The “This is how I…” series continues. In each video, I give you a behind the scenes look into my daily life with Arthrogryposis. I have a spot in my room where I can reach my drinks without calling for assistance every time. We line them up and make...
how long shall i stay? who will say? will you show me the way? do i think of a plan…wait for a man… or decide what to do when i think i can? for what do i wait? why do i hope? how much longer can i cope? what age will i be? when will i see? who will...
enter, go in the tent for the night note the moon, the fading light feel the wind, watch the trees soar make a bed on the earth’s floor talk, laugh until you can no more hear the people and dogs next door wait for the coming of the day see the sun as dark goes...
This is how I…WRITE. Today I show you the way I can write any note I like. My writing tools can’t be: A) too short, B) too big around, in order for me to hold the pen or pencil...
In the eyes of the world, I am weak. I have a physical disability that is very visible. I use a wheelchair outside of my house and I need hands-on help every day. These exact weaknesses make me strong. These limits teach me how to advocate. Self-advocacy is about more...
this is how I…take a walk. In this first video of the blog series, I talk about how I enjoy time outdoors. A physical disability means I need mobility equipment (my power wheelchair) and a side-kick (like a friend) to come along for whatever fun I...