Symptoms – my mnd shuffle

Living with it.

For most, living with mnd is a short-term sufferer thing. Now don’t get me wrong… I am very pleased to be in the category of long-term.. it’s the sufferer part that bugs me. I think people forget what it must be like for those affected to do everyday tasks. Ever since I started to takeContinue reading “Living with it.”

Vlogging and fundraising.

So, some of you may have seen on my social media that I am looking to fundraise. The reasons are simple: As a patient with ever growing mobility issues, the harsh reality of every day tasks is that they just get worse. Many of my regular subscribers will already know my views on certain things.Continue reading “Vlogging and fundraising.”

2023

Well, here we are, 2023 and I’ve been absolutely shite at posting on my blog. You’ll be eased to know there are about 6 draft posts from the year, none of which made it to the actual blog for reasons that I’ll not go into details with – other than to say, I didn’t feelContinue reading “2023”

Legacy.

‘Tis the season and all that jazz… It’s been a while for the handful of people that follow this and I’m confident you have forgotten about it anyway. It’s been a while since I posted and not much interesting has happened as far as I am concerned anyway. This coming year marks the time inContinue reading “Legacy.”

The big Low.

So, as many of you man have realised by now, I’m not one for feeling sorry for myself. That said, the majority of my mental health issues, doesn’t come from having a terminal disease: it comes from the lifestyle change that inevitably follows it. I think we’d all agree this is “life changing” or atContinue reading “The big Low.”

Things…

So, it’s been that time again when O have to go for the MOT with the miriad of specialists. It’s always an anxious time because of the nature of the diseases, it always seems like I’m walking (more hobbling) on a knife edge. I hate it. But it is what it is… I needed toContinue reading “Things…”

Update

Hello everyone and first; Sorry. Sorry its been a long time since I posted anything, life has trundle by and I’ve written and rewritten the post for the last few months. Not much seems to have happened since August, and yet, once again it feels like so much has. The annoying thing with this yearContinue reading “Update”

Others with mnd

I have recently started engaging with other people affected by MND outside of my family circle. As mentioned previously in other posts, the blogs are somewhat one sided. It is very interesting to hear others comme ting and talking about the other side of things. You know, the S word? Weirdly, it’s kinda accepted differentlyContinue reading “Others with mnd”

Updating the world wide whatsit..

I really am shit at this, so my apologies for the lack of updates on here.. As we begin to return to slightly normal life post lockdown, I am slowly becoming more and more less mobile. It could be as simple as a lack of exercise, but I was warned that things could go thisContinue reading “Updating the world wide whatsit..”

Mobility issues.

It’s been a while and for that I apologise. I’m sure all 4 of you are worried sick. (Jk, probably not even that many subs) I recently visited my physiotherapist for a check in. Unlike my doctor specialists, she is probably the most useful person I’ve seen. In her years of practice I am herContinue reading “Mobility issues.”