Skip to content

LadywithMS

  • HOME
  • BLOG
  • MEDIA
  • MULTIPLE SCLEROSIS
  • SEARCH
LadywithMS

Category: Chronic disease

Policy: When MS health policy is ill

This post was originally published in the Asia and the Pacific Policy Society’s Policy Forum on Wednesday 27 May 2015, World MS […]

Reading about MS: Time for a few confessions

People with MS write about MS I’m a reader. And since being diagnosed with Multiple Sclerosis, I’d developed […]

What we don’t talk about: Depression, disability and dying

We all ignore chronic disease, until we can’t We all know someone with chronic disease. And we all […]

The gut and (MS) health: It isn’t sexy, but it is important

Your gut is important, don’t ignore it I started to hear about how important the gut was to […]

Writing about chronic disease: Wheeler Centre Hot Desk Fellowship

Wheeler Centre Hot Desk Fellowship This blog isn’t what I would describe as the happiest you can find, […]

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, […]

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 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 […]

Posts navigation

Previous 1 2 3 4 Next
© Astrid Edwards 2014-2022