Sorry about my absence lately, school has pretty much overtaken my life, and I have had to concentrate on that rather than my social media, but something prompted me to post today. I will write a more thorough update later, but what I really want to say, I already said in my Facebook status, and can be said by the following obituary.
http://www.emersonfuneralhome.com/fh/obituaries/obituary.cfm?o_id=1816039&fh_id=10418#.UKF8NzNtrw8.facebook
My Facebook Status from 11/12/12:
Nobody should die from Chiari. It's a very treatable disease. The medical community must educate themselves, and research must be conducted to alleviate deaths that continue to happen from this disease and it's related processes. Sleep apnea is treatable. Scoliosis is treatable. Ehlers Danlos Syndrome is manageable. Tethered Cord syndrome is treatable. Idiopathic Intercranial Hypertension is treat
able/manageable. Not all problems that can come with Chiari are listed, but listen people, most of them can be treated or managed, and it's the medical communities ignorance of this disease process that keeps people in pain, and is now taking the lives of children, young adults and adults alike. I'm sorry for ranting, but I don't want to become a statistic. I'm happy I found out that I have Chiari so that I can hopefully avoid an unspeakable fate, but physicians and researchers have to listen to patients first; listen to their stories of pain, lost jobs, memories, physical function. The key word here is listen. Listen to an underrepresented population that speaks loudly in cries of pain. Rant over.
This makes me feel even more passionate about finding ways to treat Chiari. PEOPLE ARE DYING, SUFFERING AND IN PAIN. SOMETHING NEEDS TO BE DONE. Katherine was 19, and she had her whole life ahead of her.
It's not right.
Until next time,
Moe

