A little round up of my tips on how to get a new life that I’m calling “My 3 Big Things to Finding Freedom in Life”
Ever since getting sick, I’ve somehow managed to continue pursuing my passions and I’ve found unexpected freedom as a result.
So, I thought I would share the 3 big things I’ve done that have led me to finding freedom in my life.
Continue reading How to Get a New Life – Chapter 10 “My 3 Big Things”
F**k It. I’m out.
Once upon a time (in 2016 to be exact), I had been sitting, pondering about officially launching this blog of mine. I had been holding off going public worrying about how it would affect the work I’d been doing. Thinking by some miracle my condition would pass (ha).
I didn’t want to look like a fraud (you know, I might roll over one day and be restored back to the manufacturer’s settings??). But realistically, I had been fooling myself thinking, at that point, that I could resume a “normal” working life. Whatever that was anymore. Dream on. My work had been suffering anyway. In fact, I had to completely rethink it.
This week, I would like to introduce you to Nikki Albert who runs the brainlessblogger blog. Nikki manages chronic migraines, fibromyalgia and major depressive disorder. Here’s her frank and insightful account of her story.
Continue reading Nikki Albert: Living well with chronic illness
Another instalment from a day in my life of living with dysautonomia and EDS!
This week is an anniversary of sorts. An anniversary that coincides with a famous horse race, The Melbourne Cup.
It marks the time I last skipped in front of the TV!
Here’s an recap from that memorable day in November 2015….
Continue reading Living with Dysautonomia and EDS – Chapter 14 “My Last Flutter with Too Much Fun”
Introducing you to Kami Lingren from Living Grace who is a truly beautiful soul. Kami has been diagnosed with Lyme and a handful of other diagnoses, with dizziness, head pain, bone and joint pain as the most debilitating symptoms. At its worst, her list of symptoms from her illness had grown to nearly 80, which she know so many others can relate to. Thankfully she’s been finally improving this year and her symptom list has become much smaller! Find out how she is living well with chronic illness by reading more…
Continue reading Kami Lingren: Living well with chronic illness
I’ve been meaning to write about Kayla for some time. We connected a few months back but it’s taken me some time to sit down and do her justice! Kayla has lived with Chronic Fatigue Syndrome (CFS)/ME since she was 12 years old. Continue reading Kayla Kurin: Living well with chronic illness