An epidemic is sweeping the nation and world: diabetes. Almost 26 million children and adults in the United States — and 346 million worldwide — have the disease. Another 79 million Americans are considered to have pre-diabetes.
Now, thanks to a generous $1.5 million gift from a member of the Diabetes Center Leadership Council who has a child with diabetes, UCSF will be among the first in the country to educate and train nurses specifically to care for diabetes patients across their lifespan by establishing a new academic minor in diabetes at the UCSF School of Nursing.
What do you think about this? Are you pleased or frustrated with efforts to educate healthcare professionals with competencies in diabetes.
As a nurse I received a pretty good education regarding diabetes. Problem is, they only taught me about Type 2 Diabetes. I'm thinking this minor in diabetes will also be about type 2 dabetes.
The link leading to the UCSF article mentions teaching both Type1 & Type2 in children and adults. It sounds really great and progressive to me.
The link to the UCSF website indicates that this education will cover both Type 1 and Type 2, pediatric and adults. I think this is great. While I think that much more is needed overall, this is definitely a step in the right direction.
As the stories in another current thread on the TuDiabetes site show, the ignorance of diabetes and related technology is all too common among doctors, nurses, and other medical professionals.
By in large, quite annoyed by the diabetes education most "white coats" receive. Nothing is devoted to the mental health component, the psychological issues which our chronic care demands.
Every little bit helps, so this sounds like a start. I contend their education should contain a panel of diabetics to present and explore ideas about the many treatments they wish to provide for us. Questions from the audience for the panel and the reverse as well.
I also propose that there should be another layer/level of the education process, a subset specifically for and using experienced diabetics. As a community we can be invaluable help to our peers, if it were encouraged more. IMHO...
The criteria in Canada :
"HOW TO BECOME A CERTIFIED DIABETES EDUCATOR
The examination Handbook contains the necessary information you may require and should answer your questions regarding eligibility and process. You will find the application form there. Please refer to the Examination Handbook and the FAQ's online prior to submitting questions to the office."
From this Patient Point of View : there are Fantastic!!,less Fantastic and even less Fantastic CDE's no matter who are the Leaders Teaching ...we have to have Hope to get the BEST and also express what we are in need off .I have had the best Insulin Pump Nurse CDE since I started pumping in 2001 ...she is about to retire :(
It's great that there will be more specific education provided for the nurse preparing for her masters. As a nurse myself, I have always seen the lack of diabetes education at the bedside level, and have often thought that with the epidemic numbers we have why don't states mandate specific CEU's required yearly like they do for HIV/AIDS, domestic violence, etc...Of course where I live now, in Maine, there are NO state required CEu's needed for licensure.
I've read news stories, etc. that there's a significant demand for nurses so it seems unlikely that the powers-that-be will make nursing more challenging or implement any sort of new paradigm to make our lives easier. I sort of have the impression, just from my own medical experiences, that they are following the "manual" closely.
In many cases, perhaps the volume of patients may contribute to pushing nurses, doctors and other medical providers, however "nice" they may be personally (and not all of them are...) to adopt a "you do this..." approach that is patently absurd with patients like us, who have to run our own shows since there's rarely useful medical support available except at appointments or via channels, email, txting or whatever, that may or may not provide the sort of "Jack Bauer", real-time solutions that PWD come up with on our own, 40 or 50 (at least!) times per day.
The network I go to has been pretty much useful and given me my space. The surgery was interesting but the surgical team were 100% on board with leaving the pump on and pretty much letting me do what I wanted with it. I dunno what would have happened if it had started bleeping at them 1/2 way through the procedure if my BG went the wrong way but, as it turned out, it was very smooth sailing.