A health, wellness and chronic illness blog that aims to articulate lifelong illness and disabilities from various perspectives.
This post is part of a series on my knee surgery and recovery journey, and how I coped with all that down time. I spent a good part of a year bed bound, in pain, and also bored. Afternoons were the toughest, as it felt like a state of limbo, where the world was speeding […]
Yes, it’s midway through 2020, and as usual – can you believe it?! As I get older, the years, months, and even weeks simply seem to fly by at breakneck speed. Yet some days are just terribly and painfully long. Strange how that works. Anyway it’s time for the June Linkup, and I would love […]
Continue reading "June 2020 Linkup Party for People with Chronic Illnesses"
Looking February…what should I say about 2020 so far? There’s been a mix of good and bad, as there always is, but let’s say that it’s been mostly awesome just for the new experiences in itself. Winter has been a fascinating season for me in every which way. The Lupus and Sjögren’s has been flaring […]
Continue reading "Coming Alive in the Winter Air (Pushing for Personal Changes & Group Advocacy)"
Why Many People with Chronic Illness Hate to be Known as ‘Sick’ From reading articles online, I’m aware that many of us with chronic illnesses don’t like to be known as sick or weak. No human being does, really. There are many reasons why one might dislike the association with their illness, such as: We […]
Continue reading "Call Me Sick Girl (Or How to Make Your Weakness Your Strength)"
The Icefall Doctors I selected “Earth’s Natural Wonders by BBC” amongst a list of Netflix series, and began munching on my dinner alone. The first chapter shone a light on the Icefall Doctors, whose job is to secure the safest route up Mount Everest for other climbers. Call me ignorant for not knowing about them […]
Continue reading "Why Humility is the Best Tool for Advocacy"