Guest guest Posted February 19, 2008 Report Share Posted February 19, 2008 I looked up some pictures of Lichen Planus?For those of you that have it, do you have the growths or shiney spots they show? Can you still have it if you do not have the skin distubances?Delicious ideas to please the pickiest eaters. Watch the video on AOL Living. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2008 Report Share Posted February 21, 2008 Okay, I had to google this prior to replying and it is "Wickham's Striae". It just means that there is a white string-type appearance over the inflammation. They just look like white strings, really. If you wipe with your finger, it will actually wipe off--well most of it, but it comes back quickly. You can probably get info on this if you just search lichen planus and wickhams striae. I am sure the web will explain better than me and sometimes it will give you pictures. I have the same thing in my mouth, as I have OLP also, but not as severe are the V area. The inflammation is what is so bothersome.Mindy>> Mindy,> > What do you mean by white streaks that wipe away??? I> know it's probably not very easy to explain but I> don't really know what you mean. > > > > > > > ____________________________________________________________________________________> Be a better friend, newshound, and > know-it-all with Yahoo! Mobile. Try it now. http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2008 Report Share Posted February 21, 2008 , I would strongly, strongly urge you to join the Yahoo LS group, which also includes women (and some men) who are dealing with LP. Clob is not the only medication used. As Melinda mentioned, estradiol has been used very successfully by many women to prevent/undo/repair fusion. And there are other meds, steroidal and otherwise, that are used to quell the inflammatory response and allow the body to heal itself. It's a very active and supportive group that could, i feel, really help you right now as you're faced with all this uncertainty. In September i was just where you were now -- freaking out over seeing my inner labia starting to fuse and not knowing if i could get back to a vuvlar specialist ( Kellogg-Spadt in Philly) in time to save it from totally disappearing on me --not to mention being so scared that my clitoris and vagina would be next. I was fortunate: the fusion has, at least for now, stopped, i've had some re-emergence of one of my labia,and my general vulvar skin condition has improved so much that said she wouldn't want to do a biopsy now even if i was open to it (which i wasn't). The information and support i got from the group was invaluable and i really think you could really benefit from it. The link is: http://health.groups.yahoo.com/group/LichenSclerosis/HollisOn Thu, Feb 21, 2008 at 1:34 AM, millburytimes wrote: > , If you really think you have LS you can also join the Yahoo LS group. They were extremely helpful to me when I was first diagnosed. nne From: VulvarDisorders [mailto:VulvarDisorders ] On Behalf Of euc1109 s Sent: Wednesday, February 20, 2008 10:57 PM To: VulvarDisorders Subject: Re: question on Lichen Planus Mindy, What do you mean by white streaks that wipe away??? I know it's probably not very easy to explain but I don't really know what you mean. __________________________________________________________ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2008 Report Share Posted February 21, 2008 I tried the link for the LS group but it didn't work and the only lichen group i see is for lichen planus- is it the same group? Also, am i correct in understanding you that if it is lichen and you treat it that if there is fusing, it can almost be reversed with treatment in some cases? Hmmm Philly- I know i could take a quick plane trip there for something like $80- maybe i'd be able to get in with her much sooner than dr. stewart if i needed to- is she hard to get an appointment with? Thanks, hgz wrote: , I would strongly, strongly urge you to join the Yahoo LS group, which also includes women (and some men) who are dealing with LP. Clob is not the only medication used. As Melinda mentioned, estradiol has been used very successfully by many women to prevent/undo/repair fusion. And there are other meds, steroidal and otherwise, that are used to quell the inflammatory response and allow the body to heal itself. It's a very active and supportive group that could, i feel, really help you right now as you're faced with all this uncertainty. In September i was just where you were now -- freaking out over seeing my inner labia starting to fuse and not knowing if i could get back to a vuvlar specialist ( Kellogg-Spadt in Philly) in time to save it from totally disappearing on me -- not to mention being so scared that my clitoris and vagina would be next. I was fortunate: the fusion has, at least for now, stopped, i've had some re-emergence of one of my labia, and my general vulvar skin condition has improved so much that said she wouldn't want to do a biopsy now even if i was open to it (which i wasn't). The information and support i got from the group was invaluable and i really think you could really benefit from it. The link is: http://health.groups.yahoo.com/group/LichenSclerosis/ Hollis > , If you really think you have LS you can also join the Yahoo LS group. They were extremely helpful to me when I was first diagnosed. nne From: VulvarDisorders [mailto:VulvarDisorders ] On Behalf Of euc1109 s Sent: Wednesday, February 20, 2008 10:57 PM To: VulvarDisorders Subject: Re: question on Lichen Planus Mindy, What do you mean by white streaks that wipe away??? I know it's probably not very easy to explain but I don't really know what you mean. __________________________________________________________ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2008 Report Share Posted February 21, 2008 , IF you would like the name of the Dr. I see here in Florida, let me know. His treatement for my LP has given me my life back! Email, me direct if you would like at doll_fin1977@... Best wishes, :)hgz wrote: , Try this. There were some extra spaces that somehow appeared in the first version: http://health.groups.yahoo.com/group/LichenSclerosis/ Yes, the fusing that can occur with LP and LS can reverse in some cases. Dee Troll, the owner of both this and the LS group, is one of the real success stories in this regard. She had years of awful undiagnosed vuvlar irritation and, after reading about and trying topical estradiol on her own, completely unfused her labia and healed her raw hamburger (her description) skin. Some women do not regain the labia or completely unfuse their clitoral hoods, but almost all, with some combo of estradiol, testosterone, and/or steroids and other non-steroidal anti-inflammatories, experience a vast improvement in their symptoms. There are excellent files on the group that will give you a wealth of information and, as i said, the people there are great and extremely helpful. Here's Kellogg-Spadt's practice's website: http://www.pelvicandsexualhealthinstitute.org/ I think i had to wait something like a month and a half or two months for an initial appointment with her, but if you were to see one of the other NP's that work with her, the wait would be shorter. My feeling was that i wanted to be seen by the head honcho for at least the first appointment, but now i like her so much, i really want to stick with her, even if it means longer waits. Good luck. I know how upsetting it is to see changes in your vulvar skin/architecture and not know what's going on. I hope you can get to someone somewhere before too long and get some answers and, if necessary, some treatment started. Hollis On Thu, Feb 21, 2008 at 1:54 PM, euc1109 s wrote: I tried the link for the LS group but it didn't work and the only lichen group i see is for lichen planus- is it the same group? Also, am i correct in understanding you that if it is lichen and you treat it that if there is fusing, it can almost be reversed with treatment in some cases? Hmmm Philly- I know i could take a quick plane trip there for something like $80- maybe i'd be able to get in with her much sooner than dr. stewart if i needed to- is she hard to get an appointment with? Thanks, hgz <hgz (AT) verizon (DOT) net> wrote: , I would strongly, strongly urge you to join the Yahoo LS group, which also includes women (and some men) who are dealing with LP. Clob is not the only medication used. As Melinda mentioned, estradiol has been used very successfully by many women to prevent/undo/ repair fusion. And there are other meds, steroidal and otherwise, that are used to quell the inflammatory response and allow the body to heal itself. It's a very active and supportive group that could, i feel, really help you right now as you're faced with all this uncertainty. In September i was just where you were now -- freaking out over seeing my inner labia starting to fuse and not knowing if i could get back to a vuvlar specialist ( Kellogg-Spadt in Philly) in time to save it from totally disappearing on me -- not to mention being so scared that my clitoris and vagina would be next. I was fortunate: the fusion has, at least for now, stopped, i've had some re-emergence of one of my labia, and my general vulvar skin condition has improved so much that said she wouldn't want to do a biopsy now even if i was open to it (which i wasn't). The information and support i got from the group was invaluable and i really think you could really benefit from it. The link is: http://health. groups.yahoo. com/group/ LichenSclerosis/ Hollis > , If you really think you have LS you can also join the Yahoo LS group. They were extremely helpful to me when I was first diagnosed. nne From: VulvarDisorders@ yahoogroups. com [mailto:VulvarDisor ders@yahoogroups .com] On Behalf Of euc1109 s Sent: Wednesday, February 20, 2008 10:57 PM To: VulvarDisorders@ yahoogroups. com Subject: Re: question on Lichen Planus Mindy, What do you mean by white streaks that wipe away??? I know it's probably not very easy to explain but I don't really know what you mean. ____________ _________ _________ _________ _________ _________ _ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ ___________________________________ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Never miss a thing. Make Yahoo your homepage. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2008 Report Share Posted February 22, 2008 Hollis, Thanks so much...Dr. 's office finally got all my stuff today and she said they should probably call me next week to set up an appointment which they're booking out until April. But, i plan on calling every few days or so to try to get in on a cancellation since my job is flexible enough to let me leave literally on a minutes notice if i need to. I'm going to pay close attention to my skin until I can finally get in to see someone and if I notice a big change in structure i'm going to convince one of my current doctors to prescribe the estrace cream even if they don't think i have it- not sure how hard that will be, but i'll keep pushing until they agree. Who knows, i could totally not have it at all, but the more i think about it from my symptoms, past treatments that haven't worked, the appearance, etc., the more i think it is a very good possibility and i'd rather know for sure and either cross it off the list or start treatment. erin --- hgz wrote: > > , > > Try this. There were some extra spaces that somehow > appeared in the > first version: > > http://health.groups.yahoo.com/group/LichenSclerosis/ > > Yes, the fusing that can occur with LP and LS can > reverse in some cases. > Dee Troll, > the owner of both this and the LS group, is one of > the real success > stories in this > regard. She had years of awful undiagnosed vuvlar > irritation and, after > reading about > and trying topical estradiol on her own, completely > unfused her labia > and healed her > raw hamburger (her description) skin. Some women do > not regain the > labia or > completely unfuse their clitoral hoods, but almost > all, with some combo > of estradiol, > testosterone, and/or steroids and other > non-steroidal > anti-inflammatories, experience > a vast improvement in their symptoms. There are > excellent files on the > group that > will give you a wealth of information and, as i > said, the people there > are great > and extremely helpful. > > Here's Kellogg-Spadt's practice's website: > > http://www.pelvicandsexualhealthinstitute.org/ > > I think i had to wait something like a month and a > half or two months > for an initial > appointment with her, but if you were to see one of > the other NP's that > work with > her, the wait would be shorter. My feeling was that > i wanted to be seen > by the > head honcho for at least the first appointment, but > now i like her so > much, i really > want to stick with her, even if it means longer > waits. > > Good luck. I know how upsetting it is to see > changes in your vulvar > skin/architecture > and not know what's going on. I hope you can get to > someone somewhere > before > too long and get some answers and, if necessary, > some treatment started. > > Hollis > > > > I tried the link for the LS group but it didn't work > and the only lichen > group i see is for lichen planus- is it the same > group? Also, am i > correct in understanding you that if it is lichen > and you treat it that > if there is fusing, it can almost be reversed with > treatment in some > cases? Hmmm Philly- I know i could take a quick > plane trip there for > something like $80- maybe i'd be able to get in with > her much sooner > than dr. stewart if i needed to- is she hard to get > an appointment with? > > Thanks, > > > hgz <hgz (AT) verizon (DOT) net> wrote: > , > > I would strongly, strongly urge you to join the > Yahoo LS group, which > also includes women > (and some men) who are dealing with LP. Clob is not > the only medication > used. As Melinda > mentioned, estradiol has been used very successfully > by many women to > prevent/undo/ repair > fusion. And there are other meds, steroidal and > otherwise, that are > used to quell the inflammatory response and allow > the body to heal > itself. > > It's a very active and supportive group that could, > i feel, really help > you right now as you're > faced with all this uncertainty. In September i was > just where you were > now -- freaking out > over seeing my inner labia starting to fuse and not > knowing if i could > get back to a vuvlar specialist ( Kellogg-Spadt > in Philly) in time > to save it from totally disappearing on me -- > not to mention being so scared that my clitoris and > vagina would be > next. I was fortunate: > the fusion has, at least for now, stopped, i've had > some re-emergence of > one of my labia, > and my general vulvar skin condition has improved so > much that > said she wouldn't want to do a biopsy now even if i > was open to it > (which i wasn't). The information and support i > got from the group was > invaluable and i really think you could really > benefit from it. The > link is: > > > http://health. groups.yahoo. com/group/ > LichenSclerosis/ > > Hollis > > > On Thu, Feb 21, 2008 at 1:34 AM, millburytimes > wrote: > > > , > > > > If you really think you have LS you can also join > the Yahoo LS group. > They > were extremely helpful to me when I was first > diagnosed. > > > > nne > > > > > > > > From: VulvarDisorders@ yahoogroups. com > <mailto:VulvarDisorders > > [mailto:VulvarDisor ders@yahoogroups .com] > <mailto:[mailto:VulvarDisorders ]> > On Behalf Of euc1109 > s > Sent: Wednesday, February 20, 2008 10:57 PM > To: VulvarDisorders@ yahoogroups. com > <mailto:VulvarDisorders > > Subject: Re: question on Lichen Planus > > > > Mindy, > > What do you mean by white streaks that wipe away??? > I > know it's probably not very easy to explain but I > don't really know what you mean. > > > > ____________ _________ _________ _________ _________ > _________ _ > Be a better friend, newshound, and > know-it-all with Yahoo! Mobile. Try it now. > http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR > 8HDtDypao8Wcj9tA cJ > <http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ> > > > > ___________________________________ > > Be a better friend, newshound, and know-it-all with > Yahoo! Mobile. Try > it now. > <http://us.rd.yahoo.com/evt=51733/*http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtD\ ypao8Wcj9tAcJ > > === message truncated === ________________________________________________________________________________\ ____ Looking for last minute shopping deals? Find them fast with Yahoo! Search. http://tools.search.yahoo.com/newsearch/category.php?category=shopping Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2008 Report Share Posted February 22, 2008 ,Sounds as if you've got a good plan formulated. Good luck.Hope there's a cancellation soon!Hollis Hollis, Thanks so much...Dr. 's office finally got all my stuff today and she said they should probably call me next week to set up an appointment which they're booking out until April. But, i plan on calling every few days or so to try to get in on a cancellation since my job is flexible enough to let me leave literally on a minutes notice if i need to. I'm going to pay close attention to my skin until I can finally get in to see someone and if I notice a big change in structure i'm going to convince one of my current doctors to prescribe the estrace cream even if they don't think i have it- not sure how hard that will be, but i'll keep pushing until they agree. Who knows, i could totally not have it at all, but the more i think about it from my symptoms, past treatments that haven't worked, the appearance, etc., the more i think it is a very good possibility and i'd rather know for sure and either cross it off the list or start treatment. erin --- hgz < hgz (AT) verizon (DOT) net> wrote: > > , > > Try this. There were some extra spaces that somehow > appeared in the > first version: > > http://health. groups.yahoo. com/group/ LichenSclerosis/> > Yes, the fusing that can occur with LP and LS can > reverse in some cases. > Dee Troll, > the owner of both this and the LS group, is one of > the real success > stories in this > regard. She had years of awful undiagnosed vuvlar > irritation and, after > reading about > and trying topical estradiol on her own, completely > unfused her labia > and healed her > raw hamburger (her description) skin. Some women do > not regain the > labia or > completely unfuse their clitoral hoods, but almost > all, with some combo > of estradiol, > testosterone, and/or steroids and other > non-steroidal > anti-inflammatories , experience > a vast improvement in their symptoms. There are > excellent files on the > group that > will give you a wealth of information and, as i > said, the people there > are great > and extremely helpful. > > Here's Kellogg-Spadt' s practice's website: > > http://www.pelvican dsexualhealthins titute.org/> > I think i had to wait something like a month and a > half or two months > for an initial > appointment with her, but if you were to see one of > the other NP's that > work with > her, the wait would be shorter. My feeling was that > i wanted to be seen > by the > head honcho for at least the first appointment, but > now i like her so > much, i really > want to stick with her, even if it means longer > waits. > > Good luck. I know how upsetting it is to see > changes in your vulvar > skin/architecture > and not know what's going on. I hope you can get to > someone somewhere > before > too long and get some answers and, if necessary, > some treatment started. > > Hollis > > > > I tried the link for the LS group but it didn't work > and the only lichen > group i see is for lichen planus- is it the same > group? Also, am i > correct in understanding you that if it is lichen > and you treat it that > if there is fusing, it can almost be reversed with > treatment in some > cases? Hmmm Philly- I know i could take a quick > plane trip there for > something like $80- maybe i'd be able to get in with > her much sooner > than dr. stewart if i needed to- is she hard to get > an appointment with? > > Thanks, > > > hgz <hgz (AT) verizon (DOT) net> wrote: > , > > I would strongly, strongly urge you to join the > Yahoo LS group, which > also includes women > (and some men) who are dealing with LP. Clob is not > the only medication > used. As Melinda > mentioned, estradiol has been used very successfully > by many women to > prevent/undo/ repair > fusion. And there are other meds, steroidal and > otherwise, that are > used to quell the inflammatory response and allow > the body to heal > itself. > > It's a very active and supportive group that could, > i feel, really help > you right now as you're > faced with all this uncertainty. In September i was > just where you were > now -- freaking out > over seeing my inner labia starting to fuse and not > knowing if i could > get back to a vuvlar specialist ( Kellogg-Spadt > in Philly) in time > to save it from totally disappearing on me -- > not to mention being so scared that my clitoris and > vagina would be > next. I was fortunate: > the fusion has, at least for now, stopped, i've had > some re-emergence of > one of my labia, > and my general vulvar skin condition has improved so > much that > said she wouldn't want to do a biopsy now even if i > was open to it > (which i wasn't). The information and support i > got from the group was > invaluable and i really think you could really > benefit from it. The > link is: > > > http://health.groups.yahoo. com/group/ > LichenSclerosis/ > > Hollis > > > > > > , > > > > If you really think you have LS you can also join > the Yahoo LS group. > They > were extremely helpful to me when I was first > diagnosed. > > > > nne > > > > > > > > From: VulvarDisorders@ yahoogroups. com > <mailto: VulvarDisorders@ yahoogroups. com> > [mailto:VulvarDisor ders@yahoogroups .com] > <mailto:[mailto: VulvarDisorders@ yahoogroups. com]> > On Behalf Of euc1109 > s > Sent: Wednesday, February 20, 2008 10:57 PM > To: VulvarDisorders@ yahoogroups. com > <mailto: VulvarDisorders@ yahoogroups. com> > Subject: Re: question on Lichen Planus > > > > Mindy, > > What do you mean by white streaks that wipe away??? > I > know it's probably not very easy to explain but I > don't really know what you mean. > > > > ____________ _________ _________ _________ _________ > _________ _ > Be a better friend, newshound, and > know-it-all with Yahoo! Mobile. Try it now. > http://mobile.yahoo.com/ ;_ylt=Ahu06i62sR > 8HDtDypao8Wcj9tA cJ > < http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ> > > > > ____________ _________ _________ _____ > > Be a better friend, newshound, and know-it-all with > Yahoo! Mobile. Try > it now. > < http://us.rd. yahoo.com/ evt=51733/ *http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ> > === message truncated === ____________ _________ _________ _________ _________ _________ _ Looking for last minute shopping deals? Find them fast with Yahoo! Search. http://tools. search.yahoo. com/newsearch/ category. php?category= shopping Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2008 Report Share Posted February 22, 2008 ,Sounds as if you've got a good plan formulated. Good luck.Hope there's a cancellation soon!Hollis Hollis, Thanks so much...Dr. 's office finally got all my stuff today and she said they should probably call me next week to set up an appointment which they're booking out until April. But, i plan on calling every few days or so to try to get in on a cancellation since my job is flexible enough to let me leave literally on a minutes notice if i need to. I'm going to pay close attention to my skin until I can finally get in to see someone and if I notice a big change in structure i'm going to convince one of my current doctors to prescribe the estrace cream even if they don't think i have it- not sure how hard that will be, but i'll keep pushing until they agree. Who knows, i could totally not have it at all, but the more i think about it from my symptoms, past treatments that haven't worked, the appearance, etc., the more i think it is a very good possibility and i'd rather know for sure and either cross it off the list or start treatment. erin --- hgz < hgz (AT) verizon (DOT) net> wrote: > > , > > Try this. There were some extra spaces that somehow > appeared in the > first version: > > http://health. groups.yahoo. com/group/ LichenSclerosis/> > Yes, the fusing that can occur with LP and LS can > reverse in some cases. > Dee Troll, > the owner of both this and the LS group, is one of > the real success > stories in this > regard. She had years of awful undiagnosed vuvlar > irritation and, after > reading about > and trying topical estradiol on her own, completely > unfused her labia > and healed her > raw hamburger (her description) skin. Some women do > not regain the > labia or > completely unfuse their clitoral hoods, but almost > all, with some combo > of estradiol, > testosterone, and/or steroids and other > non-steroidal > anti-inflammatories , experience > a vast improvement in their symptoms. There are > excellent files on the > group that > will give you a wealth of information and, as i > said, the people there > are great > and extremely helpful. > > Here's Kellogg-Spadt' s practice's website: > > http://www.pelvican dsexualhealthins titute.org/> > I think i had to wait something like a month and a > half or two months > for an initial > appointment with her, but if you were to see one of > the other NP's that > work with > her, the wait would be shorter. My feeling was that > i wanted to be seen > by the > head honcho for at least the first appointment, but > now i like her so > much, i really > want to stick with her, even if it means longer > waits. > > Good luck. I know how upsetting it is to see > changes in your vulvar > skin/architecture > and not know what's going on. I hope you can get to > someone somewhere > before > too long and get some answers and, if necessary, > some treatment started. > > Hollis > > > > I tried the link for the LS group but it didn't work > and the only lichen > group i see is for lichen planus- is it the same > group? Also, am i > correct in understanding you that if it is lichen > and you treat it that > if there is fusing, it can almost be reversed with > treatment in some > cases? Hmmm Philly- I know i could take a quick > plane trip there for > something like $80- maybe i'd be able to get in with > her much sooner > than dr. stewart if i needed to- is she hard to get > an appointment with? > > Thanks, > > > hgz <hgz (AT) verizon (DOT) net> wrote: > , > > I would strongly, strongly urge you to join the > Yahoo LS group, which > also includes women > (and some men) who are dealing with LP. Clob is not > the only medication > used. As Melinda > mentioned, estradiol has been used very successfully > by many women to > prevent/undo/ repair > fusion. And there are other meds, steroidal and > otherwise, that are > used to quell the inflammatory response and allow > the body to heal > itself. > > It's a very active and supportive group that could, > i feel, really help > you right now as you're > faced with all this uncertainty. In September i was > just where you were > now -- freaking out > over seeing my inner labia starting to fuse and not > knowing if i could > get back to a vuvlar specialist ( Kellogg-Spadt > in Philly) in time > to save it from totally disappearing on me -- > not to mention being so scared that my clitoris and > vagina would be > next. I was fortunate: > the fusion has, at least for now, stopped, i've had > some re-emergence of > one of my labia, > and my general vulvar skin condition has improved so > much that > said she wouldn't want to do a biopsy now even if i > was open to it > (which i wasn't). The information and support i > got from the group was > invaluable and i really think you could really > benefit from it. The > link is: > > > http://health.groups.yahoo. com/group/ > LichenSclerosis/ > > Hollis > > > > > > , > > > > If you really think you have LS you can also join > the Yahoo LS group. > They > were extremely helpful to me when I was first > diagnosed. > > > > nne > > > > > > > > From: VulvarDisorders@ yahoogroups. com > <mailto: VulvarDisorders@ yahoogroups. com> > [mailto:VulvarDisor ders@yahoogroups .com] > <mailto:[mailto: VulvarDisorders@ yahoogroups. com]> > On Behalf Of euc1109 > s > Sent: Wednesday, February 20, 2008 10:57 PM > To: VulvarDisorders@ yahoogroups. com > <mailto: VulvarDisorders@ yahoogroups. com> > Subject: Re: question on Lichen Planus > > > > Mindy, > > What do you mean by white streaks that wipe away??? > I > know it's probably not very easy to explain but I > don't really know what you mean. > > > > ____________ _________ _________ _________ _________ > _________ _ > Be a better friend, newshound, and > know-it-all with Yahoo! Mobile. Try it now. > http://mobile.yahoo.com/ ;_ylt=Ahu06i62sR > 8HDtDypao8Wcj9tA cJ > < http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ> > > > > ____________ _________ _________ _____ > > Be a better friend, newshound, and know-it-all with > Yahoo! Mobile. Try > it now. > < http://us.rd. yahoo.com/ evt=51733/ *http://mobile. yahoo.com/ ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ> > === message truncated === ____________ _________ _________ _________ _________ _________ _ Looking for last minute shopping deals? Find them fast with Yahoo! Search. http://tools. search.yahoo. com/newsearch/ category. php?category= shopping Quote Link to comment Share on other sites More sharing options...
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