Guest guest Posted February 23, 2001 Report Share Posted February 23, 2001 Dear Jean: When Kaufman uses her own materials she is adimant about the children completing the card. There were times that my son would get so angry with her he would shut down. When that happens his SL:P should back down a bit, do something else and return to it. I am assuming that after a card or two is attempted by your son there is a toy to play with or a game. that he and the therapist are playing as they work the sounds. Stay in the room for as long aqs you have to. Sandy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2003 Report Share Posted September 22, 2003 No doubt to me -choose door number one -! I highly recommend Kaufman first, and not because she made me an honorary SLP, but because she can start you on an appropriate therapy path which is proven in many of our children to work while you explore what caused the apraxia. Kaufman is a professional advisor to both the nonprofit CHERAB Foundation, as well as Speechville.com and has also spoken for us probono at many events now. Her Kaufman approach is just brilliant. Again however -I recommend using it along with other multisensory therapies (and so does who I've talked to this about) In addition - also offers a video consult which is $100 -obviously not comprehensive -but do-able for most. Even if it ends up that your child's analysis comes out positive to toxins -that only means your child is probably then like most of ours http://www.cherab.org/news/Save.html Your child (even if there is a toxic cause to the condition) will still require appropriate therapy in addition to any alternative treatment. I'm positive there are environmental factors to this. After all in Texas (a pocket area) instead of an article about EFAs in formula -there is one about " Toxic Rocket Fuel Found In Milk Samples From Texas Supermarkets " http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/es034735q and they are looking for people to be tested for toxins in Ohio (so if you live in this pocket area you can do this for free!) " Groups to measure toxins in residents " http://www.mariettatimes.com/news/story/0919202003_new03sytix.asp Perhaps this is why most of our children respond so dramatically to EFAs, in addition to remyelinating properties -EFAs I'm told have strong detox properties as well. (talk to your doctor and try them...they work!) Most of our children respond to this simple dietary change alone, however there are a few who are reported to require more dramatic dietary changes as well as other alternative holistic interventions that you could do (under a respected MD's care) And for who is looking for an inexpensive Kaufman Kit -why not ask here if anyone is wanting to sell theirs. Children move from Kit 1 to Kit 2... I can tell you after spending thousands and thousands of dollars on therapy -the one hundred plus bucks for 's kit is well worth it -and something you can use and home and travel with -and bring with your child to preschool or therapy for them to borrow if they are not prepared. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2003 Report Share Posted September 22, 2003 Mandy: Where are you located? You mention going to the Pfeiffer Clinic, so that leads me to believe you are in the Chicago area? If so, I live in Gurnee, Illinois and I bought the first Kaufman set of cards,,,,we could share them? We hardly use them anymore anyway. Also, I think it is a great idea to get all of those bio-medical testing done, however, not everyone will agree. REgardless, I researched the Pfeiffer Clinic and other doctors and decided on Dr. Hicks who is primarily out of Lake Geneva, Wisconsin, but in on Wednesdays in Grayslake, Il. He and his group are fantastic! Let me know. Kim > Hello again everyone... > > I again have a question...we have a chance to make an appointment to > have our son (3.7yrs./speech apraxia) see Kaufman with > the Kaufman Children's Center for speech in Michigan. If you aren't > familiar with her work...she created the Kaufman Praxia Test and > Kaufman Kits to work with Apraxia. We really are interested and > excited in making an appointment with her. > > I guess my question is this..has anyone seen her weather it be on an > evalution or seminar and can give us some insight into this. We > really have to look hard at what we do for just due to the > fact that EVERYTHING we do for him comes out of our pocket. > > We are really searching hard on what the " right " technique/therapy is > for . I see so many different posts on what everyone else > does..but it's difficult to judge what is " right " for your child. > > We have already made an appoitment to go to the Pfeiffer Treatment > Center in Chicago to have 's hair,urine and blood tested to see > if he is maybe laking in certain minerals/vitamins. > > We deffinetly couldn't do both of these... Kaufman and > Pfeiffer...so this is the delima we are in. Do we go traditional with > Kaufman or go the other way with Pfeiffer? I'm not asking for > anyone to " tell " me what to do..I'm just looking for some insight. We > just want the best for our son and are having trouble finding out > what the best for is. > > Again...Thank you in advance! > > Mandy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 Hello... I am the one looking into the Kaufman center.... Kaufman is the one who created the Kaufman Praxis Test and the Kaufman Kits are a technique in helping apraxia. We are more than likely not going to go after all...like someone else just mentioned...we already have the diagnosis of apraxia and all she can do is show us how to use her Kaufman method. But we would still have to find a SLP in Ohio that is educated in this method. Do you have a diagnosis of apraxia? Hope this helps...let me know if you would like more information!! Mandy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 Hi , I know Kaufman is suppose to be great and but it sounds like the apraxia has already been diagnosed. Yes she may tell you that her technique will really help him, but then you are back to finding an SLP in Ohio who will use them. On the other hand maybe the video tape idea which is much cheaper could allow you to do both. If you are looking to test hair, urine, etc.. maybe go with someone else's thought I think it was Kim and go to a DAN Dr. Not sure if because they are Dr.'s you will then be covered. denise > We deffinetly couldn't do both of these... Kaufman and > Pfeiffer...so this is the delima we are in. Do we go traditional with > Kaufman or go the other way with Pfeiffer? I'm not asking for > anyone to " tell " me what to do..I'm just looking for some insight. We > just want the best for our son and are having trouble finding out > what the best for is. > > Again...Thank you in advance! > > Mandy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 Hello I do not mean to intrude but what is Nanct kauffman Centre. Is there someone who could explain how she can help ? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 Hi Mandy, I'm in a rush (again) so hope that this point comes across. You wouldn't take your child to see Kaufman solely to let you know if your child has apraxia. Kaufman and her techniques/methods and advice have greatly assisted many children in our group who live in other states or countries through coordinating an appropriate therapy program with local therapists. I love the Kaufman technique (together with other multisensory approaches) http://www.kidspeech.com is 's website. Ohio is not a state that is lacking in resources, support or members. In fact CHERAB of Ohio is there - http://www.cherabofohio.org You can join their online group as well. Other members from Ohio -what are your views on this? I know from our Jersey group -chelation had a patchy response -worked dramatically well for a few -no change at all for others who complained about expense on top of it not working. On the other hand those from Jersey who traveled to see Kaufman -the percentage who rave about success is high. Woods RN from Westchester NY isn't even active on our grouplist anymore her son (mild CP and apraxia) is doing so well on appropriate therapy/EFAs - she had tried both (and more) and highly recommends . Email me off list and I'll see if will let me give you her number if you want to talk to her. For those of you who are in local support groups and can see the numbers from others in your area that you know - to prove what I'm saying is right or wrong -correct me please if I'm wrong. Can't get much more toxic of an area than Jersey -and if chelation isn't the magic bullet for even a solid half there -than where? Again -EFAs are in my opinion the closest we have to a magic bullet in almost all areas. And in the cases where chelation works -take away the EFAs and see if you find the same results. Sure chelation is something to explore -read both pros and cons from reputable sources. Since I'm sure you've read the former -read this for the latter: http://www.quackwatch.org/01QuackeryRelatedTopics/chelation.html (Yes we know that many MDs are still learning what some here already know -but that doesn't mean you should not at least read the cons from some medical doctors and see what they have to say too. We need mutual respect between parents and professionals -and that includes medical professionals. Just my viewpoint -feel free to disagree. I'm always looking to learn more. and I know this subject is deeply split here.) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 > Sure chelation is something to explore -read both pros and cons from > reputable sources. Since I'm sure you've read the former -read this > for the latter: > http://www.quackwatch.org/01QuackeryRelatedTopics/chelation.html > (Yes we know that many MDs are still learning what some here already > know -but that doesn't mean you should not at least read the cons > from some medical doctors and see what they have to say too. We > need mutual respect between parents and professionals -and that > includes medical professionals. Just my viewpoint -feel free to > disagree. I'm always looking to learn more. and I know this subject > is deeply split here.) > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2003 Report Share Posted November 11, 2003 Thanks for sharing! Whem is your appt.? Please keep us posted. Kate, Mom to (and ) who turned 3 today!!!! > I just wanted to let everyone know that I attended one of 's > workshops here in Indianapolis just a few weeks ago. My son's SLP > had attended the same workshop (Evaluation and Treatment of Apraxia) > last year in Michigan and we were talking about it one day. I > checked out 's website and found the date for the workshop. I > was one of about 10 moms in the audience of about 150. > actually made a point to sit with the mothers (and a few fathers) at > lunchtime and address any special questions or concerns we had. Her > website gives information on sending a video to her for evaluation > ($100 fee) and I talked to her about it because I was going to do > it. However, she honestly admitted that there might be some things > that she would miss and her written evaluation might be skewed as a > result. Instead, she recommends visiting the Center. Even though > it is a 5 hour drive from my home and the appointment is only 1 1/2 > hours long, I am taking my son to her. She shows videotapes of > children she has treated in " before " and " after " situations. Based > on those tapes and her explanation of her method, I consider her a > real godsend. Seeing those children (mostly boys, incidentally) > progress from being able to barely approximate a word to speaking > spontaneous sentences really gave me hope that Ian will one day be > an " after. " I was literally crying during the videotapes. After > our appointment I will post what happened. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2003 Report Share Posted November 11, 2003 Another very popular subject! is one of my favorite people in the world -she is such a bubble! (I call happy people bubbles) has spoken pro bono at any conference I've help to book -here are just some. Her presentations are both informative and energetic. http://www.cherab.org/news/scientific.html http://www.cherab.org/programs/Kaufman.html http://www.cherab.org/news/nc2003-conference.html Here is an archive from about a month ago on her -I'm sure may pop in and have something else to add! (Mandy did you see ever see ?!) ~ From: " kiddietalk " <kiddietalk@...> Date: Mon Sep 22, 2003 12:52 pm Subject: Re: Kaufman No doubt to me -choose door number one -! I highly recommend Kaufman first, and not because she made me an honorary SLP, but because she can start you on an appropriate therapy path which is proven in many of our children to work while you explore what caused the apraxia. Kaufman is a professional advisor to both the nonprofit CHERAB Foundation, as well as Speechville.com and has also spoken for us probono at many events now. Her Kaufman approach is just brilliant. Again however -I recommend using it along with other multisensory therapies (and so does who I've talked to this about) In addition - also offers a video consult which is $100 -obviously not comprehensive -but do-able for most. Even if it ends up that your child's analysis comes out positive to toxins -that only means your child is probably then like most of ours http://www.cherab.org/news/Save.html Your child (even if there is a toxic cause to the condition) will still require appropriate therapy in addition to any alternative treatment. I'm positive there are environmental factors to this. After all in Texas (a pocket area) instead of an article about EFAs in formula -there is one about " Toxic Rocket Fuel Found In Milk Samples From Texas Supermarkets " http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/es034735q and they are looking for people to be tested for toxins in Ohio (so if you live in this pocket area you can do this for free!) " Groups to measure toxins in residents " http://www.mariettatimes.com/news/story/0919202003_new03sytix.asp Perhaps this is why most of our children respond so dramatically to EFAs, in addition to remyelinating properties -EFAs I'm told have strong detox properties as well. (talk to your doctor and try them...they work!) Most of our children respond to this simple dietary change alone, however there are a few who are reported to require more dramatic dietary changes as well as other alternative holistic interventions that you could do (under a respected MD's care) And for who is looking for an inexpensive Kaufman Kit -why not ask here if anyone is wanting to sell theirs. Children move from Kit 1 to Kit 2... I can tell you after spending thousands and thousands of dollars on therapy -the one hundred plus bucks for 's kit is well worth it -and something you can use and home and travel with -and bring with your child to preschool or therapy for them to borrow if they are not prepared. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2004 Report Share Posted January 31, 2004 As you already know - I am sooo happy and excited for you. good luck with everything and keep me posted. And oh by the way D.H. will look at a tape too! Email me and we can talk! Adrienne > I think this is my time to speak up! > > I just sent in a tape of my daughter Lindsey to Kaufman. It was a > really good tape of the 'true' Lindsey. I covered a lot just to make sure > she saw all sides of Lindsey's. I targeted into her face and mouth the > whole time. When I looked back at the tape,I was amazed at what I saw. When > you see a whole TV of your child talking,you see things that you didn't see > before. > I also taped her having a apraxia test with her SLP. I feel VERY confident > that got the true picture. > > In a matter of days called me and had SO many suggestions! She needs > to talk with Lindseys SLP to go over it all,but we have a plan! I'm just not > sure what it is yet lol! > Lindsey definitely has verbal and oral apraxia. She needs alot of work with > oral motor. We will be be doing s therapy program > talktoolstm.com for the oral motor and another plan for the verbal apraxia. > For the first time in a long time I feel REALLY hopeful. Lindsey will be 8 > in June so we have lots of work to do with her. It would have helped I'm > sure if we got the help from Kaufman earlier,but I was unable to go to > her,and when I found out she did video consultations,I started taping the > same day! > > I couldn't have asked for a more perfect time too. is having a work > shop next Fri in Ft Lauderdale Florida, just 2 1/2 house from my home. > really stressed how important it was for Lindseys speech pathologist > to be there,and she said she will when I called her! > > Jennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2006 Report Share Posted October 24, 2006 I live in MI and I take my 3.10 son to Kaufman center. It's an hr drive so we go 1x per week. He was evaluated by and we currently see an associate for services. Hmmmm... I have to be honest because I think it's important people don't put NK too high on a pedistal. My eval was a little disappointing and I left there feeling like she dumped a bucket of cold water over my head. . But I must say I am impressed with the whole operation and we are dropping about 800. per month ykkkks. So with that kind of " cake " one best be feeling mighty fuzzy I got the very strong impression that she is not all that " on board " with biomeds, which confused me a lot since she is so promoted with the Late Talker book. But matters not because I am comfortable that it is top notch therapy. So you discuss your biomed " plan " with your very well seasoned and active DAN! Dr whom you are totally comfortable. Also, if you already have an apraxia dx...Going for an eval with would be repetitive and just cost you 300.00. Just don't do it because you've read that she is the " goddess " of apraxia and you just have to get some face time with her. > > Has anyone on the board taken their child to see Kaufman in > Wisconsin(I think that is where she is). I have read that she does > intensive work with kids who have apraxia for 1-4 weeks. I know of her > apraxia cards, but not much else. Our son has made great gains in > speech in the past year, from not even being able to imitate a sound > to being able to approximate words. We still have a long way to go as > far as getting the words to really sound like what he means, and also > getting him to spontaneously use words. I guess that is the biggest > challenge. He prefers to melt down instead of using a word, or even a > sign for that matter. If anyone has used or has any ideas on > getting spontaneous speech I would love to hear about it. > Thanks, > beth in Atlanta > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2006 Report Share Posted October 24, 2006 I took my daughter to Kaufmann in March of this year. 's office is West Bloomfield, MI. I think that you can do a web search to get her website name. You can even email on her website. is excellent. My daughter has verbal apraxia and she's made tremendous process since my daughter went to see her in December of last year. Maddi's speech therapist used the videos as training videos since apraxia is quite rare and requires much different approach than regular speech therapy. Please don't feel discouraged. My daughter at 18 months could only make vowel sounds. Now at three, she's talking in 3-5 word sentences. I went to when I had the same frustration of not getting words. In a few months, my daughter improved leaps and bounds. Oddly enough, my daughter was very sick for three weeks (even hospitalized with Kawasaki disease) and she started talking in words and very short sentences. I would recommend 's summer program to you. We didn't go to it, but your speech therapist sounds good, so he/she may not need training. Your son might just benefit from intensive therapy. Good luck! If you need more info., feel free to email me at kosantowski@.... grodinmorrison <grodinmorrison@...> wrote: Has anyone on the board taken their child to see Kaufman in Wisconsin(I think that is where she is). I have read that she does intensive work with kids who have apraxia for 1-4 weeks. I know of her apraxia cards, but not much else. Our son has made great gains in speech in the past year, from not even being able to imitate a sound to being able to approximate words. We still have a long way to go as far as getting the words to really sound like what he means, and also getting him to spontaneously use words. I guess that is the biggest challenge. He prefers to melt down instead of using a word, or even a sign for that matter. If anyone has used or has any ideas on getting spontaneous speech I would love to hear about it. Thanks, beth in Atlanta --------------------------------- Messenger with Voice. Make PC-to-Phone Calls to the US (and 30+ countries) for 2¢/min or less. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2006 Report Share Posted October 24, 2006 I took my daughter to Kaufmann in March of this year. 's office is West Bloomfield, MI. I think that you can do a web search to get her website name. You can even email on her website. is excellent. My daughter has verbal apraxia and she's made tremendous process since my daughter went to see her in December of last year. Maddi's speech therapist used the videos as training videos since apraxia is quite rare and requires much different approach than regular speech therapy. Please don't feel discouraged. My daughter at 18 months could only make vowel sounds. Now at three, she's talking in 3-5 word sentences. I went to when I had the same frustration of not getting words. In a few months, my daughter improved leaps and bounds. Oddly enough, my daughter was very sick for three weeks (even hospitalized with Kawasaki disease) and she started talking in words and very short sentences. I would recommend 's summer program to you. We didn't go to it, but your speech therapist sounds good, so he/she may not need training. Your son might just benefit from intensive therapy. Good luck! If you need more info., feel free to email me at kosantowski@.... grodinmorrison <grodinmorrison@...> wrote: Has anyone on the board taken their child to see Kaufman in Wisconsin(I think that is where she is). I have read that she does intensive work with kids who have apraxia for 1-4 weeks. I know of her apraxia cards, but not much else. Our son has made great gains in speech in the past year, from not even being able to imitate a sound to being able to approximate words. We still have a long way to go as far as getting the words to really sound like what he means, and also getting him to spontaneously use words. I guess that is the biggest challenge. He prefers to melt down instead of using a word, or even a sign for that matter. If anyone has used or has any ideas on getting spontaneous speech I would love to hear about it. Thanks, beth in Atlanta --------------------------------- Stay in the know. Pulse on the new .com. Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2006 Report Share Posted October 24, 2006 A variety of cues can be used to try to stimulate prompted/spontaneous speech. Many you may have tried before without as much success and maybe it is time to try them again now that he is able to verbalize more. Use a sign or gesture yourself to give a prompt. In this, we are not really expecting the child to sign back (although they may), but to say the word we are signing. Say the first sound or syllable of the word only and wait for the child to produce the word. Use a gestural cue for the first sound of the word to help prompt the child to say the word. Using " pat " phrases may also be helpful. So, practice short phrases and and short words. E.g. " I-want-___ " with pauses. Use pictures to help prompt the child to say a familiar word. Remember too that if upset or once frustrated that the child may have difficultly getting out what they want to say even with their best efforts. Katina > > Has anyone on the board taken their child to see Kaufman in > Wisconsin(I think that is where she is). I have read that she does > intensive work with kids who have apraxia for 1-4 weeks. I know of her > apraxia cards, but not much else. Our son has made great gains in > speech in the past year, from not even being able to imitate a sound > to being able to approximate words. We still have a long way to go as > far as getting the words to really sound like what he means, and also > getting him to spontaneously use words. I guess that is the biggest > challenge. He prefers to melt down instead of using a word, or even a > sign for that matter. If anyone has used or has any ideas on > getting spontaneous speech I would love to hear about it. > Thanks, > beth in Atlanta > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2006 Report Share Posted October 25, 2006 Beth, Check out the verbal behavior style of ABA. There are 2 groups ( and verbalbehavior) that cover this area. Kaufman by the way also uses the vb style of ABA in her clinic. The vb style focuses on using language in a functional, spontaneous way by getting the person to request things, thus learning the power of language (I speak, I get). There are other parts of ABA vb style that I really like such as errorless learning, pairing the staff with fun activities so the child enjoys the therapy, etc. My son has gone from totally non-verbal to be able to spontaneously request things that to these methods. Dave > > > > Has anyone on the board taken their child to see Kaufman in > > Wisconsin(I think that is where she is). I have read that she does > > intensive work with kids who have apraxia for 1-4 weeks. I know of > her > > apraxia cards, but not much else. Our son has made great gains in > > speech in the past year, from not even being able to imitate a sound > > to being able to approximate words. We still have a long way to go as > > far as getting the words to really sound like what he means, and also > > getting him to spontaneously use words. I guess that is the biggest > > challenge. He prefers to melt down instead of using a word, or even a > > sign for that matter. If anyone has used or has any ideas on > > getting spontaneous speech I would love to hear about it. > > Thanks, > > beth in Atlanta > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2006 Report Share Posted October 25, 2006 We took Josh a couple of years ago (going on 3 three years now!) for an eval. She's in West Bloomfield, Michigan. I absolutely and strongly urge anyone to take their kid to her at least for an eval. We found that, while we couldn't stay in Michigan for treatment, her evaluation and report were gold when it came to getting services in the schools. She is fantastic with the kids, she's a kick of a person, and the whole experience was incredible! Sherry (and Josh) grodinmorrison <grodinmorrison@...> wrote: Has anyone on the board taken their child to see Kaufman in Wisconsin(I think that is where she is). I have read that she does intensive work with kids who have apraxia for 1-4 weeks. I know of her apraxia cards, but not much else. Our son has made great gains in speech in the past year, from not even being able to imitate a sound to being able to approximate words. We still have a long way to go as far as getting the words to really sound like what he means, and also getting him to spontaneously use words. I guess that is the biggest challenge. He prefers to melt down instead of using a word, or even a sign for that matter. If anyone has used or has any ideas on getting spontaneous speech I would love to hear about it. Thanks, beth in Atlanta Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 I had to admit my stupidity, but what is ABA? Suzanne [ ] Re: Kaufman Beth, Check out the verbal behavior style of ABA. There are 2 groups ( and verbalbehavior) that cover this area. Kaufman by the way also uses the vb style of ABA in her clinic. The vb style focuses on using language in a functional, spontaneous way by getting the person to request things, thus learning the power of language (I speak, I get). There are other parts of ABA vb style that I really like such as errorless learning, pairing the staff with fun activities so the child enjoys the therapy, etc. My son has gone from totally non-verbal to be able to spontaneously request things that to these methods. Dave > > > > Has anyone on the board taken their child to see Kaufman in > > Wisconsin(I think that is where she is). I have read that she does > > intensive work with kids who have apraxia for 1-4 weeks. I know of > her > > apraxia cards, but not much else. Our son has made great gains in > > speech in the past year, from not even being able to imitate a sound > > to being able to approximate words. We still have a long way to go as > > far as getting the words to really sound like what he means, and also > > getting him to spontaneously use words. I guess that is the biggest > > challenge. He prefers to melt down instead of using a word, or even a > > sign for that matter. If anyone has used or has any ideas on > > getting spontaneous speech I would love to hear about it. > > Thanks, > > beth in Atlanta > > > <!-- #ygrp-mlmsg {font-size:13px;font-family:arial,helvetica,clean,sans-serif;} #ygrp-mlmsg table {font-size:inherit;font:100%;} #ygrp-mlmsg select, input, textarea {font:99% arial,helvetica,clean,sans-serif;} #ygrp-mlmsg pre, code {font:115% monospace;} #ygrp-mlmsg * {line-height:1.22em;} #ygrp-text{ font-family:Georgia; } #ygrp-text p{ margin:0 0 1em 0; } #ygrp-tpmsgs{ font-family:Arial; clear:both; } #ygrp-vitnav{ padding-top:10px; font-family:Verdana; font-size:77%; margin:0; } #ygrp-vitnav a{ padding:0 1px; } #ygrp-actbar{ clear:both; margin:25px 0; white-space:nowrap; color:#666; text-align:right; } #ygrp-actbar .left{ float:left; white-space:nowrap; } ..bld{font-weight:bold;} #ygrp-grft{ font-family:Verdana; font-size:77%; padding:15px 0; } #ygrp-ft{ font-family:verdana; font-size:77%; border-top:1px solid #666; padding:5px 0; } #ygrp-mlmsg #logo{ padding-bottom:10px; } #ygrp-vital{ background-color:#e0ecee; margin-bottom:20px; padding:2px 0 8px 8px; } #ygrp-vital #vithd{ font-size:77%; font-family:Verdana; font-weight:bold; color:#333; text-transform:uppercase; } #ygrp-vital ul{ padding:0; margin:2px 0; } #ygrp-vital ul li{ list-style-type:none; clear:both; border:1px solid #e0ecee; } #ygrp-vital ul li .ct{ font-weight:bold; color:#ff7900; float:right; width:2em; text-align:right; padding-right:.5em; } #ygrp-vital ul li .cat{ font-weight:bold; } #ygrp-vital a { text-decoration:none; } #ygrp-vital a:hover{ text-decoration:underline; } #ygrp-sponsor #hd{ color:#999; font-size:77%; } #ygrp-sponsor #ov{ padding:6px 13px; background-color:#e0ecee; margin-bottom:20px; } #ygrp-sponsor #ov ul{ padding:0 0 0 8px; margin:0; } #ygrp-sponsor #ov li{ list-style-type:square; padding:6px 0; font-size:77%; } #ygrp-sponsor #ov li a{ text-decoration:none; font-size:130%; } #ygrp-sponsor #nc { background-color:#eee; margin-bottom:20px; padding:0 8px; } #ygrp-sponsor .ad{ padding:8px 0; } #ygrp-sponsor .ad #hd1{ font-family:Arial; font-weight:bold; color:#628c2a; font-size:100%; line-height:122%; } #ygrp-sponsor .ad a{ text-decoration:none; } #ygrp-sponsor .ad a:hover{ text-decoration:underline; } #ygrp-sponsor .ad p{ margin:0; } o {font-size:0;} ..MsoNormal { margin:0 0 0 0; } #ygrp-text tt{ font-size:120%; } blockquote{margin:0 0 0 4px;} ..replbq {margin:4;} --> Quote Link to comment Share on other sites More sharing options...
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