An insulin pump is a little gadget that's about
the size of a pager or a deck of playing cards. It's run by
batteries and contains enough insulin for about 2-3 days. It has
a small thin tube that runs from the pump to your body and pumps this
insulin continuously 24 hours a day.
Check out our new Insulin
Pumpers Web Site for more detailed information
Inside the pump there's a
container for insulin and a small microchip that tells it how much
insulin to pump into your body. It sends the insulin through a thin
piece of long tubing to a tiny, soft piece of plastic or a tiny needle
inserted under your skin. From there the insulin enters your body just
as when you give yourself an injection of insulin.
The
insulin pump is the best way to keep blood sugars under control.
The insulin pump will deliver insulin more the way your body normally
would have if things were working properly for diabetics. There
are well over 100,000 diabetics using the insulin pump today and the
more word gets around, more people will be put on an insulin pump.
When
you use an insulin pump. You have more freedom to eat what you
want and when you want to. No more schedules and injecting
yourself 2, 3 or more times a day. I've been a diabetic for most
of my life and I'm now just getting put on an insulin pump after more
than 6 months of talking to my doctor about it. This to me will
be my cure for the time being.
Remember!
An insulin pump is not a cure all for diabetes. It's going to
give you freedom in a way, but you have to keep on top of your
diabetes a little more than you have been. This means you have
to learn to use your pump correctly, test your blood sugar at least 4
times a day (6-8 times is better) and you're going to have to buckle
down and watch your diet more closely. This means counting every
carbohydrate you eat in order to tell the pump how much insulin to
give yourself.
Ok.. Now on with the techy
stuff.
Ok.. You have your little pump.
Batteries are installed and you've had your basic training by your
doctor on how to use your pump. You should already have your
pump programmed by following your pump's manual. At time time,
you should have the time and date set and the basal rate
set.
Remember the Pumpers Golden
Rule: Take care of your diabetes first and your pump second.
Also, always have a syringe and a bottle of insulin handy in case your
pump should fail. If anything happens to your pump and it stops
delivering insulin, or your blood sugar suddenly rises for no apparent
reason, you'll need to inject yourself with a dose of insulin
specified by your doctor.
That needle or little piece of
plastic is called a cannula. It stays in your body. It must be taken
out and replaced every 2 or 3 days. In fact you change it yourself. It
is almost like giving yourself an injection. The cannula fits over a
small needle, which you push into your skin. When you pull the needle
out, bingo! The cannula stays in your body. It is now inserted.
Once the cannula is inserted and
the tubing is hooked up, your pump can begin delivering insulin to
you. Using buttons on the outside of the pump, you can program it to
give you exactly the insulin dose you need.
OK, I follow you so far...
Now for some tricky new words:
you program the pump to give two different types of insulin doses: the
basal dose and the bolus dose.
The basal dose is a steady stream
of insulin that flows in all the time. It imitates the continuous
insulin that a functioning pancreas would provide. Although older
pumps used to give you the same rate of insulin all the time, the
latest pumps you can program to give different basal rates over the
day - for instance, giving you more during the day, less at night, and
more again in the early morning hours when your body needs it. You can
even reduce it if you are having a very busy active day.
The bolus is an extra little shot
of insulin you tell the pump to give you before you are going to eat a
meal. Once you've got the food in front of you, you work out roughly
how much carbohydrate you're going to eat, program the correct insulin
based on this, and the pump does the rest. You can easily take more
insulin during the meal if you want to eat more than you thought.
What insulin do I use?
The pump only uses the clear
soluble insulins, like Actrapid or Humulin S, or Humalog, which is
fast acting. This means two things:
-
You can program your insulin
doses right when you need them. You don't have to worry about
unexpected things coming up, or delayed meals.
-
It means your body absorbs
the insulin better, because soluble insulins most resemble the
insulin your body makes. Long-acting cloudy insulins tend to be
more unpredictable.
So how does this all work in
practice?
People who wear the pump take
only one shot every two or three days - that's the cannula insertion.
They have a lot more options when it's time to eat. They don't have to
eat at any particular time. And their bodies are getting insulin a lot
more like they would if their pancreases were working. That means they
feel better most of the time.
If pumps are so good, why
doesn't everyone have one?
But before you rush off to your
doctor and demand an insulin pump, you need to know a little more.
Getting a pump means you have to be on top of your diabetes. When
you're on the pump, you have to be diligent about testing. That means
4 times a day at least. (But you should be testing that much anyway.)
You also have to be willing to
learn a lot about your diabetes and a lot about your pump. You always
need to know what it's doing and how you're feeling. Not only do you
have to be able to program it, but you must be able to tell if
something's wrong with it.
What sort of things can go
wrong?
As with any medical device,
little things can happen. The tubing can get crunched, the battery can
die, the cannula in your skin can get infected or disconnected from
the tubing. Even though pumps have several different alarm systems to
tell you when these things happen, they are not foolproof. You have to
keep on top of it.
But no doubt about it, most
people who go on a pump say it has made their lives a lot better. They
get to play sports without worrying as much about going low. They get
to eat what they want. They get to sleep in because they can let the
pump manage their insulin. They can stay out late for the same reason!
What about things like having a
bath, sleeping or swimming?
Pumps come in waterproof models,
if you need them. But most pumps can tolerate a little bit of water
anyway, so you don't need to worry about getting rained on. But if you
want to swim, most people just disconnect the tubing, leaving the
cannula in place. They reconnect when finished. You also disconnect
when you take a bath or shower, or when having sex. It's normally OK
to disconnect for up to an hour.
When you sleep you can just put
the pump under your pillow or on the bedside table. The tubing is long
enough. Some people just let the pump lie next to them in bed.
How many people use a pump?
The number of people that use
pumps varies a lot from country to country. For example, in Germany
about 1 in 7 people on insulin uses a pump. In America it's about 1 in
8. In Britain it is about 1 in 1000. This reflects differing opinions
amongst healthcare professionals, and differences in healthcare
funding policies.
Check
out a short history of how insulin pumps have come along through
the years.