Diagnosing MS: Why it is so hard
MS is hard to diagnosis MS is a boutique disease. It is difficult to define and to diagnose. […]
Advocating for MS: Being a National Advocate for MS Australia
So, some good news As of March 2015, I am a National Advocate for MS Australia, the peak […]
Having an MS relapse: Why the ED is a bad place for an invisible disease
Spoiler alert: If you are one of my more squeamish friends or family, don’t read this post. Also, […]
Eating for MS Part 2: Wahls, Paleo and doing my own thing
The Wahls Protocol and the Paleo Diet Even considering writing this post takes me far too close to […]
Asking doctors to disclose: What do you want to know?
What do you know about your doctor? And your medication? If you take medication, you should know why you […]
Living with MS: Five moments I knew I am sick
I’m bored with MS Living with MS is not pleasant. But one gets used to it. It becomes […]
Preparing for the future: The coming neurological epidemic
The cost of Multiple Sclerosis I blogged last week about the cost of my medication, Gilenya. I now […]
Treating MS Part 2: Thank god for the Australian PBS
Thank god for the Australian PBS As I wrote last week, Gilenya is my new best friend: a […]
Treating MS Part I: The good news and the bad news
So, this is one of those posts I’m hoping family and friends read (as I talked about last […]