Search Results for: distress

Stress, distress & burn out

mum and son cuddle

Diabetes can affect you physically, emotionally, socially & psychologically. This is also relevant for family members and caregivers who can experience the same emotions and reactions to diabetes as the person who has been diagnosed.

Diabetes requires self management on a daily basis. This means you need to be in the driver’s seat and you should be at the centre of your diabetes management team. Diabetes is often an unpredictable and tricky disease to manage. It can be frustrating and feel pointless. Diabetes can be difficult to control no matter what sometimes and it can complicate life in general!

Diabetes tests and targets can raise stress

Targets in diabetes are important, such as blood glucose levels (BGL), HbA1c or A1c (the average BGL over the past 8 – 12 weeks), blood pressure and so on. However this can make you feel like you are “sitting an exam” every day.

The results of BGL checks, managing your weight, choosing healthy foods, managing insulin ratios and exercise, etc etc can lead to guilt, worry and stress. If you start to feel you are “not doing the right thing” and/or you are “not getting the right results”, it can lead to diabetes distress and you may end up blaming yourself. As a parent this can help your child as you model to them, these are more helpful and empowering ways to talk about their diabetes.

Talking about “high and low” blood glucose and not “good and bad” can be a healthy place to start.

It is important to remember that these targets are guides to your health and diabetes management. The results on your home blood glucose monitor are a tool to helping you and your health care team to make adjustments and work towards a healthy you.

These numbers are not ends in themselves. How you choose to use them will depend on the type of diabetes you have, how long you have had it and your personal needs and choices.

mum and son cuddle

  Diabetes Distress

Diabetes may lead to specific problems and increased stress, which we often call “diabetes distress”.

Daily life and general stress levels can affect your diabetes control. How well your diabetes is going can in turn affect your general stress levels – so it is a bit of a chicken and egg. It is very important to get the general stress in your life under control, as this will assist with your diabetes management. Likewise, feeling settled with your diabetes management will decrease your overall stress.

If you are struggling with stress at work, or in your personal life, it can be harder to manage diabetes and it suffers. We all experience stress and life would be boring without some stress! People say they would rather not have stress in their lives, but in fact we need a balance between just enough stress and not too much, to keep us alive and active. Not all stress is bad believe it or not.

Some of the things that can lead to diabetes distress are:

  • Worry about food changes
  • Management of blood glucose levels
  • Weight management
  • Going onto insulin/medication
  • Hypos (low BGL)
  • Depression & mood swings – have been shown to be higher in people with diabetes
  • Relationship & sexual problems
  • Work stress, discrimination in relation to your diabetes
  • Disclosure – wondering if you should tell people about your diabetes
  • Lack of understanding or support from family/friends
  • Guilt, fear, worry, panic & anxiety about diabetes and your future
  • Risk of Complications
  • Feeling alone and isolated
  • Seeing or hearing about all the things that can go wrong
  • Feeling out of control
  • Other mental health problems such as an eating disorder
  • Feeling overhwelmed and exhausted
  • Lack of information

aust outback with moon

Minding Diabetes

Here is a great tool from the NDSS which we had some input into. You can check your emotional health and hop back across here for some support – http://mindingdiabetes.com.au/

It is not all doom and gloom!

It is not inevitable that you will have all or any, of these problems. You may or may not experience some ups and downs with your diabetes and this might lead to increased stress.

We are all different.

What is important is to understand that diabetes is in itself a full time job and managing it can bring increased stress. This can make it easier to be gentle on yourself when things get tough and to seek support in managing.

What is stress?

In basic terms if what you are being asked to do at this point in time is too much for you, you will experience stress. What you can handle will vary from day to day and even within a day and will vary from person to person. This means your ability to cope with stress will also vary.

Stress is made up of many things: the experiences we have, pathways within our body and brain, the responses we have to stressful situations and events and outcomes of this stress.

Stress is caused by a range of different events or circumstances.

Different people experience different aspects and identify with different definitions.

Stress and worrying

Even imagined change can be a stress. This is what we tend to call “worrying”. If you worry that you will not have enough money to pay your rent, or that you might suffer the complications of diabetes, that can lead to increased negative stress. This kind of stress is in your control to manage – you can tune into the way you are thinking about things and stop this worry in its tracks, thus minimising the impact on your body and your life.

Regular relaxation and time out can help you to minimise worry. Talking to other people about your worries, rather than keeping them to yourself, can also help.

“Catastrophising” when something goes wrong also increases your stress – this is the “it’s the end of the world”; “everything happens to me” kind of thinking. If one small thing goes wrong it is easy to start linking it to all the other things that have happened and then see this as “the end of the world”. Learning how to keep this thinking in check can really help minimise stress.

A major source of stress is overdoing things. If you push yourself too much you have less rest time. Eventually you will “hit the wall. If ongoing, permanent damage may be done.

hypo anxiety

What happens to our body when under stress?

Fight or flight response

When faced with a threat an automatic response is set off in our body – the fight or flight response.

This was an essential tool for human survival, developed over many thousands of years living in wild and dangerous places. To us, living in today’s world, it is often an ineffective response, which can actively prevent us from responding usefully to a problem situation – just think about road rage!!

Fight or flight is a response to anything which is perceived as a threat, or a potential threat by our body – it is not something we necessarily think about – it just happens.

This begins when certain primitive parts of the brain send a message to the adrenal glands which release a number of hormones including adrenaline, whose purpose is to prepare the body for vigorous emergency action.

The main changes that follow are below:

  • Non-essential processes are immediately switched off by our body. Things we don’t need right now are turned off.In particular, if the body is digesting food, that is stopped immediately, and people can notice a feeling of churning or ‘butterflies’ in the stomach, or feeling nauseous or sick.
  • A number of other changes follow, to make the muscles as strong as possible
    • The liver releases stored glucose into the bloodstream.
    • Fats are released into the bloodstream from the fat stores in the body. These are fuel for the muscles, so oxygen is needed to burn them – and so the breathing increases. Those under stress may notice feeling breathless.
    • The body needs to get fuel to the muscles – (remember, the body thinks this is a life or death emergency) – so the heart begins beating far faster – some people notice palpitations.
    • Blood pressure rises, some people notice feeling hot or cold – breaking into a sweat, as the body seeks to spread out the heat that will be generated by vigorous muscular activity, for which body is preparing.
    • Becoming ready for instant action, muscle tension increases, and a person may notice shaking, or becoming restless and fidgeting.

Some people feel like this often and if this pattern is continued for long enough, chronic headaches, backache and other physical complaints may result i.e. chronic stress.

man in meditation sunset
At the same time as all this muscle action is happening, blood supply to the front parts of the brain, responsible for higher levels of reasoning is reduced, while the blood supply to the more primitive parts, near the brain stem, is increased.

These parts of the brain are responsible for automatic, or instinctive, or impulsive decision making & behaviour.

A person undergoing a stress response may be prone to impulsive thinking and behaviour – which they may thoroughly regret later – this means we can say and do things without thinking clearly.

There are a number of ways in which chronic stress can impact on your body and general health:

  • Brain -fatigue, aches & pains, crying spells, depression, anxiety/panic attacks, sleep disturbance
  • Gastrointestinal Tract – Ulcer, cramps & diarrhoea, colitis, irritable bowel
  • Glandular System – Thyroid gland malfunction
  • Cardiovascular (important for diabetes) – High blood pressure, heart attack, abnormal heart beat, stroke
  • Skin – Itchy skin rashes
  • Immune System – Decreased resistance to infections

How does stress affect diabetes?

Stress can cause BGL’s to rise.

Feelings of distress, especially when intense and long lasting, can show an increase in HbA1c (or A1C) with this typically higher in those struggling with difficult conditions at work, home or problems such as depression. Yet laboratory studies have not shown that stress consistently raises BGL – some studies show that it does and some show that it does not!

Many people report that stress does raise their BGL and we know that when life becomes busy, stressful and overwhelming, diabetes can take a back seat. In this case the stress raises BGL as the situation causing the stress interferes with diabetes management, rather than a direct effect on blood glucose levels.

The best answer to how stress affects diabetes is taken from Dr William Polonsky – “Diabetes Burnout” book :

  • Stress can have a negative effect on diabetes self management, but only for certain people at certain times
  •   Stress can have a direct and immediate effect on BGL but only for certain people at certain times

If you are significantly distressed over a long period of time it is likely that you will begin to have problems managing your diabetes. Stress might affect your ability to exercise or follow a meal plan for example. In this case it is how you understand and respond to stressful events that is the key to managing diabetes when under stress. Interestingly not all types of stress appear to make BGL rise.

Situations where you feel trapped (in that you can not make changes) or where you feel things are out of your personal control appear to be most likely to influence BGL directly.

How sensitive are you to Stress?

Some of us are more sensitive to stress than others. Scientists believe that there are 3 types of people:

  1. Stress insensitive – BGL not directly affected by stress
  2. BGL rises under conditions of stress
  3. BGL drops when stressed

Some people might experience elements of all of these at different times. You can experiment to see what happens to your BGL when under stress. This might be by tracking your BGL when under a particular stress to see what happens and/or checking BGL prior to and following a relaxation session over a week or so, to see if your BGL decreases.

woman sleeping in field

Diabetes Burn Out

Diabetes Burn Out is a common problem. If you are under too much stress in particular, this is a potential risk. Diabetes is like a “job” and the day to day effort to manage can become overwhelming. This is especially true when the results are not what you would like them to be and you know you have done all you can and worked hard.

Burn out is much more than feeling a little down. It is an overwhelming feeling of helplessness and hopelessness that you can not go on with your diabetes management – people often give up at this point and depression can also occur.

If you think Diabetes Burn Out has or may happen to you these tips may help:

  • Think about what particular areas of diabetes are causing you problems. Sometimes people say it is “just diabetes” that is the problem, but often there are specific areas that are causing problems and you are actually doing ok with other areas. It can be helpful and very positive to see that it is not everything about your diabetes that is difficult. For example you may be ok with checking your blood glucose and exercising, but not so happy with the way you are managing your food intake. Seeing the things you are doing well with gives you something to build on and gives perspective.
  • Consider what’s happening in your life that might be conflicting with diabetes care? What is making it harder at the moment for you to manage diabetes? What blocks and barriers are there and how might you deal with these other parts of your life? Sorting these things out will in turn make diabetes management easier.
  • Work out what your expectations are for your diabetes management at the moment? What are your targets? What do you want?
  • And are your goals realistic right now? Sometimes we expect too much, or too little of ourselves. You may need to work harder, or ease off on your diabetes management depending on what else is happening in your life and with your health.
  • Look at whether there difficult emotions you need to deal with? Emotions such as sadness, anger and grief may be present due to diabetes diagnosis, depression or another event in your life. These emotions can be uncomfortable but very important. Acknowledging and accepting these feelings, then working through them so you can move on with your life can help.
  • Finally do not suffer in silence. Always seek support if needed. This may be from your usual doctor, diabetes educator of other team member. A friend, family member or someone else you trust. A counsellor or psychologist. Or a service such as ours where you can access counselling, support and understanding in one place.

candles and zen stones

Stress and Relaxation

Too much “fight/flight” activity or in other words too much stress, without corresponding rest and relaxation leads to distress. Importantly you can “bank” your rest and relaxation times. By practicing regular relaxation and rest times, no matter what the stress levels are in your life, you allow your body to heal itself and stay strong in the face of the inevitable stresses of our lives.

This may be listening to quiet music, getting out in the garden, walking in the sunshine, playing a game with your child, or using guided relaxation practices. We highly recommend learning and practicing guided relaxation. It gives a much deeper relaxed state for the body and mind than many other things and can make a large difference to depression and anxiety.

We have a number of relaxation practices here on our relaxation pages. We use and recommend Dr Gillian Ross’s relaxation CDs. You can listen to some of these on our relaxation pages.

Stress Management and Exercise

Exercise is critical to overall health. The current recommendation for adults is 30 minutes moderate every day if you can and at least 4 – 5 times week (60 minutes a day for children). We now have so many convenience machines and often sedentary lifestyles, that structured exercise is even more important. This does not need to be at the gym!

Walking is one of the best forms of exercise and it is free! Swimming and water based exercise are great for people with mobility problems. If you need help to work out the best exercise for you, an exercise physiologist can be great. You can access one via a diabetes care plan – just ask your GP to refer you to someone as part of your 5 allied health care visits. They can then set this up and work out an exercise plan that will work for you and your abilities. Hop across and have a look at our Diabetes and Exercise page.

If you have type 1 diabetes this is a fantastic resource Allan Bolton.

Apart from the obvious physical health benefits exercise is also vital to stress management as it encourages that parasympathetic (rest and relaxation) response, calms body and mind and uses excess energy and muscular tension.

Go to our Relaxation and Meditation pages for information about these practices

Case Study: George Mellows (Part 4) – A visit to the Diabetes Educator

sunset walk

George Mellows is aged 55. He lives with his wife and his two teenage children, aged 15 and 19.

George works Monday to Friday 8.30 am until 4.30 pm . He works at a desk in a sedentary role, getting minimal activity in his working day. George has not played any sport for some time, but he does enjoy playing lawn bowls.

Everything Is Possible

*** Previous Posts: Part 1 here ; Part 2 here ; Part 3 here ***

healthy food spread

George has now had diabetes 3 months. He has had a consultation with his dietitian and found some healthy choices to make that not only fit with his diabetes self care plan but also things he enjoys!

This past 2 weeks George has been measuring his blood glucose level with a view of discussing the results with the diabetes educator. George feels confident that he can identify the causes of hyperglycaemia

On diagnosis, George’s doctor commenced George on Metformin 500mg in the evening with dinner. This has not changed.

The table below is his most recent blood glucose levels. George has highlighted the blood glucose levels that are over his target in red.

Click to enlarge
Click to enlarge

The Visit

Self-management means having a daily management plan, setting goals, solving problems and taking responsibility. But it certainly does not mean you are on your own. Mutual trust and respect between yourself and your doctor and other members of the health care team, as well as regular communication with them, are vital to effective self-management.

Previously, traditional care was based on doctors and health professionals being seen as the experts responsible for the diagnosis and management of care. It was accepted that people’s lives should be fitted around their diabetes with goals set by the health professionals.

But this approach is not effective. Diabetes requires daily management. Doctors are not available every day, leaving responsibility for day-to-day care on the patient and the family.

In addition, good results are difficult to achieve if the person involved is not an active participant or does not understand the reasons behind management decisions.

Patient Empowerment takes a new approach. It moves the focus from the doctor to the patient. It involves fitting diabetes into your lifestyle with you making the choices and taking charge of your management and the consequences.” Diabetes Australia

Tools

On arrival in the consultation room George was asked by the receptionist to complete:

* The Diabetes Distress Scale (download here DDS and HERE )

* The Diabetes Knowledge Questionnaire (download here DIABETES KNOWLEDGE QUESTIONNAIRE (old rtf format) )

George felt a little uncomfortable initially using these ‘tools‘ to complete these ‘tests’. However, the diabetes educator saw George acting a little uncomfortable in the waiting room and explained that the purpose of these tools would be to individualise the visit based on the knowledge and needs of George.

George felt more comfortable with this explanation, and managed to complete both before the visit started in person. *He also felt that it might have been good to complete these at home before the visit.*

"Enjoying a good quality of life is my goal" George
“Enjoying a good quality of life is my goal” George

How did you feel about completing those tools George?” the diabetes educator asked as they sat down to start the session.

At first it was a little like being in school; but when you saw I was puzzled about them, and explained how we could use them in this session, I felt like I was going to be listened to, not just spoken at and told what I should and shouldn’t do” replied George.

The diabetes educator then used these with George to open and lead the session. George was also a little surprised at this, expecting the diabetes educator to be focussed on his blood glucose levels.

The diabetes educator started with the knowledge questionnaire, only asking George about the question he had gotten incorrect. By the end of the first 20minutes George was feeling that he was learning new things despite al of the reading and research he had been doing on the internet.

George hadn’t even considered the importance of foot-care, despite being aware that diabetes can effect the nerves and the blood supply to parts of the body.

Diabetes Distress

Diabetes may lead to specific problems and increased stress, which we often call diabetes distress”.

Daily life and general stress levels can affect your diabetes control. How well your diabetes is going can in turn affect your general stress levels – so it is a bit of a chicken and egg. It is very important to get the general stress in your life under control, as this will assist with your diabetes management. Likewise, feeling settled with your diabetes management will decrease your overall stress.

If you are struggling with stress at work, or in your personal life, it can be harder to manage diabetes and it suffers. We all experience stress and life would be boring without some stress! People say they would rather not have stress in their lives, but in fact we need a balance between just enough stress and not too much, to keep us alive and active. Not all stress is bad believe it or not.

Some of the things that can lead to diabetes distress are:

  • Worry about food changes
  • Management of blood glucose levels
  • Weight management
  • Going onto insulin/medication
  • Hypos (low BGL)
  • Depression & mood swings – have been shown to be higher in people with diabetes
  • Relationship & sexual problems
  • Work stress, discrimination in relation to your diabetes
  • Disclosure – wondering if you should tell people about your diabetes
  • Lack of understanding or support from family/friends
  • Guilt, fear, worry, panic & anxiety about diabetes and your future
  • Risk of Complications
  • Feeling alone and isolated
  • Seeing or hearing about all the things that can go wrong
  • Feeling out of control
  • Other mental health problems such as an eating disorder
  • Feeling overwhelmed and exhausted
  • Lack of information

Blood Glucose Levels

Towards the end of the session the diabetes educator and George decided to take a careful look at the blood glucose levels that George had been measuring.

The diabetes educator asked “George, why do you test your blood glucose level?”

George was a little taken aback by this question. He thought that everybody just had to, that it was a part of having diabetes.

After a moment he said: ” To determine if my diabetes self care plan is working well, or if there needs to be some changes to my meal planning, or my exercise, or to my diabetes medication.”

George identified clearly the things that would impact on his blood glucose level, and also identified that weekdays at lunchtimes when he didn’t move very much was a problem for him.

dreamstime_m_5280572 (2)

Future Planning

The plan at the end of the session was to make an appointment with an exercise physiologist and a podiatrist, and then return to the diabetes educator in 6 months (unless he felt the need to return sooner).

George also had a plan to talk with his manager to have 60 minutes for lunch and go for a 20 minute walk each working day after he had eaten. This meant that he would have to work back an extra 30 minutes. But he also felt it was well worth it if it meant having a better quality of life, and potentially a longer working life (by minimising the risks to his health caused by high blood glucose levels).

 

George felt that he had achieved quite a lot in his first few months of living with diabetes, but was also aware that this was only the beginning of a lifelong journey.

 

Sweet Bytes Newsletter January 2015

diabetes dino collage

 

Welcome 2015

Happy New Year everyone! Hope you had some time for family, loved ones, peace and relaxation. Diabetes does not rest however and certainly gave me a whipping over the break….how did you go? I am writing a blog post about things that make you go hmmmm when you have diabetes – hit me with yours and I will include them!

helen Very excited to announce that my diabetes Apps are up on the Google play store and will be on Apple soon! One is Diabetes Minder which tracks BGL and stress and how they are connected as well as being able to add reminders for taking meds or blood tests etc the second is for women in pregnancy – Diabetes Pregnancy Pal x

https://play.google.com/store/apps/details?id=com.appexperts.diabets.minder

Helen E xxx

 

 

diabetes dino collage

DIABETES CAN’T STOP ME

As a person living with type 1 diabetes since childhood and working in diabetes for many years, Helen Edwards wanted to offer families a resource which takes some of the stress and worry out of managing diabetes. Growing up with her own diabetes struggles, working as a social worker for 25 years and using play therapy in her practice; as well as having hundreds of conversations with families about their daily lives with diabetes, all led to the creation of Diabetes Dino®. We hope you and your child enjoy reading and playing with Diabetes Dino® and Dragon, and that they can help you to have a calmer, happier and healthier relationship with diabetes.

http://www.diabetescounselling.com.au/store/#!/Hard-Copy-Books-&-Toys/c/11295493/offset=0&sort=normal

 

team

OUR DIABETES COUNSELLING AND EDUCATION TEAM

Diabetes Counselling Online has a team of qualified health care professionals. This includes a psychologist, mental health social worker, counsellor, diabetes educators and a dietitian. Most of these people also live with diabetes themselves and/or have many years experience working in diabetes care. We therefore bring an understanding of life with diabetes to our work.

 

While our focus is on counselling and mental health, we also offer general advice regarding diabetes management.

Our team can not make changes to your individual diabetes management but we can work with you to develop plans for how you can address this with your usual health care team.
We offer short term e-counselling and e-consults primarily via email. We can also offer telephone and/or Skype sessions in some cases. At present this may be an addition to your e-counselling or education and can be negotiated with your counsellor or other team member, once you get started.

Often counselling and education occur at the same time as issues can be related to both mental health wellbeing and diabetes management. We will decide the best person to work with you based on your needs and the experience and skills across our team.

http://www.diabetescounselling.com.au/counselling-and-diabetes-education/

 

20 THINGS I HATE ABOUT DIABETES

Helen Edwards

BGL

Sometimes I get sick of telling people that their diabetes will be ok, and they will be ok, and everything will be ok. Not because I don’t believe that to be true, I do. I think everything WILL be ok. But damn it, diabetes is NOT always ok. I am exhausted at the moment- are you? It is that whole end of year, nearly at Christmas, we can see the finish line thing.

My 6 year old Maxwell got up today and fell asleep on the couch for a minute or two, and then jumped awake shouting, “I wasn’t asleep!”He gets that from his Dad.

And my 15 year old couldn’t manage day 4 of work experience. I know his problem.

The thing is, not only am I exhausted from working bloody hard and sleeping very little all year. I am exhausted from managing diabetes. Do you know what I mean? It has NOT been ok. I have had swings from highs to lows and sudden hypos that freaked me out and stubborn highs. My gut problems from gastroparesis continue to play with me. And some days lately I have felt like maybe it WON’T be ok…..

So here are 20 things I hate about diabetes (coz we all have to get this crap out sometimes – try it, it helps!) Feel free to share and comment if you feel the same or want to add to the list

1) It’s so damn unpredictable and never ending

2) Finding spots for finger pricks after 35 years and up to 20 tests a day is pretty hard – you should see my fingers, they are a mess…..

3) There are no perfectly 100 % accurate blood glucose monitors and do you KNOW how much difference a 1 or 2 mmol reading can make to some of us with type 1??

4) My skin is stuffed and finding sites for my pump continues to be a delight of each and every day

5) Hypos, especially sudden ones where I go under 3 mmol freak me out

6) Hypers, especially unexpected ones where I go over 16 mmol freak me out

7) People ask me all the time in airports to “take the pager off” as I go through the scanner

8) It is exhausting

9) The general public don’t get it. They think it is simple.

10) It has damaged areas of my body that I am terrified will just get worse…

11) Exercise is a debacle, you need a PhD and even then your theories will be challenged every time you go out for a run

12) There is no spontaneity

13) Leaving home to go out involves lugging a suitcase with you

14) Carbs Carbs Carbs you are such a challenge – can’t live with em, can’t live without em

15) I worry that my children will get diabetes

16) I worry about losing my blood machine or breaking my pump, or forgetting to put it on after a shower – being reliant on machines to keep you alive is stressful

17) It costs a LOT and we should have a concession card- all of our lives

18) It keeps me awake at night- sometimes sitting up to make sure my levels are not too high or too low before going to sleep

19) All the “I quit sugar” people give me the shits

20) It is for life. It isn’t going anywhere fast. The promised cures never come. This is IT.

Rant over.

Oh and you know it WILL be ok. It always is in the end. But sometimes you just gotta get this stuff out. If you are feeling like me- please comment and share. You will feel better trust me and at least we know we are all in it together next time you are sitting up at night, or screaming at your blood glucose machine.

Helen

xx

Helen Edwards has lived with type 1 diabetes since 1979. She is Mum to 3 sons, the founder of Diabetes Counselling Online, a diabetes educator, social worker and PhD Candidate studying diabetes distress in pregnancy for women with type 1 diabetes. She is also a successful Interiors Blogger and Stylist at www.recycledinteriors.org and runs creative workshops, an online store and studio in Adelaide – just for a life outside of diabetes.

 

Diabetes at Primary School

Helen Wilde, Senior Counsellor

Something to think about as Term 1 draws closer

Anne Marks, a PhD candidate from the University of Western Sydney is conducting an Australian study exploring parent’s, teacher’s and diabetes educator’s experiences of intensive insulin therapy for children in early primary school.

If you are a parent, teacher or diabetes educator caring for a child with type 1 diabetes who is;
* attending kindergarten, year 1 or 2
* using intensive insulin therapy (insulin pump or 4 daily injections) and receiving an insulin injection or pump bolus at school

contact Anne Marks [email protected] for further information.

The study involves an interview which can be conducted in person or via telephone.

Participants must live in Australia.

 

HYPOGLYCAEMIA AT SCHOOL

David Mapletoft

Children of all ages require a safe and effective plan for those times when not under primary school diabetestheir parents supervision

‘Hypo’ or a low blood glucose level is one of the fears for all people living with diabetes.

A low blood glucose level will often occur unexpectedly, sometimes without an obvious cause.

For the child with diabetes, a low blood glucose level may lead to loss of concentration and behaviour change – possibly disruptive behaviours.

Talk to your child’s school about diabetes to help your child attain an education without discrimination

Education and Care Services National Act and Regulations: Australia

“In January 2012 new national legislation (Education and Care Services National Act and Regulations) requires a type 1 diabetes policy for all services providing or intending to provide education and care on a regular basis to children under the age of 13 years. This includes outside school hours programs. More information on the medical conditions section of this legislation can be found on the Australian Children’s Education and Care Authority website http://www.acecqa.gov.au/national-regulations” from HERE (Diabetes Australia Victoria)

As a parent of a child living with diabetes it is in your best interest to communicate with the headmaster of your child’s school before or at enrolment

Duty of Care

Schools have a legal responsibility to provide:

a safe environment

adequate supervision

When the school knows that certain students have diabetes, staff (including relief staff) need to know enough about diabetes to ensure the safety of those students (especially in regard to hypoglycaemia and safety in sport). Parents/guardians have a responsibility to advise the school of their child’s medical condition and the particular requirements for the management of their child’s diabetes. For children with special requirements, a written individual management plan incorporating medical recommendations should be developed with the school in collaboration with the parents/guardians and doctor. This should be attached to the student’s records. from Diabetes Australia

Hypoglycaemia Symptoms

A very good multimedia presentation from the Royal Childrens Hospital, Melbourne, can be found HERE

Managing Hypo

Managing hypoglycaemia

Hypoglycaemia (“Hypo”) means a low level of glucose in the blood. This is a blood glucose value of less than 4.0 mmol/L.

Hypoglycaemia can be caused by:

Too much insulin

Vigorous exercise without extra carbohydrate

Missing or delayed meals

Not eating all serves of carbohydrate

Alcohol intake

If you would like to share, or debrief, about your experiences please visit our Forum orFacebook

Research

“The management of type 1 diabetes in Australian Primary Schools” by Diabetes Nurse Practitioner, Associate Lecturer UWS Anne Marks HERE

Children using insulin pump therapy were more likely (97%) to receive insulin at school than children using injections (55%)

Children in the study who were able to self-administer insulin were more likely to receive insulin (93%) at school than children who were unable to self-administer insulin (65%)

Parent Concerns:

62% reported that they had current concerns about diabetes management at school

Difficulty participating in school activities

Inclusion at meal times

Lack of independence

Missing school, classroom activities or time with peers

Safety

Lack of staff to assist with care

Impact on parental employment

Increased workload of teachers who are willing to assist with care

 

Other Resources

Helping the Student with Diabetes to Succeed

sample-emergency-care-plans-for-hypoglycemia-and-hyperglycemia-508

Kind Regards,

David, Diabetes Educator @ Diabetes Counselling Online

 

 

DIGITAL MEDICS

Paid advertisement

Facebook 484x252

 

“Are you living with insulin dependent diabetes? Digital Medics introduces the new Smartplus digital insulin pen and mobile diabetes management app.

The Smartplus Insulin Pen is a new digital insulin delivery device, which was launched in Germany in 2012 and is sold in over 20 countries in Europe. The pen boasts not just 0.5U accuracy but increments of 0.1U.

To inject insulin – dial up the dose on the LCD display, press the ACT button and a precision motor delivers the insulin. The pen stores and displays around 2 months worth of injection doses, including the date and time of the injection.

The pen has a rechargeable battery, which has a lifespan of 300 recharge cycles (approx. 5 years).

The pen supports insulin cartridges from Eli Lilly and Sanofi-Aventis, which means that Humalog, Humulin, Apidra and Lantus insulin are supported. The pen is also compatible with ‘standard’ pen needles.

Furthermore you can download your insulin injections and glucose levels to your computer using our DiabeticPlus Software. The data is made available to your mobile devices such as the iPhone, iPad and Android devices.

The mobile apps feature a logbook, daily profile table, reports and charts for statistical and medical analysis.”

 

BREAKFAST WITH DIABETES

Sally Marchini

Many people have been asking me about their breakfast choices lately, so hopefully this blog will help to answer some of your own breakfast questions. lyndal-breakfast2

They usually want to know how to choose a good breakfast cereal, how much of it to have to keep them feeling satisfied til morning tea without disrupting their blood glucose results too much, what they can have instead of cereal that is quick and easy and still healthy and how to enjoy a breakfast out without tipping the scales too much.

Before starting though I’d like to remind you to not make any changes to your current diabetes routine without first checking with your own health care professionals. These are meant as general guidelines only.

Why do we need it?

As people with diabetes, breakfast is important to us for several reasons:

It helps to get our blood glucose levels off to a nice level start, especially when we include a moderate amount of low-GI carbs

It helps us to manage our appetite better as the day progresses, especially so we don’t end up very hungry and tempted to make poor choices

It fuels our brain so we can mentally function better and cope better with the curve-balls that diabetes can throw at us

It helps to reduce insulin resistance by providing us with the low-GI energy that our bodies need to function better

What should be in it?

A good starting place is a reminder that with each meal we should include low-GI carb sources, preferably 2 carbohydrate serves as a minimum, and a protein serve to ensure we have the slow release of glucose to keep our brain fuelled for peak performance and our tummies happy so we don’t crave poor food choices by morning tea. Extra fibre also doesn’t go astray.

How to choose a good breakfast cereal?

If you recall our earlier blog on label reading, when reading cereal packet labels we should be looking for whole grains,nuts and fruit with little or no added sugar or oil in the ingredients listing if possible. Ideally we’d like the fibre to be at around the 10-15g/100g level, but if it isn’t then extra can be added in the form of bran, psyllium or chia seeds to boost it.

Remember too that if you have nuts included in your cereal it may fall outside of the total fat value of 10g/100g, TABLEsaturated fat 2g/100g targets that we aim for, but as long as there are no other fats listed then all the fat is from the nuts so it’s okay.

So if you’ve got the whole grains and the nuts and the dried fruit and the low-fat milk or plain yogurt for added protein and low-GI carb, you should find all the reasons listed above satisfied for the importance of your breakfast.

How much of it should I have?

Certainly an important consideration as too much could upset your glycemic control, rather than helping it, and could also contribute to unwanted weight gain.

Everyone is different and the answer will depend on your activity levels, on your hunger and of course on your diabetes management objectives.

This is where it’s important to check with your own d-team, preferably an Accredited Practising Dietitian, about how much is right for you.

What can I have instead of cereal?

So many clients I see tell me they don’t like cereal, and that’s fine. We all have different tastes. There are many other breakfast options that are suitable for people with diabetes.

Multigrain toast and muffins with an egg or baked beans for added protein and extra veggies to help you meet your 5 veggie serves are awesome. Avocado and fresh tomato on toast (no need for a spread) is also a great way to get started. And peanut butter works on toast to give you the extra protein serve to keep you feeling fuller for longer.

Fruit smoothies also work well for those of you who struggle to eat in the mornings.

Cooked breakfasts are also wonderful when you have a little more time, and including veggies in there is a great idea.

I actually really like the ideas included in this blog by one of our Diabetes Counselling Online Facebook group members, Dr Lyndal Parker Newlyn: The Beauty of Breakfast that also talks about why it’s so important to get into this healthy habit.

What about eating out for breakfast?

Eating out can work well if you remember the diabetes basics about low-fat, low sodium and whole grains.

Choose meals like a bircher museli with fresh fruit and plain yogurt, or spinach, mushrooms and tomatoes on multigrain toast, or served with baked beans for that low GI carb with protein included.

And enjoy a coffee made on low-fat milk for the good low-GI carb and protein hit.

Traditional breakfast ideas that should be reviewed for better diabetes management

The first thing that springs to mind is fruit juice. Traditionally many Australians enjoy a glass of juice with their breakfast. With diabetes it’s not an ideal option when you consider that we’re aiming for two pieces of fruit per day and a glass of juice provides the carb energy of closer to 4 pieces of fruit without the fibre.

Avoid crumpets – yes, even the wholemeal ones. Not only do they have a high glycemic index but they’re also high in sodium (sodium bicarbonate is used to make the holes) and most people like to have butter or margarine on them which adds unneeded extra fats.

Doubling up – Some of my clients tell me they have both cereal and toast, and unless you’re having a half serve of each, you probably don’t need to have both. This is where many of my clients see a rise in their BGL readings 2 hours after breakfast, when basically they’ve just had too much for their system to manage.

What do you eat for your diabetes breakfast?

Please share below what your favourite breakfast ideas are, in case they spark someone’s tastebuds into action. We have different tastes, so the more ideas we can share the better!

 

Hello, are you okay?

Viv McKenna

My neighbour was found dead in his bed today.

rosePeter was a grumpy old man who alienated most of the other residents of our small retirement village. Originally from England, he had one sister alive, with whom he’d had an argument three Christmases ago and they hadn’t spoken since. Apart from me, only two other people here would even speak him.

Peter had type 2 diabetes which he was proud to have well controlled by diet, exercise and metformin since he was diagnosed over 20 years ago.

I was talking to him last Thursday when he told me he had been having difficulty with his breathing and had been to the doctor. Peter was upset that he’d had to give up his morning walks which he previously took rain, hail or shine. His doctor had prescribed an inhaler which he was going to get the next day. I suggested he make sure to learn how to use it properly otherwise he wouldn’t get the benefit from it. That was our last conversation.

This afternoon, Frank knocked on my door to ask when I’d last seen Peter. He had been upstairs to visit him but found everything locked and the blinds still down. He’d knocked and called but there had been no answer. Frank said he had last seen Peter on Saturday and I agreed. We talked about the possibility of him having gone into the city in a taxi which would explain why his car was in the garage and Frank went off to phone the hospital to see if he had gone to the chest clinic there.

Not long after, the maintenance man and the housing manager from our complex were at Peter’s door trying to dismantle the lock and gain entrance. They ended up having to break the window to get in and found Peter in his bed.

So Peter died as he had lived – alone. If it hadn’t been for Frank, it could have been days before he was missed.

And it made me think. How many of us, especially those of us who are getting older, have multiple chronic illnesses and live alone, have made sure that our loved ones know where the spare key is. How often do we go without making contact with those closest to us – do we do so daily, every two or three days?

Unlike Peter, I’m one of the fortunate ones with family and friends who care about me and with whom I have regular contact. I worry that I am being a nuisance if I make contact too often, but now I think it is probably a good idea to talk about it with my children and work out a regular time frame they would feel comfortable with – it only needs to be a text or fb message.

It’s also important that your medications are recorded somewhere. I have one of the excellent St John’s Ambulance record booklets which you can stick on your fridge – they’re available from most chemist shops and some doctors’ surgeries for a gold coin donation. That way if the ambulance has to take you to hospital they can easily locate your medication record which will assist your emergency care team.

I feel sad for Peter – he was grumpy and difficult to get along with but he grew wonderful roses and enjoyed a chat out the back.

 

Member’s Story

Dave Barnes

From DCO’s Mens Facebook group site

Diabetes is sometimes like riding a bike in a headwind, you may have the best gear and a strong pair of legs to crunch the peddles but you just feel like you are working hard for every metre forward.
As a bloke I am am always conscious when and if the condition will take my ability away to work, to drive, to play physical sport, to enjoy sex, to not put the added burden of complications on my spouse and my family.
I grew up with a father who had it, he had all the mess that goes with it included heart disease, stroke, kidney failure and all resulting in a long slow death. It continues to haunt me and is a key reason I work so hard to stay active and fearless.

I am active but the fearless bit is a bit of a furphy.dave barnes
Right now in my life I am starting to forget things. Every day things but I am forgetful and I am thinking is this because of diabetes? Some days my eyes hurt and get tired and I think is this the diabetic retinopathy playing with me? Some days I get agro at the smallest of things, some times I feel depressed and think, is this my diabetes and my blood sugars?
In reflecting on these some of them are diabetes and some of them are just, life. I think it is good to put some reflection into the every day grind. It’s wise to put some perspective of who I am and where I am at as a man and as a diabetic.
For the former, I think I’m doing ok; I have two beaut kids who are well, smart and active. I have a wife who is honest with me and does so much for us all. I have a job and I get to train for triathlon. As a guy I am OK. As a diabetic I have OK HB1C’s but my eyes are the first of my aging signs of diabetes. I need to “watch out for those.” I takes me a long time to do a wee which is to do with some diabetic thing which is another sign I am not 21 any more.
In a nut shell I’m doing OK but it is a battle that needs to be fought. Diabetes is not the type of illness like cancer that strikes like a blitzkrieg and kills like a thief in the night. It is like land erosion; don’t look after the land then the land starts cracking up and good earth turns to salt. In response, I have to see doctors, endo’s, pump people, eye people, feet people regularly to keep in check. My battle plan is that because If do These things I stay ahead of the game and don’t get played by the condition.
So fella’s enjoy your low carb beers and the nine to five and some sex with your lady and cricket with your mates. But remember to take care of yourself and to add some time for reflection so you can work out just what is important and what is not. In regards to diabetes, best thing as a bloke to know is to talk to your mates and if you can’t find any, come here to this site and have a chat or a rant. It’s OK, your wife can’t hear you!

 

For St. Valentine’s Day

Diabeadies® by Vivi are a range of bracelets, custom made by one of our founding members, Vivienne McKenna

The bracelet shown is a single strand stretch moonstone bracelet with hand-made gemstone & hand-made

Tibetan silver framed charm. We also have matching earrings. moonstone

All bracelets are CUSTOM MADE using only genuine gemstones and Tibetan or Sterling silver frames and mounts, with some rhinestone and Swarovski crystal highlights. Other gemstones available are Amethyst, Jade, Aquamarine, Sapphire, Garnet and Rose Quartz. Please allow 5 – 7 days for Viv to make them and then post them out. All post will be tracked.

http://www.diabetescounselling.com.au/store/#!/Diabeadies®/c/10606339/inview=product41125084&offset=0&sort=normal

 

How to stand up to the fear of diabetes

http://www.dreamstime.com/royalty-free-stock-photo-fear-concept-choice-acronym-bravery-life-image44534735

I was thinking the other day that if someone could just come up with a way to check blood glucose that does not require turning your fingers into blackened stubs, where multiple areas bleed when you squeeze for one blood test, and they could eliminate hypos, I would be ok with having diabetes.

There are many parts of it I dislike, but these are two of my most hated. In fact the hypos thing is probably the biggest fear for me. And that is the bottom line toughest part of life with diabetes when we break it all down isn’t it, the fear.

It is not that you have to eat healthy, be active, get your rest, plenty of sunshine, check your feet, visit more doctors than usual and reduce your stress. These are all good for you. It is not that you have to take medications or have multiple daily injections or lived attached to a machine, even though that is annoying and sometimes frustrating. It is not even the fact you have a chronic disease that can’t be cured. It is the cold hard fear.

It’s waking up in the morning with a high blood glucose level and having to decide whether to eat breakfast or wait, worrying about whether you are going to end up higher and feel like crap, or dive into a hypo from your correction dose of insulin, and feel like crap….It is sitting up late at night when everyone else is in bed, waiting to see if your levels are going to settle as they have been too high or too low. It’s managing the swings and ups and downs, often alone and not knowing when it will stop.

It is going out on a run, to the gym, dancing, drinking, on holidays, hiking, skiing, having sex, even a walk around the block – and not knowing if you might end up low or high. It is the fear of the unknown. And the fear of the known. The fear that gets drilled into you when you get diagnosed and reminded to you every time you look at a national diabetes week, or world diabetes day poster. It’s sleeping, waking, eating, fasting, sitting, standing, lying, existing – with FEAR.

It’s exhaustion. Which makes fear worse.

It’s all those things that can go wrong, break, stop working, fall off or be chopped off. It is blindness and dialysis and horrible feet. It’s not having babies, or having babies and then trying not to breathe the entire time you are pregnant in case it messes up your blood sugar and harms your precious baby.

It’s working hard in your career and your life dreams and not knowing if your diabetes will cause a problem you don’t want your colleagues to find out about. It’s failing exams because your levels were so high you couldn’t think straight. The stress of losing your license when your job is driving trucks. Losing your ability to make love. Losing your partner. Losing your grip.

Yes indeed, diabetes is a whole lot about fear and a whole lot less about the mechanics of it all, a whole lot less about the actual act of caring for your diabetes. People will tell you that you are “non compliant”, not managing well, not getting it. That is bullshit. You are probably scared. You are probably confused. You are probably exhausted.

Fear creeps up on you, takes hold of you, hangs around in dark corners, jumps out at you from under the bed.

Fear is a bitch.

And if someone could only take away that fear for me, I would be pretty ok with having diabetes, it is not the worst thing to have. The truth is, nobody is going to do that for you but YOU. If you are like me, and fear has a grip on your life with diabetes at times, the only way we can stand up to that fear is together, and alone.

We must take time to notice these fears, to pull them out from under the covers. We must take time to shine a light on them, share them – please don’t suffer fear in silence. Learn how to be more mindful, how to manage fears, how to be more centered, more peaceful. You don’t need to learn how to be more brave – people with diabetes are some of the bravest people I have ever had the pleasure of knowing – and trust me over 15 years working in diabetes I have known many thousands.http://www.dreamstime.com/royalty-free-stock-photo-fear-concept-choice-acronym-bravery-life-image44534735

By sharing these fears we reduce them. We feel safer, as there is safety in numbers. Fear will always be part of life with diabetes. It is scary. But we can reduce how much it impacts on our daily lives by setting up networks of support, help when we need it, talking about it and facing it head on. And in those moments when you are scared shitless, just remember we are all here holding your hand. We have your back and you CAN do it.

What do you fear most about life with diabetes – please share and get these things out into the spotlight

Helen

xx

Helen Edwards has lived with type 1 diabetes since 1979. She is Mum to 3 sons, the founder of Diabetes Counselling Online, a diabetes educator, social worker and PhD Candidate studying diabetes distress in pregnancy for women with type 1 diabetes. She is also a successful Interiors Blogger and Stylist at www.recycledinteriors.org and runs creative workshops, an online store and studio in Adelaide – just for a life outside of diabetes.

 

http://www.dreamstime.com/royalty-free-stock-photos-free-hugs-russia-image21316188

20 things I hate about diabetes

couple hands

bgl rouletteSometimes I get sick of telling people that their diabetes will be ok, and they will be ok, and everything will be ok. Not because I don’t believe that to be true, I do. I think everything WILL be ok. But damn it, diabetes is NOT always ok. I am exhausted at the moment- are you? It is that whole end of year , nearly at Christmas, we can see the finish line thing.

My 6 year old Maxwell got up today and fell asleep on the couch for a minute or two, and then jumped awake shouting, “I wasn’t asleep!”He gets that from his Dad. :)

And my 15 year old couldn’t manage day 4 of work experience. I know his problem.

The thing is, not only am I exhausted from working bloody hard and sleeping very little all year. I am exhausted from managing diabetes. Do you know what I mean? It has NOT been ok. I have had swings from highs to lows and sudden hypos that freaked me out and stubborn highs. My gut problems from gastroparesis continue to play with me. And some days lately I have felt like maybe it WON’T be ok…..

So here are 20 things I hate about diabetes (coz we all have to get this crap out sometimes – try it, it helps!) Feel free to share and comment if you feel the same or want to add to the list

1) It’s so damn unpredictable and never ending

2) Finding spots for finger pricks after 35 years and up to 20 tests a day is pretty hard – you should see my fingers, they are a mess…..

3) There are no perfectly 100 % accurate blood glucose monitors and do you KNOW how much difference a 1 or 2 mmol reading can make to some of us with type 1??

4) My skin is stuffed and finding sites for my pump continues to be a delight of each and every day

5) Hypos, especially sudden ones where I go under 3 mmol freak me out

6) Hypers, especially unexpected ones where I go over 16 mmol freak me out

7) People ask me all the time in airports to “take the pager off” as I go through the scanner

8) It is exhausting

9) The general public don’t get it. They think it is simple.

10) It has damaged areas of my body that I am terrified will just get worse…

11) Exercise is a debacle, you need a PhD and even then your theories will be challenged every time you go out for a run

12) There is no spontaneity

13) Leaving home to go out involves lugging a suitcase with you

14) Carbs Carbs Carbs you are such a challenge – can’t live with em, can’t live without em

15) I worry that my children will get diabetes

16) I worry about losing my blood machine or breaking my pump, or forgetting to put it on after a shower – being reliant on machines to keep you alive is stressful

17) It costs a LOT and we should have a concession card- all of our lives

18) It keeps me awake at night- sometimes sitting up to make sure my levels are not too high or too low before going to sleep

19) All the “I quit sugar” people give me the shits

20) It is for life. It isn’t going anywhere fast. The promised cures never come. This is IT.

Rant over.

Oh and you know it WILL be ok. It always is in the end. But sometimes you just gotta get this stuff out. If you are feeling like me- please comment and share. You will feel better trust me and at least we know we are all in it together next time you are sitting up at night, or screaming at your blood glucose machine.

Helen

xx

Helen Edwards has lived with type 1 diabetes since 1979. She is Mum to 3 sons, the founder of Diabetes Counselling Online, a diabetes educator, social worker and PhD Candidate studying diabetes distress in pregnancy for women with type 1 diabetes. She is also a successful Interiors Blogger and Stylist at www.recycledinteriors.org and runs creative workshops, an online store and studio in Adelaide – just for a life outside of diabetes.