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Posts Tagged ‘vitrectomy’


Hi,

I have some very exciting Diabetes gadgets to try which over the next few weeks I will put to good use and let you know my thoughts.

I currently have the New BT Device from Menarini (Glucomen) which wirelessly connects your GlucoMen BG meter to either you Apple or Android device so you can view results, secondly I have a New GlucoRX BG Meter to try which I had never seen before and I am very excited to give it a try a let you know what it’s like.

If you can’t wait that long then please click the following links for more info :

GlucoLog BT Device.

GlucoRX BG Meters.

Thanks for reading.

Andrew

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Roche Accu-Chek New Mobile BG Meter.

I thought it was about time I wrote a Blog review of my Roche Accu-Chek Mobile which I have been using for a fair few months now after speaking to the team at Roche who as ever are more than happy to help. I particularly like the fact they have a large range of meters to suit most tastes and requirements.

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The meter I have been using is the latest version and somewhat slimmer than the previous version which certainly appeals to me, it certainly looks the part, I even like the packaging lol. I called the Customer Service Team to ask if it was possible to send me a meter and the team took some details from me so I was registered for replacement batteries etc and within a day or so my lovely meter arrived, with a cartridge of test strips in the box. I had also ordered a new carry case to keep my lovely new meter safe and clean which looked great and protected the Accu-Chek Mobile perfectly. It is ideal for going out and popping in your pocket but it is not the smallest meter however on the flipside of this the screen is great and I have seen larger BG meters.

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For me the fact you have a cassette of 50 strips in the meter and the lancet also has 5 finger sticks included you do not need to worry about taking anything else out with you, I will get to the technical details soon.

I must say this is one of the best meters I have tried but each manufacturers BG meter has its own merits and will appeal to different people with Diabetes, I like a large clear backlit screen due to my poor eyesight, however some people with Diabetes want a tiny meter to fit in their pocket or even meters that check their ketones – technology for us is changing fast.

Here is the technical info from Roche :

The NEW Strip Free Accu-Chek® Mobile Blood Glucose Meter System.

The new Strip Free Accu-Chek Mobile system with 50 tests in one cassette eliminates the need to handle or dispose of single test strips. This makes it easier for you to test virtually whenever, wherever.

It includes everything that is needed to perform a test making blood glucose monitoring more convenient, especially for insulin-using people with diabetes.

  • All-in-one system: test whenever, wherever.
  • 50 tests in one cassette: no more strips.
  • 4 simple steps: fast, easy testing.

View Product Details

** Please click on the “View Product Details” link above for more in depth info.

As with all BG meters out in the market now they all seem to provide very accurate results in literally seconds compared to when I was first diagnosed and had to wee on a colour changing stick – nice I know J.

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Mike – I hope you don’t mind me borrowing a Blog from your site as I believe it will help many newly diagnosed people with Diabetes.

Don’t forget to check out Mike’s great Blog site EVERY DAY UPS AND DOWNS, A DIABETES BLOG

Newly diagnosed? Read Jennifer’s advice.

When I began looking around t’internet for information about managing diabetes I kept coming across something called “Jennifer’s Advice” which made a lot of sense to me and though it seems to be written with type 2 in mind, it applies equally well to type 1 diabetes (with the addition of bg tests before each meal and some more elastic post-meal test timings, I would suggest). In fact to my mind T2s on diet and exercise should test pre-meal too as it helps to isolate the action of the food at that particular meal.

Unfortunately I don’t know who Jennifer is, but I have taken the liberty of reproducing her advice here in the hope that some might find it useful.
Jennifer’s Advice to newly diagnosed diabetics – Test, test, test

Written by Jennifer, November 2008

Sounds like you’re planning to take control of your diabetes… good for you.

There is so much to absorb… you don’t have to rush into anything. Begin by using your best weapon in this war, your meter. You won’t keel over today, you have time to experiment, test, learn, test again and figure out just how your body and this disease are getting along. The most important thing you can do to learn about yourself and diabetes is test test test.

The single biggest question a diabetic has to answer is: What do I eat?

Unfortunately, the answer is pretty confusing. What confounds us all is the fact that different diabetics can get great results on wildly different food plans. Some of us here achieve great blood glucose control eating a high complex carbohydrate diet. Others find that anything over 75 – 100g of carbs a day is too much. Still others are somewhere in between.

At the beginning all of us felt frustrated. We wanted to be handed THE way to eat, to ensure our continued health. But we all learned that there is no one way. Each of us had to find our own path, using the experience of those that went before, but still having to discover for ourselves how OUR bodies and this disease were coexisting. Ask questions, but remember each of us discovered on our own what works best for us. You can use our experiences as jumping off points, but eventually you’ll work up a successful plan that is yours alone.

What you are looking to discover is how different foods affect you. As I’m sure you’ve read, carbohydrates (sugars, wheat, rice… the things our Grandmas called “starches”) raise blood sugars the most rapidly. Protein and fat do raise them, but not as high and much more slowly… so if you’re a T2, generally the insulin your body still makes may take care of the rise.

You might want to try some experiments.

First: Eat whatever you’ve been currently eating… but write it all down.

Test yourself at the following times:

Upon waking (fasting)
1 hour after each meal
2 hours after each meal
At bedtime

That means 8 x each day. What you will discover by this is how long after a meal your highest reading comes… and how fast you return to “normal”. Also, you may see that a meal that included bread, fruit or other carbs gives you a higher reading.

Then for the next few days, try to curb your carbs. Eliminate breads, cereals, rice, beans, any wheat products, potato, corn, fruit… get all your carbs from veggies. Test at the same schedule above. [Note: this advice is for T2s on diet and exercise/some oral meds, if you are T1 and on fixed doses you should be eating a measured quantity of carbs at each meal to match your insulin dose T2s on insulin and other injected meds need to reduce carbs with more caution to avoid hypos. Testing after meals will help you see how steady or spiky your levels are when you eat different foods. M]

If you try this for a few days, you may find some pretty good readings. It’s worth a few days to discover. Eventually you can slowly add back carbs until you see them affecting your meter. The thing about this disease… though we share much in common and we need to follow certain guidelines… in the end, each of our bodies dictate our treatment and our success.

The closer we get to non-diabetic numbers, the greater chance we have of avoiding horrible complications. The key here is AIM… I know that everyone is at a different point in their disease… and it is progressive. But, if we aim for the best numbers and do our best, we give ourselves the best shot at heath we’ve got. That’s all we can do.

Here’s my opinion on what numbers to aim for, they are close to non-diabetic numbers.
Fasting Under 6
One hour after meals Under 8
Two hours after meals Under 6.5

or for those in the mg/dl parts of the world:
FBG Under 110
One hour after meals Under 140
Two hours after meals Under 120

Recent studies have indicated that the most important numbers are your “after meal” numbers. They may be the most indicative of future complications, especially heart problems.

Listen to your doctor, but you are the leader of your diabetic care team. While his/her advice is learned, it is not absolute. You will end up knowing much more about your body and how it’s handling diabetes than your doctor will. Your meter is your best weapon.

Just remember, we’re not in a race or a competition with anyone but ourselves… Play around with your food plan… TEST TEST TEST. Learn what foods cause spikes, what foods cause cravings… Use your body as a science experiment.

You’ll read about a lot of different ways people use to control their diabetes… Many are diametrically opposed. After a while you’ll learn that there is no one size fits all around here. Take some time to experiment and you’ll soon discover the plan that works for you.

Best of luck!
Jennifer

Thanks again Mike Every Day Ups and Downs, a Diabetes Blog

http://www.mypump.co.uk
http://www.mypumpblog.com
T @ MyPump1

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Hi all,

Yet again it is time for my annual Eye Hospital Appointment in London at the Western Eye Hospital Nr Paddington, London on Thursday 7th March 9.10am.

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I left home at 7.00am (Time to grab a coffee at the local shop mmmm) to catch the 7.30am train again to Paddington which takes about 1 hour so not too bad as it goes direct but also gets very busy, my appointment was 9.10am – yeah right (they always run late).

Firstly I was seen by the nurse straight away to check my vision as normal and this has remained unchanged since last year which is good news, I still have big problems with night vision due to all the laser I have had in the past to help my retinopathy, I have also had two Vitrectomy Operations at the Western Eye Hospital going back a few years. I also have damage to my central vision in my right eye but it’s amazing how you cope. I was also given the drops to dilate my pupils which sting like hell for a few seconds but help the doctors see the back of your eyes easier.

20 minutes passed which gives the drops time to work and I was called by the photographer who takes images of the back of your eyes to check for any anomalies and also another machine which checks your macular condition again by a photograph.

Another 45 minutes passed and I was called by the Eye Consultant (Yes panic setting in by now) but at least I was being seen really fast which was great. I sat down with the Consultant who looked at the images of my eyes and macular condition the n she had a good look at my eyes with a very bright light. There is quite a lot of scaring to the backs of my eyes where. I also have some sort of weird eyelid infection which has been there for ages so the consultant had a good push of that and decided I needed some SPECIAL cream but would probably need it cutting mmmm lovely.

So the outcome of this check up was all good news as my eye site was stable with no changes since last year and my macular was in good condition which is such a huge relief and hard to explain what a constant worry it is.

I know we already know this but it is so important to keep your regular Diabetes check ups just to make sure everything is in order, I am a prime example (I know show off) as it was Vision Express who originally spotted my eye issues going back probably 8 years in which they immediately contacted my local eye clinic – thanks to Vision Express and of course the Western Eye Hospital.

Take care

Andrew

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Elgringo’s Retina Screen from Mike at Diabetes In Spain

By on January 22, 2013  in Ramblings
Thanks to Mike for this Blog – I wanted to share as I am due for my Annual Eye Check Up and Retina Screening in a few weeks.

730760 10151349075483518 944538258 n Elgringos Retina Screen

Yep, that’s mine!

Hey Guys!

Just checking to see how everyone is doing!  Hope you are all doing fantastically well!

Moving on, I had my Annual Retina Screening at my local clinic.  I’m sure we know how important having our eyes etc.. checked on a regular basis whilst trying to avert the dreaded Diabetes Retinopathy.  So this quick, painless and non intrusive method is a brilliant way to make sure our eyes stay in great shape.

I took a pic of mine (scared the nurse to death when I asked to snap a pic) although I won’t have the results for up to 2 weeks.  I am hopeful that all is ok this time!

 Elgringos Retina Screen

Diabetic Eye Screening

For those who wonder what it all looks like, here is a image courtesy of the UK NHS Diabetic Eye Screening service.  I would have taken self portrait but a) the room was dark b) I had a hand over one eye and c) I was being blinded by the flash going off millimeters away from the centre of my eye! icon smile Elgringos Retina Screen

Stay healthy!

Mike – Diabetes In Spain

PS: The picture was taken cause I’m a nosey bugger and it also forms part of my photo project over at www.elgringo365.com

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Hi all,

So the end of British Summer time has finally hit us all with vengeance and at 5.00pm tonight it was almost dark which is awful.

As you may already know I have had numerous trips to eye clinics due to suffering with Diabetes Retinopathy for the past 7 years which is really awful and was a real scary shock when I was first told, it was Vision Express that actually discovered the problem and instantly booked me into my Diabetes eye clinic. The problem really started after I had small blood vessels at the back of my eyes burst which affected my vision and made it very cloudy in both eyes. The treatment started with laser to burn around the blood vessels which prevents any new weak blood vessels from forming which then burst. Laser itself is very uncomfortable indeed and I have had approx 10,000 burns in each eye which I am told is the limit but this does seem to have stopped the bleeding which is great news and I am so thankful to the Eye Specialists. After all the laser it still left my vision cloudy so meant I had to have what’s called a Vitrectomy in each eye which basically entails having the clear jelly in your eye removed (Your eye replaces this fluid), I can honestly say this operation is not nice at all and means you have dissolvable stitches in your eyeball (Gross I know). Having said all that If this had not been done I would certainly not be typing this Blog even though one eye has very poor vision and both eyes have awful night vision.

So to the present day – my eyes seem to be stable at the moment and my latest eyesight test did not show any problems, even my prescription had not changed apart from my short sight vision which has got slightly worse. My next Diabetes eye check up is at the Western Eye Hospital in a few weeks time so fingers crossed I get the all clear but I am a little worried.

One of the worst things I am left with is very poor small detail reading in both eyes meaning typing Blogs like this I have to have the page zoomed in to make the words larger, damage to my central vision in my right eye meaning details in my right eye is near on impossible to read, also my night vision is really bad and means I am unable to drive in poor light so this time of year is even worse as it is dark late afternoon. It means I have to carry a very bright torch with me that literally lights the whole path/road that cost me a fortune and even then it is really hard to see if I am on my own walking home from work, without a super bright torch I would literally be stuck and please let me know of any pocket torch companies who make super bright torches. We just take our vision for granted and I am also guilty of this in the past.

Thanks for reading and please feel free to comment.

Andrew Borrett

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I live in Berkshire, UK with my wife, 19 month old son Jake and 4 week old baby daughter Amy – I also have my own Diabetes web site called http://www.mypump.co.uk .

I have had Type 1 Diabetes all my life which is 40 years and technology/treatment has changed so much for the better since I was a baby. It would have been around 1972 when I was first diagnosed with Diabetes as my parents noticed I would be drinking a lot and lethargic. I still remember when I was a very small child that my Mum used to inject me with my insulin using a stainless steel and glass syringe which was very big and did used to be quite painful to say the least but I only had one injection per day. Diabetes back then was far more difficult to control and your Blood Glucose or sugar levels where monitored using a urine stick rather than the high tech blood glucose meters we use today from Bayer Diabetes Care, Roche – Accu Chek, Lifescan etc which are far more accurate. When I was very young I did spend quite a lot of time in hospital from very bad Hypo’s where I actually would go into a Diabetic Coma and find myself waking up in Hospital which was awful. As time went on my control got better and of course technology also got better with small syringes and better insulin plus not forgetting the blood glucose meters we use today. Diabetes treatment changed fairly rapidly with me going from one injection per day to two which at the time was a huge step for me and then going onto an insulin pen with four to five injections per day (what a pain literally).
I never thought I would have any complications from Diabetes but unfortunately in 2003 after a visit to Vision Express opticians they said I had signs of Retinopathy eye complications and sent me to a specialist straight away. It was confirmed that I had Diabetes Retinopathy and would need laser treatment in both eyes to save my sight. I ended up having 10,000 burns of laser in each eye to try and stop tiny blood vessels bursting in my eye. The laser was very uncomfortable but did help but because the Retinopathy was so bad I then ended up having a Vitrectomy operation in each eye, this operation is not nice at all and involves a tube being placed in your eye and the clear liquid being taken out – your eye naturally replaces this cloudy fluid with its own clear liquid. My site now is stable but the operations have still taken there toll as my night vision is very bad (i.e. I can not see to drive a car) and my left eye central vision is damaged. I do think things could be far worse and I just hope they stay stable. I got to the point where I seemed to be injecting myself 4-6 times per day which is surely enough for anyone and this is why I spoke to my Diabetes team about the Insulin Pump. So after being on injections for almost 36 years I was lucky enough to have funding from my local PCT for an Insulin Pump which is amazing and has really changed my life for the better as it is so easy to use. I use a Medtronic Paradigm 722 and an Animas 2020 pump (No not at the same time lol) with each pump having plus/minus points but far better than constantly having injections for food or correction dose’s. An Insulin Pump basically delivers a small dose of insulin 24/7 as a background dose called a Basal Rate and each time you have a meal or snack you give yourself a boost of insulin to counteract the food called a Bolus dose. The pump did take some getting used to at first but once the tiny canular is inserted into the same are as you would inject you hardly know it is there. The pump itself is a similar size to a mobile phone and can be worn in normal places 24/7 and even while you are in bed (you do get used to it). One major thing you need to do when on an Insulin Pump is Carbohydrate Count to ensure the Bolus dose you give is enough to cover the food you have just eaten (See Diabetic Friend) but yet again this gets easy with time. My last Hba1c taken in June 2010 was 7.5 which I think is pretty damn good.

I hope you enjoy my Blog and please do not hesitate to contact me if you have any questions at all http://www.mypmump.co.uk or why not follow me on Twitter @MyPump1).

Thanks for reading.

Andrew Borrett My Pump

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