Jul 24, 2006 09:44
I am currently working on a website for my tarot readings, when this is done, I have been inspired to build another website for FMS.
I know that such websites are a dime a dozen, but I want to share my experiences. Support, lack of support, etc. I thought I would also share book lists, online communities (like this one), Good doctor lists, I think you get the idea.
Here are some of the names I thought of:
Ulookfine2me.com
fibrosurvivalresources.com
Any other ideas?
I'm feeling sort of down this morning. Since I broke out with shingles in 2003 there has been a constant back and forth as to whether I am "really" sick, whether I am doing "enough", could I be "doing more", etc. I have to tell you, and I am sure you know, it really isn't doing anything towards helping me get better. ::SIGH::My hubby is great. The mil is great is spurts. Mostly when she feels guilty. This place often saves me, even though I don't post here much. I guess sometimes I am paranoid that the inlaws will somehow read this and jump on me. Silly I know.
Like the time back in the spring of 2004 when I knew I shouldn't be driving, and the then fiance was always up way before me, and went to have coffee with his mom who lived next to the kids school, but she thought I should be driving them to school, so she had a fit that I needed to be driving them to school, SO, I did and had a panic attack in an intersection due to the medications I was on. I read in in my regular LJ recently. I knew I shouldn't be driving the MD told me as well, her response was "Oh well, see now you know, you wouldn't have known if you didn't try." When actually I had. ::SIGH::
This has been my battle all along. Every step along the way. I think we have all had these battles and the more safe havens we can provide for each other the better.
SO, that said. I am open to suggestions my friends. Fire away. What would you like to see?