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, my name is Heidi and I am the co-founder and manager of Little Buttons Charity Preschool. I would like to raise money to install aircon units into preschool to ensure we can open during any further heat waves and ensure the wellbeing of children and staff.
</div>

Little Buttons Charity Preschool

<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_177905808772333_r.jpg" width="100%" />
<div>Go fund me take a percentage of all donations
</div>
<div><br />
</div>
<div>*UPDATE*
</div>
<div><br />
</div>
<div>We went for Margo's first round of stem cell treatment at the end of April and followed this with intense physiotherapy and hyperbaric oxygen - none of this would have been possible without you all, so thank you! We have already noticed Margo is more alert &amp; has better head control.
</div>
<div><br />
</div>
<div>We are now fundraising for the second round of stem cell treatment and intense physiotherapy in Paris, and a second week of intense physiotherapy in Jersey. Unfortunately we didn't factor into the fundraising total how expensive flights and accommodation would be so we have increased the total amount required. We appreciate every donation massively. Thank you.
</div>
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_1779058136852565_r.jpg" width="100%" />
<div><br />
</div>
<div><br />
</div>
<div>Margo’s Marvellous Mind: Our Journey to Stem Cell Therapy
</div>
<div><br />
</div>
<div>Margo is a fighter. Born on September 9th, 2023, as one of triplets, she faced a traumatic start to life.
</div>
<div>After a high-risk pregnancy and an emergency C-section, Margo suffered a severe brain injury due to oxygen deprivation.
</div>
<div><br />
</div>
<div>Doctors initially feared she might not survive. Today, Margo lives with the effects of having about 10% of her brain remaining, including high muscle tone and seizures that require heavy medication.
</div>
<div>But Margo is so much more than a statistic—she is aware, she loves sunshine and cuddles, and she is working incredibly hard with her physio and neurology teams to gain head control and strength.
</div>
<div><br />
</div>
<div>The Current Mission: A Race Against Time
</div>
<div>We are focused on a critical window of neuroplasticity.
</div>
<div>Research shows that the greatest benefits for brain injuries occur within the first nine months to a year.
</div>
<div>While our original plans for a clinic in the Netherlands changed after they ceased trading, we have found a superior facility in Europe that offers advanced stem cell therapy.
</div>
<div><br />
</div>
<div>How Your Support Helps
</div>
<div><br />
</div>
<div>We have raised enough for Margo’s first treatment.
</div>
<div>However, to give her the best outcome, we need to reach our goal of £150,000 to cover:
</div>
<div>• Stem Cell Treatments: We are aiming for 6 sessions, with each session costing approximately £22,000.
</div>
<div>• Travel from Guernsey, and accommodation
</div>
<div>. A week block intensive physiotherapy post stem cell treatment.
</div>
<div><br />
</div>
<div>Join Margo’s Journey
</div>
<div><br />
</div>
<div>We are a family doing everything we can to give Margo the world. If you cannot donate, please consider sharing this page to help us reach more people.
</div>
<div>• Follow her on Instagram: @margos_marvellous_mind
</div>
<div>• Follow her on TikTok: <a href="https://www.tiktok.com/" target="_blank" rel="noreferrer noopener"><a href="https://www.tiktok.com/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.tiktok.com/</a></a>@margos_marvellous_mind?_r=1&amp;_t=ZS-93mmu9OzbSp
</div>
<div><br />
</div>
<div>Thank you for helping us fight for Margo’s marvellous mind.
</div>
<div><br />
</div>
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_1767820879591038_r.jpeg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_1767820824105298_r.jpeg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_1767820782144663_r.jpeg" width="100%" />
<div><br />
</div>
<div><br />
</div>
<div><br />
</div>
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/82476643_1730133638262844_r.jpeg" width="100%" />
<div><br />
</div>

Margo’s stem cell journey

<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787288267131418_r.jpg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_178728817481267_r.jpg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_178728804861450_r.jpg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787287995939951_r.jpg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787287860140195_r.png" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787287824452135_r.png" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787287781133589_r.png" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787287739107081_r.png" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787243210473675_r.jpg" width="100%" />
<div><br />
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/104588841_1787243143267139_r.jpg" width="100%" />
<div>Please Help Crissi Continue Her Fight Against Brain Cancer.
</div>
<div><br />
</div>
<div>UPDATE: Due to your immense support and generosity Crissi is currently in Munich having individualised Dendritic Cell immunotherapy with Dr Gansauge at the LDG clinic. We have been advised that this will remain active in her body for the next 3-4 months. It is our hope that this treatment can be repeated in 4 months time but of course this would be dependent of raising enough funds to cover a 2nd course of treatment. There has been so much publicity about the lack of brain cancer treatment options in the U.K. over the last few weeks with so many people having to go abroad for treatments that will give them a chance of life. I pray that Mr Burnham and his government listen to this public outcry of inhumanity and brings the U.K. up to date with treatments available in Europe and the rest of the world. Thank you for reading our story
</div>
<div><br />
</div>
<div>In 2016, our world changed forever.
</div>
<div><br />
</div>
<div>Crissi was diagnosed with a Grade 4 Glioblastoma brain tumour — one of the most aggressive and devastating forms of brain cancer.
</div>
<div><br />
</div>
<div>At Southampton Hospital, she had already endured major brain surgery, only to be rushed back into theatre just 12 hours later after suffering a bleed on her brain. She then spent a week fighting for her life in ICU before we were called into a side room and given the news no family is ever prepared to hear.
</div>
<div><br />
</div>
<div>The biopsy confirmed it was a Grade 4 Glioblastoma.
</div>
<div><br />
</div>
<div>The surgeons had managed to remove only 60–70% of the tumour. Radiotherapy and chemotherapy would follow, but then the consultant quietly said the words that shattered us all:
</div>
<div><br />
</div>
<div>“12 to 18 months survival.”
</div>
<div><br />
</div>
<div>In that moment, our hearts broke.
</div>
<div><br />
</div>
<div>But while we crumbled around her, Crissi did not.
</div>
<div><br />
</div>
<div>She chose to fight.
</div>
<div><br />
</div>
<div>And for the last 10 years, she has fought this cruel disease with every ounce of strength, courage, and determination imaginable.
</div>
<div><br />
</div>
<div>Brain cancer changes a person forever. We grieved deeply for the “old” Crissi, but the woman who emerged after surgery showed us a different kind of strength — pure, selfless, and full of love. Even on her darkest days, she still smiles warmly at strangers and says:
</div>
<div><br />
</div>
<div>“Now you have a lovely day.”
</div>
<div><br />
</div>
<div>That is who Crissi is.
</div>
<div><br />
</div>
<div>The strongest, kindest, most courageous soul we know.
</div>
<div><br />
</div>
<div>Crissi met her husband, Dave McMahon, in 1995, and the love they share is something truly special — unwavering, loyal, and deeply pure. For the last decade they have stood shoulder to shoulder, facing every surgery, every scan, every setback, and every heartbreak together.
</div>
<div><br />
</div>
<div>Now they need your help.
</div>
<div><br />
</div>
<div>A routine MRI scan in August 2025 was devastatingly misreported as “stable” with “no action required.” Tragically, no contrast dye was used during the scan — something essential for identifying tumour regrowth — and the images were not reviewed by a specialist neuroradiologist.
</div>
<div><br />
</div>
<div>As a result, active disease was missed and allowed to grow untreated for 10 months.
</div>
<div><br />
</div>
<div>Even more heartbreakingly, when Crissi later attended A&amp;E with frightening neurological symptoms, she was sent home and told it was simply fatigue.
</div>
<div><br />
</div>
<div>The consequences these failures have been catastrophic. (THESE ARE NOT FAILURES OF ANY NHS HOSPITALS)
</div>
<div><br />
</div>
<div>Crissi has now been told that potentially life-extending immunotherapy treatment is not available through the Guernsey healthcare system or the NHS.
</div>
<div><br />
</div>
<div>Her only hope now is to travel to Germany for specialist treatment.
</div>
<div><br />
</div>
<div>Dave and Crissi are desperately trying to raise funds to access potentially life-saving immunotherapy treatment, including Dendritic Cell Therapy in Berg, Germany, at the LDG clinic.
</div>
<div><br />
</div>
<div>But time is no longer on our side.
</div>
<div><br />
</div>
<div>These treatments are extremely expensive, and every day matters.
</div>
<div><br />
</div>
<div>We are asking, from the bottom of our hearts, if you can please help in any way possible. No donation is too small. Every single contribution brings Crissi one step closer to accessing treatment and continuing the fight she has battled so bravely for the last decade.
</div>
<div><br />
</div>
<div>If we are fortunate enough to raise more than is needed for treatment, every remaining penny will be donated to brain tumour charities to help other families facing this devastating disease.
</div>
<div><br />
</div>
<div>Please donate if you can, and if you are unable to donate, please share Crissi’s story.
</div>
<div><br />
</div>
<div>Thank you for helping us fight for more time with someone we love beyond words.
</div>
<div>Crissi is now in the amazing hands of the Christie hospital Manchester
</div>
<div><br />
</div>
<div>UPDATE
</div>
<div>Through your generosity I have now managed to fly to Munich and complete 1 round of the Dendritic cell therapy. This will remain active in my body for the next 3-4 months my dream is to be able to access a 2nd round of this treatment to give me the best chance for the NHS to catch up with the rest of the world
</div>

Please Help Crissi keep fighting

<div><strong>****UPDATE AUGUST 2022 **** </strong>
</div>
<div><br />
</div>
<div><strong>Romy has endured 9 months of intense treatment with courage and grace but we are still only half way through her treatment plan. We would like to thank every single person and organisation that has donated to our fundraiser, a thank you email was sent out several months back but in case you missed it we would like to thank you from the bottom of our hearts these funds are helping with living expenses and to pay our mortgage back home while we live in the whirlwind of treatment away from our normal lives. We created a blog to keep everyone updated on Romys progress romyocean.gg</strong>
</div>
<div>--------------
</div>
<div><br />
</div>
<div>Guernsey reception class pupil Romy McGahy just 4 was recently diagnosed with stage 4 cancer.
</div>
<div> 
</div>
<div>This has been a devastating shock for her entire family having only just started school and then suddenly now their worlds have turned upside down.
</div>
<div> 
</div>
<div>Romy is having to undergo aggressive chemotherapy, a big operation and further treatment and the road ahead is going to be long.
</div>
<div> 
</div>
<div>Her parents, Helen and Tom and little sister Zephyr are now in Southampton to be with her as she undergoes her treatment at Southampton hospital they want to be there as much as possible every step of her journey.
</div>
<div> 
</div>
<div>We are hoping to raise some money to help the family through this awful time
</div>
<div> 
</div>
<div>Romy's Mum, Helen says: " Romy had been poorly for 4 weeks in Guernsey and had not eaten a single proper meal in that time, she had abdominal pain and the Dr had diagnosed mesenteric adentitis (swelling of the lymph nodes) which would resolve on its own in time, however we were referred to a specialist just to check things the following week. After a visit to A&amp;E a few days later due to some neck pain the drs checked her bloods and all looked normal so we were sent home, we went for a fairly routine ultrasound scan the next day where the sonographer (looking for the enlarged lymph nodes or appendicitis) found an 18cm tumour in her tummy. Romy never went home after that ultrasound scan and after one night on the ward in Guernsey, 24 hours later, exactly one month before her 5th birthday, we were in Southampton on the Piam Brown ward, a specialist children's Cancer ward in Southampton General Hospital. Romy was diagnosed with Neuroblastoma, a cancer almost always found in children which makes up just 6% of childhood cancers. Romys neuroblastoma has been characterised as high-risk neuroblastoma as it has spread to other areas of the body, around 50% of children with high-risk category neuroblastoma will be cured of their disease. Children with high risk neuroblastoma require intensive treatment from the start because their neuroblastoma cells are highly cancerous and more aggressive in the body. In the blink of an eye our world has been turned upside down and our beautiful daughter is on a terrifying unknown path."
</div>
<div><br />
</div>
<div>As Romy's uncle Nathan Crabb is UK registered he is registered as the beneficiary and will pass all money raised directly to Romy's parents.
</div>

Help Romy McGahy aged 4 and her family

Richard Vahey

Richard Vahey

Richard Vahey

Featured causes

Little Buttons Charity Preschool

Margo’s stem cell journey

Please Help Crissi keep fighting

Help Romy McGahy aged 4 and her family

About me