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I would type it 8-9/10.

Could it be lorezepam which is prescribed at 1 mg , 2 mg orally?

(Sedative)

On Fri, 17 Mar 2000 10:01:25 EST Shellwipp@... writes:

> Good Friday Morning All,

>

> Can anyone help with these?

>

> This pt. has wrist pain and I am wondering how to type this: In the

>

> beginning, her wrists were hurting at about a eight or nine over 10

> pain

> level OR should it be 8-9/10 or something else?

>

> This pt. has increased stress and is presently taking Celexa. I

> have

> arranged for her to take *ir-iz-a-pam* one mg.

>

> TIA,

> : )

>

>

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  • 2 weeks later...
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In a message dated 03/31/2000 8:06:40 PM Central Standard Time,

JadeCheyenne@... writes:

Hi ,

For #1 could the doc be saying *per* staph aureau? For #2 I think you are

exactly right about the cillin. The accounts I have want slang and

abbreviations typed out. I can't find *cillin* as a word. If it were me, I

would type penicillin. For #3, The

turbinates are not obstructed would be correct. On #4 he is probably

referring to Levothroid and just not pronouncing it clear. On #5 it may be

*hydroxyamphetamine* I am not sure about *parobid*. And for #6 could the doc

possibly be saying *probably laryngis*? Just a thought. I couldn't find

anything else and I know my docs do that all the time. I hope I helped a

little. Don't ya just love it when the docs are clear as mud? : )

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At 09:05 PM 3/31/00 EST, JadeCheyenne@... wrote:

>

>1. The patient states that he cultured his nose and has a s/l Pir staph

>aureau cultured and requesting an antibiotic. Surgical history is that of

>septoplasty with s/l S and R inferior turbinates performed on 12/14/98.

I think " S and R " is actually SMR (submucous resection).

>

>3. Which would be better to say: The turbinates are not obstructive or The

>turbinates are not obstructed.

I would choose " obstructive " . The nasal turbinates themselves do not get

obstructed per se, but they can get congested, swollen, and boggy, thereby

causing obstruction to the nasal passageways. Consequently they would be

obstructive. This is why they are sometimes resected.

>

>5. She is allergic to s/l hydroxyamine and s/l parobid.

There is a hydroxyzine (tranquilizer), but there may be others also that

resemble this. I really can't find any " bid " words that might fit here.

There is Pavabid, which is a vasodilator (treatment for ischemias) but

would hesitate on that because ofthe " r " sound you are picking up.

Sorry I can't be of more help.

Judy

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Jade, Here are some of the answers.

1. I am not sure about the pir part but it is Staph aureus that was cultured.

Also I don't know about the S and R, sorry.

2. I would type " cillin " family in quotes. Do not type penicillin, as has been

suggested by another post, since there are other cillin drugs, methicillin and

oxacillin for example.

3. The inferior turbinates are not obstructed.

4. I hear Levothyroid all the time and am glad that you took the time to find

out it is not a word. Many doctors do not realize that Levothroid does not have

the " y " in it, as the generic form is levothyroxine.

5. Sorry, not sure about hydroxyamine. How about Pavabid, with sloppy

handwriting it would look a lot like parobid.

6. I am not sure about this but could it somehow be presby larynges or some

such? presby is a word beginning which denotes relationship to old age. No, I

could not find presby larynges anywhere, but am wondering.

MG

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In a message dated 04/05/2000 7:19:12 PM Central Daylight Time, fureyd@...

writes:

Hi Dana,

I didn't see any responses to your questions so here is what I have found.

The rest I will keep checking on. I hope this helps.

: )

s/l Nortate for cea. This is Noritate

s/l ectinakeratosis on the lip is treated with cryosurgery. This is actinic

keratosis

and one more a med or lotion (not sure) for multiple seborrheic keratoses

s/l

eccidex. I think this one may be Actinex, it is a topical.

>>

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In a message dated 04/05/2000 7:19:12 PM Central Daylight Time, fureyd@...

writes:

Dana,

I figured out a couple more.

s/l Trias Gel 6% at bedtime ( for acne and This is Triaz

moles)

Eczema is treated with s/l deselen lotion. Could this be Desitin?

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  • 1 month later...
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Deborah Browder wrote:

> 1. Grams percent is transcribed as grams% always.

>

> 2. I have two possible solutions for you. The first is lymphocytic colitis,

> which can sound like follitis. The other is lymphocytic folliculitis.

>

> Hope that helped!!

Did it ever! I can't believe I couldn't hear " colitis, " but he mumbled kind of

an " f " sound in there and threw me completely. Thanks!!!

Jayni

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On Tuesday, May 16, 2000 at 7:18 AM or thereabouts, Jayni wrote the

following about Questions:

Jayni> Deborah Browder wrote:

>> 1. Grams percent is transcribed as grams% always.

According to Stedman's Abbreviations, g% is an acceptable

abbreviation. I'd be interested in knowing the source for the

definitive answer given above.

Thanks.

Chuck

--

=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=

Chuck Mattsen mattsen@...

http://www.users.uswest.net/~mattsen

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Random Thought/Quote for this Message:

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  • 2 months later...
Guest guest

Lily Beekman wrote:

<< Question: I have read that you should not exercise if

your blood sugar readings are to high, why not? Since

exercise will cause the blood sugar numbers to come

down. >>

I'm stumped right now ... can't recall if that magic number is 200 or 250?

Anyway, I think their reasoning is that you could possibly develop lactic

acidosis (a rare condition, but fatal half the time!).

<< Question: I read a couple of weeks ago that glucose

#'s may become elevated when it is extremely hot.

Well, summer has hit, and my sugars seem high, when I

haven't really eaten anything out of whack. What does

the heat have to do with blood sugar control? >>

My hunch is dehydration, which reduces blood volume to a surprising degree.

(I managed to seriously overmedicate myself with blood pressure meds when I

was dehydrated.) As blood volume is reduced, all the components in our

bloodstream represent a larger percentage of the total ... sort of like

boiling something sweet down to make a syrup.

Susie

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  • 11 months later...
Guest guest

Nooo-body has ever heard of IgA nephropathy until someone says you have it!

Your nephrologist doesn't sound to be very communicative. I have never heard

of a nephrologist telling a patient that other organs are likely to fail

sooner than the kidneys because of IgA nephropathy. However, what they will

sometimes say to reassure a patient is that the odds are you will live to a

ripe old age and something else will get you before the kidneys do.

It's very rare (and debatable) for IgAN itself to affect other organs,

although it's not impossible, and it mostly happens in cases where the IgAN

itself is secondary to another disease like lupus and scleroderma, for

example. Your nephrologist would have known and told you if you had this,

unless he or she is totally incompetent.

Now, nephrologists are usually very careful about offering predictions like

6 or 7 years, because it's almost impossible to guess until the later stages

of renal failure. Are you certain your lab results are normal?

If you have uncontrolled high blood pressure though, what happens is that

this accelerates the rate of losing kidney function (because the high blood

pressure itself damages the kidneys, on top of what the IgAN is doing to

them). So, it's very, very important to work on blood pressure to keep it

around 120/80. This can mean dietary modifications, exercise, but

eventually, most of us who have high blood pressure induced by IgAN end up

on 2 or 3 different blood pressure meds at the same time. Also, what your

nephrologist may have meant is that the high blood pressure itself is a risk

factor for other things besides the kidneys - like cardiovascular things. A

stroke or a heart attack from long-time, uncontrolled high blood pressure

will affect you a lot more than chronic kidney failure does. BUT, you do

have to make sure that you really do have high blood pressure. This means it

has to be measured correctly and on successive visits. The little home

machine sometimes aren't very reliable on some people, plus people often

forget that what matters is the at rest blood pressure (that means

comfortably seated for at least 5 minutes, arm well-supported at heart

level, not right after eating, and preferably not for a couple of hours

after having anything with caffeine in it).

The percentage of people who end up in complete renal failure from IgAN

varies according to different sources, but it's in the area of 30%, that is,

30% or so of patients end up in end-stage renal failure between 10 and 25

years after diagnosis. Don't hold me to those exact percentages though --

but if they are correct, the majority will never reach end-stage renal

disease, and there is no good way to predict who will and who won't, unless

the disease is obviously rapidly-progressive.

Don't know why you feel like you do, especially since we don't know your lab

numbers for creatinine and proteinuria.

Pierre

Questions

> Well lets see, About three years ago I was diagnosed

> with IGA nep. I had never heard of it, or known any one

> that ever had any type of Kidney problem.

>

> I was only able to see a nephrologist one time before I

> lost my insurance. And asking an M.D. questions about

> how can I tell if the pain in my sides are a result of my

> kidneys, or is it being caused by the pinched nerves in my

> low back?? Well let's just say " NOT "

>

> I have always been vary active, and now there are times that all

> I want to do is stay in bed. " I just feel like crap "

>

> My blood pressure is way high even though I am taking pills.

>

> When I did have a chance to talk with the neprologist he told

> me that the problem with having IGA is that it attacks other

> organs, and that I would more than likely have more serious

> problems before my kidneys finally shut down.

>

> He said that I would probably have a hart attack, due to the

> blood pressure problem.

>

> He told me that he figured that it would take about 3-7 years.

> And that was almost three years ago. I told myself that he was

> full of it, But with the way that I have been feeling (I wounder)

>

> I know that there is no way out of this world alive " BUT "

> Not knowing what to expect or having access to answers is the pits.

>

>

>

>

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It seems to me that you need to see a nephrologist,

right now. Ask your GP about a referral. I don't know

that much about your medical system and I am a rabidly

patriotic Canadian (big fan of the socialized

medicine) so I'd rather not get into the issue of

medical insurance but it seems to me that whatever

your situation, you need to move heaven and earth to

get your butt, (and your kidneys) into a nephro, now.

There has to be some kind of contingency plan in the

USA for people who can't afford insurance -- ask your

doctor what it is. Call the hospital, ask them, sheesh

go to emergency if you have to but see a specialist.

And if it means selling something to pay for it, even

your car or your home, I'd say do it. A comfortable

standard of living is pretty meaningless if you're not

alive.

What I'm trying to say is; Take this seriously. Forget

the support groups until you've seen a doctor.

Untreated IgA leads to kidney failure and untreated

kidney failure is fatal.

--- lemac100us@... wrote:

<HR>

<html><body>

<tt>

Well lets see, & nbsp; About three years ago I was

diagnosed<BR>

with IGA nep. & nbsp; & nbsp; I had never heard of it, or

known any one <BR>

that ever had any type of Kidney problem.<BR>

<BR>

I was only able to see a nephrologist one time before

I <BR>

lost my insurance. & nbsp; And asking an M.D. questions

about<BR>

how can I tell if the pain in my sides are a result of

my <BR>

kidneys, or is it being caused by the pinched nerves

in my<BR>

low back?? & nbsp; & nbsp; & nbsp; Well let's just say

& quot;NOT & quot;<BR>

<BR>

I have always been vary active, and now there are

times that all <BR>

I want to do is stay in bed. & quot;I just feel like

crap & quot;<BR>

<BR>

My blood pressure is way high & nbsp; even though I am

taking pills.<BR>

<BR>

When I did have a chance to talk with the neprologist

he told<BR>

me that the problem with having IGA is that it attacks

other <BR>

organs, & nbsp; and that I would more than likely have

more serious<BR>

problems before my kidneys finally shut down.<BR>

<BR>

He said that I would probably have a hart attack, due

to the <BR>

blood pressure problem.<BR>

<BR>

He told me that he figured that it would take about

3-7 years.<BR>

And that was almost three years ago. & nbsp; I told

myself that he was <BR>

full of it, & nbsp; But with the way that I have been

feeling (I wounder)<BR>

<BR>

I know that there is no way out of this world alive

& quot;BUT & quot;<BR>

Not knowing what to expect or having access to answers

is the pits. <BR>

<BR>

<BR>

</tt>

<br>

<tt>

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  • 3 weeks later...
Guest guest

In a message dated 7/29/2001 8:19:30 PM Pacific Daylight Time,

redkat313@... writes:

<< Also, I was wondering what other feedback people had on

milk and afib?? I love milk-I don't drink as much as I use to-but I

was beginning to wonder if it could have something to do with my

attacks. Also, my doctor says my digoxin level only needs to be

checked a couple times a year-I was under the impression that it was

suppose to be checked once a month or every 2 months. Does anybody

really know??? >>

Hi, Kathy,

My brother who is in permanent afib takes Digoxin, and his Dig level is

checked only once a year now. Initially, it was checked every few days, then

weeks, and finally months. Regarding the milk, I have thought that afib

might be connected with milk, especially after a gastroenterologist told me

that I may have lactose intolerance. Consequently, I decided to completely

eliminate milk from my diet to see if the afib was affected, even though I

have not yet had the lactose intolerance test. Because my afib usually

starts with a sensation of extreme discomfort in the lower intestinal area

(not the solar plexus for me, Vicki), I reasoned that anything I can do to

help the stomach problem might also eliminate the afib. Cutting the milk

and other dairy products has indeed helped the stomach, but I still have some

problems although not as severe. The afib was apparently not affected by

cutting the milk because I went into afib on schedule two days ago after two

milkless weeks. I haven't given up hope, though. I will continue to avoid

the milk, have the intolerance test, and see what happens with the afib.

Best wishes,

in Seattle

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Guest guest

> Hi Group,

> It's me again!! Just had a few questions. First of all, what is

> ablations?

>

>

Hi Kathy,

At this present time AF can be treated in three ways .

Medications

Surgery ie the Maze

Ablation.

The Maze procedure developed by DR , this is very invasive surgery and in

most cases the heart has to be stooped. There are surgical leasons cut into

the Atria wall , 22 of these. This enables the faulty electoral circuits to

be isolated and stops we hope AF.It is a very effective solution for AF and

has a cure rate of 90%+.

An ablation is the same but it is much less invasive a Catheter is put into

on of your veins , usually in your groin. A map is built of your Atria

showing where the itinerant pulses are coming from that may cause your AF.

Then burned away using RF freqency. The cure rate for this procedure is

around 40%.

This is a new development in the treatment of AF , its about Four year sold.

This is the way that medical teams are looking at the treatment of Af and in

years to come will prove effective for a cure for us all.

regards

C

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  • 9 years later...

Thanks Casey, Ive read your blog and saw a video of you on youtube (I think) you

seem like a really lovely person and have a great humour!

Louise

>

> If you have any questions, Please keep asking! Never feel embarrased with your

questions.

>

>

> Casey Morton: ----------------------------------

> IMDSA Self-Advocate/Spokesman www.imdsa.org

> Morton Programs Management: Founder.  www.linkedin.com

>

> Blog: http://caseymorton30.blogspot.com/ 

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

>

>

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Well, I'm just here to help. Louise, remember if you have any questions please

ask.

Casey Morton: ----------------------------------

IMDSA Self-Advocate/Spokesman www.imdsa.org

Morton Programs Management: Founder.  www.linkedin.com

Blog: http://caseymorton30.blogspot.com/ 

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

 

Subject: Re: Questions

To: MosaicDS

Date: Thursday, August 12, 2010, 2:14 PM

 

Thanks Casey, Ive read your blog and saw a video of you on youtube (I think) you

seem like a really lovely person and have a great humour!

Louise

>

> If you have any questions, Please keep asking! Never feel embarrased with

your questions.

>

>

> Casey Morton: ----------------------------------

> IMDSA Self-Advocate/Spokesman www.imdsa.org

> Morton Programs Management: Founder.  www.linkedin.com

>

> Blog: http://caseymorton30.blogspot.com/ 

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

>

>

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