How Does Antiphospholipid Syndrome Affect The Body? (Beyond the Blood to Major Organs)

You may have heard of the rare blood clotting disorder, Antiphospholipid Syndrome, but did you know that it isn’t ‘just’ about the blood? This article is part of the Antiphospholipid Syndrome (APS) resource library that I’m building up on my site from a patient perspective. It consists of findings from research journals, as well as […]

When Autoimmune Disorder Ravages Your Face (and How That Led to My Body Dysmorphic Disorder) - Guest Post by: Julia Métraux | A Chronic Voice

*Note from A Chronic Voice: Julia is passionate about writing and contributes to various online publications. She aims to raise awareness on rare diseases and mental health, and we’re honoured to have her share her story with us here today. The stress of living with either chronic illness, permanent injury, or mental illness is one […]

The Annoying Thing About Living with Antiphospholipid Syndrome… (My Personal Experiences)

Do you have a friend or know someone living with Antiphospholipid Syndrome (APS), or another blood clotting disorder? It can be a real pain, and interferes with treatments for many other chronic illnesses. I’m not discounting the severity of any other disease, but today I’d like to share with you on how having APS can […]

Why I Need to See 10 Different Doctors on a Regular Basis: Click to read or pin to save for later | www.achronicvoice.com

Why the Need to See So Different Doctors? Autoimmune disorders are a complex beast; no two patients are the same, despite having a shared illness. There is no standard medication, like antibiotics to treat a common flu. Every patient’s custom combination of drugs comes from trial and error, and we often need to see different […]