Personalised Charity Cards - Making A Difference Cards
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Passover Cards for Medical charities
Once you've selected your favourite charity you can choose from personalised passover cards where you can add photos and custom text, or from our huge range of non-personalised cards that we are sure will make them smile on their special day.
Looking for a specific charity? Try filtering the list using the search bar below:
APP is the national charity for women and families affected by postpartum psychosis (PP). PP is a severe mental illness which begins suddenly following childbirth, affecting around 1400 women each year in the UK. We offer provide support and information for those affected by PP.
Charity Registered in England and Wales no. 1139925. Company Limited by Guarantee no. 7466643.
We’re the UK’s leading dementia charity. We provide information and support, improve care, fund research, and create lasting change for people affected by dementia. Our vision is a world without dementia.
AMMF - The Cholangiocarcinoma Charity is dedicated to raising awareness and funding research for cholangiocarcinoma, a rare bile duct cancer. They support patients and families through information resources, advocacy, and collaboration with researchers and healthcare professionals to improve diagnosis, treatment, and outcomes for those affected by this disease.
The UK’s only registered charity dedicated to raising awareness and furthering information about Avoidant/Restrictive Food Intake Disorder. As a not-for-profit, we work to provide individuals, parents, carers and medical professionals with up-to-date relevant information, research and support.
Ark Cancer Centre Charity is fundraising to help provide supportive care and services, complementary therapies, and an enhanced environment in a NHS cancer treatment centre at Basingstoke and North Hampshire Hospital.
Bowel Research UK is funding life-changing research into bowel cancer and other bowel diseases. Every year over 16,000 people die from bowel cancer in the UK and over a million suffer from bowel disease. By researching cutting edge treatments and investing in the best science, Bowel Research UK are saving and improving people’s lives
Breathing Matters’ mission is to raise awareness and inspire fundraising for research into pulmonary fibrosis and lung infection. Breathing Matters strives to improve the lives of every pulmonary fibrosis, bronchiectasis and lung infection sufferer by funding research into treatments and cures, and by spreading awareness and knowledge of these conditions.
Burning Nights CRPS Support is working to support all those affected by Complex Regional Pain Syndrome (CRPS), from awareness and education to campaigning and support services, we're on a mission to ensure no-one affected by CRPS is alone. CRPS is a debilitating chronic condition that affects approximately 15,000 people in the UK every year. Please show your support in any way you can.
Cancer Lifeline South West offer vital support to individuals and their families when confronted with a cancer diagnosis. Services include emotional counseling, practical guidance, and group support sessions. Cancer Lifeline South West provide a caring and nurturing environment where those dealing with cancer can access the help they need, fostering a sense of community and emotional well-being during their cancer journey.
Cardiac Risk in the Young (CRY) is a UK charity focused on preventing young sudden cardiac deaths through awareness, screening, research, and bereavement support for families affected by these tragic health issues.
The Chilterns Neuro Centre is a charity based in Wendover, Buckinghamshire, which supports people affected by multiple sclerosis (MS), Parkinson’s and stroke survivors. We currently work with more than 700 members, building a community in which people affected by these conditions can live life to the full.
CLAPA (Cleft Lip and Palate Association) supports individuals with cleft lip and/or palate, alongside their families. They provide information, resources, and networking opportunities, fostering understanding and acceptance. CLAPA also advocates for improved healthcare services and raises awareness about clefts, aiming to enhance the quality of life for those affected by these conditions.
We’re here for the cure. Cure Parkinson’s is working with urgency to find new treatments to slow, stop and reverse Parkinson’s. Our funding and innovation has redefined the field of Parkinson’s research, enabling the world’s leading researchers to prioritise the next generation of drugs for clinical trial. Together we will conquer Parkinson’s.
The Cystic Fibrosis Trust is fighting for a life unlimited for everyone affected by cystic fibrosis. Cystic fibrosis (CF) is a life-limiting condition that makes it difficult to breathe
& causes vulnerability to infection. Our mission is to create a world where being born with CF no longer means a lifelong burden of care and an early death, when everyone living with the condition will be able to look forward to a long, healthy life.
DEBRA is the national charity that supports individuals and families affected by Epidermolysis Bullosa (EB) – a painful genetic skin blistering condition which, in the worst cases, can be fatal. There are at least 5,000 people living with this devastating condition in the UK and 500,000 worldwide.
As the UK’s leading diabetes charity, our mission is that by bringing people together to work in partnership, we will support those living with diabetes, prevent type 2 diabetes, make research breakthroughs, and ultimately find a cure
Dystonia is a neurological movement disorder that is estimated to affect at least 100,000 people in the UK. Dystonia UK exist to give hope and support to everyone living with dystonia and to create UK and worldwide awareness.
Friends of Rosie is a volunteer-led charity that provides funding for children’s cancer research to get new ideas off the ground. Without our help many research projects would never get underway, meaning critical breakthroughs in childhood cancer research being left undiscovered.
Headway Luton provides a wide range of quality care and personal support to meet the individual needs of individuals aged 18 years and above who have acquired brain injuries. They offer support, advocacy, ABI related advice, and information to clients, their families, and/or carers residing in Luton and its surrounding areas. Headway Luton is dedicated to serving the diverse communities within these regions.
Headway Somerset exists to support individuals with acquired brain injury (ABI) and their families. In Somerset every year about 3000 people have a hospital admission due to ABI.
We aim to support and encourage as many people in the local community as we can who suffer from cardiovascular disorders, circulatory disorders, chronic lung disease or long term conditions such as cancer, stroke, TIA or diabetes.
Our Charity will collaborate with agencies and partners in the community and work closely with the Walsall Clinical Commissioning Group to ensure that the service meets the requirements of the local population.
We raise awareness about the dangers of persistent heartburn, gastro-oesophageal reflux disease (GORD) and Barrett's oesophagus. Sometimes these conditions can lead to more serious conditions such as oesophageal cancer. Many people are unaware of this and we are trying to change that.
Hope Against Cancer’s mission is to fund innovative research that leads to improved treatments and better outcomes for cancer patients in Leicestershire and Rutland. We do this by working in partnership with local universities and hospitals to ensure that Leicestershire remains a centre of excellence for cancer research and treatment to achieve the greatest impact in the local and national fight against cancer.
We understand that time is a crucial factor for patients, and in 2007 we launched the world’s first ever Mobile Cancer Care Unit (previously Mobile Chemotherapy Unit) to bring vital cancer care closer to patients, enabling them to spend more time with family, friends and loved ones.
We develop, build, provide and maintain MCCUs to support patients who are going through cancer treatment by alleviating the stresses and strains of travelling for appointments, along with reducing hospital waiting times.
Kingston Hospital Charity is the official charity of Kingston Hospital NHS Foundation Trust. Kingston Hospital Charity's mission is to work with colleagues from across Kingston Hospital, as well as key partners and stakeholders, to help ensure every patient experiences outstanding care and the best possible outcome.
Leukaemia UK believe research has the power to stop leukaemia devastating lives. Despite decades of incredible progress, only half of leukaemia patients live longer than five years after their diagnosis. Leukaemia UK won’t stop until they change this.
Long Covid Support provide peer support, advocacy and research involvement into the long-term effects of SARS-CoV2.
Our goal is to improve the futures of people with Long Covid by ensuring equitable access to high quality healthcare, employment rights and welfare services.
Mencap is the leading voice of learning disability. Everything we do is about valuing and supporting people with a learning disability, and their families and carers.
Our vision is a world where people with a learning disability are valued equally, listened to and included.
Meningitis Now is the UK's leading meningitis charity. We save lives and rebuild futures by funding research, raising awareness and providing support for people whose lives have been affected by meningitis.
Our vision is a future where no-one in the UK loses their life to meningitis and everyone affected gets the support they need to rebuild their lives.
We are a team of nurses, doctors, surgeons, and other crew members from all over the world, donating our time to help on board the world’s largest non-governmental floating hospital. As a floating hospital, we can sail directly to some of the world’s poorest people to deliver life-saving medical care and provide safe, state-of-the-art facilities in which to treat them.
We provide advice and support to empower anyone experiencing a mental health problem. We campaign to improve services, raise awareness and promote understanding. We won't give up until everyone experiencing a mental health problem gets support and respect.
The Motor Neurone Disease Association (MNDA) supports individuals affected by motor neurone disease (MND) through funding research, providing information and resources, and offering care and support services. They advocate for better access to treatments and services, raise awareness about MND, and promote collaboration among healthcare professionals to improve the quality of life for those living with the condition.
We are the only charity in the UK dedicated to transforming the diagnosis, treatment and care of people living with axial Spondyloarthritis (axial SpA). Together we can help more people tackle the challenges of living with the condition sooner.
The National Tremor Foundation is a UK based charity that aims to provide help, support and advice to all those living with neurological tremor irrespective of age.
At NeST, we care because we understand. Our founders have the perfect balance of expertise and empathy and they know just how challenging it can be living with the condition yourself or caring for a child who has it. Over ten years ago, our founder David Yearsley felt isolated when his son James developed Nephrotic Syndrome as a child.
Nerve Tumours UK provides support and information, as well as campaigns and raises awareness on behalf of over 26,500 people in the UK who have NF the group name for Neurofibromatosis Type 1 (NF1), NF2-related-Schwannomatosis (NF2) and Schwannomatosis (SWN) . Nerve Tumours UK are here to improve lives for people with NF, by making sure those affected have access to the help.
NETA is a charity which aims to support people in the North East with aphasia and their families. NETA does this by funding the NETA Aphasia Support Centre, which offers long term support to people with aphasia, offering opportunities to take part in a variety of groups.
NETA also aims to raise awareness of aphasia in the general public as too few people understand what aphasia mean
The North West Pre-hospital Critical Care Charity are a group of volunteers who have one common goal and that is to help those in need. Their volunteer responders are called by the ambulance service to attend serious accidents or incidents in which our extended skills or expertise are needed. They include time-served Doctors with a range of backgrounds including General Practice, Emergency Medicine, Anaesthesia and Surgery or Paramedics working as Critical Care Paramedics or Advanced Paramedics.
Northumbria Blood Bikes is a registered charity established by local volunteers to deliver essential blood and urgent medical supplies, out of hours, between hospitals and other healthcare sites in North East England. We cover Darlington, Durham, Gateshead, Newcastle Upon Tyne City, North Tyneside, Northumberland, South Tyneside and Sunderland.
The OPA has led the fight against oesophageal and gastric cancers for over 30 years. Our purpose is to support patients, their families and carers and raise awareness of these cancers and their prevention. Whatever stage you're at the OPA is here to help you.
Pelvic Partnership supports individuals affected by pelvic girdle pain (PGP) during pregnancy and postpartum. They provide evidence-based information, resources, and a community for those experiencing PGP. The organisation also raises awareness of the condition, collaborates with healthcare professionals, and advocates for better care and understanding of pelvic pain among the public and medical communities.
The Pernicious Anaemia Society raises awareness and provides support for individuals affected by pernicious anaemia. They offer information, resources, and advocacy to ensure patients receive proper diagnosis and treatment. The society fosters a community for sharing experiences and promotes research to enhance understanding of the condition, ultimately aiming to improve the lives of those impacted.
Polio Survivors Network provides an information service including regular newsletters for polio survivors, their families, friends and health professionals. Thank you.
Prevent Breast Cancer is the only UK charity funding ground-breaking research solely aimed at preventing breast cancer for future generations. Our research will one day bring about a world where breast cancer is preventable and thousands are saved from ever experiencing this terrible disease.
Prostate Scotland are a Scottish charity set up to provide information, advice and help on prostate health and diseases test and treatments. Nearly 1 in 2 men in Scotland will be affected by prostate disease at some stage of their lives and 1 in 10 are likely to develop prostate cancer. Prostate Scotland provides men and their families and partners with information about the prostate.
PSC Support is the UK’s only charity dedicated to beating the rare, autoimmune disease, primary sclerosing cholangitis (PSC). We provide patients and families with high-quality, accessible information and the support, collaborate with healthcare providers to improve clinical care, and shape and fund critical research so that we can live in a world without PSC.
Since 1996, QVH Charity has provided funding for equipment and other improvements that are above and beyond what the NHS funds to help support the life changing care provided at Queen Victoria Hospital.
Now more than ever, we are investing in initiatives that will make a real difference to staff and patients.
Resourcing Effective Accessible Community Healthcare in Bwindi, South West Uganda. REACH Bwindi is a UK charity supporting the lives and work of the communities of Bwindi, Uganda, with the aim of relieving or preventing poverty.
We are the only UK charity dedicated solely to working for people affected by inherited sight loss. Our vision is a world where everyone with inherited sight loss is able to live a fulfilling life. The information and support we provide helps people to lead better lives, today. And, we invest in medical research to accelerate the search for treatments for the future.
We give young girls and women the knowledge to build confidence they need to find their way forward. Rising Girl aims to help girls build a brighter future, working in some of the most deprived areas of the UK. Our 6-8 week programme Rise Together educates, inspires and empowers young women so that they value their education and seek out opportunities.
Without anaesthesia, emergency operations cannot be performed and in developing countries many patients do not survive, especially women in childbirth and children.
Safe Anaesthesia Worldwide was formed to ensure that the benefits of anaesthesia are available wherever needed so that patients can receive the treatment they need, safely and painlessly.
Sarcoma UK is a national charity that funds vital research, offers support for anyone affected by sarcoma cancer and campaigns for better treatments. It is the only cancer charity in the UK focusing on all types of sarcoma. Our mission is to ensure everyone affected by sarcoma receives the best treatment, care, information and support available and to create the treatments of the future.
Shine provides specialist support from before birth and throughout the life of anyone living with spina bifida and/or hydrocephalus, as well as to parents, families, carers and professional care staff. Shine enables people to get the best out of life.
Smile Train is the largest cleft-focused organisation with a model of true sustainability - providing training, funding, and resources to empower local medical professionals in 70+ countries to provide 100%-free cleft surgery and other forms of essential cleft care in their own communities.
We help hospitals to set up teams of volunteers, to give companionship and emotional support to patients in the final days of their life. The volunteers sit with patients, play their favourite song one last time, or simply hold their hand.
No one should have to face death alone.
We also provide phone support to anyone facing the end of life. Get in touch if you would like support.
The Children's Hyperinsulinism Charity supports families affected by hyperinsulinism, a rare but serious condition causing low blood sugar in children. They provide information, resources, and emotional support while funding research to improve diagnosis and treatment options. The charity raises awareness, helping healthcare professionals better understand the condition and ensuring affected families receive the care they need.
The Murray Parish Trust supports children’s emergency services across the South of England by raising money and awareness to support projects at key trauma centres, to enable pioneering research and provide life-saving equipment.
We are a national charity dedicated to supporting the highest standards of practice, research and training in music therapy. We receive no statutory funding and are completely reliant on donations.
Our mission is to support the Royal Orthopaedic Hospital to deliver the best care possible. Our projects help to ensure all patients have an amazing experience when they visit the hospital. Donations have enabled the development of staff, funded enhanced equipment & enabled pioneering research.
We offer support and friendship to Treacher Collins families and individuals. To seek to gain greater knowledge and understanding of Treacher Collins Syndrome and to offer advice to families and individuals on various aspects of the syndrome.
We also aim to help develop a clear policy on areas such as facial surgery, hearing aids and genetic counselling for Treacher Collins families and individuals.
TSC is a genetic condition that can lead to growths in various organs of the body, but those most commonly affected are the brain, eyes, heart, kidney, skin and lungs.
We support individuals and families affected by TSC. Our dedicated advisers and active community are here for you.
Twins Trust is the only UK-wide charity dedicated to improving the lives and wellbeing of families with twins, triplets or more. Multiple birth families face unique challenges and we are there for them, every step of the way. We offer support and information to parents and professionals, raise awareness, invest in research and campaign for the best possible outcomes for our families.
We’re the 10 million people living with arthritis in the UK. We’re the carers, researchers, health care professionals, friends, parents, runners and fundraisers all united in our ambition to make a difference. We’ll keep working until nobody has to tolerate the pain, isolation and fatigue of arthritis.
The World Transplant Games Federation organises international sporting events for organ transplant recipients. These games promote organ donation awareness, celebrate the success of transplant recipients, and provide a platform for participants to showcase their post-transplant health and vitality through competitive sports. They encourage a healthy, active lifestyle and inspire hope for those awaiting organ transplants worldwide.
Young Epilepsy is the only UK charity dedicated to creating better lives for children and young people with epilepsy, providing world class diagnosis, assessment and rehabilitation for children and young people with epilepsy, and offering information and support to families in crisis.
Here in the UK we run a clinic and advocacy programme in East London that provides medical care, information and practical support to vulnerable people, helping them access the healthcare they need.
Kent and Medway Medical School (KMMS) is an exciting collaboration between Canterbury Christ Church University and the University of Kent and builds on our existing high-quality clinical teaching and research strengths.
Our nurses work night and day, in people’s homes across the UK, providing hands-on care and vital emotional support. Our hospices offer specialist round-the-clock care. And we help people throughout their illness by giving practical information, support from trained volunteers and being there when someone wants to talk
Every hour, someone in the UK is told they have parkinson's. Because we're here, no one has to face Parkinson's alone. We bring people with Parkinson's, their carers and families together via our network of local groups, our website and free confidential helpline.
Prostate Cancer UK's top priority is funding research to stop prostate cancer killing men. We’re investing millions to find better treatments and better tests that can spot fast-growing cancers early, and could be used in a screening programme to save thousands of lives.
Every year, more than 400,000 people learn how to save a life through our training programmes, including hundreds of thousands of young people. Our volunteers provide first aid in their communities, keeping people safe at events, and working alongside the NHS in response to 999 calls. We’re also always campaigning to raise awareness of first aid and directly educate the public.