> markswis@...

> Donna/Indiana

> Mom to 4 sons, Carl 18 (ADD)

> Hayden (DSI,Speech Delay, Seizure Disorder, Possible PDD-NOS),

(DSI), Trevor(NT) 33 months

> Scrapbook Addict

> To view my scrapbook and family go to:

> http://albums.photopoint.com/j/AlbumIndex?u=200373&a=2424512

> " The mother of a disabled child will never take for granted a " spoken

word " . She will never consider a " step " ordinary. When her child says

" momma " for the first time, she will be present at a miracle and know it "

Erma Bombeck

>

>

>

>

>

[Guest guest]

We saw Dr. Chez years ago. At one point he thought my son had spinal

muscular atrophy which is always fatal. When the diagnosis was changed to

myasthenia gravis he literally was jumping up and down for joy and I thought

it was because that is not considered a fatal disease. Then he starts

saying this is so rare, most ped neuros go through their whole career

without ever seeing one case 'cause the odds are literally one in a million,

and something was said about how he might be able to get something published

in a med journal and things like that, so then I was left wondering was he

happy for my son and for us or was it a feather in his cap to have a patient

with such a rare disease? (Sounds strange and sort of perverted,but I have

heard that some patients are considered " status symbols " among doctors, and

I dealt with this in another instance with a different doctor.) I really

don't know which it was. The night before he was perfectly willing to let

my son die while he was in respiratory arrest when we had no definitive

diagnosis at the time and he seemed much more interested in him after the MG

diagnosis and he was NOT happy when we changed hospitals and doctors.

Re: Dr. Chez, in ILL............

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