Melissa’s Rap: May is Lyme disease awareness month. This disease has greatly impacted me and my family, as I was diagnosed CDC-positive with Lyme on Cinco de Mayo 2011. I spent the next two years treating with IV antibiotics, oral antibiotics, herbs, supplements and other treatments. To this day, I see effects of the disease in my low immune function, brain fog, and fatigue. Now that I know what I know about Lyme and its coinfections(Lyme rarely travels alone), I am diligent about prevention and work to educate others about how to prevent this debilitating disease. Continue reading →
From a young age, my health has been a roller coaster of sorts. I am grateful that the things I have had to deal with are what they are. I am clear that many suffer from far worse ailments. But, I do hope that my story helps me connect with others who have had similar experiences, and sheds some light on what it is like to live with multiple chronic conditions.
When I was 10, I was diagnosed with Scoliosis, curvature of the spine. My spine was and still is an S. Despite my doctor’s attempts, we couldn’t seem to slow the process, so when it degraded to a 60° curve on the bottom and a 30° curve on top, he recommended surgery. When I was 12, I underwent a surgery called Harrington rod implantation with fusion. Three rods were fused to my spine to prevent it from curving further, and to minimize the current curvature. My curvature went down to 15° and 30°. Continue reading →