Hello everyone, I want to give fair warning this is not
about living with the disease though it is about living with the disease. I
want to vent or rant or whatever you want to call it today. For the last three
years I have been on the Animas® One Touch® Ping® as my insulin pump. I have
heard many people speak badly about it and others speak good; though my
personal experience has been great with it. Here is the rant, my wonderful
insurance company has decided to no longer support the One Touch® Meter and
test strips, but they are still supporting the pump. This is just great the
meter that syncs with my pump directly for dosing communication is no longer
supported, let’s just rip the pump away and put me back on shots it would be
less complicated than what I am going to have to do now. As if the bag I have
to take with me with emergency supplies is not large enough with all the
glucose tabs, dextrose pens, spare insets, spare cartridges, extra bottle of
insulin, site dressings and a whole host of other things; I now must carry two
Glucose meters. The first is this new brand that has been jammed down my throat
by the insurance company; the second is my One Touch®. Now if I wanted to spend
over $200 a month buying my own test strips I can very well keep using my
current meter, but as hard as times are I am lucky to pay gas at times let
alone $200 in test strips.
So now I have the new meter that I take my glucose level on,
then I have to pull out my old meter and use it. This meter monitors how much “insulin
on board” I currently have, for those who do not know “insulin on board” is
just a way of saying the amount of insulin that is left in my body since my
last bolus dose combined with my normal hourly dose. Each hourly dose is
distributed a micro dose every three minutes to equal my actual hourly dose. I
enter the amount of carbs I am about to eat, then enter the glucose level from
the other meter, then the One Touch® tells me how much I am to bolus dose to
keep my insulin in line with my carbs and current glucose level. Then here is
what I love the meter communicates with the pump via wireless communication and
transmits all the entered information, then actually delivers the correct
dosage. I do not touch the pump it stays in my pocket. I want these insurance
people to live on what they allow for us as diabetics, we are sort of the
outcast of society since we are the biggest insurance cost according to
insurance companies. I guess that means we do not deserve the right treatment.
Sorry rant over.
Hi John,
ReplyDeleteI was hoping to get in touch with you about your blog with a quick question. Do you think you could email me when you see this? Thanks so much.
Cameron
cameronvsj(at)gmail.com