In spite of the fact I was living with no running water and only the sparsely-available electricity of a small solar panel in a fifth-wheel I called ‘home’ with a husband as temporary as the broken-down RV, I applied to Southern New Hampshire University...
The reality of living in the Pacific Northwest as a disabled person during a housing crisis In October 2018, the day before my 52nd birthday, my doctor prescribed a power chair for my worsening disabilities related to my exposure to the antibiotic, Levaquin. I live in a low-income apartment complex in Olympia, Washington. They have a little blue... Continue Reading →
This virus came as the 30th anniversary of the Americans for Disabilities Act began and it has highlighted our FAILED inclusion of people with disabilities as well as our utter failure to educate our population that being different is okay and should NOT BE FATAL.
For weeks we worked with my physicians to discover that although my swallow reflex was completely intact, I could no longer feel that area of my throat, which caused me to panic.
After lifetimes of confusing medical problems, an answer is now clear for many "When you hear hoofprints, think horses." That is what doctors in training are taught. Physicians are specifically trained not to think outside of the diagnostic box, then are confused as to why people with rare issues often do not get diagnosed until they have... Continue Reading →
When I entered the family history center that stormy April afternoon, I had one thing on my mind; I had never seen a photo of my father’s father. I was 46 and I had never seen my grandfather’s face. I typed his name into the search bar on the site, Newspapers.com, “George R. Slighte,” the results came back instantly.