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I NEVER have a fever regardless of how sick I am. I can feel like death warmed

over and no fever. I'm just a strange duck *lol*

Re: Question

janissa@... wrote:

>

> Sounds like it might be gastroenteritis, honey -- fancy name for a stomach

> bug. We are having TONS of people in the ERs right now with this, some

> with fever, some not.

Interesting Em, I thought in order for it to be a bug, you had to have a

temp. I got something very similar on Halloween night. Started by

throwing up, then getting hot and cold, and diarrhea. The vomiting

stopped after the evening, but I spent the next two weeks with very

loose stools. Any time I peed, I had no control over my bowels. I

thought since I didn't run a temp, it wasn't a bug. Gradually

everything became normal.

Darcy

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Your email made me laugh! I absolutely never run a fever either. I remember

being a kid in the nurses office with a fever of 99 degrees and no-one would

let me go home! My temp on a normal day is in the low 97's. As well, my

blood pressure is always really low! Last time I was at the hospital for a

proceedure, it was 95/52 and the nurse was a bit funky with processing me

along!

Missy

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<<

I NEVER have a fever regardless of how sick I am. I can feel like death

warmed over and no fever. I'm just a strange duck *lol*

>>

I very seldom have a fever either. My temperature runs from 96.7 to 97.6.

If I hit 98, I have a temperature. Try and convince a doctor that when your

temp is what is considered normal is a temp and you are sick. I seldom do

run a temp even when I am very sick. Doctors just don't want to believe that

you are so sick that you can hardly move with the flu, let's say, until your

temp is at least 100.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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<<

I NEVER have a fever regardless of how sick I am. I can feel like death

warmed over and no fever. I'm just a strange duck *lol*

>>

I very seldom have a fever either. My temperature runs from 96.7 to 97.6.

If I hit 98, I have a temperature. Try and convince a doctor that when your

temp is what is considered normal is a temp and you are sick. I seldom do

run a temp even when I am very sick. Doctors just don't want to believe that

you are so sick that you can hardly move with the flu, let's say, until your

temp is at least 100.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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<<

I NEVER have a fever regardless of how sick I am. I can feel like death

warmed over and no fever. I'm just a strange duck *lol*

>>

I very seldom have a fever either. My temperature runs from 96.7 to 97.6.

If I hit 98, I have a temperature. Try and convince a doctor that when your

temp is what is considered normal is a temp and you are sick. I seldom do

run a temp even when I am very sick. Doctors just don't want to believe that

you are so sick that you can hardly move with the flu, let's say, until your

temp is at least 100.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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patidu@... wrote:

> Try and convince a doctor that when your

> temp is what is considered normal is a temp and you are sick. I seldom do

> run a temp even when I am very sick.

Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick " . The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first.

Darcy

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patidu@... wrote:

> Try and convince a doctor that when your

> temp is what is considered normal is a temp and you are sick. I seldom do

> run a temp even when I am very sick.

Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick " . The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first.

Darcy

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patidu@... wrote:

> Try and convince a doctor that when your

> temp is what is considered normal is a temp and you are sick. I seldom do

> run a temp even when I am very sick.

Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick " . The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first.

Darcy

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< Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick. " The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first. >>

Darcy,

I think that I have just about heard just about everything and the something

like this comes along and I realize that there are still many strange

happenings around.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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< Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick. " The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first. >>

Darcy,

I think that I have just about heard just about everything and the something

like this comes along and I realize that there are still many strange

happenings around.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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< Now imagine having a coworker who lives and dies by a

thermometer/temperature who want to get an " office thermometer so we can

check out temperature before asking the boss to go home so he'll believe

we're sick. " The moment those words fell from her lips, I vetoed it and

told them that I was smart enough to know when I needed to go home and

didn't need to check a thermometer first. >>

Darcy,

I think that I have just about heard just about everything and the something

like this comes along and I realize that there are still many strange

happenings around.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Hi

I take Ultram also, it really doesn't help alot just takes the edge off so I can

stand it. I take Celebrex for the arthritis pain in my hands, knees and spine.

You may want to see if you can try that and see if it does help. You may have

arthritis also. Mine is a very mild case but the fibro makes it extremely more

painful than it would normally be.

I do have a question for everyone: How much trouble is the Fibro fog? My short

term memory is atrocious! I can't even remember a phone number long enough to

dial it! One thing I do that seems to help my congnitive brain is to play

majong on the computer. It seems to help me focus correctly.

Also my mind works really weird. When I type many words have the correct letters

but they are either (now get this!) jumbled or completely backward like in a

mirror OR this one is good, they are the correct letters IF I were to put my

hands opposite than what they are on the keyboard - like my left where my right

is etc. The letters would be like if I typed " set " but it will come out " ko[ "

too weird huh? I spend most of my typing time fixing my words. I type " eht " all

the time for " the " . Does anyone have this problem? My daughter is getting really

good at reading my words as I don't fix them when we are instant messaging

because it is so hard for me to type to begin with so we decided that I

shouldn't fix it.

Well I have rambled enough. :o)

AlyceAnn

Hello group~ i have posted quite awhile back and read all your posts

as i can but lately i had problems with my new insuraqnce co. not

paying for my ultram prescription;we appealed it and again got turned

down..now it's our 2nd appeal and i had to give ins. co. a list of

all meds tried,side effect,etc just to get them to cover my meds

still in the 2nd appeal(next i will go back on patients assistance

where i am on disability and cannot afford $95.00 a

month)..lol..anyhow i'm still waiting and i'd like to ask others out

there if there is some soothing things one can do when fibro has

severly affected the lower spine especially to a point that sitting

hurts and i have to lay flat on bed..also can bearly get from a

sitting position to a standing one and near scream aloud every time

(now mobility is being affected too)....I know this will be with me

chroniclly but for the time being i am just looking for some

suggestions on soothing great pain i have til my meds are covered

soon again..thanks for reading and any help is greatly appreciated

and still glad to be here(ps have fms0cfs 20yrs but this is the worst

it's ever been!!) Mitzi

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Hi

I take Ultram also, it really doesn't help alot just takes the edge off so I can

stand it. I take Celebrex for the arthritis pain in my hands, knees and spine.

You may want to see if you can try that and see if it does help. You may have

arthritis also. Mine is a very mild case but the fibro makes it extremely more

painful than it would normally be.

I do have a question for everyone: How much trouble is the Fibro fog? My short

term memory is atrocious! I can't even remember a phone number long enough to

dial it! One thing I do that seems to help my congnitive brain is to play

majong on the computer. It seems to help me focus correctly.

Also my mind works really weird. When I type many words have the correct letters

but they are either (now get this!) jumbled or completely backward like in a

mirror OR this one is good, they are the correct letters IF I were to put my

hands opposite than what they are on the keyboard - like my left where my right

is etc. The letters would be like if I typed " set " but it will come out " ko[ "

too weird huh? I spend most of my typing time fixing my words. I type " eht " all

the time for " the " . Does anyone have this problem? My daughter is getting really

good at reading my words as I don't fix them when we are instant messaging

because it is so hard for me to type to begin with so we decided that I

shouldn't fix it.

Well I have rambled enough. :o)

AlyceAnn

Hello group~ i have posted quite awhile back and read all your posts

as i can but lately i had problems with my new insuraqnce co. not

paying for my ultram prescription;we appealed it and again got turned

down..now it's our 2nd appeal and i had to give ins. co. a list of

all meds tried,side effect,etc just to get them to cover my meds

still in the 2nd appeal(next i will go back on patients assistance

where i am on disability and cannot afford $95.00 a

month)..lol..anyhow i'm still waiting and i'd like to ask others out

there if there is some soothing things one can do when fibro has

severly affected the lower spine especially to a point that sitting

hurts and i have to lay flat on bed..also can bearly get from a

sitting position to a standing one and near scream aloud every time

(now mobility is being affected too)....I know this will be with me

chroniclly but for the time being i am just looking for some

suggestions on soothing great pain i have til my meds are covered

soon again..thanks for reading and any help is greatly appreciated

and still glad to be here(ps have fms0cfs 20yrs but this is the worst

it's ever been!!) Mitzi

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Hi

I take Ultram also, it really doesn't help alot just takes the edge off so I can

stand it. I take Celebrex for the arthritis pain in my hands, knees and spine.

You may want to see if you can try that and see if it does help. You may have

arthritis also. Mine is a very mild case but the fibro makes it extremely more

painful than it would normally be.

I do have a question for everyone: How much trouble is the Fibro fog? My short

term memory is atrocious! I can't even remember a phone number long enough to

dial it! One thing I do that seems to help my congnitive brain is to play

majong on the computer. It seems to help me focus correctly.

Also my mind works really weird. When I type many words have the correct letters

but they are either (now get this!) jumbled or completely backward like in a

mirror OR this one is good, they are the correct letters IF I were to put my

hands opposite than what they are on the keyboard - like my left where my right

is etc. The letters would be like if I typed " set " but it will come out " ko[ "

too weird huh? I spend most of my typing time fixing my words. I type " eht " all

the time for " the " . Does anyone have this problem? My daughter is getting really

good at reading my words as I don't fix them when we are instant messaging

because it is so hard for me to type to begin with so we decided that I

shouldn't fix it.

Well I have rambled enough. :o)

AlyceAnn

Hello group~ i have posted quite awhile back and read all your posts

as i can but lately i had problems with my new insuraqnce co. not

paying for my ultram prescription;we appealed it and again got turned

down..now it's our 2nd appeal and i had to give ins. co. a list of

all meds tried,side effect,etc just to get them to cover my meds

still in the 2nd appeal(next i will go back on patients assistance

where i am on disability and cannot afford $95.00 a

month)..lol..anyhow i'm still waiting and i'd like to ask others out

there if there is some soothing things one can do when fibro has

severly affected the lower spine especially to a point that sitting

hurts and i have to lay flat on bed..also can bearly get from a

sitting position to a standing one and near scream aloud every time

(now mobility is being affected too)....I know this will be with me

chroniclly but for the time being i am just looking for some

suggestions on soothing great pain i have til my meds are covered

soon again..thanks for reading and any help is greatly appreciated

and still glad to be here(ps have fms0cfs 20yrs but this is the worst

it's ever been!!) Mitzi

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Yes, yes & YES!! Well, to everything except the Ultram and Celebrex<g>.

Ultram makes me throw up, and I don't trust the new 2 inhibitors, so

won't take Celebrex or Vioxx - just stick with good old Relafen and it

works pretty well. But the other stuff - the memory and especially the

typing?? YES!! You don't want to know how many words I've had to correct

to get this far into the email<g>. My memory is getting a bit better, but

every time I have a med change, it goes south again - so I'm thinking that

it's more a product of the medications than fibro-fog - or at least a

combination of the two. My meds were adjusted up again last week, so I'm

expecting to be pretty fogged out for at least a couple of weeks....<sigh>

But the typing is constant - and it's not just typing - I do it when I'm

writing too!! I wrote a note on a piece of paper to my husband a few weeks

back - it was late at night, I was exhausted, and the fog was REALLLLYYY

thick - when I tried to read it the next morning, it was completly

illegible!! Not from bad handwriting, but because there were extra words

in, things were spelled completely wrong, and I kept going off on tangents

that had nothing to do with the note! It was quite bizarre, and made me

glad that I've gotten in the habit of proofreading everything that I write

at least twice, 'cause now I REALLY need it! LOL!

-

At 09:10 PM 12/8/01 -0500, you wrote:

>Hi

>I take Ultram also, it really doesn't help alot just takes the edge off so

I can stand it. I take Celebrex for the arthritis pain in my hands, knees

and spine. You may want to see if you can try that and see if it does help.

You may have arthritis also. Mine is a very mild case but the fibro makes

it extremely more painful than it would normally be.

>

>I do have a question for everyone: How much trouble is the Fibro fog? My

short term memory is atrocious! I can't even remember a phone number long

enough to dial it! One thing I do that seems to help my congnitive brain

is to play majong on the computer. It seems to help me focus correctly.

>

>Also my mind works really weird. When I type many words have the correct

letters but they are either (now get this!) jumbled or completely backward

like in a mirror OR this one is good, they are the correct letters IF I

were to put my hands opposite than what they are on the keyboard - like my

left where my right is etc. The letters would be like if I typed " set " but

it will come out " ko[ " too weird huh? I spend most of my typing time fixing

my words. I type " eht " all the time for " the " . Does anyone have this

problem? My daughter is getting really good at reading my words as I don't

fix them when we are instant messaging because it is so hard for me to type

to begin with so we decided that I shouldn't fix it.

>

>Well I have rambled enough. :o)

>AlyceAnn

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Yes, yes & YES!! Well, to everything except the Ultram and Celebrex<g>.

Ultram makes me throw up, and I don't trust the new 2 inhibitors, so

won't take Celebrex or Vioxx - just stick with good old Relafen and it

works pretty well. But the other stuff - the memory and especially the

typing?? YES!! You don't want to know how many words I've had to correct

to get this far into the email<g>. My memory is getting a bit better, but

every time I have a med change, it goes south again - so I'm thinking that

it's more a product of the medications than fibro-fog - or at least a

combination of the two. My meds were adjusted up again last week, so I'm

expecting to be pretty fogged out for at least a couple of weeks....<sigh>

But the typing is constant - and it's not just typing - I do it when I'm

writing too!! I wrote a note on a piece of paper to my husband a few weeks

back - it was late at night, I was exhausted, and the fog was REALLLLYYY

thick - when I tried to read it the next morning, it was completly

illegible!! Not from bad handwriting, but because there were extra words

in, things were spelled completely wrong, and I kept going off on tangents

that had nothing to do with the note! It was quite bizarre, and made me

glad that I've gotten in the habit of proofreading everything that I write

at least twice, 'cause now I REALLY need it! LOL!

-

At 09:10 PM 12/8/01 -0500, you wrote:

>Hi

>I take Ultram also, it really doesn't help alot just takes the edge off so

I can stand it. I take Celebrex for the arthritis pain in my hands, knees

and spine. You may want to see if you can try that and see if it does help.

You may have arthritis also. Mine is a very mild case but the fibro makes

it extremely more painful than it would normally be.

>

>I do have a question for everyone: How much trouble is the Fibro fog? My

short term memory is atrocious! I can't even remember a phone number long

enough to dial it! One thing I do that seems to help my congnitive brain

is to play majong on the computer. It seems to help me focus correctly.

>

>Also my mind works really weird. When I type many words have the correct

letters but they are either (now get this!) jumbled or completely backward

like in a mirror OR this one is good, they are the correct letters IF I

were to put my hands opposite than what they are on the keyboard - like my

left where my right is etc. The letters would be like if I typed " set " but

it will come out " ko[ " too weird huh? I spend most of my typing time fixing

my words. I type " eht " all the time for " the " . Does anyone have this

problem? My daughter is getting really good at reading my words as I don't

fix them when we are instant messaging because it is so hard for me to type

to begin with so we decided that I shouldn't fix it.

>

>Well I have rambled enough. :o)

>AlyceAnn

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Yes, yes & YES!! Well, to everything except the Ultram and Celebrex<g>.

Ultram makes me throw up, and I don't trust the new 2 inhibitors, so

won't take Celebrex or Vioxx - just stick with good old Relafen and it

works pretty well. But the other stuff - the memory and especially the

typing?? YES!! You don't want to know how many words I've had to correct

to get this far into the email<g>. My memory is getting a bit better, but

every time I have a med change, it goes south again - so I'm thinking that

it's more a product of the medications than fibro-fog - or at least a

combination of the two. My meds were adjusted up again last week, so I'm

expecting to be pretty fogged out for at least a couple of weeks....<sigh>

But the typing is constant - and it's not just typing - I do it when I'm

writing too!! I wrote a note on a piece of paper to my husband a few weeks

back - it was late at night, I was exhausted, and the fog was REALLLLYYY

thick - when I tried to read it the next morning, it was completly

illegible!! Not from bad handwriting, but because there were extra words

in, things were spelled completely wrong, and I kept going off on tangents

that had nothing to do with the note! It was quite bizarre, and made me

glad that I've gotten in the habit of proofreading everything that I write

at least twice, 'cause now I REALLY need it! LOL!

-

At 09:10 PM 12/8/01 -0500, you wrote:

>Hi

>I take Ultram also, it really doesn't help alot just takes the edge off so

I can stand it. I take Celebrex for the arthritis pain in my hands, knees

and spine. You may want to see if you can try that and see if it does help.

You may have arthritis also. Mine is a very mild case but the fibro makes

it extremely more painful than it would normally be.

>

>I do have a question for everyone: How much trouble is the Fibro fog? My

short term memory is atrocious! I can't even remember a phone number long

enough to dial it! One thing I do that seems to help my congnitive brain

is to play majong on the computer. It seems to help me focus correctly.

>

>Also my mind works really weird. When I type many words have the correct

letters but they are either (now get this!) jumbled or completely backward

like in a mirror OR this one is good, they are the correct letters IF I

were to put my hands opposite than what they are on the keyboard - like my

left where my right is etc. The letters would be like if I typed " set " but

it will come out " ko[ " too weird huh? I spend most of my typing time fixing

my words. I type " eht " all the time for " the " . Does anyone have this

problem? My daughter is getting really good at reading my words as I don't

fix them when we are instant messaging because it is so hard for me to type

to begin with so we decided that I shouldn't fix it.

>

>Well I have rambled enough. :o)

>AlyceAnn

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Hi Mitzi

Have you had your lower back x-rayed or had a milogram or MRI? That kind of

pain sounds more like a spinal problem than plain FMS. Actually, it sounds very

much what I went through in the late '80's and early '90's. I eventually had

surgery and after about a year of recuperation, that excruciating pain was

gone. It still hurts somewhat, but never enough to cause me to take to my bed.

Just a thought.

Lyndi

kissndolphin wrote:

> Hello group~ i have posted quite awhile back and read all your posts

> as i can but lately i had problems with my new insuraqnce co. not

> paying for my ultram prescription;we appealed it and again got turned

> down..now it's our 2nd appeal and i had to give ins. co. a list of

> all meds tried,side effect,etc just to get them to cover my meds

> still in the 2nd appeal(next i will go back on patients assistance

> where i am on disability and cannot afford $95.00 a

> month)..lol..anyhow i'm still waiting and i'd like to ask others out

> there if there is some soothing things one can do when fibro has

> severly affected the lower spine especially to a point that sitting

> hurts and i have to lay flat on bed..also can bearly get from a

> sitting position to a standing one and near scream aloud every time

> (now mobility is being affected too)....I know this will be with me

> chroniclly but for the time being i am just looking for some

> suggestions on soothing great pain i have til my meds are covered

> soon again..thanks for reading and any help is greatly appreciated

> and still glad to be here(ps have fms0cfs 20yrs but this is the worst

> it's ever been!!) Mitzi

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Hi Mitzi

Have you had your lower back x-rayed or had a milogram or MRI? That kind of

pain sounds more like a spinal problem than plain FMS. Actually, it sounds very

much what I went through in the late '80's and early '90's. I eventually had

surgery and after about a year of recuperation, that excruciating pain was

gone. It still hurts somewhat, but never enough to cause me to take to my bed.

Just a thought.

Lyndi

kissndolphin wrote:

> Hello group~ i have posted quite awhile back and read all your posts

> as i can but lately i had problems with my new insuraqnce co. not

> paying for my ultram prescription;we appealed it and again got turned

> down..now it's our 2nd appeal and i had to give ins. co. a list of

> all meds tried,side effect,etc just to get them to cover my meds

> still in the 2nd appeal(next i will go back on patients assistance

> where i am on disability and cannot afford $95.00 a

> month)..lol..anyhow i'm still waiting and i'd like to ask others out

> there if there is some soothing things one can do when fibro has

> severly affected the lower spine especially to a point that sitting

> hurts and i have to lay flat on bed..also can bearly get from a

> sitting position to a standing one and near scream aloud every time

> (now mobility is being affected too)....I know this will be with me

> chroniclly but for the time being i am just looking for some

> suggestions on soothing great pain i have til my meds are covered

> soon again..thanks for reading and any help is greatly appreciated

> and still glad to be here(ps have fms0cfs 20yrs but this is the worst

> it's ever been!!) Mitzi

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< But the typing is constant - and it's not just typing - I do it when I'm

writing too!! >>

This can't help when writing but don't you have a spell check on your

computer. I couldn't do without mine. I use to be a great speller but know,

forget it.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Thanks for the suggestion Irene, but unfortunately, my email program

actually doesn't have a spellchecker on it! It's an older free program

(not even available anymore that I can find!)that I keep using because I

like the way it works, and I don't like the newer programs - they do too

many things automatically that I'd rather do manually. But the lack of a

spellcheck is a downside to it. Luckily, I can usually catch most of the

problems by diligent proofreading (something I wish more people would do

sometimes<g>). The other problem that I have - and I'd love to know if

anyone else does - is not being able to come up with the right word. It

doesn't have to be a " hard " word either - it's like my mind just " forgets "

words sometimes and someone either has to remind me (good thing my husband

& I have been together long enough that we read each others' minds!) or I

have to just sit until it comes to me - rather embarrassing sometimes

during a conversation!! Or I'll do stuff like calling the refrigerator the

microwave, etc. Anyone else run into this??

- (btw - I don't get offended if people point out spelling or usage

mess-ups in my emails, so anyone that sees anything, feel free to write me

privately and tell me about it :-)

At 03:05 PM 12/9/01 EST, you wrote:

>This can't help when writing but don't you have a spell check on your

>computer. I couldn't do without mine. I use to be a great speller but

know,

>forget it.

>

>Take care,

>Irene

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Thanks for the suggestion Irene, but unfortunately, my email program

actually doesn't have a spellchecker on it! It's an older free program

(not even available anymore that I can find!)that I keep using because I

like the way it works, and I don't like the newer programs - they do too

many things automatically that I'd rather do manually. But the lack of a

spellcheck is a downside to it. Luckily, I can usually catch most of the

problems by diligent proofreading (something I wish more people would do

sometimes<g>). The other problem that I have - and I'd love to know if

anyone else does - is not being able to come up with the right word. It

doesn't have to be a " hard " word either - it's like my mind just " forgets "

words sometimes and someone either has to remind me (good thing my husband

& I have been together long enough that we read each others' minds!) or I

have to just sit until it comes to me - rather embarrassing sometimes

during a conversation!! Or I'll do stuff like calling the refrigerator the

microwave, etc. Anyone else run into this??

- (btw - I don't get offended if people point out spelling or usage

mess-ups in my emails, so anyone that sees anything, feel free to write me

privately and tell me about it :-)

At 03:05 PM 12/9/01 EST, you wrote:

>This can't help when writing but don't you have a spell check on your

>computer. I couldn't do without mine. I use to be a great speller but

know,

>forget it.

>

>Take care,

>Irene

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  • 2 months later...

Jen,

I know it is a shock to see how up and out the foot is! If you go to

the photos section and look in Calebs album you can see what his and

his friend Edens casts looked like the day of their Tenotomies were

done at the U of Iowa. It is picture #7.

Also about the dorsoflexion, Calebs was not great at first and did

improve in the shoes. Now his is fine.

And I am always for Dr. Ponseti's opinion!!!! Who would know more

than he would?

Best of luck, you are in our prayers

and Caleb 3-31-01

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Jen,

I know it is a shock to see how up and out the foot is! If you go to

the photos section and look in Calebs album you can see what his and

his friend Edens casts looked like the day of their Tenotomies were

done at the U of Iowa. It is picture #7.

Also about the dorsoflexion, Calebs was not great at first and did

improve in the shoes. Now his is fine.

And I am always for Dr. Ponseti's opinion!!!! Who would know more

than he would?

Best of luck, you are in our prayers

and Caleb 3-31-01

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Jen,

I know it is a shock to see how up and out the foot is! If you go to

the photos section and look in Calebs album you can see what his and

his friend Edens casts looked like the day of their Tenotomies were

done at the U of Iowa. It is picture #7.

Also about the dorsoflexion, Calebs was not great at first and did

improve in the shoes. Now his is fine.

And I am always for Dr. Ponseti's opinion!!!! Who would know more

than he would?

Best of luck, you are in our prayers

and Caleb 3-31-01

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