Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

Samuel Weidenhofer

Patriotic Kenny Foundation

Ben Saunders - Flawless Cleaning

The Dogist

Peter Bond

Amy Jandrisevits

Ask Uncle Jack

That Good News Girl

Tess Bohne

FowlMouthFarmer

Latonja and Taylor Richardson

Officer Richard Craig

Flavor Flav

John Wolfe

Khloe

<div>Hi Everyone,
</div>
<div>Our names are Jack, Luke and Aidan Kelly. We are twelve, ten and nine years old.
</div>
<div><br />
</div>
<div>On July 10th we will be making our first journey to Tír na nÓg in Tanzania to visit the children in the home and school which was founded by our Auntie Louise.
</div>
<div><br />
</div>
<div>We decided to organise a triathlon to raise money before we leave. All the money raised is going towards a new astro pitch and running track at the primary school.
</div>
<div><br />
</div>
<div>On June 1st, in Fenit, we will swim 300m, cycle 10km and run the first 2.5km in Ireland. We will run the final 2.5km in Tanzania with the children from Tír na nÓg.
</div>
<div><br />
</div>
<div>We hope you can help!
</div>
<div>Thank you,
</div>
<div>The Kelly Brothers
</div>

The Kelly Brothers Triathlon for Tír na nÓg

<div>Hi everyone,
</div>
<div>My name is Sarah and I will be running the Edinburgh marathon on the 25th May. I am fundraising for Make-A-Wish and Tír na nÓg and every cent raised will be shared equally between these two amazing charities
</div>
<div>Make-A-Wish is a chosen charity of someone very dear to me, who has inspired me with their never-ending strength and determination during their journey through cancer. I hope I make you proud ❤️
</div>
<div>Tír na nÓg is an orphanage run by my friend and colleague, Louise Quill. An unstoppable lady and hero to the children in Tanzania ❤️
</div>
<div>These two charities are changing lives every day and any donation would be greatly appreciated,
</div>
<div>Thanks everyone,
</div>
<div>Sarah xxx
</div>

Tír na nÓg orphanage & Make-A-Wish

<div><strong>Aim of fundraiser:</strong>
</div>
<div><br />
</div>
<div>Hi, we created this page (Shane and Stephanie parents) initially to help raise funds for Theo’s future, ensuring he has everything he needs to thrive as we didn't know what the path ahead looked like for him. Luckily Theo is doing brilliantly since receiving gene therapy in December 2021. As we look ahead, our goal is to provide him with the best possible care and support, while also enabling him to access critical medical, physio, and occupational therapy appointments.
</div>
<div><br />
</div>
<div>We have some exciting news that we have bought a <a href="https://www.trexorobotics.com/" target="_blank" rel="noreferrer noopener">Trexo robotic walker</a> but we still have a long way to go to fully pay for it as they offer a payment plan. This incredible device offers children with mobility challenges the ability to walk and experience greater independence. The Trexo will assist Theo by improving his strength, endurance, and overall movement, providing a transformative impact on his quality of life.
</div>
<div><br />
</div>
<div>We didn't want to waste time and wanted to get it for him as soon as possible. Luckily Trexo robotics offer financing and so we will have it in September 2024 to get him started on his walking journey. Money raise will go directly to paying off the unit.
</div>
<div><br />
</div>
<div>With your generous support, we can secure the Trexo and ensure Theo has access to the treatments and therapies that will give him the best opportunities for growth and development. Your contributions will go directly toward these essential resources, helping us give Theo the brightest possible future.
</div>
<div><br />
</div>
<div><strong>Theo's Story:</strong>
</div>
<div><br />
</div>
<div>Theo was born on April 29th, 2021, and on August 19th, 2021, our world was changed when he was diagnosed with SMA Type 1 (spinal muscular atrophy). This is a severe genetic condition that affects infants, often limiting their movement, and making it difficult for them to breathe, eat, and swallow. Without intervention, children with SMA Type 1 struggle to sit up unassisted and face serious challenges in their development.
</div>
<div><br />
</div>
<div>Thankfully, recent advances in medicine have brought new hope to families like ours. These breakthrough therapies target the root cause of SMA, offering children like Theo a chance for a better quality of life. On December 8th, 2021, Theo received Zolgensma, a cutting-edge gene therapy that gives him the opportunity to fight this disease. We are incredibly grateful that this treatment became available just in time for Theo in Ireland.
</div>
<div><br />
</div>
<div>While this therapy is a major step forward, Theo’s journey is far from over. He still requires extensive care, including regular medical appointments, physiotherapy, and specialised equipment to help him reach his full potential. That’s why we are sharing his story and asking for your support. Any donation, no matter how small, will go directly toward ensuring Theo receives the best care, therapy, and equipment, like the Trexo robotic walker, to help him live life to the fullest.
</div>
<div><br />
</div>
<div><strong>Theo's day to day needs:</strong>
</div>
<div><br />
</div>
<div>Theo requires specialised care at home. His daily routine includes using a BiPAP machine during naps and at night to support his breathing. He also receives enteral feeding, and we monitor him closely to ensure his comfort and health.
</div>
<div><br />
</div>
<div>His care involves:
</div>
<div><br />
</div>
<ul>
<li>BiPAP respiratory support during sleep
</li>
<li>Physiotherapy and use of a cough assist machine
</li>
<li>Regular hospital visits and weekly therapy sessions, including occupational therapy, speech therapy, and hydrotherapy
</li>
</ul>
<div><br />
</div>
<div>As Theo continues to grow stronger, his therapy needs will increase, but we are committed to giving him the best support possible.
</div>
<div><br />
</div>
<div><strong>Theo's future needs:</strong>
</div>
<div><br />
</div>
<div>Looking ahead, Theo will continue to need:
</div>
<div><br />
</div>
<ul>
<li>Specialised equipment, personalised to suit his needs as they evolve.
</li>
<li>Hospital visits and potentially extended stays, as well as ongoing private physiotherapy.
</li>
<li>Hydrotherapy to aid in flexibility, mobility, and strength development.
</li>
<li>Home adaptations to ensure his living environment is accessible as he grows.
</li>
</ul>
<div><br />
</div>
<div>Thanks for your help, love and support.
</div>
<div> 
</div>
<div>Shane, Stephanie and Theo :)
</div>

Help Theo live his best life with SMA 1

<div>On 22nd April 2023, family and friends will walk the 23km/14miles between Bantry and Church Cross, connecting Maud's two homes.
</div>
<div><br />
</div>
<div>Please show your support by donating what you can. All proceeds raised will go directly to Cork Cancer Connect, a charity Maud has helped to raise funds for in the past.
</div>
<div><br />
</div>
<div>Thanks in advance for your contribution to this cause.
</div>

Maud's Miles - Charity Walk

<div>Last Sunday morning 8th of January, Joe Toms, Marie, Ciara, Niamh, Niall, Aoife Fenton-Toms of Muingaphuca, Caragh lake, lost their family home to a lightning strike. While we, their friends are very grateful that there was no loss of life. They have lost ALL their possessions. we the friends of the Toms Fenton-Toms, Would like to raise some funds, to try and get them back on their feet. Costs have already started to come in, it is so very overwhelming for them and their children. Any donation big or small is so welcome at this extremely challenging and highly emotional time. Everything needs to be replaced, like clothes, underwear, medications, and so much more, which isn't covered by insurance. They have to start from scratch. As a community we ask you to give what you can please to help at this awful time.
</div>

Killorglin Family Fenton-Toms lost their home.

<p>Hi, my name is Kevin and I'm setting up this gofundme for my good friend's Geraldine and Andrews daughter Alannah. Here is their story. 
</p>
<p><br />
</p>
<p>Alannah is a happy, bubbly 4-year-old from Killorglin, Co. Kerry. Alannah lives with her dad Andrew, mom Geraldine, Aunty Caitlin and baby brother Adam. She goes to preschool and loves building lego, going to the beach, art, glitter and all things unicorn! 
</p>
<p><br />
</p>
<p>When Alannah was 5 months old her parents noticed marks on her body called cafe au lait stains. Cafe au Lait stains are a type of birthmark characterized by flat patches on the skin, which can be indicators of an underlying illness. 
</p>
<p><br />
</p>
<p>In January 2019, aged 2 Alannah was diagnosed with Neurofibromatosis Type 1 (NF1), a condition that can cause benign tumours to grow on nerve tissue.
</p>
<p><br />
</p>
<p>That summer Alannah began feeling dizzy, having falls and wobbles which became more frequent. Geraldine contacted the family GP, who sent Alannah to Cork University Hospital where an MRI found a bilateral optic pathway glioma (slow growing tumour). The tumour was blocking part of Alannah's brain and caused hydrocephalus, a condition where an accumulation of cerebrospinal fluid (CSF) occurs within the brain.
</p>
<p>Alannah’s parents were told that an ambulance was booked to bring Alannah to Temple Street Children's Hospital immediately. A biopsy of the tumour was taken and thankfully it was benign. 
</p>
<p><br />
</p>
<p>A few days later Alannah underwent her second brain surgery and had a VP shunt fitted, to help alleviate the pressure caused by the hydrocephalus. Alannah attends physiotherapy and occupational therapy to help with the difficulties the brain tumour and hydrocephalus have caused.
</p>
<p><br />
</p>
<p>The decision was made to monitor the tumour with regular MRIs and eye exams every 3 months in Crumlin.
</p>
<p>Alannah is under the care of a team of specialists in Crumlin Children’s Hospital including an oncologist, ophthalmologist and the neurophysiologist, her favourite doctor, who performs an EEG (electroencephalogram). The EEG is a test that detects electrical activity in the brain.
</p>
<p><br />
</p>
<p>On Alannah’s last visit to the eye clinic the doctor noted a decline in the vision in her left eye. The eye tests and EEG were repeated. It was decided that Alannah would start chemotherapy for 70 weeks in the hope that it will prevent any further damage to her eyesight.
</p>
<p><br />
</p>
<p>On the 14 May 2021 Alannah had a port fitted that she has christened Polly. 
</p>
<p>The port is used to administer chemotherapy, take weekly bloods and give antibiotics if needed. 
</p>
<p><br />
</p>
<p>On 15th May 2021 Alannah had her first dose of chemotherapy.
</p>
<p><br />
</p>

Alannah and Polly's Fight for Sight

Killorglin basketball club is one of Kerry's oldest basketball clubs set up in the late 1950's, having taken a brief  step back from competition, the club re-launched in 1999 competing locally.  <br /><br />The club has grown from strength to strength since then and in 2015 launched themselves to compete nationally, after three great seasons the team Keanes SuperValu were promoted to Super League having won the Basketball Ireland National League in 2017/18 season.  <br /><br />Our club is our basketball family and we have grown and strengthened over the years, creating special moments, memories &amp; developed some fine basketball players now and our future stars are emerging through our juvenile system.  <br /><br />Unfortunately due to this current Covid 19 pandemic, not only did our third Super League season finish early and our final games cancelled,  so have our fundraising events. <br /><br />The club have decided to launch a virtual challenge and help tip us off into a fantastic  20/21 season.  Funds raised will help develop and nuture our future super stars and ensure we compete locally &amp; nationally <br /><br />Our #AroundTheWorldBball challenge in 40 seconds will do just that! We challenge you juniors &amp; seniors alike to try your hand scoring at each 5 spots and do so successfully within the 40 seconds.  Send us your videos and we will share across our social media channels from July 26th to July 28th .  All those who participate will be entered in a draw for some fantastic prizes.  <br /><br />All your efforts, donations and contributions will be very much appreciated and will go a long way to help our club and our future stars.<br /><br />Yours in sport, <br />Killorglin CYMS Basketball Club

Killorglin CYMS #AroundTheWorld

<p><strong>Do 5km </strong><br /><strong>Donate €5<br /></strong><strong>Nominate 5 people to do the same </strong>
</p>

<p>Hi my name is Fiona and I am a healthcare professional from Meath. After seeing my friends on Instagram participating in a UK version of this campaign I have decided to start an Irish one to help our own  heroes in the HSE. 
</p>

<p>The Irish are renowned worldwide for the warm welcomes and caring nature. In this challenging time we are asked to come together by staying apart. Our frontline heroes go to work every day and risk their own health to help others. I ask you to help them by joining in this fundraiser and showing your support. 
</p>

<p>Please remember whilst participating to stay within your 2km boundary and to practise social distancing. 
</p>

<p>All money raised will be donated to local hospitals so they can continue the good fight not just now but for years to come.
</p>

<p>The hospitals benefiting from this campaign will be Beaumont, St James, Mater Miserdei, Connolly hospital Blanchardstown, Our Lady of Lourdes Drogheda, Limerick University Hospital, Mercy University Hospital Cork, Waterford University Hospital.<br /><br />I plan to liaise with hospital staff directly  to gather information on what they need and what they would benefit from and either source it directly or donate the relevant amount. 
</p>

<p>Ní neart go cur le chéile - There is strength in unity  <br /><br />All funds will be managed through The Mater Foundation (Charity Registration No: CHY9768) , who will assist in distributing the funds across the hospitals and causes regarding frontline workers. 
</p>

Run for our HSE heroes

I am seeking to raise funds for two charities in Kerry that are close to my heart and require the funding for retention and expansion of vital services<br />The charities are: <strong>Comfort For Chemo Kerry</strong> &amp; <strong>Down Syndrome Kerry.<br /><br /><br /></strong>I am taking on the task of climbing Kilimanjaro which would normally be difficult but especially for me as I suffer from Acrophobia (no not spiders, I'm afraid of heights).<br />It is 5895m above sea level and there's me that won't climb a step ladder. <br /><br />I know that the two charities will be very grateful and so would I if you could donate whatever you can and share and encourage your friends and colleagues to do the same.

Shane Buckley's Kerry To Kilimanjaro

Sarah Pigott

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Sarah Pigott

Sarah Pigott

Featured causes

The Kelly Brothers Triathlon for Tír na nÓg

Tír na nÓg orphanage & Make-A-Wish

Help Theo live his best life with SMA 1

Maud's Miles - Charity Walk

Killorglin Family Fenton-Toms lost their home.

About me