her own diabetes blog where she writes about everyday things and how they relate to diabetes.
Here, Jane shares 3 things she’s learned from her patients with diabetes:
- Every person with diabetes is unique. Unfortunately, due to time constraints, budgets, and the need to be as efficient as possible, health care has become very standardized, which can lessen the ability to offer more individualized care.”In my diabetes education practice, I’m very fortunate to have 60 minutes to meet with each patient — which is a lot compared to what some health care providers have. The remaining challenge, though, is how many times I get to meet with that patient and follow-up, either because they’re too busy or their insurance won’t pay for more than one visit in a certain amount of time.”
- There are common threads for everyone with diabetes. People clearly benefit from being part of a community. There is a fine line, she says, between keeping within the structure of the standardized system and making sure the patients gets specifically what they need and want in their appointment.”Gradually, I see my patients getting more active online. Locally, I don’t see people getting involved in diabetes-related groups, but I am noticing patients finding support and encouragement from other people with diabetes in online communities. Having a connection makes a tremendous difference. I have noticed there seems to be more online interactions with type 1 patients than those with type 2, but that is gradually changing, and I am referring more and more of my patients to online communities.”
- It’s not about me! Jane’s strongest focus when communicating with her patients is to inform, motivate and support them, rather than lecture or tell them what to do.”I’ve heard health care professionals say, ‘I got my patient to do this,’ and ‘I got my patient to do that.’ It’s not about me or your physician, and what I ‘convinced’ you to do as my patient. It’s about what they do in their life. I’m here to facilitate my patients’ progress, and educate them. I am not trying to convince or force or sway someone to do something.”
Stay tuned for more articles and interviews with Jane over the next few months! Do you have questions or articles from the perspective of a CDE living with diabetes that you’d like to read? Post your comments and suggestions here and we’ll be sure to consider them!
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Australian JDRF-funded researchers have discovered two particular proteins are essential in the development of autoimmune diseases including type 1 diabetes.
The study found that the absence of these two proteins, called Bim and Puma, led to an accumulation of ‘self-reactive’ immune cells that attacked different organs of the body. In healthy individuals, the body protects itself from autoimmune disease by forcing these self-reactive immune cells to die or become inactive.
This study, published by Professor Andreas Strasser and his colleagues at the Walter and Eliza Hall Institute of Medical Research, showed that the death of self-reactive immune cells was an important component of protecting the body against autoimmune disease.
The results of this study could impact not only the direction of type 1 diabetes prevention research, but also research into other autoimmune diseases. Future research can target these proteins to investigate the potential for preventing the onset of type 1 diabetes. This research will also pave the way to further understand the root causes of autoimmune diseases.
To support similar research studies into type 1 diabetes, please donate at www.jdrf.org.au/giving.
Its great that research like this is making small steps