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<div>Hi my name is Keira and I am Maximus’s mum, or Mighty Max as we like to call him. 
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<div>Maximus is 7 years old and has been fighting brain cancer since he was just 10 months old. 
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<div>In just under 7 years he has had 6 brain tumours, 28 doses of chemotherapy, 93 sessions of radiotherapy, numerous surgeries and blood transfusions and developed some life changing conditions due to all of this. 
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<div>He does not know what it is like to live “a normal” life. I am fundraising to try my best to give him this and raise money to try to get him life saving treatment over in Germany as the tumours keep returning and their is no longer anything else that the NHS can do to cure him.
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<div>Maximus was diagnosed on 2nd October 2017 at just 10 months old. A day we will never forget! A 6cm tumour in the back of his tiny little brain which was diagnosed as an Ependymoma, at the time we were told that he had a 50% chance of survival and that it would most probably come back. Over the years, as it has come back the chances of survival have gotten much lower. 
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<div>After years of research and our own personal experiences, we now know that Ependymoma does not typically respond to any known chemotherapy and that radiotherapy and surgery can be effective in only a few patients. However when these tumours reappear there is no effective therapy, and we are just simply buying time. Treatment options have remained unchanged for the past 30 years but quite recently there has been a huge advancement in Immunotherapy to treat cancer.
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<div>Immunotherapy induces the immune system to fight against these tumours and the UK have started using it to treat other cancers, but unfortunately it is not available here for the cancer that Max has. Therefore we need to go to Germany where they will be able to use personalised treatment to hopefully save my beautiful, caring and kind little boy. 
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<div>This advanced treatment is incredibly expensive and on top of treatment costs we will require travel, accommodation and insurance, possibly for a number of years. We cannot simply afford this by ourselves and we are relying on the kindness and generosity of you to help us save Maximus. 
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<div>No matter how big or small, we will be extremely grateful for any donation or even awareness that you can make to help us.
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<div>Thankyou for taking the time to read this. 
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<div>lots of love and hope 
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<div>Keira (Mighty Max’s Mum) 
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Find a cure for Mighty Max

<div>Hi, I’m Andy, the head coach of a girl’s football team in Cheshire – the Chester Nomads Zebras under 11s.
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<div>We are so lucky to have 13 committed girls in our squad who try their best every time they step onto the pitch - in the blazing sunshine, freezing cold, wind or pouring rain! 
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<div>They train hard, play to win, work together and have a brilliant time along the way. Their ongoing growth and development is fantastic to see and both parents and coaches are so proud of them and can’t wait to see their journey continue.
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<div>They are currently in their first season in a boy's league and have had a really strong start to the season, with some hard-fought victories and strong performances.
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<div>We have really struggled to get any sponsorship since the team was formed. They've had to play in second hand kits and use second hand equipment when the older boy's teams have finished with them. 
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<div>The girls have already held their own fundraising event - a sponsored walk (up a mountain, in Halloween fancy dress, on a very windy day!) and the money raised was used to buy waterproof training jackets, kits and training equipment. 
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<div>Our fundraising continues, as it is necessary just to make sure that they can continue to do what they love. 
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<div>We have created an amazing opportunity for the girls.... 
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<div>In October 2024, they have the chance to travel to Madrid, where they would have coaching sessions with youth team coaches from both Real and Atletico Madrid, tours of both stadiums and games against local opposition.
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<div>We would LOVE for the whole squad to go on this trip and we're sure it would be both educational and inspiring for them.
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<div>As you can imagine, there are significant costs involved in something like this and the only way that most of the girls would be able to attend is if we raise money through donations and sponsorship. 
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<div>We would be so grateful if you were able to offer some support to our amazing squad to help them to continue their football journeys.
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<div>Thanks for reading! :-) 
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Chester Nomads Zebras U11 girl's football team

<div>Hi my name is Hugo. I'm 10 years old.
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<div>I'm trying to raise money to find a cure for my condition. I have Nephrotic Syndrome which is a rare kidney disorder.
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<div>I have Been designing and Hand drawing cards then selling them to raise money for NeST Charity Trust.
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<div>Nephrotic syndrome is a kidney disorder that causes your body to pass too much protein in your urine.
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<div>Currently there is no cure, just medication to stableilise.
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<div>If you would like to buy my cards but have no cash, just scan the QR Code and donate the money direct
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Help find a cure for Nephrotic Syndrome

<div>Chester Nomads football club brings football to the community of Chester and surrounding areas where in addition to the great seniors teams it also caters for over 200 children. There are teams from the age of 7 to 16 and a development club for 5 to 7 year olds. We are run partly by volunteer coaches and parents. The girls under 12s Jaguars team have an amazing opportunity to take part in the Gothia Cup in Sweden 2024 where we want to win for our community and our country … but we need your support! The Gothia Cup is the largest youth football tournament in the world with 1600 teams from 170 countries… there’s nothing quite like it.
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<div>This is a once in a lifetime opportunity for our girls to build confidence and skill by playing the world’s greatest teams. The parents and girls are currently doing a lot of fundraising to help but as the tour cost exceeds £500 per person we need to raise money to meet the shortfall - that's where you can help us achieve our aim. We are really grateful for any contributions and words of support you can give.
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Get The Jags Team to the World Youth Cup 2024

Dear Friends,<br /><br />I am usually a private person and do not like sharing this information. However, unfortunately, my mother, 66 years young, suffered a heart attack in Bolivia (Home), where she was treated and somewhat stabilized; however, due to inadequate treatment, she developed heart failure and is now requiring a Double Bypass (possible triple bypass) surgery and mitral valve replacement via open heart surgery.<br /><br />The problem is that there is only one capable doctor in Bolivia who can perform this operation (in a different city from where my parents reside). As this is a critical situation, she is in need of immediate medical care and that particular physician does not have availability to accommodate her in a timely manner. She has developed fluid in her lungs and has difficulty breathing. La Paz is also 12,000 ft above sea level and does not allow her to get adequate oxygen perfusion during this hard time. Thus, we have decided to take her to Chile, where she will be at sea level and can obtain immediate care from better doctors. <br /><br />After the surgery is done, she will need to stay in a foreign country for two to three months to recover with my dad.<br /><br />Due to all the reasons above and because we have already invested a lot of cash thus far to keep her stable while in Bolivia this past December, we are turning on this site with the goal of helping us offset the financial burden that has been placed upon myself and my family. Unfortunately, medical care in Bolivia is not the same as it is here in the United States; all medical treatment received thus far, and that will be done in the future, <strong>will all be cash pay</strong>. That being said, this fund will not cover all of the expenses but it will definitely be a significant contribution.<br /><br />All mothers are precious and I want to do everything I possibly can to keep my beloved mother healthy and close to us for as long as possible.<br /><br />Therefore, my family and I are asking for any help that you are willing to provide in order to prolong my mother's life. No matter how big or small your generosity WILL make a difference.<br /><br />Thank you for taking the time to read this and we are forever grateful for your love and support.<br /><br />Love, <br />Omar &amp; The Liendo Family

URGENT Medical Matter; Mom's Open Heart Surgery

Neil Zarac

Neil Zarac

Neil Zarac

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