I am totally confused though as to why this should be a fight! From what I have read and now experienced first-hand, I am increasingly convinced that some Doctor’s seem to have a negative mind-set towards T2 patients. I think they believe we have largely brought this upon ourselves, are an unnecessary drain on NHS resources and should just shut-up and take the meds they prescribe. It sounds as if many have not updated their knowledge or thinking on the subject since they left training decades ago. And then we have the system itself unwilling or unable to change the advice they are offering. Thankfully though, I know that is not true of all doctors. Up to that point, I have had nothing but good support and sensible advice.
Yes that's the impression I have had from some of my GP's too. It's very demoralising at times.
Can't wait for your next set of results though.
Oh dear, our sympathies. You got one of "them".
Same here Guys.Agree with you all! The GP,s treat people as if they are "rabid dogs" and need to be put down! After 5 months of aches and pains,she finally sent me for a blood test,which proved to be diabetes type 2!
I suffer with a mental illness too,Combat PTSD after serving in Iraq War,and take many meds.The doc thought all my symptoms were related to the PTSD! When clearly,now It wasnt! Waste of time are the Docs.
Just finished my GP appointment today to follow up on the results ... I left feeling probably the worst I have felt since my diagnosis. I have worked very hard in the last 2 months. I am a pretty resilient person (I like to think) but I walked out thinking what’s the point.
Know what you mean.<snip>
My PHQ-9 was nearly off the scale as was the GAD-7... so basically severe depression and anxiety.........
<snip>
Gosh it does frustrate me when I read stories such as yours @Klangley
I am a nurse specialist - not in diabetes I hasten to add! - and if I heard another health professional talking to a patient that way, I would be taking them to one side for a SERIOUS talking to!
I work with patients with an incurable disease called Myeloma - a cancer of the plasma cells. And never for a moment would I dream of dismissing any positive progress they made, or being anything other than positive about their future. Sometime I have patients who choose not to have treatment. In those instances we make sure that they are fully aware of the treatment options available to them, but if they choose not to proceed, we SUPPORT them fully in their decision. Caring for patients HAS to be a holistic approach, not a prescriptive one. My patients often know as much (if not more) about their disease than I do - and any health professional worth their salary will use this expertise! I have learned a lot over the years, and continue to learn things from my patients.
So, let me make this absolutely clear, the way you felt when you left that GP surgery is a reflection on the Doctors POOR practice and in no way a reflection on you.
You have done fantastically well in reducing your HbA1c - I hope mine shows such a great improvement when I have my first test since diagnosis next month.
As for the medication issues - their role is to give you the facts and help you decide if it's right for you.
Quite frankly she's simply showing her ignorance in her inability to give you a satisfactory explanation.
Whatever you are doing is working well for you - keep up the good work xxxx
From a personal point of view, I would check the practice website, see if there is a go who has an interest in Diabetes and INSIST that you get an appointment with them, it really does help if the doctor has an interest in the subject, I know it helped me when I was first diagnosed.
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