Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Challis! Your an angel! Im so grateful to be part of this group. You are a very wise lady! Your strength and understanding and caring shine right through the computer screen. When you speak about your mom it touches my heart. Me and my mom are very close too,I would be lost without her. We all deal with so much in so many different ways but what is so amazing is how we all come together and make eachother stronger. I would be lost without my family and all you are part of my family. So you had better get cozy and keep blessing us with you being here ok! Luv ya cassy --- MSersLife wrote: > Uh oh. Maybe it's all from breastfeeding then? LOLOL > > Ah, so it isn't only your daughter who does the things you described? You must all feel quite at home in one anothers abode. LOL > > I do, in fact, meet the criteria in the DSM, though I appreciate what you're trying to do as a former professional. Maybe I'm wrong in assuming you're merely trying to offer comfort? In the form of " not to worry, you don't quite fit this " ? No comfort needed, really. It's all just part of life and, for me, not something terrible. For many it is and it can be debilitating even. For me it's not and even when my, or my sons', symptoms rear up harder we've managed well over all. It hasn't always been easy, but we do manage. > > I've smiled over some of the posts regarding this issue, thinking " here are people with MS and they offer me support and encouragement for these things? " Such wonderful, caring and loving people. Living with MS and yet our TS/OCD/ADD garners such warmth and comfort. (Did you know I adore the people on this list, for their compassion, love and wisdom and so much more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, and that is not 'only' in MS, OCD, AD/HD, but in Bipolar Disorder, Autism, Diabetes, et al. I look at others on this list, hearing what they live with, what has come in their lives, and I marvel at their strength and determination. The ability to embrace what is happening and arm themselves with information and move through life overcoming their obstacles. > > It certainly isn't an easy task and all things cannot be " overcome " , but these people whom I respect so deeply have found a way to make it theirs and adjust as needed. > > I watch my Mother, for one, with her MS and as it progresses and changes she adapts. I know she doesn't want to experience fatigue, an exhaustion unlike any simple " sleepiness " , the lack of understanding from others, the struggle to accomplish the simplest of tasks. The cognitive dysfunction, the changes in the way her intelligence shows itself to others. Oh, and my Mother is a brilliant woman. This isn't something I needed to be an adult to recognize, nor even her child with a clear bias. She is intelligent, strong, independent, sharp and amazing in so many ways. The cognitive dysfunction puts roadblocks up, but these things are still there. How frustrating to know it and yet be unable to express it in the way of ten years ago, or even tomorrow. Her body does not allow her to do the things she used to, the things she wants so badly to do. Even to walk through a store, go from aisle to aisle, shelf to shelf, comparing prices and quality and thinking clearly in > the process, picking and choosing and placing any item she wants in the cart and then buying and taking it home. To carry bags into the house, to put groceries away, to be able to continue with a day and for shopping to be nothing more than a chore accomplished. Such simple things and yet such great things. Her pain is immense and I don't know how anyone manages life with such pain. My shoulder hurts and I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take a pill and make it go away. They deal with it each moment, all through their day. They try to sleep through it, they wake the next day and begin again, they don't always know what will come, but they hold heads high and flex those inner muscles and move forward. Such things can be overwhelming and depressing, but their strength carries them through and they manage. Not in a slight way, but manage in a way that should impress anyone. > > And each person dealing with so much still looks to others and sees a struggle and offers love and support. ) > > Clearly reading bits and pieces won't give an idea of what life is truly like in my home and with my own OCD, or even that of my sons. Now, if I knew we were doing an intake and eval, === Message Truncated === ________________________________________________________________________________\ ____ Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games. http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Challis! Your an angel! Im so grateful to be part of this group. You are a very wise lady! Your strength and understanding and caring shine right through the computer screen. When you speak about your mom it touches my heart. Me and my mom are very close too,I would be lost without her. We all deal with so much in so many different ways but what is so amazing is how we all come together and make eachother stronger. I would be lost without my family and all you are part of my family. So you had better get cozy and keep blessing us with you being here ok! Luv ya cassy --- MSersLife wrote: > Uh oh. Maybe it's all from breastfeeding then? LOLOL > > Ah, so it isn't only your daughter who does the things you described? You must all feel quite at home in one anothers abode. LOL > > I do, in fact, meet the criteria in the DSM, though I appreciate what you're trying to do as a former professional. Maybe I'm wrong in assuming you're merely trying to offer comfort? In the form of " not to worry, you don't quite fit this " ? No comfort needed, really. It's all just part of life and, for me, not something terrible. For many it is and it can be debilitating even. For me it's not and even when my, or my sons', symptoms rear up harder we've managed well over all. It hasn't always been easy, but we do manage. > > I've smiled over some of the posts regarding this issue, thinking " here are people with MS and they offer me support and encouragement for these things? " Such wonderful, caring and loving people. Living with MS and yet our TS/OCD/ADD garners such warmth and comfort. (Did you know I adore the people on this list, for their compassion, love and wisdom and so much more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, and that is not 'only' in MS, OCD, AD/HD, but in Bipolar Disorder, Autism, Diabetes, et al. I look at others on this list, hearing what they live with, what has come in their lives, and I marvel at their strength and determination. The ability to embrace what is happening and arm themselves with information and move through life overcoming their obstacles. > > It certainly isn't an easy task and all things cannot be " overcome " , but these people whom I respect so deeply have found a way to make it theirs and adjust as needed. > > I watch my Mother, for one, with her MS and as it progresses and changes she adapts. I know she doesn't want to experience fatigue, an exhaustion unlike any simple " sleepiness " , the lack of understanding from others, the struggle to accomplish the simplest of tasks. The cognitive dysfunction, the changes in the way her intelligence shows itself to others. Oh, and my Mother is a brilliant woman. This isn't something I needed to be an adult to recognize, nor even her child with a clear bias. She is intelligent, strong, independent, sharp and amazing in so many ways. The cognitive dysfunction puts roadblocks up, but these things are still there. How frustrating to know it and yet be unable to express it in the way of ten years ago, or even tomorrow. Her body does not allow her to do the things she used to, the things she wants so badly to do. Even to walk through a store, go from aisle to aisle, shelf to shelf, comparing prices and quality and thinking clearly in > the process, picking and choosing and placing any item she wants in the cart and then buying and taking it home. To carry bags into the house, to put groceries away, to be able to continue with a day and for shopping to be nothing more than a chore accomplished. Such simple things and yet such great things. Her pain is immense and I don't know how anyone manages life with such pain. My shoulder hurts and I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take a pill and make it go away. They deal with it each moment, all through their day. They try to sleep through it, they wake the next day and begin again, they don't always know what will come, but they hold heads high and flex those inner muscles and move forward. Such things can be overwhelming and depressing, but their strength carries them through and they manage. Not in a slight way, but manage in a way that should impress anyone. > > And each person dealing with so much still looks to others and sees a struggle and offers love and support. ) > > Clearly reading bits and pieces won't give an idea of what life is truly like in my home and with my own OCD, or even that of my sons. Now, if I knew we were doing an intake and eval, === Message Truncated === ________________________________________________________________________________\ ____ Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games. http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 As the newbie....I like you even though the thought of you organizing your kitchen doing that elvis hip lip twitch taebo scares me a little..LOL I kid!! I kid!! Re: Re: We ARE amusing people--in this group!/Challis Challis! Your an angel! Im so grateful to be part ofthis group. You are a very wise lady! Your strengthand understanding and caring shine right through thecomputer screen. When you speak about your mom ittouches my heart. Me and my mom are very close too,Iwould be lost without her. We all deal with so much inso many different ways but what is so amazing is howwe all come together and make eachother stronger. Iwould be lost without my family and all you are partof my family. So you had better get cozy and keepblessing us with you being here ok! Luv yacassy--- MSersLife@yahoogrou ps.com<smyelingroovy@ yahoo.com> wrote:> Uh oh. Maybe it's all from breastfeeding then? LOLOL> > Ah, so it isn't only your daughter who does thethings you described? You must all feel quite at homein one anothers abode. LOL> > I do, in fact, meet the criteria in the DSM,though I appreciate what you're trying to do as aformer professional. Maybe I'm wrong in assumingyou're merely trying to offer comfort? In the form of"not to worry, you don't quite fit this"? No comfortneeded, really. It's all just part of life and, forme, not something terrible. For many it is and it canbe debilitating even. For me it's not and even whenmy, or my sons', symptoms rear up harder we've managedwell over all. It hasn't always been easy, but we domanage.> > I've smiled over some of the posts regarding thisissue, thinking "here are people with MS and theyoffer me support and encouragement for these things?" Such wonderful, caring and loving people. Living withMS and yet our TS/OCD/ADD garners such warmth andcomfort. (Did you know I adore the people on thislist, for their compassion, love and wisdom and somuch more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, andthat is not 'only' in MS, OCD, AD/HD, but in BipolarDisorder, Autism, Diabetes, et al. I look at otherson this list, hearing what they live with, what hascome in their lives, and I marvel at their strengthand determination. The ability to embrace what ishappening and arm themselves with information and movethrough life overcoming their obstacles.> > It certainly isn't an easy task and all thingscannot be "overcome", but these people whom I respectso deeply have found a way to make it theirs andadjust as needed.> > I watch my Mother, for one, with her MS and as itprogresses and changes she adapts. I know she doesn'twant to experience fatigue, an exhaustion unlike anysimple "sleepiness" , the lack of understanding fromothers, the struggle to accomplish the simplest oftasks. The cognitive dysfunction, the changes in theway her intelligence shows itself to others. Oh, andmy Mother is a brilliant woman. This isn't somethingI needed to be an adult to recognize, nor even herchild with a clear bias. She is intelligent, strong,independent, sharp and amazing in so many ways. Thecognitive dysfunction puts roadblocks up, but thesethings are still there. How frustrating to know itand yet be unable to express it in the way of tenyears ago, or even tomorrow. Her body does not allowher to do the things she used to, the things she wantsso badly to do. Even to walk through a store, go fromaisle to aisle, shelf to shelf, comparing prices andquality and thinking clearly in> the process, picking and choosing and placing anyitem she wants in the cart and then buying and takingit home. To carry bags into the house, to putgroceries away, to be able to continue with a day andfor shopping to be nothing more than a choreaccomplished. Such simple things and yet such greatthings. Her pain is immense and I don't know howanyone manages life with such pain. My shoulder hurtsand I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take apill and make it go away. They deal with it eachmoment, all through their day. They try to sleepthrough it, they wake the next day and begin again,they don't always know what will come, but they holdheads high and flex those inner muscles and moveforward. Such things can be overwhelming anddepressing, but their strength carries them throughand they manage. Not in a slight way, but manage in away that should impress anyone.> > And each person dealing with so much still looksto others and sees a struggle and offers love andsupport. )> > Clearly reading bits and pieces won't give an ideaof what life is truly like in my home and with my ownOCD, or even that of my sons. Now, if I knew we weredoing an intake and eval, === Message Truncated === ____________ _________ _________ _________ _________ _________ _Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games.http://get.games. yahoo.com/ proddesc? gamekey=monopoly herenow Be a better Heartthrob. Get better relationship answers from someone who knows.Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 As the newbie....I like you even though the thought of you organizing your kitchen doing that elvis hip lip twitch taebo scares me a little..LOL I kid!! I kid!! Re: Re: We ARE amusing people--in this group!/Challis Challis! Your an angel! Im so grateful to be part ofthis group. You are a very wise lady! Your strengthand understanding and caring shine right through thecomputer screen. When you speak about your mom ittouches my heart. Me and my mom are very close too,Iwould be lost without her. We all deal with so much inso many different ways but what is so amazing is howwe all come together and make eachother stronger. Iwould be lost without my family and all you are partof my family. So you had better get cozy and keepblessing us with you being here ok! Luv yacassy--- MSersLife@yahoogrou ps.com<smyelingroovy@ yahoo.com> wrote:> Uh oh. Maybe it's all from breastfeeding then? LOLOL> > Ah, so it isn't only your daughter who does thethings you described? You must all feel quite at homein one anothers abode. LOL> > I do, in fact, meet the criteria in the DSM,though I appreciate what you're trying to do as aformer professional. Maybe I'm wrong in assumingyou're merely trying to offer comfort? In the form of"not to worry, you don't quite fit this"? No comfortneeded, really. It's all just part of life and, forme, not something terrible. For many it is and it canbe debilitating even. For me it's not and even whenmy, or my sons', symptoms rear up harder we've managedwell over all. It hasn't always been easy, but we domanage.> > I've smiled over some of the posts regarding thisissue, thinking "here are people with MS and theyoffer me support and encouragement for these things?" Such wonderful, caring and loving people. Living withMS and yet our TS/OCD/ADD garners such warmth andcomfort. (Did you know I adore the people on thislist, for their compassion, love and wisdom and somuch more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, andthat is not 'only' in MS, OCD, AD/HD, but in BipolarDisorder, Autism, Diabetes, et al. I look at otherson this list, hearing what they live with, what hascome in their lives, and I marvel at their strengthand determination. The ability to embrace what ishappening and arm themselves with information and movethrough life overcoming their obstacles.> > It certainly isn't an easy task and all thingscannot be "overcome", but these people whom I respectso deeply have found a way to make it theirs andadjust as needed.> > I watch my Mother, for one, with her MS and as itprogresses and changes she adapts. I know she doesn'twant to experience fatigue, an exhaustion unlike anysimple "sleepiness" , the lack of understanding fromothers, the struggle to accomplish the simplest oftasks. The cognitive dysfunction, the changes in theway her intelligence shows itself to others. Oh, andmy Mother is a brilliant woman. This isn't somethingI needed to be an adult to recognize, nor even herchild with a clear bias. She is intelligent, strong,independent, sharp and amazing in so many ways. Thecognitive dysfunction puts roadblocks up, but thesethings are still there. How frustrating to know itand yet be unable to express it in the way of tenyears ago, or even tomorrow. Her body does not allowher to do the things she used to, the things she wantsso badly to do. Even to walk through a store, go fromaisle to aisle, shelf to shelf, comparing prices andquality and thinking clearly in> the process, picking and choosing and placing anyitem she wants in the cart and then buying and takingit home. To carry bags into the house, to putgroceries away, to be able to continue with a day andfor shopping to be nothing more than a choreaccomplished. Such simple things and yet such greatthings. Her pain is immense and I don't know howanyone manages life with such pain. My shoulder hurtsand I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take apill and make it go away. They deal with it eachmoment, all through their day. They try to sleepthrough it, they wake the next day and begin again,they don't always know what will come, but they holdheads high and flex those inner muscles and moveforward. Such things can be overwhelming anddepressing, but their strength carries them throughand they manage. Not in a slight way, but manage in away that should impress anyone.> > And each person dealing with so much still looksto others and sees a struggle and offers love andsupport. )> > Clearly reading bits and pieces won't give an ideaof what life is truly like in my home and with my ownOCD, or even that of my sons. Now, if I knew we weredoing an intake and eval, === Message Truncated === ____________ _________ _________ _________ _________ _________ _Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games.http://get.games. yahoo.com/ proddesc? gamekey=monopoly herenow Be a better Heartthrob. Get better relationship answers from someone who knows.Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 It would be something now, wouldn't it? roflmhoSharon This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Re: Re: We ARE amusing people--in this group!/Challis Challis! Your an angel! Im so grateful to be part ofthis group. You are a very wise lady! Your strengthand understanding and caring shine right through thecomputer screen. When you speak about your mom ittouches my heart. Me and my mom are very close too,Iwould be lost without her. We all deal with so much inso many different ways but what is so amazing is howwe all come together and make eachother stronger. Iwould be lost without my family and all you are partof my family. So you had better get cozy and keepblessing us with you being here ok! Luv yacassy--- MSersLife@yahoogrou ps.com<smyelingroovy@ yahoo.com> wrote:> Uh oh. Maybe it's all from breastfeeding then? LOLOL> > Ah, so it isn't only your daughter who does thethings you described? You must all feel quite at homein one anothers abode. LOL> > I do, in fact, meet the criteria in the DSM,though I appreciate what you're trying to do as aformer professional. Maybe I'm wrong in assumingyou're merely trying to offer comfort? In the form of"not to worry, you don't quite fit this"? No comfortneeded, really. It's all just part of life and, forme, not something terrible. For many it is and it canbe debilitating even. For me it's not and even whenmy, or my sons', symptoms rear up harder we've managedwell over all. It hasn't always been easy, but we domanage.> > I've smiled over some of the posts regarding thisissue, thinking "here are people with MS and theyoffer me support and encouragement for these things?" Such wonderful, caring and loving people. Living withMS and yet our TS/OCD/ADD garners such warmth andcomfort. (Did you know I adore the people on thislist, for their compassion, love and wisdom and somuch more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, andthat is not 'only' in MS, OCD, AD/HD, but in BipolarDisorder, Autism, Diabetes, et al. I look at otherson this list, hearing what they live with, what hascome in their lives, and I marvel at their strengthand determination. The ability to embrace what ishappening and arm themselves with information and movethrough life overcoming their obstacles.> > It certainly isn't an easy task and all thingscannot be "overcome", but these people whom I respectso deeply have found a way to make it theirs andadjust as needed.> > I watch my Mother, for one, with her MS and as itprogresses and changes she adapts. I know she doesn'twant to experience fatigue, an exhaustion unlike anysimple "sleepiness" , the lack of understanding fromothers, the struggle to accomplish the simplest oftasks. The cognitive dysfunction, the changes in theway her intelligence shows itself to others. Oh, andmy Mother is a brilliant woman. This isn't somethingI needed to be an adult to recognize, nor even herchild with a clear bias. She is intelligent, strong,independent, sharp and amazing in so many ways. Thecognitive dysfunction puts roadblocks up, but thesethings are still there. How frustrating to know itand yet be unable to express it in the way of tenyears ago, or even tomorrow. Her body does not allowher to do the things she used to, the things she wantsso badly to do. Even to walk through a store, go fromaisle to aisle, shelf to shelf, comparing prices andquality and thinking clearly in> the process, picking and choosing and placing anyitem she wants in the cart and then buying and takingit home. To carry bags into the house, to putgroceries away, to be able to continue with a day andfor shopping to be nothing more than a choreaccomplished. Such simple things and yet such greatthings. Her pain is immense and I don't know howanyone manages life with such pain. My shoulder hurtsand I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take apill and make it go away. They deal with it eachmoment, all through their day. They try to sleepthrough it, they wake the next day and begin again,they don't always know what will come, but they holdheads high and flex those inner muscles and moveforward. Such things can be overwhelming anddepressing, but their strength carries them throughand they manage. Not in a slight way, but manage in away that should impress anyone.> > And each person dealing with so much still looksto others and sees a struggle and offers love andsupport. )> > Clearly reading bits and pieces won't give an ideaof what life is truly like in my home and with my ownOCD, or even that of my sons. Now, if I knew we weredoing an intake and eval, === Message Truncated === ____________ _________ _________ _________ _________ _________ _Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games.http://get.games. yahoo.com/ proddesc? gamekey=monopoly herenow Be a better Heartthrob. Get better relationship answers from someone who knows.Yahoo! Answers - Check it out. Fussy? Opinionated? Impossible to please? Perfect. Join Yahoo!'s user panel and lay it on us. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2007 Report Share Posted July 3, 2007 I was so overcome by emotions after reading what Challis wrote about me. I never think people see me that way. But I know Challis understands what it's like to have the fatigue and all the other lovely stuff that goes along with it. Isn't Challis the sweetest daughter for the things she said, Cassy? I'm glad to hear that you and your mom have a very close relationship too. loveSharon This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Re: Re: We ARE amusing people--in this group!/Challis Challis! Your an angel! Im so grateful to be part of this group. You are a very wise lady! Your strength and understanding and caring shine right through the computer screen. When you speak about your mom it touches my heart. Me and my mom are very close too,I would be lost without her. We all deal with so much in so many different ways but what is so amazing is how we all come together and make eachother stronger. I would be lost without my family and all you are part of my family. So you had better get cozy and keep blessing us with you being here ok! Luv ya cassy --- MSersLife@yahoogrou ps.com <smyelingroovy@ yahoo.com> wrote: > Uh oh. Maybe it's all from breastfeeding then? LOLOL > > Ah, so it isn't only your daughter who does the things you described? You must all feel quite at home in one anothers abode. LOL > > I do, in fact, meet the criteria in the DSM, though I appreciate what you're trying to do as a former professional. Maybe I'm wrong in assuming you're merely trying to offer comfort? In the form of "not to worry, you don't quite fit this"? No comfort needed, really. It's all just part of life and, for me, not something terrible. For many it is and it can be debilitating even. For me it's not and even when my, or my sons', symptoms rear up harder we've managed well over all. It hasn't always been easy, but we do manage. > > I've smiled over some of the posts regarding this issue, thinking "here are people with MS and they offer me support and encouragement for these things?" Such wonderful, caring and loving people. Living with MS and yet our TS/OCD/ADD garners such warmth and comfort. (Did you know I adore the people on this list, for their compassion, love and wisdom and so much more? Oh, I've said it previously? lolol). Many others onlist live with far more than we do, and that is not 'only' in MS, OCD, AD/HD, but in Bipolar Disorder, Autism, Diabetes, et al. I look at others on this list, hearing what they live with, what has come in their lives, and I marvel at their strength and determination. The ability to embrace what is happening and arm themselves with information and move through life overcoming their obstacles. > > It certainly isn't an easy task and all things cannot be "overcome", but these people whom I respect so deeply have found a way to make it theirs and adjust as needed. > > I watch my Mother, for one, with her MS and as it progresses and changes she adapts. I know she doesn't want to experience fatigue, an exhaustion unlike any simple "sleepiness" , the lack of understanding from others, the struggle to accomplish the simplest of tasks. The cognitive dysfunction, the changes in the way her intelligence shows itself to others. Oh, and my Mother is a brilliant woman. This isn't something I needed to be an adult to recognize, nor even her child with a clear bias. She is intelligent, strong, independent, sharp and amazing in so many ways. The cognitive dysfunction puts roadblocks up, but these things are still there. How frustrating to know it and yet be unable to express it in the way of ten years ago, or even tomorrow. Her body does not allow her to do the things she used to, the things she wants so badly to do. Even to walk through a store, go from aisle to aisle, shelf to shelf, comparing prices and quality and thinking clearly in > the process, picking and choosing and placing any item she wants in the cart and then buying and taking it home. To carry bags into the house, to put groceries away, to be able to continue with a day and for shopping to be nothing more than a chore accomplished. Such simple things and yet such great things. Her pain is immense and I don't know how anyone manages life with such pain. My shoulder hurts and I want to whine and go to bed until it's gone. LOL But so many of the listers here cannot take a pill and make it go away. They deal with it each moment, all through their day. They try to sleep through it, they wake the next day and begin again, they don't always know what will come, but they hold heads high and flex those inner muscles and move forward. Such things can be overwhelming and depressing, but their strength carries them through and they manage. Not in a slight way, but manage in a way that should impress anyone. > > And each person dealing with so much still looks to others and sees a struggle and offers love and support. ) > > Clearly reading bits and pieces won't give an idea of what life is truly like in my home and with my own OCD, or even that of my sons. Now, if I knew we were doing an intake and eval, === Message Truncated === ____________ _________ _________ _________ _________ _________ _ Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games. http://get.games. yahoo.com/ proddesc? gamekey=monopoly herenow Get the free Yahoo! toolbar and rest assured with the added security of spyware protection. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2007 Report Share Posted July 3, 2007 Yes. She is sooo sweet. It just melted my heart reading all that. You are all those things Sharon! You are both some of the most loving caring people I have ever known. I know how it feels to have a mom thats also like your best friend and I think its one of the greatest gifts in this world. Now,you 2 have got to get closer to eachother already. ;o) --- MSersLife wrote: > I was so overcome by emotions after reading what Challis wrote about me. I never think people see me that way. But I know Challis understands what it's like to have the fatigue and all the other lovely stuff that goes along with it. Isn't Challis the sweetest daughter for the things she said, Cassy? I'm glad to hear that you and your mom have a very close relationship too. > > love > Sharon > > This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. > > > > > > > Re: Re: We ARE amusing people--in this group!/Challis > > > > > > > > > > > > > > Challis! Your an angel! Im so grateful to be part of > > this group. You are a very wise lady! Your strength > > and understanding and caring shine right through the > > computer screen. When you speak about your mom it > > touches my heart. Me and my mom are very close too,I > > would be lost without her. We all deal with so much in > > so many different ways but what is so amazing is how > > we all come together and make eachother stronger. I > > would be lost without my family and all you are part > > of my family. So you had better get cozy and keep > > blessing us with you being here ok! Luv ya > > cassy > > --- MSersLife@yahoogrou ps.com > > <smyelingroovy@ yahoo.com> wrote: > > > Uh oh. Maybe it's all from breastfeeding then? > > LOLOL > > > > > > Ah, so it isn't only your daughter who does the > > things you described? You must all feel quite at home > > in one anothers abode. LOL > > > > > > I do, in fact, meet the criteria in the DSM, > > though I appreciate what you're trying to do as a > > former professional. Maybe I'm wrong in assuming > > you're merely trying to offer comfort? In the form of > === Message Truncated === ________________________________________________________________________________\ ____ Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. http://answers.yahoo.com/dir/?link=list & sid=396545469 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2007 Report Share Posted July 3, 2007 I want to live closer to Challis and that may just happen one of these days. :)Sharon This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Re: Re: We ARE amusing people--in this group!/Challis > > > > > > > > > > > > > > Challis! Your an angel! Im so grateful to be part of > > this group. You are a very wise lady! Your strength > > and understanding and caring shine right through the > > computer screen. When you speak about your mom it > > touches my heart. Me and my mom are very close too,I > > would be lost without her. We all deal with so much in > > so many different ways but what is so amazing is how > > we all come together and make eachother stronger. I > > would be lost without my family and all you are part > > of my family. So you had better get cozy and keep > > blessing us with you being here ok! Luv ya > > cassy > > --- MSersLife@yahoogrou ps.com > > <smyelingroovy@ yahoo.com> wrote: > > > Uh oh. Maybe it's all from breastfeeding then? > > LOLOL > > > > > > Ah, so it isn't only your daughter who does the > > things you described? You must all feel quite at home > > in one anothers abode. LOL > > > > > > I do, in fact, meet the criteria in the DSM, > > though I appreciate what you're trying to do as a > > former professional. Maybe I'm wrong in assuming > > you're merely trying to offer comfort? In the form of > === Message Truncated === ____________ _________ _________ _________ _________ _________ _ Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. http://answers. yahoo.com/ dir/?link= list & sid= 396545469 Looking for a deal? Find great prices on flights and hotels with Yahoo! FareChase. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2007 Report Share Posted July 3, 2007 Aww. I know you do. I know how much you both miss eachother. --- MSersLife wrote: > I want to live closer to Challis and that may just happen one of these days. > > Sharon > > This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. > > > > > > > Re: Re: Re: We ARE amusing people--in this group!/Challis > > > > > > > > > > > > > > Yes. She is sooo sweet. It just melted my heart > > reading all that. You are all those things Sharon! You > > are both some of the most loving caring people I have > > ever known. I know how it feels to have a mom thats > > also like your best friend and I think its one of the > > greatest gifts in this world. Now,you 2 have got to > > get closer to eachother already. ;o) > > --- MSersLife@yahoogrou ps.com <wobbletowalk@ yahoo.com> > > wrote: > > > I was so overcome by emotions after reading what > > Challis wrote about me. I never think people see me > > that way. But I know Challis understands what it's > > like to have the fatigue and all the other lovely > > stuff that goes along with it. Isn't Challis the > > sweetest daughter for the things she said, Cassy? I'm > > glad to hear that you and your mom have a very close > > relationship too. > > > > > > love > > > Sharon > > > > > > This email is a natural hand made product. The > > slight variations in spelling and grammar enhance its > > individual character and beauty and in no way are to > > be considered flaws or defects. > > > === Message Truncated === ________________________________________________________________________________\ ____ Need a vacation? Get great deals to amazing places on Yahoo! Travel. http://travel.yahoo.com/ Quote Link to comment Share on other sites More sharing options...
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