Took a break for a month
Last month I did not post anything about my pain and suffering. I got lazy I guess. At the same time, jobs started ramping up again. I've gone …
I am originally from Detroit, Michigan, but I have lived in California for the past 11 years. I went to school to be a teacher but after moving to California, I started working in the computer industry because it pays much better. After years of continual job changes (that is the nature of the computer industry), a company I was working for fired me for being out sick 1-3 days per month. I gave full disclosure of my condition. They waited until after I had my surgery, which diagnosed me with stage III Endometriosis, to hire me as a full timer. I came back to work and within a couple of months began missing work again from the illness. The company changed its tune and started harrassing me. I pleaded with them that they had full disclosure, doctor's and surgeon's notes, the works. They replied, "we thought the surgery would cure you." That's what started the fight - they had been told there is no cure for this illness. They didn't care, they wanted me gone, even though I was a top performer in the company. So I filed a complaint with the state's labor board. As soon as I was fired, the labor board got all the paperwork I'd saved, took my case and launched an investigation against the company. Nine months later, the dispute was settled - the company has to pay me lost wages, remove the stain of 'fired' from my record, provide me with a positive reference, and give sensitivity training on disability issues to their employees. I've had Endo for 21 years, and for that long, doctors kept telling me either it was all in my head, it's part of being a woman, or that I *only* had Dysmenorrhea (painful period). So this is not my first fight against an establishment. I finally found a doctor in 2006 who believed me, and she did the surgery in 2007. Unfortunately, the disease is stage III, which is 'moderate', and was too close to my bladder to remove all of the disease. After surgery, I tried Yasmin - a hormone mix of synthetic estrogen and progesterone, but that made me clinically insane and suicidal. So now I'm back to doing what I did all the years before surgery - managing the pain through dietary modification, exercise and pain medication. At present, I am re-employed in a field I used to work in 12 years ago - I've gone back to the field of child care and currently work as a private nanny. I have respect and trust from real people, not corporate overlords. I have my sanity back!
Spending time with my honey, IRC, online research, genealogy, astrology, travel, writing, bicycling, walking
zept replied to their discussion post The labor board settled! I win! in the Endometriosis support group 12:13am
Thank you Valerie, I am glad that I went through it because I knew I had to. I knew I wanted to, despite…
zept replied to Jamie510’s discussion post Analgesic in the Endometriosis support group 5:16pm
Found an article on the athlete's death from overuse of topical analgesics: http://tinyurl.com/5867np…
zept replied to deborahmarkus’s discussion post New and nervous in the Endometriosis support group 1:07pm
Sounds like it could be endo, but the only way to find out is to talk to your GYN about your symptoms…
zept gave Anastacia a High Five 12:48pm
Aww, thank you!…
Last month I did not post anything about my pain and suffering. I got lazy I guess. At the same time, jobs started ramping up again. I've gone …
Saturday morning I awoke from nightmares of gushing everywhere and as expected, upon awakening, I really was starting to gush. Thankfully I awoke …
The following post is from my personal journal, so I'm pasting it here. This entry is from Friday, May 9, 2008:
I was really out of it …
My period is a tricky bastard. It arrived on May 6 around 10:30pm. I medicated with Ibuprofen 600 and felt moderate cramps come on before the meds …
T-minus one day til bleedy doom, and I've only had very minor symptoms. Much better than some months, when I'm feeling crampy, cranky and …
Have had Endo for 21 years. Just had surgery to diagnose it in Feb, 2007. Surgery didn't work. Hormones made me psycho. I'm managing the pain through medication and diet.