Cleft Lip and Palate
Positive experiences of cleft and advice to others
From among all the interviews we conducted there were lots of stories of positive experiences. Families appreciated the support they had received from professionals, friends and others in their communities, schools and other services. There was a strong feeling of wanting to ‘give something back’ to the cleft community. This concept was formed on the basis of being grateful for the support of organisations such as Cleft Lip and Palate Association (CLAPA), CLAPA Edge and Changing Faces and for the treatment received through the regional cleft lip and palate services provided by the NHS (see ‘Cleft treatment pathway’). Some people were involved in giving advice to others through social media forums and others took part in fundraising and awareness raising activities for the cleft community in the U.K.
I really, really don’t think it has, because he is quite a robust kid. And he’s been quite fortunate with the schools he’s gone to, I think, they’ve been supportive and he’s not had to change schools very often. Well he was at primary junior school and then we changed him to senior school but…
Is he aware of any other children with a cleft at all?
Interestingly there’s a lad that’s just come to his school that has got a cleft, that we’ve met before.
Yeah OK.
But apart from that, no. And he’s a bit resistant now to come to any of the events that I get involved with. He just, it’s not cool anymore. But I wouldn’t push him.
You’d say he’s fine with his own identity then?
Yeah, oh yeah, yeah, yeah, yeah and…
Not, not needing to…
No not need, well, you know, I think…
Not needing to be part of…
No, any kind of…
…of a, yeah, of a group?
Yeah but I think he, I think he knows, hopefully, through what I do and get involved with, that, you know, he’s not on his own.
Yeah.
He’s not some kind of, well I don’t want to use the word “freak” because that’s awful, but he’s not that kind of, he isn’t on his own with what he’s got as a condition and what he’s been through and what he might have to... he knows that, I think, because of what I talk about and what I do with the, with CLAPA and the branch. And, you know, we have Christmas parties, we have summer parties, he doesn’t want to come to them anymore, and that’s fine, I’m not going to push him. But he knows that... there are loads of other kids out there like him. I’d like to think he does, hope I’m not putting [laughs] words into his mouth, or thinking things that he’s not thinking. But, you know, you kind of sometimes do that as a parent. But I’ve tried really hard to... to make him… feel... like it’s just something he can talk about, or hopefully accepts what it is, and that it’s no big thing really, you know. And so yeah, no, thankfully, God, he hasn’t had, I really hope he doesn’t at any point, he hasn’t had any bullying.
Well the only other one was , yeah, was just was CLAPA, but also just, yeah, groups on Facebook really and just getting in contact with, with parents. I mean my wife’s been more into that than myself.
OK.
Just yeah going on Facebook and sort of hooking up with other mums and... things like that. But that’s been pretty much her... her domain really.
Yeah so was this kind of a positive aspect of what you’ve been going through?
Yeah I think so. I mean and, and also hearing, obviously, my wife, we chat and stuff, and she relays what she’s learnt from other people, what they’re going through and stuff. And so it’s just, yeah, I would say it’s very positive. I mean I think that’s a big thing, I mean in society, where we should, when sort of people are going through things, actually you share with one another what’s going on, and encourage one another and say, “Look, hey you’re not in it by yourself, we’re going, we’re going through it as well.” And, and because you do think you’re very, oh you’re thinking, “Oh no, it’s only us, why has it happened to us?” all this kind of stuff. And you always have these questions.
Sure.
And it’s when you can say, “Look, it’s not just us, it’s, we, there’s another family there, there’s another family there,” and, and then you can chat to them and encourage them. And, as I say, my wife still contacts this little family who’ve had a little boy who had the cleft palate.
Yeah.
And it actually perhaps sparks up friendships as well which you wouldn’t necessarily have had. And just, yeah, just encouraging one another really, but yeah.
OK great. So is there any advice you would give to other families or health professionals at all, in the way people communicate about cleft lip and palate?
I would say... just, yeah, just be honest and about how you’re feeling. Because I think it’s the worst thing to kind of shut up your feelings and sort of think, “Oh it’s, it’s,” you know, saying it’s all OK and you’re fine with it. And ask questions as well when you’re seeing particular specialists and the cleft nurse team.
Diane: I just think the best advice is to stick to, if you’re going to do research, I think stick to... the proper...
Andy: Official sites.
Diane: Official websites, like the CLAPA website or the hospital has got their dedicated website. Or to speak to a cleft team and see if they can put you in contact with a family who has gone through it, because I think that’s the best
Andy: I certainly think so, yeah.
Diane: The best route to go down: somebody who has been through it, or to read stories on the CLAPA website of people that, you know, their stories. Rather than just go ploughing on Google and finding, oh, all sorts of negative, I think.
Andy: I think that’s what it boils down to, because there was a lot of stuff from like America with the stories and things like that…
Diane: Which are very different.
Andy: And it’s different levels of care and different systems. And you can’t kind of…
Diane: Yeah, just to be careful I think.
Andy: You know, you can’t compare that, you know, because they haven’t got an NHS over there. And like I said, there’s different levels all over the place; it’s kind of, yeah. I certainly think that, from my perspective is... to deal with this kind of message as well then, you know, some NHS departments maybe need to re-look at how they deliver the messages and what support is available when they do deliver them at the time, you know, and that help and support. Because, certainly from our perspective, and I think from somebody else as well that we know as well, it was pretty much... delivered.
Diane: Quite abrupt yeah.
Andy: That kind of way as well. So I think, you know, I think they need to be aware about what can happen and how you can deal with it.
Parents and individuals also had advice to give to others regarding how to research cleft-related issues with regard to treatment and living with the condition.
Mark: Well my biggest advice would be don’t go on the internet like Beck did, which I know for some situations you could find it reassuring, but it did throw up a lot of other things. The CLAPA website was great for the photos, because it is nice to see before and after, because you want to know what you’ve got to go through.
Becky: Yeah, yeah.
Mark: You know, and it’s it was nice there. But obviously just go into sites which are recommended, not sites which are just made up by people, because they can be quite negative.
Becky: Yeah, yeah. And my advice would be just to go with your emotions, if you’re feeling, you know, to go through like, you know, you probably when, if you have a diagnosis, is to go with those feelings. You know, sometimes you know, that shock, that loss, just to let it, you know, just to, to come over you and just and deal with that. And even if you’re having, you know, really negative thoughts, I think you’ve got to go there sometimes.
Mark: Yeah you have to.
Becky: You know, if you’re feeling angry, to go there. Because I think, you know, it’ll come out in other ways otherwise. But just to recognise, “Yeah, I’m feeling like this,” but at the end of the day, you know, from, you know, it’s not a major thing, it can be sorted. And, you know, to write things down if you’re not sure about anything. But it’s not, it’s really not such a big deal. You know, from the initial diagnosis you think, “Oh my goodness,” you want your child to be... sort of normal or perfect, but what is, but it’s stuff that can be dealt with. And it’s, I think from…
Mark: Yeah it can all be overcome.
Becky: It can be, it can all be, you know, overcome really.
Mark: But like ask these health professionals, because they are there for support. And don’t be afraid, however stupid the question is.
Becky: Any stupid question, some of the questions I’ve asked.
Mark: Write it down, you know.
Becky: Was just thinking, but I thought, no, if that’s…
Mark: But he didn’t think they were silly, were they?
Becky: Definitely not.
Mark: He was, you know, very good, you know.
Becky: Yeah.
Mark: “Please just ask.”
Becky: Yeah.
Mark: And keep annoying them. Because we do, we ring up with any question at all, don’t we?
Becky: Yeah and sometimes sort of, you know, I know with the CLAPA website they’ve got things like parent contacts information if you... I didn’t personally use that but, you know, for some people that might be useful. But, you know, sort of or even speaking to people, you know, like the local team can put you in contact with people.
And you know, the nurse, seeing photographs before and after, or speaking to families like say with the feeding concerns, different things like that, you know, probably families who have experienced it, they’ve been there, and they probably have come up with a, you know, a solution and you know, it’s to gather that information sometimes, isn’t it?
Mark: Yeah definitely.
Great OK. And, sorry, just to go back to the written side of information.
Becky: Yeah.
What kind of written information would you like to see at that point of diagnosis?
Becky: I just, I think it was just like perhaps a simple leaflet would have been helpful. Because like once we first had the diagnosis, it’s like sort of because I think sometimes at that particular stage, all according, you could be perhaps a bit too overwhelmed with too much information. But just something simple about like, you know, should you need to contact somebody, like perhaps a website with some, you know, information on which is like recommended, somebody to contact. Or like sort of some of the most common questions, just like sort of on the leaflet, which is something quite basic. You know, you’ve had a diagnosis, what is it you know, what can be done about it? And just basic stuff at that stage I think would be useful.
Mark: But also I think visual pictures as well.
Becky: Yeah, yeah I think
Mark: Because the pictures were the best thing, because the hours we spent looking at before and after photos…
Becky: Yeah I, when we had…
Mark: …trying to make comparisons to what we were having.
Some of the younger adults we spoke with had received good information and support from other people born with clefts they had met through ‘CLAPA Edge’. CLAPA Edge is the Cleft Lip and Palate Association’s organisation for young people who were born with cleft lip and/or palate and incorporates a youth council for the discussion of cleft care. The ‘Adult Voices ‘ network provides a forum for adults born with cleft to discuss issues of living with the condition and accessing treatment as an adult. Adult Voices is associated with the CLAPA Facebook pages.
Maybe you could summarise your experience of being born with a cleft lip and palate?
Yeah... so the first experiences I remember of it are being bullied because of it. But then I moved schools and... had more operations and so it started to improve. And then I started... to not really care about it anymore. And then through more treatment... I’m at where I am today, and it’s a positive experience now.
And what advice would you have for other young people who are born with a cleft lip or palate?
To not like let people get to them, to like not listen to the bullying and try and get it sorted as soon as possible. And then just be positive, because it makes them unique, and so it’s a good thing, not something to be ashamed about, so yeah.
OK thanks. And you mentioned earlier that you’ve been involved with CLAPA again recently, can you perhaps explain what’s brought you back into that, into that world, and what you’ve given to the organisation?
Yes well it’s just like we were waiting for a normal orthodontic appointment, and I saw a flier for the CLAPA football weekend, and then I went on that, and then I found out more information about the youth council, and then I went on that. And then I became too old for the youth council, so I am now a volunteer for CLAPA, so I helped out on residential weekends or part of the like... sorting out money, so wherever they need help really.
So some of it is practical help and some of it is more, would you say more emotional?
Yeah.
You know, do you have contact with other people with clefts and?
Yeah like there’s loads of like different meetings, and you meet new people, and you hear their experiences, so it can help some people, yeah.
A lot of people don’t know a lot of people with clefts.
OK yeah.
In terms of you might have a good support network from your friends and your family but... if they don’t... completely understand it’s quite good to be able to talk to somebody else. And I think... being able to... to get in touch with other people with cleft, whether it be over email or if you’re close enough to like meet up, that’s definitely important.
So like a buddy scheme or something?
Yeah like and it’s just, especially when you’re younger and, you know, things like treatments have been mentioned, obviously to like cleft teams and... other professionals involved in your treatment that is every day to them; that is what they do. They deal with, they deal with so many patients and their treatments will be similar so... but to you, that treatment, you’ve, you’ve never had it before, you don’t know what to expect, so it can be quite daunting for somebody.
Yeah.
And not knowing what to expect or and it’s kind of hard to remember that people, you know, it’s their job to talk about it, that you kind of need to be able to talk to somebody as well. ...Like it would have been good with someone who had been through it, and you’re able to get in touch with them and like ask any questions.
Sure.
And they can answer you from someone who has been through it, rather than just a professional saying, you know, what their thoughts are. Someone who has actually been through it, it kind of gives you a bit of a... makes you feel a wee bit more comfortable about it.
OK thanks. So where have you gone for information yourself over the years? Do you use the internet for information?
Yeah I
And what do you think of the quality of the information?
Yeah I think it’s... there could possibly be more patient opinions out there, more views from people with cleft, even if it’s just people asking, not so much even if it’s just the information up there from patients, people able to ask questions. It would be quite good if there was something more accessible online in terms of asking questions, and someone who had had the same treatment or, yeah, the same treatment be able to get back to you and answer your questions. Rather than it just being ...because a lot of the information that’s out there is just what a cleft is, these are the potential surgeries that people will need to go through, but there’s not actually a lot of ‘this is what it’s actually like to have this treatment’ or... which I think would be quite beneficial to a lot of people. It would probably put a lot of people at ease a wee bit more.
Yeah I understand, yeah.
Yeah but I know there’s like ... there is a lot of information out there, and there are quite a lot of social interactions out there as well, but it would be quite good if it could just be widened a wee bit.
Widened yeah?
Yeah.
OK and is there a group, a CLAPA group for young people or?
I know there’s a CLAPA website aimed at the younger people, CLAPA Edge, I think.
CLAPA Edge?
Yeah.
I’d say my main bit of advice, if I was going to give anyone advice, is try not to... let what other people say get to you.
Just... I’d almost say surround yourself with positive people and if anyone sort of is negative or says things or... affects you in any way, just... don’t let them bother you; ignore them.
I think just because you’ve got a cleft lip and palate, it doesn’t make you different or it shouldn’t; you’re the same as everyone else, it shouldn’t matter at all. I think it’s one of the most... regrettable things I did was letting someone make me think that because I looked different I should be treated different and... should allow myself to be bullied. And... now I think about it, I think it’s quite a... silly thing to let myself think.
It’s easy to say that in hindsight, yeah.
Yeah I mean people said it to me at the time but sort of... you don’t know. But... now, now I think about it, it is really true.
Last reviewed June 2017.
Natalie’s son was born with cleft lip and palate but through having good experiences at school and socially he has developed a strong identity.
Natalie’s son was born with cleft lip and palate but through having good experiences at school and socially he has developed a strong identity.
SHOW TEXT VERSION
PRINT TRANSCRIPT
Is he aware of any other children with a cleft at all?
Interestingly there’s a lad that’s just come to his school that has got a cleft, that we’ve met before.
Yeah OK.
But apart from that, no. And he’s a bit resistant now to come to any of the events that I get involved with. He just, it’s not cool anymore. But I wouldn’t push him.
You’d say he’s fine with his own identity then?
Yeah, oh yeah, yeah, yeah, yeah and…
Not, not needing to…
No not need, well, you know, I think…
Not needing to be part of…
No, any kind of…
…of a, yeah, of a group?
Yeah but I think he, I think he knows, hopefully, through what I do and get involved with, that, you know, he’s not on his own.
Yeah.
He’s not some kind of, well I don’t want to use the word “freak” because that’s awful, but he’s not that kind of, he isn’t on his own with what he’s got as a condition and what he’s been through and what he might have to... he knows that, I think, because of what I talk about and what I do with the, with CLAPA and the branch. And, you know, we have Christmas parties, we have summer parties, he doesn’t want to come to them anymore, and that’s fine, I’m not going to push him. But he knows that... there are loads of other kids out there like him. I’d like to think he does, hope I’m not putting [laughs] words into his mouth, or thinking things that he’s not thinking. But, you know, you kind of sometimes do that as a parent. But I’ve tried really hard to... to make him… feel... like it’s just something he can talk about, or hopefully accepts what it is, and that it’s no big thing really, you know. And so yeah, no, thankfully, God, he hasn’t had, I really hope he doesn’t at any point, he hasn’t had any bullying.
Matt’s daughter was born with a cleft palate and being able to share experiences with other people through direct contact and social media made things easier for the family.
Matt’s daughter was born with a cleft palate and being able to share experiences with other people through direct contact and social media made things easier for the family.
Sex: Male
SHOW TEXT VERSION
PRINT TRANSCRIPT
OK.
Just yeah going on Facebook and sort of hooking up with other mums and... things like that. But that’s been pretty much her... her domain really.
Yeah so was this kind of a positive aspect of what you’ve been going through?
Yeah I think so. I mean and, and also hearing, obviously, my wife, we chat and stuff, and she relays what she’s learnt from other people, what they’re going through and stuff. And so it’s just, yeah, I would say it’s very positive. I mean I think that’s a big thing, I mean in society, where we should, when sort of people are going through things, actually you share with one another what’s going on, and encourage one another and say, “Look, hey you’re not in it by yourself, we’re going, we’re going through it as well.” And, and because you do think you’re very, oh you’re thinking, “Oh no, it’s only us, why has it happened to us?” all this kind of stuff. And you always have these questions.
Sure.
And it’s when you can say, “Look, it’s not just us, it’s, we, there’s another family there, there’s another family there,” and, and then you can chat to them and encourage them. And, as I say, my wife still contacts this little family who’ve had a little boy who had the cleft palate.
Yeah.
And it actually perhaps sparks up friendships as well which you wouldn’t necessarily have had. And just, yeah, just encouraging one another really, but yeah.
OK great. So is there any advice you would give to other families or health professionals at all, in the way people communicate about cleft lip and palate?
I would say... just, yeah, just be honest and about how you’re feeling. Because I think it’s the worst thing to kind of shut up your feelings and sort of think, “Oh it’s, it’s,” you know, saying it’s all OK and you’re fine with it. And ask questions as well when you’re seeing particular specialists and the cleft nurse team.
Andy and Diane encourage parents to look at UK based information from reliable sources such as CLAPA. They also question the information given through the NHS and how it is delivered.
Andy and Diane encourage parents to look at UK based information from reliable sources such as CLAPA. They also question the information given through the NHS and how it is delivered.
SHOW TEXT VERSION
PRINT TRANSCRIPT
Andy: Official sites.
Diane: Official websites, like the CLAPA website or the hospital has got their dedicated website. Or to speak to a cleft team and see if they can put you in contact with a family who has gone through it, because I think that’s the best
Andy: I certainly think so, yeah.
Diane: The best route to go down: somebody who has been through it, or to read stories on the CLAPA website of people that, you know, their stories. Rather than just go ploughing on Google and finding, oh, all sorts of negative, I think.
Andy: I think that’s what it boils down to, because there was a lot of stuff from like America with the stories and things like that…
Diane: Which are very different.
Andy: And it’s different levels of care and different systems. And you can’t kind of…
Diane: Yeah, just to be careful I think.
Andy: You know, you can’t compare that, you know, because they haven’t got an NHS over there. And like I said, there’s different levels all over the place; it’s kind of, yeah. I certainly think that, from my perspective is... to deal with this kind of message as well then, you know, some NHS departments maybe need to re-look at how they deliver the messages and what support is available when they do deliver them at the time, you know, and that help and support. Because, certainly from our perspective, and I think from somebody else as well that we know as well, it was pretty much... delivered.
Diane: Quite abrupt yeah.
Andy: That kind of way as well. So I think, you know, I think they need to be aware about what can happen and how you can deal with it.
Becky and Mark say that looking for information on the internet can be misleading and advise looking at recognised sites such as CLAPA. They also advise to look at ‘before and after’ images of babies that have had cleft surgery.
Becky and Mark say that looking for information on the internet can be misleading and advise looking at recognised sites such as CLAPA. They also advise to look at ‘before and after’ images of babies that have had cleft surgery.
SHOW TEXT VERSION
PRINT TRANSCRIPT
Becky: Yeah, yeah.
Mark: You know, and it’s it was nice there. But obviously just go into sites which are recommended, not sites which are just made up by people, because they can be quite negative.
Becky: Yeah, yeah. And my advice would be just to go with your emotions, if you’re feeling, you know, to go through like, you know, you probably when, if you have a diagnosis, is to go with those feelings. You know, sometimes you know, that shock, that loss, just to let it, you know, just to, to come over you and just and deal with that. And even if you’re having, you know, really negative thoughts, I think you’ve got to go there sometimes.
Mark: Yeah you have to.
Becky: You know, if you’re feeling angry, to go there. Because I think, you know, it’ll come out in other ways otherwise. But just to recognise, “Yeah, I’m feeling like this,” but at the end of the day, you know, from, you know, it’s not a major thing, it can be sorted. And, you know, to write things down if you’re not sure about anything. But it’s not, it’s really not such a big deal. You know, from the initial diagnosis you think, “Oh my goodness,” you want your child to be... sort of normal or perfect, but what is, but it’s stuff that can be dealt with. And it’s, I think from…
Mark: Yeah it can all be overcome.
Becky: It can be, it can all be, you know, overcome really.
Mark: But like ask these health professionals, because they are there for support. And don’t be afraid, however stupid the question is.
Becky: Any stupid question, some of the questions I’ve asked.
Mark: Write it down, you know.
Becky: Was just thinking, but I thought, no, if that’s…
Mark: But he didn’t think they were silly, were they?
Becky: Definitely not.
Mark: He was, you know, very good, you know.
Becky: Yeah.
Mark: “Please just ask.”
Becky: Yeah.
Mark: And keep annoying them. Because we do, we ring up with any question at all, don’t we?
Becky: Yeah and sometimes sort of, you know, I know with the CLAPA website they’ve got things like parent contacts information if you... I didn’t personally use that but, you know, for some people that might be useful. But, you know, sort of or even speaking to people, you know, like the local team can put you in contact with people.
And you know, the nurse, seeing photographs before and after, or speaking to families like say with the feeding concerns, different things like that, you know, probably families who have experienced it, they’ve been there, and they probably have come up with a, you know, a solution and you know, it’s to gather that information sometimes, isn’t it?
Mark: Yeah definitely.
Great OK. And, sorry, just to go back to the written side of information.
Becky: Yeah.
What kind of written information would you like to see at that point of diagnosis?
Becky: I just, I think it was just like perhaps a simple leaflet would have been helpful. Because like once we first had the diagnosis, it’s like sort of because I think sometimes at that particular stage, all according, you could be perhaps a bit too overwhelmed with too much information. But just something simple about like, you know, should you need to contact somebody, like perhaps a website with some, you know, information on which is like recommended, somebody to contact. Or like sort of some of the most common questions, just like sort of on the leaflet, which is something quite basic. You know, you’ve had a diagnosis, what is it you know, what can be done about it? And just basic stuff at that stage I think would be useful.
Mark: But also I think visual pictures as well.
Becky: Yeah, yeah I think
Mark: Because the pictures were the best thing, because the hours we spent looking at before and after photos…
Becky: Yeah I, when we had…
Mark: …trying to make comparisons to what we were having.
Alex was born with a cleft lip and palate and experienced bullying when she was younger. Her experience has been more positive as an adult and has volunteered to work with the CLAPA Youth Council (CLAPA Edge).
Alex was born with a cleft lip and palate and experienced bullying when she was younger. Her experience has been more positive as an adult and has volunteered to work with the CLAPA Youth Council (CLAPA Edge).
SHOW TEXT VERSION
PRINT TRANSCRIPT
Yeah... so the first experiences I remember of it are being bullied because of it. But then I moved schools and... had more operations and so it started to improve. And then I started... to not really care about it anymore. And then through more treatment... I’m at where I am today, and it’s a positive experience now.
And what advice would you have for other young people who are born with a cleft lip or palate?
To not like let people get to them, to like not listen to the bullying and try and get it sorted as soon as possible. And then just be positive, because it makes them unique, and so it’s a good thing, not something to be ashamed about, so yeah.
OK thanks. And you mentioned earlier that you’ve been involved with CLAPA again recently, can you perhaps explain what’s brought you back into that, into that world, and what you’ve given to the organisation?
Yes well it’s just like we were waiting for a normal orthodontic appointment, and I saw a flier for the CLAPA football weekend, and then I went on that, and then I found out more information about the youth council, and then I went on that. And then I became too old for the youth council, so I am now a volunteer for CLAPA, so I helped out on residential weekends or part of the like... sorting out money, so wherever they need help really.
So some of it is practical help and some of it is more, would you say more emotional?
Yeah.
You know, do you have contact with other people with clefts and?
Yeah like there’s loads of like different meetings, and you meet new people, and you hear their experiences, so it can help some people, yeah.
Iona suggests that there could be an online service which enable people born with clefts to communicate with others who have had similar treatment to themselves.
Iona suggests that there could be an online service which enable people born with clefts to communicate with others who have had similar treatment to themselves.
SHOW TEXT VERSION
PRINT TRANSCRIPT
OK yeah.
In terms of you might have a good support network from your friends and your family but... if they don’t... completely understand it’s quite good to be able to talk to somebody else. And I think... being able to... to get in touch with other people with cleft, whether it be over email or if you’re close enough to like meet up, that’s definitely important.
So like a buddy scheme or something?
Yeah like and it’s just, especially when you’re younger and, you know, things like treatments have been mentioned, obviously to like cleft teams and... other professionals involved in your treatment that is every day to them; that is what they do. They deal with, they deal with so many patients and their treatments will be similar so... but to you, that treatment, you’ve, you’ve never had it before, you don’t know what to expect, so it can be quite daunting for somebody.
Yeah.
And not knowing what to expect or and it’s kind of hard to remember that people, you know, it’s their job to talk about it, that you kind of need to be able to talk to somebody as well. ...Like it would have been good with someone who had been through it, and you’re able to get in touch with them and like ask any questions.
Sure.
And they can answer you from someone who has been through it, rather than just a professional saying, you know, what their thoughts are. Someone who has actually been through it, it kind of gives you a bit of a... makes you feel a wee bit more comfortable about it.
OK thanks. So where have you gone for information yourself over the years? Do you use the internet for information?
Yeah I
And what do you think of the quality of the information?
Yeah I think it’s... there could possibly be more patient opinions out there, more views from people with cleft, even if it’s just people asking, not so much even if it’s just the information up there from patients, people able to ask questions. It would be quite good if there was something more accessible online in terms of asking questions, and someone who had had the same treatment or, yeah, the same treatment be able to get back to you and answer your questions. Rather than it just being ...because a lot of the information that’s out there is just what a cleft is, these are the potential surgeries that people will need to go through, but there’s not actually a lot of ‘this is what it’s actually like to have this treatment’ or... which I think would be quite beneficial to a lot of people. It would probably put a lot of people at ease a wee bit more.
Yeah I understand, yeah.
Yeah but I know there’s like ... there is a lot of information out there, and there are quite a lot of social interactions out there as well, but it would be quite good if it could just be widened a wee bit.
Widened yeah?
Yeah.
OK and is there a group, a CLAPA group for young people or?
I know there’s a CLAPA website aimed at the younger people, CLAPA Edge, I think.
CLAPA Edge?
Yeah.
Elliott was bullied when he was younger and regrets that he let it happen to him. His advice is to surround yourself with positive people.
Elliott was bullied when he was younger and regrets that he let it happen to him. His advice is to surround yourself with positive people.
SHOW TEXT VERSION
PRINT TRANSCRIPT
Just... I’d almost say surround yourself with positive people and if anyone sort of is negative or says things or... affects you in any way, just... don’t let them bother you; ignore them.
I think just because you’ve got a cleft lip and palate, it doesn’t make you different or it shouldn’t; you’re the same as everyone else, it shouldn’t matter at all. I think it’s one of the most... regrettable things I did was letting someone make me think that because I looked different I should be treated different and... should allow myself to be bullied. And... now I think about it, I think it’s quite a... silly thing to let myself think.
It’s easy to say that in hindsight, yeah.
Yeah I mean people said it to me at the time but sort of... you don’t know. But... now, now I think about it, it is really true.
Copyright © 2024 University of Oxford. All rights reserved.