Hi everyone,
I've been lurking on the board lately but haven't posted in quite a long time. I first had symptoms in January of 2008. Like most of you, the symptoms got worse and I endured a long search for answers. I had a pretty severe case of Lyme and co-infections. In addition to boat loads of oral meds, I did two rounds of IV Rocephin in the Fall of 2009 and during the Spring of 2011. During the last round on IVs, I developed clots in both arms as a result of my PICC lines. Not fun!! So I resorted to daily IM injections of Rocephin for many months. Also, not fun. However, I am happy to report that I have been off all medications for 9 months and doing quite well physically. I am convinced I suffered some minor but permanent damage to some joints but I haven't observed any signs of relapse...yet. However, I think the years of terrible suffering took a major toll on me mentally. It's still a stuggle. I also have constant fear of relapse.
I somehow managed to excel in my job (infectious disease research scientist) even when I was VERY sick. In fact, I was able to support 70% of my salary and benefits by acquiring federal and private grants. Unfortunately, research funding is non-existent and I lost my job. To make matters worse I wasn't given unemployment benefits because I was not considered an employee (I was considered to be in 'training' despite have worked constantly since I graduated in 2006). To make matters worse, the employment situation seems hopeless and my family is in major debt due to medical bills and student loans.
I'll keep on fighting. I remember the days when ALL I wanted was to not be in constant pain. I am grateful that my health has improved. I am also grateful for this forum and others like it as it gave me comfort and support when I was at my lowest. So, thank you all! To those that are stuggling, hang in there. I'm living proof that feeling better can be a reality!