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Hello everyone, only me again. I'm going to do a bit of a different type video this one.

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I'm going to explain exactly what I've had going on over the last few years and how we've

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got to where we've got to. It's been a bit of a long road, I'll be totally honest with

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you. We started out about 10 years ago, come back from working down in the Olympics doing

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security and I come back and I had very numb feet which is a bit strange. I didn't really

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think much of it, I thought you know, is what it is. Probably somewhat silly so I ignored

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it for a really really really long time and it never really went away. It sort of became

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a little bit less of a problem now and then and then it became almost a permanent problem.

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So I went to the doctors, they gave me some antibiotics thinking it was probably an infection.

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Lo and behold that did not work, not even close. And then I just carried on ignoring

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it, I got used to it and thinking oh do you know what, obviously something's gone a little

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bit wrong but such is life, we carry on and we keep trying. As time went by, and I'm talking

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a good few years, as time went by, it almost felt like it started working its way up my

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legs a little bit and my legs started feeling a little bit numb. And again it was a bit

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uncomfortable but I got so used to it with my feet I'm thinking you know what, I don't

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need to be going backwards and forwards to the doctors, there's people out there that

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need that service a lot more than I do so you know, let's leave them to it and let's

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carry on. I was able to, I started playing a bit of six-a-side football which I'd seen

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we eventually won the league, just putting that one out there, but when I was running

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around I was falling over a lot. Now I would run literally a couple of feet and it would

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feel like my legs didn't exist. I would just end up flat on my face because my legs weren't

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there. So to an extent I had to stop playing and more sort of on the touchline, leaving

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the rest of the team to it. They did good, they did very good. But again, I ignored it.

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You know this is the kind of thing that I'd always done, I just ignored things. And that

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again almost seemed to work its way up towards these sort of areas, top of my belly and my

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chest area. It started feeling like a band, really sort of squeezing quite tight. And

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thinking to myself, I was a bit overweight, thinking to myself, that's got to be a weight

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issue. So I made a bit of an effort and over the course of ten months I managed to drop

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three stone, which I have to admit has made me feel better in myself, it really has. I

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feel a bit in that respect a bit healthier. But the band feeling never went away. In fact

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it got worse to the point where it would sort of go and I'd have a few weeks without feeling

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anything there at all. Within the last few months it's got to a point where that band

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feeling is permanent, it's there all the time. And some days it's not so bad, other days

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it's to a point where it's actually quite scary. And I'm on tablets which do help a

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bit but it's still there, it's not nice. I'm at a point where I'm suffering quite badly

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with fatigue. I don't need to do a great deal of things before actually I feel like I just

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can't move. My thighs, knees, feet, across my chest, it's just my back, lower back, it's

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agony. And I can't walk that far anymore. The other day when we was at the zoo for instance,

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did very little walking, had to use my wheelchair. Lighten the mood a little bit. When I'm walking

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I'm permanently walking with a crutch. Supposed to be two crutches and I keep getting told

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I'm not using them but I find using two quite difficult. I struggle along with one. My crutches

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have got names. I've got Sticky Sticky Stick Stick and Sticky Stick Sticky Stick. I've

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also, bit of a name for the wheelchair, he's the DeLorean. And the reason for that name,

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because let's be totally honest, if I could get him to go to 88 mile an hour and go back

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in time, I wouldn't have MS in my life. Let's be totally honest about that. So it's a bit

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of a name for the wheelchair. You've got to try and keep these things light hearted. I

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have, that's my way of dealing with things. I need to keep light hearted, I need to keep

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fun. But let's be totally honest, not every day is fun. There is very much days where

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I don't even want to get out of bed. I feel absolutely awful. And for want of a better

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term, I paint a smile on and do what I can. Because for me personally, not everyone needs

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to see when I'm struggling. But when I am, I am very lucky. And something I've got to

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say is that I have a very good support network. My wife is absolutely incredible. She's always

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there. She notices when I'm not right. And she gets me to talk. And it helps a lot. I've

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got my dad, I've got my brother, and I've got the kids. They all do an incredible job

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of helping. They really do, no matter what the situation, they are right there by my

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side. And it is massively appreciated. Going back a little bit to February, when it was

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first said to me by the doctor to expect the diagnosis of MS, I'd already had one failed

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NHS MRI scan because terrified of them. Absolutely terrified. I have since overcome that, and

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I will do a video at some point where I actually discuss how I've overcome that. Because hopefully

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that could help other people. Because I'll be honest with you, I've gone from shaking

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like a leaf in the wind in an MRI scanner to being able to lay there relatively calmly.

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And I managed to have my brain scan done. But when the second private scan, I had the

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results come back, I had to go to the doctors. And me, again, being a bit of a joker, I walked

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in, first thing I said to the doctor, he sat there blessing, and I said, okay, this is

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where you're going to tell me that scan shows absolutely nothing and it was a waste of time.

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He said to me, Mr. Parkley, I can't say that, come and sit down for a minute. And he explained

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that there was two patches of demyelination on my spine. And he advised me that I must

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have a brain scan to confirm. But he said to me to expect a diagnosis of MS. That wasn't

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easy. Because genuinely, I was expecting just, you know, it's something and nothing. I walked

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out of that doctor's office. I cried. It was not easy. I rang my wife, I told her. And

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she put a smile back on my face pretty quickly. She calmed me down. I then rang my dad, explained

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it to him. We then sat down and had a chat. Wasn't the easiest conversation in the world,

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but altogether, we got there. And we managed to make it seem a lot calmer. It certainly

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didn't feel okay. But there was a calmness because I'd spoken about it. And we did some

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research. I got booked in for that brain scan. And as I say, I went through it, which was

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absolutely incredible the fact that I managed to go through it. Because honestly, I'm terrified

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of them scanners. But now, not so much. Going forward, I'd had a conversation with the

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EMS Society. And they were incredible. They gave me some absolutely brilliant advice.

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They gave me some incredible help and explained to me what to expect going forward, which

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has been brilliant. And that is why next month, myself, dad and Richard, we're doing a 5K

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sponsored walk. I tell you now, I won't be walking 5K unless I'm really, really lucky.

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A couple of hundred yards tops. But if I have to go in the wheelchair, I will do so because

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that charity has done some incredible things, not just for me, but for other people as well.

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And I will do what I can to support them and help. So that's something I'm quite looking

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forward to. I've written lists of things I was going to talk about in this video. But

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in all fairness, I don't really think it's necessary me going through them. It's very

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much a case of, from what I'm understanding from other people and from what I'm dealing

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with myself, EMS is very much a one person at a time job. Not everyone is the same. Not

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every case is the same. It's different. And everyone handles it their own way. And that's

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perfect. That's how you have to be, in my opinion, as you handle these things on your

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own, in your head. But then you take advice, you take support from everyone else. Because

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quite honestly, in life you can't handle everything on your own. You always need that support.

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And there's charities out there that can help if you need them. And as I say, my recommendation

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very much would be the MS Society because they've been brilliant for me. And as I say,

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this video was very much a case of just sort of getting this out of there, explaining to

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an extent what I'm going through. And kind of just try and give people a bit of an idea

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that it's not easy. It's not easy. But I'm trying to do what I can to make it as easy

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as I can for myself. And I will, if anyone needs to talk or anyone wants a bit of support,

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there's charities out there. I'm here. I'm quite happy. I'll have a conversation. It's

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not a problem at all. I'm not going to try and keep you all too long. I say we're probably

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pushing on a 14 or 15 minute video here. But if there's any questions or anyone wants to

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have a chat with me about what I've said, by all means, by all means, my inbox is open.

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Have a conversation with me. Not a problem at all. Thank you all for listening. I do

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appreciate it. And as you can all see, I've got my glasses on and I'm getting used to

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it.

