Re: (unknown)

[Guest guest]

California? Nebraska? Hawaii?

I hear there are Mcs in China now too

----- Original Message -----

> Hello! Pre and Post Operative Gastric Reduction Duodenal Switch

> Patients, Family Members and Support people! Please come and join us

> to keep and increase muscle mass, get those heart and lungs in better

> shape and prevent DVT, and help melt the fat mass and keep those

> bones nice and strong! McFarland (5 miles south of Delano on 99) is

> having a Christmas walk/run December 16, 2000 race begins 11:00am

> Registration between 9-10:30am inside the Recreation Mouser Center

> 100 S. Second St. just south of Mcs take Sherwood ave. west off

> of Hwy99

> Cost until Dec.11 $17 Race Day $20 under 17yr $12 you call for pre-

> registration form to be postmarked by Dec. 13 for $17

> price. Hope to see you all there!

>

>

>

>

>

>

[Guest guest]

There IS one in SPAIN!!!!! LOL!!

loriann

Re: (unknown)

California? Nebraska? Hawaii?

I hear there are Mcs in China now too

----- Original Message -----

> Hello! Pre and Post Operative Gastric Reduction Duodenal Switch

> Patients, Family Members and Support people! Please come and join us

> to keep and increase muscle mass, get those heart and lungs in better

> shape and prevent DVT, and help melt the fat mass and keep those

> bones nice and strong! McFarland (5 miles south of Delano on 99) is

> having a Christmas walk/run December 16, 2000 race begins 11:00am

> Registration between 9-10:30am inside the Recreation Mouser Center

> 100 S. Second St. just south of Mcs take Sherwood ave. west off

> of Hwy99

> Cost until Dec.11 $17 Race Day $20 under 17yr $12 you call for pre-

> registration form to be postmarked by Dec. 13 for $17

> price. Hope to see you all there!

>

>

>

>

>

>

[Guest guest]

FYI Mc's is in over 100 countries.

T

Kansas

[Guest guest]

Sorry!!! I have to add my 2cents here. Don't concentrate on the staff so much. If their really nasty, move on. No one should have to take any abuse. It's better to look for a competent dr. who's extremely skilled at what he's doing. Staff is not worth fighting over.

[Guest guest]

I wonder if they filled my Dec 6th clinic visit and Dec 7th surgery date

that I canceled but they called to remind me to go to.......

BTW, I think her name is

----- Original Message -----

> ,

> If you want to publically chastise me, kindly get your facts

> straight. I was quoting sandy, she said the staff was " horrid " and i

> put horrendous in quotations for that reason, personally i think

> they just suck------chuckle

> As far as hanging up on Ivonne, after the first phone call and her

> refusal to adress the december surgery date and repeating over and

> over again, " We are booking surgery dates for the end of jan, into

> feb " , i did hang up.

> She then called my house later that afternoon looking for a Dale

> somebody. I said as i would with anyone, you have the wrong number

> and hung up, she called right back, i again told her you have the

> wrong number, she then questions me telling her she has the wrong

> number, that is when i identified myself and she used it as an

> opportunity to launch into how ivette said she had " worked closely

> with me to get my blood donated and to get me a unit number " Whatever

> a unit number is? Then again launches into we arebooking surgeries

> late jan, early feb, that is when i halted her and said " i have not

> made up my mind " and hung up.

> I generally work and play well with others, and i address questions

> that people ask me to the best on my ability, never did she answer my

> questions.

> I could accept being told, " doctor had other surgeries that were more

> pressing, or we thought we could book you in, in dec., which by the

> way was never my resquest, however that is not possible,or even

> doctor is taking a day off and is going to loll in bed " ,but don't act

> oblivious or obtuse to my questions and don't act like it is in some

> way on me.

> As far as calling or requesting a phone conference, i already sent

> two e-mails that were not responded to, so be it.

> I am not in the habit of being rude to people,i work with people on a

> daily basis,and don't have problems

> This or any postings of mine were never intended to become a pissing

> contest, however i am not a person to remain quiet when i feel

> wronged nor to not advocate for others that might not know that this

> is not the way it should be when you deal with doctor's and their

> office or nurses or hospitals, etc.

> I wish everyone luck in their choices,

> ciar

>

>

>

>

>

>

[Guest guest]

I was amazed at how much you pay for insurance. We have no insurance here

and only pay $3.30 for the run of the mill stuff like colistin, ceclor etc.

(Im not sure about new stuff on the market). And although our taxes pay for

the public hsp system, we dont have any out of pocket expenses when she's

discharged. We are very lucky and we are thankful for all our hsp does for

us. Do you have a cf clinic at all? Does it belong to a hsp. Sometimes

its maddening that cf takes a back seat to other things, I think its because

they all LOOK healthy and thats frustrating.

(unknown)

> Hi ......

>

> I live in South Africa and have a daughter with CF ............

>

> In order for her to get the minimum treatment, which excludes such things

as

> CVS's or IVF's, which are not available in South Africa and need to be

> imported and consider this - for one US dollar it costs us nearly 8 Rand,

> this makes it IMPOSSIBLE for the average person on the street to afford

any

> treatment other than that available, being a 3rd world country means no

> " super drugs " .

>

> Due to CF being " not as important " as AIDS, there is no government

> assistance, and all the money needed to run the CF clinic is collected via

> donations.

>

> I pay such high premiums towards the medical aid (Nearly 50% of my salary)

> in order to cover my daughter for the basics, that is 1 monthly visit,

> creon, and " some " , not all of her antibiotics. This after a LONG battle to

> get them to cover her, as in their eyes " she is too much of a RISK " . I

still

> have to pay out of my own pocket for the medication they will NOT cover.

>

> A second child with CF ??????

>

> YOU TELL ME !!!!!!!!!

> _________________________________________________________________________

> Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

>

>

> ***********************

> This is a secular list.

> ***********************

>

>

> PLEASE do not post religious emails to the list.

>

>

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

>

>

> The opinions and information exchanged on this list should

> IN NO WAY

> be construed as medical advice.

>

> PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

>

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

>

>

> Our webpage is at http://www.eohio.net/malbright/cfparents.htm

>

> _________________________________________________

> Post message: cfparentsegroups

> Subscribe: cfparents-subscribeegroups

> Unsubscribe: cfparents-unsubscribeegroups

> List owner: cfparents-owneregroups

> _________________________________________________

>

> WE HAVE A CHAT PAGE!!!

> /chat/cfparents

> _________________________________________________

>

>

>

[Guest guest]

That's okay, ; I always adored Eeyore! (Pooh, too!),

n Rojas

[Guest guest]

,

I am on Tobi every other month and the only probem I ever have with it is

that it does seem to make my voice a little raspy, esp my singing voice which

I notice when I am in the car, which is a disappointment for me but a

blessing for whomever I am driving with!!! I do notice though that it

really helps my lungs when I am not well, and when I do get sick it is

usually when I am not on Tobi and that is what they put me on. I don't feel

as though it suppresses my immune system, though you might be onto something.

Good luck!

-le

[Guest guest]

I had my oldest daughter tested twice , because i could not beleive it

either. but both said the same thing C.F.... My daughters are 15 and 19 yrs

old. both with cf. patty

[Guest guest]

Yes, Shantell did last month. As it turned out, she had a vitamin K

deficiency. She was coughing up quite a bit of blood from that. She also

then started coughing up mucous. The doctors gave her vitamin K shots, the

bleeding stopped. She was put on IV's for three weeks, Tobramyicin and

Ceftazadine for the infection. She's on a ADEK vitamin supplement now.

They can check her K level with a blood test. Hope that's all it is,

, mom of Shantell 19yr wcf

(unknown)

Has anyone experienced coughing up blood before having much

congestion? We have had the blood before but it usually after having

some congestion. After coughing up blood Jess has been more congested

than I have ever heard her .

We are going in the hospital next Monday for IVs after a week of

TOBI and 4 treatments a day.

Dana 11 w/CF & G-tube Philip 4 wo/CF

PLEASE do not post religious emails to the list.

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

The opinions and information exchanged on this list should

IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS.

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

[Guest guest]

Tisha-

I'm so sorry to hear that Bryce is having such a hard time. It must be

so hard for you to see him having so much pain etc. You don't say how many

creon he already takes, but my first thought is that you are on the right

track by trying to increase his creon slowly to see if that has any effect

on his stools. Poor thing, of course he is weak with so much diarrhea. My

son is 6 and he takes 6 creon with his meals and 3 with each fat containing

snack. While he sometimes has loose stools, that is now the exception,

rather than the rule.

From what I have learned over the years, 99 is not a borderline test

result at all- it is definitely positive. If I am remembering correctly, a

sweat test over 60 is considered positive. From the sound of his symptoms,

there doesn't seem to be much doubt. I can't imagine why they never did a

DNA test to find out more definitively whether it was cf. It is totally

understandable why all of you would be having a hard time accepting the

diagnosis- we have ALL been there. It is a process that we all go through-

it does not happen overnight. Unfortunately, in your case it has been made

more difficult by so much uncertainty.

I'm glad to hear that you are going to have an appointment tomorrow - is

that person a cf doctor? One of the first things I would want to find out

is the exact status of his pulmonary situation, in addition to clearing up

his digestive problems. You would want him to have a pulmonary function

test, as well as cultures to see if he is growing any of the bacteria that

people with cf sometimes grow.

Please continue to use this group as a place to ask questions so that you

can be your son's advocate. I'm so upset that they dragged their feet for so

long when he was clearly having such a hard time.

Let us know how you make out tomorrow.

Take care,

Debi

>

>Reply-To: cfparents

>To: cfparents

>Subject: (unknown)

>Date: Sun, 22 Apr 2001 19:15:13 -0000

>

>MY SON BRYCE WAS DX'D WITH CF LAST WEDNESDAY. HE IS 10 YRS WEIGHS

>52LBS, AND WAS HOSPITALIZED WITH A BOWEL OBSTRUCTION. HE HAS SUFFERED

>WITH THE DIGESTIVE PROBLEMS SINCE BIRTH. AT THE AGE OF 4 HE SEEN A

>PED. GASTRO DR AT RILEY'S, HE DX'D BRYCE WITH A MALABSORPTION DISODER

>OF THE PANCREASE. STARTED HIM ON CREON. AND HE SEEMED TO BE FINE FOR

>AWHILE. SINCE THEN HE HAS BEEN HOSPITALIZED 4 TIMES. 2 TIMES WITH

>PNEUMONIA AND ABD PAIN, AND DIARRHEA. HE HAS BEEN TESTED FOR CF AT

>LEAST THREE TIMES. HE WAS ALWAYS VERY CLOSE TO THE POSITVE RANGE. AND

>RIGHT AT THE NUMBER IN 99. BUT THE DR TOLD ME HE DIDN'T WANT TO MAKE

>THAT DX AT THAT TIME, HE WANTED TO WAIT. THIS TIME HE WAS TESTED

>TWICE AND BOTH TIMES WERE VERY POSITIVE. HE RAN SOME BLOOD WORK TO

>FIND OUT HIS VIT D LEVELS AND SOMETHING ELSE THAT I DON'T KNOW WHAT

>IT WAS. THE DR IS GOING TO CALL THE CHILDREN'S HOSPITAL IN CHICAGO,

>NORHTWESTERN UNIVERSITY, DR SUSAN MCCOLLEY, ON MONDAY TO SET UP HIS

>FIRST APPT. MY SON IS HAVING A HARD TIME EXCEPTING THIS AND I GUESS I

>AM TOO. RIGHT NOW HE IS HAVING AT LEAST 12-15 DIARRHEA STOOLS. HE IS

>IN SO MUCH PAIN, AND IS VERY WEAK. I FEEL SO BAD FOR HIM. I TALKED TO

>A PARENT WHO'S DAUGHTER HAD THIS DISEASE. SHE ASKED WHAT WAS GOING ON

>WITH HIM AND SHE SUGGESTED THAT I GIVE HIM MORE OF HIS CREON. I DID

>AND IT SEEMED TO HELP CUT DOWN ON THE NUMBER OF STOOLS. BUT HE IS SO

>WEAK RIGHT NOW. HE'S VERY UPSET AND WONDERS WHY THIS HAS HAPPENED TO

>HIM. I JUST NEED SOME HELP. THAT IS WHY I AM SENDING THIS MESSAGE TO

>ALL OF YOU. WHAT CAN WE EXPECT? WHAT COMES NEXT? THANKS, TISHA

>

_________________________________________________________________

Get your FREE download of MSN Explorer at http://explorer.msn.com

[Guest guest]

Tisha,

your on the right path now.

take him to see pulmonary, get his stools straightened out, sounds like you

need more enzymes and maybe an antacid(zantac,prilosec,etc.)

then you need to go to the library and check out some books, you can look

on the internet, there is alot of info to learn / live .

they also have things for kids , if he can't talk to you about it have him

talk to someone else.

when you go to clinic appt. they should do PFT'S, chest x-ray and you

should meet a bunch of people. you will be overwhelmed, but you will make

it.

chris

mom of 3

brandon 12 yrs w cf

On Sun, 22 Apr 2001 19:15:13 -0000, cfparents wrote:

> MY SON BRYCE WAS DX'D WITH CF LAST WEDNESDAY. HE IS 10 YRS WEIGHS

> 52LBS, AND WAS HOSPITALIZED WITH A BOWEL OBSTRUCTION. HE HAS SUFFERED

> WITH THE DIGESTIVE PROBLEMS SINCE BIRTH. AT THE AGE OF 4 HE SEEN A

> PED. GASTRO DR AT RILEY'S, HE DX'D BRYCE WITH A MALABSORPTION DISODER

> OF THE PANCREASE. STARTED HIM ON CREON. AND HE SEEMED TO BE FINE FOR

> AWHILE. SINCE THEN HE HAS BEEN HOSPITALIZED 4 TIMES. 2 TIMES WITH

> PNEUMONIA AND ABD PAIN, AND DIARRHEA. HE HAS BEEN TESTED FOR CF AT

> LEAST THREE TIMES. HE WAS ALWAYS VERY CLOSE TO THE POSITVE RANGE. AND

> RIGHT AT THE NUMBER IN 99. BUT THE DR TOLD ME HE DIDN'T WANT TO MAKE

> THAT DX AT THAT TIME, HE WANTED TO WAIT. THIS TIME HE WAS TESTED

> TWICE AND BOTH TIMES WERE VERY POSITIVE. HE RAN SOME BLOOD WORK TO

> FIND OUT HIS VIT D LEVELS AND SOMETHING ELSE THAT I DON'T KNOW WHAT

> IT WAS. THE DR IS GOING TO CALL THE CHILDREN'S HOSPITAL IN CHICAGO,

> NORHTWESTERN UNIVERSITY, DR SUSAN MCCOLLEY, ON MONDAY TO SET UP HIS

> FIRST APPT. MY SON IS HAVING A HARD TIME EXCEPTING THIS AND I GUESS I

> AM TOO. RIGHT NOW HE IS HAVING AT LEAST 12-15 DIARRHEA STOOLS. HE IS

> IN SO MUCH PAIN, AND IS VERY WEAK. I FEEL SO BAD FOR HIM. I TALKED TO

> A PARENT WHO'S DAUGHTER HAD THIS DISEASE. SHE ASKED WHAT WAS GOING ON

> WITH HIM AND SHE SUGGESTED THAT I GIVE HIM MORE OF HIS CREON. I DID

> AND IT SEEMED TO HELP CUT DOWN ON THE NUMBER OF STOOLS. BUT HE IS SO

> WEAK RIGHT NOW. HE'S VERY UPSET AND WONDERS WHY THIS HAS HAPPENED TO

> HIM. I JUST NEED SOME HELP. THAT IS WHY I AM SENDING THIS MESSAGE TO

> ALL OF YOU. WHAT CAN WE EXPECT? WHAT COMES NEXT? THANKS, TISHA

>

_______________________________________________________

Send a cool gift with your E-Card

http://www.bluemountain.com/giftcenter/

[Guest guest]

Tisha,

Im so sorry for your family. For Bryce it probably hard suddenly have to

stick to a regime like physio etc. when all his life he hasnt had to do

that. Im sure they do all the testing, x-ray's etc. in his first visit or

so and then show you and Bryce all the things that need to be done. Do you

have a cf association near where you live? If you do maybe Bryce could meet

with some of the other cf kids (careful which ones due to infections) and

then he can see they a normal (hate that word) and play and do all the

things he probably thinks will change. Maybe they have outings etc. This

list is wonderful and you'll find such nice people on it. I wish Id found

it in the early zombie-like stage where you can hardly believe this is

happening. I didnt find it until Eilish was over 2, but am so glad I did

and you will be to.

(mummy to Liam 6 wocf & Eilish 3.6 wcf)

(unknown)

> MY SON BRYCE WAS DX'D WITH CF LAST WEDNESDAY. HE IS 10 YRS WEIGHS

> 52LBS, AND WAS HOSPITALIZED WITH A BOWEL OBSTRUCTION. HE HAS SUFFERED

> WITH THE DIGESTIVE PROBLEMS SINCE BIRTH. AT THE AGE OF 4 HE SEEN A

> PED. GASTRO DR AT RILEY'S, HE DX'D BRYCE WITH A MALABSORPTION DISODER

> OF THE PANCREASE. STARTED HIM ON CREON. AND HE SEEMED TO BE FINE FOR

> AWHILE. SINCE THEN HE HAS BEEN HOSPITALIZED 4 TIMES. 2 TIMES WITH

> PNEUMONIA AND ABD PAIN, AND DIARRHEA. HE HAS BEEN TESTED FOR CF AT

> LEAST THREE TIMES. HE WAS ALWAYS VERY CLOSE TO THE POSITVE RANGE. AND

> RIGHT AT THE NUMBER IN 99. BUT THE DR TOLD ME HE DIDN'T WANT TO MAKE

> THAT DX AT THAT TIME, HE WANTED TO WAIT. THIS TIME HE WAS TESTED

> TWICE AND BOTH TIMES WERE VERY POSITIVE. HE RAN SOME BLOOD WORK TO

> FIND OUT HIS VIT D LEVELS AND SOMETHING ELSE THAT I DON'T KNOW WHAT

> IT WAS. THE DR IS GOING TO CALL THE CHILDREN'S HOSPITAL IN CHICAGO,

> NORHTWESTERN UNIVERSITY, DR SUSAN MCCOLLEY, ON MONDAY TO SET UP HIS

> FIRST APPT. MY SON IS HAVING A HARD TIME EXCEPTING THIS AND I GUESS I

> AM TOO. RIGHT NOW HE IS HAVING AT LEAST 12-15 DIARRHEA STOOLS. HE IS

> IN SO MUCH PAIN, AND IS VERY WEAK. I FEEL SO BAD FOR HIM. I TALKED TO

> A PARENT WHO'S DAUGHTER HAD THIS DISEASE. SHE ASKED WHAT WAS GOING ON

> WITH HIM AND SHE SUGGESTED THAT I GIVE HIM MORE OF HIS CREON. I DID

> AND IT SEEMED TO HELP CUT DOWN ON THE NUMBER OF STOOLS. BUT HE IS SO

> WEAK RIGHT NOW. HE'S VERY UPSET AND WONDERS WHY THIS HAS HAPPENED TO

> HIM. I JUST NEED SOME HELP. THAT IS WHY I AM SENDING THIS MESSAGE TO

> ALL OF YOU. WHAT CAN WE EXPECT? WHAT COMES NEXT? THANKS, TISHA

>

>

>

>

> PLEASE do not post religious emails to the list.

>

>

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

>

>

> The opinions and information exchanged on this list should

> IN NO WAY

> be construed as medical advice.

>

> PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

>

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

>

>

>

[Guest guest]

I just wanted to add to this - I had suggested an antacid too and then

remembered that sometimes people being treated for pancreatic problems (not

CF) are given non-enteric coated enzymes. You might want to check on that

also. Perhaps it is time to switch to enteric coated ones (if he has been

getting the other type). I also don't know how the antacid would effect

non-enteric coated enzymes. Just another thought.

Lori

Mom to Scout 2 wCF

Re: (unknown)

Tisha,

your on the right path now.

take him to see pulmonary, get his stools straightened out, sounds like you

need more enzymes and maybe an antacid(zantac,prilosec,etc.)

then you need to go to the library and check out some books, you can look

on the internet, there is alot of info to learn / live .

they also have things for kids , if he can't talk to you about it have him

talk to someone else.

when you go to clinic appt. they should do PFT'S, chest x-ray and you

should meet a bunch of people. you will be overwhelmed, but you will make

it.

chris

mom of 3

brandon 12 yrs w cf

On Sun, 22 Apr 2001 19:15:13 -0000, cfparents wrote:

> MY SON BRYCE WAS DX'D WITH CF LAST WEDNESDAY. HE IS 10 YRS WEIGHS

> 52LBS, AND WAS HOSPITALIZED WITH A BOWEL OBSTRUCTION. HE HAS SUFFERED

> WITH THE DIGESTIVE PROBLEMS SINCE BIRTH. AT THE AGE OF 4 HE SEEN A

> PED. GASTRO DR AT RILEY'S, HE DX'D BRYCE WITH A MALABSORPTION DISODER

> OF THE PANCREASE. STARTED HIM ON CREON. AND HE SEEMED TO BE FINE FOR

> AWHILE. SINCE THEN HE HAS BEEN HOSPITALIZED 4 TIMES. 2 TIMES WITH

> PNEUMONIA AND ABD PAIN, AND DIARRHEA. HE HAS BEEN TESTED FOR CF AT

> LEAST THREE TIMES. HE WAS ALWAYS VERY CLOSE TO THE POSITVE RANGE. AND

> RIGHT AT THE NUMBER IN 99. BUT THE DR TOLD ME HE DIDN'T WANT TO MAKE

> THAT DX AT THAT TIME, HE WANTED TO WAIT. THIS TIME HE WAS TESTED

> TWICE AND BOTH TIMES WERE VERY POSITIVE. HE RAN SOME BLOOD WORK TO

> FIND OUT HIS VIT D LEVELS AND SOMETHING ELSE THAT I DON'T KNOW WHAT

> IT WAS. THE DR IS GOING TO CALL THE CHILDREN'S HOSPITAL IN CHICAGO,

> NORHTWESTERN UNIVERSITY, DR SUSAN MCCOLLEY, ON MONDAY TO SET UP HIS

> FIRST APPT. MY SON IS HAVING A HARD TIME EXCEPTING THIS AND I GUESS I

> AM TOO. RIGHT NOW HE IS HAVING AT LEAST 12-15 DIARRHEA STOOLS. HE IS

> IN SO MUCH PAIN, AND IS VERY WEAK. I FEEL SO BAD FOR HIM. I TALKED TO

> A PARENT WHO'S DAUGHTER HAD THIS DISEASE. SHE ASKED WHAT WAS GOING ON

> WITH HIM AND SHE SUGGESTED THAT I GIVE HIM MORE OF HIS CREON. I DID

> AND IT SEEMED TO HELP CUT DOWN ON THE NUMBER OF STOOLS. BUT HE IS SO

> WEAK RIGHT NOW. HE'S VERY UPSET AND WONDERS WHY THIS HAS HAPPENED TO

> HIM. I JUST NEED SOME HELP. THAT IS WHY I AM SENDING THIS MESSAGE TO

> ALL OF YOU. WHAT CAN WE EXPECT? WHAT COMES NEXT? THANKS, TISHA

>

_______________________________________________________

Send a cool gift with your E-Card

http://www.bluemountain.com/giftcenter/

PLEASE do not post religious emails to the list.

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

The opinions and information exchanged on this list should

IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS.

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

[Guest guest]

hi tisha ..im so sorry about your son..i know how you feel..my daughter was

diagnosed with cf when she was 2 months old..shes now 9 months old and she

only weighs 12 lbs. her right lung has been collapsed for 6 months now and

they are trying everything to get it to reinflate..she also has the reflux

problem and she slowly asperated into her lung after she eats and thats why

its so hard to get her lung to reinflate...shes on 7 breathing treatments a

day and on 5 different medications...if you give your son at least 2 ina half

or 3 creons at every time he eats it should cut his diahrea and should get

his stools for thicker...you are in my prayers cause im going through the

same thing and i hope he gets better...my prayers are with ya hun...

love,]

elizabeth

mother of 9 month girl with cf

[Guest guest]

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[Guest guest]

Jan, Your Spanky and Skeeter are the cutest. I love animals.

I have a minatue schnauzer and Akita. And 2 adorable cats. Deana

On Wed, 6 Jun 2001 13:35:46 -0400 (EDT) janicelpn@... writes:

> As promised here is the pics of my fur-boys. Spanky is 2 and Skeeter

> is

> 8 weeks......I need to get more pics of the baby, will let you know

> when

> I do. In the mean time you can see my guys here:

>

> http://community.webtv.net/janicelpn/JGsSkeeterDoo

> http://community-2.webtv.net/janicelpn/SPANKYthelittle

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

Jan, Your Spanky and Skeeter are the cutest. I love animals.

I have a minatue schnauzer and Akita. And 2 adorable cats. Deana

On Wed, 6 Jun 2001 13:35:46 -0400 (EDT) janicelpn@... writes:

> As promised here is the pics of my fur-boys. Spanky is 2 and Skeeter

> is

> 8 weeks......I need to get more pics of the baby, will let you know

> when

> I do. In the mean time you can see my guys here:

>

> http://community.webtv.net/janicelpn/JGsSkeeterDoo

> http://community-2.webtv.net/janicelpn/SPANKYthelittle

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

Jan, Your Spanky and Skeeter are the cutest. I love animals.

I have a minatue schnauzer and Akita. And 2 adorable cats. Deana

On Wed, 6 Jun 2001 13:35:46 -0400 (EDT) janicelpn@... writes:

> As promised here is the pics of my fur-boys. Spanky is 2 and Skeeter

> is

> 8 weeks......I need to get more pics of the baby, will let you know

> when

> I do. In the mean time you can see my guys here:

>

> http://community.webtv.net/janicelpn/JGsSkeeterDoo

> http://community-2.webtv.net/janicelpn/SPANKYthelittle

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

Thanks !

I know it will all come together at some point...am just hoping it's

sooner rather than later......

elle

> Elle,

> Wow, is it that hard to get things down there? I didn't know the

import charges were so much. Wouldn't it be nice to have everything

just go smoothly for a change!? I hope it all works out for you.

take care.

>

>

> 16wks

> ep 12-00

>

> ----- Get more from the Web. FREE MSN Explorer download :

http://explorer.msn.com

[Guest guest]

Thanks !

I know it will all come together at some point...am just hoping it's

sooner rather than later......

elle

> Elle,

> Wow, is it that hard to get things down there? I didn't know the

import charges were so much. Wouldn't it be nice to have everything

just go smoothly for a change!? I hope it all works out for you.

take care.

>

>

> 16wks

> ep 12-00

>

> ----- Get more from the Web. FREE MSN Explorer download :

http://explorer.msn.com

[Guest guest]

Thanks !

I know it will all come together at some point...am just hoping it's

sooner rather than later......

elle

> Elle,

> Wow, is it that hard to get things down there? I didn't know the

import charges were so much. Wouldn't it be nice to have everything

just go smoothly for a change!? I hope it all works out for you.

take care.

>

>

> 16wks

> ep 12-00

>

> ----- Get more from the Web. FREE MSN Explorer download :

http://explorer.msn.com

[Guest guest]

Elle, Me too!! (smile) Re: (unknown) Thanks !I know it will all come together at some point...am just hoping it's sooner rather than later......elle> Elle,> Wow, is it that hard to get things down there? I didn't know the import charges were so much. Wouldn't it be nice to have everything just go smoothly for a change!? I hope it all works out for you. take care.> > > 16wks> ep 12-00> > ----- Get more from the Web. FREE MSN Explorer download : http://explorer.msn.com