Podcasts about cystic fibrosis ireland

Today marks 65 Roses Day, the national fundraising and awareness campaign for Cystic Fibrosis Ireland. Joining us is Claire Merrigan from Gorey, whose young son Mason lives with CF. Claire shares what this day means to their family, the challenges they face, and the importance of community support. We also reflect on the origin of the campaign's name — a touching mispronunciation that has come to symbolise hope and resilience.

Alice Ward is a surfer and film maker based in Sligo. Together with João Tudella, she has made a film which has already won several awards. Entitled Salt and part-funded by Cystic Fibrosis Ireland, it aims to spread awareness about living life with her own CF condition, and the positive benefits she derives from spending time in the Atlantic.

Today is 65 Roses Day, which is the National Fundraising Day for Cystic Fibrosis Ireland. On Friday's Morning Focus, Peter O'Connell was joined by Deborah Kett from Crusheen, Deborah is a mother to 21 year old Hannah who is living with cystic fibrosis. Cystic Fibrosis Ireland hope to raise €300,000. Deborah will be at Dunnes Stores in Ennis today as part of the fundraising drive.

The power of the GAA is best seen when the people who are its lifeblood support a cause. The sense of a community united for the greater good is what makes the GAA different and special. On Free State, Joe and Dion talk about how the GAA makes a difference and why it contrasts with the one-way street of fandom in the Premier League. Joe explains the importance of the 65 Roses Day, the Fundraising Day for Cystic Fibrosis Ireland, and the phenomenal work the charity is doing. Joe also explains why his views on Mickey Harte haven't changed despite Derry's success and why Jurgen Klopp wouldn't be a great GAA man.Free State with Joe Brolly and Dion Fanning is a Gold Hat Production in association with SwanMcG.For more on Free State: https://freestatepodcast.com/To get in touch with the podcast: info@freestatepodcast.com Hosted on Acast. See acast.com/privacy for more information.

10am-11am Tentative plans to amalgamate the dioceses of Galway, Tuam, Clonfert, Achonry, Killala and Elphin  Connacht Tribune Headlines  Galway people urged to support Cystic Fibrosis Ireland ahead of 65 Roses Day – Friday, 12th April  Action Tuam Entrepreneur Competition    'Galway Talks' broadcasts every weekday morning from 9am on Galway Bay FM.

Cystic Fibrosis Ireland's annual fundraising day, 65 Roses Day, which is taking place on Friday, April 12th. We speak to a mother who is advocating for her son. Joining Pat on the show was Louise Dowling is Mum to Aaron who has cystic fibrosis (CF). Aaron carries two rare CF gene mutations. This means that Aaron is considered part of the 10% of the CF population who is not eligible for access to life- changing modulator drug therapies. Also joining Louise was Professor Paul McNally is an Associate Professor of Paediatrics in Royal College of Surgeons Ireland (RCSI) in Dublin. He is a consultant in paediatric respiratory medicine and Director of Research and Innovation in Children's Health Ireland.

An Ennis woman whose dog was tragically killed after being startled by fireworks is reminding Halloween revellers of the dangers associated with the day. Following the discharge of a firework near Clíodhnadh Sheedy's family farm on the outskirts of Ennis last Thursday evening, her one-year-old Rottweiler, Bear, became confused and ran out on the road where he was hit by a car and suffered fatal injuries. Under Irish law, possessing unlicensed fireworks, which includes all fireworks except the likes of party poppers and sparklers, carries a fine up €10,000 or can result in five years in prison. Ambassador at Cystic Fibrosis Ireland and Ennis native Chlíonadh Sheedy says regardless of a pet's temperament, they become completely disorientated once they hear fireworks.

51 year old Rory Tallon works with Cystic Fibrosis Ireland as a CF Patient Advocate as part of CFI's member service team. Rory has CF and was recently featured in our Living with cystic fibrosis podcast volunteering  for CF Ireland. In this podcast he's talking about dating someone with CF.   It happens more than people may know and he tells us why as he explains his relationship with former girlfriend, Jean, and losing her to the disease.Rory is married to Sarah and they have two daughters.Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website: https://thebonnellfoundation.orgBonnell Foundation email: thebonnellfoundation@gmail.comThanks to our sponsors:Genentech: https://www.gene.comViatris: https://www.viatris.com/en

Limerick harpist, Siobhan Brady, has broken the Guinness World Record for the highest harp concert after climbing and performing on top on Mount Kilimanjaro to raise funds for Cystic Fibrosis Ireland. She joins Gillian to tell her about the experience. Hosted on Acast. See acast.com/privacy for more information.

Set to break her previous Guinness World Record, Limerick harpist Siobhán Brady is gearing up to perform on the summit of Mount Kilimanjaro. In 2018 she set the Guinness World Record for Highest Harp Concert at Singla Pass, India a height of over 16,000ft. All funds for this performance will go towards Cystic Fibrosis Ireland. Hosted on Acast. See acast.com/privacy for more information.

Today is 65 Roses Day! - A national fundraising day for Cystic Fibrosis Ireland. Cystic fibrosis Patient Ambassador, Aoife Rafter told Ciara this morning on the show about her experience with Cystic Fibrosis.

Today is 65 Roses Day! - A national fundraising day for Cystic Fibrosis Ireland. Cystic fibrosis Patient Ambassador, Aoife Rafter told Ciara this morning on the show about her experience with Cystic Fibrosis.

Listen By:Season 7Season 6Season 5Season 4Season 3Season 2Season 1Podcast Categories:Fertility and pregnancyGuest interviewsInfectious diseaseRespiratory healthSkincareSkincare for babiesMy somewhat political views!Listen By:Season 7Season 6Season 5Season 4Season 3Season 2Season 1Podcast Categories:Fertility and pregnancyGuest interviewsInfectious diseaseRespiratory healthSkincareSkincare for babiesMy somewhat political views!Listen By:Season 7Season 6Season 5Season 4Season 3Season 2Season 1Season 7Season 6Season 5Season 4Season 3Season 2Season 1Podcast CategoriesGuest interviewsFertility and pregnancyInfectious diseaseRespiratory healthSkincareSkincare for babiesMy somewhat political views!John Test PageGuest interviewsFertility and pregnancyInfectious diseaseRespiratory healthSkincareSkincare for babiesMy somewhat political views!John Test PageA WonderCare PodcastReal Lives: Eva's Cystic Fibrosis Journey with Rachel MurrayPlay EpisodePause EpisodeMute/Unmute EpisodeRewind 10 Seconds1xFast Forward 30 seconds00:00/00:52:20SubscribeShareAmazonApple PodcastsGoogle PodcastsSpotifyRSS FeedShareLinkEmbedDownload file | Play in new window | Duration: 00:52:20 | Recorded on 21/09/2022Subscribe: Amazon | Apple Podcasts | Google Podcasts | Spotify Amazon Apple Podcasts Google Podcasts Spotify Real Lives: Eva's Cystic Fibrosis Journey with Rachel MurrayThis week I chat with Rachel Murray as we deep dive into Cystic Fibrosis.  We discuss the impact it has had on their daughter Eva.  We get to know Rachel and hear about her deep joy on the safe arrival of her gorgeous little girl Eva two years ago.Rachel and Jason found out that Eva has Cystic Fibrosis three weeks after her birth.  Rachel explains the process involved and how they coped with their daughter's diagnosis. We hear all about their journey and how they have coped since.  Most importantly we learn that there is hope and Eva's future looks brighter everyday.I discuss the genetic aspect to cystic fibrosis and the medications used in it's treatment.  Rachel explains how important it is that every child that is clinically eligible to benefit from new medications should have access to them.  We have come a long way in Ireland but there is more work to be done.  No family, child or adult living with Cystic Fibrosis should be excluded from a life of possibility.Cystic Fibrosis Ireland is an incredible resource for anyone affected by CF in Ireland.  It contains so much information and up to date advice and I urge every patient and healthcare provider to spend some time checking it out.I am so grateful for hearing all about Eva's Cystic Fibrosis journey with Rachel Murray.  Rachel is a passionate mum who see's the optimism  in medical advancement. Season 2 PartnershipI am so thrilled to be partnering with Salin plus for an entire Season packed with lots of respiratory health information! This 100% natural salt therapy device is suitable for both adults and children!  Tune in to learn more!Support this PodcastSimply following and reviewing this podcast can make a huge difference!  If you enjoy this episode ‘Real Lives: Eva's Cystic Fibrosis Journey with Rachel Murray' I would be so grateful if you could follow or subscribe to the show!I aim to support parents and appreciate every one of you who take the time from your day to learn something new along with me!  We have episodes where I explain medical conditions and offer lots of tips and advice from my perspective as a Pharmacist mum.  We also chat with experts about a whole range of medical and parenting challenges. Of course I can't forget our little voices episodes where I chat with kids and hear things from their point of view!  I'm also extremely grateful to everyone who contributes to a real lives episode – I learn so much from these and am privileged to be able to share your story which will help people who find them in a similar situation in life.You can check out all of my previous episodes by clicking right here!Get Involved!Email Sheena@wonderbaba.ie Sale!Salin Plus Air Purifier PLUS 1 Replacement Filter€157.95 €204.00Add to basketSale!Salin Plus Air Purifier PLUS 2 Replacement Filters€187.45 €250.00Add to basket Hosted on Acast. See acast.com/privacy for more information.

Real Lives: Eva's Cystic Fibrosis Journey with Rachel Murray This week I chat with Rachel Murray as we deep dive into Cystic Fibrosis. We discuss the impact it has had on their daughter Eva. We get to know Rachel and hear about her deep joy on the safe arrival of her gorgeous little girl Eva two years ago. Rachel and Jason found out that Eva has Cystic Fibrosis three weeks after her birth. Rachel explains the process involved and how they coped with their daughter's diagnosis. We hear all about their journey and how they have coped since. Most importantly we learn that there is hope and Eva's future looks brighter everyday. I discuss the genetic aspect to cystic fibrosis and the medications used in it's treatment. Rachel explains how important it is that every child that is clinically eligible to benefit from new medications should have access to them. We have come a long way in Ireland but there is more work to be done. No family, child or adult living with Cystic Fibrosis should be excluded from a life of possibility. Cystic Fibrosis Ireland is an incredible resource for anyone affected by CF in Ireland. It contains so much information and up to date advice and I urge every patient and healthcare provider to spend some time checking it out. I am so grateful for hearing all about Eva's Cystic Fibrosis journey with Rachel Murray. Rachel is a passionate mum who see's the optimism in medical advancement. Season 2 Partnership I am so thrilled to be partnering with Salin plus for an entire Season packed with lots of respiratory health information! This 100% natural salt therapy device is suitable for both adults and children! Tune in to learn more! Support this Podcast Simply following and reviewing this podcast can make a huge difference! If you enjoy this episode 'Real Lives: Eva's Cystic Fibrosis Journey with Rachel Murray' I would be so grateful if you could follow or subscribe to the show! I aim to support parents and appreciate every one of you who take the time from your day to learn something new along with me! We have episodes where I explain medical conditions and offer lots of tips and advice from my perspective as a Pharmacist mum. We also chat with experts about a whole range of medical and parenting challenges. Of course I can’t forget our little voices episodes where I chat with kids and hear things from their point of view! I’m also extremely grateful to everyone who contributes to a real lives episode – I learn so much from these and am privileged to be able to share your story which will help people who find them in a similar situation in life. You can check out all of my previous episodes by clicking right here! Get Involved! Email Sheena@wonderbaba.ie

Cystic Fibrosis Ireland questions whether a CF drug for 35 children will be fairly assessed by the National Centre for Pharmaco-Economics (NCPE) following recent newspaper comments and Phillip Watt, CEO of Cystic Fibrosis Ireland reacts

Today is 65 Roses Day, which is the National Fundraising Day for Cystic Fibrosis Ireland. On Friday's Morning Focus, Alan Morrissey was joined by Chlíonadh King, Ennis woman with Cystic Fibrosis. Photo (c)Cystic Fibrosis Ireland

Rory Mahon from ROM in Sligo spoke with Francie about the 65 Roses Day Challenge for Cystic Fibrosis Ireland. Rory told Francie why they were undertaking this personal challenge and what it entailed. To donate click here: https://www.idonate.ie/fundraiser/11431001_david-o-reilly-s-page.html All Podcasts can be found on Spotify, Apple Podcast, Soundcloud or wherever you find your podcasts. Just search OceanFmIreland. The Francie Boylan Show airs weekdays 11am – 2pm

On todays show Ray is joined by Clodagh O'Hagan who is raffling off her pink piano to raise money for Cystic Fibrosis Ireland, Dr?David Robert Grimes is in studio to talk about vaccine hesitancy and resistance and Ray catches up with Eddi Reader from a studio in Glasgow.

Ray is joined by Clodagh O'Hagan who is raffling off her pink piano to raise money for Cystic Fibrosis Ireland, a charity close to her heart as the daughter of her friend Rachel Murray was born with CF. Rachel Also joined Ray on the line.

Philip Watt, Chairperson, Irish Donor Network and CEO Cystic Fibrosis Ireland

My guest on this episode is Cystic Fibrosis Association of Ireland ambassador, Emma Hempton. Emma is a vibrant young woman who adores music and has a lust for life and lives it to the best of her ability. On this platform, she shares what it is like living with CF, the challenges she faced throughout her life, with memories of her childhood, adolescent years, and also the times she and her family were close to saying their goodbyes. Yet as you listen to Emma, her story is one of strength, of determination, of resilience and I believe it will encourage you to take another look at your life and ask yourself are living every moment and making the best of what is in front of you? Emma has an ability to tell a story and hook the listener on every word with her soft tones. Her calmness and serenity ring through. Today is April 9th otherwise known as 65 roses day. A day created to help raise awareness and funds for the people of Ireland who battle live with Cystic Fibrosis. There are 1400 people in Ireland living with this genetic, chronic, terminal lung disease and to date, there's no cure. CF Having an ambassador like Emma Hempton, I'm certain that Cystic Fibrosis Ireland will raise the much-needed funds. While you're listening, head over to www.65rosesday.ie and donate what you can. At 21 years old, Emma has a grip on life and a passion for living. That passion is there in us all, we just have to start looking in the right places and finding out what living really means to us. Please do one thing today, head to 65rosesday.ie and donate to help Emma and the people affected by CF. Your support matters. Thank you for listening. For anyone who wants to find out more about Cystic Fibrosis please head to https://www.cfireland.ie/ Also, check out their Instagram page cf_ireland #65rosesday #cysticfibrosis #cfireland

There has been a lot of commentary concerning the ongoing Beacon Hospital vaccination controversy - one that has a lot of people feeling dismayed and disappointed. But what is the feeling from those who are in real need of a vaccination, like those suffering from long-term illnesses such as Cystic Fibrosis? Philip Watt, Chairperson of the Irish Donor Network and CEO of Cystic Fibrosis Ireland joins Susan to discuss. Listen and subscribe to Newstalk Breakfast with Susan Keogh on Apple Podcasts, Google Podcasts and Spotify.      Download, listen and subscribe on the Newstalk App.    You can also listen to Newstalk live on newstalk.com or on Alexa, by adding the Newstalk skill and asking: 'Alexa, play Newstalk'.

However tough the past year has been for all of us, it’s challenged those facing a higher risk, due to underlying conditions, such as Cystic Fibrosis, even more. And, here in Ireland we have one of the highest rates of Cystic Fibrosis across the world. So, the work of Cystic Fibrosis Ireland is never done. Maria Driscoll’s husband Kevin suffered from Cystic Fibrosis. She told us about the important work they do along with Louise Galvin, Ireland rugby player, Kerry GAA footballer and Cystic Fibrosis Ireland ambassador. You can support the by donating online at 65RosesDay.ie or by taking part in a 65 Roses Team Challenge.

Dr. Peter Sloane, Dr. Frances O'Hagan, Gerald Barry, Assistant Professor of Virology at UCD and Philip Watt, CEO of Cystic Fibrosis Ireland, join the programme to react to the news that use of the AstraZeneca vaccine has been suspended.

Philip Watt, Chief Executive of Cystic Fibrosis Ireland, gives his reaction to changes in the priority groups for vaccination, and we hear from transplant recipient Orla Tinsley.

Today we welcome the 117th addition to our Local Selection series from Dublin DJ, promoter and Seshin collective's Gavin Conway. From playing Croatia's Ultra Festival twice, Phever FM shows and running the popular Seshin Collective nights, as well as hosting a stage takeover at Life Festival in 2019, it's fair to say prior to the Covid lockdown and restrictions Gavin was busy on the DJ front. Having held residencies in Dublin's Wright Venue, Tamangos, Babylon and Berlin D2 playing his signature style of soulful and club house music, this mix explores what you'd expect to hear from his DJ sets, radio shows or Seshin parties. Back in May, when the countries restrictions were somewhat relaxed, you might have caught Gavin, his Seshin crew and friends taking part in the incredible charity drive supporting Cystic Fibrosis Ireland, where they constructed a mobile DJ booth and walked from Malahide to Portmarnock all while banging out house music in aid of charity. Today, Gaving takes over the Local Selection mix series, as he provides us an hour of house music to soundtrack your Wednesday afternoon. Gavin Conway -------------------- SC: @gavin.conway.92 FB: www.facebook.com/seshinnights Four Four Magazine --------------------------- FB: www.facebook.com/FOURFOURDANCE/ IG: www.instagram.com/fourfourmagazine/ Web: www.fourfourmag.com/

Well known Clara man John "Chucky' Dunne passed away this year, aged 35 from Cystic Fibrosis. His Uncle Lloyd Bracken has recorded this song "drink a beer' in his memory and to raise funds for Cystic Fibrosis Ireland. Lloyd tells Chucky's story here...

Covid 19 has dried up fundraising efforts for many charities, The sixth annual Woodie’s Heroes campaign is set to be out of this world as the 1,400 colleagues of the DIY, Home and Garden store walk to the moon in a bid to raise vital funds for Down Syndrome Ireland, Cystic Fibrosis Ireland, Autism Assistance Dogs Ireland, and ISPCC Childline. Drum and Inch native Marie Brennan spoke to Fran Curry on Tipp Today this morning.

Over the last number of weeks since all sport was stopped players from all SSE Airtricity League Premier Division clubs have been competing in a FIFA 20 tournament on Playstation as part of the Extratime.ie e-sports cup in aid of Cystic Fibrosis Ireland.   Jaze Kabia of Shelbourne, Cameron Saul of Finn Harps, Cian Kelly from St Pats, Daniel Kelly of Dundalk, Daniel Grant of Bohemians, Daire O'Connor from Cork City, Ronan Coughlan of Sligo Rovers, Tyreke Wilson of Waterford, Darren Cole from Derry City and Aaron McEneff of Shamrock Rovers all took part.    After the group stages and Semi-Finals Shamrock Rovers represented by Aaron McEneff and Tyreke Wilson of Waterford have progressed to tonight's Final which can be watched live on the Extratime.ie You-Tube channel.   Ahead of the decider both McEneff and Wilson took time out to speak to tournament commentator Oisin Langan about the game itself but also how themselves, their families and their teammates have been handling the stoppage of football due to Covid 19.  

On Friday's show Niall Boylan Spoke to Bevan Murphy who lives with Cystic Fibrosis. Today is the annual fundraising day for Cystic Fibrosis Ireland. Bevan spoke about life with Cystic Fibrosis during COVID 19See omnystudio.com/listener for privacy information.

On Friday's show Niall Boylan Spoke to Bevan Murphy who lives with Cystic Fibrosis. Today is the annual fundraising day for Cystic Fibrosis Ireland. Bevan spoke about life with Cystic Fibrosis during COVID 19 See omnystudio.com/listener for privacy information.

On Friday's programme, we heard from Killaloe teenager Jade Needham. The 18 year old has cystic fibrosis, and told us how she has been cocooning for the best part of a month, so that she doesn't catch COVID-19. She appealed to all of us to follow social distancing guidelines, and also issued a fundraising appeal on behalf of Cystic Fibrosis Ireland, who should have been holding their annual 65 Roses Day fundraiser today.

Declan Marron & Tom O Connor chat with Kevin Burke (Author of One Night in Dudelange) about next seasons new third tier European competition, about UCD's Europa League adventure in 2015 and the logistics of Irish sides planning for European Football. (3.30)Dave Donelly dials in to discuss the FAI's managerial headache with both Mick McCarthy and Stephen Kenny seemingly have claims to the throne. (38.38)All of this and Robbie Benson being abused in a Tesco in Luxembourg, Tom's new fitness regime and whether the IRN BRU/Tunnex Cup could influence our european places. Extratime.ie eSports Cup Page with all donations going to Cystic Fibrosis Ireland:https://www.idonate.ie/fundraiser/11384612_extratime-ie-esports-cup-page.htmlSupport the show (https://www.patreon.com/extratimecom)

It's an esports bonanza with our upcoming Extratime.ie spports Cup for Cystic Fibrosis Ireland. And we get the prospect and quite a bit of trash talk fromThe players involved - Ronan Coughlan (12.35), Daire O'Connor (16.21), Keith Ward (22.03), Jack Byrne (25.59), Tyreke Wilson (29.00) and Cameron Saul (31.43). Host Declan Marron and Dave Donnelly also chat about the further delay to Irish Football until mid June and how you can help out clubs in the meantime.(2.50)Donate to Cystic Fibrosis Ireland:https://www.idonate.ie/fundraiser/11384612_extratime-ie-esports-cup-page.htmlHow To Help Your LOI Club Guide:https://www.extratime.ie/articles/24630/how-to-help-your-league-of-ireland-club-financially-during-the-coronavirus-shutdown---a-guide/Support the show (https://ko-fi.com/X8X6D5R1)

We had Gaz Bailey in to talk about his 65 Day Challenge for Cystic Fibrosis Ireland.

Keith grew up in Greystones, Co. Wicklow, Ireland and followed his father path into business and sales. He followed a normal path of school, study, first job, career, marriage, first child… His normal life path was changed abruptly when their second child was diagnosed with Cystic Fibrosis just weeks after birth. He and his family had to quickly adapt to a New Normal . Keith sits on the board of Cystic Fibrosis Ireland and is the current Treasurer. He values the family unit, community and the importance of getting involved to make sure that change happens For more information on CF_Ireland visit https://www.cfireland.ie/ (https://www.cfireland.ie) For more about Keith check out https://twitter.com/keithmccabe27 (Twitter ), https://www.instagram.com/keithmccabe2/ (Instagram )or https://www.linkedin.com/in/mccabekeith/ (Linkedin) ___________________________________________________________________ Keith’s Music Choice Stranger on the shore – Aker Bilk All Night Long – Lionel Ritchie Children – Tokyo Myers I Lived – One Republic Giant – Rag n Bone Man Something just like this – Coldplay with The Chainsmokers Hourglass – Mindy Gledhill _____________________________________________________________   All music is available on Spotify in the https://open.spotify.com/user/asplendori/playlist/52RfJG6gxwmVUazdOX8m9G?si=Wcl3A8-QSHa3J_K29yzWzQ (Social Fabric Playlist) Support this podcast

See http://www.president.ie/en/diary/details/president-receives-members-of-cystic-fibrosis-ireland

Cystic Fibrosis Ireland has launched it's one in 1,000 campaign.

Shownotes:   Pat Divilly is an author, speaker and health and wellness coach who has fast become one of Irelands leading authorities on health and wellness.   He has raised hundreds of thousands of euros through various events for Irish charities including Console and Cystic Fibrosis Ireland.   In this episode we delve into:   How and why Pat got into into health and fitness.   Pat's definition of health.   How can other men take the first steps to help improve their mental health.   What Pat did that helped him when he suffered with poor mental health.   What advice he would give himself back when things weren’t going well.   How important has self awareness been in your journey from adversity to where you are now.   The importance of belief.   How he turned Failure into Success   Inspiration vs Desperation   What caused Pat to commit fully to change?   How getting a balanced life, work and family is so important to Pat.   Being vulnerable and open.   Revealing emotions as a man.   Critics and how he deals with them.   10 day challenge for listeners:   Take action on what you learnt.   Write down 3 things each night of things you want to do the next day that are important.   Top 3 tips to live a healthy and happy life   1) Gratitude   2) Action Steps   3) Journalling/goal setting       Find out more about Pat and his work:       Website:   http://www.patdivilly.com/       Facebook:   https://www.facebook.com/PatDivillyFit         Other Resources: (Non Affiliate Links)   Headspace App– Start a free 10 day introduction into Mindfulness Meditation. This is the app I use everyday and how I started into Mindfulness Meditation.     Enjoying The Podcast?   Then I would really appreciate if you could please Subscribe to the podcast on iTunes and leave an honest 5 star rating so that the Choose Health Podcast can help more people improve their health.   Darragh       Share The Love Below        

Food & Wine Magazine reviewer, Rachael Kealy, talks about her visit to Brick Lane in Cork. Kerry Chef John Fitzmaurice, formerly of the Mustard Seed in Ballingarry, Co Limerick, talks about life in his new position as Head Chef at Moloughney's in Clontarf. Sharon Noonan meets cancer survivor Patricia Daly at the WAPF Wise Traditions Conference in Thomond Park. Yes Chef Magazine's Shane Smith is on the phone to talk about a charity cycle by chefs in May 2016 to raise funds for Cystic Fibrosis Ireland.

Don 70ú clár, bhí clár lán, bríomhar againn! Bhí an bhean Bhrasaíleach-Ghaelach Natália Danzmann sa stiúideó linn ag labhairt faoin bhféile Carnaval sa Bhrasaíl agus chualamar agallamh a rinne sí féin le Cristóir Ó Faoláin a bhí ag cóisir Carnaval i mBaile Átha Cliath. Chomh maith labhair Eoin faoi scéalta móra idirnáisiúnta na seachtaine, cúrsaí eacnamaíochta na Gréige san áireamh agus labhair Lisa faoi Shiúlóid urraithe atá á eagrú sa Bheilg ag Cystic Fibrosis Ireland (breis eolais ag cfireland.ie). Ar deireadh, bhí Brían Ó hAirt linn ón suíomh Language Hunters linn ag insint dúinn faoin ngréasán iontach do chainteoirí mionteangacha atá á reachtáil in Oregon agus ar líne ar languagehunters.org