Hanukkah Cards for Medical charities

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.

For more information visit app-network.org

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.

For more information visit alzheimers.org.uk

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.

For more information visit ammf.org.uk

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.

For more information visit https://www.arfidawarenessuk.org

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.

For more information visit arkcancercharity.org.uk

The Asthma and Allergy Foundation provides education, support, and resources for individuals affected by asthma and allergies. They aim to improve quality of life through awareness campaigns, research funding, and advocacy for better healthcare policies. Their initiatives also focus on fostering understanding and management of these conditions within communities and promoting healthier environments.

For more information visit asthmaandallergy.org.uk

At Blood Bikes Wales we gear up to provide a completely free courier service for the NHS, relying solely on volunteers and donations to offer this service. This is not possible without your support

For more information visit bloodbikes.wales

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

For more information visit https://www.bowelresearchuk.org/

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.

For more information visit breathingmatters.co.uk

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.

For more information visit burningnightscrps.org

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.

For more information visit cancer-lifeline.org

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.

For more information visit //c-r-y.org.uk

Children's Cancer Research Fund 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.

For more information visit childrenscancerresearchfund.co.uk

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.

For more information visit chilternsmscentre.org

Cleft Lip and Palate Action (CLAPA) is the national charity for people affected by cleft lip and palate in the United Kingdom. We support people to take control of their journey, connect with others, and use their voices to impact the future of care.

For more information visit ww.clapa.com

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.

For more information visit cureparkinsons.org.uk

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.

For more information visit //cysticfibrosis.org.uk

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.

For more information visit debra.org.uk

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

For more information visit diabetes.org.uk

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.

For more information visit doctorsoftheworld.org.uk

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.

For more information visit dystonia.org.uk

FOP Friends was established to raise money and awareness for the rare genetic condition Fibrodysplasia Ossificans Progressiva (FOP)

For more information visit fopfriends.com

Haemochromatosis UK is dedicated to raising awareness and providing support for individuals affected by hereditary haemochromatosis. They offer information, resources, and advocacy to improve diagnosis and treatment. The organisation works to educate healthcare professionals and the public about the condition, aiming to enhance quality of life for those impacted by iron overload disorders.

For more information visit huk.org.uk

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.

For more information visit headwayluton.com

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.

For more information visit headwaysomerset.org.uk

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.

For more information visit www.heartcare.org.uk

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.

For more information visit heartburncanceruk.org

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.

For more information visit hopeagainstcancer.org.uk

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.

For more information visit hopefortomorrow.org.uk

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.

For more information visit khc.org.uk

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.

For more information visit leukaemiauk.org.uk

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.

For more information visit longcovid.org

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.

For more information visit mencap.org.uk

Meniere's & Vestibular UK helps people with vestibular (inner ear) disorders. We provide essential support and information to enable people to cope positively and get the right diagnosis. We are a voice for sufferers and raise awareness within the medical community and wider public for greater understanding. We work towards a brighter future through investment in vital medical research.

For more information visit meandve.org.uk

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.

For more information visit meningitisnow.org

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.

For more information visit mercyships.org.uk

Mesothelioma UK is a charity dedicated to improving the lives of those affected by mesothelioma, a type of cancer linked to asbestos exposure. They provide information, support, and resources for patients, families, and healthcare professionals. The charity also promotes research and raises awareness about the disease to help improve diagnosis and treatment outcomes.

For more information visit mesothelioma.uk.com

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.

For more information visit www.mind.org.uk

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.

For more information visit mndassociation.org/about-us/

My Shining Star Children’s Cancer Charity supports children diagnosed with cancer and their families. They provide financial assistance for treatments, essential equipment, and respite services. The charity also offers emotional support and creates memorable experiences for the children, helping to alleviate the challenges of cancer and improve their quality of life during treatment.

For more information visit myshiningstar.co.uk

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.

For more information visit nass.co.uk

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.

For more information visit www.tremor.org.uk

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.

For more information visit nstrust.co.uk

Nerve Tumours UK provides support and information, as well as campaigns and raises awareness on behalf of over 26,500 children and adults 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 help.

For more information visit nervetumours.org.uk

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

For more information visit neta.org.uk

North West First Responder Group provides vital emergency medical support by training volunteers to respond to medical emergencies in their communities. They work alongside local healthcare services to ensure rapid response to incidents, offering essential care until professional medical teams arrive. Their commitment enhances community safety and helps save lives through prompt action and first aid training.

For more information visit nwfrg.co.uk

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.

For more information visit nwpcc.charity

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.

For more information visit northumbriabloodbikes.org.uk

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.

For more information visit //opa.org.uk

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.

For more information visit pelvicpartnership.org.uk

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.

For more information visit pernicious-anaemia-society.org

Polio Survivors Network provides an information service including regular newsletters for polio survivors, their families, friends and health professionals. Thank you.

For more information visit poliosurvivorsnetwork.org.uk

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.

For more information visit preventbreastcancer.org.uk

Prostate Scotland is a Scottish charity set up to inform, support and advance on prostate cancer and disease in Scotland. 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.

For more information visit prostatescotland.org.uk

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.

For more information visit pscsupport.org.uk

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.

For more information visit www.supportqvh.org

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.

For more information visit reachbwindi.com

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.

For more information visit www.RetinaUK.org.uk

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.

For more information visit risinggirl.co.uk

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.

For more information visit safe4all.org.uk

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.

For more information visit sarcoma.org.uk

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.

For more information visit //shinecharity.org.uk

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.

For more information visit smiletrain.org.uk

Kawasaki Disease is the leading cause of acquired heart disease in children in the U.K. It’s time we changed that…
…Together we will.

For more information visit www.societi.org.uk

SUDEP Action is dedicated to raising awareness of epilepsy risks and tackling epilepsy deaths including Sudden Unexpected Death in Epilepsy

For more information visit sudep.org

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.

For more information visit //annerobsontrust.org.uk

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.

For more information visit hyperinsulinism.co.uk

The ME Association is a UK-based charity dedicated to supporting individuals affected by myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS). They provide information, guidance, and advocacy to improve the quality of life for those living with these conditions, whilst also funding research to better understand and treat ME/CFS.

For more information visit meassociation.org.uk

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.

For more information visit themurrayparishtrust.com

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.

For more information visit www.musictherapy.org.uk

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.

For more information visit www.roh.nhs.uk

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.

For more information visit treachercollins.org.uk

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.

For more information visit tuberous-sclerosis.org

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.

For more information visit //twinstrust.org

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.

For more information visit versusarthritis.org

We believe that every child with cancer, wherever they live in the world, should have equal access to the best possible treatment and care.

We partner specialised healthcare professionals from high income countries to those in low income ones to improve treatment standards.

For more information visit //worldchildcancer.org

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.

For more information visit wtgf.org

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.

For more information visit https://www.youngepilepsy.org.uk

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.

For more information visit

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

For more information visit mariecurie.org.uk

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.

For more information visit parkinsons.org.uk

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.

For more information visit

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.

For more information visit sja.org.uk