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I thought this was the BPD not the DS??? I can't read the language

to figure it out.. but recalling (dimly) what a precious poster wrote.

, Seattle

> sounds good Nick......I would hope though if anyone goes that far

from home

> that they take someone with them just in case...(same as with Spain

except

> Dr B is beloved by all who have gone there)

> He does sound too good to be true!! (the fee) glad he is another

option.

>

> Judie

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In a message dated 10/20/2001 6:34:51 PM Central Daylight Time,

bohlinjt@... writes:

> Hi! My name is Katrina and I'm investigating DS! I'm looking for

> all the info I can get. I live in NW Indiana. Anyone know of

> doctors in my area (Indiana, Illinois, or Michigan) that do this type?

> Any help would be great.

>

> Thanks,

> Trina

>

>

>

Trina,

I live south of Chicago and went to Dr. Hess in Bowling Green, OH. It is a

very easy drive straight out I-80 and then just a little south when you get

to toledo. From my house it takes 4.5 hours of very easy driving.

Dawn--South Suburban Chicago area

Dr. Hess, Bowling Green, OH

BPD/DS

4/27/00

www.duodenalswitch.com

267 to 165 5' 4 "

size 22 to size 10

have made size goal

no more high blood pressure, sore feet, or dieting

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  • 3 years later...
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Allo Mélissa,

Je suis aussi de Québec. Je vais te contacter en privé si tu veux. J'ai un

garçon de 20 mois qui a le RSS. Pour tous ceux qui veulent me parler en

français mon adresse est isalac2@....

****

Hi everybody, I'm from Quebec too. I don't want to bother you in French so if

you want to talk with me in French you can contact me in private at

isalac2@.... I have a 20 months old son with RSS.

Mélissa wrote:

Hi everyone

my name is melissa and i'm 20 years old. I live in Québec

(Canada) and i would like to talk with other person like me, with

the siLver syndrome. I speak french but i try to speak

english.

Bonjour tous le monde,

Je m'apelle Mélissa et j'ai 20 ans je vis au

Canada et je parle Français mais j'essaie de me débrouiller en

anglais. Je suis très contente de voir qu'il y a d'autre gens comme

moi avec le syndrome de silver russell. J'aimerais beaucoup parler

avec des gens qui ont la même chose que moi. Merci

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

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