“Don’t miss out on something that could be great just because it could also be difficult” I wasn’t sure whether or not to post this because…
Last year for Dysautonomia Awareness Month I shared my story of medical gas-lighting and struggles to diagnosis for one of my chronic conditions Postural Orthostatic Tachychardia…
The other night I had a flare. I think it was a combination of overdoing things and having a weaker immune system at the moment. I immediately…
So I haven’t found self-isolation too hard, stressful or different from my normal life. Why? Because my life changed when I was officially diagnosed with Myalgic…
Having a chronic illness can feel like I am fighting a battle everyday but one thing I find extremely helpful is reading little words of inspiration.…
What you don’t see. They say a picture tells a thousand words… but a picture only shows so much. A picture shows what happened in one…
Endometriosis Awareness Month is now coming to a close but how could I let it end without sharing a post on my blog? If you follow…
Just a small post today to address the craziness that is going on lately. Life is uncertain. Nothing is guaranteed and things don’t always go to…
Starting the new year is a hopeful time, we make new resolutions, goals and there is an overwhelming ‘new year, new me’ culture. However, the new…
A few weeks ago I was reflecting on how much my life has changed since becoming sick. Of course it has changed for the worse… but…