There are times that I am dismayed at what I read on Facebook about people navigating diabetes care for themselves or their child. Today, I was asked for my comment on a situation where a child with type 1 was being threatened with the removal of her pump because her HbA1c was higher than target.
This really gets my blood boiling for a number of reasons. Let me count the ways!
- A pump is not a luxury. It is a way of delivering insulin. Let’s be clear about that. It is a tool that we use in the management of our diabetes.
- The only person who has the right to determine how their diabetes will be managed is the person with the faulty pancreas (or their parents in the case of young children).
- HCPs are there to work with us and be guided by what we need and what we are asking for. Equally, we look to them for support, education, advice and information about our diabetes management. We do not look to them to be told off or judged.
- Punishing a PWD by removing a management tool is just plain stupid. Like it or not, I need to give myself insulin and I choose to use a pump to do that. If I’m feeling a little unmotivated and don’t have the capacity to be checking my BGLs, taking away my pump is not suddenly going to give me an injection (bad, bad pun) of motivation.
- Scare tactics DO NOT WORK. I’m going to say that again. Scare tactics DO NOT WORK. Also, scare tactics DO NOT WORK.
- The person in charge at all times is the person with diabetes. Let’s be clear about that too. The PWD is up front, directing traffic. HCPs, diabetes organisations, friends and family are there to support the person in charge.
- This is going to sound crass, and I don’t mean it to, but HCPs need to remember that they are being paid to do our bidding. They are providing us with a service. And that means, if we don’t like the service, they get sacked and we find someone who will give us the service we need.
- Threatening to remove a pump is bullying behaviour and it absolves the HCP of any responsibility in the management of their patient. I will never blame my HCP if my A1c is out of range or I am not checking my BGL. I would ask that they don’t blame me and threaten me.
- Deciding to take away a pump because HbA1c is too high is placing far too much importance on the value of the HbA1c! It’s just a number that gives an average. But not much more.
- Also, by using results of an HbA1c check as a reason to threaten to remove someone’s pump is forgetting about the considerable emotional impact of diabetes. Just as an out of target A1c is not a reason to rap someone over he knuckles, an in-target A1c is not necessarily an indication that everything is A-okay.
I know that it is not always easy to be your own advocate, but it’s times like this that you really need to be able to stand up for yourself (or your child), or bring along someone who can. Being clear about what you want and need is important – and that includes being clear about what you won’t accept.
5 comments
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September 6, 2013 at 5:24 am
endocrinegremlin
Mostly I agree. I do think it is a slightly different ball game in the UK though. They don’t have the funding to provide the number of pumps desired so if you don’t use it ‘properly’ I can understand why they get upset about it. to them, that is a three grand machine they could have given to someone else on the list that needs it urgently too. I mean, I had to sign a contract ffs. But, yeah, the HBA1C is not the whole story. It doesn’t tell the doctor how many tests you do, how many hours you’ve spend pouring over numbers, how many different things you’ve tried to lower it. I mean, I wrote a post earlier in the year about how my HBA1c is a lie. It suggests I have really good control and yet it comes from swings and roundabouts and my diabetes is so bad I can’t work or study. But yes, trying to terrorise diabetics into good control never has worked and never will and I can’t believe this hasn’t penetrated the doctor’s skulls yet.
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September 6, 2013 at 12:11 pm
Cas
Hi Renza
It makes my blood boil too.. Totally agree with you. Who do they think they are to make those judgements? There are so many variables and factors behind a hbac number. No one besides the pwd knows what it’s like.
Isn’t life tricky enough? Hcps should be supportive.
Cas
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September 6, 2013 at 1:22 pm
Mairi-anne
The PWD or child in our case decides the best insulin therapy for each individual. (and as we buy our pumps) it should be a partnership decision. As a mum I dont go into my HCP and say why is the HBA1C so High, what did YOU eat, what do YOU do. I dont do it to them – dont do it to my child. And if we were on a pump and they threatened to “take us off” I would question whether they were really part of my support network and had the best interests of my child in mind. We are a team, any HCP we choose will work with us – not against us. In the BIG scheme of living positively with T1 – these are but numbers… look at the big picture. Encourage and empower DO NOT be negative or judgemental. EVER
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September 6, 2013 at 4:35 pm
Kerryn Shrimpton
Great Blog again Renza – Chloe is not pumping so I don’t quite get how that side of it all works! I totally agree with what you are saying here and was shocked to read some FB comments to the effect that pumps would be taken away! Simply I just don’t get it!
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September 7, 2013 at 2:26 am
fifteenwaitfifteen
Ugh, I couldn’t imagine someone saying that to me as an adult, but saying it to a child??? And completely agree – scare tactics do NOT work.
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