Takling life with Chronic Fatigue Syndrome
What happens when someone with Chronic Fatigue Syndrome and a whole host of other invisible ailments tries to keep up with normal humans for a week and a half? Let’s find out!
An intimate look at the reality of how chronic illness alters romantic relationships and how we view ourselves.
Living on disability comes with the added stress of knowing you may be ripped off of it at any point for any reason – completely vulnerable to the whims of someone you’ve never met.
How what started as a social welfare net turned into a punishment.
It’s no real secret that Western Medicine is deeply uncomfortable admitting that there is a mind and body connection when it comes to the health of an individual. This often mixes with a deep unspoken systematic misogyny that colors a
Relationships are hard. They’re even harder when invisible illness is involved.
You know what’s hard about having a body that’s a constant disappointment? Having a brain that isn’t. I need a vast amount of intellectual stimulation or I am stir crazy but this is often pretty impossible to accomplish when my
I must admit that when the Corona Virus hit the US it was at the worst time possible for me. After a year and a half “down” where I did almost nothing except go to the grocery and feed store
A trip to Boston both throws me into relapse and gives me hope.
I have a very busy day with friends and travel – fully expecting I’d have to pay for it.