Author Davee Jones

I try to host a health related post each week in The Locker. I like to share my experiences in the hopes of helping someone else. I've decided to make a little turn and have a guest host for the next few weeks. My friend Brian is a beast. He cycles more miles in a year than I probably drive in my car. He has a passion for health, and shares an equal passion to eradicate MS. Please be kind to Brian and give him a warm welcome. Hugs- My name is Brian Jones. I am an avid cyclist riding to rid the world of Multiple Sclerosis. As we embark on a new year, I want to share some highlights of the South Central US chapter of the National MS Society: 9 Bike MS events raised approximately $24.7 million. 32 Walk MS events raised approximately $3.2 million. 11 leadership events raised approximately $840k. Their network of human service professionals is connecting people affected by MS to solutions that address the challenges and obstacles in their l...

10/22/2014 I’ve decided to use my blog not only to writing, music, and other facets of entertainment, but, also to share my journey. I’ve had significant health problems for almost three years. Thank you for listening, periodically, I will have a new installment chronicling my journey- SOMEWHAT STARTING OVER I stopped and thought about the number of doctors I’ve seen since January 2013. As close as I can get to the numbers include: 3 Rheumatologists, 1 cardiologist, 1 vascular doc, 1 Ob/GYN, 3 neurologists, 1 oncologist, 1 gastroenterologist, 1 immunologist/allergy doc, 1 hematologist, one pain management doc, 3 orthopedists, one spine specialist, and three ER visits. I’ve given at least 200 vials of blood, taken 100 xrays, 3 CT scans, 1 MRI, and several urine tests. I’m in a serious relationship with BC/BS. I will say, and I almost hesitate to go out loud with it, but, I think I might be on the right track. Finally. You see, other than all the problem...

Good morning!   I’ve decided to use my blog not only to writing, music, and other facets of entertainment, but, also to share my journey. I’ve had significant health problems for almost three years. Initially, a rheumatologist diagnosed me with systemic lupus (SLE) on June 19, 2013. However, the medication wasn’t working and I kept getting worse and developing new symptoms. So, after second, third, and fourth opinions, my neurologist believes instead I have fibromyalgia.   In April 2014 I visited yet another rheumatologist who I hoped would be familiar with autoimmune disorders. Following an extensive intake during my initial appointment, I found a place where the doctor also listened to me. Based upon my blood work, the doctor believes I have Sjogren’s Syndrome. She also made the diagnosis of Fibromyalgia and pre-lupus. I’ve never heard of pre-lupus, but, hopefully it stays in the “pre” category. Thank you for listening, each week I will have a new installment chron...