Paris Hilton

Jimmy  Darts

Flavor Flav

SB Mowing

Kalina Silverman / @makebigtalk on Instagram

The Dogist

Patriotic Kenny Foundation

Pattie Gonia

Little Miss Flint

Carlos Eduardo Espina

Samuel Weidenhofer

Ben Saunders - Flawless Cleaning

Peter Bond

That Good News Girl

Ask Uncle Jack

Amy Jandrisevits

FowlMouthFarmer

Tess Bohne

Latonja and Taylor Richardson

Officer Richard Craig

<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.
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<div><br />
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<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.
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<div><br />
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<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>We are the <strong>Mounthawk Masterminds</strong>, a team of students from <strong>Mercy Secondary School Mounthawk</strong>, and we are incredibly proud to have been selected to represent Ireland at the <strong>FIRST LEGO League Open International Championship in Greece this May 2026.</strong>
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<div><br />
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<div>FIRST LEGO League (FLL) is a global STEM competition where students design, build, and program robots while also developing innovative solutions to real-world problems. Teams are judged on Robot Design, Robot Game, Innovation Project, and Core Values such as teamwork, respect, and inclusion.
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<div>Following an extremely successful All-Ireland Final, our team was chosen based on our outstanding performance across all four areas of the competition. Being selected is a huge honour and a once-in-a-lifetime opportunity.
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<div><br />
</div>
<div><strong>Who We Are:</strong>
</div>
<div>Our team is made up of seven students from 1st Year to Transition Year, all with a shared passion for STEM. Since September, we have spent countless hours designing, building, and programming our LEGO Spike Prime robot, while also developing an innovative project and growing as a team for this year’s competition.
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<div><br />
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<div><strong>Our Innovation Project:</strong>
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<div>This year, we tackled a real-world problem: how archaeologists safely explore tight, dangerous, or unstable excavation spaces.
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<div>We designed and built an Archaeology Access Rover, powered by a Yahboom Raspberry Pi, with a camera and sensors to explore these areas safely and send back live data. The robot was programmed using Python, giving us experience in real-world coding, robotics, and problem-solving.
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<div><br />
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<div><strong>The Opportunity:</strong>
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<div>At the Open International in Greece, we will compete against <strong>56 of the top teams from around the world</strong>. The event includes robot games, judging sessions, innovation presentations, and collaboration with teams from different countries, making it an incredible learning and cultural experience.
</div>
<div><br />
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<div><strong>Why We Need Your Help</strong>
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<div>While this is an amazing achievement, the cost of getting to Greece is significant. We need to fund:
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<ul>
<li>Flights
</li>
<li>Accommodation
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<li>Competition fees
</li>
<li>Equipment and travel costs
</li>
</ul>
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<div><br />
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<div>We are actively fundraising, but we need support from our community to make this possible.
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<div><br />
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<div><strong>How You Can Support Us</strong>
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<div>Any donation, no matter how small, will help us represent our school, community, and country on the international stage.
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<div>If you’re unable to donate, sharing this page would mean so much to us.
</div>
<div><br />
</div>
<div>Thank you for supporting young students in STEM and helping us achieve something truly special.
</div>
<div><strong>Let’s get the Mounthawk Masterminds to Greece!</strong>
</div>

Help the Mounthawk Masterminds Represent Ireland in Greece!

<div>My name is Niall O'Brien.  I'm 28.
</div>
<div><br />
</div>
<div>I decided I wanted to run the Dublin City Marathon on October 29th. However to do this, I was told I'd need to raise money for a charity. So I decided that if I was going to do this, I wasn't just going raise money for some random charity just to secure me a place. I might as well raise money for a cause that I can get behind.
</div>
<div><br />
</div>
<div>Which is why I chose the Irish Cancer Society. My older sister. Laura, died from Lung Cancer back in 2014 at the age of 27. My dad had a cancerous tumour removed from his stomach back in 2019, and I myself had to undergo chemotherapy for testicular cancer back in 2020. Thank God I'm alright now, but experience has never left me. Fair to say that cancer has been an unwelcome presence in my families life, as well as many others.
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<div><br />
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<div>I say I'd like to raise €2,000, but realistically, I'd like to raise as much money as I possibly can. A portion of the money raised will be used to secure my place at the starting line, the rest will be donated to the charity.
</div>
<div><br />
</div>
<div>Any money you can donate will be greatly appreciated xxx
</div>
<div><br />
</div>
<div><br />
</div>

Running the Dublin Marathon

<div>Hi my name is Laura Baker and I am running the Tralee half marathon on the 29th of October 2023. Running is a massive challenge for me and I’ve decided to push myself to my absolute limit for a great cause. I work as a special needs assistant in the amazing Autism class in Derryquay National School located in Derrymore, Co. Kerry. A really important part of this class is bringing the children on weekly outings such a local shops ,cafes, playgrounds, swimming and horse riding to name a few.These outings are vital for the children’s life skills &amp; social skills and the children love it. As our school is located in the countryside transport costs are high and it’s impacting the amount of activities we can do with the children. I’m hoping by me running and raising some money we can make a huge difference to the children’s school year ahead .
</div>
<div>Any donations will be hugely appreciated.
</div>
<div><br />
</div>
<div>On behalf of the children in Múinteoir Lucy's class in Derryquay "thank you!"
</div>

I’m running 21k for Derryquay!

The Tralee Soup Kitchen was set up in 2012 to provide a free three course meal for those in need in our community. The money raise will go directly back into The Tralee Soup Kitchen so we can continue to provide this service. In donating to The Tralee Soup Kitchen you are helping those in need to avail of a meal they go without. We are so grateful for all the support we get.

Tralee Soup Kitchen

<div>Hi, I'm Emma and I'm raising funds so that I can treat my cancer in more than one way and have the very best chance of survival against stage 4 breast cancer. I believe my life can be extended by incorporating several other treatments into my regime, and clinics in Europe and America have seen success using dendritic cell therapy, mistletoe treatments and immunotherapy. The clinics offer other therapies like hyperthermia, immune stimulation therapy and red light therapy which have been shown to improve quality of life and slow tumor growth. People often ask me how they can help, with your support I can access these treatments and prolong my life.
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<div><br />
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<div>For those of you who may not know my story, in April 2021 at 38, with a 1-year-old dote of a son, I was diagnosed with stage 3 breast cancer. What followed was a year of harrowing treatments, chemotherapy, a mastectomy and radiation. Treatment finished in April 2022 and for 8 months, life felt normal until December when a routine scan showed lots of cancer in my liver. The cancer had metastasized, and it was now stage 4. I'm taking medicine daily and monthly shots, regular scans and we're trying to keep it contained in the liver, however, it is considered incurable, and I will continue to take this medicine until I become resistant or too ill to continue taking it. This is where complementary medicine can help.
</div>
<div><br />
</div>
<div>I need to be around for as long as possible with my son Joel and partner Paul. Being around also means I need to feel as well as possible, and wellness throughout a stage 4 illness is made possible through integrative, holistic cancer therapies often not available on the HSE or NHS. I remain optimistic in the face of this illness, and I am inspired by people who have healed and recovered from cancer. Pursuing complementary medicines alongside conventional medicine, I believe I can feel much healthier, less tired and more empowered. And more like myself. Research shows that individuals who take their health into their own hands live longer which is why I believe being proactive and pursuing further treatments will help.
</div>
<div><br />
</div>
<div>This is how I plan to spend funds raised, on supplementing my mainstream treatment with complementary therapies, visiting the clinics in Spain and Germany for treatment and ensuring I am comfortable for as long as possible. Paying for added therapy via this Go Fund Me means that our family can continue to live our normal lives as cancer does take a financial toll...on top of everything else.
</div>
<div><br />
</div>
<div>Thank you for donating or sharing, I really appreciate the support.
</div>

Help Emma get the cancer treatments she needs.

<div>Hi my name is Michael Moriarty Juvenile Chairman of St Pats GAA Blennerville. We are fundraising for our u12 football team who have been selected to represent Kerry in a blitz in Croke Park on April 12th. This is a fantastic honour for our club and a great opportunity for our u12 stars to play in Croke Park. We are fundraising in support of this trip to help with travel and other costs. Any donation you can give is much appreciated.
</div>
<div>Regards,
</div>
<div>Michael
</div>

St Pats u12 Croke Park Football Blitz

<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.

<div>Three years ago, our whole world was thrown into turmoil when our youngest son, Fionn, had to be rushed to Crumlin Children’s Hospital. He was in kidney failure. 
</div>
<div>For over a week, Dr Mary Waldron and her expert team in the Renal Unit worked tirelessly to save his life. Words will never be able to describe our immense gratitude that they were successful. It was a world we knew nothing about previously but we were confident that Fionn couldn’t have been in a better place.
</div>
<div>This Halloween, we are raising funds to ensure that this team can continue to provide care to families like us.  We would be grateful for any donation you can make here as part of the Children’s Health Foundation Trick or Treat for Sick Children initiative. 
</div>
<div><br />
</div>

Fionn’s fundraiser

<p>Hi all, my name is Ann Eager and I am undertaking a charity cycle ride (over 500kms) from Derry Beag, Co Donegal to Derrymore,  Co Kerry.  The cycle will commence on Monday 27th September and will finish on Saturday 2nd October.
</p>
<p>The cycle is in aid of the Intensive Care Unit, Beaumont Hospital, Dublin and the Cardiac Rehabilitation Unit, University Hospital Co Kerry.
</p>
<p>This cycle is in memory of my late sister Pauline Lynch, who sadly passed away unexpectedly in December 2019. Pauline was an amazing family person, full of life and always smiling. Pauline was the life and the soul of every party and would bring a smile to the saddest of faces. This is reflected in her three beautiful children.
</p>
<p>Pauline was admitted to Beaumont ICU after she suddenly collapsed in Dublin and she received amazing care by all staff in Beaumont and although everything possible was done she passed away peacefully in December 2019. As a family we will always be eternally grateful for the care and treatment given to Pauline during this very stressful period.
</p>
<p>I am hoping to work with you, our community, to raise enough money for new equipment for both Beaumont ICU and the Cardiac Rehab Unit in UHK. Both units do amazing life saving work and this is my way of giving back. So if you would like to donate, no matter how small I am hoping to make a difference so it can help others.
</p>
<p>I will update the gofundme page regularly and I will have an Instagram and Facebook age also. Please remember to share this cause far and wide so we can help more people in our community to avail of the new equipment we can purchase for the two units. Collection buckets will be in the Town of Tralee for people who would like to support locally, and sponsorship cards will be available also.
</p>
<p>If you would like to help in any way then please get in touch via the email below
</p>
<p>Thank you so much in advance for your support.
</p>

Charity Cycle for Beaumont ICU & UHK Cardiac Rehab

<strong><iframe media_type="0" media_id="3kkzBx9M2m8" class="youtube-replace" title="YouTube video player" style="margin-bottom:20px;width:560px;height:315px;" src="//www.youtube.com/embed/3kkzBx9M2m8/?rel=0" frameborder="0" allowfullscreen="1"></iframe>The ‘Help Rose Bloom’ Campaign</strong><br /><br /><strong>About the Campaign</strong><br /><br />We are a group of family, friends and local community members fundraising on behalf of Rose O Flaherty.  This is Rose’s plight in her own words: <em><strong>“Mommy, when will I be able to hold your hand to walk to school?”</strong></em><br /><br />Rose, from Ballymacelligot, Tralee, Co Kerry, is only 4 years old and was diagnosed with a rare and serious genetic neuromuscular condition called Spinal Muscular Atrophy (SMA), Type 1, when she was 9 months old.  SMA 1 children typically have a life expectancy of 2 years.  Currently, there is no cure for SMA.  However, there are treatments available to help manage symptoms and reduce discomfort.<br /><br />Rose is a gorgeous determined girl who is defying medical odds.  She has already learned to stand with aid for 10-15 seconds thanks to intensive ongoing physiotherapy.  However, extremely difficult and heart-breaking questions such as <em><strong>“Mommy, when will I be able to hold your hand to walk to school?”</strong></em> and <em><strong>“Mommy, why can’t I play like the other kids?”</strong></em> are now common questions for Rose.   After turning 4 recently, she said <em><strong>“Mommy, I don’t want to be 4, I want to be a baby forever because I can’t walk”</strong></em>.  This is Rose's very sad reality, but highly indicative of the level of awareness that Rose already has in her brilliant and clever mind. <br /><br />Her parents dream that one day Rose will walk (aided) and be able to do the simple things that we take for granted like, being able to move from a lying to a sitting position.  There is a treatment plan as detailed in Rose’s Story (attached), but we need your support.  We would be very grateful if you could take the time to read Rose’s story and consider how you can lend your support to her campaign.<br /><br /><strong>Rose’s Story</strong><br />Roses parents began to notice that she wasn’t meeting the milestones that their first child easily achieved at an early stage and began to worry.  When they realised that she did not have the strength to hold her head or her upper body at a stage when most or all children would have been able to do so, when she struggled at weaning stage to take any solids and as she began to have recurrent chest infections by the age of 4 months, they began to further investigate why this was the case.  Following comprehensive testing Rose was diagnosed at 9 months with SMA type 1.  Rose began her treatment of Spinraza shortly afterwards.  This diagnosis turned Roses, her parents and her family’s world upside down and in one sentence Rose’s future became very uncertain and a future that would depend on the support of her family, the medical profession and the community at large.<br /><br />Rose currently receives Spinraza via a lumbar puncture, this treatment has put a stop to the progression of her SMA but cannot reverse the toll it’s taken on her little body.  Rose will be in personally funded physiotherapy throughout her lifetime to ensure she remains as strong as she can.  She will need to receive Spinraza every 4 months for the rest of her life.<br /><br />Rose’s parents, Karen and Thomas, are very progressive regarding her treatments and lifestyle management and their determination with Rose’s therapies has led to a very impressive progression in her physical abilities.  Her progress has even surprised the medical professionals and Rose continues to exceed their expectations.  This progression is mainly due to the intensive physiotherapy which Rose attends twice a week and the incorporation of extensions of her physiotherapy routine at home on a daily basis.  After 3 years of twice weekly physiotherapy, Rose can now stand with aid for 10-15 seconds, which is MAJOR for a child with SMA Type 1, but as you can imagine, the journey ahead is daunting.  This private physiotherapy alone comes at a cost of approximately €10,000 per year.   Caring for Rose is a full-time job and Karen provides this care as well as running the house and being mom to Rose’s older sister, 6-year-old Kate, while Thomas is away working as a truck driver.  She regularly meets with her multidisciplinary healthcare team to ensure that Rose is getting the best possible treatment and her determination is also a fundamental element in Rose’s progress.  <br /><br />This Summer, Rose will undergo Spinal Surgery to insert spinal rods which will hopefully treat a significant curvature on her spine caused by scoliosis, due to the postural muscle weakness within her body.  Early intervention is key to long-term success in treating this aspect of the condition.  The surgery is considered high risk for Rose due to her condition but necessary so that Rose can progress further.  As Rose is undergoing this surgery at such a young age, she will require twice yearly medical procedures to adjust the spinal rods that will be fitted during the initial surgery, to compensate for her growing body.  <br /><br />For you or I, even 1 surgery per year would be daunting, however, for 4 year old Rose, she now faces 5 major medical procedures on a yearly basis for the foreseeable future to treat her SMA and her scoliosis.<br /><br />The current Covid pandemic has raised some serious concerns for Rose as respiratory illnesses are a common feature of SMA Type 1.  This could also be detrimental to Rose as her lack of muscle tone in general can make common infections very serious.  Previously Rose has been hospitalised as a result of what would be considered minor chest infections to her peers.  This has made Rose's life quite isolated, so while she may see her cousins often enough, she does not see her friends for any social outings.  Karen does her best to ensure that Rose lives with a relatively normal quality of life but needs to protect her from these common ailments.  Keeping Rose healthy while providing a normal life is a constant worry and battle for her family, Karen, Thomas and her big sister Kate. <br /><br />Extremely difficult and heart-breaking questions such as "Mommy, when will I be able to hold your hand to walk to school" and "Mommy, why can’t I play like the other kids” are now common questions for Rose.   After turning 4 recently, she said "Mommy, I don’t want to be 4, I want to be a baby forever because I can’t walk".  This is Rose's very sad reality, but highly indicative of the level of awareness that Rose already has in her brilliant and clever mind.  It is Karen and Thomas’s dream that one day Rose will walk (aided) and be able to do the simple things that we take for granted like, being able to move from a lying to a sitting position.  Not only would this be a monumental triumph for her it would also be a monumental triumph for everybody who has and will be involved in her painful yet beautiful journey.<br /><br />We would move mountains for our children to give them the best possible life and facing a life with SMA 1 comes with extremely unique mountains.<br /><br />There is a long list of equipment, facilities and therapies that Rose will need to ensure a decent quality of life.  As she grows, so does this list but there are certain standards that must be achieved now to give Rose the physical environment to maintain her progress and build further on it.  In the immediate future, Rose’s condition will require a wheelchair accessible ground floor extension and alterations to the existing family home to address the needs of a wheelchair dependent occupant.  There are also many pieces of equipment that Rose will need as she grows and learns to gain her own independence, such as a wheelchair, an ergonomic car seat, a wheelchair accessible family car and more.  There are also many other pieces of equipment which have been recommended by her physiotherapist which are cost prohibited for the family at present.  There are a range of further therapies available which also come with a cost but would certainly improve Rose’s quality of life.  Rose requires extensive hospital visits which incur their own costs and because Karen is the primary carer, there is only a single wage coming into the house.<br /><br />It has and will continue to be a long and expensive process to provide all the treatments necessary to allow Rose the best standard of living that can be achieved under the circumstances.  Karen and Thomas have been managing with these therapies to date, however, they are simply unable to personally finance the vast array of expenditure required for the immediate future.<br /><br />We would like to thank you for your support during our campaign.<br /><br />Please check out our website for further information and links to our social media accounts.<br /><br /><a href="http://www.helprosebloom.ie">www.helprosebloom.ie<br /><br /></a>

Help Rose Bloom

Come along to this wonderful work shop all based around Self-care and Healing on  Summer Solstice weekend June 20th &amp; 21st .<br /><br />To purchase a ticket please donate €10 and you will be invited into our private Facebook Group where this wonderful event take place. <br /><br />All the proceeds will go directly to Women's Aid,  A leading national organisation that has been working in Ireland to stop domestic violence against women and children since 1974.<br /><br />For anyone who may be suffering from Abuse you can contact 1800 341 900  24 Hours a Day,&amp; Days a week. Don't suffer in Silence!<br /><br />We will have presentations on Make Up, Meditation, Reflexology, Weightloss, Hormonal Health, Essential Oils, Yoga, Hair Care,  Angel Healing, Journaling, Affirmations, Fashion, Skin care, Crystals, Culture and much more!<br /><br />Amazing Prizes to be won over the Weekend including Therapy's, Consultations, Essential Oil Blends, Hair Care Products, Skin care products and much more.<br /><br />Invest in your self while supporting this wonderful Cause.<br /><br />Woman's Aid Charity no. CHY6491

Source your inner sunshine.

Suzanne Ennis

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Survicate

Suzanne Ennis

Suzanne Ennis

Featured causes

The Kelly Brothers Triathlon for Tír na nÓg

Help the Mounthawk Masterminds Represent Ireland in Greece!

Running the Dublin Marathon

I’m running 21k for Derryquay!

Tralee Soup Kitchen

About me