Sometimes the only way to truly process what it’s like to live with chronic illness is through metaphors and analogies.
I wrote my book to guide others through the day-to-day discoveries that a new chronic illness diagnosis can bring.
Maybe my travels in, through, and back out again will help someone else. That is the theory… but it can only happen if they read it, right?
Want to make a difference this year? Help me get my book out in the world where readers can find it.
It’s really simple: Buy a copy for yourself, a friend, your doctor’s office, your library, or order a copy from your local bookstore… trust me, this small act will #makeadifference — 100% of my sales profits benefit @acceleratedcure4ms , and by doing so, you support the arts, artists, the small press, people with MS, and medical research.
More info: http://www.intentiontremorbook.com
#Janniversary #ms #mslife #msawareness🎗 #multiplesclerosis #poetry #medicalmemoir #pacificnorthwest #intentiontremor #msresearch #smallpress #livingwithms