Thursday, November 17, 2005

New Update

   Well I have been on the Cymbalta for long enough and it’s not not working for the pain. Going to the Pain Dr on Thursday and asking for an increase on my Avinza. Not many more options for me, I had so much hope for the Cymbalta.

    Due to pain politics  he probably won’t get an increase even though I’ve been on this dose for 15 months. Now I have pain in my upper neck area which is sharp and my ROM is bad.

    What is need is an entire set of artificial disks and I’ll be ok but that’s not an option. At least not in the near future.Will let you know what happens.

Friday, October 21, 2005

TO PEOPLE WITHOUT CHRONIC PAIN

Having chronic pain means many things change, and a lot of them are invisible. Unlike having cancer or being hurt in an accident, most people do not understand even a little about chronic pain and its effects, and of those that think they know, many are actually misinformed.In the spirit of informing those who wish to understand. These are the things that I would like you to understand about me before you judge me... Please understand that being sick doesn't mean I'm not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit, sometimes I probably don't seem like much fun to be with, but I'm still me-- stuck inside this body. I still worry about school, my family, my friends, and most of the time I'd still like to hear you talk about yours, too. Please understand the difference between "happy" and "healthy". When you've got the flu, you probably feel miserable with it, but I've been sick for years. I can't be miserable all the time. In fact, I work hard at not being miserable. So, if you're talking to me and I sound happy, it means I'm happy. That's all. It doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm getting better, or any of those things. Please don't say, "Oh, you're sounding better!" or "But you look so healthy!¨ I am merely coping. I am sounding happy and trying to look normal. If you want to comment on that, you're welcome.Please understand that being able to stand up for ten minutes doesn't necessarily mean that I can stand up for twenty minutes, or an hour. Just because I managed to stand up for thirty minutes yesterday doesn't mean that I can do the same today. With a lot of diseases you're either paralyzed, or you can move. With this one, it gets more confusing everyday. It can be like a yo-yo. I never know from day to day, how I am going to feel when I wake up. In most cases, I never know from minute to minute. That is one of the hardest and most frustrating components of chronic pain.Please repeat the above paragraph substituting, "sitting", "walking", "thinking", concentrating, "being sociable" and so on ... it applies to everything. That's what chronic pain does to you. „ Please understand that chronic pain is variable. It's quite possible (for many, it's common) that one day I am able to walk to the park and back, while the next day I'll have trouble getting to the next room. Please don't attack me when I'm ill by saying, "But you did it before!" or Oh, come on, I know you can do this!¡¨ If you want me to do something, then ask if I can. In a similar vein, I may need to cancel a previous commitment at the last minute. If this happens, please do not take it personally. If you are able, please try to always remember how very lucky you are--to be physically able to do all of the things that you can do.Please understand that "getting out and doing things" does not make me feel better, and can often make me seriously worse. You don't know what I go through or how I suffer in my own private time. Telling me that I need to exercise, or do some things to get my mind off of it¨ may frustrate me to tears, and is not correct if I was capable of doing some things any or all of the time, don't you know that I would? I am working with my doctor and I am doing what I am supposed to do. Another statement that hurts is, "You just need to push yourself more, try harder..." Obviously, chronic pain can deal with the whole body, or be localized to specific areas. Sometimes participating in a single activity for a short or a long period of time can cause more damage and physical pain than you could ever imagine.Not to mention the recovery time, which can be intense. You can't always read it on my face or in my body language. Also, chronic pain may cause secondary depression (wouldn't you get depressed and down if you were hurting constantly for months or years?), but it is not created by depression. Please understand that if I say I have to sit down/lie down/stay in bed/or take these pills now, that probably means that I do have to do it right now - it can't be put off or forgotten just because I'm somewhere, or am right in the middle of doing something. Chronic pain does not forgive, nor does it wait for anyone. If you want to suggest a cure to me, please don't. It's not because I don't appreciate the thought, and it's not because I don't want to get well. Lord knows that isn't true. In all likelihood, if you've heard of it or tried it, so have I. In some cases, I have been made sicker, not better. This can involve side effects or allergic reactions. It also includes failure, which in and of itself can make me feel even lower. If there were something that cured, or even helped people with my form of chronic pain, then we'd know about it. There is worldwide networking (both on and off the Internet) between people with chronic pain. If something worked, we would KNOW. It's definitely not for lack of trying. If, after reading this, you still feel the need to suggest a cure, then so be it. I may take what you said and discuss it with my doctor. If I seem touchy, it's probably because I am. It's not how I try to be. As a matter of fact, I try very hard to be normal. I hope you will try to understand. I have been, and am still, going through a lot. Chronic pain is hard for you to understand unless you have had it. It wreaks havoc on the body and the mind. It is exhausting and exasperating. Almost all the time, I know that I am doing my best to cope with this, and live my life to the best of my ability. I ask you to bear with me, and accept me as I am. I know that you cannot literally understand my situation unless you have been in my shoes, but as much as is possible, I am asking you to try to be understanding in general. In many ways I depend on you - people who are not sick. I need you to visit me when I am too sick to go out... Sometimes I need you help me with the shopping, cooking or cleaning. I may need you to take me to the doctor, or to the store. You are my link to the normalcy of life. You can help me to keep in touch with the parts of life that I miss and fully intend to undertake again, just as soon as I am able. I know that I asked a lot from you, and I do thank you for listening. It really does mean a lot.

Sunday, October 16, 2005

A Fine Sunday


And I'm inside on the couch and I would love to get out and do things.To get some exercise , play tennis , go to flea market,take a hike in the woods. Don't know how I keep myself together and keep from going crazy. Pain,,sleep ,eat,take meds,lay on couch and watch Tv if I feel like it, that's about what I do.

Sunday, September 25, 2005

Morning

Just a typical Sunday morning here, not much sleep last night. Woke up a hundred times and seemed to be awake more than asleep.
Anyone ever bought pharmacy drugs online ? I am looking for my Cymbalta since I can't find a Dr. who will write a script.The prices really vary and you can get generics that aren't even available here yet.

Friday, September 23, 2005

Pain Sucks


Pain Sucks
have not been going well. My Cymbalta which was helping with the pain is no longer working and I cannot get anyone to increase the dosage.This sure does suck. It's hard not to think about the pain since it is basically all over. Moves from my lower back to neck, legs and arms always ache and hands are numb.Don't see how I can keep this up much longer, my quality of life has dropped down to a 2 and I stay on the couch most of the day

Thursday, September 22, 2005

http://www.livejournal.com/userinfo.bml?user=cheekwa

Thursday, September 01, 2005

The Hell Down South


I feel so sorry for those millions of people without their homes from the hurricane. Seems like the goverment is not acting fast enough and things are gonns geta lot worse down there I fear.

WeII the cat got out of the hat

Everyone knows about my suicidal thoughts now in my family and things have gotten pretty weird. Mom calls and crying and I don't think she really knows what to say but I love you and I am past the point of tears where the pain has hardened my heart to others feelings.I don't want any of you guys compassion for me. Just an understanding of what the chronic patient goes through in life with their spouse,family,Doctor and the DEA which is screwing us over and society in general.