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At 6:26 PM +0000 10/5/01, unreel2me@... wrote:

>Hi Everyone,

>

>My name is Amy and I have been researching WLS for about 2 years. I

>have just recently discovered the DS procedure and I am very curious

>about why people who have had RNY are so against it. Are they

>jealous because it was not available to them?

Could be. Then, their physicians warn them about the " dangers " of

malabsorption, etc., ans, of course, since physicians are demi-gods,

they buy into it.

>It sounds like the

>superior method of WLS and I can't wait until more surgeons learn to

>do it.

>I am currently trying to get an approval to go to California for the

Why California? Where do you live?

>surgery but every surgeon I have come across is requiring a down

>payment of at least $12K!

From what I read on this list, Rabkin might charge $12K, but

Keshishian charges a lot less ($2000 or $4500?). Nick, what say you

as one of Dr. K's latest patients?

>Yikes! Anyone out there have very recent

>experience with Blue Cross/Blue Shield covering a California surgeon?

What's this California obsession?

>I am extremely anxious to get on with this surgery, I am afraid I may

>have to resort to the " old fashioned " RNY after all.

Think long and hard about that. This isn't like a choice between

vanilla and strawberry ice cream. It's more like a choice between

riding buses or taking cabs (if not limousines). And it is a

life-long choice.

--Steve

--

Steve Goldstein, age 61

Lap BPD/DS on May 2, 2001

Dr. Elariny, INOVA Fairfax Hospital, Virginia

Starting (05/02/01) BMI = 51

BMI on 09/27 = 41 (-66 lb.)

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  • 1 month later...

Hi ette,

What province are you in, I'm in Orangeville, Ontario.

, mom of 3 1/2 Autism Spectrum Disorder

> I'm new to the group. We suspect that our three year old son

is

> somewhere on the autism spectrum but we are still awaiting a

diagnosis.

> We live in Canada and there is a huge wait in the health care

system. I

> just found out that our health plan will pay for most of a private

> diagnosis so we are going that route. In the meantime, I am in the

> process of putting on a GFCF diet. He has been on the diet for

> about 2 weeks but we have had some slip ups as a result of this all

> being so new. Interestingly enough I am recognizing some of the

> regressions I have been reading about on this message board -

chewing

> his sleeves, night waking, an unbelievable tantrum at the doctor's

> office today. I would be interested in hearing from other people in

> Canada about Canadian GFCF products, other alternative therapies I'm

> hearing about hear, and if it is possible to find a doctor that will

> support me. I told my GP about the diet today and gave me a look

that

> told me she thought it was pitiful that I was resorting

to " alternative

> therapies " that would not work. This site has been a wealth of

info.

> Thanks to everyone.

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  • 3 years later...

Hi, . How wonderful to have another NZ member! And you

already have plans to go to the convention. That is terrific.

The convention will be one of the best experiences you will ever

have. It is like being with one huge family, even though you will

not have met most of the people there. It is the one time that I

feel I can relax and let my son be part of a group where he does not

stand out, but really fits in. Of course, he is 16 now and will be

17 by the time of the convention (YIKES!!!), but he loves it as much

as I do and is comforted by the large number of kids who have g-

tubes as he does. No one stares, no one questions that he is really

the age that he is (most think he is 12 at best) and a whole lot of

people like to see him as a glimpse into the future for their own

children. He is happy to oblige.

Hint: If you really want to make friends with s, bring

her some Tim Tams. After being taught by Forsyth, I showed

her the Tim Tam Implosion. She is as hooked as I am. (Fortunately

my Aussie friend ne brought me a supply of them last summer

and they are stored in my freezer to last me a long while.)

Jodi Z

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  • 4 weeks later...

Hi ,

Welcome to the group, you've found a great bunch of people here.

We do have an adult in our group who's from Scotland, she has RSS.

My daughter Olivia has just turned 5 and has RSS.

This is a very resourceful group of people and we're all willing

to answer any questions that you may have.

What was your son's birth weight? and his weight now?

Leah, mom to 9 and Olivia 5, 19lbs, 34 " , RSS, OI, lots of

meds

>

> Hi, my name is . I'm from Scotland. My son, Blair, is 14

months

> old and was diagnosed with RSS 2 months ago. I would love to chat

to

> other parents about his condition. Are there any ish families

in

> the group?

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Hi ,

Where about in Scotland are you? I'm ish - but I won't be much

use to you as I now live in New Zealand (married to a kiwi!!) -

however, my parents and wider family are all in Fife and we do get

home for a visit every couple of years. On our last trip home we

consulted with the endo at the " Sick Kids " in Edinburgh - he was

really nice and we really just made the contact on the off chance

that we decide to move back to Scotland at some point in the future.

There was a family on this list serve from Inverness - but I haven't

heard from them for about 18mths.

When we went to the sick kids in Edinburgh the endo thought he had

about 20 RSS patients at that time.

How is Blair doing? Do you have good care for him where you are?

Best Wishes

>

> Hi, my name is . I'm from Scotland. My son, Blair, is 14

months

> old and was diagnosed with RSS 2 months ago. I would love to chat

to

> other parents about his condition. Are there any ish families

in

> the group?

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Hi Leah and Tonya,

Thank you both for replying, you all sound so friendly. It's great to have

so many people to share things with. Blair was born at 37 weeks and weighed

3lbs13oz. At 14 months now he probably weighs about 17 lbs and is about 62cm. We

feel very lucky because he doesn't have alot of the symptoms that so many of

the kids have. He has small stature, low set ears and a slight blue tinge to

the white of his eyes but that seems to be it. He is a good eater, great

sleeper and the best natured boy i've ever known. He has been walking since the

age of 1 and can say a few words. He is incredibly handsome with a great

sense of humour. I would love to hear from you all.

Best Wishes from (mum to Greg age6 nonRSS and Blair 14 months RSS)

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Hi karen my name is kim and i'm an rss adult age 26 and live in scotland. In Oct

2003 i attended a child growth foundation conference in england and net a family

from glasgow, have you joined the CGF?,as they could maybe put you in contact

with any rss families in scotland, i'm on aol ( mightyatom2@...) if you want

to email me or instant message me privately anytime.Look forward to hearing from

you soon

Hi, my name is . I'm from Scotland. My son, Blair, is 14 months

old and was diagnosed with RSS 2 months ago. I would love to chat to

other parents about his condition. Are there any ish families in

the group?

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- Welcome to the group. I have a daughter - 15 1/2 months - she was born

full term at 4# 10oz, 18 1/2 " . She has been diagnosed SGA with ?RSS - we get

different oppinions from different Dr.s. walked at 13 months, says about

6 words - she is very bright and social. Now at 15 months she weighs 15lb 15oz

and is 27 " long. She has been my easiest baby yet - good sleeper - always

happy. You have found a great group here. Jane - mom to 2 boys (wild ones) and

, SGA ?RSS and holding her own with 2 big brothers.

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  • 1 year later...
Guest guest

Hello Group

My name is , I recently had the surgery on My 31st

2006. At the time i weighed at 347 and stood at 5'9. After my first

week i was 327, now im at 333. I called my doc nurse she said it was

normal to gain weight if im excersing and lifting weights, and that

muscle mass weighs more, which i knew. but im a lil concerned cuz i can

drink alot of water in a sitting and eat a can of soup enterily as

well, im hoping i havent stretched out my pouch. Has anyone else

experienced this?

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Guest guest

Puerto--First of all you posted when lots of us are or were busy leaving town or preparing for the upcoming holiday. The day after you posted there were only 3 posts! The next day there were only 8 posts! The next day only 9!

Secondly, in your original post (see below) you asked if anyone else had experienced this. Since no one replied to you --apparently they had not. So why get mad about that.

Thirdly, what were you thinking? Eating a whole can of soup when the Binder clearly states you should only be having only 1/4 cup, 3 times per day. As far as the water it has been said time and again "sip, sip, sip." Have you stretched your pouch? I'm sure you have. You went through the pain of surgery so why not work your "tool" the way it was meant to be, instead of testing it to see how much you can get away with. In the end you only hurt yourself. Your anger and vile comments are misdirected.

on 6/27/06>> Hello Group> > My name is , I recently had the surgery on My 31st > 2006. At the time i weighed at 347 and stood at 5'9. After my first > week i was 327, now im at 333. I called my doc nurse she said it was > normal to gain weight if im excersing and lifting weights, and that > muscle mass weighs more, which i knew. but im a lil concerned cuz i can > drink alot of water in a sitting and eat a can of soup enterily as > well, im hoping i havent stretched out my pouch. Has anyone else > experienced this?> > >

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