Pituitary Advocate Groups

The PNA is an international non-profit organization for patients with pituitary tumors and disorders, their families, loved ones, and the physicians and health care providers who treat them.

 

The PNA was founded in 1992 by a group of acromegalic patients in order to communicate and share their experiences and concerns. The PNA has rapidly grown to become the world's largest and fastest growing patient advocacy organization devoted to the treatment and cure of pituitary disorders.

 

Located in the USA- Serving Internationally

Pituitary World New Logo.png

PWN connects thought leaders to patients, creating access to critical expertise. We are re-framing the conversation by creating a network of highly informed professionals and people affected by pituitary disorders. 

Our mission is to bring you state-of-the-art and up-to-date information pertaining to health related matters of importance to those with pituitary tumors and other related disease processes. By publishing this information about what happens when the pituitary gland starts acting up and how it affects people, we hope to increase awareness so more people are diagnosed properly and early.

For all of us affected, we hope this information will be helpful, make life better and happier! Located online-Covering topics for both USA & International

Located in Argentina - Serving all of Latin America

APEHI es una asociación destinada a una obra de interés general que tiene por objeto la promoción, protección y defensa de la salud, facilitar el acceso a la atención médica y hacer respetar los derechos que asisten a toda persona con diagnóstico de enfermedad hipofisaria ocasionada por: - un tumor: acromegalia, prolactinoma, enfermedad de cushing adenomas no funcionantes; - o no tumorales: hipopituitarismo, diabetes insípida; - como así también enfermedades asociadas: tumores o lesiones no tumorales fuera de la hipofisis que afecten la función hipofisaria.

 

 

 

 

 

 

 

 

National Brain Tumor Society is fiercely committed to finding better treatments, and ultimately a cure, for people living with a brain tumor today and anyone who will be diagnosed tomorrow. This means effecting change in the system at all levels.

 

 

Location Nationwide

Over 13 Years For Cushing's Patients

Межрегиональная Благотворительная Общественная Организация пациентов с патологией гипофиза "ВЕЛИКАН"

Целью пациентской организации является желание помогать друг другу и для поддержки пациентов с диагнозом Акромегалия, их друзей и семьи. Пациенты, как правило, имеют тысячи вопросов и существует определенная нехватка «ветеранов» этого заболевания, кто мог бы на них ответить.

Located in Russia 

We give support, information and we bring people together. We provide information to health professionals and we campaign to raise awareness of issues facing pituitary patients, theirfamilies and carers.

 

Located in London- Serving the UK

If you have an advocate group you would like me to consider adding please contact: Sharmyn@hormones411.org

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