Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
Please God, grant me the strength to change what I cannot accept, the courage to accept what I cannot change, and the wisdom to know the difference.
Sorry if I mis-quoted. I think I got the meaning right.
peaceful night to all.
It was a very difficult struggle to go through and then I realized it was myself that I was fighting with. Why fight myself? I didn't choose this life, it chose me. Why blame myself? So I've spent that energy instead on living as positively of a life as possible. Living my life to the fullest with what I have of ME to do it with. I research, I try to find ways to improve my life all the time.
I do go through phases of sorrow for what was. Grief never leaves, but it can become more bearable.
Just because I say I accept it that is not the end all game. I dont want to live with regret or live being mad. I really do think I have the same life as I did but just with different limitations.
Some good things have come from my pain and that I am thankful for.
I recall telling my therapist that I had no choice but to accept what was done because I couldnt have my organs back. She told me I didnt have to accept it. By that I think she meant that I need to grieve and its ok to fight the system and try to change it. She also said that I dont have to forgive my gyn. I know forgiveness is supposed to be freeing and doesnt condone the wrong but it doesnt feel like that. I dont know if Ill ever be able to forgive or truly accept this injustice.
Thanks, jancam, for starting this discussion.
I know they mean well with statements like, "Technology has come a long way, and they are coming up with new techniques everyday". Well, whomever said that is not living with a rare disorder in which there has not been any money spent on research. And we have not found any new info in the field for 50 years. They figure, hey it's rare, why would we spend our funding on that. There's no celebrity suffering with it, let's leave it alone and let them deal with pain management for the rest of their lives. Obviously I'm angry right now, I'm going through Solumedrol infusions this week to hopefully ease some of my symptoms in my hands, and the swelling that comes along with it. I have already met my deductible for the year about two weeks ago. How sad is that? I just want to stop thinking about all of it, but I can't, it never goes away.
Someone on here said something about terminally ill patients. I guess that it may be easier for them to deal, because they see the end. Not saying that that is better, probably easier for them to accept. When you have a life long illness that is going to cause you pain for the rest of your life, you tend to hope that the rest of your life isn't going to be so long. We see no end to our misery. Just when you feel a little better, someone pulls the rug out from under you and laughs in your face as you experience yet another symptom to add to a long pathetic collection.
And it doesn't mean I accept it forever.
I surrender to the moment but I do not give up trying to get better.
Working towards healing is what keeps me going and accepting the pain in each moment is what keeps me sane.