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Hi, (the other) Vicki...insulin may be a good choice for you...excellent

control is definitely obtainable with insulin. (It does take some trial and

error, however, to find your correct dose). As far as fear of needles...we

all start out that way, I guess, but pretty fast it becomes just something

you do. Considering the alternatives of diabetic complications due to

prolonged high BGs (and you know what they are, smile) a little needle prick

is well worth it. Pretty soon giving yourself insulin shots becomes second

nature. Trust me. Vicki in Portland, Or.

In a message dated 04/06/2002 10:31:17 AM US Mountain Standard Time,

vmossman2@... writes:

> Woudl insulin be a better choice for

> me (much as I fear needles?) My primary goal is to have excellent control

> with no more complications than I have currently!

>

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<< Pretty soon giving yourself insulin shots becomes second

nature. >>

I am getting so use to it I do it in a hurry now. I don't even think about

it anymore cause if I do I don't want to do it. My daughter wants to learn

how to give me a shot. YIKES they want to stick me with needles.

Kathy

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Vicki Mossman wrote:

> OK - all this talk about sulfonylureas has got me concerned for sure!

>

> I'm confused and not sure what to do. Woudl insulin be a better

> choice for me (much as I fear needles?) My primary goal is to have

> excellent control with no more complications than I have currently!

Hi Vicki,

I was doing well in my control with Diet and Exercise until I had foot

surgery in March 2001. I tend to do things rather aggressively and

walked myself into the ground! My right foot actually had three

individual surgical procedures at the same time.

Anyway, my BGs went through the roof no matter what I did. I tried to

wait things out to see if they would come back down, but they did not. I

went to the Doc who started me off with Glucophage, then Glucophage XR,

then added Actos. With all these oral meds max'd out, my BGs barely

budged. I was expecting my Doc to suggest a sulfonylurea and was ready

to argue with her. Instead, she suggested Insulin - Lantus at bedtime

and Humalog before each meal. Since taking exogenous Insulin would

preserve my own beta cells, I decided to try Insulin, even though I

dreaded the needle. Well - long story short - I seldom even feel the

shot (poking my finger hurts FAR more - even at the light settings), my

BG's began to come down nicely. It has taken some tweaking, but the

control is back and I am pleased. As I begin walking again this year

(with more sense), I am hoping that the need for the Glucophage and

Insulin will diminish or go away completely. If it does not go away

completely though, I am still glad to have control again. To me, dosing

on a per meal basis with a good Insulin like Humalog make s far more

sense than trying to take a set amount of a sulfonylurea and then " feed "

it all day/night long. Just my humble opinion! :o)

Rick

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Vicki Mossman wrote:

> OK - all this talk about sulfonylureas has got me concerned for sure!

>

> I'm confused and not sure what to do. Woudl insulin be a better

> choice for me (much as I fear needles?) My primary goal is to have

> excellent control with no more complications than I have currently!

Hi Vicki,

I was doing well in my control with Diet and Exercise until I had foot

surgery in March 2001. I tend to do things rather aggressively and

walked myself into the ground! My right foot actually had three

individual surgical procedures at the same time.

Anyway, my BGs went through the roof no matter what I did. I tried to

wait things out to see if they would come back down, but they did not. I

went to the Doc who started me off with Glucophage, then Glucophage XR,

then added Actos. With all these oral meds max'd out, my BGs barely

budged. I was expecting my Doc to suggest a sulfonylurea and was ready

to argue with her. Instead, she suggested Insulin - Lantus at bedtime

and Humalog before each meal. Since taking exogenous Insulin would

preserve my own beta cells, I decided to try Insulin, even though I

dreaded the needle. Well - long story short - I seldom even feel the

shot (poking my finger hurts FAR more - even at the light settings), my

BG's began to come down nicely. It has taken some tweaking, but the

control is back and I am pleased. As I begin walking again this year

(with more sense), I am hoping that the need for the Glucophage and

Insulin will diminish or go away completely. If it does not go away

completely though, I am still glad to have control again. To me, dosing

on a per meal basis with a good Insulin like Humalog make s far more

sense than trying to take a set amount of a sulfonylurea and then " feed "

it all day/night long. Just my humble opinion! :o)

Rick

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Vicki Mossman wrote:

> OK - all this talk about sulfonylureas has got me concerned for sure!

>

> I'm confused and not sure what to do. Woudl insulin be a better

> choice for me (much as I fear needles?) My primary goal is to have

> excellent control with no more complications than I have currently!

Hi Vicki,

I was doing well in my control with Diet and Exercise until I had foot

surgery in March 2001. I tend to do things rather aggressively and

walked myself into the ground! My right foot actually had three

individual surgical procedures at the same time.

Anyway, my BGs went through the roof no matter what I did. I tried to

wait things out to see if they would come back down, but they did not. I

went to the Doc who started me off with Glucophage, then Glucophage XR,

then added Actos. With all these oral meds max'd out, my BGs barely

budged. I was expecting my Doc to suggest a sulfonylurea and was ready

to argue with her. Instead, she suggested Insulin - Lantus at bedtime

and Humalog before each meal. Since taking exogenous Insulin would

preserve my own beta cells, I decided to try Insulin, even though I

dreaded the needle. Well - long story short - I seldom even feel the

shot (poking my finger hurts FAR more - even at the light settings), my

BG's began to come down nicely. It has taken some tweaking, but the

control is back and I am pleased. As I begin walking again this year

(with more sense), I am hoping that the need for the Glucophage and

Insulin will diminish or go away completely. If it does not go away

completely though, I am still glad to have control again. To me, dosing

on a per meal basis with a good Insulin like Humalog make s far more

sense than trying to take a set amount of a sulfonylurea and then " feed "

it all day/night long. Just my humble opinion! :o)

Rick

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Vicki Mossman wrote:

> How do you figure out which type of insulin to use and what dosage to

> use? I'm beginning to think I should discuss the possibility with my

> doctor at my next visit this month.

Hi Vicki,

As Phyllis W. mentioned, your Doctor would set an initial dosage

schedule for you. Since the advent of Humalog, more and more doctors are

prescribing it for the daytime mealtime Insulin needs, although there

are still plenty of occasions when a different regimen is called for.

Humalog is fast acting and does not last as long as other types of

Insulin (thinking R & N here). In many people, that is exactly what they

need. Others, especially those with diabetic digestion problems (help me

folks - my mind is going blank on the condition), food is digested and

absorbed more slowly and a longer acting Insulin is sometimes needed in

those cases. He may also recommend a " basal " insulin such as Ultra Lente

(UL) or Lantus. This insulin would cover the background insulin needs

(if required). Dosages of either or both would be adjusted over a period

of time. The docs are not anxious to give anyone a hypoglycemic event,

so they'll make changes slowly over a period of time. Once you've been

at it for a while, you'll eventually learn how insulin affects you as an

individual and it will be easier for you to make minor tweaks as the

need arises.

>

> Also, how does the cost of insulin and syringes compare with

> Glucophage and/or Glyburide?

>

In my case, everything is $10.00 per prescription fill. I am able to

make the insulin last longer than any oral meds, so for me it is

cheaper. This is an insurance YMMV issue though.

>

> Thanks for everyone's comments!

You're welcome. My input on this particular subject is only meant to

say, don't be afraid of Insulin. Everyone's situation is different, but

I truly believe that it's a great drug and when used properly, can boost

your enjoyment of life. We can't get this diabetes " monkey " off our

backs, but sometimes we can knock it unconscious for a while!

Rick

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I prefer using Ultralente for background twice a day as it's virtually

peakless. And I use fast-acting Humalog, dose matched to carbs eaten at that

meal. This works really good for me. Vicki

In a message dated 04/06/2002 4:56:55 PM US Mountain Standard Time,

vmossman2@... writes:

>

> How do you figure out which type of insulin to use and what dosage to use?

> I'm beginning to think I should discuss the possibility with my doctor at

> my

> next visit this month.

>

>

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The word you're thinking of, Rick, is " gastroparesis, " , i.e. delayed stomach

emptying. Hey, you're too young for senior moments! Vicki

In a message dated 04/06/2002 7:44:48 PM US Mountain Standard Time,

rick@... writes:

> Others, especially those with diabetic digestion problems (help me

> folks - my mind is going blank on the condition), food is digested and

> absorbed more slowly and a longer acting Insulin is sometimes needed in

> those cases.

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The word you're thinking of, Rick, is " gastroparesis, " , i.e. delayed stomach

emptying. Hey, you're too young for senior moments! Vicki

In a message dated 04/06/2002 7:44:48 PM US Mountain Standard Time,

rick@... writes:

> Others, especially those with diabetic digestion problems (help me

> folks - my mind is going blank on the condition), food is digested and

> absorbed more slowly and a longer acting Insulin is sometimes needed in

> those cases.

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Vicki Mossman wrote:

<< I have been on 1000 mg Glucophage 2 x day, 5 mg Glyburide 2 x day for

several years. (Actually it was 2.5 mg of Glyburide 2 x a day for several

years, and it was increased to 5 mg twice a day about 6 months ago). After

an A1c of 8 a few months ago, my doctor had me add Avandia 4 mg once a day.

His intention was for me to take the Glucophage and Avandia and be able to

stop the Glyburide.

I also began eating low carb the end of January. My bg's came down nicely,

and I began to lose some weight (I've lost 22 since the end of January). >>

All that sounds good, Vicki. I can tell you about my sister, who was

diagnosed type 2 about 45 years ago. She was on Glyburide or Diabeta or

another sulfonylurea for many years. About a year ago, she was maxed out on

three different diabetes meds, and her HbA1c's just kept climbing ... 9, 10,

11. The doctor told her it was time for insulin. She is terrified of

needles! She began low-carbing, lost 40 pounds, went off the sulfonylurea,

has cut her other meds by two-thirds, and feels much better. Her HbA1c's are

around 7.

After several years on sulfonylureas, you may never be able to achieve an

HbA1c below 6.0, but I want you to know that with your present regimen of

good diet and weight loss, your changes of maintaining good health are very

good. Many type 2's find it easier to lose weight on the Glucophage and off

sulfonylureas, which in many cases cause weight gain.

<< Woudl insulin be a better choice for me (much as I fear needles?) >>

You could give it a try. Two-thirds of insulin users are type 2's. But what

I've seen is that you need to exercise regularly and have your weight in

normal range so as to minimize insulin resistance, so you don't have to use

too much of it. I have heard of type 2's who use 100 units daily, several

hundred ... even one good soul who was shooting a thousand units!

<< BTW, my physician is an internal medicine doctor; I like him very much,

but not sure of his expertise in diabetes care. I'm on an HMO and require

referral to see any other doctor. Also, the town I live in doesn't even

have an endo! >>

Aah, I sympathize ... We live in a small town too. My husband's doctor

refuses to diagnose my husband as diabetic or prescribe the appropriate

tests until his *fasting* readings reach the 120s. I'm about ready to feed

Rob a glazed donut before the finger-stick, to get his doctor's attention!

Susie

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Art Mc asked about sulfonylureas. They were the only form of medicine

available for type 2's until about five years ago. They work by forcing the

pancreas beta cells to churn out even more insulin, to try to overcome our

insulin resistance. Here, from http://www.rxlist.com, are some popular

brands:

Glucotrol, Diabeta, Glyburide, Micronase, Glynase

Susie

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Rick wrote:

<< Others, especially those with diabetic digestion problems (help me

folks - my mind is going blank on the condition) >>

Gastroparesis. I struggle with that word myself.

Susie

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Rick wrote:

<< Others, especially those with diabetic digestion problems (help me

folks - my mind is going blank on the condition) >>

Gastroparesis. I struggle with that word myself.

Susie

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Phyllis N. wrote:

<< I guess Amaryl is one of these, even though it is fairly new. Is this

correct? I wonder if my problems are linked to this. >>

Yes, Amaryl is one of those drugs, dear.

Susie

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Kathy wrote:

<< A while back there was someone that said about Glyburide type of drug

will wear out your pancreas. My Aunt is on Glipizide and I think that is

similar to glyburide and I had said something about it wearing out your

pancreas and she is frightened now and what I was wondering is there any

sites I can direct her to? >>

Studies say that within six years of commencing use, 60 percent of type 2's

on sulfonylureas will lose pancreas function. It goes about treating

diabetes in the wrong way ... pummeling the pancreas to churn out even more

insulin, when what is needed is an approach to improve insulin resistance,

so that the pancreas beta cells don't have to work so hard. That is

accomplished by lowering carbohydrate intake, weight lifting, weight loss,

and regular exercise.

Because of the long history of sulfonylurea use, this notion that type 2

diabetes is inevitably " progressive " has developed. Doctors feed their

patients sulfonylureas; they see their patients' pancreases fail; they

eventually move them on to injected insulin; complications develop. Never do

the doctors recognize their own role in prescribing wrong medications!

Susie

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This is very concerning to me. I took glucotrol for 8 years, then they

switch me to Amaryl about 2 years ago.

1/2 of an Amaryl will bring my blood sugar down more than all other drugs

combine. I used to take Avandia, glucophage and amaryl and my blood sugars

were never good. Then I took 2000mg of glucophage a day and my levels were

still not that good. Then I say not good, I am talking about 190 in the

morning and 135 in the afternoon. I have never had the blood sugar levels

that people on this list talk about, even on Atkins. They were always about

the same as above.

Now I am taking only 1/2 of an Amaryl, eating about 100 carbs a day and my

blood sugar is 150 in the morning and 100 at night. It has never been

better. I had a C-peptide test about 6 months ago and my insulin production

was normal.

Now I am just confused. Which is more important to take the Amaryl and have

good blood sugars or protect my pancreas?

The glucophage makes my legs hurt really bad, after good use of it for 8

years??????????????? So I have recently stopped it. I tried over 15 times

stopping and starting it over the last two months to see if I could tolerate

it. I would stop for 2 days - leg pain gone away. Then I would take only

500mg a day just to see, hoping my legs had gotten better, in 24 hours, my

legs would ache so bad, I could barely walk.

Also, when I take Actos, my heart races like it is coming out of my chest,

so I stopped it after 2 days of use. I repeated this 4 times in 2 years

hoping something else had effected my heart, with the same results.

The Avandia - which I have only tried once for about 3 months, made my

ankles swell up like watermelons, every night, so I stopped it.

Now, I am just upset and feel that no one can help me get better. Does

anyone know of any new medication or can anyone give me any advice on the

Amaryl?

Last A1C was 6.5

Thanks,

Phyllis N

<<Studies say that within six years of commencing use, 60 percent of type

2's

on sulfonylureas will lose pancreas function. It goes about treating

diabetes in the wrong way ... pummeling the pancreas to churn out even more

insulin, when what is needed is an approach to improve insulin resistance,

so that the pancreas beta cells don't have to work so hard. That is

accomplished by lowering carbohydrate intake, weight lifting, weight loss,

and regular exercise.>>

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Studies say that within six years of commencing use, 60 percent of type 2's

on sulfonylureas will lose pancreas function. It goes about treating

diabetes in the wrong way ... pummeling the pancreas to churn out even more

>>>>>>>>>>>>>>>>>>>>>>

I finally had my appt with the Endo last Thursday and brought the above up.

She said it was BS. Told me that a twenty year study of 7000 people in the

UK had disproved it. She was also dead against low carbing. No big

surprises there and I don't have the test results back yet, but from looking

at my readings book over the last couple of months she suggested I reduce

the glyburide from 5 to 2.5 per day and keep the metformin at 2000 for now,

but did leave room for cutting that as well. She was very pleased that I

had lost twenty pounds since my last visit and DID agree that weight lifting

is a good thing for Diabetics to do. I just hope that the HB1ACXXXX>>????

comes back good (last time it was a little below 10) so that I can wag that

in her pretty face:-).

Art

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Studies say that within six years of commencing use, 60 percent of type 2's

on sulfonylureas will lose pancreas function. It goes about treating

diabetes in the wrong way ... pummeling the pancreas to churn out even more

>>>>>>>>>>>>>>>>>>>>>>

I finally had my appt with the Endo last Thursday and brought the above up.

She said it was BS. Told me that a twenty year study of 7000 people in the

UK had disproved it. She was also dead against low carbing. No big

surprises there and I don't have the test results back yet, but from looking

at my readings book over the last couple of months she suggested I reduce

the glyburide from 5 to 2.5 per day and keep the metformin at 2000 for now,

but did leave room for cutting that as well. She was very pleased that I

had lost twenty pounds since my last visit and DID agree that weight lifting

is a good thing for Diabetics to do. I just hope that the HB1ACXXXX>>????

comes back good (last time it was a little below 10) so that I can wag that

in her pretty face:-).

Art

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Art Mc wrote:

<< Told me that a twenty year study of 7000 people in the UK had disproved

it. >>

She is talking about the UKPDS. That study didn't study sulfonylurea use,

but the risks of complications if diabetics didn't achieve tight control.

Unfortunately for us, some people with initials after their names think they

know it all. You can look up info about the UKPDS on the internet. Here's a

good place to start: http://www.dtu.ox.ac.uk/index.html?maindoc=/ukpds/

Susie

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Art Mc wrote:

<< Told me that a twenty year study of 7000 people in the UK had disproved

it. >>

She is talking about the UKPDS. That study didn't study sulfonylurea use,

but the risks of complications if diabetics didn't achieve tight control.

Unfortunately for us, some people with initials after their names think they

know it all. You can look up info about the UKPDS on the internet. Here's a

good place to start: http://www.dtu.ox.ac.uk/index.html?maindoc=/ukpds/

Susie

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