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Re: CONTACTING WHITEMAN

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Hi Anne,

Not sure about new patients - we were new just this month. Never know unless you call. I found everyone helpful. Carla had a baby girl the week before we got there. Just got the 14-page report yesterday. We were there 2/4-6/04.

Here is the phone number:

I do know that a typed letter with condensing J.D.'s years helped tremendously. Plus I scanned pictures throughout his years and placed on one page to see the growth pattern.

We go back in May.

Good luck.

Darlene

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confirmed that Dr. Whiteman is not taking any new patients.

Possibly in September he will be. They are referring people to other

docs in the genetics dept who she says are not mito experts.

This request was not for me but for another family. I feel sad that

there are so few choices for families to go to get expert advice once

the diagnosis is made.

We are fortunate to have a local doctor that is not afraid of the

disease and not too proud to listen to me and to national mito

experts who he consults by phone. But there seems to be such a

paucity of physicians who are willing to dive in and learn and care

for kids like ours.....they fall back on " i'm not a metabolic expert "

and I guess just assume someone else will care for the child. Makes

me feel blessed for the doctor we have but angry and sad that now

another practice is closed for families who despertaley need help.

We desperately need more primary physicians to come forward and be

willing to learn along side the family and not be so scared of the

disease!

Anne

Anne

> Hi Anne,

> Not sure about new patients - we were new just this month.

Never know unless you call. I found everyone helpful. Carla had a

baby girl the week before we got there. Just got the 14-page report

yesterday. We were there 2/4-6/04.

> Here is the phone number:

> I do know that a typed letter with condensing J.D.'s years

helped tremendously. Plus I scanned pictures throughout his years

and placed on one page to see the growth pattern.

> We go back in May.

> Good luck.

> Darlene

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Share on other sites

confirmed that Dr. Whiteman is not taking any new patients.

Possibly in September he will be. They are referring people to other

docs in the genetics dept who she says are not mito experts.

This request was not for me but for another family. I feel sad that

there are so few choices for families to go to get expert advice once

the diagnosis is made.

We are fortunate to have a local doctor that is not afraid of the

disease and not too proud to listen to me and to national mito

experts who he consults by phone. But there seems to be such a

paucity of physicians who are willing to dive in and learn and care

for kids like ours.....they fall back on " i'm not a metabolic expert "

and I guess just assume someone else will care for the child. Makes

me feel blessed for the doctor we have but angry and sad that now

another practice is closed for families who despertaley need help.

We desperately need more primary physicians to come forward and be

willing to learn along side the family and not be so scared of the

disease!

Anne

Anne

> Hi Anne,

> Not sure about new patients - we were new just this month.

Never know unless you call. I found everyone helpful. Carla had a

baby girl the week before we got there. Just got the 14-page report

yesterday. We were there 2/4-6/04.

> Here is the phone number:

> I do know that a typed letter with condensing J.D.'s years

helped tremendously. Plus I scanned pictures throughout his years

and placed on one page to see the growth pattern.

> We go back in May.

> Good luck.

> Darlene

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