Wednesday, November 9, 2005
Just because.....
Well, I'm still awake. :o( Not a good thing for my pain. Less sleep, more pain. All fibros know that one. I want to ask all of the readers a question that have fibromyalgia. Do any of you suffer from "fibro fog?" And, isn't this the correct term? I would appreciate it if I was corrected if I'm wrong. It's just for my own personal sanity. I am tired of people thinking that I'm making it up to use it to my advantage. Thats all. I'm not at all. I'm hoping I will be able to get sleepy soon. I had something that hurt and upset me tonight, but I'm glad it happened because now I know the truth. I guess I am that neive. <----can't spell. :o) Oh well, glad it's over now. Going to find a web site to see about the "fibro fog." When I do find it, I will post it. :o) http://www.fibromyalgia.md/viewtopic.php?t=20
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6 comments:
I'm sorry that she feels that way honey. But you know honey, people who have never had to do without anything don't understand people who have. And just because you have cable and aol,don't mean squat. You and Jim have worked really hard to get what you have and that's means alot to you guy's,because you worked for it. Some people just get it handed to them. I don't understand these christians that go out of there way to judge people. In my Bible it says judge not lest ye be judged. You did nothing wrong honey,your a good person,and you try to treat everybody the same way. As for the Fibro fog,yes you do have it. I'm sorry she feels that way. I thought she was a better prson than that. Oh well honey it's her loss if she loses you as a friend. Just pray for her honey.
Love,Love
Mom
Thats what I thought...you don't judge. And it her her loss, certainly not mine.
Lisa
And yes...Jim and I have worked most of our lives to have what we do have. Nothing was given to us. Thats why we take care of what we have to make it last longer. The reason I bought that new chair for on the porch was for my back. The other chairs that I bought about 7 years ago at the good will are starting to fall apart. What else was I suppose to do?
Lisa
Lisa,I just read link about Fibrofog, and your not the only one who has it. I thought your neighbor was a nurse,so why don't she believe you? Good question huh?
Love ya!
Mom
Lisa, I am not sure if you will remember me, but I am one of Jeremy's Aunt's. We came to visit one day after Nena had Kayden. I am one of kelley's sister. I hope you don't mind but kelley passed along this site to me. She knows what my husband is going thru and thought it might help. My husband has had 3 back surgery's and still in alot of pain. He has a lot of nerve damage down both legs. I just wanted to say THANK YOU for the the fibro site. A year or so again the dr said Sean had a mild case of fibro. After reading some of your journals and this website I think he has gotten worse. He gets really bad knots in the bottom of his feets, he says it feels like he is walking on golf balls, and your mention today of the fibro fog, just seem to click. i thought it was from all the different type of medicine he takes but after reading i think it might be something more. I have also passed along the fibro site for him to look at. I just want him to know he isn't the only one going thru this. THANK YOU AGAIN.
Robin...You're very welcome. :o) Yes, I do remember you! :o) I relate to what your husband says about walking on golfballs. My feet our the same way. Sometimes I've had to walk on the sides of my feet. And yes, it is so hard to remember things, or while I'm talking, I'll forget what I was going to say, or forget how to spell a certain word, and it's very frustrating. It really seems to be getting worse for me. I'm so glad that what I write helps you and your husband. :o) Even if I help just one person, it makes me feels like this journal is worth writing in everyday, even if others don't like what I write. It's just my life, and what I have to go through and deal with. :o) Please, feel free at anytime if you have any questions about fibromyalgia to write me, ok. :o)
Lisa
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