Hello
@Pipp and
@EllieM . Thanks for the replies.
Sorry. I probably should have clarified—I’m not looking for a diagnosis here. I am aware of the site rules. Though, if anybody does have experiences with neuropathic itching and have experienced similar symptoms to me, I welcome you to share them if you’re comfortable.
I guess what I’m looking for is advice on who it’s best to speak with out of the GP and the DSN and how I can get either one to take me seriously. I don’t have anybody in my daily life whom I can talk to about my diabetes outside of medical professionals, so I’m mostly dealing with these situations by myself. So, forgive me if I’m rambling with my thoughts.
I think what’s getting me concerned about this itching is how strange it is. Because of how conflicting my symptoms feel, it doesn’t seem like it quite fits into either criteria to be classed as one thing or the other. I’ve had eczema itching before. I developed it long before I was diagnosed with diabetes due to it running in my family. But back then, it was restricted to certain areas of my body and showed visible skin irritation. Additionally, since this itching started four months ago, I sometimes think I might have been fleetingly feeling things like slight pain or tingling or crawling on my body. So, it’s making me question myself a lot. Especially because my itching does not improve with my blood sugar levels. It seems unaffected regardless of how high or low they are, which I don’t know if that’s a good thing or a bad thing.
Logically, I feel I need to speak to the DSN about my symptoms. They are specialised in diabetes and I think they would take me more seriously than my GP. Then again, that’s exactly what I thought when I spoke with the diabetic consultant and they basically went ‘Sorry, we can’t help with this. Go to your GP.’ I’m worried the DSNs might say the same, even despite having my diabetes history on record.
On the other hand, my GP don’t have my full diabetes history (even though they should; I’ve chased this up with them and the hospital with little success in the past) and despite expressing my concerns about my diabetes control, they don’t seem worried about it. Furthermore, they keep citing my most recent blood test as the reason why they think I’m fine. Though, as far as I’m aware, a full blood count isn’t a reliable detector for nerve damage. I think there’s a specific test for it that I need to have, so I fear they might be making judgements based on the wrong test. I’m also worried that if I try to go back to them before finishing their treatment plan, they might not take me seriously because I haven’t followed it through. I’m trying to be as honest and as transparent about my symptoms as I can be so they have all the information, yet I feel this is backfiring on me.
Is it worth speaking to the DSN first and seeing what they have to say? Does anybody know if they could help me and potentially refer me to whoever I need to see to check for neuropathy? Or am I going to have to go through my GP instead?