Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 hey kim.you will come threw this because you are strong.everything seems crazy right now but eventually it will get better..I dont know if your disease will slow down,i know its awful im in the same boat.but no matter how bad we get,we have to keep the faith,and hope.hope can get us threw very far.and sometimes its the only thing we can hold on to,but I have learned threw my struggles and sickness that my hope and faith,and love for my family is keepn me hangn on.so most days suck,but I still have my love for my family and all of you..some days I think its the only thing keepn me here.not cuz im sorry for myself but because im so sick and dont have a clue were ill be in a week or a day.pray pray pray kim.ill tell u 1 thing im the closest ive ever been to god,and hes holdn mine and my familys hand walking us threw this dredful mess.you are in my thoughts and prayers and remember there is always a light at the end,sometimes we just have to search for it...keep us posted.hugs,cassy [klatour1@...] wrote: I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle. None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act makes me feel exhausted, i get zappy feelings through out my whole body and my legs feel like they are full of lead. I think my head is full of lead too...can't remember peoples names (that I should know) and feel like I am in a fog. It is difficult to hold a conversation and pay attention through out it. I'm sorry for whining, I know many of you have been there on and off for years. Please just reassure me that I will come through this. Kim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 Cassy- You will get through this. It's very tough right now. Especially if you are of an independent nature. When you're used to doing everything, it's hard to have to sit back and watch others do it for you. But, when you think about it, it makes you feel very humble. You realize that what you're used to having can be gone in a flash. The simple things that we take for granted. The use of our hands, our vision, walking, dressing, bathing, combing our hair, brushing our teeth, Just the act of lifting our fork and putting it in our mouths without poking an eye out. These things we normally do without giving it a thought. When we lose it, that's when we miss it. Remember, you are blessed and you are still a blessing to others. Through God, anything is possible. I'm keeping you in my prayers. You will see the light again. God bless...Val -- Re: Just needing to vent to those who know... hey kim.you will come threw this because you are strong.everything seems crazy right now but eventually it will get better..I dont know if your disease will slow down,i know its awful im in the same boat.but no matter how bad we get,we have to keep the faith,and hope.hope can get us threw very far.and sometimes its the only thing we can hold on to,but I have learned threw my struggles and sickness that my hope and faith,and love for my family is keepn me hangn on.so most days suck,but I still have my love for my family and all of you..some days I think its the only thing keepn me here.not cuz im sorry for myself but because im so sick and dont have a clue were ill be in a week or a day.pray pray pray kim.ill tell u 1 thing im the closest ive ever been to god,and hes holdn mine and my familys hand walking us threw this dredful mess.you are in my thoughts and prayers and remember there is always a light at the end,sometimes we just have to search for it...keep usposted.hugs,cassy[klatour1cogeco (DOT) ca] wrote:I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle.None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act makes me feel exhausted, i get zappy feelings through out my whole body and my legs feel like they are full of lead. I think my head is full of lead too...can't remember peoples names (that I should know) and feel like I am in a fog. It is difficult to hold a conversation and pay attention through out it.I'm sorry for whining, I know many of you have been there on and off for years. Please just reassure me that I will come through this.Kim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 Kim I am so sorry you are going through all of this. I don't have MS but hubby is in the process of getting diagnosed with MS or possibly Lupus. We go to the neuro on Mon. I have been through breast cancer and the best thing I can tell you is try to take it day by day or even hour by hour. Not knowing is the absolute WORST. You will be in my prayers. Hugs nne Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.htmlBreastCancerStories.comhttp://www.breastcancerstories.com/content/view/433/161/Angel Feather Loomerwww.angelfeatherloomer.blogspot.comCheck out my other ornaments atwww.geocities.com/chucky5741/bcornament.htmlLots of info and gifts at:www.cancerclub.com Just needing to vent to those who know... I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle.None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act makes me feel exhausted, i get zappy feelings through out my whole body and my legs feel like they are full of lead. I think my head is full of lead too...can't remember peoples names (that I should know) and feel like I am in a fog. It is difficult to hold a conversation and pay attention through out it.I'm sorry for whining, I know many of you have been there on and off for years. Please just reassure me that I will come through this.Kim No virus found in this incoming message.Checked by AVG Free Edition.Version: 7.1.410 / Virus Database: 268.17.4/643 - Release Date: 1/21/2007 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 thanks val.your such a sweetie.I have found the light.it is everything I have.my family,god,the greatness of the world,all of u! I have lost most functions.but to me as long as im still alive watching my family grow,and enjoying everything life has to offer,then im at peace...thanks for the lovely words,you are a blessing...hope your well today val...,hugs,cassy [tgrl@...] wrote: Cassy- You will get through this. It's very tough right now. Especially if you are of an independent nature. When you're used to doing everything, it's hard to have to sit back and watch others do it for you. But, when you think about it, it makes you feel very humble. You realize that what you're used to having can be gone in a flash. The simple things that we take for granted. The use of our hands, our vision, walking, dressing, bathing, combing our hair, brushing our teeth, Just the act of lifting our fork and putting it in our mouths without poking an eye out. These things we normally do without giving it a thought. When we lose it, that's when we miss it. Remember, you are blessed and you are still a blessing to others. Through God, anything is possible. I'm keeping you in my prayers. You will see the light again. God bless...Val -- Re: Just needing to vent to those who know... hey kim.you will come threw this because you are strong.everything seems crazy right now but eventually it will get better..I dont know if your disease will slow down,i know its awful im in the same boat.but no matter how bad we get,we have to keep the faith,and hope.hope can get us threw very far.and sometimes its the only thing we can hold on to,but I have learned threw my struggles and sickness that my hope and faith,and love for my family is keepn me hangn on.so most days suck,but I still have my love for my family and all of you..some days I think its the only thing keepn me here not cuz im sorry for myself but because im so sick and dont have a clue were ill be in a week or a day.pray pray pray kim.ill tell u 1 thing im the closest ive ever been to god,and hes holdn mine and my familys hand walking us threw this dredful mess.you are in my thoughts and prayers and remember there is always a light at the end,sometimes we just have to search for it.. keep us posted.hugs,cassy [klatour1@...] wrote: I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle. None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 {{{Cassy}}} <wink, wink> Just got a call from the daughter who just had her baby. She said the baby is in NICU. Even though he was born healthy, he was still born too soon, so they have him hooked up to a machine. His lungs aren't fully developed. He was supposed to be born, March 3rd. He was born last night at 7:51 PM. His name in Landen . She said it may be awhile before he is allowed to go home. Just wanted to tell you about it. I'm not very EXCITED...(Yeah, right.) GBU....Valene -- Re: Just needing to vent to those who know... thanks val.your such a sweetie.I have found the light.it is everything I have.my family,god,the greatness of the world,all of u! I have lost most functions.but to me as long as im still alive watching my family grow,and enjoying everything life has to offer,then im at peace...thanks for the lovely words,you are a blessing...hope your well today val...,hugs,cassy[tgrlearthlink (DOT) net] wrote:Cassy-You will get through this. It's very tough right now. Especially if you areof an independent nature. When you're used to doing everything, it's hard tohave to sit back and watch others do it for you. But, when you think aboutit, it makes you feel very humble. You realize that what you're used tohaving can be gone in a flash. The simple things that we take for granted.The use of our hands, our vision, walking, dressing, bathing, combing ourhair, brushing our teeth, Just the act of lifting our fork and putting it inour mouths without poking an eye out. These things we normally do withoutgiving it a thought. When we lose it, that's when we miss it.Remember, you are blessed and you are still a blessing to others. ThroughGod, anything is possible. I'm keeping you in my prayers. You will see thelight again.God bless...Val -------Original Message-------From: cassandra workmnDate: 01/22/2007 10:55:37 AMTo: MSersLife Subject: Re: Just needing to vent to those who know...hey kim.you will come threw this because you are strong.everything seemscrazy right now but eventually it will get better..I dont know if yourdisease will slow down,i know its awful im in the same boat.but no matterhow bad we get,we have to keep the faith,and hope.hope can get us threw veryfar.and sometimes its the only thing we can hold on to,but I have learnedthrew my struggles and sickness that my hope and faith,and love for myfamily is keepn me hangn on.so most days suck,but I still have my love formy family and all of you..some days I think its the only thing keepn me herenot cuz im sorry for myself but because im so sick and dont have a clue wereill be in a week or a day.pray pray pray kim.ill tell u 1 thing im theclosest ive ever been to god,and hes holdn mine and my familys hand walkingus threw this dredful mess.you are in my thoughts and prayers and rememberthere is always a light at the end,sometimes we just have to search for it..keep usposted.hugs,cassy[klatour1cogeco (DOT) ca] wrote:I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle.None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act.... Font Lucida Handwriting Art by Engelbreit Tube by Tut Ripples In Time Email Me April, 2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 Are you keeping a journal of your symptoms? Not all doctors will look at it but some will. If the doc won't look at a journal then also have a list of your worst symptoms in order of severity. Most will look at that. I'm so sorry to hear you are having such a bad time. Where do you live again? I can't remember. Have you registered with your local chapter of the National MS Society? If not, please do that. They will send an info packet out to the newly diagnosed. They can also tell you about local MS support groups or programs that they run. What day is your appointment?Sharon Just needing to vent to those who know... I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle. None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act makes me feel exhausted, i get zappy feelings through out my whole body and my legs feel like they are full of lead. I think my head is full of lead too...can't remember peoples names (that I should know) and feel like I am in a fog. It is difficult to hold a conversation and pay attention through out it. I'm sorry for whining, I know many of you have been there on and off for years. Please just reassure me that I will come through this. Kim Get amazing travel prices for air and hotel in one click on Yahoo! FareChase Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 ahh how cute..and what a cute name!im sure he will be fine.my neice was just recenly born 3 mons premature.and it was a rocky road,but now shes almost 3 lbs. And had numerous problems.but that was at 3 mons preemie.and she wasnt even 2 pds.wow your little 1 is 6 lbs. And was 6 wks. Preemie...thats a good size...congrats again...will you be able to see him soon?hugs, cassy [tgrl@...] wrote: {{{Cassy}}} <wink, wink> Just got a call from the daughter who just had her baby. She said the baby is in NICU. Even though he was born healthy, he was still born too soon, so they have him hooked up to a machine. His lungs aren't fully developed. He was supposed to be born, March 3rd. He was born last night at 7:51 PM. His name in Landen . She said it may be awhile before he is allowed to go home. Just wanted to tell you about it. I'm not very EXCITED...(Yeah, right.) GBU....Valene -- Re: Just needing to vent to those who know... hey kim.you will come threw this because you are strong.everything seems crazy right now but eventually it will get better..I dont know if your disease will slow down,i know its awful im in the same boat.but no matter how bad we get,we have to keep the faith,and hope.hope can get us threw very far.and sometimes its the only thing we can hold on to,but I have learned threw my struggles and sickness that my hope and faith,and love for my family is keepn me hangn on.so most days suck,but I still have my love for my family and all of you..some days I think its the only thing keepn me here not cuz im sorry for myself but because im so sick and dont have a clue were ill be in a week or a day.pray pray pray kim.ill tell u 1 thing im the closest ive ever been to god,and hes holdn mine and my familys hand walking us threw this.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2007 Report Share Posted January 22, 2007 Well Cassy, Grandma was having a senior moment. I got all my information mixed up. Pooh! My grandson's name is actually , not Landen . That's the name she was going to name him, but her in-laws talked her out of it, because of Landon.(Go figure) They say he may have to stay in the hospital for at least 3 weeks. I'm hoping no longer than that. I'd like to see him come home sooner. They are going to monitor him. They told my daughter that if he didn't improve within that time, he could have to stay there until his expected due date. That is March 13. Man, I had it all mixed up. Don't ever give me any instructions to give to someone else, unless it's in writing....My memory is only this____long. Oh, by the way...I'm really good at keeping secrets!!! As you can imagine. Thanks again for the congrats. I'm passing them on to Mommy and Daddy. God bless....Valene -- Re: Just needing to vent to those who know... ahh how cute..and what a cute name!im sure he will be fine.my neice was just recenly born 3 mons premature.and it was a rocky road,but now shes almost 3 lbs. And had numerous problems.but that was at 3 mons preemie.and she wasnt even 2 pds.wow your little 1 is 6 lbs. And was 6 wks. Preemie...thats a good size...congrats again...will you be able to see him soon?hugs, cassy[tgrlearthlink (DOT) net] wrote:{{{Cassy}}}<wink, wink>Just got a call from the daughter who just had her baby. She said the babyis in NICU. Even though he was born healthy, he was still born too soon, sothey have him hooked up to a machine. His lungs aren't fully developed. Hewas supposed to be born, March 3rd. He was born last night at 7:51 PM. Hisname in Landen . She said it may be awhile before he is allowed to gohome.Just wanted to tell you about it. I'm not very EXCITED...(Yeah, right.) GBU....Valene -------Original Message-------From: cassandra workmnDate: 01/22/2007 12:50:02 PMTo: MSersLife Subject: Re: Just needing to vent to those who know...thanks val.your such a sweetie.I have found the light.it is everything Ihave.my family,god,the greatness of the world,all of u! I have lost mostfunctions.but to me as long as im still alive watching my family grow,andenjoying everything life has to offer,then im at peace...thanks for thelovely words,you are a blessing...hope your well today val...,hugs,cassy[tgrlearthlink (DOT) net] wrote:Cassy-You will get through this. It's very tough right now. Especially if you areof an independent nature. When you're used to doing everything, it's hard tohave to sit back and watch others do it for you. But, when you think aboutit, it makes you feel very humble. You realize that what you're used tohaving can be gone in a flash. The simple things that we take for granted.The use of our hands, our vision, walking, dressing, bathing, combing ourhair, brushing our teeth, Just the act of lifting our fork and putting it inour mouths without poking an eye out. These things we normally do withoutgiving it a thought. When we lose it, that's when we miss it.Remember, you are blessed and you are still a blessing to others. ThroughGod, anything is possible. I'm keeping you in my prayers. You will see thelight again.God bless...Val -------Original Message-------From: cassandra workmnDate: 01/22/2007 10:55:37 AMTo: MSersLife Subject: Re: Just needing to vent to those who know...hey kim.you will come threw this because you are strong.everything seemscrazy right now but eventually it will get better..I dont know if yourdisease will slow down,i know its awful im in the same boat.but no matterhow bad we get,we have to keep the faith,and hope.hope can get us threw veryfar.and sometimes its the only thing we can hold on to,but I have learnedthrew my struggles and sickness that my hope and faith,and love for myfamily is keepn me hangn on.so most days suck,but I still have my love formy family and all of you..some days I think its the only thing keepn me herenot cuz im sorry for myself but because im so sick and dont have a clue wereill be in a week or a day.pray pray pray kim.ill tell u 1 thing im theclosest ive ever been to god,and hes holdn mine and my familys hand walkingus threw this.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2007 Report Share Posted January 23, 2007 {{{{Kim}}}}} Once you get treatment hopefully some of your symptoms will go away. I can't believe they haven't given you neurontin or something like that for eht feelings in teh legs and such. Keep on the docs. x0x0x0 ShirleyKim Latour wrote: I am feeling a little down today. It feels like YEARS (although I know its been more like weeks...9 to be exact) since I have been my capable self. I am relying on others for most things...including care of my children to a certain extent, my house work, laundry, shopping etc and I HATE it. I worry about burning them out...and ending up alone in this terrible struggle.None of the doctors in this area know anything about tumefactive MS, they are totallly freaked out and will not even conduct an assessment. I have an appointment at a MS clinic at the end of the week..but it seems so long away. I am struggling with many symptoms, and I am scared. I don't know weather to hope for treatment or not..they all have such potentially scary side effects! I am worried about when I will be able to return to work...if I will. I can not feel my hands or feet, my balance is awful, EVERY act makes me feel exhausted, i get zappy feelings through out my whole body and my legs feel like they are full of lead. I think my head is full of lead too...can't remember peoples names (that I should know) and feel like I am in a fog. It is difficult to hold a conversation and pay attention through out it.I'm sorry for whining, I know many of you have been there on and off for years. Please just reassure me that I will come through this.Kim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2007 Report Share Posted January 23, 2007 I just want to thank everyone who responded to my post. I am feeling better...I find that giving in to the desire to sleep is very helpful in maintaining a stable mood. However, it is discouraging to sleep sooo much. My appointment is this Friday at the MS clinic. I will go with a healthy serving of hope, journal in hand with your support in mind. Kim > > Sharon.....What a great idea to have a journal....Even if is just a squared off calender type.That may even be best as the Dr can see at a glance your activity. > > > Just needing to vent to those who know... > > > I am feeling a little down today. It feels like YEARS (although I > know its been more like weeks...9 to be exact) since I have been my > capable self. I am relying on others for most things...including > care of my children to a certain extent, my house work, laundry, > shopping etc and I HATE it. I worry about burning them out...and > ending up alone in this terrible struggle. > > None of the doctors in this area know anything about tumefactive MS, > they are totallly freaked out and will not even conduct an > assessment. I have an appointment at a MS clinic at the end of the > week..but it seems so long away. I am struggling with many > symptoms, and I am scared. I don't know weather to hope for > treatment or not..they all have such potentially scary side > effects! I am worried about when I will be able to return to > work...if I will. > > I can not feel my hands or feet, my balance is awful, EVERY act > makes me feel exhausted, i get zappy feelings through out my whole > body and my legs feel like they are full of lead. I think my head > is full of lead too...can't remember peoples names (that I should > know) and feel like I am in a fog. It is difficult to hold a > conversation and pay attention through out it. > > I'm sorry for whining, I know many of you have been there on and off > for years. Please just reassure me that I will come through this. > > Kim > > > > > > > > Get amazing travel prices for air and hotel in one click on Yahoo! FareChase > > > > > _____________________________________________________________________ _______________ > Finding fabulous fares is fun. > Let Yahoo! FareChase search your favorite travel sites to find flight and hotel bargains. > http://farechase.yahoo.com/promo-generic-14795097 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2007 Report Share Posted January 24, 2007 Kim you will be in my prayers for your appointment. Hugs nne Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.htmlBreastCancerStories.comhttp://www.breastcancerstories.com/content/view/433/161/Angel Feather Loomerwww.angelfeatherloomer.blogspot.comCheck out my other ornaments atwww.geocities.com/chucky5741/bcornament.htmlLots of info and gifts at:www.cancerclub.com Just needing to vent to those who know...> > > I am feeling a little down today. It feels like YEARS (although I > know its been more like weeks...9 to be exact) since I have been my > capable self. I am relying on others for most things...including > care of my children to a certain extent, my house work, laundry, > shopping etc and I HATE it. I worry about burning them out...and > ending up alone in this terrible struggle.> > None of the doctors in this area know anything about tumefactive MS, > they are totallly freaked out and will not even conduct an > assessment. I have an appointment at a MS clinic at the end of the > week..but it seems so long away. I am struggling with many > symptoms, and I am scared. I don't know weather to hope for > treatment or not..they all have such potentially scary side > effects! I am worried about when I will be able to return to > work...if I will. > > I can not feel my hands or feet, my balance is awful, EVERY act > makes me feel exhausted, i get zappy feelings through out my whole > body and my legs feel like they are full of lead. I think my head > is full of lead too...can't remember peoples names (that I should > know) and feel like I am in a fog. It is difficult to hold a > conversation and pay attention through out it.> > I'm sorry for whining, I know many of you have been there on and off > for years. Please just reassure me that I will come through this.> > Kim> > > > > > > > Get amazing travel prices for air and hotel in one click on Yahoo! FareChase > > > > > _________________________________________________________________________> Finding fabulous fares is fun. > Let Yahoo! FareChase search your favorite travel sites to find flight and hotel bargains.> http://farechase.yahoo.com/promo-generic-14795097> No virus found in this incoming message.Checked by AVG Free Edition.Version: 7.1.410 / Virus Database: 268.17.6/646 - Release Date: 1/23/2007 Quote Link to comment Share on other sites More sharing options...
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