mark guymer’s supportive words

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You’re listening to the Cornwall Cancer Cafe podcast with me, Matthew and me, Emma. Thanks

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to the National Lottery Community Fund for supporting this podcast. So this week we are back with

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Mark Gaimer, the Chief Executive of Cancer Support UK, who I asked recently to give some tips.

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Before we go into those, I’m just going to emphasise that I’m not a doctor. Are you

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a doctor, Emma? I’m not a doctor, I’m not a counsellor, I’m not a specialist. I’m not

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a specialist or a counsellor or nothing like that. What are you? I’m a person with lived

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experience. What are you? I think that sort of sums me up as well, yes. How funny,

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how funny that is. Bravo. Bravo. And both of us appreciate hugs. We do, we appreciate big

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because when you give a hug, you get a hug. And that empathy is very important to us,

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having gone through a cancer diagnosis and things like that. And in many ways,

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that is the theme, really, of what we’re talking about with Mark Gaimer. So I asked him

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for top five supportive words and phrases, because people find language very difficult,

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don’t they? They do. And yeah, any tips he can give, obviously, in his position,

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he’s got a lot of experience, a lot of people under him with that specialist knowledge,

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the specialist knowledge that we don’t have because we’re not specialists.

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Cancer Support UK do run a cancer coach scheme as well. And this is all the sorts

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of things that they’re involved with learning. Oh, fantastic. Let’s hear all about it.

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So let’s go to Mark Gaimer to hear his first tip. OK, so my first word, top five words,

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supportive word is empathy. And I’ve deliberately chosen this because we know that one of the

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challenges that people face or we hear that they face when they’ve had a cancer diagnosis is

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how they respond to people interacting with them. And often they say that one of the things they

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find difficult is where people come up to them and they sort of do that. I describe it as the

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sympathetic face, which is that oh, you know, poor you type expression. And often it will be

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show sympathy because the human nature is that’s how we feel we should respond.

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And sometimes that’s how we want to respond. Whereas empathy, when you try and actually

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place yourself a little bit more in trying to understand how the person telling you what

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they’re telling you is feeling, can actually have a really different impact and can really

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feel much more supported. So that’s my first supportive word, empathy.

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And it’s interesting he there is talking about empathy is about understanding as well.

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Yeah, I guess rather than saying, oh, I’m so sorry that you’re not very well,

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maybe say, how are you doing? That sort of thing.

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And keep it very open language so that you’re not forcing your thoughts on someone.

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Yeah, so by not saying, oh, I’ve got a friend who’s suffering with da da da,

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and they’re doing this, that and the other, rather than forcing their perceived knowledge on

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you, they are asking you for how are you? What are you doing? How are you doing?

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Have you had people tell you how to deal with your cancer?

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I’ve had people suggest various different things, or they’ve told me about friends

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or family that have had types of skin cancer. But my skin cancer is melanoma.

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And there are also there are different types of skin cancer out there, all very different.

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So I think there’s a lack of understanding out there. But,

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you know, people are just trying to help, aren’t they?

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People do mean well. And that is very important, because when people are they’re

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trying to do that.

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Yeah, I think they are. So yeah, let’s let’s hear what Mark has to say about.

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Connection.

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Connection.

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My second supportive word is connection. And this is something that we we have a

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little strapline on our website at Cancer Support UK. And one of the words on there

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is connection. And the reason for that is that we know people can very quickly

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describe themselves as feeling isolated. And initially you may think, well, you know,

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is that physical isolation? Is that people who live on their own or

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haven’t got a strong network around them? But often it’s people who have

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big friends and family network around them, they can just as easily

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become isolated and and feel unconnected to people.

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And so one of the things that we focus on, and which I think is a way that you can

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be supportive, is by thinking about how you stay connected with someone, not just

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physically being present, but actually being there for them

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emotionally as they go on this this difficult and challenging journey.

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Here to support you, the Cornwall Cancer Cafe podcast.

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Share this podcast on your social media so others may benefit.

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One of the things that a lot of people talk about as well

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is how lonely a cancer experience can be.

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Yeah, I think I’m thinking back to when I was first diagnosed.

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I think the isolation for me was around. First of all, I didn’t know enough about my cancer,

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so I felt isolated because I didn’t know enough about it.

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And then I felt a little bit isolated when my friends didn’t know enough about it.

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So going back to the empathy before where they were trying to be supportive,

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but didn’t know enough about it, and it just made me feel a little bit isolated

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because they were trying to talk about something they didn’t know enough about.

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How did you have anything like that?

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A lot, yes. And I also found myself almost self-isolating because I

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wasn’t sure how to express what was going on within me

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in a way that other people could understand.

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Well, that’s interesting.

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Do you feel that you’re more able to express yourself now?

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I do, yes, because once you’ve gone on a fairly long journey,

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you do learn an awful lot of coping tips, mechanisms,

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and sometimes you just throw caution to the wind and just give it a go.

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Yeah, I was going to say, I think as you travel along your journey,

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there are times that you need to just express how you’re feeling,

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and if people around you get battered, then you just have to apologize afterwards for it.

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Did you do that sort of thing yourself as well?

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Yes, I do apologize. Sometimes I felt that in my attempt to connect,

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I published almost every day what I was going through on Facebook.

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It was like an ongoing traumatic diary.

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An onslaught of Matty’s journey.

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And I actually, at many points, felt sorry for my

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friends and followers for what I was subjecting them to.

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But I suppose those that were really interested probably read each of them,

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and they were there for you.

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They were, and they actually found my honesty about it quite useful as well

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for themselves because some of them had other members or family or friends who’ve

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experienced all sorts of things.

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And so just to get that insight is useful for other people as well.

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Yeah, and of course there is the other side of it where people don’t want to talk about it

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at all. So yeah, there’s an everywhere in between, of course.

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And we’ve spoken about this before about living on your own.

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And sometimes when you live on your own you need to work harder

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to form those ways of connecting and explaining how you’re feeling that day.

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Yes, but also it’s quite handy living on your own sometimes

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because when you want to have those dark moments,

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you can just sit on the sofa in your living room and have them.

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You don’t have to go and hide yourself away to have them.

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What about the lighter moments now?

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I think we’ve got some sort of thoughts on that from Mark Gimer.

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My third supportive word is joy, which may surprise you a little bit,

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but despite the most challenging of times that people go through,

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something that we hear again and again is the importance of just finding

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those little moments of joy. And it can be the simplest of things.

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It can be a big thing. It could be an organised treat or a get together.

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But sometimes it can be just that little note

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that someone leaves you saying they’re thinking of you.

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It can be very small acts of kindness,

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but what we know is that those little moments of joy become incredibly important.

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One of the best examples I can think of recently that people may be familiar with

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is if you listen to Chris Hoy, who’s had his own cancer diagnosis

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and he’s done a BBC documentary,

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I think he talks very eloquently about the importance of finding those moments,

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those moments of joy, those little moments that are uplifting and positive.

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And he explains very clearly how that’s been important to him.

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Funny enough, he’s talking about joy.

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And Cancer Support UK sent me a care package in the post,

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which has some sweets, some teas, some treats and things to ease the day.

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Care packages do bring that sort of soft joy

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that someone has thought about it very carefully to be empathetic with you.

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Yeah, I had a care package from my skin cancer nurses

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when I got back from hospital from having the lymph nodes removed of my neck.

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There was this beautiful scarf arrived in the post for me

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and it was perfect because I’d had this operation on my neck

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and I thought they’ve thought about this.

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They’ve sent me this beautiful soft scarf and I still use it regularly.

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Absolutely blew me away.

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I was, you know, it made me cry thinking this is an amazing thing.

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But moving on from that, I’ve talked to my mum and dad quite a lot

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and they said that since I’ve had my diagnosis, they’ve seen more of me.

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So it’s also about choosing moments,

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the moments that you want to enjoy,

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the people that you want to be with, the things that bring you joy.

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I found it in many times almost permission to be sillier than normal.

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Sillier than normal?

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No, I’ve mentioned at many points about humour

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and we’ve had some chats with people who’ve got interesting takes on humour.

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One of the things that gave me joy was in many ways

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winding up some of the nurses on Headland Unit.

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Oh, I bet they love that.

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Who’s the most popular person on the Headland Unit?

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I think one of the things that I used to enjoy doing is because

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when you’re linked up to your cannula and having an infusion,

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they flush the line, don’t they?

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Yeah.

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And this nurse said, oh, flush.

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I went, ah, it saved every one of us.

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And did they say that’s not the first time you’ve heard that?

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And I did it nearly every time.

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I’ve like known it.

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I could have carried that on.

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You should have told me it’s too late now.

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So, anyone listening to this going for a treatment at the Headland Unit?

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Every time they say flush, yeah, now you’ve all got to do it.

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Everyone’s got to do that now.

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So, joy can be, you know, enjoying a bit of humour.

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A bit of humour.

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Right, okay.

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So, we are moving back to the tips and the words and the phrases

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from Cancer Support UK’s Chief Executive, Mark Gimer.

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Let’s go for number four.

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So, my fourth supportive word is comfort.

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And this, again, is another word that we use at Cancer Support UK a lot.

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Comfort is one of the things that we provide through our cancer kits

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that we send out to people who have had a cancer diagnosis.

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And you can find comfort in different ways.

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But I think everybody, when they’re facing a challenging time,

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will have moments where they feel low,

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will feel like they need something around them

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to just make them feel a bit more comforted.

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That can be through the actions of a person,

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but sometimes it can just be through a comforting item.

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So, one of the items that we send out in our cancer kits is lemon and ginger tea.

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And what we know is that many people who go through a treatment like chemotherapy

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will lose a sense of taste.

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And just having that moment where you can taste something,

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the lemon and ginger tea is something which people tell us they can still taste.

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And it just gives them that moment of comfort

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that they can still taste something despite everything they’re going through.

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And it gives them a real lift.

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So, comfort is my fourth word.

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You’re listening to the Cornwall Cancer Café podcast.

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Visit our website www.cancercafepodcast.org

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Also got to mention that Cancer Support UK send out to children

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soft toys as well for comfort for children going through cancer treatments,

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which I think is lovely.

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It is lovely but heartbreaking at the same time, isn’t it?

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But yeah, it’s interesting you saying about comfort

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because we were talking about care packages as well.

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So, I didn’t go through chemotherapy.

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So, I didn’t lose my taste.

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But I know others that did and where I’ve joked about, you know,

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all chocolate is a real go-to for comfort.

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Some of the ladies I’ve spoken to have completely lost their taste for chocolate.

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I did.

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Yeah.

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And I was amazed the first time I heard it.

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Shocked even.

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Oh no, these poor people, they can’t enjoy chocolate anymore.

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Tastes a really weird thing because I had a stem cell transplant

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and I was told before my stem cell transplant,

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during your stem cell transplant,

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you’ll probably experience the taste of sweet corn.

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I thought, what?

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Sweet corn, not popcorn.

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What?

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And I thought this was just some sort of leg pull.

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Oh, to get back at you.

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No, but when I had my stem cell transplant, yes,

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there was a distinct taste of sweet corn that filled my mouth.

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So, yeah, so I can’t actually eat sweet corn now

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without the memory of my stem cell transplant.

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So, did it put you off sweet corn for a while?

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Well, I did have sweet corn.

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Mother put some sweet corn in something the other week

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and I recounted this as, oh, are you okay?

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Yeah, I can eat it, I can eat it.

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But it just brings back the memory, that’s all.

224
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Yeah, lovely.

225
00:17:41.360 –> 00:17:45.580
But comfort, he also mentioned about people and about,

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I suppose part of that comfort is someone just turning up

227
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and checking in on you.

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Or inviting you out for a cup of coffee or,

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I mean, I had friends that I hadn’t seen for a while.

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Soon as they heard my diagnosis, they were straight,

231
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well, I was going to say straight on the phone,

232
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but straight on the phone and messaging me saying,

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come out for a cup of tea, come out for a cup of coffee.

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We’d love to see you, come and talk to us.

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And it was really refreshing just to go out

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and be outside of that immediate circle of family

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and friends that had been there supporting you,

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which it was amazing that immediate family was there,

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00:18:25.760 –> 00:18:29.840
but so lovely that other friends from further afield

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were rallying around, so very comforting there.

241
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And it is amazing that the people who put their hands up

242
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and say, I’m here for you, isn’t it?

243
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Yeah.

244
00:18:42.700 –> 00:18:43.920
Those people you just didn’t expect.

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Yeah, yeah, so if you’re one of those people,

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if you’ve heard that one of your friends has had a diagnosis

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and you think, oh, should I reach out to them?

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Yes, yes, you should, because give them the opportunity

249
00:18:55.060 –> 00:18:56.960
to say, yes, I’d like to see you,

250
00:18:57.040 –> 00:18:59.100
or it’s not the right time for me,

251
00:18:59.240 –> 00:19:02.040
but you could make such a difference to that person.

252
00:19:02.860 –> 00:19:04.820
Even if it’s on my case,

253
00:19:04.940 –> 00:19:06.800
people were taking me to hospital,

254
00:19:06.920 –> 00:19:09.300
picking me up from hospital, things like that.

255
00:19:09.560 –> 00:19:14.640
And so one friend of mine took me to hospital,

256
00:19:14.640 –> 00:19:17.420
picked me up, and then took me for a pizza

257
00:19:17.420 –> 00:19:19.440
and a cup of coffee and something afterwards.

258
00:19:19.740 –> 00:19:21.560
Yeah, that was fantastic, isn’t it?

259
00:19:22.020 –> 00:19:25.420
So, yes, that was comfort from Mark Guymore.

260
00:19:26.120 –> 00:19:30.520
The number five on his top five supportive words

261
00:19:30.520 –> 00:19:33.640
and phrases, let’s find out what that is.

262
00:19:33.800 –> 00:19:38.520
And my final supportive word is compassion.

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00:19:39.740 –> 00:19:42.660
And compassion, it’s a big word,

264
00:19:42.660 –> 00:19:44.140
it can mean many different things,

265
00:19:44.140 –> 00:19:46.720
but the way I think about it in this context

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is people showing compassion to themselves.

267
00:19:50.780 –> 00:19:52.860
So it’s really important

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00:19:52.860 –> 00:19:56.140
that you’re not too hard on yourself,

269
00:19:57.050 –> 00:20:01.240
you don’t sort of allow this situation

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00:20:01.240 –> 00:20:04.400
to sort of spiral a little bit

271
00:20:04.400 –> 00:20:07.180
and you start becoming, very easily in fact,

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00:20:07.400 –> 00:20:10.300
you can become overly critical of yourself

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00:20:10.300 –> 00:20:12.300
and how you’re handling this situation.

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The reality is we’re all different,

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00:20:15.420 –> 00:20:17.540
we’ll all handle it in different ways,

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00:20:17.680 –> 00:20:19.420
depending on the type of people we are

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00:20:19.420 –> 00:20:21.320
and how we deal with these things.

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00:20:21.680 –> 00:20:23.800
And that’s okay, that’s normal.

279
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And I think having a moment of compassion

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00:20:26.120 –> 00:20:28.060
to sit back and say to yourself,

281
00:20:28.100 –> 00:20:31.040
do you know what, this is difficult for me,

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00:20:31.680 –> 00:20:36.160
I am finding this challenging can be really important.

283
00:20:36.480 –> 00:20:40.340
But it also applies to obviously other people,

284
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if you’re working with a colleague who’s had a diagnosis,

285
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how can you be a little bit more understanding

286
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and compassionate towards that individual

287
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in the right way so that they feel supported.

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Being compassionate to yourself

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00:20:57.380 –> 00:21:00.100
is very, very difficult.

290
00:21:00.600 –> 00:21:04.240
From my point of view, I found that so difficult.

291
00:21:05.340 –> 00:21:08.700
Yeah, I’m sat here thinking after listening to him,

292
00:21:08.700 –> 00:21:10.940
thinking about the number of times

293
00:21:10.940 –> 00:21:12.300
I was told that I could die.

294
00:21:12.460 –> 00:21:14.460
Now I’m sure you’ve had the same thing.

295
00:21:15.560 –> 00:21:17.460
The first time I heard it, I thought,

296
00:21:18.080 –> 00:21:18.840
ah, don’t be silly.

297
00:21:19.300 –> 00:21:21.560
And then it was repeated and repeated.

298
00:21:21.960 –> 00:21:25.060
And you begin to believe that actually,

299
00:21:25.180 –> 00:21:28.580
oh my goodness, I could die, I could die.

300
00:21:28.580 –> 00:21:30.700
And I did start putting my affairs in order.

301
00:21:31.580 –> 00:21:33.060
I started sorting things out,

302
00:21:33.140 –> 00:21:35.680
so writing passwords down and writing things down

303
00:21:35.680 –> 00:21:37.820
so that if something did happen to me,

304
00:21:38.700 –> 00:21:40.820
my family would be able to find everything

305
00:21:40.820 –> 00:21:42.180
that they needed to.

306
00:21:44.120 –> 00:21:47.960
And then you have days where you feel indestructible.

307
00:21:49.460 –> 00:21:51.640
And yeah, so it’s a journey, isn’t it?

308
00:21:52.480 –> 00:21:55.460
I think for my point with this

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00:21:55.460 –> 00:21:57.280
being compassionate to yourself,

310
00:21:57.880 –> 00:22:00.720
I remember going to a hope course,

311
00:22:00.880 –> 00:22:02.420
or as I call it, a cope horse,

312
00:22:03.480 –> 00:22:06.240
where it was about being kind to yourself.

313
00:22:06.240 –> 00:22:07.860
And they gave you little cards

314
00:22:07.860 –> 00:22:11.000
to put in your wallet about being kind to yourself.

315
00:22:12.540 –> 00:22:17.200
And I found that so tricky because I’m so often,

316
00:22:17.700 –> 00:22:19.200
previously, the previous me,

317
00:22:19.280 –> 00:22:23.200
the former version of me was always very,

318
00:22:23.340 –> 00:22:27.160
I castigated myself for not getting things right

319
00:22:27.160 –> 00:22:31.940
or not thinking properly and all those sorts of things.

320
00:22:32.660 –> 00:22:35.740
Oh, Matthew, you’re being so stupid, you know?

321
00:22:35.740 –> 00:22:36.820
And all that sort of,

322
00:22:36.860 –> 00:22:41.620
that sort of very aggressive language to myself.

323
00:22:41.980 –> 00:22:44.340
And I wasn’t being compassionate to myself.

324
00:22:44.600 –> 00:22:47.340
And it took me a while to get over that.

325
00:22:48.100 –> 00:22:51.200
And even still, in recovery,

326
00:22:51.540 –> 00:22:55.820
I’ve been, well, now 18 months plus in remission

327
00:22:55.820 –> 00:22:57.540
from my third line of treatment.

328
00:22:59.240 –> 00:23:01.360
And you find yourself,

329
00:23:01.500 –> 00:23:03.080
oh, I’m gonna lie in bed a bit longer.

330
00:23:03.120 –> 00:23:05.060
I’m just gonna go back to bed after lunch

331
00:23:05.060 –> 00:23:05.800
for a sleep.

332
00:23:06.160 –> 00:23:09.940
And the little devil on your shoulder says,

333
00:23:10.560 –> 00:23:13.520
oh, you’re such a lazy person you are,

334
00:23:13.920 –> 00:23:17.040
where actually, no, I’m not a lazy person.

335
00:23:17.080 –> 00:23:19.500
I’m just someone who is in recovery.

336
00:23:19.620 –> 00:23:20.800
I’ve been through a lot.

337
00:23:20.820 –> 00:23:23.920
And I need that time and space

338
00:23:23.920 –> 00:23:26.640
to just get myself together.

339
00:23:27.480 –> 00:23:29.700
Yeah, you mentioned about being in recovery.

340
00:23:30.760 –> 00:23:35.880
I think also I’m now taking various drugs and things

341
00:23:36.420 –> 00:23:40.100
to help me along the way for the pain,

342
00:23:40.200 –> 00:23:42.100
for the pain, not for, yeah,

343
00:23:42.260 –> 00:23:44.820
not recreational drugs, because that would be naughty.

344
00:23:47.020 –> 00:23:49.300
I don’t know what you’re talking about.

345
00:23:50.900 –> 00:23:52.040
Where was I going with that?

346
00:23:52.040 –> 00:23:52.680
Oh, yeah.

347
00:23:53.600 –> 00:23:54.580
See, this is the thing.

348
00:23:55.120 –> 00:23:55.820
So, funny enough,

349
00:23:55.820 –> 00:23:57.480
I spoke to my doctor about it the other day,

350
00:23:57.480 –> 00:24:00.080
and I said, I hate the way I am now.

351
00:24:00.720 –> 00:24:03.040
Before cancer, I was on it.

352
00:24:03.040 –> 00:24:04.340
I could remember everything.

353
00:24:04.500 –> 00:24:06.060
I was organized.

354
00:24:06.660 –> 00:24:08.360
I could get lots done.

355
00:24:09.160 –> 00:24:12.260
Since cancer, and I know part of it is PTSD,

356
00:24:12.740 –> 00:24:14.760
part of it is I’m now on these,

357
00:24:15.440 –> 00:24:18.040
the drugs, my prescription drugs.

358
00:24:18.820 –> 00:24:21.480
And it’s all affected how my brain works

359
00:24:21.480 –> 00:24:22.760
and how I feel emotionally.

360
00:24:23.300 –> 00:24:24.220
But also, as you said,

361
00:24:24.220 –> 00:24:27.480
we are still recovering from a very traumatic experience.

362
00:24:27.880 –> 00:24:30.160
So, I’m trying to do things every day.

363
00:24:30.300 –> 00:24:32.420
And then a bit like we talked about earlier,

364
00:24:32.540 –> 00:24:34.080
if you try and do something,

365
00:24:34.480 –> 00:24:38.560
it absolutely wipes you out and then you need to sleep.

366
00:24:38.660 –> 00:24:41.280
But then the guilt drops in, doesn’t it?

367
00:24:41.380 –> 00:24:42.200
You know, you shouldn’t be sleeping.

368
00:24:42.260 –> 00:24:43.940
You should be doing this or this or this.

369
00:24:44.320 –> 00:24:45.820
And we also talked about, you know,

370
00:24:45.940 –> 00:24:47.460
are we well enough to work?

371
00:24:47.720 –> 00:24:49.320
And I think we both know

372
00:24:49.320 –> 00:24:50.640
that we’re not well enough to work,

373
00:24:50.640 –> 00:24:53.180
because if we did a day’s work,

374
00:24:53.180 –> 00:24:55.420
that would be it for the rest of the week, wouldn’t it?

375
00:24:56.060 –> 00:24:58.480
Yesterday, I went to a careers fair

376
00:24:59.620 –> 00:25:03.040
at Liz Kerrano, a new county hall in Truro.

377
00:25:03.740 –> 00:25:07.140
And I was thinking I’ve got to sort of

378
00:25:07.140 –> 00:25:11.760
get my mind in place to sort of reboot life in that way.

379
00:25:12.580 –> 00:25:16.080
And I looked through all of the sorts of things

380
00:25:16.080 –> 00:25:18.700
that were on offer as jobs you could apply for.

381
00:25:19.480 –> 00:25:20.820
I said, no, I can’t do that.

382
00:25:20.980 –> 00:25:22.120
No, I can’t do that.

383
00:25:22.120 –> 00:25:23.700
Nope, I won’t be able to cope with that.

384
00:25:23.780 –> 00:25:25.340
Nope, won’t be able to cope with that.

385
00:25:25.340 –> 00:25:26.560
And you start to think,

386
00:25:26.560 –> 00:25:28.740
you’re not really there, are you?

387
00:25:29.460 –> 00:25:34.220
No, so yeah, so you have to be compassionate about yourself

388
00:25:36.500 –> 00:25:39.960
and allow yourself to recover.

389
00:25:41.280 –> 00:25:43.060
And so I said to you,

390
00:25:43.060 –> 00:25:47.620
when you came through the door today to do this recording,

391
00:25:47.920 –> 00:25:49.680
that I’ve been to that careers fair

392
00:25:49.680 –> 00:25:51.540
and I was a bit sort of wiped out.

393
00:25:51.540 –> 00:25:52.280
You’re okay.

394
00:25:52.460 –> 00:25:54.820
So, well, I mean, in this way,

395
00:25:54.820 –> 00:25:56.880
I’m not being compassionate to myself today

396
00:25:56.880 –> 00:25:59.980
because I know I’ve got stuff I need to do.

397
00:26:00.060 –> 00:26:01.800
But what I did say is,

398
00:26:01.940 –> 00:26:04.260
tomorrow, Saturday and Sunday,

399
00:26:04.760 –> 00:26:08.320
I am going to do absolutely nothing

400
00:26:08.320 –> 00:26:09.580
apart from doing the shopping.

401
00:26:10.480 –> 00:26:12.760
But you might get some nice things in the shopping

402
00:26:12.760 –> 00:26:15.060
that you can enjoy and treat yourself

403
00:26:15.060 –> 00:26:17.020
and have some joy from it.

404
00:26:17.440 –> 00:26:18.320
Yes, brilliant.

405
00:26:18.320 –> 00:26:21.320
So we’ve been talking about Mark Gimer

406
00:26:22.080 –> 00:26:25.420
from Cancer Support UK’s tips.

407
00:26:25.480 –> 00:26:27.840
We’re going to have some more tips from him

408
00:26:27.840 –> 00:26:29.700
in another episode.

409
00:26:30.920 –> 00:26:33.520
So what have you learned overall today, Emma?

410
00:26:35.960 –> 00:26:38.200
To find the joy in things,

411
00:26:39.420 –> 00:26:41.620
to forgive yourself,

412
00:26:41.660 –> 00:26:46.300
but also to try and see the good in everybody,

413
00:26:46.300 –> 00:26:51.940
give people the space to come and help you.

414
00:26:51.960 –> 00:26:55.440
But also if that space is not right for you at the time,

415
00:26:55.940 –> 00:26:58.520
you’re allowed to be negative at that point

416
00:26:58.520 –> 00:27:01.240
and then you can ask for forgiveness afterwards.

417
00:27:01.840 –> 00:27:03.760
Something positive we can all do

418
00:27:03.760 –> 00:27:08.980
is if you can help us by sharing our social media posts,

419
00:27:09.020 –> 00:27:12.980
we have a Facebook feed or a page,

420
00:27:12.980 –> 00:27:16.960
look up Cornwall Cancer Cafe podcast on Facebook

421
00:27:16.960 –> 00:27:19.220
and you can follow us on there.

422
00:27:19.540 –> 00:27:24.120
And then share on Facebook, whatever, social media.

423
00:27:24.740 –> 00:27:27.500
You can go to our website as well

424
00:27:27.500 –> 00:27:31.320
and share links direct from the website.

425
00:27:31.660 –> 00:27:33.040
Have a look around the website too.

426
00:27:33.040 –> 00:27:34.280
We’ve got some blogs

427
00:27:34.280 –> 00:27:37.880
and we’ve got a diary of things going on in Cornwall

428
00:27:37.880 –> 00:27:40.840
which can support you

429
00:27:40.840 –> 00:27:44.460
as you are going through your cancer experience.

430
00:27:45.500 –> 00:27:47.680
And yeah, so we’re just looking about

431
00:27:47.680 –> 00:27:50.460
a bit of caring and sharing on that side of things.

432
00:27:50.880 –> 00:27:51.820
Yeah, caring and sharing.

433
00:27:51.860 –> 00:27:54.320
I was just thinking about my little tagline

434
00:27:54.320 –> 00:27:55.640
about hugs and things.

435
00:27:56.180 –> 00:27:58.000
When you see people say to them,

436
00:27:58.020 –> 00:27:58.620
do you want a hug?

437
00:27:58.660 –> 00:28:00.180
And if they say yes, give them a hug

438
00:28:00.180 –> 00:28:01.600
because you’ll get a hug back.

439
00:28:02.320 –> 00:28:06.220
And we’ve got a video on our video page

440
00:28:06.220 –> 00:28:07.560
with Amanda Winwood

441
00:28:07.560 –> 00:28:10.880
and have a look at cosmetics.

442
00:28:12.020 –> 00:28:14.900
And she loves, she’s called the queen of hugs

443
00:28:15.720 –> 00:28:17.000
amongst many people.

444
00:28:17.740 –> 00:28:20.640
So yeah, she really loves

445
00:28:20.640 –> 00:28:22.640
giving those sort of supportive hugs.

446
00:28:23.380 –> 00:28:26.920
So that’s almost about it this week.

447
00:28:27.060 –> 00:28:29.800
And thank you very much for listening

448
00:28:29.800 –> 00:28:31.740
and supporting this project.

449
00:28:31.760 –> 00:28:33.200
So we’ve been brought to you

450
00:28:33.200 –> 00:28:35.820
by the National Lottery Community Fund

451
00:28:35.820 –> 00:28:38.960
and we will be bringing you a lot more

452
00:28:38.960 –> 00:28:40.360
in the coming weeks.

453
00:28:40.840 –> 00:28:42.720
So just take care of yourselves.

454
00:28:43.280 –> 00:28:44.320
Yep, look after yourselves.

455
00:28:44.580 –> 00:28:46.140
Big hugs, give a hug, get a hug.

456
00:28:53.720 –> 00:28:55.960
Thanks to the National Lottery Community Fund

457
00:28:55.960 –> 00:28:57.700
for supporting this podcast.