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Hello, welcome to the next show. I know on just all of my social medias I've told everyone

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what this show is going to be about. So the first thing I'd like to do is welcome you

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all. Welcome to another show. I'd like to say again a massive thank you to everyone

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for watching, listening, everything that you're doing because it's massively gratefully appreciated.

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With the show today, it's going to be a bit different. I know I say that quite a lot,

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but it's going to be a bit different because predominantly I'm literally going to explain

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the emotional impact that the MS diagnosis has had on me. I'm going to do that explaining

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from the first minute that I was told about it right up to today. So please bear with

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me because I'm hoping it doesn't, but this could be a little bit emotional because we

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are talking about emotions. Yeah, okay. But yeah, I think it's only right to get this

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sort of side of it out and about. I know I have mentioned bits and pieces on other shows.

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Yeah, this one, I want to dedicate the show to it. Well, let's start right from the very

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start. It's probably the best place to start. Let's be honest. As I've said in a couple

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of shows, when things were first going on about MRI scans and whatever else, MS was

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nothing but a condition I'd heard of in passing. Nothing to do with me, nothing to do with

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family, nothing to do with really anyone I knew. I knew the condition existed, but that

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was it. I didn't have a clue what the condition was, how the condition would affect people.

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And I knew nothing. I literally knew nothing. And when I sat there that day with my GP after

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the second open scan, and as I've made clear previously, I'm a laughing joker. And I stood

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there in the doctor's office and I made the joke that he was about to tell me it was a

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wasted time, there was no need for the scans, nothing was on him. And he looked at me and

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he said to me, Mr Parker, sit down. And he said lots and lots of different words to me.

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I'm going to be honest, he said lots and lots of different things. He was explaining about

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demyelination, he was explaining about what to expect going forwards. And then he said

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to me that I need to expect, once I've seen a neurologist, I need to expect the diagnosis

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of multiple sclerosis. Now, as I've said, I'd heard of condition, I've been a first

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aider for many, many years. I knew nobody that had MS. So to say it was something genuinely

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I knew nothing about. I'd be lying to you if I said I knew what MS was, I didn't. Didn't

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have a clue. And I'll be honest with you, when he told me that, pretty much everything

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else he said while I was sat with him was a blur. I literally didn't hear or understand

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anything else that he'd said to me. All I heard was expect the diagnosis of multiple

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sclerosis. And that was it. I sort of closed off. We finished the meeting and I left his

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office. I mean, at the time I was still having mobility issues, which again, we now know

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what they were. But at that time, I thought I was just going to cut the tablets and I'd

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be okay. Until after that meeting, and I come out. And I walked out of the doctor's office.

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I had a smile on my face. You know, people were seeing me. In my head, all I could think

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was what do you mean I've got MS? What does that mean for me? What does that mean for

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my family? And as I said, I walked out of the doors into the fresh air. And I took a

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step to the side away from the doors. I broke. I absolutely broke. I bawled my eyes out.

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I could not stop the tears coming down my face. I rang Lisa and told her what the doctor

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had said. She, bless her heart, did everything she possibly could to keep me calm. And to

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an extent, I'll be honest, it really did help. I finished the conversation with Lisa.

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I rang my dad. And I said, you know, I want to pop over. This is what he said. So me,

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dad, Lisa, we sat there. And we sort of chewed it all over. We discussed it all. And again,

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I'd be honest with you. I didn't understand what was going on. I've got to say that.

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I did not understand what was going on. It wasn't till, I think it was probably the

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day after. And I went for a bath. And I laid there in that bath. And I cried. I absolutely

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broke. As I say, I broke outside the doctor's office. I cried. This, when I was in the bath,

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was something totally different. I genuinely had all these feelings, all these thoughts,

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literally smacked me in the face. And I have to say it, I've got to be totally straight,

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because this is what this show's about. It's me being straight. Because there's people

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out there that are going to have had the same sort of feelings I've had, all worse. And

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there's people out there that maybe one day are going to have similar conversations with

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their doctor. And towards the back end of the show, I want to explain how I've dealt

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with it all. But yeah, I had one really horrific thought go through my head, which was, how

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much time have I got left with my family? Because I knew nothing. I knew nothing. I

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genuinely was terrified. I was thinking, have I only got a few months left? A few years

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tops? Where do we go from here? What happens? I didn't understand what was going on. I

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got to say that I didn't understand what was going on. I didn't really think anything

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through. I was struggling. And I couldn't process what had been said. I really couldn't

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process it at all. I mean, I spoke to Lisa a lot. But again, there were certain things

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I held back because I didn't know how to say them. There's things that for many months,

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I'll be honest, for many months, I didn't know what to say, how to say. I didn't know

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what I should think. I didn't know how to think. I was struggling. And I'll be honest

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with you, I tried really hard to keep it from family and friends. And I think I actually

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succeeded. But I was in a dark place. I was in a real, real struggle to think too far

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ahead in my life. And what I did do is I made contact with a support group. And I did post

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up a post on there when I'd been formally diagnosed. And I also sort of sat back and

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just read other people's stories and whatever else. And it helped quite a lot. I'm going

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to be honest with you, it helped quite a lot to see what people that are actually going

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through this say and think. I tried really hard to avoid Dr. Google. Because let's be

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honest with you, you can stub your toe and Dr. Google is going to tell you things that

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are actually going to scare the life out of you. Don't get me wrong, there was bits and

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pieces that yes, I did look at. And I regret it. I genuinely regret it. Because again,

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it's not the way forward. Reading Google, no. I went onto the NHS website and read things.

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And that is fine. It's the National Health Service. It's there to give advice and whatever

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else. So that actually helped quite a lot. I've got to say that I learned bits and pieces.

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And I managed to get myself to a more calmer point. I managed to get myself to a point

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where I'm thinking, okay, I've got MS. MS is horrible. MS is evil. I'm struggling physically,

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really struggling. I need to keep fighting. I need to keep going. And again, I'm very,

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very lucky. I've got an incredible support network. I really have. And I totally respect

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people out there who don't have the same. If you don't, there's charities out there.

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The one main charity I would absolutely recommend, certainly if you're in the UK, is the MS Society.

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That's purely because that's the charity that I've spoken to on a few occasions. And I have

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to say they've been superb each and every time. They really have. Now, again, going

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back to other sort of feelings that I've had, I mean, some of the sort of things that I've

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thought and have gone through my head are, am I good enough? Am I what my family need?

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Would my family do better than me in the state I'm in? And yeah, some of them thoughts have

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been there more than once. But what I have always, always tried to do is battle my way

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through them. Now, what I will say is doing this podcast has been an absolute, it's done

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so much for me. Again, I've said it previous, I sit here in this brick shed, my studio,

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no, it's a brick shed, stop it. No, studio, brick shed. Sorry, just playing. But yeah,

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I sit here and I just look at my phone and I've got my microphone, I've got my sound

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board, sometimes I've got my notes and I just talk, I get things off my chest. Sometimes

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not nice things, sometimes just have a bit of fun and a bit of a laugh and a joke. Either

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way, that helps me because I'm talking. I'm getting things off my chest, which actually

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I really need to do. I've got the website now and I've got the social media accounts

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and I'm really going to town on that because I want others to see that, yeah, I mean, this

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is life changing. It's not a game, it's not fun, it's horrific, it is life changing. But

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you don't have to let it destroy what you've got in terms of your life and everything else.

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There are, as I've said, there are charities out there that can help, there is people out

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there that can help. If you can, use that. I'd strongly recommend it. I mean, other feelings

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that I've had going a bit further forward, because again, I mean, all those sort of feelings

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I've had for many, many months and hidden a lot back, going forward up towards present

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day, when I went for my first ocrevus treatment, I was so far in denial right up until the

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point that I sat down in the chair and they put the drip in my arm. I was genuinely thinking

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they were going to say to me, oh, is this okay? We've got it wrong. You haven't got

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MS. There's some other condition. Again, take some tablets, you'll be perfectly fine. I

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was really hoping for that. Honestly, I was genuinely hoping for it and I'm thinking that's

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what's going to happen. They're going to realise that they've got it wrong. No, no, I'd got

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it wrong. I thought the right thing for me to say, yeah, I'd got it wrong because I hadn't

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processed what was going on. I hadn't wanted to accept it and I still don't, but I am going

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to move forward with it and I am going to continue to fight it. Yes, I have got multiple

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sclerosis. Fine. Don't like it. Not happy about it. None of us are ever going to be

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happy about it, but you know what? I'm at a point now where I've kind of, I'm not going

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to say come to terms with it because I haven't. I've still got days where I sit there and

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think, no, no, no, no, no, this can't be right. But what I have got is thoughts and feelings

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where I'm saying to myself, do you know what? You need to accept it and you need to move

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forward with it because it can't hold you back. Don't let it hold you back. Do what

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you can to push yourself as far forward as possible. And that's what I'm going to do.

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That's definitely what I'm going to do. I'm going to continue to fight. I am going to

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continue to battle with it because that's what this thing is. It's a fight. It's a battle.

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We go to war with it, so to speak. But yeah, pushing forward, I'm going to be a lot more

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open to my emotions with it. I am going to start talking a lot more and I'm going to

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try and find a way of, I'm going to say accepting because I can't really think of any other

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term to use. I'm going to try and accept it and find a way to live alongside it. It's

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probably about the only way I can put it because the only option I've got is to live alongside

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it. But honestly, the things that I do, like I say, the podcast, the website, the social

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medias and me personally, I try and make a bit of a joke of it. I know not everyone will

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and I fully respect that. For me, I try and make a bit of a joke of it to take away its

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power. Because if I take the mickey out of it, for me personally, if I take the mickey

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out of it, to an extent it loses that grip it's got on me. Again, that's just how I

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handle it. That's what I'm doing with it because quite honestly, I know no other way. I'm looking

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for other routes. I'm looking for other things that I can do to try and fight it. I'm just

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hoping, just hearing my story, hearing what I'm going through, how I'm dealing with it,

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what I've done, I'm just hoping other people out there can also find a way.

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Well I think I've kept you all long enough. As I say, this is actually quite a hard episode

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for me to record because it's not the sort of thing I'd normally talk about in such depth.

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But 20 minutes I think is probably long enough to keep you all. I do appreciate you all listening.

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I really do. I know this isn't necessarily going to be an easy listen for some. I'm sorry

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for that. But honestly, I think this is an episode that needed to get out there a little

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bit. Well, thank you all for listening and I will speak to you all again soon. Thank

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you. Bye bye.

