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Social Chat This is a place for daily chit-chat and other discussions that are not directly related to a neurological or mental health issue. |
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02-10-2008, 07:54 PM | #11 | |||
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Elder
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Cheryl Dx: MS 2001 CRPS 2009 “When everything seems to be going against you, remember that the airplane takes off against the wind, not with it.” - Henry Ford |
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02-10-2008, 07:57 PM | #12 | |||
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Legendary
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Thank you from the bottom of my heart though. I really appreciate the thought.
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Eastern Australian Daylight Savings Time and my temperature . Last edited by Koala77; 02-10-2008 at 09:36 PM. Reason: word omitted |
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"Thanks for this!" says: | tovaxin_lab_rat (02-10-2008) |
02-10-2008, 08:02 PM | #13 | |||
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Magnate
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(Now if everyone sent a book, you'd be in BIG trouble!) Koala, buried in books, lol....
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Anybody who doesn't think a dog can smile has never dropped a piece of bacon. |
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02-10-2008, 08:05 PM | #14 | |||
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Legendary
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And that was not a hint!
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Eastern Australian Daylight Savings Time and my temperature . |
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02-11-2008, 12:00 PM | #15 | |||
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Member
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I agree we definately deserve treats after txs!
We give up so much and we should be rewarded for the fact that we keep fighting and trying things to keep ourselves healthy despite this disease. Especially given that there aren't any treatments as of yet that are "guarenteed" to help, every time we step up to the plate even thought it "may or may not" help we should be rewarded! Some times I think that's the hardest thing for others to understand, we don't know which treatment really is making a difference verses "our" natural disease course. Further more any treatment can just stop helping us at any time. Yet many of us keep the faith that "it", meaning what ever tx you choose, will help even if others have failed. Some times I wonder if even we realize how truly hopefull and opptimistic we all are. After all we keep trying despite the odds, we persevere. We take those daily, weekly, monthly shots, we join medical studies, we donate blood for research, we answer questionaires, we come here to help each other and answer questions. We continue to fight despite a lack of concrete evidence that we are making a difference, in the face of dissapointment when that new "wonder drug" turns out not to be so wonderful, we don't give up. So yes we deserve a treat every now and then! Sorry I've been forim jumping and was thinking I was in MS social chat, so alot of my post refers to my feelings on MS. But every one else deserves a treat too!!!
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To talk about "conquering" the uncertainty of MS is to miss the point: MS is uncertain; one of its foremost attributes is uncertainty. BARBARA D. WEBSTER You learn to be a man and a warrior by sharing and by keeping promises. Kenneth Maryboy DX w/MS 2/12/07 on Copaxone 3/07 Last edited by ckepi; 02-11-2008 at 12:11 PM. Reason: Clarifing |
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"Thanks for this!" says: | braingonebad (02-11-2008), Koala77 (02-11-2008) |
02-11-2008, 12:18 PM | #16 | |||
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Member
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Have you tried going online to your library site? If your library is small, find out what the nearest big one is and go to theirs. Some libraries will mail you a book. You can mail it back. I'm just suggesting this in case you can't get out. Garage sales have cheap books (usually 10 or 25 cents; occasionally a bit more). I also use Amazon and do the 'used' book thing. I got my DH a book for a penny. Of course i still had to pay shipping and handling, but that still made the book cheap. I also dislike the MRI. I'm not afraid of it, I just don't like to lay there with a 'dead' mind listening to the grinding of the MRI. So I ask for earphones and I take a book on cd or a music cd I like. That helps. If you can't do that then ask for a sedative and go to sleep. Tomorrow I go for a nerve conduction test (I've never had one before). I just hate tests and I am always wary of the unknown. Tootsie
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AKA DianeD |
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"Thanks for this!" says: | braingonebad (02-11-2008), Koala77 (02-11-2008) |
02-11-2008, 07:13 PM | #17 | |||
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Magnate
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On and on She just keeps on trying And she smile when she feels like crying on and on, on and on.... Your post brought that to mind. I ask myself why I do it. My pessimistic side does not want another *experiment*. My daredevil side says *You can't win if you don't play*. And the daredevil wins. At any rate it's an adventure. I'm not brave, optimistic or so much hopeful, I don't think. I don't know what anybody else's motives are. I try the meds and the shots and whatever because they seem like the lesser of the evils. Feels like I have nothing to lose and I'll never know if it'll help if I don't try. Scary, sucky way to live. Thing is, after an LP 4 ESIs etc - I can let a lot of other stuff slide where before I never could. People talking on cell phones in the grocery is just not that bad after the needles in the neck. Annoying, but not painful, you know? When I say "I've had worse days" - the days with the needles are the ones I'm usually referring to. That said, there are scarier, suckier ways to live than the needle days too and I'm dang glad I don't have to live those.
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