yeh I must've gone real lowI tend to take a lot longer to recover from those night ones I miss.
As you get more sensitive and aware of hypos, the body does take its time getting the fug out of your head, and it usually would take a good night's sleep to get back to normal.
I have had so many memory lapses in work and at home and doing the chores, shopping etc. I think it so hard to remember what you have forgotten.
Or is it the other way around?
That you have forgotten to remember?
I don't know!
It will come back to me!
Yeh it's definitely my brain that is the last to recover. It is pretty hard to describe to someone what it feels like as it isn't just the exhausted feeling... it's more like my brain has been zapped. Of course I know it has been zapped literally of glucose and it's recovering. A bit like a flat battery I suppose. But it is definitely nothing I ever felt prior to diabetes and having hypos... so really people wouldn't have a clue what it's like unless they've had a hypo. Although on saying that my epilepsy friend describes how she feels after a seizure and it is very similar to how I am after a hypo. But of course epilepsy seizures are caused by imbalances in the brain.
Sorry to read about your experience this morning. Hope you are feeling better now (or asap).
From what you have described it sounds very similar to what I've heard termed 'fibro fog'. When the fibromyalgia affects the brain function we can do literally anything, and forget anything! Yesterday I was looking at a sign that said contactless payments under £30 and then asked about apple pay on a purchase that was over £150 (just one of the silly (and potentially less problematic) things fibromyalgia has made me do!). Although I've done things such as you describe, forgotten to lock my car at times and the list is endless.
Yes, I've heard about the fibro fog. I guess this is similar to that. I've been asked if I have fibro before but I don't think I do. The reason is apparently I have conditions that are linked to it (ic, migraines, pcos). I do get pain throughout my body but it's only really been like that since being on meds so I figure it's my meds doing it. I'm on baclofen which weakens my muscles. I'm on amitriptyline which one of the side effects it gives me is nerve pain under the skin and it can shoot pain anywhere at any time all over my body... sometimes in quite a few places. I know it's the drug as when they took me off it that symptom stopped. When they put me back on it, it started again. So yeh it's hard to figure things out once you get diagnosed with a few things. Is it a new condition or just meds? Usually 9/10 just the meds.
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