- Claiming My Shadow Self
- Letting Go and Holding On
- Walking the Walk for the Seventh Time
- Stress and the Shadow Man
- The Descent – A Video Excerpt
- Fear and Covid-19
- Looking for the Oracle
- The Descent and Smashing Tropes
- The Story Within My Self – Love and Lemonade out now!
- The Stone Man Speaks
- The Whispering of the Trees
- Listening to the Body is the Hardest Thing to Do
- What Max Shadow Taught Me
- We Are Warriors
- Disabled and Fabulous
- Please Help Save the MS Clinic!
- We Are All Rock Stars!
- The Fractured Mirror
- Little Yellow Magnet – Available Now!
- Little Yellow Magnet – It’s Almost Here!
- From This Moment
- A Hard Way To Learn a Lesson
- Stepping Out of the Box and Breaking the Routine
- I’m Alive For This Moment
- The Lion and the Internal Orchestra
Category Archives: Brain Fog
Before I was diagnosed with relapse and remitting Multiple Sclerosis, I thought I could cure myself. Someone had said that it was all about mind over matter. I could choose not to be sick. I could choose my destiny and … Continue reading
As much as I’m thankful for the multiple sclerosis and what it’s taught me, there are times that it makes me angry and pisses me off. There is so much that I try to do and, most days, I succeed. … Continue reading
I’ve been struggling a lot lately. I’ve been trying to break out of the box that I’ve put myself in. That box is built on routine. When I was first diagnosed with multiple sclerosis, this routine helped. It helped me … Continue reading
I’d like to take a moment to talk about pain. Everyone experiences pain differently. Maybe it’s muscle pain or internal pain. Perhaps it’s a mixture of both. For myself, there is no rhyme and reason to it. My Multiple Sclerosis … Continue reading
On December 30th, 2012, I woke up to find that my world as I knew it had changed. I woke not knowing how to move my body. It was no longer mine and I was no longer able to control … Continue reading
The other day, when I was talking to someone, I mentioned how meditation was really helping me deal with my Cerebral Palsy and Multiple Sclerosis. She looked at me, her mouth drawn into a frown of sympathy, and said “Oh, … Continue reading
I am in pain of some sort twenty-four hours a day, seven days a week. I never get a vacation or a day off, I never get to go on a holiday from the pain. It is my constant companion … Continue reading
I’ve come to realise that I’ve been living in fear. When the MS hit in January of 2013, it took everything from me: my mobility, my independence, my freedom. I was a prisoner inside of my own body. I fought … Continue reading
Today marks the start of four weeks I’ve walked without my cane. For the first two weeks, I brought with me to work and when I went out. For the past week and a half, I’ve left it at home. … Continue reading