Guest guest Posted October 18, 2005 Report Share Posted October 18, 2005 Hi. I don't post here regularly, but do read the posts, on and off that come through my yahoo. I learn a lot from them. But today, I'm really struggling.......... I've done everythign I can to get away from this illness, mentally and physically, only to have so many days like this to remind me of what the reality is..... The last several nights, I've been unable to sleep more than a couple of hours. I'm awake all through the night. IT's so frustrating! I take alprazolam for sleep, but don't want to up my dosage of .05 because then the next day, it's hard to function. BUt it is if I don' tget sleep either. I'm cognitively deficient as well. Everything just hurts. My head, my eyes......my car broke down and I'm a single mom of six. My son's have had to accompany me to the store......which means walking. It hurts. It just plain hurts to walk. I make it there and back, but I'm exhausted afterwards. It is so frustrating! I suffer a great deal of anxiety over this illness, and I also suffer trying to convey what it is to live with this crap everyday. Has anyone got any idea how to convey this? When I feel reasonably well one day, I might be sick as a dog the next, I might not sleep that night that leads to weeks of no sleep...which aggravates everything else. WHen I feel reasonably well, it's easy to go comfie into denial again, only to pay for that denial. I have anxiety disorder, as well as PTSD. I find myself literally being dishonest about those things too. Not wanting to talk about it because of the stigma attached......not only to fibro, as well as the other multitude of illnesses I have, but also the mental health issue. That also makes it really hard. I don't want to whine. I'm tired of feeling this way. I'm tired of the denial, I'm tired of the confusion and frustration over the feeling great one day, then like shit the next. I realize that harsh, but it makes me so angry and feel so defeated sometimes. Right now I am under pressure (once again) by the state who has me on their welfare system due to not being able to work while I wait for the SSI application to be decided, to be pushed to work. One of my workers, from my perception, wants to boot me out to do something she thinks I can do, but I keep telling her that I can't. It is interesting because she has MS. SHe's a super nice lady and has always treated me with respect, ALWAYS, but there's this underlying thing that says she's not believing what I'm saying.....she has a husband and a nanny to take care of her children while she works, and when she gets home. I don't have that. My kids have me and that is all. It is too unhealthy for me to have a relationship wtih my family and they are unsupportive as well as my ex's family. When everything seems so big and overwhelming, to live as I do everyday, and I don't mean to suggest that others don't have it really hard, cuz I've seen some of the stuff that is posted in here and it blows my mind.......but I HAVE NO HELP. I get therapy (mental healthy) by a very good therapist. But I don't have family and I haVE one friend on whom I can rely upon to take me places if I need it. My best friend, but I try not to ask too much because she has a hubby and kids and responsibilities to attend to and I don't want to burden her. How do I explain this to people? I can't even get the words out as to what it is to live in this body and this mind every single day and try to take care of my children and hope and pray to God they have a healthier existence than I do when they eventually leave home, emotionally and physically. I'm just so tired. I hurt all over. But I hurt in my heart too. I don't know how to convey......... Does anyone have any suggestions for me? I would surely appreciate some Kelli Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.