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...
Hi, nice to meet you, so very sorry to hear of your situation. Seems like you are in the same boat as the rest of us, between a rock and a hard place. I have had epi injections, radio frequency ablations and facet injections. I'm not sure if the ablations are the same thing you are talking about. Those burn the nerve endings so you will not feel pain. For me however, they did the exact opposite. I have to agree with LBF, maybe you should get a referal to another pm doc. It never hurts to get a second oinion, and maybe they will have a different take on treatments for you.
In regards to you other question about wanting to do something nice for yourself when you get bad news or have a bad day, yes I do. I will go tan, get my hair done, but myself something that I've wanted for a while. I think this helps us cope with all the crap we deal with daily and maybe for a few hours we get to forget the crappy day we were having, Kim.
Reginaann, the pain meds help, but they don't cover all the pain, and I can't take them at all when I'm at work, out and about, etc. Any stronger pain meds it seems like I just can't tolerate. Thanks for the good thoughts :) I'm tempted to go buy new shoes and clothes too, but I'm super broke! It's hard to treat yourself when you have no money ;)
Kim, the injections I had are different than what you're describing, although yours sound interesting. You didn't find them helpful though? That's a bummer. Glad to hear I'm not alone in needing to do something special for myself! Right now I'm working on finding a new PCP and just starting all over. I'm not feeling like mine is working that hard for me anymore, and she's super far away. Just got my labs retaken today, so once the nephrologist looks at them and tells me I'm ok, I'll make the switch. Maybe this new woman will be able to help me.
Sarah
Usually once a Ddr finds out what's wyour caserong they do seem to gear shift down when they are just maintaining your disorder. I have had several Drs do that. It doesnt mean they dont care they just feel that they cant do anything else to help improve your case.
I have had over 10 nerve blocks and no Dr has told me that. I even asked that question and the Pain Management Dr said no to the nerve blocks scarring the nerve. The nerve blocks have helped my pain reduce by over 35% lower. But my disease my nerves are dying on the inside. The inside or Axons are dying and no one can tell me why. I have been in pain 24 hrs a day every day of the year since July,1996.
At first Drs could not tell me what was wrong, so they blamed me. They said it was all in my head. Well I knew that Dr was too afraid to say he didnt know, so the blame had to go somewhere. I hate when I have to find a new Dr. New Drs always start with the "Giuenie pig Syndrome". They try and putme on old simular meds that didnt work, but he thought 'we it will work because I'm ordering it'. Over and over again I have to suffer wjile they play, I HATE THAT!!!!
Currently the Dr I have is afraid of my pain meds i'm on, hes a pulmunoligist and he has no exprience with Oxycontin, so my dosage is too low and pain control is not good, my lowest pain number level in always 7, and i'm misseriable. I wasnt suppose to be in this nursing home for only 1 monrh. That was almost 3 yrs ago. Also I cant find any one to do my nerve block.
Sarah, if I were you I would get 2 more opinions about the damage the nerve blocks could cause, in order to make your decision, and you might have to weigh out the good the blocks do for you vs the possible bad scarring of the nerve. It may be worth it to take the chance, especially since the blocks do give you good pain relief.
I suggest you pray and ask our Lord what you should do. He always knows what's best for us. I was only allowed 3 nerve blocks a year. That was the rule my Dr set, but I dont know why he did that. Unfortunately he's retired now and I cant ask him, but I will call his old partner and ask him about this and will let you know what he says. Okay?
Well It's been nice to meet you and hope to hear from you again.
Denise