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 […]
CLICK HERE to submit your own entry, and to read about what others are up to as well! Regrouping April was a bit of a whirlwind month for me. There was the post-dengue fever recovery, my birthday, and work to catch up on. There was also the loss of some pets – our first, only […]
*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 […]
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 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 […]
Stress. It is an oft-forgotten factor in the equation to good health. Sometimes the tolerance for it is even glorified. More emphasis is placed on diet, exercise and sleep, with stress relief as a byproduct or afterthought. Why? Is it because these factors are more tangible and easily measured or monitored, while stress is a […]