Guest guest Posted August 22, 1993 Report Share Posted August 22, 1993 Hi Everyone, I saw the Rheumatologist today. The one who diagnosed me with Fibro in the first place back in 1995. (I thought it was '96, but the nurse told me that the chart says '95) Guess what? His disposition hasn't changed one bit in the 6 years since I saw him. He said he really doesn't understand what I want from him, that he can't do anything for me that my PCP can't. He said he is already sure I have Fibro, what more do I want? Tho, he was willing to admit I had gotten much worse than when he diagnosed me. Remember he told me 6 years ago, that Fibro is *not* progressive, nor disabling. I told him that I belong to several FMS support groups online and have done alot of reading. That I believe that I could have CFS and/or MPS, in addition to the Fibro. And that several of my doctors think I have Arthritis as well and asked if he could examine me and run some tests for these illnesses. He said that it's not necessary, that since I have FMS, I most likely have those things too. He implied FMS, CFS and MPS are all the same thing. He said that I shouldn't worry whether I have those or not, because nothing much can be done for them anyway. (AAAHHH!) He was insistent that I stop using the 3 different anti-inflammatory drugs my other doctors prescribed because of the danger to my stomach. He told me out of the Salsalate, Clinoril and Vioxx, that I should only continue the Vioxx. Then said he doesn't know why they have me taking any of it because NSAIDs doesn't help Fibro anyway. I told him because they believe I have Arthritis too, but they hoped he being the specialist, would run tests and confirm it. He looked at me like I was from Mars. He told me there is nothing he, or any other doctor can do for me. Only *I* can make myself better by losing weight, exercising and getting enough rest. He said the Depression is mostly the problem. (Tho I've had Fibro since around 1984 and wasn't depressed till a couple of years ago) He also told me that I *know* I have severe FMS. Why I am looking for other things to be wrong with me? Why can't I just accept his diagnosis? Just to shut me up, he ordered x-rays of my hands (tho the pain is worse in the back of my neck, both hips, lower back and knees). He also ordered blood work, CBC w/Diff, Comprehensive Metabolic, ESR and RF Latex Quantitative. Ok, Kathy D., Dawn, some of you nursing folks, I know all of them but the last one. I see my Thyroid doctor tomorrow morning and my PCP in the afternoon. I get the results of the Lipids Profile and the Thyroid Panel to see if it's time to get ready for scans for the Cancer again (Yippee...Not!) The PCP is going to run an EKG and probably more blood work (Oh joy!). She already told me on the phone, she will refer me to a Neurologist to try to find out why I'm suddenly having near " black out " spells. My Psychiatrist took me off the Serzone this past Monday to see if not taking it will help me not to sleep all the time. I was having trouble falling asleep, now I can't stay awake. I'm wanting to go lay down right now. Sorry this was so long... {{{Hugs}}} Jacqui Jacqui McCallister Age: 38 Dx'd: 1995, but symptoms since 1984 Location: Ridgeview, West Virginia Divorced, no kids. One furbaby, Jasmine, my Himalayan Hobbies: Internet, Country, Rock and Gospel music, TV, Trivia games ICQ#: 126676406 Yahoo Messenger ID: jacqui_mccallister " I'm not confused, I'm just well mixed. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 1993 Report Share Posted August 23, 1993 Hi Lorraine, This was the first time I'd seen this doctor since he diagnosed me in 1995. He didn't want to see me back, but my Thyroid doctor insisted I see him again because I have so many new problems. He as much as said if the Depression is treated, all the other symptoms will go away. He talked to me like I am a Hypocondriac. I wish to goodness I were *sigh*. I asked him how I am supposed to do *vigorous exercise* (His exact words) when I am too exhausted and aching to get off the couch long enough to go to the bathroom half the time? He just looked at me and said I have to be willing to help myself. Thanks for listening Lorraine .Take care! :-) {{{Hugs}}} Jacqui Re: My Trip To The Rheumy Hello Jacqui I can't understand why your Rheumatologist is so negative towards you. It must exasperate you to go to see him. As for losing weight and exercising, well that's a near impossibility and depression, no wonder you have felt depressed with the attitude of the medical staff you have seen, telling by you all that you wrote. They don't realise that they are as much to blame for people being depressed by their attitude towards their patients. I have had Fibro all my life but only found out about 7 years ago after a great many test and painful examinations. But I was determined I wouldn't let it drag me down or let the medical profession drag my spirit down into depression. I feel I am the winner in this. I have arthritis but found that since I returned back to drinking plenty of milk every day the arthritis has eased off greatly. The muscle pain I take very strong pain meds.. which helps relieve at least a bit of the pain. But going back to your arthritis and any other conditions that you have, surely it is better the doctors help alleviate some of the pain and other problems you face than to have all of the problems without anything to relieve at least some of it. I have various illness with the Fibro and I take a cocktail of medication daily as without them I wouldn't be able to eat, breath, or be able to move around at all. Although I do suffer pain when I do move around but at least I have just a few things to cope with than have every health problem I have fighting for attention of my body every day. Keep at the doctor or find another who is more willing to help you. How would they feel if they had multiple illnesses, they would get help for as many as they possible could. Keep fighting for what you need as we have as much right to help with our illness as any one else has. God bless in your quest. Lorraine UK --- persephene wrote: <HR> <html><body> <tt> Hi Everyone,<BR> <BR> I saw the Rheumatologist today. The one who diagnosed me with Fibro in the first place back in 1995. (I thought it was '96, but the nurse told me that the chart says '95) <BR> <BR> Guess what? His disposition hasn't changed one bit in the 6 years since I saw him. He said he really doesn't understand what I want from him, that he can't do anything for me that my PCP can't. He said he is already sure I have Fibro, what more do I want? Tho, he was willing to admit I had gotten much worse than when he diagnosed me. Remember he told me 6 years ago, that Fibro is *not* progressive, nor disabling. <BR> <BR> I told him that I belong to several FMS support groups online and have done alot of reading. That I believe that I could have CFS and/or MPS, in addition to the Fibro. And that several of my doctors think I have Arthritis as well and asked if he could examine me and run some tests for these illnesses.<BR> <BR> He said that it's not necessary, that since I have FMS, I most likely have those things too. He implied FMS, CFS and MPS are all the same thing. He said that I shouldn't worry whether I have those or not, because nothing much can be done for them anyway. (AAAHHH!)<BR> <BR> He was insistent that I stop using the 3 different anti-inflammatory drugs my other doctors prescribed because of the danger to my stomach. He told me out of the Salsalate, Clinoril and Vioxx, that I should only continue the Vioxx. Then said he doesn't know why they have me taking any of it because NSAIDs doesn't help Fibro anyway. I told him because they believe I have Arthritis too, but they hoped he being the specialist, would run tests and confirm it. He looked at me like I was from Mars. <BR> <BR> He told me there is nothing he, or any other doctor can do for me. Only *I* can make myself better by losing weight, exercising and getting enough rest. <BR> <BR> He said the Depression is mostly the problem. (Tho I've had Fibro since around 1984 and wasn't depressed till a couple of years ago) He also told me that I *know* I have severe FMS. Why I am looking for other things to be wrong with me? Why can't I just accept his diagnosis? <BR> <BR> Just to shut me up, he ordered x-rays of my hands (tho the pain is worse in the back of my neck, both hips, lower back and knees).<BR> He also ordered blood work, CBC w/Diff, Comprehensive Metabolic, ESR and RF Latex Quantitative. Ok, Kathy D., Dawn, some of you nursing folks, I know all of them but the last one. <BR> <BR> I see my Thyroid doctor tomorrow morning and my PCP in the afternoon. I get the results of the Lipids Profile and the Thyroid Panel to see if it's time to get ready for scans for the Cancer again (Yippee...Not!) The PCP is going to run an EKG and probably more blood work (Oh joy!). She already told me on the phone, she will refer me to a Neurologist to try to find out why I'm suddenly having near " black out " spells. <BR> <BR> My Psychiatrist took me off the Serzone this past Monday to see if not taking it will help me not to sleep all the time. I was having trouble falling asleep, now I can't stay awake. I'm wanting to go lay down right now. <BR> <BR> Sorry this was so long...<BR> <BR> {{{Hugs}}}<BR> Jacqui<BR> <BR> Jacqui McCallister<BR> Age: 38<BR> Dx'd: 1995, but symptoms since 1984<BR> Location: Ridgeview, West Virginia<BR> Divorced, no kids. One furbaby, Jasmine, my Himalayan<BR> Hobbies: Internet, Country, Rock and Gospel music, TV, Trivia games<BR> ICQ#: 126676406<BR> Yahoo Messenger ID: jacqui_mccallister<BR> <BR> <BR> <BR> " I'm not confused, I'm just well mixed. " <BR> <BR> <BR> <BR> [Non-text portions of this message have been removed]<BR> <BR> </tt> <br> <!-- |**|begin egp html banner|**| --> <table border=0 cellspacing=0 cellpadding=2> <tr bgcolor=#FFFFCC> <td align=center><font size= " -1 " color=#003399><b> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 1993 Report Share Posted August 23, 1993 Hi Lorraine, This was the first time I'd seen this doctor since he diagnosed me in 1995. He didn't want to see me back, but my Thyroid doctor insisted I see him again because I have so many new problems. He as much as said if the Depression is treated, all the other symptoms will go away. He talked to me like I am a Hypocondriac. I wish to goodness I were *sigh*. I asked him how I am supposed to do *vigorous exercise* (His exact words) when I am too exhausted and aching to get off the couch long enough to go to the bathroom half the time? He just looked at me and said I have to be willing to help myself. Thanks for listening Lorraine .Take care! :-) {{{Hugs}}} Jacqui Re: My Trip To The Rheumy Hello Jacqui I can't understand why your Rheumatologist is so negative towards you. It must exasperate you to go to see him. As for losing weight and exercising, well that's a near impossibility and depression, no wonder you have felt depressed with the attitude of the medical staff you have seen, telling by you all that you wrote. They don't realise that they are as much to blame for people being depressed by their attitude towards their patients. I have had Fibro all my life but only found out about 7 years ago after a great many test and painful examinations. But I was determined I wouldn't let it drag me down or let the medical profession drag my spirit down into depression. I feel I am the winner in this. I have arthritis but found that since I returned back to drinking plenty of milk every day the arthritis has eased off greatly. The muscle pain I take very strong pain meds.. which helps relieve at least a bit of the pain. But going back to your arthritis and any other conditions that you have, surely it is better the doctors help alleviate some of the pain and other problems you face than to have all of the problems without anything to relieve at least some of it. I have various illness with the Fibro and I take a cocktail of medication daily as without them I wouldn't be able to eat, breath, or be able to move around at all. Although I do suffer pain when I do move around but at least I have just a few things to cope with than have every health problem I have fighting for attention of my body every day. Keep at the doctor or find another who is more willing to help you. How would they feel if they had multiple illnesses, they would get help for as many as they possible could. Keep fighting for what you need as we have as much right to help with our illness as any one else has. God bless in your quest. Lorraine UK --- persephene wrote: <HR> <html><body> <tt> Hi Everyone,<BR> <BR> I saw the Rheumatologist today. The one who diagnosed me with Fibro in the first place back in 1995. (I thought it was '96, but the nurse told me that the chart says '95) <BR> <BR> Guess what? His disposition hasn't changed one bit in the 6 years since I saw him. He said he really doesn't understand what I want from him, that he can't do anything for me that my PCP can't. He said he is already sure I have Fibro, what more do I want? Tho, he was willing to admit I had gotten much worse than when he diagnosed me. Remember he told me 6 years ago, that Fibro is *not* progressive, nor disabling. <BR> <BR> I told him that I belong to several FMS support groups online and have done alot of reading. That I believe that I could have CFS and/or MPS, in addition to the Fibro. And that several of my doctors think I have Arthritis as well and asked if he could examine me and run some tests for these illnesses.<BR> <BR> He said that it's not necessary, that since I have FMS, I most likely have those things too. He implied FMS, CFS and MPS are all the same thing. He said that I shouldn't worry whether I have those or not, because nothing much can be done for them anyway. (AAAHHH!)<BR> <BR> He was insistent that I stop using the 3 different anti-inflammatory drugs my other doctors prescribed because of the danger to my stomach. He told me out of the Salsalate, Clinoril and Vioxx, that I should only continue the Vioxx. Then said he doesn't know why they have me taking any of it because NSAIDs doesn't help Fibro anyway. I told him because they believe I have Arthritis too, but they hoped he being the specialist, would run tests and confirm it. He looked at me like I was from Mars. <BR> <BR> He told me there is nothing he, or any other doctor can do for me. Only *I* can make myself better by losing weight, exercising and getting enough rest. <BR> <BR> He said the Depression is mostly the problem. (Tho I've had Fibro since around 1984 and wasn't depressed till a couple of years ago) He also told me that I *know* I have severe FMS. Why I am looking for other things to be wrong with me? Why can't I just accept his diagnosis? <BR> <BR> Just to shut me up, he ordered x-rays of my hands (tho the pain is worse in the back of my neck, both hips, lower back and knees).<BR> He also ordered blood work, CBC w/Diff, Comprehensive Metabolic, ESR and RF Latex Quantitative. Ok, Kathy D., Dawn, some of you nursing folks, I know all of them but the last one. <BR> <BR> I see my Thyroid doctor tomorrow morning and my PCP in the afternoon. I get the results of the Lipids Profile and the Thyroid Panel to see if it's time to get ready for scans for the Cancer again (Yippee...Not!) The PCP is going to run an EKG and probably more blood work (Oh joy!). She already told me on the phone, she will refer me to a Neurologist to try to find out why I'm suddenly having near " black out " spells. <BR> <BR> My Psychiatrist took me off the Serzone this past Monday to see if not taking it will help me not to sleep all the time. I was having trouble falling asleep, now I can't stay awake. I'm wanting to go lay down right now. <BR> <BR> Sorry this was so long...<BR> <BR> {{{Hugs}}}<BR> Jacqui<BR> <BR> Jacqui McCallister<BR> Age: 38<BR> Dx'd: 1995, but symptoms since 1984<BR> Location: Ridgeview, West Virginia<BR> Divorced, no kids. One furbaby, Jasmine, my Himalayan<BR> Hobbies: Internet, Country, Rock and Gospel music, TV, Trivia games<BR> ICQ#: 126676406<BR> Yahoo Messenger ID: jacqui_mccallister<BR> <BR> <BR> <BR> " I'm not confused, I'm just well mixed. " <BR> <BR> <BR> <BR> [Non-text portions of this message have been removed]<BR> <BR> </tt> <br> <!-- |**|begin egp html banner|**| --> <table border=0 cellspacing=0 cellpadding=2> <tr bgcolor=#FFFFCC> <td align=center><font size= " -1 " color=#003399><b> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 1993 Report Share Posted August 23, 1993 Hi Lorraine, This was the first time I'd seen this doctor since he diagnosed me in 1995. He didn't want to see me back, but my Thyroid doctor insisted I see him again because I have so many new problems. He as much as said if the Depression is treated, all the other symptoms will go away. He talked to me like I am a Hypocondriac. I wish to goodness I were *sigh*. I asked him how I am supposed to do *vigorous exercise* (His exact words) when I am too exhausted and aching to get off the couch long enough to go to the bathroom half the time? He just looked at me and said I have to be willing to help myself. Thanks for listening Lorraine .Take care! :-) {{{Hugs}}} Jacqui Re: My Trip To The Rheumy Hello Jacqui I can't understand why your Rheumatologist is so negative towards you. It must exasperate you to go to see him. As for losing weight and exercising, well that's a near impossibility and depression, no wonder you have felt depressed with the attitude of the medical staff you have seen, telling by you all that you wrote. They don't realise that they are as much to blame for people being depressed by their attitude towards their patients. I have had Fibro all my life but only found out about 7 years ago after a great many test and painful examinations. But I was determined I wouldn't let it drag me down or let the medical profession drag my spirit down into depression. I feel I am the winner in this. I have arthritis but found that since I returned back to drinking plenty of milk every day the arthritis has eased off greatly. The muscle pain I take very strong pain meds.. which helps relieve at least a bit of the pain. But going back to your arthritis and any other conditions that you have, surely it is better the doctors help alleviate some of the pain and other problems you face than to have all of the problems without anything to relieve at least some of it. I have various illness with the Fibro and I take a cocktail of medication daily as without them I wouldn't be able to eat, breath, or be able to move around at all. Although I do suffer pain when I do move around but at least I have just a few things to cope with than have every health problem I have fighting for attention of my body every day. Keep at the doctor or find another who is more willing to help you. How would they feel if they had multiple illnesses, they would get help for as many as they possible could. Keep fighting for what you need as we have as much right to help with our illness as any one else has. God bless in your quest. Lorraine UK --- persephene wrote: <HR> <html><body> <tt> Hi Everyone,<BR> <BR> I saw the Rheumatologist today. The one who diagnosed me with Fibro in the first place back in 1995. (I thought it was '96, but the nurse told me that the chart says '95) <BR> <BR> Guess what? His disposition hasn't changed one bit in the 6 years since I saw him. He said he really doesn't understand what I want from him, that he can't do anything for me that my PCP can't. He said he is already sure I have Fibro, what more do I want? Tho, he was willing to admit I had gotten much worse than when he diagnosed me. Remember he told me 6 years ago, that Fibro is *not* progressive, nor disabling. <BR> <BR> I told him that I belong to several FMS support groups online and have done alot of reading. That I believe that I could have CFS and/or MPS, in addition to the Fibro. And that several of my doctors think I have Arthritis as well and asked if he could examine me and run some tests for these illnesses.<BR> <BR> He said that it's not necessary, that since I have FMS, I most likely have those things too. He implied FMS, CFS and MPS are all the same thing. He said that I shouldn't worry whether I have those or not, because nothing much can be done for them anyway. (AAAHHH!)<BR> <BR> He was insistent that I stop using the 3 different anti-inflammatory drugs my other doctors prescribed because of the danger to my stomach. He told me out of the Salsalate, Clinoril and Vioxx, that I should only continue the Vioxx. Then said he doesn't know why they have me taking any of it because NSAIDs doesn't help Fibro anyway. I told him because they believe I have Arthritis too, but they hoped he being the specialist, would run tests and confirm it. He looked at me like I was from Mars. <BR> <BR> He told me there is nothing he, or any other doctor can do for me. Only *I* can make myself better by losing weight, exercising and getting enough rest. <BR> <BR> He said the Depression is mostly the problem. (Tho I've had Fibro since around 1984 and wasn't depressed till a couple of years ago) He also told me that I *know* I have severe FMS. Why I am looking for other things to be wrong with me? Why can't I just accept his diagnosis? <BR> <BR> Just to shut me up, he ordered x-rays of my hands (tho the pain is worse in the back of my neck, both hips, lower back and knees).<BR> He also ordered blood work, CBC w/Diff, Comprehensive Metabolic, ESR and RF Latex Quantitative. Ok, Kathy D., Dawn, some of you nursing folks, I know all of them but the last one. <BR> <BR> I see my Thyroid doctor tomorrow morning and my PCP in the afternoon. I get the results of the Lipids Profile and the Thyroid Panel to see if it's time to get ready for scans for the Cancer again (Yippee...Not!) The PCP is going to run an EKG and probably more blood work (Oh joy!). She already told me on the phone, she will refer me to a Neurologist to try to find out why I'm suddenly having near " black out " spells. <BR> <BR> My Psychiatrist took me off the Serzone this past Monday to see if not taking it will help me not to sleep all the time. I was having trouble falling asleep, now I can't stay awake. I'm wanting to go lay down right now. <BR> <BR> Sorry this was so long...<BR> <BR> {{{Hugs}}}<BR> Jacqui<BR> <BR> Jacqui McCallister<BR> Age: 38<BR> Dx'd: 1995, but symptoms since 1984<BR> Location: Ridgeview, West Virginia<BR> Divorced, no kids. One furbaby, Jasmine, my Himalayan<BR> Hobbies: Internet, Country, Rock and Gospel music, TV, Trivia games<BR> ICQ#: 126676406<BR> Yahoo Messenger ID: jacqui_mccallister<BR> <BR> <BR> <BR> " I'm not confused, I'm just well mixed. " <BR> <BR> <BR> <BR> [Non-text portions of this message have been removed]<BR> <BR> </tt> <br> <!-- |**|begin egp html banner|**| --> <table border=0 cellspacing=0 cellpadding=2> <tr bgcolor=#FFFFCC> <td align=center><font size= " -1 " color=#003399><b> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 22, 2001 Report Share Posted August 22, 2001 Hello Jacqui I can't understand why your Rheumatologist is so negative towards you. It must exasperate you to go to see him. As for losing weight and exercising, well that's a near impossibility and depression, no wonder you have felt depressed with the attitude of the medical staff you have seen, telling by you all that you wrote. They don't realise that they are as much to blame for people being depressed by their attitude towards their patients. I have had Fibro all my life but only found out about 7 years ago after a great many test and painful examinations. But I was determined I wouldn't let it drag me down or let the medical profession drag my spirit down into depression. I feel I am the winner in this. I have arthritis but found that since I returned back to drinking plenty of milk every day the arthritis has eased off greatly. The muscle pain I take very strong pain meds.. which helps relieve at least a bit of the pain. But going back to your arthritis and any other conditions that you have, surely it is better the doctors help alleviate some of the pain and other problems you face than to have all of the problems without anything to relieve at least some of it. I have various illness with the Fibro and I take a cocktail of medication daily as without them I wouldn't be able to eat, breath, or be able to move around at all. Although I do suffer pain when I do move around but at least I have just a few things to cope with than have every health problem I have fighting for attention of my body every day. Keep at the doctor or find another who is more willing to help you. How would they feel if they had multiple illnesses, they would get help for as many as they possible could. Keep fighting for what you need as we have as much right to help with our illness as any one else has. God bless in your quest. Lorraine UK --- persephene wrote: <HR> <html><body> <tt> Hi Everyone,<BR> <BR> I saw the Rheumatologist today. The one who diagnosed me with Fibro in the first place back in 1995. (I thought it was '96, but the nurse told me that the chart says '95) <BR> <BR> Guess what? His disposition hasn't changed one bit in the 6 years since I saw him. He said he really doesn't understand what I want from him, that he can't do anything for me that my PCP can't. He said he is already sure I have Fibro, what more do I want? Tho, he was willing to admit I had gotten much worse than when he diagnosed me. Remember he told me 6 years ago, that Fibro is *not* progressive, nor disabling. <BR> <BR> I told him that I belong to several FMS support groups online and have done alot of reading. That I believe that I could have CFS and/or MPS, in addition to the Fibro. And that several of my doctors think I have Arthritis as well and asked if he could examine me and run some tests for these illnesses.<BR> <BR> He said that it's not necessary, that since I have FMS, I most likely have those things too. He implied FMS, CFS and MPS are all the same thing. He said that I shouldn't worry whether I have those or not, because nothing much can be done for them anyway. (AAAHHH!)<BR> <BR> He was insistent that I stop using the 3 different anti-inflammatory drugs my other doctors prescribed because of the danger to my stomach. He told me out of the Salsalate, Clinoril and Vioxx, that I should only continue the Vioxx. Then said he doesn't know why they have me taking any of it because NSAIDs doesn't help Fibro anyway. I told him because they believe I have Arthritis too, but they hoped he being the specialist, would run tests and confirm it. He looked at me like I was from Mars. <BR> <BR> He told me there is nothing he, or any other doctor can do for me. Only *I* can make myself better by losing weight, exercising and getting enough rest. <BR> <BR> He said the Depression is mostly the problem. (Tho I've had Fibro since around 1984 and wasn't depressed till a couple of years ago) He also told me that I *know* I have severe FMS. Why I am looking for other things to be wrong with me? Why can't I just accept his diagnosis? <BR> <BR> Just to shut me up, he ordered x-rays of my hands (tho the pain is worse in the back of my neck, both hips, lower back and knees).<BR> He also ordered blood work, CBC w/Diff, Comprehensive Metabolic, ESR and RF Latex Quantitative. Ok, Kathy D., Dawn, some of you nursing folks, I know all of them but the last one. <BR> <BR> I see my Thyroid doctor tomorrow morning and my PCP in the afternoon. I get the results of the Lipids Profile and the Thyroid Panel to see if it's time to get ready for scans for the Cancer again (Yippee...Not!) The PCP is going to run an EKG and probably more blood work (Oh joy!). She already told me on the phone, she will refer me to a Neurologist to try to find out why I'm suddenly having near " black out " spells. <BR> <BR> My Psychiatrist took me off the Serzone this past Monday to see if not taking it will help me not to sleep all the time. I was having trouble falling asleep, now I can't stay awake. I'm wanting to go lay down right now. <BR> <BR> Sorry this was so long...<BR> <BR> {{{Hugs}}}<BR> Jacqui<BR> <BR> Jacqui McCallister<BR> Age: 38<BR> Dx'd: 1995, but symptoms since 1984<BR> Location: Ridgeview, West Virginia<BR> Divorced, no kids. One furbaby, Jasmine, my Himalayan<BR> Hobbies: Internet, Country, Rock and Gospel music, TV, Trivia games<BR> ICQ#: 126676406<BR> Yahoo Messenger ID: jacqui_mccallister<BR> <BR> <BR> <BR> " I'm not confused, I'm just well mixed. " <BR> <BR> <BR> <BR> [Non-text portions of this message have been removed]<BR> <BR> </tt> <br> <!-- |**|begin egp html banner|**| --> <table border=0 cellspacing=0 cellpadding=2> <tr bgcolor=#FFFFCC> <td align=center><font size= " -1 " color=#003399><b> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2001 Report Share Posted August 23, 2001 MPS For give me for bein dumb, but what is MPS? Thanks ever so much...Shay Join my new Diabetic Recipes group @ http://groups.yahoo.com/group/Recipes4Diabetes God Bless You All, Shay/Shalynn and the rescue gang; Max, Samson I, Samson II, Walter, Bogie, Jake, Ralph, Curly (Tazz), Sebastian, Tina Marie, Bear & Zeuss Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2001 Report Share Posted August 23, 2001 Does anyone take Stadol Nasal spray for their pain with the fibro and other related pains? Thanks, Shay Join my new Diabetic Recipes group @ http://groups.yahoo.com/group/Recipes4Diabetes God Bless You All, Shay/Shalynn and the rescue gang; Max, Samson I, Samson II, Walter, Bogie, Jake, Ralph, Curly (Tazz), Sebastian, Tina Marie, Bear & Zeuss Quote Link to comment Share on other sites More sharing options...
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