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>Help Our Boxing Club Find a New Home!
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<div>Hi! My name is Andrea, and I’m new to the boxing world. But in my short time here, I’ve seen firsthand the kindness, dedication, and community spirit that make this club so special.
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<div>For years, our incredible boxing club has been training athletes—some of whom have gone on to become champions—in the underground of a church. Despite the limited space and resources, the club continues to provide a safe and supportive environment for people of all ages and backgrounds.
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<div>Now, we need your help to take the next step! We are raising €400,000 to build a brand-new facility that will give our boxers the space, equipment, and opportunities they deserve. A proper gym means better training, more chances for young athletes to excel, and a stronger future for our club.
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<div>Every donation, big or small, brings us closer to making this dream a reality. Join us in building something truly special—one punch at a time!
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<div>Donate today and help us fight for the future!
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<div>Follow our Instagram and TikTok @Athloneboxingclub for regular updates on our progress!
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Athlone Boxing Club's Future Build

<p>Hi guys its Michelle.. I was diagnosed 6 years ago with cervical cancer 3 years ago I was told I was terminal with 2/3 years I have 4 kids and 2 bonus kids and we as a family would love nothing more than to make fun and loving memories have never been on a family holiday my kids never left the country yet they are 12 12 8 8 6 and 5 and they have really been having a hard year with my health I've been hospitalised for weeks and worry and stress and frustration we wud love nothing better than to escape it all for a week or 2 so I'm asking even if u can't donate maybe you could share ❤️ thank you all so very much xx can I just say a massive massive thank you to all who has donated and shared so far xxx 
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please support to send us on a family holiday

This is my incredible and very precious friend Elaine. <br />Elaine is 37 years old and she has Ehlers Danlos syndrome (EDS). <br /><br />EDS is a cruel, painful and in some circumstances life threatening genetic connective tissue disorder. <br />EDS has no cure. <br />EDS is a thief that has stolen so much from my friend and her family<br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/51794068_1602276590513884_r.jpeg" width="100%" media_type="3" alt="51794068_1602276590513884_r.jpeg" /><br />Both Elaine and her very precious 6 year old daughter Ruby have EDS and both suffer unimaginably each day with countless symptoms including dislocations, subluxations, chronic pain, fatigue, vertigo, violent spasms, and chronic digestive problems such as Gastoparesis which causes Elaine to vomit blood daily. <br />Recently Elaine and Ruby have received diagnoses of spinal instability including Atlanta Axial Instability (AAI) and Cranio Cevical Instability (CCI) <br /><br />This in short this means that a person’s skull is very dangerously unstable on the top of their spines and in Elaine's case there is also instability further down in her spine also. <br />Both Elaine and her daughter have compressed jugular veins too. <br />Elaine urgently needs spinal fusion surgery at the top of her spine at C0-C2 and also at C4-C5 and she also needs to have her jugular veins decompressed surgically. <br /><br /><iframe media_type="0" media_id="m4r7Qy7vNck" class="youtube-replace" title="YouTube video player" style="margin-bottom:20px;width:560px;height:315px;" src="//www.youtube.com/embed/m4r7Qy7vNck/?rel=0" frameborder="0" allowfullscreen="1"></iframe><br />Elaine and her daughter Ruby receive no care for their EDS under the national health system where they live, despite Elaine and others campaigning for care for years now. <br />EDS care is massively neglected.<br /><br />People with EDS need specialist care, and the surgery that Elaine so badly needs is not available at all for people with EDS under the national health system. <br />This family have no choice but to appeal for help to pay for EDS care and for this life saving surgery with a private specialist in Barcelona, Spain. <br /><br />Elaine has bravely cared for Ruby who has been sick since she was a baby, and for her family for years. She has pushed aside her own chronic illness, pain and horrendous symptoms. <br /><br />But now her symptoms are completely debilitating and she badly needs help. <br />Elaine's older son Jordan now assists her in caring for Ruby and for herself. <br />This amazing and incredibly brave family have fought through and daily fight through the unspeakable hell of EDS. <br /><br />This surgery unfortunately can not cure EDS, but it can alleviate the violent and debilitating spasms that now plague her body daily, relieve the pain in her head and spine, and stop her from deteriorating further<br />Please help Elaine continue to live, her family needs her. <br /><br />We are waiting for the final quote for Elaine's surgery but the costs in all will be around €80,000. <br />We will update this target if needed. <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/51794068_1602277261397334_r.jpeg" width="100%" media_type="3" alt="51794068_1602277261397334_r.jpeg" /><br />My heart felt appeal for Elaine's surgery comes from a friendship found in a similar journey...<br />Just a few months ago my little 11 year old daughter and myself who both also have EDS, had surgery with the very same incredible surgeon who will perform Elaine’s Surgery! <br /><br />This surgery saved our lives, and gave us both a future! <br />Please please give this incredible Mum the same chance I have been given. <br />Even the smallest amount given by many individuals can make all the difference! <br />Please give what ever you are able, as often as you are able, to help Elaine have her urgently needed surgery, as soon as possible! <br /><br />As I mentioned, Elaine’s wonderful little girl Ruby has many on going health care needs because of her EDS, and she will unfortunately at some time also need to have surgery. <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/51794068_1602277155264447_r.jpeg" width="100%" media_type="3" alt="51794068_1602277155264447_r.jpeg" /><br />I will link below to Ruby’s separate go fund me which is run by Elaine. <br />If you can, please give also to help her.<br />You can follow Ruby’s on going health care journey on Facebook at “Ruby’s Journey”<br /><br />Thank you all so so much for helping me help my precious friend. <br />Please share this go fund me anywhere and everywhere you possibly can, please let everyone know what an amazing lady Elaine is, and how much she needs your help! <br /><br />Leanne Hill<br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/51794068_1602277410237935_r.jpeg" width="100%" media_type="3" alt="51794068_1602277410237935_r.jpeg" /><br /><a href="https://www.gofundme.com/f/8b87y-ruby039s-healthcare" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.gofundme.com/f/8b87y-ruby039s-healthcare</a>

Saving Elaine

Hi, this is Ruby, she is 5 years old and has no medical care in Ireland. <br /><br />Every hospital appointment ends in how they can't help her, one hospital told us "your daughter has to many issues for us to help her", "we can't help" so we have no choice but to travel for health care. <br /><br />Last May we thought our worst fears had come true and we had lost her as nothing I did was bringing her around.  Our local hospital told us how lucky she was to be alive but we were sent home because they didn't know how to help her, I was terrified so I rang a doctor in London who is one of the very few who can see pass Ruby's smiles. That itself was brilliant.  This winter was horrific and we fear for the next one as I felt I was struggling to keep her here, every 7 mins pulling her up to breathe all night long. In December a respected Doctor told me Ruby needs health care so she can grow up.<br /><br />Ruby is diagnosed, hEDS (suspected Vascular), MCAS, chronic fatigue, Dysautonomia or autonomic dysfunction, Hypomobitlity of the throat, enlarged tonsils, sleep apnea, chromosome deletion 18, eyes dislocation, loss of eye sight and absent seizures,  GERD, hiatus hernia  she spends most nights having to be pulled up so she will breathe, she is extreme pain constantly and every time she runs or walks a distance she dislocates her bones so she uses a wheelchair, her throat issues mean she can go for days even weeks without eating at a time, due to pain she can also be awake for days before covid she only managed 2 half days of school a week on a good week but loved school. This is to name  some of her conditions and we were told more will follow when she is old enough to be diagnosed officially. <br /><br />Ruby has traveled to London where she sees a great specialist but because we can't get it writing from our hospitals that they can't  help her or there is no consultant in Ireland to refer her we can't avail of any of the medical aboard schemes. <br />I have contacted the minster for health numerous times and have spoken Leo Varadkar.<br /><br />Ruby needs to have genetics done in London as she was refused here even after 4 appeals, she needs an upright MRI, she needs to be seen by her specialist, a knowledgeable ENT, Ophthalmologists, cardiology,  respiratory, genetics, Gastroenterologist, orthopaedic, ot, physio,  pain management  and many of our EDS friends and a specialist I have seen believe/suspect Ruby also has neck instability and chiari so she also needs this to be investigated to cross it of but it is almost certain as I have these conditions. These are just a few of the areas I know off that she needs to be seen in but most likely more will be added after her tests. <br /><br />Ruby is a very happy child, you will very rarely see her without her smile or lipstick.  She lights up my day every day and sees the good in everything. We are doing the go fund me as we just want her to receive treatment and grow up.  Sadly trips aboard add up very fast. We are lucky to have wonderful friends. <br /><br />Thank you so much for reading and supporting if you can. <br /><br /><br /><a href="https://www.facebook.com/RubysEDSJourney/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/RubysEDSJourney/</a>

Ruby's Journey (medical care)

Tara  Berry

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Tara Berry

Tara Berry

What Tara cares about

Tara’s featured causes

Athlone Boxing Club's Future Build

please support to send us on a family holiday

Saving Elaine

Ruby's Journey (medical care)