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Anne,

I'm still up if you are...If you need me, holler. We can chat or you

could call me? Sorry, I don't have long distance right now. :(

" Anne . " wrote:

> Any one up, & around at this hour?

>

>

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Hyten wrote:

Anne,

I'm still up if you are...If you need me, holler. We can

chat or you

could call me? Sorry, I don't have long distance right now. :(

i am

hanging in there... I am tired, but I can't sleep... it seems to be starting

up again... this annoys the hell out of me!!!

does

someone think I need yet one more allergy? especially one that is

life threatening... I actually I was allergic to ragweed before but

I only got the sniffles, hay fever type stuff.

It

is 0545 Saturday September 9th now, and I have one of the coolest

friends!! (across the street) was just leaving for work, and

saw my light on, so she went back into house to call me and make sure I

was okay.... it is nice to have friends that really care.

I

am hoping for a nap soon!

Love

Always!

Anne

P.S.

I have long distance, I'll take you up on that soon, but at a more decent

hour since you have children.

"Anne ." wrote:

> Any one up, & around at this hour?

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Hyten wrote:

Anne,

I'm still up if you are...If you need me, holler. We can

chat or you

could call me? Sorry, I don't have long distance right now. :(

i am

hanging in there... I am tired, but I can't sleep... it seems to be starting

up again... this annoys the hell out of me!!!

does

someone think I need yet one more allergy? especially one that is

life threatening... I actually I was allergic to ragweed before but

I only got the sniffles, hay fever type stuff.

It

is 0545 Saturday September 9th now, and I have one of the coolest

friends!! (across the street) was just leaving for work, and

saw my light on, so she went back into house to call me and make sure I

was okay.... it is nice to have friends that really care.

I

am hoping for a nap soon!

Love

Always!

Anne

P.S.

I have long distance, I'll take you up on that soon, but at a more decent

hour since you have children.

"Anne ." wrote:

> Any one up, & around at this hour?

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  • 11 months later...

-Kim-

GREAT NEWS! I bet you are relieved. Now you can focus on your trip

and get excited.

lee-- In cholesteatoma@y..., " Kim " <kiekeboe4you@y...> wrote:

> Hi Everyone.

> Well seen my ENT on Tuesday and he said everything is great with

my

> ear. He said " It's the best healing cavity I've seen all week " Hmm

> well that sounds promising, I guess. Everything is okay to go

flying,

> on wild crazy amusement park rides and other things so that is

good.

> A big weight was lifted off my shoulders as I thought something

would

> prevent me from going on my trip.

> Anyways, I gave my ENT this site. I'm hoping he joins or checks

it

> out. He said it's great that I started this group. I think so too.

I

> enjoy talking with others who know what I'm going through or have a

> loved one that is also going thru this. We are not alone. :-)

> Well, that's it. I hope everyone is well and healthy. 6 more days

&

> I'm outta here. Not sure how much I'll be able to check in, but

I'll

> try my best.

> Hugz,

> Kim

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  • 5 months later...
Guest guest

" netlarry1976 " <lbalsley@...> writes:

> Hello everyone. I'm new to the group. In fact, I've not even been

> diagnosed yet-- I've never even heard of cholesteatoma until

> yesterday (I woke up (yet again) with a blood-covered pillow, hands,

> arms, and neck) and decided to do some net searching to find out why

> this was happening. That's when I discovered www.cholesteatoma.org

> and was amazed.. if I were a gambling man, I would bet that this is

> what has been bothering me for the past 8 months. Almost non-stop ear

> drainage, that foul-smelling odor, headaches, the past history of ear

> problems (I've has tubes several times as a child and a typanoplasty

> in 1988), etc, that my GP continually pushes off with antibiotics and

> drops.

>

> I have an appointment with an ENT on March 12th and am very anxious

> to get a diagnosis so we can get this " fixed " . Can anyone provide

> some suggestions on what I should ask my doctor, what I should be

> concered about, what I should listen for when he talks to me?

>

> Any assistance anyone can provide would be greatly appreciated!

Hi Larry, and welcome to the group. I'm assuming you're male - nice

to see another chap in here if that's the case :-)

Firstly, and I don't want to come across as condescending when I say

this - I wouldn't advise going into the appointment with a

preconceived idea of what your diagnosis is going to be. I would

just describe your symptoms as clearly as you can, and wait and see

what conclusions the ENT specialist comes to after they've examined

your ear(s).

That being said - I agree that your symptoms sound likely to be

c-toma, but I'm not an ENT specialist ;-) You can always get a second

opinion if you're unhappy with the outcome of this visit (and if the

consultant bristles at the mention of getting a second opinion, you

*definitely* need to get one!).

In the event that you *are* diagnosed with c-toma, you will require at

least one operation to remove it. The questions I would ask would

relate to how many of these procedures the consultant has carried out,

and how frequently they do so. From reading others experiences the

best consultants/surgeons (for this type of problem) are those who

have been doing this for a long time, and carry out the operations

frequently (we're talking multiple times a week).

As an example, my consultant has been performing these operations for

15 years, and typically does 2-4 a week. He also teaches others how

to do them, both in this country (UK), and around the world (he's in

Nepal during March on a teaching trip).

Good Luck with your appointment, and let us know how you get on.

You'll find this group a brilliant source of encouragement and support

(I know I have :-).

--

Pete

pete@...

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

MaVerick - Open Source MultiValue Database Management System

Check out the website -> http://www.maverick-dbms.org

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Guest guest

> Hello everyone. I'm new to the group. In fact, I've not even been

> diagnosed yet-- I've never even heard of cholesteatoma until

> yesterday (I woke up (yet again) with a blood-covered pillow,

hands,

> arms, and neck) and decided to do some net searching to find out

why

> this was happening. That's when I discovered www.cholesteatoma.org

> and was amazed.. if I were a gambling man, I would bet that this is

> what has been bothering me for the past 8 months. Almost non-stop

ear

> drainage, that foul-smelling odor, headaches, the past history of

ear

> problems (I've has tubes several times as a child and a

typanoplasty

> in 1988), etc, that my GP continually pushes off with antibiotics

and

> drops.

>

> I have an appointment with an ENT on March 12th and am very anxious

> to get a diagnosis so we can get this " fixed " . Can anyone provide

> some suggestions on what I should ask my doctor, what I should be

> concered about, what I should listen for when he talks to me?

>

> Any assistance anyone can provide would be greatly appreciated!

>

> Thank you,

> Larry

Hello Larry,

I also self diagnosed in May of 2001, I finally saw a regular MD,

then an ENT, had a CT scan, and was told it was c-toma, got an

appointment with an ENT surgeon, one of the top 5 in Onrario ( I was

very lucky) and I had my first surgery the 14th of February this year.

Pete is right again, explain exactly what your symptoms are, some

doctors will tell you right out it's c-toma, some will want a CT

scan, just because some doctors aren't as familiar with it.

My Doctor told me, the c-toma had most likely been growing for 20

years, it's a very slow grower, and almost never cancerous, my

surgery took 4 hours, I was in recovery for 2 hours, I was released

the next day, and my husband and I made the 6 hour drive back home on

Saturday.

The doctor had me on IV antibiotics all night, and gave me a

prescription for tylenol 3, plus more antibiotics to take by mouth,

the c-toma had come very close to impeding the brain, and they wanted

to be on the safe side.

It's been almost 3 weeks, and I'm not back to work yet, I'm still

very dizzy, but some people are back to work in a week, I'm 46, and

not really a spring chicken any more. Ha Ha

If you'll notice on the left side of the screen when you open the

message board, there's a link to bookmarks, open it, and read all you

can, we've spent hours reading and researching, that's why it's

there, I go back to Sudbury for my post-op checkup the 11th of March,

and he'll remove the packing at that time also.

The group here is wonderful, we'll help all we can, good luck to

you Larry, and keep us posted.

Jan G. Kap. Ontario

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Guest guest

Larry,

Your symptoms sounds identical to what our son experienced. Get to a doctor you trust (it may take a few tries) and push for a diagnosis. We didn't push hard enough and our son's c-toma became pretty bad.

Now a question for everyone. How much time lapsed between the first and second surgery?? Our first surgery was 4 months ago so I am getting a bit anxious knowing that another may be right around the corner.

Thank you for all the support and knowledge. It helps so much!!

-----Original Message-----From: jangodinca [mailto:jangodinca@...]Sent: Sunday, March 03, 2002 2:45 PMcholesteatoma Subject: Re: Hello...> Hello everyone. I'm new to the group. In fact, I've not even been > diagnosed yet-- I've never even heard of cholesteatoma until > yesterday (I woke up (yet again) with a blood-covered pillow, hands, > arms, and neck) and decided to do some net searching to find out why > this was happening. That's when I discovered www.cholesteatoma.org > and was amazed.. if I were a gambling man, I would bet that this is > what has been bothering me for the past 8 months. Almost non-stop ear > drainage, that foul-smelling odor, headaches, the past history of ear > problems (I've has tubes several times as a child and a typanoplasty > in 1988), etc, that my GP continually pushes off with antibiotics and > drops.> > I have an appointment with an ENT on March 12th and am very anxious > to get a diagnosis so we can get this "fixed". Can anyone provide > some suggestions on what I should ask my doctor, what I should be > concered about, what I should listen for when he talks to me?> > Any assistance anyone can provide would be greatly appreciated!> > Thank you,> LarryHello Larry, I also self diagnosed in May of 2001, I finally saw a regular MD, then an ENT, had a CT scan, and was told it was c-toma, got an appointment with an ENT surgeon, one of the top 5 in Onrario ( I was very lucky) and I had my first surgery the 14th of February this year. Pete is right again, explain exactly what your symptoms are, some doctors will tell you right out it's c-toma, some will want a CT scan, just because some doctors aren't as familiar with it. My Doctor told me, the c-toma had most likely been growing for 20 years, it's a very slow grower, and almost never cancerous, my surgery took 4 hours, I was in recovery for 2 hours, I was released the next day, and my husband and I made the 6 hour drive back home on Saturday. The doctor had me on IV antibiotics all night, and gave me a prescription for tylenol 3, plus more antibiotics to take by mouth, the c-toma had come very close to impeding the brain, and they wanted to be on the safe side. It's been almost 3 weeks, and I'm not back to work yet, I'm still very dizzy, but some people are back to work in a week, I'm 46, and not really a spring chicken any more. Ha Ha If you'll notice on the left side of the screen when you open the message board, there's a link to bookmarks, open it, and read all you can, we've spent hours reading and researching, that's why it's there, I go back to Sudbury for my post-op checkup the 11th of March, and he'll remove the packing at that time also. The group here is wonderful, we'll help all we can, good luck to you Larry, and keep us posted. Jan G. Kap. Ontario

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Guest guest

My two surgeries were a year apart.

Jane

>From: " A. Behr " <behr@...>

>Reply-cholesteatoma

><cholesteatoma >

>Subject: RE: Re: Hello...

>Date: Mon, 4 Mar 2002 07:34:47 -0500

>

>Larry,

>

>Your symptoms sounds identical to what our son experienced. Get to a doctor

>you trust (it may take a few tries) and push for a diagnosis. We didn't

>push

>hard enough and our son's c-toma became pretty bad.

>

>Now a question for everyone. How much time lapsed between the first and

>second surgery?? Our first surgery was 4 months ago so I am getting a bit

>anxious knowing that another may be right around the corner.

>

>Thank you for all the support and knowledge. It helps so much!!

>

>

>

>

> Re: Hello...

>

>

>

> > Hello everyone. I'm new to the group. In fact, I've not even been

> > diagnosed yet-- I've never even heard of cholesteatoma until

> > yesterday (I woke up (yet again) with a blood-covered pillow,

> hands,

> > arms, and neck) and decided to do some net searching to find out

> why

> > this was happening. That's when I discovered www.cholesteatoma.org

> > and was amazed.. if I were a gambling man, I would bet that this is

> > what has been bothering me for the past 8 months. Almost non-stop

> ear

> > drainage, that foul-smelling odor, headaches, the past history of

> ear

> > problems (I've has tubes several times as a child and a

> typanoplasty

> > in 1988), etc, that my GP continually pushes off with antibiotics

> and

> > drops.

> >

> > I have an appointment with an ENT on March 12th and am very anxious

> > to get a diagnosis so we can get this " fixed " . Can anyone provide

> > some suggestions on what I should ask my doctor, what I should be

> > concered about, what I should listen for when he talks to me?

> >

> > Any assistance anyone can provide would be greatly appreciated!

> >

> > Thank you,

> > Larry

>

>

>

> Hello Larry,

> I also self diagnosed in May of 2001, I finally saw a regular MD,

> then an ENT, had a CT scan, and was told it was c-toma, got an

> appointment with an ENT surgeon, one of the top 5 in Onrario ( I was

> very lucky) and I had my first surgery the 14th of February this year.

> Pete is right again, explain exactly what your symptoms are, some

> doctors will tell you right out it's c-toma, some will want a CT

> scan, just because some doctors aren't as familiar with it.

> My Doctor told me, the c-toma had most likely been growing for 20

> years, it's a very slow grower, and almost never cancerous, my

> surgery took 4 hours, I was in recovery for 2 hours, I was released

> the next day, and my husband and I made the 6 hour drive back home on

> Saturday.

> The doctor had me on IV antibiotics all night, and gave me a

> prescription for tylenol 3, plus more antibiotics to take by mouth,

> the c-toma had come very close to impeding the brain, and they wanted

> to be on the safe side.

> It's been almost 3 weeks, and I'm not back to work yet, I'm still

> very dizzy, but some people are back to work in a week, I'm 46, and

> not really a spring chicken any more. Ha Ha

> If you'll notice on the left side of the screen when you open the

> message board, there's a link to bookmarks, open it, and read all you

> can, we've spent hours reading and researching, that's why it's

> there, I go back to Sudbury for my post-op checkup the 11th of March,

> and he'll remove the packing at that time also.

> The group here is wonderful, we'll help all we can, good luck to

> you Larry, and keep us posted.

> Jan G. Kap. Ontario

>

>

>

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My surgeries were 8 months apart. Now my son Cody has had a ctoma in each ear, and only one surgery each. The right ear is 2 years out and left ear is 1 year out.

Angie

>From: " A. Behr"

>Reply-cholesteatoma >

>Subject: RE: Re: Hello... >Date: Mon, 4 Mar 2002 07:34:47 -0500 > >Larry, > >Your symptoms sounds identical to what our son experienced. Get to a doctor >you trust (it may take a few tries) and push for a diagnosis. We didn't push >hard enough and our son's c-toma became pretty bad. > >Now a question for everyone. How much time lapsed between the first and >second surgery?? Our first surgery was 4 months ago so I am getting a bit >anxious knowing that another may be right around the corner. > >Thank you for all the support and knowledge. It helps so much!! > > > > > Re: Hello... > > > > > Hello everyone. I'm new to the group. In fact, I've not even been > > diagnosed yet-- I've never even heard of cholesteatoma until > > yesterday (I woke up (yet again) with a blood-covered pillow, > hands, > > arms, and neck) and decided to do some net searching to find out > why > > this was happening. That's when I discovered www.cholesteatoma.org > > and was amazed.. if I were a gambling man, I would bet that this is > > what has been bothering me for the past 8 months. Almost non-stop > ear > > drainage, that foul-smelling odor, headaches, the past history of > ear > > problems (I've has tubes several times as a child and a > typanoplasty > > in 1988), etc, that my GP continually pushes off with antibiotics > and > > drops. > > > > I have an appointment with an ENT on March 12th and am very anxious > > to get a diagnosis so we can get this "fixed". Can anyone provide > > some suggestions on what I should ask my doctor, what I should be > > concered about, what I should listen for when he talks to me? > > > > Any assistance anyone can provide would be greatly appreciated! > > > > Thank you, > > Larry > > > > Hello Larry, > I also self diagnosed in May of 2001, I finally saw a regular MD, > then an ENT, had a CT scan, and was told it was c-toma, got an > appointment with an ENT surgeon, one of the top 5 in Onrario ( I was > very lucky) and I had my first surgery the 14th of February this year. > Pete is right again, explain exactly what your symptoms are, some > doctors will tell you right out it's c-toma, some will want a CT > scan, just because some doctors aren't as familiar with it. > My Doctor told me, the c-toma had most likely been growing for 20 > years, it's a very slow grower, and almost never cancerous, my > surgery took 4 hours, I was in recovery for 2 hours, I was released > the next day, and my husband and I made the 6 hour drive back home on > Saturday. > The doctor had me on IV antibiotics all night, and gave me a > prescription for tylenol 3, plus more antibiotics to take by mouth, > the c-toma had come very close to impeding the brain, and they wanted > to be on the safe side. > It's been almost 3 weeks, and I'm not back to work yet, I'm still > very dizzy, but some people are back to work in a week, I'm 46, and > not really a spring chicken any more. Ha Ha > If you'll notice on the left side of the screen when you open the > message board, there's a link to bookmarks, open it, and read all you > can, we've spent hours reading and researching, that's why it's > there, I go back to Sudbury for my post-op checkup the 11th of March, > and he'll remove the packing at that time also. > The group here is wonderful, we'll help all we can, good luck to > you Larry, and keep us posted. > Jan G. Kap. Ontario > > >

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Guest guest

At 05:06 PM 3/4/2002 -0600, you wrote:

> >

> >Now a question for everyone. How much time lapsed between the first and

> >second surgery?? Our first surgery was 4 months ago so I am getting a bit

> >anxious knowing that another may be right around the corner.

> >

> >Thank you for all the support and knowledge. It helps so much!!

> >

> >

> >

My second surgery was seven months out, but was a planned " second look "

with prosthesis placement. Good thing my surgeon went in again, the demon

was back! Third surgery was 18 months later, prosthesis had slipped due to

regrowth. So far, so good. No more c-toma after two years. Hope to keep

it that way!

Diane Brunet

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  • 6 months later...

Hey Becca. Welcome. Glad you came out of lurk mode. Many of us here

have wild schedules like you so we can relate. I am not doing an

official challenge but basically I am doing the best I can. I am

pleased with how things are going. I need a lifestyle change not a 12

week quick fix.

Good luck

--

- In @y..., B <vtpeach1@y...> wrote:

> I guess it's about time I introduce myself... I've

> been lurking long enough. I'm Becca working mom of a

> wild almost-2 year old. Today is my first day of my

> first challenge. I've been geared to start it before,

> but my energy and enthusiasm fizzled long before I

> even started. Today went well. I didn't get the

> workout I had hoped for, but I made it through. Ü

> Please excuse the fact that I sometimes may be a few

> days behind on threads and posts. I work as a medical

> lab technician on second and third shifts most weeks.

> And my hubby has decided to go back to school, so I'm

> the financial provider and care giver. Some days I

> might not have time to pee, let alone get on the

> computer, lol. But I'm doing this challenge for ME. I

> haven't been happy with my body since having my

> daughter. What little muscle definition I had went

> right out the window!! I'm not setting a goal for the

> body of a 's Secret model or anything... but

> having a butt like Tamilee Webb would be nice. Ü Take

> care.

>

> Becca

>

> __________________________________________________

> - We Remember

> 9-11: A tribute to the more than 3,000 lives lost

> http://dir.remember./tribute

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  • 3 weeks later...

Hey dear,

Okay one thing, when your sick you need to rest. You body needs to fight

what it is doing in order to be healthy Just try to stretch and make good

food choices. I had the same issue and have been off of serious workouts

for about 2 weeks. I have been stretching and doing some ball workouts to

do something.

Now lets talk about food. You can always get a small cooler and take items

with you. so you can pack your favorite snack. Prepare for the next day.

Maybe make extra dinner, then you can take some leftovers for a meal. Also,

you can take Sandwich with you.

Can you cook in bulk? Then on the weekend, you can boil up some eggs, cook

up some protein and rice say, and freeze it in portion sizes. Then you have

something you can take when your really busy. Have fruits around, like

apples, oranges, so you can grab on the go.

I always try to cook in bulk, because my college schedule can go crazy on

one days notice and then I have stuff in the freezer to eat.

I hope this helps

At 02:54 PM 10/02/2002 -0400, you wrote:

>So, I let myself slide the past few days as well after I was sick *sigh*

>Of course, I am disappointed in myself, but I am not going to let that get

>me down entirely! I had already printed out 12 weeks worth of planning

>sheets and I am not letting all of that paper go to waste =)

>Today was a fairly legitimate reason for not making it to the fitness

>center. I had two one hour breaks, the first I had done some homework, as

>planned. The second I ended up having to speak to a teacher about a paper

>that I had gotten back and it ended up running longer than I thought it

>would, so I didn't have time to work out. I am bound and right determined

>to at least do a fairly short PM Yoga routine tonight. I need to unwind!

>Tomorrow my classes start at 8 a.m. and since I have to drive an hour

>first and get kids ready before then...it will make for a long time. I

>have found that I do well with planning my food for the day, but not

>implementing my plan. I know that I don't have enough time to make food

>in the morning, but I haven't been preparing it the night before, so that

>has been a downfall for me. Mostly, I am just so tired at the end of the day!

>I do have use of a microwave at school, which I didn't know before, so

>that is a bonus. I just can't refrigerate things. So, my favourite snack

>of the cottage cheese/jello mixture isn't a very good idea since it gets

>pretty raunchy by the time I can get to it. Occasionally I can find a ham

>sandwich on whole wheat bread in the cafeteria. The selections that they

>have are not bad overall, but they don't really fit into BFL and I really

>just want to stick with that for this first 12 weeks.

>I WANT TO SUCCEED!! LoL Just had to remind myself.

>So, I know people ask all of the time, but any suggestions?

>

>Thanks!

>nortina

>

>

>

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Norita,

I'm in school too and eating is the biggest problem I'm having right

now! I put all my food for the day into a small ice chest and leave

it in the car. I get back there when I have time. For those times

that I need to eat and cannot get back to the car (why is it that

even the nearest parking is still a long walk to the buildings?!) I

have a small lunchbox style cooler that I can fit one meal into. If I

don't have time to even eat real food, I have a bar.

It is not easy with the school schedule, but with a little

determination I'm going to figure it out!

Alys

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  • 1 month later...

> as for me...dennis is now seeking sole custody of cameron... i have

temp cust

> until april. sigh.... please say prayers for our little family...

>

> love to all leah

>

> Leah,

I'm so sorry that you're going through all this legal stuff with your

ex and kids. I thank God everyday for my loving husband. Again, I'm

praying for you and I'm truely sorry. :(

Love,

>

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I will pray too, sorry you are going through all this, shawna.

Re: hello...

>

> > as for me...dennis is now seeking sole custody of cameron... i have

> temp cust

> > until april. sigh.... please say prayers for our little family...

> >

> > love to all leah

> >

> > Leah,

>

> I'm so sorry that you're going through all this legal stuff with your

> ex and kids. I thank God everyday for my loving husband. Again, I'm

> praying for you and I'm truely sorry. :(

>

> Love,

>

> >

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  • 7 months later...
Guest guest

Hey there ! Long time since I've heard from you. I'm glad you're

getting the show back on the road! I've been wondering what's been

happening. Have you been lurking here and on the forum all this time? Keep

us updated on your progress. We miss hearing from you.

LouAnne

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Guest guest

Thanks Everyone! I am still keeping my hopes up. Praying also! smile! Still

waiting to hear back from my audie in Spokane!

cawlaw <cawlaw@...> wrote:

Hey there ! Long time since I've heard from you. I'm glad you're

getting the show back on the road! I've been wondering what's been

happening. Have you been lurking here and on the forum all this time? Keep

us updated on your progress. We miss hearing from you.

LouAnne

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  • 4 months later...

Thanks for replying to my message. Sorry to hear that the owner is not doing well. I added the group to my buddy list, for AIM, too, and wondered if you liked to chat, and of so we could sometime. I love to talk, both IM and chat room, and right now the only chat room I ever went to has lots of people in it that like to argue and fight. I went there looking for support and friends that understand disabilities, pain, etc. The name of the group is Disabled Support for crying out loud...LOL! You'd think that's what everyone would be doing! I met lots of great people there, too, and keep in touch with them either IM or email.

See, I even TYPE alot!! LOL!

Anyway, again, thanks, and see you sometime, I hope!

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Hi Kathy,

WIll love to talk with you! Just want to let you know that your posts are

already reaching the Group now, so don't worry!

I'm Ling, and I have Type 2 diabetes and occipital neuralgia.

Feel free to contact me via email or through messager if you have it

installed!

Regards, Ling

Hello...

> Hi there! I got the invitation to join your group, sent it back, and

> never got any other notification, until I looked at another

> gtoup I am in, and saw your group name in My Groups section. I would

> love to get to know you, and take place in any chats and messages

> that you have. Emails, too. Somehow no emails was put by my name. I

> love to chat IM anytime, though I am on AOL, too, as KathBlueEyes.

> I have many back and leg troubles, diabetes, aleep apnea, and close

> to Narcolepsy...on and on...LOL...Have a great sense of humor,too.

> I guess this is long enough for one message. My ID is

> Katholdme@... if you need it. Have a great weekend!

> Kathy :o)

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Welcome aboard Kathy! I think you'll like it here. We have all kinds

of probs between us, hope we can help.

Looking forward to chatting w you.

> Hi there! I got the invitation to join your group, sent it back,

and

> never got any other notification, until I looked at another

> gtoup I am in, and saw your group name in My Groups section. I

would

> love to get to know you, and take place in any chats and messages

> that you have. Emails, too. Somehow no emails was put by my name. I

> love to chat IM anytime, though I am on AOL, too, as KathBlueEyes.

> I have many back and leg troubles, diabetes, aleep apnea, and close

> to Narcolepsy...on and on...LOL...Have a great sense of humor,too.

> I guess this is long enough for one message. My ID is

> Katholdme@y... if you need it. Have a great weekend!

> Kathy :o)

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  • 5 months later...
Guest guest

Come on guys,

If 50 % of us on this list sent this young man $10 each , he'd have over

$10,000.

THINK OF THE PUBLICITY HE AND LPA COULD GET IN WHAT MUST BE THE SMALL

TOWN OF JASPER, TENNESSEE.

To say nothing of how enterprizing he is !!!

, my check is in tomorrow's mail.

Good Luck!!

Marge Carlisle.

On Mon, 3 May 2004 15:50:08 -0400 lhookey@... writes:

>

>

> Hi. I'm using my mom's e-mail.

>

> I am Hookey and I am a 9 year old achon. I have decided to

> walk in the

> Relay for Life here in my community in Jasper, Tennessee. This is a

> 12 hour

> walk, starting at 7:00 p.m. and ending at 7:00 a.m. the next

> morning. It is on

> June 4 and 5. The team who asked me to participate is my physical

> therapist's

> office who treated me when I had surgery to straighten my bowed

> legs. They are

> all adults and I am the only child. I am trying to raise as much

> money as I can

> to try and get more than the adults on my team.

>

> I am going to TRY to walk all night, but don't know if I can or not,

> but I'm

> going to try. I wanted to see if any of you could sponsor me in my

> mission.

> All donations are tax deductible and you can make the check payable

> to the

> American Cancer Society. If you can't sponsor me, just cheer for me

> that I can

> walk as much as possible for this good cause. Any amount will be

> gladly

> accepted.

>

> If you can help me with sponsorship, please send it to me at the

> address below

> before the May 28th deadline:

>

> Hookey

> 144 Drive

> Jasper, Tennessee 37347

>

>

>

>

>

> P.S. My mom helped me with this e-mail. Thank you for your help.

>

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

> Hookey

> 423-756-6859, ext. 516

> lhookey@...

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

> ******************* CONFIDENTIALITY NOTICE *******************

> The information contained in this e-mail message is legally

> privileged and confidential, and is intended only for the use

> of the addressee. If you are not the intended recipient,

> please be aware that any dissemination, distribution or copy

> of this e-mail is prohibited. If you have received this e-mail

> in error, please immediately notify us by reply e-mail and

> delete this message and any attachments. Thank you.

>

> Please also advise us immediately if you or your employer does

> not consent to receipt of Internet email for confidential

> messages of this kind.

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

>

>

>

>

>

>

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Guest guest

,

You don't know how much your will and strength has touched

me. My favorite Uncle in the world passed away from cancer at 38

years old. I will be right along side you in spirit as far as you

can make it.

You are doing a great thing, not only for Little People but

for everyone that has or knows anyone affected by this desease.

You are the rock that this foundation is built on, and for

that, my check is in the mail to you right now, and you go out there

and get em'!

All our wishes and good thoughts are with you.

, Annette, and Gretchen Strasbaugh

>

>

> Hi. I'm using my mom's e-mail.

>

> I am Hookey and I am a 9 year old achon. I have decided

to walk in the

> Relay for Life here in my community in Jasper, Tennessee. This is

a 12 hour

> walk, starting at 7:00 p.m. and ending at 7:00 a.m. the next

morning. It is on

> June 4 and 5. The team who asked me to participate is my physical

therapist's

> office who treated me when I had surgery to straighten my bowed

legs. They are

> all adults and I am the only child. I am trying to raise as much

money as I can

> to try and get more than the adults on my team.

>

> I am going to TRY to walk all night, but don't know if I can or

not, but I'm

> going to try. I wanted to see if any of you could sponsor me in

my mission.

> All donations are tax deductible and you can make the check

payable to the

> American Cancer Society. If you can't sponsor me, just cheer for

me that I can

> walk as much as possible for this good cause. Any amount will be

gladly

> accepted.

>

> If you can help me with sponsorship, please send it to me at the

address below

> before the May 28th deadline:

>

> Hookey

> 144 Drive

> Jasper, Tennessee 37347

>

>

>

>

>

> P.S. My mom helped me with this e-mail. Thank you for your help.

>

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

> Hookey

> 423-756-6859, ext. 516

> lhookey@m...

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

> ******************* CONFIDENTIALITY NOTICE *******************

> The information contained in this e-mail message is legally

> privileged and confidential, and is intended only for the use

> of the addressee. If you are not the intended recipient,

> please be aware that any dissemination, distribution or copy

> of this e-mail is prohibited. If you have received this e-mail

> in error, please immediately notify us by reply e-mail and

> delete this message and any attachments. Thank you.

>

> Please also advise us immediately if you or your employer does

> not consent to receipt of Internet email for confidential

> messages of this kind.

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

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Guest guest

,

Great going, you're doing more than you'll ever know for a great cause.

I've lost three grandparents and two aunts to cancer, and my wife has lost

her two parents to it too. My father had Prostate Cancer two years ago, and

so far has beaten it, thanks to medical research funded by the American

Cancer Society. So I can appreciate what you are doing. What amounts are you

taking, like a dollar a mile, or hour, or is it more like five dollars an

hour. Please let me know, so I can be one of your many sponsors, OK.

Rob Tille

Hello...

>

>

> Hi. I'm using my mom's e-mail.

>

> I am Hookey and I am a 9 year old achon. I have decided to walk

in the

> Relay for Life here in my community in Jasper, Tennessee. This is a 12

hour

> walk, starting at 7:00 p.m. and ending at 7:00 a.m. the next morning. It

is on

> June 4 and 5. The team who asked me to participate is my physical

therapist's

> office who treated me when I had surgery to straighten my bowed legs.

They are

> all adults and I am the only child. I am trying to raise as much money as

I can

> to try and get more than the adults on my team.

>

> I am going to TRY to walk all night, but don't know if I can or not, but

I'm

> going to try. I wanted to see if any of you could sponsor me in my

mission.

> All donations are tax deductible and you can make the check payable to the

> American Cancer Society. If you can't sponsor me, just cheer for me that

I can

> walk as much as possible for this good cause. Any amount will be gladly

> accepted.

>

> If you can help me with sponsorship, please send it to me at the address

below

> before the May 28th deadline:

>

> Hookey

> 144 Drive

> Jasper, Tennessee 37347

>

>

>

>

>

> P.S. My mom helped me with this e-mail. Thank you for your help.

>

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

> Hookey

> 423-756-6859, ext. 516

> lhookey@...

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

> ******************* CONFIDENTIALITY NOTICE *******************

> The information contained in this e-mail message is legally

> privileged and confidential, and is intended only for the use

> of the addressee. If you are not the intended recipient,

> please be aware that any dissemination, distribution or copy

> of this e-mail is prohibited. If you have received this e-mail

> in error, please immediately notify us by reply e-mail and

> delete this message and any attachments. Thank you.

>

> Please also advise us immediately if you or your employer does

> not consent to receipt of Internet email for confidential

> messages of this kind.

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

>

>

>

>

>

>

> ===

>

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  • 6 months later...

Hi ,No we don't know every thing, but we do know what won't work OK...Having gone though all the sale pitches and all,,What we were doing was pointing out that herbal method are not going to cure the disease OK..That when it gets right down to the nity gritty A Medical Doctor is needed..But everybody is entitled to their own way of dealing with this OK..It is not condemnation, it is our right to express a opinion..Sorry if that bothers you, but somethimes it well feel like a whole herd of brothers and sister in your business..And I am glad you state your opinion...Thank you..Kathy b..emily34756 <emily34756@...> wrote: Hello all...I know I am new and just joined, but I want to get something off my chest here.Kathy Brunow

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