I have a functional capacity exam tomorrow. I am scared of how much pain it will cause but I know it's important to go through it and do the best I can. It's supposed to lasts 5 hours (I assume some of that time is to build in some breaks though...I hope anyway). I just know I will be in a flare up after (well...probably during)...and that my pain will probably be elevated for days or weeks after. I've never been to one of these before and I am so nervous. Hopefully it is worth it.

I haven't done one of those, but it sounds intimidating. However I know that many of my disability appointments took far less time than what they quoted to me. One they said 2 hours and I was in with the doctor for about 30 mins. The other time (about 15 mins for me) was filling out a form. Perhaps they allowed more time because some people need more time for the form, but certainly not an hour for two pages.

I hope it doesn't make you too miserable.

Just got home. Left the house at 8am and got back after 5:30pm. The appointment took the full 5 hours and I am pretty sure I didn't even complete all the tests (many she stopped me very early on). My right thumb is about all that's working right now but wanted to update you guys. She said multiple times that she appreciated the effort I put in. She wants me to email her the next 3 days to let her know how I am doing...and if this moment in time is any judge I think I will be in bad shape for several days. Not quite a 10...but very close to it and she said I will also probably be very sore on top of the pain. I'm already arranging for help the next few days because I know I will need it more so than even usual. Have to wait until the boyfriend gets home but Im going to probably have him help me into the bath tub after the little one goes to bed and then help put some Lidoderm patches on to help mitigate this pain because everything hurts. Fingers crossed that it was worth it...

I hope you feel better soon Catra. I don't understand why they put you through that pain. My dr told me that aggravating rsd can cause more flare ups. It doesn't sound like they know what rsd really is. If I were you I would check with a dr who is educated about rsd and see what he thinks. In the meantime, I will pray your flare ups subside soon. I am sorry I didn't see this post sooner. I was having alot more pain then usual due to my rsd the past few days and haven't been online that much. Sending virtual hugs and healing thoughts your way my friend.

It does seem counter intuitive to make the injured do things which will cause them to have flares. Before I was diagnosed I went through one of these exams and I tried valiantly to overcome my weaknesses so that I could continue to work. I know now that RSD is not one of those "over do it and you will be fine" issues. It is "over do it to suffer for days, if not weeks."

My latest trial is trying 1lb weights on my legs to see if I can build up to greater weight so that I can eventually walk on a treadmill. I did have a negative response from yesterday's wearing of 2 hours, my RSD foot shocked me all night long, even frankincense oil did not help. I will just have to use the weights for fewer hours. This response is also likely because I worked out on a stationary bike in the morning and also attended a balance class in the afternoon. Too much in one day.

I agree...it's definitely an overdo it and you will pay for days, if not weeks condition. I went in with eyes open though because the functional capacity exam is my best chance to receive the benefits I need from the insurance companies. It is incredibly frustrating to know that I felt I NEEDED to put myself in this pain just to "prove" what my doctor and I already know...and there's still no guarantee that the report with show what I want it to because I did the absolutely best I could and used every ounce of effort I had in me...and there's always a chance that the "one off" effort (despite it's consequences) will show more than I can consistently do. But...I have to have faith because I know I did my part that the test takes all of that into account...because it's really all I have besides my doctor's notes, records, and opinions (which weren't enough to prevent the initial denial of benefits so that is why we felt the need to go forward with the FCE).

Thank you guys. I wanted to reply yesterday but my hands have been in a severe bone crushing flare since Wednesday night.

The functional capacity exam isn't for treatment or even diagnosis. The reason I needed to get one was so that it will serve as a form of "proof" for the courts/insurance companies on how the pain impacts my ability to function and perform tasks...ie...work. There is no test that can measure pain...but a functional capacity exam is (supposedly) designed to assess a person's ability to work and perform tasks.

I definitely went all in and did the best I could but an paying for it. I haven't slept more than 2 hours since the test because the pain is just awful...but my hands are by far the worst. I have to email the therapist who did the test every day for 3 days after the test to update her on my condition...so that is supposed to be included in the report as well.

Fingers crosses...the report that we get helps prove our case to the insurance companies so that I can get the benefits that I need.