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Amy,

Your children's problems certainly sound like they might be diet

related. One thing you might want to do is keep a detailed food diary for a

few weeks before you start the diet. You might be able to pinpoint some

common denominators and save yourself some legwork later. Keep up on the

diary as you embark on the diet and make sure to note symptoms like the

eczema, tantrums etc.

Pat in Ohio

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Welcome! I'm new at this too but am learning so much! Hey, are you going to

get them evaluated at all? I took my daughter to a developmental pediatrician

for diagnosis. Also, are you into scrapbooking? I love it! But I've done

nothing with it since our diagnosis...one month ago. Hugs,

H, mom to 3 yrs, PDD; and 23 months

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In a message dated 07/07/2001 6:09:07 AM Central Daylight Time,

armywife1993@... writes:

<< Hi, my name is Lori and I just joined the list. I have a question

regarding the dumping syndrome. I understand with the DS procedure

you don't have it. I am a big sweets eater right now and think that

the dumping syndrome would be a benefit for me post-op. (that might

sound crazy but it's true) Can anyone tell me if they loved sweets

pre-op and how you are doing post-op? I really prefer the DS

procedure but given my love for sweets I wonder if the RNY would be

the better procedure for me to have. Any info would be greatly

appreciated. You can email me personally if you like.

Thanks so much,

LORI

>>

I was a sweets eater pre-op. I did not eat many sweets early post op (first

6 months or so). They did not appeal to me. Now I eat my share of sweets.

I probably would get a few more pounds off if I didn't, but I am very happy

at the weight I am at WITH my sweets. You have to remember that most of the

sweets that appeal to us are a sweet/fat combination. An example is ice

cream. I eat the really good stuff that is high in fat. But with the BPD/DS

most of the fat doesn't count, so it doesn't turn out to be that calorie

ladden for us. My weight is VERY stable and I eat sweets whenever I want

which is sometimes several times a day.

YMMV

Dawn--Chicago metro--south

Dr. Hess, Bowling Green, OH

BPD/DS

www.duodenalswitch.com

267 to 165 5'4 "

size 22 to size 10

have made size goal, weight goal may need to be adjusted.

no more high blood pressure, sore feet, or dieting!

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Lori:

You need to research everything you can to determine which surgery is best

for you. Two sites that I can recommend are:

Our moderator has put together a wonderful site with a wealth of

information:

http://www.duodenalswitch.com

This is a site that is owned by NYU. Click the link about surgery

procedure, it will give you a very good explanation of the three types of

surgeries.

http://thinforlife.med.nyu.edu/

Most of the members on this list have had the DS procedure or are pre-op.

We have chosen this procedure for a variety of reasons and I am sure at the

recommendation of our doctors. Many of the doctors do more than one type of

surgery. You need to make any decision on your own with the help of your

doctor. However, I will tell you that I am very pleased with my outcome. I

have never dumped and do not want to dump. I personally believe that the

disease of Morbid Obesity has punished and restricted our lives enough. If

you at the stage in this journey that you are seriously considering WLS

surgery, you know what I mean. I do not need to be burdened with the

dumping syndrome to feel like I've done the right thing. When you have WLS

surgery many things will change. It is different for each person, but you

will have a different perspective about food and what you eat. Immediately

after my surgery and for about 5-6 months there were things that I either

could not eat or had no desire to eat. I am 9 months out now and I can eat

anything. There are still things that I do not want to eat. I also do not

consume any carbonated beverages, as they have a tendency to fill me up and

make me gaseous. I do not miss them. I just do not eat as much and my

weight is coming down.

Also, you need to really understand what the dumping syndrome entails. Read

as much as you can about it because for some people it can be very

debilitating for several hours. When I was doing the research for my

surgery I remember reading a post from a guy on another list. He recounted

a story where he had taken a church group bus tour to Atlantic City. This

person had the RNY surgery. There was a buffet table there and he asked the

caterer what was in some of the dishes to be sure he wasn't eating anything

with sugar. On the way home on the bus, he was hit with the dumping

syndrome. He spent the next several hours curled up in a fetal position on

a Greyhound bus because there was something in the buffet he should not have

eaten. I knew I did not want to live like that. Some people look at the

dumping syndrome as a watchdog, I did not go through this process to be

punished like that.

You may also read on other surgical list that the DS surgery causes you to

be a bathroom hermit and have nothing but odorous gas. This is not true.

You will go through an initial period immediately after surgery that you may

experience more visits than you are accustomed to having. Much of that is

your due to your body making the adjustment from the surgery, the anesthetic

as it clears your system and your ability to become accustomed to the way

food will react with the changes that have been made with your digestive

system. In addition, as with any WLS surgery, you should consume more water

to flush out your system (we should do this for our health without the

surgery) and thus this prompts more visits. I do have more BMs that I did

before, but then I only went once per day before. However, they do not

restrict my life in any negative way.

Good luck to you in your decision and hopefully your eventual surgery.

Kathie from MD

Lap DS, Dr Gagner, Mount Sinai, NY

New here

> Hi, my name is Lori and I just joined the list. I have a question

> regarding the dumping syndrome. I understand with the DS procedure

> you don't have it. I am a big sweets eater right now and think that

> the dumping syndrome would be a benefit for me post-op. (that might

> sound crazy but it's true) Can anyone tell me if they loved sweets

> pre-op and how you are doing post-op? I really prefer the DS

> procedure but given my love for sweets I wonder if the RNY would be

> the better procedure for me to have. Any info would be greatly

> appreciated. You can email me personally if you like.

>

> Thanks so much,

>

> LORI

>

> armywife1993@...

>

>

> ----------------------------------------------------------------------

>

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Lori,

I am 11 weeks out from my DS surgery and I can say that I not only do not

crave sweets, I don't even take them when they are offered. They just hold

no appeal for me now. I did have a bite of cake and ice cream once, at about

five or six weeks out. I was able to tolerate it well, but it just was no

big thrill. I wish I could explain it better than that!

That said, if I really wanted something I would have it. But after eating

protein, and trying to get in a bit of veggies, etc., I just don't have room

for it at this point. But if I really, really wanted something I would have

a bite.

My mother had weight loss surgery around 25 years ago. Whatever the nature

of the surgery, she most definitely came away with dumping syndrome. One of

my most vivid memories is that of my mother passing out on the floor of a

restaurant after eating pasta. It was terribly frightening. She used to

think she just had to " lie down " after eating certain things, and it was only

then that she realized she was actually passing out.

I don't think I, personally, could handle feeling sick on a regular basis. I

could not tolerate that as part of my life for the duration. Now, 11 weeks

post DS surgery, I feel perfectly fine 99.9% of the time. I feel great, can

eat anything I want (small amounts) and feel satisfied. And I am losing

weight! Not as fast as some, but I am losing. I can't imagine anything

better than this.

Just my 2-cents...

Dawna

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HI LORI, MY NAME IS MELANIE TAYLOR AND I WILL BE HAVING THE DS ON JULY THE 10TH.I HAVE BEEN TOLD THE RNY IS BETTER FOR SWEET EATERS AND I WOULD SUGGEST YOU TALK WITH OTHER RNYERS TO GET MORE INFO..HOPE U FIND WHAT U R LOOKING FOR HERE.WE R A GOOD GROUP OF PEOPLE AND LOVE TO HELP ANYONE WE CAN.WELCOME ABOARD AND HAPPY RESEARCHING. MELANIE TAYLOR armywife1993@... wrote: Hi, my name is Lori and I just joined the list. I have a question regarding the dumping syndrome. I understand with the DS procedure you don't have it. I am a big sweets eater right now and think that the dumping syndrome would be a benefit for me post-op. (that might sound crazy but it's true) Can anyone tell me if they loved sweets pre-op and how you are doing post-op? I really prefer the DS procedure but given my love for sweets I wonder if the RNY would be the better procedure for me to have. Any info would be greatly appreciated. You can email me personally if you like.Thanks so much,LORIarmywife1993@...----------------------------------------------------------------------

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Hi Lori,

Since I'm pre-op for the DS, you know which surgery I think provides better

quality of life -- and that's what I'm after. With the DS, after the

recovery period you can eat fairly normal small meals that include most

foods. Your stomach functions properly, you don't have the problems with

getting things " stuck " or dumping - which is an awful experience. With the

RnY you can ony eat tiny amounts, and most people say their food choices are

extremely restricted FOR LIFE. There is also more of a problem with B

vitamin absorption because of the tiny stomach pouch. As someone who has a

failed VBG I know how awful it feels to have things get " stuck " and have to

throw up. After 10 years, I still have that experience, and can't eat most

meats, raw vegetables or fruits.

At a recent DS support group meeting I heard that DS patients who lose the

most weight are ones who avoid simple sugars and exercise. The DS will not

prevent simple sugars from being absorbed.

I would really encourage you to look at any WL surgery as a tool, and to

talk to as many people as you can about quality of life long term after the

surgery. All the WL surgeries require some changes in life style after the

surgery. I've heard many people say the dumping syndrome with the RnY will

prevent them from eating sugar and fat, but many people who have the RnY

never do dump! Research, research, research and talk to lots of people about

how they feel, what they can eat, how their health is, etc. longer term.

Take your time about making this decision.

I also should add that there are many people who come to this group and

research this surgery who have had a RNY that failed and who want a revision

to DS. I could be wrong, but it is my understanding that revision from rny

to DS is quite difficult.

Only you can make the decision about what is right for you. I send you all

best wishes for making the right decision.

Peace,

Robyn

New here

> Hi, my name is Lori and I just joined the list. I have a question

> regarding the dumping syndrome. I understand with the DS procedure

> you don't have it. I am a big sweets eater right now and think that

> the dumping syndrome would be a benefit for me post-op. (that might

> sound crazy but it's true) Can anyone tell me if they loved sweets

> pre-op and how you are doing post-op? I really prefer the DS

> procedure but given my love for sweets I wonder if the RNY would be

> the better procedure for me to have. Any info would be greatly

> appreciated. You can email me personally if you like.

>

> Thanks so much,

>

> LORI

>

> armywife1993@...

>

>

> ----------------------------------------------------------------------

>

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Dawn wrote:

> I was a sweets eater pre-op. I did not eat many sweets early

> post op (first 6 months or so). They did not appeal to me.

> Now I eat my share of sweets.

I could have written these very words. All true for me too.

> I probably would get a few more pounds off if I didn't, but I

> am very happy at the weight I am at WITH my sweets.

A big ditto here too. I often feel like I'm " cheating " because I truly

do not limit myself, except for the limitation imposed by my stomach

size. I indulge in sweet treats throughout the day, but usually just a

bite here and there -- a Dove Promise or two, or a cookie or two. I was

never, and still am not one to overindulge or do the " whole bag of

cookies " type of thing.

> You have to remember that most of the sweets that appeal to us

> are a sweet/fat combination. An example is ice cream. I eat

> the really good stuff that is high in fat. But with the BPD/DS

> most of the fat doesn't count, so it doesn't turn out to be

> that calorie ladden for us.

Yep. Delphine told me ages ago that if I wanted to have milk, for

example, I'd be better off having whole milk, since it is lower in sugar

ounce-for-ounce than skim milk. Same for ice cream -- eat the premium

stuff, since the proportion of fat is higher, we won't absorb as much of

the premium stuff as we would of a " skimmer " ice cream that is higher in

sugar per serving.

My whole life, ice cream has been my indulgence, and I ate it every

single day without fail. For the first year post-op, I didn't have it as

much. But now, I'm pretty much back into my routine of having 2-3 scoops

of ice cream as my evening snack, and I do this more days than not.

I'm not advocating my way for anyone else! None of the DS docs are going

to give us " permission " to be reckless about sugars, and Dr. Rabkin

might want to bop me one if I admitted to him how many treats I indulge

in. LOL. But from day one, I have been pretty stubborn in my reluctance

to " artificially " limit myself, or to adopt a " diet mindset " . I

researched the DS and my intent was to have faith in all the clinical

data, which shows us maintaining our weight loss over the long term.

I'm at the end of my weight loss window now, so I'm in a nervous spot

where I'm watching the scale and hoping and praying that all the

research will hold true for me! :) Only time will tell on that one.

Never thought getting HERE would be harder than the losing stage, but it

kinda is, since I'm in the " waiting for the other shoe to drop " stage

right now. It can be unnerving!

M.

---

in Valrico, FL, age 38

Starting weight 299, now 156

Starting BMI 49.7, now 26.0

Lap DGB/DS by Dr. Rabkin 10-19-99

http://www.duodenalswitch.com

Direct replies: mailto:melanie@...

_________________________________________________________

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I hope that I un-crave sweets post too! Re: New here Lori,I am 11 weeks out from my DS surgery and I can say that I not only do notcrave sweets, I don't even take them when they are offered. They just holdno appeal for me now. I did have a bite of cake and ice cream once, at aboutfive or six weeks out. I was able to tolerate it well, but it just was nobig thrill. I wish I could explain it better than that!That said, if I really wanted something I would have it. But after eatingprotein, and trying to get in a bit of veggies, etc., I just don't have roomfor it at this point. But if I really, really wanted something I would havea bite.My mother had weight loss surgery around 25 years ago. Whatever the natureof the surgery, she most definitely came away with dumping syndrome. One ofmy most vivid memories is that of my mother passing out on the floor of arestaurant after eating pasta. It was terribly frightening. She used tothink she just had to "lie down" after eating certain things, and it was onlythen that she realized she was actually passing out.I don't think I, personally, could handle feeling sick on a regular basis. Icould not tolerate that as part of my life for the duration. Now, 11 weekspost DS surgery, I feel perfectly fine 99.9% of the time. I feel great, caneat anything I want (small amounts) and feel satisfied. And I am losingweight! Not as fast as some, but I am losing. I can't imagine anythingbetter than this.Just my 2-cents...Dawna----------------------------------------------------------------------

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Hello everyone is there anyone here that has recently had surgery done by

Dr, Elariny in Va.

>

>Reply-To: duodenalswitch

>To: " Yahoo Group " duodenalswitch >

>Subject: Re: New here

>Date: Sat, 7 Jul 2001 15:18:02 -0700

>

>I hope that I un-crave sweets post too!

>

> Re: New here

>

>Lori,

>

>I am 11 weeks out from my DS surgery and I can say that I not only do not

>crave sweets, I don't even take them when they are offered. They just hold

>no appeal for me now. I did have a bite of cake and ice cream once, at

>about

>five or six weeks out. I was able to tolerate it well, but it just was no

>big thrill. I wish I could explain it better than that!

>

>That said, if I really wanted something I would have it. But after eating

>protein, and trying to get in a bit of veggies, etc., I just don't have

>room

>for it at this point. But if I really, really wanted something I would

>have

>a bite.

>

>My mother had weight loss surgery around 25 years ago. Whatever the nature

>of the surgery, she most definitely came away with dumping syndrome. One

>of

>my most vivid memories is that of my mother passing out on the floor of a

>restaurant after eating pasta. It was terribly frightening. She used to

>think she just had to " lie down " after eating certain things, and it was

>only

>then that she realized she was actually passing out.

>

>I don't think I, personally, could handle feeling sick on a regular basis.

>I

>could not tolerate that as part of my life for the duration. Now, 11 weeks

>post DS surgery, I feel perfectly fine 99.9% of the time. I feel great,

>can

>eat anything I want (small amounts) and feel satisfied. And I am losing

>weight! Not as fast as some, but I am losing. I can't imagine anything

>better than this.

>

>Just my 2-cents...

>

>Dawna

>

>----------------------------------------------------------------------

>

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In a message dated 7/9/01 1:15:05 AM, duodenalswitch writes:

<<

I hope that I un-crave sweets post too!

>>

Hi! I have not craved sweets much post-op. It got to the point where I

didn't even like the Viactiv chewable calciums in the first three weeks

post-op! LOL

Now if I have a 'sugar fix', it's almost always fruity flavored stuff

(usually drinks or ice cream), not chocolate. I wasn't a tremendous

chocoholic before but I certainly don't enjoy it now. I try to really watch

the intake of drinks, having only one glass of juice in the a.m. (not every

day even) and watered down halfway (I love grapefruit juice and also orange

juice). I have a wonderful flavored iced tea/iced tea milk when I go to

Chinatown every week (I'm sure that's LOADED with sugar, man). But, I just

don't 'crave' chocolate or sweets to any great degree. :):)

Good news, right?

all the best,

lap ds with gallbladder removal

January 25, 2001

five months post-op and still feelin' fab! :)

pre-op: 307 lbs/bmi 45

now: 239 (ok - maybe I'm going down South again???? Let's hope so!)

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i had surgery with Dr. Elariny on May 15, 2001

--- Sitton Sitton@...> wrote:

> Hello everyone is there anyone here that has

> recently had surgery done by

> Dr, Elariny in Va.

>

>

> >

> >Reply-To: duodenalswitch

> >To: " Yahoo Group " duodenalswitch >

> >Subject: Re: New here

> >Date: Sat, 7 Jul 2001 15:18:02 -0700

> >

> >I hope that I un-crave sweets post too!

> >

> > Re: New here

> >

> >Lori,

> >

> >I am 11 weeks out from my DS surgery and I can say

> that I not only do not

> >crave sweets, I don't even take them when they are

> offered. They just hold

> >no appeal for me now. I did have a bite of cake

> and ice cream once, at

> >about

> >five or six weeks out. I was able to tolerate it

> well, but it just was no

> >big thrill. I wish I could explain it better than

> that!

> >

> >That said, if I really wanted something I would

> have it. But after eating

> >protein, and trying to get in a bit of veggies,

> etc., I just don't have

> >room

> >for it at this point. But if I really, really

> wanted something I would

> >have

> >a bite.

> >

> >My mother had weight loss surgery around 25 years

> ago. Whatever the nature

> >of the surgery, she most definitely came away with

> dumping syndrome. One

> >of

> >my most vivid memories is that of my mother passing

> out on the floor of a

> >restaurant after eating pasta. It was terribly

> frightening. She used to

> >think she just had to " lie down " after eating

> certain things, and it was

> >only

> >then that she realized she was actually passing

> out.

> >

> >I don't think I, personally, could handle feeling

> sick on a regular basis.

> >I

> >could not tolerate that as part of my life for the

> duration. Now, 11 weeks

> >post DS surgery, I feel perfectly fine 99.9% of the

> time. I feel great,

> >can

> >eat anything I want (small amounts) and feel

> satisfied. And I am losing

> >weight! Not as fast as some, but I am losing. I

> can't imagine anything

> >better than this.

> >

> >Just my 2-cents...

> >

> >Dawna

> >

>

>----------------------------------------------------------------------

> >

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Hello ,

Welcome, and sorry you have to be here. As some of the others already

wrote in, it is extremely difficult to figure out where the end is in this

terrible disease, as it affects different people in different ways. I

believe your doctor is as unsure as anyone else, since the disease is so

rare. As our internist put it- " I will probably never see another case

like this in my lifetime " .

Of all the symptoms you mentioned that your wife is experiencing, I would

probably say that the two most alarming are the sleep apnea and swallowing

problems. Sleep apnea can cause sudden death, as the patient stops

breathing. Has she had a sleep study? Many of the MSA patients, including

my husband, use a CPAP at night to help with the brething difficulties.

The swallowing problems could cause fluid to leak in to the lungs, which

in turn can cause pneumonia. This is also one of the more common causes of

death in MSA patients, along with respiratory failure.

I hope you can glean some help and moral support from this group. They

have been a tremendous help to me and have given both me, my husband and

our doctor invaluable advice and resources to help fight this terrible

disease.

Best Wishes,

Maciejewski,

caregiver to Jeff, age 37, dx 2000

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Hello ,

Welcome, and sorry you have to be here. As some of the others already

wrote in, it is extremely difficult to figure out where the end is in this

terrible disease, as it affects different people in different ways. I

believe your doctor is as unsure as anyone else, since the disease is so

rare. As our internist put it- " I will probably never see another case

like this in my lifetime " .

Of all the symptoms you mentioned that your wife is experiencing, I would

probably say that the two most alarming are the sleep apnea and swallowing

problems. Sleep apnea can cause sudden death, as the patient stops

breathing. Has she had a sleep study? Many of the MSA patients, including

my husband, use a CPAP at night to help with the brething difficulties.

The swallowing problems could cause fluid to leak in to the lungs, which

in turn can cause pneumonia. This is also one of the more common causes of

death in MSA patients, along with respiratory failure.

I hope you can glean some help and moral support from this group. They

have been a tremendous help to me and have given both me, my husband and

our doctor invaluable advice and resources to help fight this terrible

disease.

Best Wishes,

Maciejewski,

caregiver to Jeff, age 37, dx 2000

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Whew..

I am overwhelmed with the messages.. :)

I made a mistake.. My wife is taking Magnesium and potassium.. Not

calcium... Sigh...

I guess you are all correct. Most Dr's have no idea what MSA/SDS is. We saw

our family Dr. today. He has no idea what this is. She was told by an

Electrophysiologist, he has been treating her PVC's for 8 years now, that

she has MSA/SDS..And sent her to a Neurologist who confirmed.

I now feel I have found a home, where I can share my frustration with this

disease, and with the comparatively low amount of research into this

disorder.

While Gwenna has not had a sleep study done, I plan to get her scheduled in

for one as soon as possible.

Peace and Love...

RE:New Here

>

> Hello ,

>

> Welcome, and sorry you have to be here. As some of the others already

> wrote in, it is extremely difficult to figure out where the end is in this

> terrible disease, as it affects different people in different ways. I

> believe your doctor is as unsure as anyone else, since the disease is so

> rare. As our internist put it- " I will probably never see another case

> like this in my lifetime " .

>

> Of all the symptoms you mentioned that your wife is experiencing, I would

> probably say that the two most alarming are the sleep apnea and swallowing

> problems. Sleep apnea can cause sudden death, as the patient stops

> breathing. Has she had a sleep study? Many of the MSA patients,

including

> my husband, use a CPAP at night to help with the brething difficulties.

> The swallowing problems could cause fluid to leak in to the lungs, which

> in turn can cause pneumonia. This is also one of the more common causes

of

> death in MSA patients, along with respiratory failure.

>

> I hope you can glean some help and moral support from this group. They

> have been a tremendous help to me and have given both me, my husband and

> our doctor invaluable advice and resources to help fight this terrible

> disease.

>

> Best Wishes,

>

> Maciejewski,

> caregiver to Jeff, age 37, dx 2000

>

>

> If you do not wish to belong to shydrager, you may

> unsubscribe by sending a blank email to

>

> shydrager-unsubscribe

>

>

>

>

>

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Whew..

I am overwhelmed with the messages.. :)

I made a mistake.. My wife is taking Magnesium and potassium.. Not

calcium... Sigh...

I guess you are all correct. Most Dr's have no idea what MSA/SDS is. We saw

our family Dr. today. He has no idea what this is. She was told by an

Electrophysiologist, he has been treating her PVC's for 8 years now, that

she has MSA/SDS..And sent her to a Neurologist who confirmed.

I now feel I have found a home, where I can share my frustration with this

disease, and with the comparatively low amount of research into this

disorder.

While Gwenna has not had a sleep study done, I plan to get her scheduled in

for one as soon as possible.

Peace and Love...

RE:New Here

>

> Hello ,

>

> Welcome, and sorry you have to be here. As some of the others already

> wrote in, it is extremely difficult to figure out where the end is in this

> terrible disease, as it affects different people in different ways. I

> believe your doctor is as unsure as anyone else, since the disease is so

> rare. As our internist put it- " I will probably never see another case

> like this in my lifetime " .

>

> Of all the symptoms you mentioned that your wife is experiencing, I would

> probably say that the two most alarming are the sleep apnea and swallowing

> problems. Sleep apnea can cause sudden death, as the patient stops

> breathing. Has she had a sleep study? Many of the MSA patients,

including

> my husband, use a CPAP at night to help with the brething difficulties.

> The swallowing problems could cause fluid to leak in to the lungs, which

> in turn can cause pneumonia. This is also one of the more common causes

of

> death in MSA patients, along with respiratory failure.

>

> I hope you can glean some help and moral support from this group. They

> have been a tremendous help to me and have given both me, my husband and

> our doctor invaluable advice and resources to help fight this terrible

> disease.

>

> Best Wishes,

>

> Maciejewski,

> caregiver to Jeff, age 37, dx 2000

>

>

> If you do not wish to belong to shydrager, you may

> unsubscribe by sending a blank email to

>

> shydrager-unsubscribe

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, hang in there you can make it. After all, how many other folks

have such a support group? Ask a question and no telling who has an

answer. But there will be some one.

God bless you as you learn along the way.

Barb in Arlington, who feels God never sleeps and I hear there are folks

on the line who can prove it.

--

Grand Parent. A thing so simple, even a small child can operate it.

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, hang in there you can make it. After all, how many other folks

have such a support group? Ask a question and no telling who has an

answer. But there will be some one.

God bless you as you learn along the way.

Barb in Arlington, who feels God never sleeps and I hear there are folks

on the line who can prove it.

--

Grand Parent. A thing so simple, even a small child can operate it.

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I'm a hanging :)

The amount of information I have already received from this site is morethan

I learned from all the other sites combined.

Peace and Love..

Re: RE:New Here

>

> , hang in there you can make it. After all, how many other folks

> have such a support group? Ask a question and no telling who has an

> answer. But there will be some one.

>

> God bless you as you learn along the way.

>

> Barb in Arlington, who feels God never sleeps and I hear there are folks

> on the line who can prove it.

>

> --

>

> Grand Parent. A thing so simple, even a small child can operate it.

>

>

>

>

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Guest guest

I'm a hanging :)

The amount of information I have already received from this site is morethan

I learned from all the other sites combined.

Peace and Love..

Re: RE:New Here

>

> , hang in there you can make it. After all, how many other folks

> have such a support group? Ask a question and no telling who has an

> answer. But there will be some one.

>

> God bless you as you learn along the way.

>

> Barb in Arlington, who feels God never sleeps and I hear there are folks

> on the line who can prove it.

>

> --

>

> Grand Parent. A thing so simple, even a small child can operate it.

>

>

>

>

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Sorry to hear you are having the same bad time my son is having right now.My

19 yr.old w/cf has been in the hospital since Dec 30 he went in with bleeding

they found he is impacted with stool.He throws up all food he is getting a

PICC line today for total IV nutrition .The doctors can't do surgery until

his lungs are better.I wish you lots of good thoughts and my hopes of a fast

recovery of both our kids.BeckyB.

PS was born with meconium illeus did your

daughter have this problem at birth?

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-thank you for the nice welcome. Kayla wasn't diagnosed till she was

5 yrs. old. She has had a picc line before and they are no fun., I'm

hoping your son feels better soon also, let us know how its going.

Jen

-- In cfparents , hlbbet@a... wrote:

> Sorry to hear you are having the same bad time my son is having

right now.My

> 19 yr.old w/cf has been in the hospital since Dec 30 he went in

with bleeding

> they found he is impacted with stool.He throws up all food he is

getting a

> PICC line today for total IV nutrition .The doctors can't do

surgery until

> his lungs are better.I wish you lots of good thoughts and my hopes

of a fast

> recovery of both our

kids.BeckyB.

> PS was born with meconium illeus did

your

> daughter have this problem at birth?

>

>

>

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Welcome, Amber. I think you will get lots of ideas here on what to do to

jump start your weight loss again. How tall are you? Keep in mind that

" normal " weight charts don't really work for us post-ops. We generally weigh

more " than we should " according to the charts, but yet wear smaller sizes

than we should as well. The most important measure should be how you feel,

not the numbers on the scale, but that is easier said than done, as almost

all of us have that magic number in mind. I hit a low of 146, I'm back up to

161, and want to get back down to 150. But for the most part I don't sweat

it...as long as I'm feeling good.

Sounds like you are doing all the right things. I will be interested in

hearing the feedback you get from other members. How much exercise are you

getting in, and what type?

KC

<< I would really

appreicate some help. I have posted to other boards and seem to get

little to know response or support. I hope things are different

here!!

Thanks to all of you!

Amber Cook>>

Homepage: http://groups.yahoo.com/group/Graduate-OSSG

Unsubscribe: mailto:Graduate-OSSG-unsubscribe

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