The American Partnership for Eosinophilic Disorders (APFED) is a 501c3 nonprofit organization founded in December 2001 by a group of mothers of young children living with eosinophil-associated diseases. Their mission is to passionately embrace, support, and improve the lives of patients and families affected by eosinophil-associated diseases through education and awareness, research, support, and advocacy.

• Facebook: https://m.facebook.com/APFED/
• Instagram: https://www.instagram.com/apfedorg/
• Twitter: https://twitter.com/APFEDorg
• YouTube: APFED
• Pinterest: https://www.pinterest.com/apfed/

Based in Virginia, the Allergy and Asthma Network was founded in 1985 to combat the inaccessibility of patient-friendly information on asthma and allergies. Through outreach, advocacy, education and research, the organisation has launched programs to help both patients and their caregivers.

• Facebook: https://www.facebook.com/AllergyAsthmaHQ/
• Twitter: https://twitter.com/AllergyAsthmaHQ

Founded in 1953, AAFA is a non-profit organization – the oldest asthma and allergy patient group in the world. AAFA seeks to support asthma and allergy patients through advocacy, education and research.

• Facebook: https://www.facebook.com/AAFANational
• Twitter: https://twitter.com/AAFA_Advocacy

At Asthma + Lung UK believe that every breath matters – and that the right to breathe freely applies to everybody, regardless of income, age, ethnicity, gender, or background. Their vision is for a world where everyone has healthy lungs. A world where lung health is prioritised through better understanding, research, treatment and support. We are dedicated to helping create a world where good lung health and the ability to breathe freely are a basic right enjoyed by all.

• Facebook: https://www.facebook.com/asthmalunguk/

Supporting those in the UK affected by all types of allergy, the charity offers a dedicated helpline and factsheets with information on symptoms and triggers. The charity is registered with the Fundraising Regulator.

• Facebook: https://www.facebook.com/allergyuk/
• Twitter: https://twitter.com/AllergyUK1

Aspergillosis Trust is a patient advocacy group to support everyone with all forms of Aspergillosis worldwide. They have a support group and information on their website. They have just become the first charity worldwide that solely deals with Aspergillosis.

• Facebook: https://www.facebook.com/groups/777282226382870
• Instagram: https://www.instagram.com/aspergillosistrust
• Twitter: https://www.twitter.com/aspertrust

AHDADER is a non-governmental organization that provides information and advice for patients with lung conditions. The group communicates research and health policy to the public in order to better support those in need.

• Facebook: https://www.facebook.com/Ahdader-Akci%C4%9Fer-Hastalar%C4%B1-Dayan%C4%B1%C5%9Fma-Derne%C4%9Fi-269508383387828/

Based on its philosophy, “Is there a more precious good for a man than health?” the association Santé Meilleure Vie Meilleure (SM-VM) has a health promotion program for all. With patients suffering from different diseases, it develops solutions to alleviate the pain and treatment of other patients. The association SM-VM organizes with the patients it has already accompanied and who have become members, information, and awareness campaigns the in the communities on the different pathologies it supports. It trains community health workers in vulnerable communities to help communities promote their health. In partnership with health facilities nationwide, SM-VM accompanies patients suffering from food allergies, cystic fibrosis, cystic fibrosis, allergy, atopic dermatitis, and asthma. It should also be noted that SM-VM accompanies patients in palliative care.

Based in Bern, aha! disseminates information about the causes, prevention and treatment of allergies and intolerances. The center is dedicated to supporting the three million people who are affected by allergies and intolerances in Switzerland.

The Asthma and Allergy Association seeks to influence society to improve standards for people with allergic diseases. The association prioritises increased accessibility to different environments for people with allergies and hypersensitivity.

• Facebook: https://www.facebook.com/astmaallergiforbundet/
• Twitter: https://twitter.com/AochAF

Sevilla Respira is a non-profit organisation that aims to raise awareness about respiratory diseases, sharing local events and programs with the community.

• Facebook: https://www.facebook.com/RespiraSevilla
• Twitter: https://twitter.com/RespiraSevilla

Pulmonary Hypertension Spain (HPE) works to promote the health, in a broad sense, of all people diagnosed with Pulmonary Hypertension and their families, to improve their quality of life in all aspects, promote and improve as far as possible their level of care, work, and social life.

• Facebook: https://www.facebook.com/HPSpain.org
• Instagram: https://www.instagram.com/hpe_org/
• Twitter: https://twitter.com/hpe_org
• YouTube: Hipertensión Pulmonar España ORG Pacientes
• LinkedIn: https://www.linkedin.com/company/hipertensionpulmonar

The Fundación Lovexair is a non-profit organization that provides care, support and guidance for those with respiratory diseases and their caregivers. The organization aims to do this by sensitizing society about the importance of early diagnosis, prevention and treatment.

• Facebook: https://www.facebook.com/FundacionLovexair/
• Twitter: https://twitter.com/Lovexair

The Spanish Federation of Allergy and Airways Diseases Patients’ Associations (FANAER) was established in 2007 by respiratory patients. The non-profit organization aims to improve care and awareness around allergies and respiratory diseases.

• Facebook: https://www.facebook.com/fenaer
• Twitter: https://twitter.com/fenaer2

APEPOC provides information on chronic obstructive pulmonary disease (COPD) and defends the rights and improves the quality of life of patients. The organization also provides healthcare services for its associates.

• Facebook: https://www.facebook.com/apepoc
• Twitter: https://twitter.com/apepoc_es

AADA (Association of people affected with Atopic Dermatitis) was founded in 2017 and focused on giving trusted information to the patients and making this disease more understandable for the population.

They give voice to the patient community to achieve the recognition and normalization of AD, defending their interests before health policymakers and offering direct support and reliable information to patients and families.

• Facebook: https://www.facebook.com/AADAes
• Instagram: https://www.instagram.com/somosaada/
• Twitter: https://twitter.com/somosAADA

The Association AAUC was founded 2012 and is a non-profit organization that groups together people affected by chronic urticaria with the aim of improving their quality of life.

• Facebook: https://www.facebook.com/urticariacronica
• Twitter: https://twitter.com/UrticariaCronic

ASMABI is an Asthma patient organization, that was founded 2019. Its mission is to create awareness for the chronic disease Asthma. ASMABI represents the group of Asthma patients in fighting for the rights for acess to health care, for psychological service, and more.

• Facebook: https://www.facebook.com/asmabi.bizkaia
• Instagram: https://www.instagram.com/asmabibizkaia/
• Twitter: https://twitter.com/AsmabiBizkaia

ALERMA is a non-profit organization, whose objective is the care, information, and training of allergic and respiratory patients. It is provincial and has about two hundred patients. Our activities revolve around the training of patients, through talks given by professionals: Pulmonologists, Allergists, Psychologists, Physiotherapists, etc. In addition to workshops on inhaler management, management of your disease, and knowledge of your disease. We also celebrate the World Days of diseases that cover the entire respiratory field: Asthma, COPD, Apnea, etc. with an information table in Hospitals and Shopping Centers. On World Asthma Day, we carried out a march along the “Paseo Marítimo” de Málaga, to deepen the idea of the need for exercise for these patients.

• Facebook: https://www.facebook.com/ALERMA-Asociaci%C3%B3n-de-Al%C3%A9rgicos-y-Enfermos-Respiratorios-de-M%C3%A1laga-337395213055249/

AEPNAA is an association that works for people with food and latex allergy and their families. AEPNAA is a non-profit entity and has received in July 2019 the Declaration of Public Utility by the Ministry of Interior of the Government of Spain. The Association has a Board of Directors, democratically elected every two years by a vote of the members of the association. For the development of its functions, AEPNAA has five working groups in charge of the different areas of work: food safety, brands, medicines, and communication and education. AEPNAA also has a Scientific Committee made up of prestigious allergists who advise the association on allergy-related issues.

• Facebook: https://www.facebook.com/Aepnaa/
• Instagram: https://www.instagram.com/somosaepnaa/
• Twitter: https://twitter.com/aepnaa1
• LinkedIn: https://www.linkedin.com/company/asociaci%C3%B3n-espa%C3%B1ola-de-personas-con-alergia-a-alimentos-yl%C3%A1tex/mycompany/
• Youtube: AEPNAA – Asociación Española de Personas con Alergia a Alimentos Y Látex
• TikTok: https://www.tiktok.com/@somosaepnaa