Sorry, my comment appears to be confusing you. I meant where did Deb learn about different approaches.
(I wrote 'the lady' rather than write 'she'.)
Not only here on DCUK and on Twitter (and probably on FB, I am not a fan of FB but I bet Deb is going on there shouting loud and clear that there is another way) but In Real Life. I have to take my hat off to the lass.Sure @Debandez
will be along soon.
the lady has written on here, the the Forum was her guiding light.
Like many distressed at news once Diagnosed...
she had a very personal reason and was invested day one, so i believe
took the fight on,.T2d V Debs..
And she is WINNING...
It helps to be proactive. At my last check they didn’t call me, I called them, but I sense at my local surgerie(s), things are improving - I am beginning to find this stuff out via PPG connections.In England (and maybe the rest of the UK) people aged 40 and above are supposed to be called in for a health check that includes the usual raft of blood tests. The exceptions to this are those with existing illnesses who already have regular checks. Those where a problem is discovered are treated accordingly. Those without problems are given repeat checks every 3 or 5 years depending on circumstances. This is what happens at my surgery. My healthy daughter and her husband were invited once they had passed the age of 40. Their tests included an HbA1c. They have recently been called again for a 5 year check, and this also included an HbA1c.
I don't know if all surgeries do this, but it was an NHS recommendation several years ago, and of course I have no idea if everyone takes up the invitation. I very much doubt it.
Not only here on DCUK and on Twitter (and probably on FB, I am not a fan of FB but I bet Deb is going on there shouting loud and clear that there is another way) but In Real Life. I have to take my hat off to the lass.
It helps to be proactive. At my last check they didn’t call me, I called them, but I sense at my local surgerie(s), things are improving - I am beginning to find this stuff out via PPG connections.
Oh I am if I need something. I get my results online and advocate for myself. Leaving messages is very hit and miss too.It helps to be proactive. At my last check they didn’t call me, I called them, but I sense at my local surgerie(s), things are improving - I am beginning to find this stuff out via PPG connections.
We all need to get round there then.Our practice is excellent for being proactive. It is easy for them because it is a large practice with half a dozen partners, half a dozen associates, several practice nurses, maternity clinic, other specialist clinics, a blood clinic. a treatment room with a theatre for minor ops that GPs can do and a new community hospital that they also run, with CT scanners, X-Ray stuff, physiotherapy unit, in patient wards, outpatient departments where consultants hold appointments, and goodness knows what else. We are very spoilt here.
Way to go! Well done.I saw my GP when I was initially diagnosed followed by diabetic nurse who prescribed statins and a dietician who gave me leaflets and the eatwell plate guidance - lucky for me I found this forum before any real damage was done. I have an hba1c test every 6-9 months followed by a diabetic review - however I’m struggling to get one at the moment due to no appointments being available but I had my hba1c test the other day and, at 37, it is still in the non-diabetic range so I’m not too concerned!
Thanks xxWay to go! Well done.
Posted my journey. All my notes (I can only apologise!) I didnt learn really, just need things to change so my passion for that is carrying me along. I saw my mum suffer. She became registered blind, sores on legs that wouldnt heal. Numb fingers and feet. Kidney issues. Stroke. Uncontrolled bs. They just kept upping her insulin! I know now that isnt the solution. How many more have suffered needlessly and even lost their lives. Hospital food for diabetics is an absolute joke. Guidelines are worse. Look at what the low fat advice has caused. Over 50 different names for sugar stuffed in practically everything we eat. Medication offered before diet advice. Statins as well as metformin I was offered. Few tweaks to my way of eating and hba1c levels plummeted. Not everyone will want to do it but everyone should be given the choice.Sorry, my comment appears to be confusing you. I meant where did Deb learn about different approaches.
(I wrote 'the lady' rather than write 'she'.)
And you discovered this approach where?Posted my journey. All my notes (I can only apologise!) I didnt learn really, just need things to change so my passion for that is carrying me along. I saw my mum suffer. She became registered blind, sores on legs that wouldnt heal. Numb fingers and feet. Kidney issues. Stroke. Uncontrolled bs. They just kept upping her insulin! I know now that isnt the solution. How many more have suffered needlessly and even lost their lives. Hospital food for diabetics is an absolute joke. Guidelines are worse. Look at what the low fat advice has caused. Over 50 different names for sugar stuffed in practically everything we eat. Medication offered before diet advice. Statins as well as metformin I was offered. Few tweaks to my way of eating and hba1c levels plummeted. Not everyone will want to do it but everyone should be given the choice.
Never seen a GP about Diabetes.
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