I'm new here!
Hi, my name is MoopyMyBuddy. I'm here because 12yrs ago I collapsed at work and have never been the same. I was fired after 14yrs, lost my children, and after many tests, my diagnosis and disability is Fibromyalgia along with depression, anxiety, neuropathy, a few other things, and daily I think Im going crazy. I have no friends. I am in a relationship for 14yrs and he has stayed by my side, which amazes me, since most days I would like to leave myself. I know this is horrible to say, I would rather have cancer and battle knowing I will get better or die. Not knowing what your day will be like, may start out good and then turn to crap within a blink of an eye. Trying to explain to people, but they can't understand because of the way you look. They think you are lazy, lying, even though you received your disability within 5mos which has been the best positive for me after hearing so many horror stories of people applying for disability. I know everyone has their own pains, cognitive issues, ways they deal, it is like fitting a circle peg into a square hole. We don't fit into anything. Sorry I have done nothing, but complaining. I am angry, tired, just want a normal life. I want to be happy, have energy. I want a miracle pill. Then, I look at those who have lost limbs, or came back with injuries they didn't have and I feel I have no right to complain. I do feel, I am dealing with this for a reason. I just don't know what they reason is. What is my purpose. I think that is what I hate the most. I no longer or I feel like I no longer have a purpose. I haven't given up yet, obviously since I am here, but I want, I need a purpose. I am hoping that by reaching out, maybe I will learn more techniques on how to cope, make a friend or two, just hear how others have learned to live with this invisible disease. Thank you #fibrowarriors