Living with Dysautonomia Post-COVID: A Personal Account

The author recounts their struggle with persistent symptoms after COVID, initially mistaken for anxiety, later diagnosed as Postural Orthostatic Tachycardia Syndrome (POTS) and mast cell activation syndrome (MCAS). They detail managing autonomic dysfunction through lifestyle adjustments and support, emphasizing the emotional impact on family and the ongoing nature of recovery.

POTS and Orthostatic Intolerance: What You Need to Know

Postural orthostatic tachycardia syndrome (POTS) is a real, disabling condition affecting the body's autonomic nervous system, blood volume, and immune response. Patients experience symptoms like dizziness, rapid heartbeat, and fatigue upon standing. Multiple overlapping mechanisms contribute to POTS, and proper diagnosis and management can significantly improve patient outcomes. Understanding and recognition are crucial.

Anti-CHRM Autoantibodies and Long COVID: Understanding the Link and Future Treatments

Long COVID presents persistent challenges, including fatigue and brain fog. Recent research highlights anti-CHRM autoantibodies, which disrupt muscarinic cholinergic receptors and could explain ongoing symptoms. Understanding these mechanisms is vital for developing targeted therapies and improving diagnostic practices, shifting the narrative that Long COVID is merely psychological to a biological basis.

Perching Stool for Long COVID and POTS Relief: How a Simple Stool Became My Recovery Sidekick

The author shares their unexpected journey with a perching stool, initially viewed with skepticism due to its unappealing design. However, it soon becomes a vital tool during their Long COVID recovery, providing comfort and stability, particularly for those with autonomic dysfunction. The stool proves functional, despite its lack of aesthetics.