Hi, my name is Shellie. I was dx'd with FM since Jan 09 but I have had it for a long time. They just didn't want to dx'd it that. They think I have other things but not sure yet, running more tests. I gave up my job due to not being able to work anymore. My kids father kicked me out of the house(now going through a divorce). They doctors had him convinced that it was all in my head(faking). My parents is now helping me until I get on my own. I have three kids and I see them when I want. Friends and family understand want I go through. Someday is ok and some days not. More not than ok. I have my sense of humor so I'm doing good.

Hi Kim I also have Fibro and I have a hard time with friends, my family understands, but my friends don't.

From today's session with Mr. Therrien:
A lady named Joanna from CA was on and asking questions: about how to get the utilities to remain on; and how she needs natural remedies, herbs, sans allopathic meds to help her.
Concerning your utilities: there are always plans; programs for people who are in need; we all know them. However there is one EVERYONE can use. I believe each state. local has a program that allows you to pay one price each month. At the end of the year; if your average is over you pay the difference; if they owe you they will either cut you a check; or you can forward it to next years bills. Some locals only will allow if you have a low income or on retirement, etc. That said I DO know of some folk setting this up no matter what the circumstance, I do know one of the conditions is that you must be in good standing… Again, each local is different. All you can do is check it out.

I have the same issues about the allopathic meds. I would like to compare notes sometime soon… Good luck! Remember this one, you are NOT alone.

hello everyone. Just wanted to introduce myself. My name is Adrianne and I was dx'd with FMS about 1 1/2 yrs ago. I'm a registered nurse, but haven't been able to work since last Sept due to FMS and OA. I have applied for SSDI and awaiting the initial determination. Love this site and am hoping to meet some new friends here.

Hey my name is Judy. I was just diagnosted last week. I also have Lupus and Sjogrens. Trying to get disability but having some problems. If anyone has suggestions please let me know. Im still trying to work 20 hours a week but it is getting hard to do.