Guest guest Posted August 20, 2002 Report Share Posted August 20, 2002 Our experience with Infectious disease doc's is they take the CDC approach that it's not lyme, it's old age, or someother ridiculous dodge. Expect an ache or pain every now or then go home, take aspirin, die, who cares, just leave me alone. If it is lyme, well then, 28 days of abx will do the trick. If it doesn't you never had lyme. Hopefully there are some good ones out there, like the one you're seeing. The ones out here in So. central PA are awful. I had one refuse to treat me even though I was symptomatic as heck. Having had symptoms for a few weeks prior to the dx is probably enough for the doc to treat you til you feel better. 28 days won't likely be enough. I wouldn't worry too much. It;s not like you had it for years. You might look into alternatives too to take starting now and continuing past the cut off date of the abx. Don't test the kids unless they develop symptoms. Even if they were bitten, remember not all ticks carry disaese. If they develop a rash and symtoms a LLMD won't bother with testing. He/she will dx clinically. Dave [ ] Thank you! Thank you everyone for your kind responses. I have to be honest - I'm scared to death now. I was feeling pretty hopeful but now - WOW. I printed your posts to give to my doctor so I know what questions to ask and what information I need. I'll try and find out if the infectious disease guy that I'm seeing in September is an " LLMD " . I have another question. I take my kids everywhere I go and chances are wherever I was when I was bit by the tick my kids were standing next to me. Should I have them tested also? Thanks again for all the information. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2003 Report Share Posted March 21, 2003 Just wanted to thank everyone for all the kind words you sent me. It really made me feel good. Thank you for that. Also, thanks for the decorating tips. I'll let you know what we come up with Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2003 Report Share Posted April 9, 2003 You are welcome for the replies. Most of our plagio cases are caused by sleep position....check out this link for causes of plagio: http://www.plagiocephaly.org/support/causes.htm And about none of us in the group had ever heard of " plagio " or flat heads until after our child had developed it. You'll be in great hands with the DOCband. Cranial Technologies (maker of the DOCband) are terrific and experts in treating plagio!! Check out their webpage for more great plagio info: http://www.cranialtech.com/ Debbie Abby's mom DOCGrad MI > Thanks to everyone who replied to my post. Baby Mo (Moira) will be > in a DOC band, I believe. That's the booklet they gave me. I've > never heard of any of this stuff, and I was in medical insurance for > years! Thankfully, at this time, we have Moira on Medicaid, and > they cover this. I've been reading that it can get rather > expensive! Since I have a 2 1/2 year old and a 4 1/2 month old, I > don't have a lot of time to sit and read, but I'll be looking > through here and getting as much info as I can when I get the chance. > > Does anyone ever tell you what they believe may have caused your > child's specific problem? I think it's one of two things with > Moira. She sleeps with us, use to sleep mostly with her head on my > arm on her right side. I can't imagine that would make her plates > overlap on the left side, though. The other thing that I wonder > about is that the Dr. who delivered her used the vacuum to get her > out, because she was sort of wedged sideways in the birth canal. > It's sounding like this may have been the culprit. Either the > vacuum, or her being wedged, or perhaps both. My older daughter > came out with the vacuum, as well, because she had turned facing the > side, not that she was wedged sideways (if that makes sense), and > she hasn't had any problem. With Moira, I was going to a midwife, > and then at the end of the pregnancy, she was transverse, plus I had > a low placenta, so the midwife and I both decided it would be best > if I went to an OB, in case I needed a C-section. She did get into > the correct position, and I was able to deliver her vaginally in the > end, but it wasn't a very good experience. She and I have both had > problems since, and I wonder how gentle the Dr. was with that > vacuum. We didn't even realize she'd used it until we had watched > the birth video, that my husband took, about 7 times, then I noticed > her, at one time, say " vacuum " , and realized what she was doing. > Didn't bother me, because, like I said, my first had it used on her > with no problem. But, this was a different state, different Dr., > different hospital, and I just wonder.... > > Any ideas? > > Caro (rowwith)...mom of Baby Mo (Moira) in Texas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2003 Report Share Posted April 9, 2003 I guess it's quite possible this was caused by her sleep position. Maybe I just don't want to think of it as being my fault, but maybe it was. My first daughter slept mostly in her bassinet and crib for the first 6 months, before she ended up in our bed (a long story). Moira has been in bed with us since night one, and I started sleeping with her on my arm because we were in a full sized bed, with my 2 1/2 year old there, as well, because I didn't want to roll over on her and I didn't want my 2 1/2 year old rolling over on her. Now we have a king sized bed, much more room, and she sleeps more just on the bed. She did have a large lump on her head, due to the vacuum I presume, for several weeks after she was born (my first daughter's vacuum lump was smaller and went away faster). Then once it went down, we noticed that the right side of her head was still bigger or higher up than her left side, and the back of her head is kind of smushed on the right side (that does look like how she sleeps, I suppose). Her pediatrician said that it wasn't that the right side was bigger or higher than the left side, it was the that the left side was depressed, which lead her to believe it was the cranio thing. Btw, her dad chose the nickname " Lumpy " for her because of her vacuum lump! LOL! Anyway, who knows. What's strange is that normally, I'd be stressing out about this terribly! Strangely, I'm very peaceful about it, and have no doubt that this will take care of her problem with no trouble. We've been praying about this for the past few weeks, since her pediatrician first said what it might be, and we've had lots of people praying for her, so I believe that's where my peace is coming from. Thanks again for everyone's welcome! I look forward to getting to know you all better! Caro (rowwith)...Baby Mo's mom > You are welcome for the replies. > Most of our plagio cases are caused by sleep position....check out > this link for causes of plagio: > http://www.plagiocephaly.org/support/causes.htm > And about none of us in the group had ever heard of " plagio " or flat > heads until after our child had developed it. > You'll be in great hands with the DOCband. Cranial Technologies (maker > of the DOCband) are terrific and experts in treating plagio!! Check > out their webpage for more great plagio info: > http://www.cranialtech.com/ > > Debbie Abby's mom DOCGrad > MI > > --- In Plagiocephaly , " rowwith " <rowwith@y...> wrote: > > Thanks to everyone who replied to my post. Baby Mo (Moira) will be > > in a DOC band, I believe. That's the booklet they gave me. I've > > never heard of any of this stuff, and I was in medical insurance for > > years! Thankfully, at this time, we have Moira on Medicaid, and > > they cover this. I've been reading that it can get rather > > expensive! Since I have a 2 1/2 year old and a 4 1/2 month old, I > > don't have a lot of time to sit and read, but I'll be looking > > through here and getting as much info as I can when I get the chance. > > > > Does anyone ever tell you what they believe may have caused your > > child's specific problem? I think it's one of two things with > > Moira. She sleeps with us, use to sleep mostly with her head on my > > arm on her right side. I can't imagine that would make her plates > > overlap on the left side, though. The other thing that I wonder > > about is that the Dr. who delivered her used the vacuum to get her > > out, because she was sort of wedged sideways in the birth canal. > > It's sounding like this may have been the culprit. Either the > > vacuum, or her being wedged, or perhaps both. My older daughter > > came out with the vacuum, as well, because she had turned facing the > > side, not that she was wedged sideways (if that makes sense), and > > she hasn't had any problem. With Moira, I was going to a midwife, > > and then at the end of the pregnancy, she was transverse, plus I had > > a low placenta, so the midwife and I both decided it would be best > > if I went to an OB, in case I needed a C-section. She did get into > > the correct position, and I was able to deliver her vaginally in the > > end, but it wasn't a very good experience. She and I have both had > > problems since, and I wonder how gentle the Dr. was with that > > vacuum. We didn't even realize she'd used it until we had watched > > the birth video, that my husband took, about 7 times, then I noticed > > her, at one time, say " vacuum " , and realized what she was doing. > > Didn't bother me, because, like I said, my first had it used on her > > with no problem. But, this was a different state, different Dr., > > different hospital, and I just wonder.... > > > > Any ideas? > > > > Caro (rowwith)...mom of Baby Mo (Moira) in Texas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2003 Report Share Posted April 9, 2003 > I guess it's quite possible this was caused by her sleep position. > Maybe I just don't want to think of it as being my fault, but maybe > it was. Oh Caro! Heavens NO NO! It's most definitley not your fault any more than the other tens of thousands of babies with plagio!!! So don't say that, please. My daughter's plagio began inutero, we noticed it on weekly ultrasounds that her head was stuck in the same position, however, we never worried about a flat head (worried she'd NEVER come out of me, BUT! hehe). It only worsened after birth because of her sleep position. Some babies get it, some don't - just like crooked teeth, some get em, some don't. Absolutely nothign you could do - especially w/o knowing of it! Can't prevent something you don't know exists, right?! But I'm so happy to read how at peace you are with this and getting her a band. She should have a rounder head in no time! I forgot to mention, Cranial Technology's average treatment time in their band is 4.5 mos., some babies are longer, some less, based on age, severity & growth spurts. Hard to estimate...but as I mentioned earlier, given Mo's young age, she'll be hitting many growth spurts over the next several mos which will round that pretty little head out nicely! It's also nice to hear how proactive your pediatrician has been with getting Mo Xrayed and referring her for a band. Many group members struggle to get their ped. to listen to their concerns. Please keep us posted Debbie Abby's mom DOCGrad MI Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2003 Report Share Posted April 9, 2003 Well, you will be in the best possible hands with the DOCband people - they really know what they are doing! There are SO many theories as to why plagio develops, but mostly it seems to happen from inuterio constraint or sleep position. Who knows who will get it - it's just impossible to say at this point. Definitely not your fault - that much is for sure! So keep us posted. At 4 1/2 months Moira (LOVE the name) should get some great correction with the DOCband! Marci (Mom to ) Oklahoma > Thanks to everyone who replied to my post. Baby Mo (Moira) will be > in a DOC band, I believe. That's the booklet they gave me. I've > never heard of any of this stuff, and I was in medical insurance for > years! Thankfully, at this time, we have Moira on Medicaid, and > they cover this. I've been reading that it can get rather > expensive! Since I have a 2 1/2 year old and a 4 1/2 month old, I > don't have a lot of time to sit and read, but I'll be looking > through here and getting as much info as I can when I get the chance. > > Does anyone ever tell you what they believe may have caused your > child's specific problem? I think it's one of two things with > Moira. She sleeps with us, use to sleep mostly with her head on my > arm on her right side. I can't imagine that would make her plates > overlap on the left side, though. The other thing that I wonder > about is that the Dr. who delivered her used the vacuum to get her > out, because she was sort of wedged sideways in the birth canal. > It's sounding like this may have been the culprit. Either the > vacuum, or her being wedged, or perhaps both. My older daughter > came out with the vacuum, as well, because she had turned facing the > side, not that she was wedged sideways (if that makes sense), and > she hasn't had any problem. With Moira, I was going to a midwife, > and then at the end of the pregnancy, she was transverse, plus I had > a low placenta, so the midwife and I both decided it would be best > if I went to an OB, in case I needed a C-section. She did get into > the correct position, and I was able to deliver her vaginally in the > end, but it wasn't a very good experience. She and I have both had > problems since, and I wonder how gentle the Dr. was with that > vacuum. We didn't even realize she'd used it until we had watched > the birth video, that my husband took, about 7 times, then I noticed > her, at one time, say " vacuum " , and realized what she was doing. > Didn't bother me, because, like I said, my first had it used on her > with no problem. But, this was a different state, different Dr., > different hospital, and I just wonder.... > > Any ideas? > > Caro (rowwith)...mom of Baby Mo (Moira) in Texas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2003 Report Share Posted July 5, 2003 well done bert, you and your family will always be in my prayers as will the rest of the group love and hugs to all anita> > From: " Bertha " <sunshinedotson@...> > Date: Fri 04/Jul/2003 17:47 GMT > > Subject: [ ] Thank you! > > > Hello everyone, > > I would like to thank all of you for your kind words, encouragement > and prayers for my children. I am hanging in there and praying a lot > too. I accepted everyone's advice and will use it to help me and my > family get through this rough road. I know if I don't take care of > me, I am no good to anyone, especially my children. So again, I > thank you all! Best wishes and LOTS of LOVE to all of you! > > HUGS... > Bert. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 24, 2003 Report Share Posted August 24, 2003 See the attached file for details Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2003 Report Share Posted August 26, 2003 See the attached file for details Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2003 Report Share Posted August 27, 2003 Julea ) The first step towards success is taken when you refuse to be a captive of the environment in which you first found yourself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2003 Report Share Posted August 27, 2003 Best of luck, Sue. Hope it all goes well for you all. Julea ) The first step towards success is taken when you refuse to be a captive of the environment in which you first found yourself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2003 Report Share Posted September 4, 2003 See the attached file for details Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2003 Report Share Posted September 4, 2003 How weird, I have no idea why this blank post " came from me " ... I think I sent someone some ES bath info. If I figure out why it's here, I won't do it again! W > See the attached file for details > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2003 Report Share Posted September 4, 2003 , it is very likely that you have a virus on your computer which sent the letter without your participation. We had not access to Internet for a day and when we called the provider they told us that the server was flooded by letters because some new virus gets into your computer through some port just while you are browsing the Internet, configures mail server on your computer and starts sending a lot of letters. Microsoft made some update of the Windows 2000 system to prevent this, but I do not know if there is antivirus software that fixes it. Margaret > > See the attached file for details > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 5, 2003 Report Share Posted September 5, 2003 , It's the virus going around... [ ] Re: Thank you! How weird, I have no idea why this blank post " came from me " ... I think I sent someone some ES bath info. If I figure out why it's here, I won't do it again! W > See the attached file for details > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 5, 2003 Report Share Posted September 5, 2003 > How weird, I have no idea why this blank post " came from me " ... I > think I sent someone some ES bath info. If I figure out why it's > here, I won't do it again! > W This is the subject header of many of the virus emails I have been receiving, and even some I have been " sending " , altho it is not me sending them, it is a spam-bot that found my email address on my site and sent emails to people purportedly " from me " . Example subjects: Re: your details Re: your application Re: approved! Re: wicked screensaver I receive 1-3 of these emails every minute, which is why I had to create a new email address. Fortunately I have no addresses in my address book, and I don't send/receive email to the [i read web-only], and I have not seen a " spam email from me " show up on any of my regular message boards, altho sometimes they show up on a board I rarely use. I sure hope this problem is fixed soon! Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 5, 2003 Report Share Posted September 5, 2003 Please see the attached file for details. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2003 Report Share Posted October 31, 2003 Hi Trish, I just checked out the pics of Carson, he is a doll. I love the hiney picture. Thanks for sharing. In order for repositioning to work it must be done 24/7. Will Carson sleep on his side? > Wow! Thanks to all you great ladies for all your wonderful and > informative replies! I spent most of my day yesterday wandering > around the net educating myself as much as possible. > I'm pretty sure that Carson does not have torticollis (sp?) He was > resisting turning his head to the left for a little while, but from > moving him around in his crib and change table he now has full > motion (or so I can tell) Also, it looks to me as if he my not have > true plagiocephaly since his head is moslty flat all the way across. > The right side is only slightly flatter (from those few months of > not realy turning is haed to the left I guess) So, the term that I > found to describe him is brachycephaly. I'm definitly no doctor, so > we'll see what the ped. says I guess. There is no way I can get to > see one before December either. > I'm trying not to put him on his back at all right now (except to > sleep), but it is so hard since he LOVES to lay under his toys and > kick and swat at them! Well, I guess for now that will be my plan of > action. I have posted a couple of pictures of him in a new folder > called Carson H. and am waiting for my batteries to re-charg in my > camera so I can take a few more! lol > > Thanks again, > Trish > Barrie, Onatrio > Ben - 2 1/2 > Carson - 5 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2003 Report Share Posted October 31, 2003 Trish, Carson's head looks like a classic case of Brachy to me. He is such a cutie!!! Thanks for sharing and let us know how things are going with you. Dustie > Wow! Thanks to all you great ladies for all your wonderful and > informative replies! I spent most of my day yesterday wandering > around the net educating myself as much as possible. > I'm pretty sure that Carson does not have torticollis (sp?) He was > resisting turning his head to the left for a little while, but from > moving him around in his crib and change table he now has full > motion (or so I can tell) Also, it looks to me as if he my not have > true plagiocephaly since his head is moslty flat all the way across. > The right side is only slightly flatter (from those few months of > not realy turning is haed to the left I guess) So, the term that I > found to describe him is brachycephaly. I'm definitly no doctor, so > we'll see what the ped. says I guess. There is no way I can get to > see one before December either. > I'm trying not to put him on his back at all right now (except to > sleep), but it is so hard since he LOVES to lay under his toys and > kick and swat at them! Well, I guess for now that will be my plan of > action. I have posted a couple of pictures of him in a new folder > called Carson H. and am waiting for my batteries to re-charg in my > camera so I can take a few more! lol > > Thanks again, > Trish > Barrie, Onatrio > Ben - 2 1/2 > Carson - 5 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2003 Report Share Posted October 31, 2003 Hi Trish - Carson is a doll! I am glad that you educated yourself on this that is exactly what I did when I found out about it too. I learned so much more on the net than I did from any DR. My sone also had slight flatening on the right side but the whole back was pretty flat as well and we are seeing great correction. Good Luck! Donna and Xavier DOCband 7/25 and 10/8 > Wow! Thanks to all you great ladies for all your wonderful and > informative replies! I spent most of my day yesterday wandering > around the net educating myself as much as possible. > I'm pretty sure that Carson does not have torticollis (sp?) He was > resisting turning his head to the left for a little while, but from > moving him around in his crib and change table he now has full > motion (or so I can tell) Also, it looks to me as if he my not have > true plagiocephaly since his head is moslty flat all the way across. > The right side is only slightly flatter (from those few months of > not realy turning is haed to the left I guess) So, the term that I > found to describe him is brachycephaly. I'm definitly no doctor, so > we'll see what the ped. says I guess. There is no way I can get to > see one before December either. > I'm trying not to put him on his back at all right now (except to > sleep), but it is so hard since he LOVES to lay under his toys and > kick and swat at them! Well, I guess for now that will be my plan of > action. I have posted a couple of pictures of him in a new folder > called Carson H. and am waiting for my batteries to re-charg in my > camera so I can take a few more! lol > > Thanks again, > Trish > Barrie, Onatrio > Ben - 2 1/2 > Carson - 5 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2003 Report Share Posted October 31, 2003 Trish, I have a 6 month old daughter, Jordyn, who has brachy. Carson's head looks a lot like hers - flat across the back and higher on top. She also doesn't have tort, so the flatness is pretty much uniform across the back of her head. You can see a picture of the top view in her folder that shows the flatness. I think that I already took out the side view picture. Good luck and let us know how it goes with repo. & Jordyn (DOCband 10/13) Dallas > Wow! Thanks to all you great ladies for all your wonderful and > informative replies! I spent most of my day yesterday wandering > around the net educating myself as much as possible. > I'm pretty sure that Carson does not have torticollis (sp?) He was > resisting turning his head to the left for a little while, but from > moving him around in his crib and change table he now has full > motion (or so I can tell) Also, it looks to me as if he my not have > true plagiocephaly since his head is moslty flat all the way across. > The right side is only slightly flatter (from those few months of > not realy turning is haed to the left I guess) So, the term that I > found to describe him is brachycephaly. I'm definitly no doctor, so > we'll see what the ped. says I guess. There is no way I can get to > see one before December either. > I'm trying not to put him on his back at all right now (except to > sleep), but it is so hard since he LOVES to lay under his toys and > kick and swat at them! Well, I guess for now that will be my plan of > action. I have posted a couple of pictures of him in a new folder > called Carson H. and am waiting for my batteries to re-charg in my > camera so I can take a few more! lol > > Thanks again, > Trish > Barrie, Onatrio > Ben - 2 1/2 > Carson - 5 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2003 Report Share Posted November 12, 2003 <To whoever made the brilliant suggestion of adding cocoa to eggnog, thank you a billion times over. I am trying to wean my kids off cold cereal and they won't drink the fruit smoothies I make. I made an eggnog today with raw goat milk kefir, cream, eggs, maple syrup, vanilla and cocoa powder and it was devoured by both girls! I just told them it was chocolate milk, which, technically, it was. I had some myself and it was so super tasty. Thank you!!> If we don't stop talking about eggnog I am going to have to leave work soon and go home and make my own! _________________________________________________________________ Frustrated with dial-up? Get high-speed for as low as $26.95. https://broadband.msn.com (Prices may vary by service area.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2003 Report Share Posted November 12, 2003 I had some > myself and it was so super tasty. Thank you!!> You're quite welcome Lynn we like it too ;-) DMM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 THANK YOU! You all have raised $1212.00 so far! Thank you! Because of you, we're all that much closer to reaching the $6k mark. Less than 20 hours to go and, along with helping fund some much-needed projects, you have the opportunity to snag some bargain merchandise. T-shirts as low as $3.00, etc. (I can tell you from experience that's a quarter less than the shirts I buy at Goodwill and those have already been worn.) You can click on the 'online store' option at http://www.nationalautismassociation.org/index.php ALL donations will go to these two projects: Projects: NAA Crisis Fund: Sometimes tragedies happen within the ASD Community. A family may lose their home, their employment, etc. The crisis fund will provide families in urgent need with financial support whether it be for emergency shelter or covering medical/funeral expenses should the unthinkable happen. SafeMinds VSD Research Project See below for more details, and once again, thank you... Lori McIlwain National Autism Association Phone: 877-NAA-AUTISM Email: Lori@... http://nationalautismassociation.org/ Don't Miss the 24-hour NAA Fire Sale starting tomorrow morning (Thursday) at 8 am! Prices on autism-themed merchandise will be marked down 50% to 70%. Items include, T-shirts, Awareness Ribbon Lapel Pins, Key Chains, License Plate Frames, Slogan Buttons, Hats, Tote Bags, Syringe Pens and more! Some items will sell for as low as $.50 for 24 hours only! Buy for your kids, your family, or yourself. Imagine the awareness you'll raise in your community while helping to raise funds for research and family programs. ALL proceeds will go to the projects listed below. The National Autism Association is a nonprofit, not-for-salary organization. Prices will be marked back up starting at 8:00 AM January 16th. Please forward this onto family and friends. With everyone's help, we all can get so much accomplished in 2004. Projects: NAA Crisis Fund: Sometimes tragedies happen within the ASD Community. A family may lose their home, their employment, etc. The crisis fund will provide families in urgent need with financial support whether it be for emergency shelter or covering medical/funeral expenses should the unthinkable happen. SafeMinds VSD Research Project Thank you! The NAA Team www.nationalautismassociation.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2004 Report Share Posted July 20, 2004 Randy, I was sorry to see you felt like there was little support here. Guess I shoulda said something earlier. Just lately have been doing more reading and not much posting. Have just had so much going on that my time on line is short. The people here, all of them, are never far from my thoughts. I do keep up with the postings, and always send up a prayer for those having rough times. Glad you got through the MRI - dang shame they did not get the sedative right - I share your " love " of the whole MRI experience. Will be thinking of you tomorrow and hoping for positive results. nne Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.