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...
So sorry to hear of your pain. I see you're in Oregon. So am I. I was DX with fibro several years ago and got psoriasis at the same time and now have some sort of joint/ tendon/connective tissue autoimmune disorder. There seems to be a lot of fibro and autoimmune problems around here. I never had these problems until I moved up here.
My mother also suffered from the same problems, so I guess where I live may be just a coincidence and this is just hereditary. I watched my mother go from healthy to crippled with pain, and I assure you, she was not doing it with a smile.
I'm up writing this right now in the middle of the night because I was trying to sleep, but I'm in so much pain that sleep was impossible.
I've been looking for a good doctor for fibro/pain/autoimmune around the Portland area for the past couple years. No luck so far. The rheumatologist that diagnosed me doesn't treat fibro, and just told me to take some Naproxen and exercise. Yeah, right.
You can have fibro without having an auto immune disorder. But I read an article that said many times people are diagnosed with fibo and they also have an underlying autoimmune disease that actually caused the nerve damage that caused the fibro. The article said that this is particularly true with Lupus. Studies showed the Lupus always came first and then fibro, so yes I do think they are connected. After I developed psoriasis, the dermatologist gave me topical steroids and when I use them, it really eases the fibro symptoms. This leads me and the doctor to conclude that either the psoriasis is causing wide spread inflammation in my tissues which puts pressure on the nerves and causes the muscle pain of fibro or I have another as yet undiagnosed autoimmune disease.
Feeling angry at this terrible disease is normal. Feeling sorry for yourself is normal. Take care and please feel free to write to me if you want to talk.
It sounds to me that checking out your current Doctor or firing your current Doctor might be a better idea..... If you are in so much pain that you are thinking the way that you are, it means that your pain is not been treated appropriatley and that you need to find a good pain management Doctor that is going to solve this issue for you.
A lot of us here are in chronic and/or intractable pain, but most of us have Doc's that treat our pain and help us with our pain levels, if this is not what's happening with you, is time to change it!
It took me 6 different Doc's to find my current pain management Doc. I never gave up, I knew that there was going to be the right fit and the right Doc for me out there, and I did find it, so now is your turn! Ask your PCP to give you a referral to a good PM Doctor in your area, and if you don't need a referral, check out this website and see if you can find a pain Doctor that can help. The website is:
www.doctorsforpain.com. Good luck to you and I hope that you can find good pain relief soon!
Hugs,