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#1
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OT - My Spoon Story
I'm *NOT* posting it here. I'm just posting a link that, if people want
to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at: http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net |
#2
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OT - My Spoon Story
On 8/19/2011 1:39 AM, CatNipped wrote:
I'm *NOT* posting it here. I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. More information he http://www.biegler.com/pstim.en.html -- ^..^ This is Kitty. Copy and paste Kitty into your signature to help her wipe out Bunny's world domination. -- The ONE and ONLY lefthanded-pathetic-paranoid-psychotic-sarcastic-wiseass-ditzy former-blonde in Bloomington! (And proud of it, too)© email me at nalee1964 (at) comcast (dot) net http://community.webshots.com/user/mgcmdjeep |
#3
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OT - My Spoon Story
On 8/19/2011 2:19 PM, Magic Mood Jeep wrote:
On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. More information he http://www.biegler.com/pstim.en.html I tried hat about 3 or 4 years ago, but it didn't help - that's why I won't let them put the electrical stimulator in my spine. But thank you for thinking of me, I appreciate it. -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at: http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net |
#4
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OT - My Spoon Story
On Aug 19, 7:27*pm, CatNipped wrote:
On 8/19/2011 2:19 PM, Magic Mood Jeep wrote: On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. *I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. *It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. * I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! *I have several friends that also have fibro.... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. * More information he http://www.biegler.com/pstim.en.html I tried hat about 3 or 4 years ago, but it didn't help - that's why I won't let them put the electrical stimulator in my spine. *But thank you for thinking of me, I appreciate it. -- Hugs, CatNipped See all our masters at: *http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", *maintained by Mark Edwards, at:http://www.professional-geek.net/rpcablog/ Email: *L(dot)T(dot)Crews(at)comcast(dot)net- Hide quoted text - - Show quoted text - You should seriously think about posting this as a blog! If you used the keywords (tag words?) RSD, and fibromyalgia, I bet you would have followers in no time. Sherry |
#5
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OT - My Spoon Story
On 8/19/2011 10:31 PM, Sherry wrote:
On Aug 19, 7:27 pm, wrote: On 8/19/2011 2:19 PM, Magic Mood Jeep wrote: On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. More information he http://www.biegler.com/pstim.en.html I tried hat about 3 or 4 years ago, but it didn't help - that's why I won't let them put the electrical stimulator in my spine. But thank you for thinking of me, I appreciate it. -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at:http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net- Hide quoted text - - Show quoted text - You should seriously think about posting this as a blog! If you used the keywords (tag words?) RSD, and fibromyalgia, I bet you would have followers in no time. Sherry Thank you Sherry. A question, and please don't worry about offending me or hurting my feelings. As I've expressed before, I have *NO* social skills, not just poor or bad social skills, really just *NONE* at all. The "But You Don't Look Sick" support site is really great and friendly and all my other posts have gotten a good number of responses, but this one has gotten not a single response. If you read the story, (and again, don't worry about hurting me, I won't mind if you haven't), do you see any reason why nobody would respond. Is there anything offensive or weird about it? I asked Ben and he said he liked it, but he has about the same amount of social skills as I which is why we're so good together. I really can't tell when something I write might be taken the wrong way - which is why I've gotten into so much trouble here. I've read it back a few times and it seems OK to me, but then again I wrote it so it would. I'm just wondering why it didn't even get an "I hear ya" response. TIA. -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at: http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net |
#6
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OT - My Spoon Story
I thought it was a beautiful piece of work but then again having read
your other stories I knew it would be Lesley Slave of the Fabulous Furballs |
#7
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OT - My Spoon Story
On 8/19/2011 8:27 PM, CatNipped wrote:
On 8/19/2011 2:19 PM, Magic Mood Jeep wrote: On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. More information he http://www.biegler.com/pstim.en.html I tried hat about 3 or 4 years ago, but it didn't help - that's why I won't let them put the electrical stimulator in my spine. But thank you for thinking of me, I appreciate it. :/ Sorry it didn't work for you... I thought this was "new"... but alas it seems to only be new *to our area* (that being southern Indiana...) One of the "girls" that has severe/constant migraines has even tried accupressure, those same spots on the ears. Didn't work for her... or at least not that she could tell... -- ^..^ This is Kitty. Copy and paste Kitty into your signature to help her wipe out Bunny's world domination. -- The ONE and ONLY lefthanded-pathetic-paranoid-psychotic-sarcastic-wiseass-ditzy former-blonde in Bloomington! (And proud of it, too)© email me at nalee1964 (at) comcast (dot) net http://community.webshots.com/user/mgcmdjeep |
#8
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OT - My Spoon Story
On 8/20/2011 4:57 PM, Magic Mood Jeep wrote:
On 8/19/2011 8:27 PM, CatNipped wrote: On 8/19/2011 2:19 PM, Magic Mood Jeep wrote: On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. More information he http://www.biegler.com/pstim.en.html I tried hat about 3 or 4 years ago, but it didn't help - that's why I won't let them put the electrical stimulator in my spine. But thank you for thinking of me, I appreciate it. :/ Sorry it didn't work for you... I thought this was "new"... but alas it seems to only be new *to our area* (that being southern Indiana...) One of the "girls" that has severe/constant migraines has even tried accupressure, those same spots on the ears. Didn't work for her... or at least not that she could tell... The device might be new, the one I used wasn't over my ear, it had electrode to attach to various nerve points on the body, and a lot were placed around the neck and behind the ear. The constant electrical tingling just irritated me. -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at: http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net |
#9
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OT - My Spoon Story
On 8/20/2011 12:29 PM, Lesley wrote:
I thought it was a beautiful piece of work but then again having read your other stories I knew it would be Lesley Slave of the Fabulous Furballs Thank you, Lesly. I do hope I haven't offended anyone there, though. You guys know me and what a tongue-tied, foot-in-the-mouth geek I am so you cut me some slack. -- Hugs, CatNipped See all our masters at: http://www.PossiblePlaces.com/CatNipped See the RPCA FAQ site, created by "Yowie", maintained by Mark Edwards, at: http://www.professional-geek.net/rpcablog/ Email: L(dot)T(dot)Crews(at)comcast(dot)net |
#10
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OT - My Spoon Story
On Aug 20, 3:00*am, CatNipped wrote:
On 8/19/2011 10:31 PM, Sherry wrote: On Aug 19, 7:27 pm, *wrote: On 8/19/2011 2:19 PM, Magic Mood Jeep wrote: On 8/19/2011 1:39 AM, CatNipped wrote: I'm *NOT* posting it here. *I'm just posting a link that, if people want to read, they will have to deliberately click and download a Word document from my web site. *It's my "Spoon Story" that I just posted on the support site Julie recommended. It's not gory, it's not explicit, it's not depressing, there should be absolutely no controversy over its contents. http://www.possibleplaces.com/Where_did_she_go.doc Please do NOT click on this link if you have no wish to read this story. * *I apologize in advance if the subject line of this post hits a "hot button". Very well written, Lori! *I have several friends that also have fibro... both with iffy medical insurance (both have small-business owners as husbands, so some things fall by the wayside...their employees have access to med insurance, but they bypass it for themselves...) Anyway, a mutual friend of ours that works in the medical/insurance billing office of (one of) the local hospitals brought in a brochure from a "new" treatment being offered by one of the pain management offices in town. It's called P-Stim, and my friends have yet to try it. |
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