31
Oct 11
Check your LADA
31
Oct 11
I Guess ‘Hello’ Is A Good Start…
So there I was, playing Bejewelled Blitz, relishing the fact that I’d finally beaten one of my friends, when up popped a notification from the Diabetes Facebook page asking if anyone was interested in blogging. I’m not sure if it was a ‘hypo’, a ‘hyper’ or the sheer exhileration of winning that made me do it, but here I am ‘blogging’!
I believe ‘Profile Pages’ will be added at a later date, but until then (and ignoring the fact that ‘a little knowledge is a dangerous thing’) I guess a small introduction won’t do any harm.
My name is David, I’m 45 and from Lincolnshire in the UK. I have a younger brother and sister who were diagnosed with Type1 diabetes within 9months of each other about 8 years ago. Last year in October, having lost 2 stone in weight because of massive muscle loss (and following tests) they diagnosed me Type2. I was prescribed Gliclazide and put on Atorvastatin. I’ve never been overweight, and because they couldn’t risk me losing any further weight, they couldn’t add Metformin to the mix to help the Gliclazide work. In addition, as I’d never had an unhealthy diet, my Dietician couldn’t really find anything to tweak that would have had a substantial effect in reducing my levels.
I had a review in September this year, and although I hadn’t gained or lost any more weight I remarked that I felt the best I’d felt in a year. My Hb1Ac result told a different story and I was referred to my Diabetes Specialist. Within two days I had what was a rather alarming call asking if I could get to the specialist that afternoon (Friday). For numerous reasons I couldn’t, so was given instructions on what to do if various scenarios/symptoms occurred over the weekend – and my file was ‘flagged’ at A&E – just in case!!! On the Monday at my appointment I had a keytones reading of 3.8, and my blood was over 32.7. I was ‘converted’ to Type1 and had my first shot of insulin (HumulinM3). Within an hour my blood was down to 15.1, and later that evening it was at 5.1 with a keytones reading 0.6. My specialist (who is the same one as my sister) said that if it wasn’t for the fact that my levels came down so rapidly, and the fact that I wasn’t new to diabetes and it’s associated issues, he would have admitted me there and then.
I’m not sure what has disappointed me most – losing my muscular thighs, pert buttocks and strong forearms, or having to inject! In fact with hindsight, I could have made a fortune as a ‘living skeleton’ last Hallowe’en! The good news for me is that I’ve already gained 6lbs and feel great. I’m also lucky that as a self-employed artist and graphic designer, I can have a regular routine to my day with set mealtimes and periods of physical activity.
‘Diabetic’ is not one of the labels that I’d have consciously collected to go with my Calvin Kleins or Dolce & Gabbana, but it’s there, and I have to deal with it. My mindset is still one of “I’m going to control my diabetes – it’s not going to control me”, and as long as I keep with that I’m sure that I’ll be fine.
I know that there will be complications along the way, and I know that sometimes it may be scary – but scary is just another emotion and sensation. From many of the threads on the Diabetes forum I also know that whatever may happen, many will have gone through it before.
Hopefully, the diversity of our family of bloggers will ensure that everyone can identify or relate to the challenges and champagne moments of our lives with diabetes and the wider issues that affect us.
Until next time… Dave.
28
Oct 11
My life with Diabetes
Hey guys,
So I’m new to this whole blogging thing, but I felt like I would feel privileged just to talk about diabetes, as over the years I have come to accept it.
So My names chelsea I’m 18 years old and lived with Diabetes since I was 8 years old. I’ve had a lot of problems with my diabetes over the years (I will talk about this at a later date), but one thing I have learnt is that although there will be bad days with it, Diabetes shouldn’t control your life it should be part of you and your identity.
I’m now living a life which I am happy with, I’m chasing for my dreams, and yes there is times where I get stressed about my diabetes, I am a perfectionist, I spent so many years wanting it to be perfect, but I came to realise that you can only do the best you can.
I basically think what I am trying to say is, just have don’t let it win, let it be part of you and who you are. I’ve learnt that and being recently diagnosed with depression, my HBA1C was 7.9% despite this stress, it just shows that you have to take things as they come.
I hope to post more on here! i feel I would love to share my experiences with people, and be in contact with people who also want to share theire experiences. Take care:)
28
Oct 11
First time – be kind !
Its all very well volunteering to write a blog – but sitting in front of a (very slow) computer screen and all of a sudden it’s a pretty daunting task. I suppose the thing to do in this first post is to share my story with you.
I am 56 years old and live in a rural area in Lancashire. I was first diagnosed with type 2 diabetes around 9 years ago. I didn’t consider myself particularly unfit or overweight (15 stones for a 5′ 10″ frame) and my lifestyle was no different or any more unhealthy than my friends. I’m a keen cook and we eat hardly any processed food and although I like a pint I tended to drink only socially – and to excess only about once a month.
On first diagnosis I was handed the standard NHS diet sheets and told to keep a diary of what I ate. The nurse seemed to think my diet was fairly healthy but my blood sugars stayed high and eventually I was prescribed Metformin and statins which brought my numbers down to a point where the nurse announced she was pleased with my progress. My weight seemed to stay fairly constant between 15 – 16 stones despite all attempts to reduce it.
That was the picture until February of this year when I decided to take charge of my life. I guess that we all need something to give us a wake-up call and get us to look at our situations afresh – in my case it was the statins that gave me the push that I needed.
The first statin that I was prescribed was simvastatin. It certainly worked as advertised and my cholesterol score came down from 6 to just under 3. After 18 months I began to notice that my memory was failing me and it became a bit of a family joke. I mentioned it to the diabetic nurse at my annual review but she seemed to think it was a consequence of growing older and nothing to worry about. Although I was still a little concerned I accepted that and got on with my life. The crunch came at Sainsburys checkout. I was standing there with a trolley full of shopping trying desperately to remember the pin numbers on my bank cards. After trying 3 different cards with a queue full of tutting shoppers behind me I finally had to admit defeat and leave the store without my shopping. I’ve never been so embarrassed in my life !
As soon as I got home I made an appointment to see my GP. He was very soothing and told me not to worry about dementia (I wasn’t) and that failing memory at my age (49 then) was probably due to stress. When I mentioned that the little leaflet inside the packet of statins gave memory loss as a possible (though rare) side effect he told me that he’d never heard of that. I was not convinced and the doctor finally agreed to change my prescription to Rosuvastatin to see if that made any difference but also arranged an appointment with a consultant and sent me off for a CT scan of my brain.
Needless to say the scan showed nothing untoward and happily my memory improved and was back to normal after 6 weeks or so on the new medication. All seemed well for a few years – my numbers were in the right area and my weight wasn’t increasing but I noticed a bit of stiffness in the joints. At my reviews I mentioned the joint pain but was told it was a normal part of getting older (where had I heard that before ?) and to take more exercise.
Crunch number two came along in February. I had got to the point were I was in pain most of the time. The pains were at their worst in my shoulder and back and had spread to my kidneys. I was also going bald ! The only way I could get to sleep at night was by propping myself up with pillows. As an ex smoker I convinced myself that I had developed cancer and that my days were numbered. I plucked up the courage to go to the GP again and got an appointment with a locum doctor. He was sympathetic and arranged a chest X-Ray for me and then asked me to undress and hop onto his couch. He started to palpate my abdomen and quizzed me about my diet and asked if I had a problem with indigestion as he suspected I might be experiencing referred pain from digestive problems. When I told him that I very rarely had any problems like that he casually mentioned that it may be a reaction to some of the medication I was taking.
When the chest X-Ray was clear I turned to the internet and googled ‘Statins side effects‘. Ten minutes later I threw the statins into the bin and waited to see what would happen. The pains began to subside almost immediately and after 4 weeks I was feeling much better with only a bit of pain in my shoulder (now almost completely gone) and was having a good nights sleep for the first time in years.
My annual diabetic review came along 4 weeks later – and as you can probably guess it wasn’t good. All my numbers were up with my cholesterol increased and my Hba1c over 7. The nurse also told me that my triglycerides were the highest she had ever seen. As I was already on 2g of Metformin a day she also suggested that I needed to take other medications to control my blood sugar and tried to persuade me to take some form of statin perhaps at a lower dose. After my experience with statins I was extremely reluctant to take any more drugs and asked her to arrange another blood test in a few weeks and that I would try to change my diet to bring my numbers down. She agreed but was obviously sceptical that anything would change much.
Back to the internet ! I looked for ways of changing my diet in order to bring my cholesterol down and found a site that recommended a low carbohydrate diet. The site had a link through to the Low Carb forum on this site and the rest, as they say, is history. Four weeks later I hopped on to the scales and astonished the nurse by being a full stone lighter. My cholesterol and HbA1c had both come down and whats more I felt like a new man.
Now I have been on my low carb diet for over 6 months I can report that I am down to 12 stone in weight and have stopped taking my Metformin. I have also started to exercise and run up to 4 miles a day. I feel better than I have done for many years and my sugar control is very good. My cholesterol is a little on the high side but I’m working on ways to change that with my consultant.
My apologies if this is all a bit long – but if you read this blog in the future (and I hope you will) I think you should know how I got to where I am now and how that has coloured my views on diabetes. I intend in future to mix my own experiences with musings on topics that interest me – in particular turning a sceptical eye on to what we are told and the assumptions that people make.
All comments are welcome but please, as it says in the title, remember that this is my first attempt and be kind.
If you have managed to get as far as this – thanks for reading !
06
Jul 11
Islet cell transplants becoming a welcome reality
It’s great to see stories where people are successfully undergoing islet cells transplants.
Kathleen Duncan has made the news this week for becoming the first woman in Scotland to receive an islet cell transplant.
A number of NHS centres around the UK are starting to roll out islet cell transplantation as a treatment procedure. The Edinburgh Royal Infirmary’s transplant unit, where Kathleen’s transplant was carried out is one of these with other islet cell transplant centres including London, Bristol, Oxford, Newcastle and Manchester.
Stopping the immune system
Those who have the transplants need to take anti-immune drugs to stop the body attacks the new insulin-producing cells in the pancreas but hopefully as more people receive the transplants, a greater understanding of how to stop the immune system attacking it’s own cells could follow.
The numbers of people who have received transplants in the UK is still low (dozens rather than treble figures) but it’ll be exciting to see how this area develops.
10
Jun 11
Could Victoza become a viable treatment for type 1 diabetes?
This week there was news from a small study that showed that Novo Nordisk’s Victoza could serve as a viable treatment for type 1 diabetes, as a supplement to insulin.
People with type 1 diabetes can often find themselves dealing with large swings in blood sugar on a near-to daily basis which can be particularly difficult to control. The study on Victoza indicated that the drug helps to reduce the swings in blood sugar and improved overall blood glucose control.
Victoza (also known as Liraglitude) is a once daily injectable medication for people with type 2 diabetes.
The drug’s action is to:
- Increase insulin secretion
- Delay stomach emptying
- Suppress meal time glucagon secretion
It is the third action, suppressing glucagon, that raises interest as potential treatment for type 1 diabetes –in addition to insulin.
Victoza and type 1 diabetes study findings
The study, which was a small one in terms of participant numbers (looking at 14 people with relatively well controlled diabetes), was of note for the following reasons:
- Participants found that the amount of insulin they needed to take was reduced by about 30% (basal and bolus)
- Average blood sugar decreased by about 15%
- The group’s collective HbA1c dropped from 6.5% down to 6.1%
One worry which people with type 1 diabetes may have is that with glucagon suppressed, whether this could lead to dangerous hypos that the body cannot respond to. With Victoza’s action reportedly taking place at meal times, I would think it only a problem for people who have lost hypo awareness, however, this is just a supposition of mine and more research may be needed to test safety from severe hypoglycemia.
The study suggested that swings in blood sugar were avoided which helped to reduce hypoglycemia as well as hyperglycemia.
Other type 2 drugs which may have benefits
Victoza is not the only type 2 diabetes medication to have been suggested as a possible aid for people with type 1 diabetes – Januvia was studied as a potential option in 2010.
Type 2 diabetes drug Januvia could help people with type 1 diabetes
The other available non-insulin injectable medication available in the UK is Byetta (Exenatide), which is also prescribed specifically for people with type 2 diabetes.
Benefits and disadvantages of Victoza and Byetta
An potential benefit of Victoza and Byetta are that they can help to suppress appetite and aid weight loss. This may be a benefit for some people with type 1 diabetes but could also be a disadvantage for those who are already slim. Participants taking Victoza in the study lost an average of 10lbs in body weight over 6 months.
Victoza and Byetta both have potential side effects which include stomach pain, nausea and vomiting.
Not recommended for use in type 1 diabetes
It should be noted that Victoza, Byetta and Januvia have not been recommended for use for people with type 1 diabetes. If you have type 1 diabetes you should not take or expect to be prescribed the drug. It is possible that these medications may be approved in future for use by type 1 diabetics but not until research can prove its safety.
Your views on Victoza
- If you have type 1 diabetes, would you be tempted to try taking an injectable medication in addition to your insulin?
- If you have type 2 diabetes and take Victoza, how do you find it?
17
May 11
Got diabetes something chronic
‘Chronic disease’ -this is the charming name that was given for the first appointment I had at my most recent practice.
I do wonder whether anyone thought that this phrase might appear maybe just a tad on the blunt side for what was in reality a simple ‘diabetic review’ appointment. It seems as though common sense has prevailed as they’ve recently changed the name of the appointment to ‘long term illness’.
Shocking ways to describe diabetes
Having been working on behalf of those with diabetes for about 4 years now, I’ve seen a fair few hard to fathom ways to describe this condition.
I think my all time favourite has to be this outrageous, 24-carat howler from the International Diabetes Federation (IDF):
“Diabetes is a chronic, debilitating and costly disease associated with severe complications, which poses severe risks for the entire world.”
“Whoa, steady on!” I thought, when I first came across this page.
In fairness, the IDF had been fighting to get recognition from the United Nations (UN) that diabetes is a serious worldwide concern that deserves greater public awareness. However, without knowing the background, it’s a very odd webpage to come across.
Edit: 2 June 2011
I’d like to draw attention to IDF CEO Ann Keeling’s comment below, which reinforces the fact that people in developing countries are a long way away from the luxuries that we have. It brings home how lucky I am to have my insulin and giving this opportunity to people in developing countries is what the IDF is campaigning for. Check out the links Ann has put in her post too.
Bizarre references to diabetes
Has anyone seen any similar confusing, thoughtless or even insulting references to our condition?
16
May 11
Cerys and the insulin gang raising money for diabetes
Cerys is 9 years old and was diagnosed with type 1 diabetes in January this year. She’s a born star, having raised money for a boy with cancer and, since being diagnosed, for diabetic charities too.
Shortly after her diagnosis Cerys wanted to raise some money for the charity Diabetes UK. Cerys organized a tea party and had about 20-30 people in her front room helping to raise money. Many of her friends, family and even school teachers came along, including the headmaster.
During the tea party she said that she felt so proud she could cry that so many people came along, including the headmaster who Cerys says is her own hero. In total, over £200 was raised.
A few months before she was diagnosed Cerys raised over £300 alone, by doing a sponsored silence, for a local boy who was sadly dying of cancer. She raised over £300 for him. With help from her parents, Cerys managed to raise, in total, over £1,000 for the cause –a fantastic effort.
Cerys even has own website now about diabetes, called The Insulin Gang, which will appeal to other children with the condition and gives them a place to talk with Cerys and other kids with diabetes as well as raise money for specific causes.
16
May 11
Behind the wheel with diabetes
As someone on insulin I have to be particularly careful when driving. More than just testing blood sugar levels before each journey I’m conscious of where my sugar levels may be pretty much throughout the whole journey. I find I tend be pretty much constantly aware of how I’m feeling to make sure I avoid low blood sugars and any danger of an accident.
Knowing whether I’m low
One situation that I tend to be very careful of is if I’m not feeling a hundred per cent. If I have even a slight cold or a mild touch of man flu, it could mask some of my hypo symptoms.
Feeling ill could mean:
- Feeling more tired
- Experience unusual changes in body temperature
- Being less sharp with making decisions
- More prone to exaggerated emotions (eg becoming annoyed at other drivers!)
These aren’t ideal for driving to start with and furthermore, they’re also all relatively common hypo symptoms for me. If, for example, I were to drive whilst feeling lethargic, it would be more difficult to spot any tiredness as a result of my blood sugar crashing down to low levels.
Keeping blood sugar levels safe whilst driving
I check my blood sugars before any journey and if the level is low I won’t set off until the level is back above 4.0 mmols/L (following the DVLA recommendations).
If my journey lasts longer than 2 hours, I’ll stop to test blood glucose levels within every 2 hours. Should the levels turn out to be low, I’ll need to wait until the levels are back up to the safe level (above 5.0 mmols/L) before setting off.
I keep a pack of glucose tablets within easy reach. If at any point I’m in doubt as to whether my levels may be low, I’ll eat a tablet or two and look to stop to test my levels.
High blood sugars
High blood glucose levels (hyperglycemia) can also be problematic for driving. High levels can lead to irritability, tiredness, poor decision making and –with particularly high sugar levels- blurred vision.
To maintain good blood sugar control, I will try and keep my levels below 8.0 mmols/L. It is not unusual for me to finish a journey with figures above 9.0 mmols/L and, whilst not ideal, I am pleased not to have been driving in hypoglycemia territory.
Managing diabetes when driving
Diabetes in general always seems to give me one extra thing to think about in most situations and with driving it’s particularly the case. It can be annoying at times, especially if I’m in a hurry to get going or if I have to find somewhere to pull in to check levels mid journey but I’ll take a little inconvenience over being unsure as to whether I’m safe to drive.
- How is driving for you? Is every journey a worry or does it have little impact?
- Does a pump rather than injections make a difference with driving?
- Anyone with tips for making sure your levels are in the right place?
- Any tips for professional drivers with diabetes?
11
May 11
Type 2 diabetes and the blame game
There are a number of discussions we probably all see going on about how people with type 2 diabetes have made themselves fat and brought it upon themselves.
- “They chose to eat this way, it’s their fault they got diabetes.”
- “People overeating are eating away at our tax money.”
- …and such like.
We know that the effects of type 2 diabetes mean that, unless aggressively countered, a vicious cycle is entered into and it takes at least a long and concerted effort to break out of it.
I find it a little hard to believe that people are totally willingly eating their way into poor health. There may be people who are eating things and knowing it’s likely not good for them but it may be worth asking whether it’s such a free choice they made to start with?
UK’s poor nutrition
Nutrition in Britain is generally poor. Cheap food is full of refined carbs, flavourings and emulsifiers to conserve shelf life, taste and appearance. These all turn out to be great in terms of profits for food producers (and distributers) but not so good for us.
So who is to blame for the rise in type 2 diabetes?
If someone is told why they’re making themselves ill and they keep doing it, then there may be some sense in apportioning blame –however, it seems not even the nutrition experts have a complete handle on why people are developing metabolic syndrome (type 2 diabetes).
Fruitless
Personally I find blaming people with type 2 diabetes to be fruitless. I don’t think it’s their fault. Most of us have grown up under conditions where the choice of what we eat has been steadily taken further away from us and put into the hands of food producers and distributors.
Rather than place blame on individuals, I would much prefer to see the root issues tackled:
- Let many more people know what a proper balanced diet should consist of
- Cut down on the harmful artificial additives in foods
- Support a move towards fresher, better quality foods
NICE (The National Institute for Clinical Excellence) has itself just laid out guidelines, for the prevention of type 2 diabetes, that supports good quality and affordable fruit and vegetables to be available in people’s locality.
Should people be blamed?
What do you think though?
Are we being soft by not blaming people? Do they need a kick up the behind to help them take notice of what’s happening?
Or, is blame the last thing that’s needed? Isn’t type 2 diabetes enough of a kick in the rear to start with?











