If this is your first visit, be sure to check out the FAQ by clicking the link above. You may have to register before you can post: click the register link above to proceed. To start viewing messages, select the forum that you want to visit from the selection below. |
|
|
|
Thread Tools | Display Modes |
#11
|
|||
|
|||
OT - My Spoon Story
On 8/20/2011 10:59 PM, Sherry wrote:
On Aug 20, 3:00 am, 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. 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 Butt-honestly. I thought it was a wonderfully written chronicle of the descent which has brought you here today. It was well-written and poignant. I still think it's excellent blog material; but in *your* blog. The one that you're gonna start. :-) Add "dancer" to your list of tag words along with RSD and fibro. You *will* collect followers. When Julie (of Julie and Julia fame), and Pioneer Woman, and scores of other "famous" bloggers started, they didn't have any readers either! Be patient. Even if you're not getting any feedback right away, doesn't it help you just throwing it all out into cyberspace? I know you. You are impatient. You get frustrated if no one answers a post within two hours. You know that is true. :-) Hang in there and be patient. I think you're really on to something. Sherry I understand. I'll confine my writing about my descent to a blog or a support web site. I know now it's not appropriate to post it here. -- 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 |
#12
|
|||
|
|||
OT - My Spoon Story
On 8/21/2011 8:47 PM, CatNipped wrote:
On 8/20/2011 10:59 PM, Sherry wrote: On Aug 20, 3:00 am, 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. 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 Butt-honestly. I thought it was a wonderfully written chronicle of the descent which has brought you here today. It was well-written and poignant. I still think it's excellent blog material; but in *your* blog. The one that you're gonna start. :-) Add "dancer" to your list of tag words along with RSD and fibro. You *will* collect followers. When Julie (of Julie and Julia fame), and Pioneer Woman, and scores of other "famous" bloggers started, they didn't have any readers either! Be patient. Even if you're not getting any feedback right away, doesn't it help you just throwing it all out into cyberspace? I know you. You are impatient. You get frustrated if no one answers a post within two hours. You know that is true. :-) Hang in there and be patient. I think you're really on to something. Sherry I understand. I'll confine my writing about my descent to a blog or a support web site. I know now it's not appropriate to post it here. Just remember to post a link to it so those of us that *do* want to follow, can... -- ^..^ 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 |
#13
|
|||
|
|||
OT - My Spoon Story
On 8/22/2011 9:49 AM, Magic Mood Jeep wrote:
On 8/21/2011 8:47 PM, CatNipped wrote: On 8/20/2011 10:59 PM, Sherry wrote: On Aug 20, 3:00 am, 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. 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 Butt-honestly. I thought it was a wonderfully written chronicle of the descent which has brought you here today. It was well-written and poignant. I still think it's excellent blog material; but in *your* blog. The one that you're gonna start. :-) Add "dancer" to your list of tag words along with RSD and fibro. You *will* collect followers. When Julie (of Julie and Julia fame), and Pioneer Woman, and scores of other "famous" bloggers started, they didn't have any readers either! Be patient. Even if you're not getting any feedback right away, doesn't it help you just throwing it all out into cyberspace? I know you. You are impatient. You get frustrated if no one answers a post within two hours. You know that is true. :-) Hang in there and be patient. I think you're really on to something. Sherry I understand. I'll confine my writing about my descent to a blog or a support web site. I know now it's not appropriate to post it here. Just remember to post a link to it so those of us that *do* want to follow, can... Thanks MMJ, as soon as I get it set up I'll do that. I've been putting it off lately because, sorry other folks, I'm having a few difficult days just know and am not much to doing anything, especially after my ill-advised walk yesterday - not that I regret it in the least! ; -- 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 |
|
Thread Tools | |
Display Modes | |
|
|
Similar Threads | ||||
Thread | Thread Starter | Forum | Replies | Last Post |
never irrigate a spoon | Rudy | Cat anecdotes | 0 | September 12th 05 12:28 PM |
hey, go measure a spoon | Angelo | Cat anecdotes | 0 | September 12th 05 12:28 PM |
lately, go waste a spoon | Mikie B. Abercrombie, DVM | Cat anecdotes | 0 | September 12th 05 10:50 AM |
RB Kitty story invite (Rocky's Story" reposted - Longish) | Steve Touchstone | Cat anecdotes | 2 | July 15th 05 07:14 AM |
He grabbed the spoon | W. Leong | Cat anecdotes | 7 | July 2nd 05 05:01 PM |