PRIMARY ALDOSTERONISM FOUNDATION

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Patient-led non-profit with a goal of advancing standards of care for primary aldosteronism. Committed to fostering actionable research/inclusive collaboration.

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Address: 3533 E Ahwatukee CT, PhoenixWeb: Sign in to see organisation websiteX (Twitter): WeArePAOrgRevenue: 35566ICO: 843216292

Primary Aldosteronism Foundation – Supporting patients and research Although it affectsmillions of patients with hypertension primary aldosteronism is mistakenly considered rare. Understanding of the disease remains fragmented and it is seldom diagnosed and treated. Although it affectsmillions of hypertensives primary aldosteronism is mistakenly considered rare. Understanding of the disease remains fragmented and it is seldom adequately diagnosed and treated.

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Anna

- How can patient collaboration enhance research efforts and improve treatment protocols for primary aldosteronism?

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Ray

💚 It's so important to raise awareness about primary aldosteronism! Many people suffer in silence due to misdiagnosis. Let's spread the word and support the incredible work of the Primary Aldosteronism Foundation! #AwarenessMatters #PatientAdvocacy

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Victor

🔍 Thank you to the Primary Aldosteronism Foundation for leading the charge in improving standards of care! Together, we can ensure that every patient receives the attention and treatment they deserve. Let's keep pushing for change! 💪 #HealthForAll #SupportTheCause

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John

- What strategies can we implement to raise awareness about primary aldosteronism among healthcare providers and the general public?

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