Pledge your support to back our campaign to introduce an allergy nurse and dietitian as part of the services offered within GP practices.
Allergy UK launched a Patient Charter in 2022 to articulate the challenges patients face in every single aspect of their lives. These range from accessing high quality care, to feeling equal in a society that dismisses their condition and disregards their needs.
It represents the voices of the allergic community; people whose lives have been impacted by a disease with no cure and who live with the anxiety, stress and mental health burden that comes with allergies; parents fearful for the safety of their children; the children and young people who experience isolation and bullying, as well as the potential effect poorly controlled allergy can have on their educational grades and subsequent job opportunities; and the people with allergy and asthma who are the first to suffer because of poor air quality.
Support our campaign
We need your help. We’re calling for patients, friends and family of patients, clinicians, and policy makers to lend their voices and support for this Patient Charter call and help us campaign for change:
Pledge your support
Tell your local politician to help raise awareness within government and achieve change
Raise awareness by sharing your experiences or showing your support.
Sign our Pledge
Now at 1,911 | Our goal: 10,000 signatures
People living with allergy have the right to a ‘Gold Standard’ of care. Pledge your support to back our campaign to introduce an allergy nurse and dietitian as part of the services offered within GP practices.
I am pledging my support to the Allergy UK Patient Charter because…
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Your Pledge Wall
I’m a registered Children’s nurse and now a university programme lead. Allergy should be embedded into all HCPs training. The most common chronic conditions in childhood but still a real lack of allergy awareness amongst most HCPs
As an allergy specialist nurse for many years, I witnessed the often serious health impact and reduced quality of life of people with allergic conditions. This will never improve until it is better understood and managed in primary care.
Our daughter has allergies and I’m getting no where with advice and help from my GP. It’s like a light has been switched on as she suddenly acquired itchy eyes and tummy aches, since April 2023. It’s heartbreaking to see her suffer, we are still without advice and paediatrician referral.
My son has allergies - we live in Northern Ireland and we do not have access to challenges without significant waiting times, or immunotherapy.
2 years ago I lost my beloved eldest sister to an allergic reaction.This was late onset at the age of 64. Although she received one Consultation, they did not identify the allergy. She was prescribed Certazine. She suddenly died at 68. As a family, we remain shocked,and devastated.
My son has severe allergies and current hospital based consultant led clinic appointments are infrequent and rushed. Being able to access support as required via the GP service would be helpful.
My daughter suffered for 5 months because of a delayed diagnosis of CMPA. GP’s failed to diagnose it and claimed it was colic. We ended up in A&E twice and my daughter was classed as failure to thrive due to refusing feeds.
Rosey Hepburn Imber
My daughter was born in lockdown and little support was provided for her allergy, don’t believe anyone should have the same experience as we did. We believe having assessable allergy support locally to hand is vital
After my daughter's death I vowed to make change. By supporting allergy UK I'm also helping my other children who have allergies.
1,911 supporters already, pledge your support now!
Tell Your Local Politician
Help them understand the importance of our campaign by sharing with them your story and our Patient Charter call.
Sarah and Max’s experience highlights the very real need for improved access to allergy services. She has agreed to share her story in the hope it will encourage others to understand why Allergy UK is making this call and motivate people to also pledge the support. we are thrilled that Sarah agreed to be the first signatory on our pledge wall.
Allergy UK developed this charter in collaboration with patients and clinical experts which reflects the challenges that patients face in every single aspect of their lives – from accessing high quality care, wherever they live in the UK, to feeling equal in a society that dismissed their condition and disregards their needs.
The Vision for the Patient Charter is to outline the ‘gold standard’ of patient rights, as defined by the allergic community and leading clinicians in the field of allergy, namely:
The Right to a Quality Standard of Care – for everyone with allergy throughout the UK
The Right to Education – to empower of patients with allergic conditions to understand and manage their condition with support from informed healthcare professionals
The Right to Equality – through the promotion of a better awareness and understanding of allergy so that people with allergic conditions are not discriminated against in any aspect of their daily lives.
For this phase of the Patient Charer, we are focusing on raising awareness of our calls for allergic patients to have the Right to a Quality Standard of Care. We have evidence to show that introducing a specialist allergy nurse and dietitian as part of GP services improves the healthcare outcomes for those living with an allergic condition.
Our call is for each Integrated Care Board (ICB) to have a fully funded specialist allergy service with a specialist allergy nurse and one specialist dietitian.
You told us, we listened...
In 2021, Allergy UK carried out a major research study to find out how people perceive allergy.
of people would like government to do more to help people with allergies.
of parents wanted specialist allergy nurses in GP surgeries.
of parents feel that sometimes their children’s allergies are not taken seriously.