Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 I have been on birth control and lupron to control bleeding since December. My blood count went down to 5.9 and I was given 3 units of blood or ? else. I do feel that even though I am stuck taking birth control and lupron now. That when my blood count dropped if my GYN would of upped my bith contol to 3 or 4 pills to stop bleeding I would of never got a blood transfusion. I was told this by 2 different Infertility doctors that they sometimes have to increase the birth control to stop bleeding. And it did work since then to slow or stop my bleeding. If you can stop the bleeding you will be able to bring your blood count up and move on to making a decision on a treatment without the threat of loosing more blood. Some group members are using Depo-Provera to conbtrol bleeding. maybe they can help. Me Im just hanging in there till my MRI results are read before I move forward to a decision. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 I have been on birth control and lupron to control bleeding since December. My blood count went down to 5.9 and I was given 3 units of blood or ? else. I do feel that even though I am stuck taking birth control and lupron now. That when my blood count dropped if my GYN would of upped my bith contol to 3 or 4 pills to stop bleeding I would of never got a blood transfusion. I was told this by 2 different Infertility doctors that they sometimes have to increase the birth control to stop bleeding. And it did work since then to slow or stop my bleeding. If you can stop the bleeding you will be able to bring your blood count up and move on to making a decision on a treatment without the threat of loosing more blood. Some group members are using Depo-Provera to conbtrol bleeding. maybe they can help. Me Im just hanging in there till my MRI results are read before I move forward to a decision. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 In a message dated 02/16/2001 5:11:01 PM Eastern Standard Time, infinityandon@... writes: << My blood count went down to 5.9 and I was given 3 units of blood >> My blood count was down to 3 this month has been 6 and no one gave me any blood. Panic I think. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 In a message dated 02/16/2001 5:11:01 PM Eastern Standard Time, infinityandon@... writes: << My blood count went down to 5.9 and I was given 3 units of blood >> My blood count was down to 3 this month has been 6 and no one gave me any blood. Panic I think. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 Your non-surgical options, I'm afraid aren't that plentiful. I spent the last 2 years trying them. First dietary changes (I read Dr. Lark's Fibroid book), then the birth control pills. They controlled my bleeding for 6 months, then stopped working. Then I tried Depo Provera to try and control the bleeding, it worked a bit at first but stopped working (some women here have had luck, however, with Depo Provera to control bleeding--I believe it's worth a try). None of these options serves to shrink fibroids, only to try and control bleeding. Potentially the drug RU-486 might help to shrink fibroids, but the availability of the drug and lack of research in this area probably mean this option is a few years away from helping you. The drug Lupron is used with some women to shrink fibroids before surgery or if a woman is very close to menopause. It turns off estrogen production, which for most women shrinks the fibroid. The drug cannot be used for longer than 6 months safely, however, because it causes menopausal symptoms, the most dangerous of them being loss in bone density. After you stop this drug the fibroids grow back it is not a fix in and of itself, only in conjunction with surgery or a looming menopause. Some people have had very bad reactions to the drug, most, I believe just have the annoying side-effects of hot-flashes and moodiness. I just had my first shot of this last week and the only side-effect I have had so far is that it completely stopped my bleeding. (Great for me, I'm not sure that will continue, though). I will be doing this for three months before surgery. An interesting note, in your case, is that Lupron is also used to treat Endometriosis. Do you know where your fibroids are located? If you have any totally in the uterine cavity (submucosal), you may be able to remove it hysteroscopically (still surgery but easier than a traditional myomectomy). These tend to cause a lot of bleeding so this may be your culprit. I'm going in for this myself in April and actually looking forward to it (then I get my life back!). As far as surgery goes, this one is relatively easy (I had one 3 years ago), with only 1 day of recovery and 1 week of restricted activity. Hope this arms you with some information. Sydney At 03:28 PM 2/16/2001 -0500, you wrote: >Hi. I was searching the web for information on fibroids and that is how I >found out about this group. I recently >had an ultrasound that showed several fibroids in my uterus. I had been >bleeding heavily and sometimes twice a month for the past 6 months and 3 >months ago my dr. prescribed the >birth control pill to try and control this. I hadn't had the ultrasound >yet. The bleeding got so much worse. I bled nearly everyday for 3 three >months. I called him to ask for help. I didn't think the pills were >helping me, but really making it worse. I requested an ultrasound and >CBC. My Hgb count is >8 and the ultrasound showed the fibroids. >I want to know what I can do that doesn't involve surgery. I haven't been >able to talk to my doctor, he'll be back in the office on Monday. I just >need some >support at this time. I don't want to have >surgery. I should tell you that I am 45 and have a history of endometriosis. >Thanks for any help you can give. >A.L. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2001 Report Share Posted February 16, 2001 Thank you very much for the information, I will definitely look at all of my options. I hope your surgery goes well. Good luck Anita uwsport Re: new diagnosis > Your non-surgical options, I'm afraid aren't that plentiful. > > I spent the last 2 years trying them. First dietary changes (I read Dr. > Lark's Fibroid book), then the birth control pills. They controlled > my bleeding for 6 months, then stopped working. Then I tried Depo Provera > to try and control the bleeding, it worked a bit at first but stopped > working (some women here have had luck, however, with Depo Provera to > control bleeding--I believe it's worth a try). > > None of these options serves to shrink fibroids, only to try and control > bleeding. > > Potentially the drug RU-486 might help to shrink fibroids, but the > availability of the drug and lack of research in this area probably mean > this option is a few years away from helping you. > > The drug Lupron is used with some women to shrink fibroids before surgery > or if a woman is very close to menopause. It turns off estrogen > production, which for most women shrinks the fibroid. The drug cannot be > used for longer than 6 months safely, however, because it causes menopausal > symptoms, the most dangerous of them being loss in bone density. After you > stop this drug the fibroids grow back it is not a fix in and of itself, > only in conjunction with surgery or a looming menopause. > > Some people have had very bad reactions to the drug, most, I believe just > have the annoying side-effects of hot-flashes and moodiness. I just had my > first shot of this last week and the only side-effect I have had so far is > that it completely stopped my bleeding. (Great for me, I'm not sure that > will continue, though). I will be doing this for three months before > surgery. An interesting note, in your case, is that Lupron is also used to > treat Endometriosis. > > Do you know where your fibroids are located? If you have any totally in > the uterine cavity (submucosal), you may be able to remove it > hysteroscopically (still surgery but easier than a traditional > myomectomy). These tend to cause a lot of bleeding so this may be your > culprit. > > I'm going in for this myself in April and actually looking forward to it > (then I get my life back!). As far as surgery goes, this one is relatively > easy (I had one 3 years ago), with only 1 day of recovery and 1 week of > restricted activity. > > Hope this arms you with some information. > > Sydney > > At 03:28 PM 2/16/2001 -0500, you wrote: > >Hi. I was searching the web for information on fibroids and that is how I > >found out about this group. I recently > >had an ultrasound that showed several fibroids in my uterus. I had been > >bleeding heavily and sometimes twice a month for the past 6 months and 3 > >months ago my dr. prescribed the > >birth control pill to try and control this. I hadn't had the ultrasound > >yet. The bleeding got so much worse. I bled nearly everyday for 3 three > >months. I called him to ask for help. I didn't think the pills were > >helping me, but really making it worse. I requested an ultrasound and > >CBC. My Hgb count is > >8 and the ultrasound showed the fibroids. > >I want to know what I can do that doesn't involve surgery. I haven't been > >able to talk to my doctor, he'll be back in the office on Monday. I just > >need some > >support at this time. I don't want to have > >surgery. I should tell you that I am 45 and have a history of endometriosis. > >Thanks for any help you can give. > >A.L. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2001 Report Share Posted February 17, 2001 when I had a severe bleed it apparantly caused lesions on my pituitary which caused very severe moods swings. It was a difficult dx, and one that is usually found on autopsy and is fairly rare, but I went to a group where women who had the same freaky thing happen to them met and talked. We are talking radical mood swings in previously " normal " women. gg ilia80@... wrote: > You are losing too much blood!!! I am post-hysterectomy (Still have ovaries) > since 1/29/01. I am 37 years old, married with two children (9 & 19). But I > had to make a decision about my health or go on suffering each month. > > My symtoms were: Periods once a month, for 5 days. I would use 4-5 pads an > hour (Soaked). I would pass large blood clots constantly. My iron level was > at 7-8 and I was getting weaker each month, sometimes no energy at all. I > was also experiencing harmonal changes so bad that I had to seek help from my > doctor. They suggested I try Prozac for a while. I tell you that Prozac > save my relationships with my friends, co-workers, and most of all my > children and husband who had to endure my awful attitude and mood swings. I > knew something was going on with my body and the fibroids were contributing > to it. After my surgery I have not taken any Prozac and I feel great and do > not need it. > > But I urge you to get as much information as possible about your illness. > But it comes down to how much you can endure. My surgery was sucessful, > considering I was cut in the same place 3 times before (2 prior C-sections). > > Please take good care of yourself and get plenty of iron supplements. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 The whole thing stinks. There are so many symptoms, so many medication side effects, the only thing that saves me is a sense of humor. There are several books available that might help. Your family and friends don't know what to do. Since a lot of lupus doesn's show, we don't always look sick. The faigue, muscle weakness, joint pain and a bunch of other stuff is hard to put into words others can understand. We understand. Here, you can laugh, cry, piss and moan and we know how you feel. I like to do as much normal stuff as I can, but I have a tendency to over-do. Learning to pace myself has been a real challenge. I suggest you learn as much as you can about the illness and keep in touch with us. We care. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 The whole thing stinks. There are so many symptoms, so many medication side effects, the only thing that saves me is a sense of humor. There are several books available that might help. Your family and friends don't know what to do. Since a lot of lupus doesn's show, we don't always look sick. The faigue, muscle weakness, joint pain and a bunch of other stuff is hard to put into words others can understand. We understand. Here, you can laugh, cry, piss and moan and we know how you feel. I like to do as much normal stuff as I can, but I have a tendency to over-do. Learning to pace myself has been a real challenge. I suggest you learn as much as you can about the illness and keep in touch with us. We care. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 I am new to this Sh#*!. I have had two attacks in two months. I don't know what my triggers are. How do most people figure this out? I am having difficulty w husband and best friend. Neither one will talk to me about lupus. Feel alone and very frustrated. Have absolutely no sex drive. I don't know if I want to be treated " normal " or otherwise. feel plain pissed off alot. I don't know what to expect and that in itslef is tough for me. Any input for a newbie? Jan Swenson Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Jan, Firstly, don't try to decide all at once how you are going to deal with this s**tty disease. It takes a while to find out what is really going on inside your body, what meds can be effective for you, and to learn how to cope with the ups and downs that come with life in the Lupus Lane. You will find that periods of work must be followed by periods of rest. Depending on how much you are flaring at any given moment will determine how much rest vs. work is the right ratio for YOU. This takes time and patience...sometimes clairvoyance. LOL But, most of all, it takes supportive friends and that is what we are here for. Your family members are welcome to join in and ask questions and vent, too. We have had many husbands or parents join the group in order to better understand what their loved one is experiencing and to learn ways to help. Once you feel comfortable with that idea, you may invite your hubby to join in. If you just want to help him get better informed, print out the copies of the articles available on a list at the main Lupies board. The web addresses for 's informational web sites are there. And, most importantly, keep writing what you feel, fears, hopes, jokes, tears. We all need it, and we all use this group to help us through. Loving hugs, MM aka: Mike one of the moderators Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Jan, Firstly, don't try to decide all at once how you are going to deal with this s**tty disease. It takes a while to find out what is really going on inside your body, what meds can be effective for you, and to learn how to cope with the ups and downs that come with life in the Lupus Lane. You will find that periods of work must be followed by periods of rest. Depending on how much you are flaring at any given moment will determine how much rest vs. work is the right ratio for YOU. This takes time and patience...sometimes clairvoyance. LOL But, most of all, it takes supportive friends and that is what we are here for. Your family members are welcome to join in and ask questions and vent, too. We have had many husbands or parents join the group in order to better understand what their loved one is experiencing and to learn ways to help. Once you feel comfortable with that idea, you may invite your hubby to join in. If you just want to help him get better informed, print out the copies of the articles available on a list at the main Lupies board. The web addresses for 's informational web sites are there. And, most importantly, keep writing what you feel, fears, hopes, jokes, tears. We all need it, and we all use this group to help us through. Loving hugs, MM aka: Mike one of the moderators Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Hi Jan. At some point, all of us were new to this S***. Not everyone is going to deal with chronic illness the same either. People have different triggers, lupus may share many of the same issues, but on the other hand, it is very unique to each individual. What may trigger you, may not trigger me, and vice versa. One thing I think that definitely is a trigger for all or most of us, is stress, overexerting one's self, poor diet, and definitely ignoring signals that your body is getting overly exhausted or strained. It is not to say, you can be feeling perfectly fine, doing all the right things, and you can still flare as well. Not all of us use the same meds either. The same holds true, what works for one, may not for another. It is not uncommon for family and friends to react this way. Some people are fortunate enough to have very understanding family and friends. Some of us have people that turn away, are in denial, do not want to deal with it, etc..... Hopefully in your case, time will help,and education will help. Misinformation and lack of knowledge are the big factors to estrange people. It is no doubt with feeling how you do, that you are not having a sex drive at this time. I myself prefer to be treated "normal", and if you need any assistance or help, ask for it. I do not want any special treatment from anyone, nor do I want anyone feeling sorry for me, or like I am some type of non productive freak either. How long since you have been dx? I mean a lot of people go through anger, depression, denial, feeling isolated, fearful, worried,confused, etc...... Not all people have the same level of disease either. Some people are more mild, and some people have major issues with lupus. There is no real way to know if a mild case will stay the same or progress slowly or suddenly. There are just no guarantees with anything. I do advise you to try and find a method of stress relief, help, counseling, whatever to deal with your frustrations. You may want to include your family or friends at some point. Mind you, this is all just my own opinion here, ok? Also, I may not always take my own advice when I should. But, I am still telling you just how I feel about it. Take care, Normi New diagnosis>I am new to this Sh#*!. I have had two attacks in two months. I >don't know what my triggers are. How do most people figure this >out? I am having difficulty w husband and best friend. Neither one >will talk to me about lupus. Feel alone and very frustrated. Have >absolutely no sex drive. I don't know if I want to be >treated "normal" or otherwise. feel plain pissed off alot. I don't >know what to expect and that in itslef is tough for me. Any input >for a newbie?>Jan Swenson>>>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Hi Jan. At some point, all of us were new to this S***. Not everyone is going to deal with chronic illness the same either. People have different triggers, lupus may share many of the same issues, but on the other hand, it is very unique to each individual. What may trigger you, may not trigger me, and vice versa. One thing I think that definitely is a trigger for all or most of us, is stress, overexerting one's self, poor diet, and definitely ignoring signals that your body is getting overly exhausted or strained. It is not to say, you can be feeling perfectly fine, doing all the right things, and you can still flare as well. Not all of us use the same meds either. The same holds true, what works for one, may not for another. It is not uncommon for family and friends to react this way. Some people are fortunate enough to have very understanding family and friends. Some of us have people that turn away, are in denial, do not want to deal with it, etc..... Hopefully in your case, time will help,and education will help. Misinformation and lack of knowledge are the big factors to estrange people. It is no doubt with feeling how you do, that you are not having a sex drive at this time. I myself prefer to be treated "normal", and if you need any assistance or help, ask for it. I do not want any special treatment from anyone, nor do I want anyone feeling sorry for me, or like I am some type of non productive freak either. How long since you have been dx? I mean a lot of people go through anger, depression, denial, feeling isolated, fearful, worried,confused, etc...... Not all people have the same level of disease either. Some people are more mild, and some people have major issues with lupus. There is no real way to know if a mild case will stay the same or progress slowly or suddenly. There are just no guarantees with anything. I do advise you to try and find a method of stress relief, help, counseling, whatever to deal with your frustrations. You may want to include your family or friends at some point. Mind you, this is all just my own opinion here, ok? Also, I may not always take my own advice when I should. But, I am still telling you just how I feel about it. Take care, Normi New diagnosis>I am new to this Sh#*!. I have had two attacks in two months. I >don't know what my triggers are. How do most people figure this >out? I am having difficulty w husband and best friend. Neither one >will talk to me about lupus. Feel alone and very frustrated. Have >absolutely no sex drive. I don't know if I want to be >treated "normal" or otherwise. feel plain pissed off alot. I don't >know what to expect and that in itslef is tough for me. Any input >for a newbie?>Jan Swenson>>>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Hi Jan! Trust me, we have all been there. What triggers the flares? It all depends. I would say the most common triggers would be stress and not enough rest. But, there are many others but they all vary from person to person. You said you have had 2 attacks. What kind of attacks exactly? What do your flares consist of? I can definitely relate to the no sex drive. When I do feel it's been long enough and give into my husband so he doesn't explode, go blind, or go insane - for the most part it's not fun. It is uncomfortable to downright painful. It is very hard to feel sexy and horny when you feel so terrible. That is normal. Also, with the medications, that is normal to have a low or non-existent sex drive. My only advice with your family is try to educate them. If they don't want to talk about it or listen just yet, maybe print out as much information as you can and let them read it on their own time. There is just way too much to try to tell people all at once. I printed out I don't know how many pages and gave to my parents to read up on it. I would tell my husband every little thing I would learn and constantly involved him in my learning process. Otherwise, he still wouldn't have a clue what I have or what I'm going through. Also, my husband and/or my Mom go with me to all of my doctor appointments. They feel involved and hear first hand what the doctors have to say. You may want to print out the information that has provided for the group at www.itzarion.com. There is a link at the bottom of this group's home page. It's full of great information and even a letter to be shared with your family. Hang in there. I know it's extremely frustrating. Just keep learning all you can and hopefully your family will come around. Laurie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Hi Jan! Trust me, we have all been there. What triggers the flares? It all depends. I would say the most common triggers would be stress and not enough rest. But, there are many others but they all vary from person to person. You said you have had 2 attacks. What kind of attacks exactly? What do your flares consist of? I can definitely relate to the no sex drive. When I do feel it's been long enough and give into my husband so he doesn't explode, go blind, or go insane - for the most part it's not fun. It is uncomfortable to downright painful. It is very hard to feel sexy and horny when you feel so terrible. That is normal. Also, with the medications, that is normal to have a low or non-existent sex drive. My only advice with your family is try to educate them. If they don't want to talk about it or listen just yet, maybe print out as much information as you can and let them read it on their own time. There is just way too much to try to tell people all at once. I printed out I don't know how many pages and gave to my parents to read up on it. I would tell my husband every little thing I would learn and constantly involved him in my learning process. Otherwise, he still wouldn't have a clue what I have or what I'm going through. Also, my husband and/or my Mom go with me to all of my doctor appointments. They feel involved and hear first hand what the doctors have to say. You may want to print out the information that has provided for the group at www.itzarion.com. There is a link at the bottom of this group's home page. It's full of great information and even a letter to be shared with your family. Hang in there. I know it's extremely frustrating. Just keep learning all you can and hopefully your family will come around. Laurie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 Hi Jan! Trust me, we have all been there. What triggers the flares? It all depends. I would say the most common triggers would be stress and not enough rest. But, there are many others but they all vary from person to person. You said you have had 2 attacks. What kind of attacks exactly? What do your flares consist of? I can definitely relate to the no sex drive. When I do feel it's been long enough and give into my husband so he doesn't explode, go blind, or go insane - for the most part it's not fun. It is uncomfortable to downright painful. It is very hard to feel sexy and horny when you feel so terrible. That is normal. Also, with the medications, that is normal to have a low or non-existent sex drive. My only advice with your family is try to educate them. If they don't want to talk about it or listen just yet, maybe print out as much information as you can and let them read it on their own time. There is just way too much to try to tell people all at once. I printed out I don't know how many pages and gave to my parents to read up on it. I would tell my husband every little thing I would learn and constantly involved him in my learning process. Otherwise, he still wouldn't have a clue what I have or what I'm going through. Also, my husband and/or my Mom go with me to all of my doctor appointments. They feel involved and hear first hand what the doctors have to say. You may want to print out the information that has provided for the group at www.itzarion.com. There is a link at the bottom of this group's home page. It's full of great information and even a letter to be shared with your family. Hang in there. I know it's extremely frustrating. Just keep learning all you can and hopefully your family will come around. Laurie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 I like to do as much normal stuff as I can, but I have a tendency to over-do. Learning to pace myself has been a real challenge. I suggest you learn as much as you can about the illness and keep in touch with us. We care. Lynn Lynn, you have just described my new spelling test for this week lol. or my life story. I just got out of the hospital yesterday and today I am over at my sisters cause I did not want to pace myself so I tried to help her by fixing up the boy;s room real cute, trying to act normal in front of my family so they wont worry over me, then came home and made dinner and straighented my own house before my guys got home to surpise them and now I did an over-do and am ill the rest of the night and cannot sleep because of it. I hate this stupid disease because it is taking from me things that I love to do and I get angry and want to do them anyway's. I am so glad I joined this group so I could know I am not crazy just a little wacky : -) Take care Carlasue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 I like to do as much normal stuff as I can, but I have a tendency to over-do. Learning to pace myself has been a real challenge. I suggest you learn as much as you can about the illness and keep in touch with us. We care. Lynn Lynn, you have just described my new spelling test for this week lol. or my life story. I just got out of the hospital yesterday and today I am over at my sisters cause I did not want to pace myself so I tried to help her by fixing up the boy;s room real cute, trying to act normal in front of my family so they wont worry over me, then came home and made dinner and straighented my own house before my guys got home to surpise them and now I did an over-do and am ill the rest of the night and cannot sleep because of it. I hate this stupid disease because it is taking from me things that I love to do and I get angry and want to do them anyway's. I am so glad I joined this group so I could know I am not crazy just a little wacky : -) Take care Carlasue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 I like to do as much normal stuff as I can, but I have a tendency to over-do. Learning to pace myself has been a real challenge. I suggest you learn as much as you can about the illness and keep in touch with us. We care. Lynn Lynn, you have just described my new spelling test for this week lol. or my life story. I just got out of the hospital yesterday and today I am over at my sisters cause I did not want to pace myself so I tried to help her by fixing up the boy;s room real cute, trying to act normal in front of my family so they wont worry over me, then came home and made dinner and straighented my own house before my guys got home to surpise them and now I did an over-do and am ill the rest of the night and cannot sleep because of it. I hate this stupid disease because it is taking from me things that I love to do and I get angry and want to do them anyway's. I am so glad I joined this group so I could know I am not crazy just a little wacky : -) Take care Carlasue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 Carlasue, A little wacky? Is that what you call it? And, here I thought I was truly insane. What a disappointment. Just kidding. LOL Actually, I treat my split personality (ies) as old friends. That way, life is never dull, and I always have company. LOL Hugs, MM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 Carlasue, A little wacky? Is that what you call it? And, here I thought I was truly insane. What a disappointment. Just kidding. LOL Actually, I treat my split personality (ies) as old friends. That way, life is never dull, and I always have company. LOL Hugs, MM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2002 Report Share Posted October 26, 2002 Carlasue, A little wacky? Is that what you call it? And, here I thought I was truly insane. What a disappointment. Just kidding. LOL Actually, I treat my split personality (ies) as old friends. That way, life is never dull, and I always have company. LOL Hugs, MM Quote Link to comment Share on other sites More sharing options...
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