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Aidan Greene: ‘I never wanted to be a stammering advocate but by being a stand-up comedian I've inadvertently become one'

Aidan Greene: ‘I never wanted to be a stammering advocate but by being a stand-up comedian I've inadvertently become one'

Irish Times3 days ago
Aidan Greene choose to
study
software engineering because he thought he wouldn't have to speak to people so much in this kind of work. 'But, of course, as with any other job, you have to collaborate and interact with other people,' says the 35-year-old
Cavan
man.
His choice of career was influenced by the fact that, at the age of four, he developed a stammer and struggled with the fear of speaking to people – particularly during his teenage years – in case he stammered.
'I used to joke that I developed my stammer when my family moved from
Northern Ireland
to the South but we only moved a mile down the road over the border from
Fermanagh
to Cavan,' says Greene, who does stand-up comedy based around his experiences of stammering.
'I never wanted to be a stammering advocate, but, by being a stand-up comedian, I've inadvertently become one because I'm open and confident about being dysfluent as part of my comedy.'
READ MORE
Greene recently spoke at the launch of the position paper on stammering from the Irish Association of Speech and Language Therapists (IASLT). Dr Mary Dwyer, speech and language therapy manager at HSE Kerry, is one of the lead authors of that paper. 'We support the rights of people who stammer to experience living without discrimination and without the expectation to conform to a norm of fluency. But we also acknowledge their right to seek increased fluency as and how they wish to do so,' says Dwyer.
About one in 20 young children stammer, but many grow out of it during their childhood. About one in 100 adults stammer openly or hide their stammer.
Greene says his mother brought him along for all kinds of treatments to help reduce his stuttering. 'At the time, it felt normal to go for these treatments, but, in hindsight, they fed into the shame. By insinuating that it's a problem to be fixed makes you think subconsciously that you are broken,' he explains.
He says he gets annoyed when people say that they had a stammer as a child and they fixed it. 'Because, statistically, many people grow out of it. I've got coeliac disease and ADHD as well, but neither of these would have made me cry at school – but stammering did.'
He tells the story about how in an effort to not treat him any differently to his classmates, his English teacher had him take his turn to read aloud during class. But, Greene's passage contained mentions of Hepzibah, one of the central characters from the Junior Certificate book Carrie's War. Hepzibah was a word he really struggled to say.
Eventually, his teacher said he didn't have to read aloud any more. 'He tried to treat me like everyone else and when it didn't work, he treated me completely differently. It would have been easier if he had asked me, 'Are you okay to read aloud'?'
As a teenager, Greene also followed the Maguire Programme, an internationally recognised coaching programme to help people overcome stuttering. 'I was probably too young to stick with the discipline of it. It's about pausing, taking a deep breath before you speak and if you start to stutter, releasing the air and starting again,' he explains.
He says the Maguire programme helped him to be relatively fluent, when fluency was his goal. But, at a certain point, he decided to embrace his stammering instead.
'A lot of my shame was built around how I thought other people perceived me. The stammering character in films is always the one to be laughed at or felt sorry for, so everything changed for me when I started to do stand-up comedy.'
While acknowledging that stand-up comedy won't work for everyone with a stammer, he says the fact that some people told him he would never be able to be a stand-up comedian actually spurred him on. 'I can't say, do what I do just because it worked for me. But you just need to learn that nobody cares about your stammer as much as you do. I hope that's a freeing thought. You have to let go of the shame around stammering. That's what held me back.'
It's such a cocky thing to think you know what someone is going to say next

Aidan Greene
Looking back on his childhood, he said that he loved to talk and was fed up feeling bad about stammering. 'I was naturally a chatterbox as a child. But I had allowed stammering to dominate my life. I was going into my final year at college when I did my first stand-up. Speaking in public was my way of giving the middle finger to the thing I used to fear.'
Greene now incorporates much of his early experience of stammering and the different ways he tried to overcome it into his comedy sketches. 'I don't ever intentionally stammer to trick the audience into thinking I'm stammering and I don't ever make fun of stammering but I make fun out of people's reactions to my stammering.'
He gets annoyed when people stammer intentionally at the end of his performances, thinking they are funny by saying 'that was vvvvery gggggood'.
[
'Finishing their sentences isn't helpful': How to talk to someone who stammers
Opens in new window
]
He also dislikes when people offer him advice. 'People say things like 'if I ever trip over my words, I breathe and relax'. And he hates when people try to finish his sentence for him. 'It's such a cocky thing to think you know what someone is going to say next. I'll change what I'm going to say if someone tries to finish my sentence for me.'
Really, he says, 'it's about treating other people as human beings and not thinking you know more about their disability than they do.'
Greene also suggests that public figures who stammer offer other stammerers lifelines when they speak in public about it. 'I think Joe Biden missed an opportunity to be a stammering advocate. I know he had lots of other important work to do but anytime he stammered, it was seen as a sign of his cognitive decline. Why didn't he own it and have some pride in it? That way he could have controlled the narrative a bit.'
[
Stammering: It's just a different way of talking
Opens in new window
]
Greene's latest project is a 14-minute film, Stutterbug, in which he stars alongside David Peter Meads, known professionally as Scroobius Pip. The latter is an English actor, podcaster and former spoken-word and hip hop recording artist who is also a stammerer. 'It's not ideal. But it's allowed me to become more comfortable with myself. It's just how I talk,' says Scroobius Pip in one of his many videos for
STAMMA
, the British Stammering Association.
The film, Stutterbug – which Greene is currently pitching at film festivals, is about how a stammering man's attempts to hide his stammer, results in him insulting sick children and ruining his chances with his college crush.
'My main hope with Stutterbug is that it will give other people who stutter the authentic representation they've never had. For people who don't stutter, I hope it will give them a chance to laugh with, and not at, people who do stutter,' says Greene.
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Aidan Greene: ‘I never wanted to be a stammering advocate but by being a stand-up comedian I've inadvertently become one'
Aidan Greene: ‘I never wanted to be a stammering advocate but by being a stand-up comedian I've inadvertently become one'

Irish Times

time3 days ago

  • Irish Times

Aidan Greene: ‘I never wanted to be a stammering advocate but by being a stand-up comedian I've inadvertently become one'

Aidan Greene choose to study software engineering because he thought he wouldn't have to speak to people so much in this kind of work. 'But, of course, as with any other job, you have to collaborate and interact with other people,' says the 35-year-old Cavan man. His choice of career was influenced by the fact that, at the age of four, he developed a stammer and struggled with the fear of speaking to people – particularly during his teenage years – in case he stammered. 'I used to joke that I developed my stammer when my family moved from Northern Ireland to the South but we only moved a mile down the road over the border from Fermanagh to Cavan,' says Greene, who does stand-up comedy based around his experiences of stammering. 'I never wanted to be a stammering advocate, but, by being a stand-up comedian, I've inadvertently become one because I'm open and confident about being dysfluent as part of my comedy.' READ MORE Greene recently spoke at the launch of the position paper on stammering from the Irish Association of Speech and Language Therapists (IASLT). Dr Mary Dwyer, speech and language therapy manager at HSE Kerry, is one of the lead authors of that paper. 'We support the rights of people who stammer to experience living without discrimination and without the expectation to conform to a norm of fluency. But we also acknowledge their right to seek increased fluency as and how they wish to do so,' says Dwyer. About one in 20 young children stammer, but many grow out of it during their childhood. About one in 100 adults stammer openly or hide their stammer. Greene says his mother brought him along for all kinds of treatments to help reduce his stuttering. 'At the time, it felt normal to go for these treatments, but, in hindsight, they fed into the shame. By insinuating that it's a problem to be fixed makes you think subconsciously that you are broken,' he explains. He says he gets annoyed when people say that they had a stammer as a child and they fixed it. 'Because, statistically, many people grow out of it. I've got coeliac disease and ADHD as well, but neither of these would have made me cry at school – but stammering did.' He tells the story about how in an effort to not treat him any differently to his classmates, his English teacher had him take his turn to read aloud during class. But, Greene's passage contained mentions of Hepzibah, one of the central characters from the Junior Certificate book Carrie's War. Hepzibah was a word he really struggled to say. Eventually, his teacher said he didn't have to read aloud any more. 'He tried to treat me like everyone else and when it didn't work, he treated me completely differently. It would have been easier if he had asked me, 'Are you okay to read aloud'?' As a teenager, Greene also followed the Maguire Programme, an internationally recognised coaching programme to help people overcome stuttering. 'I was probably too young to stick with the discipline of it. It's about pausing, taking a deep breath before you speak and if you start to stutter, releasing the air and starting again,' he explains. He says the Maguire programme helped him to be relatively fluent, when fluency was his goal. But, at a certain point, he decided to embrace his stammering instead. 'A lot of my shame was built around how I thought other people perceived me. The stammering character in films is always the one to be laughed at or felt sorry for, so everything changed for me when I started to do stand-up comedy.' While acknowledging that stand-up comedy won't work for everyone with a stammer, he says the fact that some people told him he would never be able to be a stand-up comedian actually spurred him on. 'I can't say, do what I do just because it worked for me. But you just need to learn that nobody cares about your stammer as much as you do. I hope that's a freeing thought. You have to let go of the shame around stammering. That's what held me back.' It's such a cocky thing to think you know what someone is going to say next — Aidan Greene Looking back on his childhood, he said that he loved to talk and was fed up feeling bad about stammering. 'I was naturally a chatterbox as a child. But I had allowed stammering to dominate my life. I was going into my final year at college when I did my first stand-up. Speaking in public was my way of giving the middle finger to the thing I used to fear.' Greene now incorporates much of his early experience of stammering and the different ways he tried to overcome it into his comedy sketches. 'I don't ever intentionally stammer to trick the audience into thinking I'm stammering and I don't ever make fun of stammering but I make fun out of people's reactions to my stammering.' He gets annoyed when people stammer intentionally at the end of his performances, thinking they are funny by saying 'that was vvvvery gggggood'. [ 'Finishing their sentences isn't helpful': How to talk to someone who stammers Opens in new window ] He also dislikes when people offer him advice. 'People say things like 'if I ever trip over my words, I breathe and relax'. And he hates when people try to finish his sentence for him. 'It's such a cocky thing to think you know what someone is going to say next. I'll change what I'm going to say if someone tries to finish my sentence for me.' Really, he says, 'it's about treating other people as human beings and not thinking you know more about their disability than they do.' Greene also suggests that public figures who stammer offer other stammerers lifelines when they speak in public about it. 'I think Joe Biden missed an opportunity to be a stammering advocate. I know he had lots of other important work to do but anytime he stammered, it was seen as a sign of his cognitive decline. Why didn't he own it and have some pride in it? That way he could have controlled the narrative a bit.' [ Stammering: It's just a different way of talking Opens in new window ] Greene's latest project is a 14-minute film, Stutterbug, in which he stars alongside David Peter Meads, known professionally as Scroobius Pip. The latter is an English actor, podcaster and former spoken-word and hip hop recording artist who is also a stammerer. 'It's not ideal. But it's allowed me to become more comfortable with myself. It's just how I talk,' says Scroobius Pip in one of his many videos for STAMMA , the British Stammering Association. The film, Stutterbug – which Greene is currently pitching at film festivals, is about how a stammering man's attempts to hide his stammer, results in him insulting sick children and ruining his chances with his college crush. 'My main hope with Stutterbug is that it will give other people who stutter the authentic representation they've never had. For people who don't stutter, I hope it will give them a chance to laugh with, and not at, people who do stutter,' says Greene.

Fermanagh farmer convicted over animals in 'poor condition'
Fermanagh farmer convicted over animals in 'poor condition'

Agriland

time06-08-2025

  • Agriland

Fermanagh farmer convicted over animals in 'poor condition'

A Co. Fermanagh farmer has been convicted in court over the condition of animals on his farm. 78-year-old Wesley Lee of Cleenish Road, Cleenish, Bellanaleck, Enniskillen was today (Wednesday, August 6) convicted at Enniskillen Court on two charges under the Welfare of Animals Act (Northern Ireland) 2011 and one under the Veterinary Medicines Regulations 2013. Lee was convicted on: Two charges of failure to ensure the needs of animals were met; One charge of failure to produce a medicine record when required. The farmer was convicted and fined £600 plus £15 offender levy and £72 summons fee. The case arose following numerous welfare inspections carried out by Department of Agriculture, Environment and Rural Affairs (DAERA) Veterinary Service officials between April 13, 2023 and September 4, 2023. During these inspections, one sheep was found to be caught on briars and was euthanised by a DAERA veterinary officer as, in their opinion, it was suffering unnecessarily. There were a number of lame animals and animals in poor condition on the premises being kept in dirty conditions without access to clean drinking water. There was no evidence of suitable pens for calving or suitable isolation pens for sick or injured animals and young calves had no access to dry lying areas. During one of the inspections, one of the sick animals died. Lee was asked to provide medicine records to demonstrate treatment of the lame and sick animals seen, but was unable to provide such. DAERA has stated that it gives high priority to the welfare of animals and operates a vigorous enforcement policy to ensure full compliance of regulatory requirements. Any breaches are investigated thoroughly and offenders prosecuted as necessary, it added. The improper use of medicines in animals presents a risk to human health, DAERA has stressed. This is of particular relevance when it comes to observing withdrawal times of medicines administered to animals which are subsequently slaughtered for human consumption. The main areas for concern are: The slaughter for human consumption of an animal before the recommended withdrawal period has been observed for drugs which may themselves have direct side effects in humans; The slaughter of animals entering the food chain containing a drug to which human pathogens are capable of developing a resistance which may reduce the effectiveness with which human diseases can be controlled by a drug. If proper medicine records are not kept, there is a risk of animals which have been treated, but whose withdrawal periods have not been observed, being slaughtered for human consumption, or sold on to another herd from which they will be slaughtered for human consumption without withdrawal times being observed.

Family in shock: ‘We found out from a WhatsApp that my mother had died by assisted suicide'
Family in shock: ‘We found out from a WhatsApp that my mother had died by assisted suicide'

Sunday World

time06-08-2025

  • Sunday World

Family in shock: ‘We found out from a WhatsApp that my mother had died by assisted suicide'

Swiss clinic criticised by family of Cavan woman (58) with history of mental illness after they were left in dark over her death plan Or at least that is what her family have been told. None of them were with the 58-year-old as she slipped away at a clinic in Switzerland. In fact, news of Ms Slough's death reached her daughter, Megan Royal, back in Dublin by WhatsApp. Ms Royal was horrified to be informed that her mother's ashes would be posted to her. Now the family of the Cavan-based woman, who had a long history of mental illness and had tried to take her own life last year, want to know how somebody's life could be ended in such a manner. Maureen Slough Ms Slough travelled to the ­Pegasos clinic in Switzerland less than a month ago, on July 8, having told her family she was going to Lithuania with a friend. Her family became suspicious and contacted her. They say she promised to return. But Ms Royal and Ms Slough's partner, Mick Lynch, would later receive a message from a volunteer for the ­Pegasos group to inform them of her death. The family immediately set about trying to find out why they were not informed by the clinic in advance, and also questioned if Ms Slough's history of mental illness was assessed by the clinic first. The Pegasos group has said in response to questions from family and friends of Ms Slough, that it received a letter from Ms Slough's daughter Megan saying she was aware of her mother's wishes and accepted them. It also says it verified the letter through an email response to Ms Royal using an email address supplied by Ms Slough. Ms Royal has said she never wrote such a letter or verified any contact from Pegasos, and now her family think Ms Slough may have forged the 'letter' and verified it using an email address she created herself. Maureen Slough with her daughter Megan News in 90 Seconds - August 6th Pegasos was asked further questions by the Irish Independent as to why it did not ring Ms Royal, and whether it sought a mental health history for Ms Slough before her death. The Pegasos group responded that Ms Slough went through an extensive assessment process leading up to her death, including an independent psychiatric evaluation confirming she was of sound mind. Her brother Philip, a UK solicitor, has now written to the Foreign, Commonwealth and Development Office in the UK, asking it to investigate the matter with Swiss authorities. In his letter, he said Pegasos did not rigorously follow its own policy to inform a family. He said while he understands Ms Slough represented to the clinic that this had been done by the letter purportedly written by Ms Royal, the clinic only sought ­confirmation through an email provided by Ms Slough. 'I am working on the assumption that my sister created this email and the clinic's procedures were woefully inadequate in verification,' he wrote. 'The Pegasos clinic has faced numerous criticisms in the UK for their practices with British nationals' 'It appears my sister provided ­Pegasos with letters of complaint to medical authorities in Éire in respect of bogus medical conditions, and that these documents were considered by Pegasos in support of her application. 'While I understand that Swiss law permits assisted dying, the Pegasos clinic has faced numerous criticisms in the UK for their practices with British nationals, and the circumstances in which my sister took her life are highly questionable.' In March, the BBC ran a report saying the Pegasos clinic allegedly helped a Welsh woman named Anne (51) end her life in January without informing her family, despite promising to change its practices following a previous case. It said that under similar circumstances, Alistair Hamilton (47) died in 2023, and the Pegasos clinic reportedly promised last year that it would always contact a person's family before carrying out an assisted death. However, Anne, whose death was first reported by ITV News, allegedly died without her family being informed. The BBC reported that Pegasos said it had attempted to phone and text Anne's brother John, but he insisted he had received no communication from the group. Dyfed-Powys Police in Wales told the BBC it is investigating her death. The Pegasos building Anne's family learnt of her intention to die only after goodbye letters ­posted to them from Switzerland arrived. Ms Royal and Ms Slough's partner, Mr Lynch, received a similar card, handwritten by her mother, in recent weeks. The grieving daughter said her mother had tried to take her own life last year following the deaths of two of her sisters, and was not in her right mind when she made her decision to go to Switzerland. Her latest granddaughter had been born just days earlier. 'They should not have allowed her to make that decision on her own. This group did not contact me, even though my mother had nominated me as next of kin. They waited until afterwards and then told me she had died listening to an Elvis Presley song,' Ms Royal said. She added that her mother had a difficult upbringing, having been brought to Ireland by her own mother and a man she had met while in a mental ­hospital in the UK. She said that despite years of trauma, her mother made a good life for herself and joined the civil service, being promoted to executive officer before retiring last year. Ms Royal said that her mother travelled alone to Switzerland and paid €15,000 to the Pegasos Swiss Association to facilitate her death two days later. 'I was actually talking to her that morning and she was full of life' 'She had told us she was going to Lithuania, but she had confided in two people that she had other plans, and ­after a series of concerned phone calls she said she would come home, but then we got the WhatsApp message to say she had died,' her daughter said. Mr Lynch said: 'I was actually talking to her that morning and she was full of life. She said she was after having her ­breakfast and she was going out to sit in the sun. Maybe she was heading off to that place. I still thought she was coming home.' The Pegasos group said Ms Slough went through an extensive assessment process ­leading up to her death, including an independent psychiatric evaluation confirming she was of sound mind. It said she was consistently forthcoming about her background and history, and provided thorough medical documentation, including from her pain-management consultant. It said she had stated repeatedly that she was in chronic pain that was unbearable to her, despite seeing the pain specialist. Pegasos logo Pegasos added that Ms Slough provided a letter from her daughter Megan, and in the letter she stated in writing that she confirmed she was fully informed regarding her mother's decision, and that she had been made fully aware of her intentions and the nature of the procedure she was seeking. It said Megan stated that she had the opportunity to discuss this matter with her mother and understood the reasons behind the decision, and the implications of her choice. Pegasos said Megan was contacted directly by email to confirm the authenticity of the letter, and that in the email, Megan confirmed that the letter was indeed hers, and that she was sorry she could not accompany her mother to Switzerland, and that she was not happy with her mother's decision but understood that she was in a great deal of pain. The letter and email are disputed by Ms Royal and Ms Slough's family. Friends of Ms Slough have been horrified by the manner of her death, and questioned everything about it, including the manner in which the Swiss group repatriates remains through the parcel post system. 'You get letters in the post, not ­people,' her friend Stephanie Daly said. Ms Slough's ashes have now arrived with her family and funeral arrangements are being made. If you have been affected by the issues raised in this article, you can call Samaritans free on 116123 or email jo@ or call Pieta on freephone 1800 247 247 or text HELP to 51444

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