MoonSpirit
Well-Known Member
- Messages
- 70
- Type of diabetes
- Type 1
- Treatment type
- Insulin
If you get the opportunity, move to somewhare like Spain.Unbelievable!
My husband thinks I must be hypo or something as I did laugh out loud when I read this----so, so funny!!!!!I was 13 when diagnosed in 1981 and I was admitted to hospital and was in there for 2 weeks being stabilised.
I was due to be discharged awaiting a final meeting with a Dr and when he came with his "entourage" this brief but ridiculous interaction took place
(This is what I remember!)
Dr - So then Bernard, we were going to discharge you today but we are going to keep you in for a few more days as we are not happy with your sugar levels.
Me - I'm not Bernard
Dr - Sorry !
Me - I'm not Bernard
Dr - Who are you ?
Me - I'm Kevin
Dr - Your not Bernard Fitzpatrick !
Me - No I'm Kevin Fitzgerald
Dr - Your notes say your Bernard Fitzpatrick
Me - I'm not Bernard Fitzpatrick I'm Kevin Fitzgerald
Dr - Nurse can you confirm this
Nurse - Yes this is Kevin Fitzgerald
Dr - I think I've got the wrong notes !
But so funny--this would make an ideal scenario for a comedy......!!!!Well from what I remember of Bernard his family kept visiting him in hospital and bringing him mars bars and coco cola and he was eating and drinking this stuff. The nurses were always having a go at his family trying their best to explain that they mustn't do this (they just didn't get it!)
He was in there long before I was even admitted and he was discharged a couple of days prior to my conversation with the consultant. It seems he may have been discharged as they thought he was me and I was in hospital longer than I should have been as thought I was him !
Scary !
I had similar at aged 8--mum took me backwards and forwards to GP. His diagnosis: that my mother should feed me!! I was only 2 stone and was hungry and ate all the time. No wee test was offered & my mum had no idea what was wrong--which is why we kept on visiting the GP. Eventually school got school doctor to give me a medical as they were very worried about me. I was admitted to hospital within 24 hours after seeing her. GP got into trouble and it turned out that he didn't believe that children got ill. Apparently I would have been dead in another 2 weeks were it not for the school doctor. (type 1 now for 54 years and thriving)!!!Believe it or not, when I was initially unwell at the age of 8, I was drastically losing weight and vommiting. My Mum took me to see a GP who said it was an 'ear infection'. My Mum forced the GP to take a urine sample which was sent away for testing.
Lets just say, I think id rather it was an ear infection over type 1, but how on Earth do you get mixed up over those 2 illnesses? Ha!! Always laughed at that one.
Last time I had retinopathy check was odd. Dr told me he could see retinopathy in my eyes but not to worry because it had healed. I have had these checks for very many years now (I took part in the research for the cameras now used, way back in the eighties too) and not once has retinopathy been diagnosed. Obviously I have never had laser treatment either so no "healing" has ever taken place or could my body have healed retinopathy and then no doc ever picked it up? I said nothing--I have had 54 years of stupid remarks--BUT then it got worse. Doc said I had thinning of the optic nerve in my left eye and that I must have noticed considerable worsening of my eye sight. I assured him that my eyesight had not changed at all and that the nurse, prior to consultation, had remarked on how well I did on eye test. He told me he wanted to see me soon for further tests with regard to optic nerve and then remarked that my eyesight must make it very difficult to carry out my job !!!! When I saw DSN she told me retinopathy check report stated "no retinopathy" and there was no mention re optic nerve either--could this have been a Kevin/ Bernard scenario, I wonder?Nurse at the retinopathy clinic after I'd just received the first letter ever saying I had background retinopathy in one eye looking through machine at my eyes.
Nurse: I can see your diabetes has been very bad
Me: My control is good (hba1c turned out to be 6.2 but I didn't know this at the time). Are you going to give me more details about the letter I've received about background retinopathy?
Nurse: You will receive another letter.
(I go to sob in the toilets)
Finally see consultant 6 months later.
Consultant looks at eyes then looks at me and notices I'm wearing glasses.
Consultant: What's your prescription
Me: -8 and -6
Him: and do you have astigmatism?
Me: Yes
Him: That's what came up on the scan you don't have any retinopathy.
I assume she was that rude because I am about 40 years younger than most who attend that clinic because I have type 1 and have had diabetes for considerably longer than most of them too.
Next misdiagnosis. Thoroughly cheerful scanner "yes you've definitely got retinopathy, I'll send these off and if they disagree they'll have an aribtration (I'm a lawyer and my mind starts going through the usual arbitration routes I use and thinking they don't apply) but I'll be right. Then hands me a booklet from RNIB which I interpret to mean I'll be blind by the time I'm 35 (30 at the time) will lose the right to drive (having only passed a year before and started to really enjoy driving). Get very depressed.
Get seen by a doctor in eye hospital about 6 months later. She looks at my eyes and says:
It's just a strong retinal reflex. Sometimes they come up funny on the pictures. There's no retinopathy.
Since those 2 experience I now don't believe a word any scanner or nurse says about my eyes.
My parents were told the 10 year cure thing when I was diagnosed in 1983..... When my friend's brother was diagnosed in 1997 she said to me "it's ok they've said there'll be a cure in 10 years". I didn't have the heart to point out they were already 4 years over on that estimate with me. Whenever I see chuggers at stations trying to raise money for cures for diabetes usually with claims of 10 years I get very very angry and have to give them a wide berth to prevent launching into a diatribe that this is a big lie. IMHO I'm not sure there ever will be a cure because diabetes medication has become such big business it's not in the drug companies' interest to have one. That's my cynical view after 32 years of type 1.
Silly things said by docs, nurses, dietician:
GP: You became hypo after eating a slice of cake because your body produced extra insulin as a result (type 1 for 54 years & obviously on insulin for 54 years--maybe if I ate high cho, sugary foods etc all the time I would be cured because it would stimulate my pancreas into producing insulin) !!!!!????--job done--it would save the NHS a fortune).
DSN: What would you prefer next time HBA1C or glucose tolerance test (I bet the latter is cheaper--never mind its lack of appropriateness)!!!!!!!!!
DIETICIAN: Do you know how much cho is in a slice of bread? ME: 2/3 oz = 10g cho DIETICIAN: 10g = what? (turned out she thought I was talking about 10g weight in spite of specifity of my answer--obviously not listening, was she)? There followed a long protracted conversation in an effort to establish facts. DIETICIAN: How many grams (weight) is in 2/3 oz of bread? ME: Look it up (had had enough by that time)!! DIETICIAN: Do you do any exercise? ME: I teach GCSE & A Level dance in a school so every day I do warm ups and practical dance exercises with each of 6 classes, that is at least 30 hours a week of exercise. END OF INTERVIEW !!!!
NURSE: (Who was a chunky monkey) you have put on weight (1/2 kilo in 3 months which made me 58 1/2 kilos)---there then followed a lecture on what I should do to lose the excessive weight!!!!!!!
CONSULTANT: I know about clinical aspects of diabetes--you only know how to manage it (thought that was my responsibility--he shouted that out too--I obviously irritated him....)!!!!
CONSULTANT: Oh dear what are you eating? Lets have a look at your HBA1C shall we? (his face fell as it was within the normal range--we moved on to another aspect of diabetes!!) I take animal insulin so eat 20g cho mid morning and afternoon otherwise hypos occur)
GP: No point bringing in a wee sample as it will be full of sugar--as I handed him a bottle--he tested it anyway--it was NAD- (
EVERY DOC/ NURSE etc: you will of course pick up infections far more easily because of high blood sugars. ME: No MEDIC: When were you last off work because of illness? ME: 10 years ago MEDIC: in hospital because of diabetes? ME: Never
GP: You have metabolic syndrome ME: I always understood that I had an auto immune disorder
CONSULTANT: CGMs are only used for diagnostic purposes and are not useful for any other purpose (did he know what they were,, I now wonder)
CONSULTANT: if you think either of your children is developing diabetes just bring them here for a test and we'll have second generation diabetics (whoopee woo) ME: With type 1 there is only a 0.1% of offspring developing diabetes (both mine ended up with chronic fatigue syndrome--which both can manage-- as a result of the same virus that can cause IDD so they obviously inherited susceptibility to developing the virus as well as an adverse reaction to it). If the father is IDD the % goes up substantially and with type 2 a person would be lucky not to develop diabetes.
MEDICS: Of course both your babies will have been big because of diabetes ME: Both were born naturally; the 1st was 7lbs and the 2nd was 6lbs 6 ozs. Neither was hypo at birth.
Most of these remarks are annoying because a) the medic hasn't listened to my answer to his/ her question b) their statements are presumptive with regard to my behaviour/ compliance (or lack of) without having read my notes or checked the validity of their own statements c) I swear that they make up what they say to make it seem as though they know what they are talking about (see point b).and d) most of these statements are not thought through so lack logic.
I get extremely annoyed now because (of my age supposedly) conversations about diabetes, with medics, are referred to as though I have type 2. So forthcoming statements and advice are irrelevant.
Why does no one ever ask how much insulin you take or how much cho you eat? Those used to be the opening questions every time you saw a doctor & can explain why sugar is lower or higher etc etc etc.
Because they now expect everyone to be using a basal bolus regime where this is considered to be much less of an issue. As a result, there is little point in answering, as someone might be eating 500g of sugar a day, taking 100u of insulin to cover it and have a normal Hba1C. In spite of this not being terribly clever.Why does no one ever ask how much insulin you take or how much cho you eat? Those used to be the opening questions every time you saw a doctor & can explain why sugar is lower or higher etc etc etc.
I had similar at aged 8--mum took me backwards and forwards to GP. His diagnosis: that my mother should feed me!! I was only 2 stone and was hungry and ate all the time. No wee test was offered & my mum had no idea what was wrong--which is why we kept on visiting the GP. Eventually school got school doctor to give me a medical as they were very worried about me. I was admitted to hospital within 24 hours after seeing her. GP got into trouble and it turned out that he didn't believe that children got ill. Apparently I would have been dead in another 2 weeks were it not for the school doctor. (type 1 now for 54 years and thriving)!!!
My mum took me to the GP after seeing me stand on tip toe at the age of 4 to drain the taps as so thirsty. She knew there was a family history of diabetes so took a urine sample along as well.I had similar at aged 8--mum took me backwards and forwards to GP. His diagnosis: that my mother should feed me!! I was only 2 stone and was hungry and ate all the time. No wee test was offered & my mum had no idea what was wrong--which is why we kept on visiting the GP. Eventually school got school doctor to give me a medical as they were very worried about me. I was admitted to hospital within 24 hours after seeing her. GP got into trouble and it turned out that he didn't believe that children got ill. Apparently I would have been dead in another 2 weeks were it not for the school doctor. (type 1 now for 54 years and thriving)!!!
Similar to the conversation that was had when I went in to hospital as a thirteen year old. On arrival, they took my bloods and the consultant said "How are you still conscious?"My most memorable (to me aged 15 and my Mum) when I was diagnosed at the GP surgery - 'I don't know how you got here today but you should be dead young lady'
I'm seen by the diabetes clinic at the hospital but also get my HBA1c done at my GP practice and I also have the same thing about paying for print outs that other people have reported. I don't mind paying, it's just the red tape if it all that annoys me.
This is how it goes for me: have my blood test, get a call a week later telling me the result is "normal". I ask for the exact number and get told only the doctor can tell me my number and usually get a lecture asking why I want to know because "if it's normal it's normal". I have to insist and then wait for a GP to call me (wasting both their time and my time) to tell me my number. Then when I go in for my next appointment and ask for a print out of my hba1c and my cholesterol results and I'm told it's £3.50. I say okay, don't worry then, I'll just write the results down (didn't have cash on me and they didn't take cards). She said no, you aren't allowed to write them down in case you don't understand them! So utterly nonsensical and ridiculous.
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