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All responses Most smiled responses
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I was told once that I resemble Katy Sagal or, more specifically, Peggy Bundy (from Married With Children). I don't see it. I think it's the red hair. I would much rather look more like Katy Sagal as Gemma in Sons of Anarchy. She kicks ass and I love her. ;)
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Apparently, there are a lot of wishfulthinkers out there. I have a sneaking suspicion you're some kind of spambot. If not, you should know how to reach me other than on Formspring. Just sayin'.
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asked by culurmepeach
I think I'm the same person all around. I don't try to "put on airs" to make people like me in real life or on the interwebz. I might be a little funnier in real life, but it may be that only I think so.
So, yeah, I'm a crabby, caring, potty-mouthed, loyal friend in real life AND on the interwebz. What you see, or read, is what you get. :) -
asked by thecabbagestalk
I had morphine after my spinal fusion surgery and it was GREAT! I'd be really happy to be on it all the time. Unfortunately, they won't do that so I have to find other ways to alleviate the pain in my back. If it's just my back that hurting, I'll use my TENS unit to help with the pain. It's definitely saved me from a lot of suffering. But when my entire body hurts (like now), it won't help anything but my back.
As for Tumblr, you can only reply to the posts that have the "Reply" option at the top of the post. Some people don't have that feature enabled. If you want to send someone a message, you can go to their Tumblr page and use the "Ask" feature. If they don't have a link, just add the word "ask" after the URL for their page. If you don't get an "ask box" that means they don't have that feature enabled, either. -
No, but I'll definitely check it out. I'm always open for new book suggestions. Thanks!
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asked by thecabbagestalk
I don't know if I can be considered to be keeping going. I do have the occasional positive thought, but I struggle from day to day just like anybody else who is chronically ill. The key to being able to finish school, or anything else for that matter, is pacing and other "chronic illness" life skills. There's a book called "The Patient's Guide to CFS and Fibromyalgia" that takes you step by step through the new and different set of life skills you need to live a life with chronic illness. I wrote about some of it on my blog at fmslife.blogspot.com. If you go there, scroll down to the very bottom where I have "FMS Life Recommendations" and click on Fibromyalgia books. It's listed there and I think some are selling it for just under $4.00 US. The reason I recommend that book above all others is that it doesn't try to explain the hows and whys of FMS or CFS, it just explains how to live and cope and function with these afflictions.
Also, if you have a lot of back pain, get a TENS unit. You'll be able to sit in class without writhing in pain or paying for it with severe back spasms later. I have some listed in my FMS Life Recommendations list, which are portable (clip onto your belt or pocket) and cheap - and very effective. -
I've queued your pain management study to my Fibromyalgia posts. I'll have to check it out, as well. Thank you for the link!
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I wasn't born in a hockey town and I wasn't raised watching hockey. When I was married, my husband started watching hockey with a friend of his who was a huge hockey fan. They explained the game to me, but I didn't really watch it much with them. When my husband and I separated, I moved back to my non-hockey hometown. My son started playing goalie for a roller blade hockey team at the YMCA. Then we got our own WCHL hockey team. I talked my BFF into going with me, and I fell in love with the game when a puck flew off the ice and hit me in the arm. I had a huge black bruise for over a week and it was like a badge of honor. A religious experience. It happened during the second game I'd ever been to and I was a die-hard fan ever since. Don't ask me to explain it. That's just how it happened.
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Jessi Bee’s Bio
Just a socially inept gimp.
