kitedoc
Well-Known Member
- Messages
- 4,784
- Location
- Adelaide, South Australia
- Type of diabetes
- Type 1
- Treatment type
- Pump
- Dislikes
- black jelly beans
But there will be other checks of health to consider. The GP is responsible for what he or she prescribes. Any issues will be sheeted home to him or her, whatever the specialist has said. There will be yearly or 2 yrly screening health checks for women's health or men's health.. And who refers you fo eye checks? Here is X who I have not seen for 15 years...? Who examines your feet, pulses etc? Who do you see regarding mental health if that is needed?I disagree - my GP does not treat my diabetes. He/she (my GP retired and I have had no reason to meet her replacement) is aware of my diabetes but it is treated by a diabetes consultant rather than a generalist. I think it is some sort of bureaucracy which mean the prescription gets signed by the GP but it makes sense for them to trust a specialist.
For women's health, there are cervical smear tests done at the surgery (but not by the GP). Breast scans are done (after a certain age) at the hospital. Foot checks, cholesterol, kidney function, blood pressure, BMI and, to a certain extent diabetes related mental health checks ("have you been frustrated by diabetes in the last year?" type questions), etc are part of the diabetes review at the hospital, retinal scans are done at the surgery (but not by the GP), other eyes test are done by and scheduled with the optician (just like mouth checks are arranged with and by the dentist), flu jabs are done by the pharmacist, ...But there will be other checks of health to consider. The GP is responsible for what he or she prescribes. Any issues will be sheeted home to him or her, whatever the specialist has said. There will be yearly or 2 yrly screening health checks for women's health or men's health.. And who refers you fo eye checks? Here is X who I have not seen for 15 years...? Who examines your feet, pulses etc? Who do you see regarding mental health if that is needed?
This is part of what helps keep GP s blinking well ignorant of diabetes.
There is something wrong with a system that does that!!!!!
Zero relationship yet GP is supposed to do scripts? Absolutely daft. I can understand others like nurses doing screening but this devalues the GP who is supposed to be involved with gatekeeper functions to keep more expensive hospital treatments, referrals to minimum. No wonder the medical system is under strain.For women's health, there are cervical smear tests done at the surgery (but not by the GP). Breast scans are done (after a certain age) at the hospital. Foot checks, cholesterol, kidney function, blood pressure, BMI and, to a certain extent diabetes related mental health checks ("have you been frustrated by diabetes in the last year?" type questions), etc are part of the diabetes review at the hospital, retinal scans are done at the surgery (but not by the GP), other eyes test are done by and scheduled with the optician (just like mouth checks are arranged with and by the dentist), flu jabs are done by the pharmacist, ...
I have zero relationship with my GP and I am not going to start going to more check ups just so they know who I am - they have to many people to deal with to have time for that.
As for knowing about diabetes, they have no need to know more than diagnosis for type 1 because after that care is handed over to a specialist. I believe the relationship is different with type 2.
I lived in Australia for two and a half years (before I had diabetes) and the relationship with GPs seemed to be similar. The only time I saw one was when I had a viral type flu thing and needed a sick note for my employer.
But how often are checks like BP and women or man health checks done if you do not see youyr GP?? The prescriber has responsibility to ensure what is prescribed is being taken etc. Insulin affects more than what endos look at !!! What is the world coming too!!!
But, But. But a prescriber is responsible for ensuring that all is well regrading that prescriptoin and others. In Oz a script with repeats lasts 6 months so that a review is required. That may seem excessive but for a BP medication there may be a need to change dose, to check of side-effects some of which as only detected on blood testing, there may be yearly checks for screening etc. Do dentists hand out lollies and never check teeth??
That a person can arbitrarily obtain insulin, a potentially deadly substance to the person , AND To Others, without a script is nuts. It degrades the NHS system to the low third world conditions of the US system. And how does that prevent waste??I haven't been taking meds on repeat for 12 months yet, but as far as I can tell from the systems messaging, my repeat is done in a 12 month trache. Obviously 12 scripts aren't signed off, but I imagine the countdown would be to some form of review/chat or whatever.
As I am currently still titrating and e-consultations are still bouncing back and forth between GP and Endo, the 12 month gate shifts with each treatment adjustment .
Things like mamography, smear tests, eye screening and so on are handled remotely, with appointments being generated from a centralised point, for services executed remotely to the surgery, or a letter is sent requiring the patient to make their appointment.
As far as dental services are concerned, if a patient is referred for specialist care (the probably most frequent of which would be adolescents for fixed orthodontic care), the specialist deals with their specialist referral, but the patient still needs to have their routine check-ups at the referring durgery.
Systems differ over the world.
Where I am right now, I can walk into a pharmacy and buy thyroid meds, inclusing liothyronine and insulin over the counter, just at my request. For the record I haven't.
I can recall a T2 member (but can't recall his name, and wouldn't name him anyway), a while ago, who had rocked up and bought himself some fast acting insulin, so that he could have carby meals as and when he chose to without, in his view, harming himself.
I have been interested to find a reliable source of T3, should it eventually be required, as it is rarely available on the NHS these days, due to cost. The NHS pays c£300 for 30 tablets, wherease I can buy 100 tablets of 100mcgr, including worldwide shipping for £47 from here.
Whilst no system is ideal, what is clear is patients need to be engaged with their own health wherever they are in the world.
That a person can arbitrarily obtain insulin, a potentially deadly substance to the person , AND To Others, without a script is nuts. It degrades the NHS system to the low third world conditions of the US system. And how does that prevent waste??
Yet others complain that if they use up insulin more quickly for legit reasons that they have trouble obtaining it ??
And with T3 and some insulins does not the NHS have the purchasing power to not be ripped off by Big Pharma? Or is the effect of splitting the NHS up into smaller units allowed this to happen ?
There is either corruption in the system itself or between NHS and Big Pharma !!
Some much for rights of equal access !!
HI @DCUKMod, Thank you for clarifying about scripts and location. I agree that the medical bureaucracy and NHS are a nightmare where lack of commonsense and understanding have evolved. Some parts of Australia are I contend heading towards this type bureaucratic decision-making by at least one Medical Colleges with ludicrous research findings used to back its recommendations and theGovernment lamely following on.To be clear, Kitedoc, I am currently in SE Asia, hence the ability to rock up to a pharmacy counter and buy those meds, if I chose to.
Well, one would have hoped that all those thousands of folks with thyroid glands unable to efficiently convert their T4 to T3 would be supported, it's just not the case, with thousands being declined or having their NHS prescritions stopped, with sometimes immediate effect.
I know of a number of people buying T3 from overseas, for c10% of the UK costs. That is a 100% sad reality.
To date, my thyroid is simply not catching on with the programmes, so I'm a bit unclear where I'll eventually end up in the meds lottery, but if I need something, I am resolute I will source it. My health and wellbeing is very important to me.
HI @DCUKMod, Thank you for clarifying about scripts and location. I agree that the medical bureaucracy and NHS are a nightmare where lack of commonsense and understanding have evolved. Some parts of Australia are I contend heading towards this type bureaucratic decision-making by at least one Medical Colleges with ludicrous research findings used to back its recommendations and theGovernment lamely following on.
Where are the appeals processes and the specialists who will argue for the proper medical knowledge and understanding?
I also contend it is easier if the bureaucracy sidelines General Practice and takes away its experience and learning base.
But then we have Dr Unwin. So how is he so effective where other GPs do not appear to be??
Sorry I only just saw your post, sorry I don't usually use forums or anything. It does go in, honestly I do listen to everyone's experiences and storys but it's just hard for me, I can't even explain it.Hi @Bladezy I think this has a lot to do with glucose tolerance. In my late teens my glucose tolerance (i.e. how high my blood sugar levels could reach before feeling unwell) was very high - nobody talked about HbA1c then. But if it sharply increased I would get very bad ketones, which would blurr my sight, make me nauseous, or even sick, give me appalling diarrhoea and lock my muscles up. Once I had been read the riot act, at the age of 21, and been lent a glucometer like a housebrick, my glucose tolerance went down to a point where I had the same symptoms as above, sometimes even if my blood sugar was only just over 10mml/ml. All I can say is that the longer your tolerance level is high, the more damage will occur to the extremes of your circulatory system, that is, eyes, feet, kidneys and private member's bill. Nobody can force you to do this, but my life would have been very different had I not ignored advice in my childhood and teens. Good luck with tackling this.
Really don't worry. If you get anything out of these posts that's all that matters. Hope life improves for you.Sorry I only just saw your post, sorry I don't usually use forums or anything. It does go in, honestly I do listen to everyone's experiences and storys but it's just hard for me, I can't even explain it.
@Kevvb1 I had pretty much the same experience when I was diagnosed, I was 21 and told take this and this and off you go. Since then Iv had minimal contact with docs/nurses. I just order my insulin when iv nearly ran out but that about it. Thats the way it's been for the last 10 years. I'm lucky in a way because my little brother is also type 1, but he has had it since he was about 8, so I knew a fair bit before hand.
@DCUKMod thank you that is a great idea, I will give it a try.
@BeccyB yeah iv been on a few different antidepressants and that but not anything that iv got along with. Tbh it's something iv lived with for about the last 12 - 15 years. It's does make things a bit awkward because I struggle to talk to people face to face, and I barely leave the house, it's hard to get anything sorted out with anyone when I get like that. Yes I will take DCUK's advice and try to write a letter and try and get some things sorted
No not at all, it's nice to know other people have had similar experiences and have made it through and also want to help others to reach the same place. I'd feel rude not coming back after you guys were nice enough to reply.I understand, I suffer with anxiety too and think there's quite a few forum members who do too. It's mostly under control for me now but I have had several 'hermit' episodes. My worst was about 2 years ago and in the end hypnotherapy worked for me - I was SO skeptical but a friend suggested it and I was pretty desperate so tried it. 3 sessions and I was back at work and socialising properly again! I've also found Mindfulness helps, try the Headspace app - the basics are free so definitely worth trying
Also, put in your letter to your GP that you are struggling with your anxiety/leaving the house and ask if there are any online resources you can access, I know my local area has a site you can get access to if you're registered with a local GP. There may also be telephone counselling available, maybe with a waiting list but I think a lot of places are using it these days.
In terms of your diabetes - if you get an appointment with a hospital team and don't think you will be able to manage it give them a ring and explain. Hopefully they will be willing to arrange a phone appointment too. They may even have a mental health team attached to them as there is a lot more awareness of the interaction with diabetes these days
Sorry if I'm overloading you with stuff, or it seems like I'm nagging you, I just want to get anything that may be useful onto this thread for you and anyone else that may read it. I'm glad you are popping back here occasionally, as @Grant_Vicat said if you get anything out of these posts then it's great.
I don't understand either to be honest, that's why I came on here originally to ask about dka. As I assumed that something must be up as I didn't ever get ill like my brother.I don't understand how being Type 1 for over 10 years you can go a week without taking any short, or long acting insulin? I also don't understand how after that time you have never heard the term DSN?
As for currently not being concerned around complications enough to make any real effort around control, I can only hope you come to realise the potential serious consequences of living this way before any real lasting damage occurs. I and many others have lived periods of our lives in denial, but sadly when things do eventually start to go wrong it can often be too late to undo the damage done. Only then do you look back and regret the way you lived with the condition.
Please don't ignore the experiences of others. Don't think that because you can live this way today, tomorrow or the future doesn't matter. If things do go wrong it will only come back on one person, and that's you. You owe it to yourself to avoid that.
I've learnt you can ignore this condition all you want but sadly it's never going away and if continually ignored, which is very easy to do, has the potential for some very serious consequences Indeed.
Honestly, if you can go a week without insulin after ten years as a T1 I'd be skeptical about the original diagnosis.I don't understand either to be honest, that's why I came on here originally to ask about dka. As I assumed that something must be up as I didn't ever get ill like my brother.
Aha well I'm deffo type 1, I can guarantee if I tested my glucose levels they'll be super high. I can tell when they're up or down. My mate always tells me I'm not a real diabetic as i don't crumple at the sight of a chocolate bar lol. After a day or two I get weak and quite thirsty but as long as I keep hydrated I don't feel too bad, but now I think about it maybe I'm just too used to it and don't notice, I'm not really sureHonestly, if you can go a week without insulin after ten years as a T1 I'd be skeptical about the original diagnosis.
Aha well I'm deffo type 1, I can guarantee if I tested my glucose levels they'll be super high. I can tell when they're up or down. My mate always tells me I'm not a real diabetic as i don't crumple at the sight of a chocolate bar lol. After a day or two I get weak and quite thirsty but as long as I keep hydrated I don't feel too bad, but now I think about it maybe I'm just too used to it and don't notice, I'm not really sure
Aha well I'm deffo type 1, I can guarantee if I tested my glucose levels they'll be super high. I can tell when they're up or down. My mate always tells me I'm not a real diabetic as i don't crumple at the sight of a chocolate bar lol. After a day or two I get weak and quite thirsty but as long as I keep hydrated I don't feel too bad, but now I think about it maybe I'm just too used to it and don't notice, I'm not really sure
MODY? I'll have a Google for that ahaYou know, I'm still wondering about that. Is there a possibility you can be MODY? They don't always need insulin, and as it's rare many get initially misdiagnosed as T1 or T2.
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