Definitely brain fogged today. I got up and put on my house coat/dressing gown/whatever, something I have done almost every day for years. Today I stood there for a while trying to figure out whether to wrap left over right or right over left. That has to be brain fog because the alternative doesn’t bear thinking about.
Next task: shower and deal with the fog that invariably goes with it - and I don’t mean the condensation on the windows.
That is a perfect example of brain fog. It’s like where your brain just will not make the appropriate connections, even when doing something you do every day.
Don’t worry too much about it, it’s not likely to herald serious permanent cognitive dysfunction, in all likelihood you’ll get up tomorrow and automatically do it up the right way.
Its just a little alarm bell that tells you something’s not quite right.
If it happens often, or if you get really worried about your cognition, ask for a referral to a neuro-psychologist. I had an assessment earlier this year (referred by my neurologist), basically she said my on/off haphazard thinking was typical of the MS brain, basically a slowing down of the cognitive functions. It will probably deteriorate gently over time (like everything else) but isn’t something that’s going to send me (any more) doolally in the short term.
Bought my son and his girlfriend socks, forgot mine! Yes, fluffy socks on my Christmas request list and what does everyone expect off me every year = socks.
I saw my MS nurse this morning. Partly it was my annual visit, but mostly it was to discuss my PIP award and sort out the medical evidence to support my request for Mandatory Reconsideration. When she read that I had ‘no memory or cognitive impairment’ she said that she doesn’t have any patients who don’t have such impairment. It’s not something that I worry about, it’s just something that sneaks up and gives me a prod from time to time, just to stop me getting complacent.
Actually, mental health was something we discussed at length. My appointments with my neuro and my MS nurse have always focused on the physical side of MS, probably because that’s where my symptoms have been most obvious. The PIP application and award have forced me to look at how I’ve been affected mentally - cognitive issues, anxiety, adverse reactions to stress or stressful situations, loss of confidence…
Today I had no problems with my dressing gown. I just didn’t recognise my phone’s ringer when hubby rang to check when I’d be finished with my MS nurse.
AD, your avatar does look like someone on whom it is starting to dawn that the re-run of ‘The Simpsons’ that he thought he was watching is, in fact, the US Presidential Election.
Time to take your mind off Grandpa’s socks cocks and loo’s with a view.
Lets think of something more topical. Do you think they will ever add a rock carving of Donald Trump - amongst the other US presidents on Mount Rushmore - Black Hills National Forest - South Dakota. He will insist on it being gold-plated.