Guest guest Posted January 19, 2006 Report Share Posted January 19, 2006 At 11:49 AM 1/19/2006, you wrote: >I don't mind speaking in front of people but it's been awhile! I founded >the local Ds support group in Rapid City, SD when we lived there and did >some speaking with that and some short blips on the news for Buddy Walk >awareness but that was all a long time ago, back in the days of just Ds! LOL! > > So, of course, I turn to you all for ideas and suggestions for my speech. The thing to remember is speaking is that unless these students have dealt with disabilities in their family they don't have a clue what you experience. The more you can help them to see about day to day struggles and joys the more they will take into their professional life and help others down the road. I am sure you are going to do fine. It is great you are doing this. Keep us informed. Peggy Lou www.parentingyourcomplexchild.com www.lighthouseparents.com http://parentingacomplexchild.blogspot.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2006 Report Share Posted January 19, 2006 Hey, Jayne!! Congratulations!!!! Liz I've been asked to speak... > Hi there, > > Recently I sent an email out to several professors at Old Dominion > University in Norfolk, VA regarding finding students to babysit for > . His private OT had suggested that I may be able to find some OT, > PT, SLP, or SPED students that are interested in some " hands on " > experience. I thought it was a wonderful idea. > > I've heard back from several of the professors and it seems my email is > circulating nicely around the campus! LOL! > > Today I received a call from a professor in the Speech Pathology > Department. She is the Advisor for ODU's chapter of The National Student > Speech Language Hearing Association. She has asked me to speak at their > next meeting January 31st! She said she's been searching for interesting > speakers and when she read my email this morning, it clicked - just how > important a parents point of view would be to the students. The > Organization is made up of about 40 Undergraduate, Graduate, and Doctoral > Students in the SLP field. There are some staff that attend the meetings > but mostly students. She wants me to speak for about 20 minutes and then > open it up to Q & A's. The whole thing lasts about an hour. > She basically wants me to tell my story and share my " wisdom " (her words > not mine) LOL. She said to just share what I think is important with > future SLP's, etc... > > I don't mind speaking in front of people but it's been awhile! I founded > the local Ds support group in Rapid City, SD when we lived there and did > some speaking with that and some short blips on the news for Buddy Walk > awareness but that was all a long time ago, back in the days of just Ds! > LOL! > > So, of course, I turn to you all for ideas and suggestions for my speech. > Fire away, I'm all ears! > Thanks so much - > Jayne > > > --------------------------------- > Yahoo! Photos > Ring in the New Year with Photo Calendars. Add photos, events, holidays, > whatever. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2006 Report Share Posted January 19, 2006 Jayne, When did you live in Rapid City? One of my best friends lived there twice (once before I knew her). She as a genetic counselor--Carol Christianson and Carol STrom (you know, got married...). It' gets to be such a small, small world! j __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2006 Report Share Posted January 19, 2006 Hi Jayne, Go for it!! Charlyne Mom to Zeb 13 DS/OCD/ASD? Jayne Hickey wrote: Hi there, Recently I sent an email out to several professors at Old Dominion University in Norfolk, VA regarding finding students to babysit for . His private OT had suggested that I may be able to find some OT, PT, SLP, or SPED students that are interested in some " hands on " experience. I thought it was a wonderful idea. I've heard back from several of the professors and it seems my email is circulating nicely around the campus! LOL! Today I received a call from a professor in the Speech Pathology Department. She is the Advisor for ODU's chapter of The National Student Speech Language Hearing Association. She has asked me to speak at their next meeting January 31st! She said she's been searching for interesting speakers and when she read my email this morning, it clicked - just how important a parents point of view would be to the students. The Organization is made up of about 40 Undergraduate, Graduate, and Doctoral Students in the SLP field. There are some staff that attend the meetings but mostly students. She wants me to speak for about 20 minutes and then open it up to Q & A's. The whole thing lasts about an hour. She basically wants me to tell my story and share my " wisdom " (her words not mine) LOL. She said to just share what I think is important with future SLP's, etc... I don't mind speaking in front of people but it's been awhile! I founded the local Ds support group in Rapid City, SD when we lived there and did some speaking with that and some short blips on the news for Buddy Walk awareness but that was all a long time ago, back in the days of just Ds! LOL! So, of course, I turn to you all for ideas and suggestions for my speech. Fire away, I'm all ears! Thanks so much - Jayne --------------------------------- Yahoo! Photos Ring in the New Year with Photo Calendars. Add photos, events, holidays, whatever. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 In a message dated 1/19/2006 2:52:53 P.M. Eastern Standard Time, jacksonsmom99@... writes: don't mind speaking in front of people but it's been awhile! I founded the local Ds support group in Rapid City, SD when we lived there and did some speaking with that and some short blips on the news for Buddy Walk awareness but that was all a long time ago, back in the days of just Ds! LOL! So, of course, I turn to you all for ideas and suggestions for my speech. You'll do great Jayne. I do this every year at a couple colleges. Once I did it at a large university here in Philly to a group of 50 students AND it was televised in other classrooms as well....talk about shaking in my shoes!!!!! I would suggest you bring pictures of ...... with his siblings, friends, at school, at play...whatever you have. Typically, what I do is do a large posterboard and I also bring handouts (Maddie's IEP, any therapy reports that were written particularly well over the years, info on SI, ABA and other behavior techniques---depending on what the professor needs addressed). My friend who teaches special education to college students usually writes up about 5 or 6 specific topics he's teaching at that time, so I can narrow it down a bit. I always bring *Maddie's book* with me too, that I had done up years ago...that's a big hit with the students. One time, years ago, I was contacted by a student at a local college asking me if she could spend a day with me and Maddie. Her professor had told the students they had to come up with their own plan for learning sensitivity in relation to families dealing with disability...that was hers. We had a great day...she even went food shopping with us. She told me that day that she was studying to be a geneticist and that before spending the day with us she firmly believed that abortion was the only option for parents upon learning their child had DS. I still have the letter she wrote me afterwards, thanking me....in it she actually said *I want to be more like you*. It's the most incredible feeling knowing you've impacted someone that way. I think you'll do the same thing, Jayne. And you'll be so happy and proud of yourself, and of !!!!!! Good luck, and let us know how it went afterwards, K? Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 In a message dated 1/20/2006 8:32:08 A.M. Eastern Standard Time, louandy@... writes: I used to think that the SLP should know how to sign. A few years ago one of 's staff was in a SLP program and she said that learning sign language was a part of her program now. Louise, I remember when Maddie was 2 and Alison was 3, we were hanging out back with the ST at the EI program Maddie was part of......Allie, AT THREE, showed her all the signs she knew and the ST turned to me and said, " Wow, she knows more than me " . That was the final straw that made me go in and ask for another SLP to work with Maddie....LOL Jayne, I forgot...I also always bring Maddie's communication pictures that we use here at home. Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Jayne what a great opportunity. I used to think that the SLP should know how to sign. A few years ago one of 's staff was in a SLP program and she said that learning sign language was a part of her program now. I don't know if it was an elective or required but she was taking classes in sign language. We haven't had any contact with SLP for a number of years so I don't know their current program. For communication with sign and using pictures to help plan his day is important. I am currently putting together a sign book for his staff that will include the name of the sign and a picture of the way he uses it, staff signs with their picture, family signs with their picture etc. A few I couldn't find in the sign books I have or the internet so I did the signs and had my picture taken doing them. Thanks to Carol who made a similar book for Trisha for the idea. Some day I may make a video of the signs. I will give your request more thought and if I come up with any other thoughts will let you know. Louise I've been asked to speak... Hi there, Recently I sent an email out to several professors at Old Dominion University in Norfolk, VA regarding finding students to babysit for . His private OT had suggested that I may be able to find some OT, PT, SLP, or SPED students that are interested in some " hands on " experience. I thought it was a wonderful idea. I've heard back from several of the professors and it seems my email is circulating nicely around the campus! LOL! Today I received a call from a professor in the Speech Pathology Department. She is the Advisor for ODU's chapter of The National Student Speech Language Hearing Association. She has asked me to speak at their next meeting January 31st! She said she's been searching for interesting speakers and when she read my email this morning, it clicked - just how important a parents point of view would be to the students. The Organization is made up of about 40 Undergraduate, Graduate, and Doctoral Students in the SLP field. There are some staff that attend the meetings but mostly students. She wants me to speak for about 20 minutes and then open it up to Q & A's. The whole thing lasts about an hour. She basically wants me to tell my story and share my " wisdom " (her words not mine) LOL. She said to just share what I think is important with future SLP's, etc... I don't mind speaking in front of people but it's been awhile! I founded the local Ds support group in Rapid City, SD when we lived there and did some speaking with that and some short blips on the news for Buddy Walk awareness but that was all a long time ago, back in the days of just Ds! LOL! So, of course, I turn to you all for ideas and suggestions for my speech. Fire away, I'm all ears! Thanks so much - Jayne -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.20/234 - Release Date: 1/18/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Hi Joan, Yes, it is a small world. I lived there 3 times thanks to the US Air Force. Ellsworth AFB is home to the B-1B Bomber, which my husband flew until we moved here to Virginia just over a year ago. I lived there from 94-96, 98-01, and 02-04. If we hadn't decided to hang our hat up at 20 years with the Air Force, I'd be headed back there in the spring of this year! It's a beautiful area with the Black Hills, Mt. Rushmore, Crazy Horse, Badlands, etc... - so much to see and do. It holds a special place in my heart after living there so many times. One of the many places I never thought I would call home but thanks to the Air Force, we've seen the world! (translation - the midwest!) Your friend's name rings a bell, I want to say she was either the only genetic counselor or 1 of 2. I want to say there was one who came in from Sioux Falls once or twice a month as well. I'm sure she knows several of my friends in the Ds community there, probably chatted with a few of them before or after their childs birth at Rapid City Regional Hospital. When did she live there? Is she still there? The name of the Ds Support Group there is called Ups of Downs. Small world! Take care, Jayne Joan Medlen wrote: Jayne, When did you live in Rapid City? One of my best friends lived there twice (once before I knew her). She as a genetic counselor--Carol Christianson and Carol STrom (you know, got married...). It' gets to be such a small, small world! j __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Thank you Louise. You make a very important point about the sign language. I was very surprised to find so many of 's SLP's along the way havn't known Sign Language. I remember having to teach his SLP when he was 2 and I thought we were never going to get ahead if I was the one constantly giving the SLP ideas - I was the one who needed new ideas. I always said that I bet that therapist went on to be a great therapist after her year of brainstorming with LOL! I don't know if it is required now for them to take Sign Language but it should be. I will talk about the importance of that and the importance of PECS too. Any other ideas are very appreciated, thanks Louise. Take care, Jayne Louise & Andy wrote: Jayne what a great opportunity. I used to think that the SLP should know how to sign. A few years ago one of 's staff was in a SLP program and she said that learning sign language was a part of her program now. I don't know if it was an elective or required but she was taking classes in sign language. We haven't had any contact with SLP for a number of years so I don't know their current program. For communication with sign and using pictures to help plan his day is important. I am currently putting together a sign book for his staff that will include the name of the sign and a picture of the way he uses it, staff signs with their picture, family signs with their picture etc. A few I couldn't find in the sign books I have or the internet so I did the signs and had my picture taken doing them. Thanks to Carol who made a similar book for Trisha for the idea. Some day I may make a video of the signs. I will give your request more thought and if I come up with any other thoughts will let you know. Louise I've been asked to speak... Hi there, Recently I sent an email out to several professors at Old Dominion University in Norfolk, VA regarding finding students to babysit for . His private OT had suggested that I may be able to find some OT, PT, SLP, or SPED students that are interested in some " hands on " experience. I thought it was a wonderful idea. I've heard back from several of the professors and it seems my email is circulating nicely around the campus! LOL! Today I received a call from a professor in the Speech Pathology Department. She is the Advisor for ODU's chapter of The National Student Speech Language Hearing Association. She has asked me to speak at their next meeting January 31st! She said she's been searching for interesting speakers and when she read my email this morning, it clicked - just how important a parents point of view would be to the students. The Organization is made up of about 40 Undergraduate, Graduate, and Doctoral Students in the SLP field. There are some staff that attend the meetings but mostly students. She wants me to speak for about 20 minutes and then open it up to Q & A's. The whole thing lasts about an hour. She basically wants me to tell my story and share my " wisdom " (her words not mine) LOL. She said to just share what I think is important with future SLP's, etc... I don't mind speaking in front of people but it's been awhile! I founded the local Ds support group in Rapid City, SD when we lived there and did some speaking with that and some short blips on the news for Buddy Walk awareness but that was all a long time ago, back in the days of just Ds! LOL! So, of course, I turn to you all for ideas and suggestions for my speech. Fire away, I'm all ears! Thanks so much - Jayne -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.20/234 - Release Date: 1/18/2006 -------------------------------------------------- Checkout our homepage for information, bookmarks, and photos of our kids. Share favorite bookmarks, ideas, and other information by including them. Don't forget, messages are a permanent record of the archives for our list. http://groups.yahoo.com/group/ -------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 ok this is the second time this came through, that is strange. lol Carol Trishasmom She isn't typical, She's Trisha! If you always do what you always did, you'll always get what you've always gotten. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Donna, Thank you so much for the fantastic ideas, they are truly wonderful. Tell me about " Maddie's book " . Donna I bet you are fantastic at public speaking. I know the professors are so glad they can turn to you to shed light on family life with a child with special needs and bring that reality into the classroom. Good for you. The posterboard is a great idea, I wanted to bring a lot of pics but I wasn't sure the best route. Do you make copies of the IEP, etc. to hand out to them? What a powerful feeling it must have been to have the student share her change in thinking right before your eyes - thanks to you and Maddie. That's just great. I will definately let you all know how it goes. I'm just trying to piece together the most important things to share. You all have been really helpful. Thanks, Jayne duffey48@... wrote: In a message dated 1/19/2006 2:52:53 P.M. Eastern Standard Time, jacksonsmom99@... writes: don't mind speaking in front of people but it's been awhile! I founded the local Ds support group in Rapid City, SD when we lived there and did some speaking with that and some short blips on the news for Buddy Walk awareness but that was all a long time ago, back in the days of just Ds! LOL! So, of course, I turn to you all for ideas and suggestions for my speech. You'll do great Jayne. I do this every year at a couple colleges. Once I did it at a large university here in Philly to a group of 50 students AND it was televised in other classrooms as well....talk about shaking in my shoes!!!!! I would suggest you bring pictures of ...... with his siblings, friends, at school, at play...whatever you have. Typically, what I do is do a large posterboard and I also bring handouts (Maddie's IEP, any therapy reports that were written particularly well over the years, info on SI, ABA and other behavior techniques---depending on what the professor needs addressed). My friend who teaches special education to college students usually writes up about 5 or 6 specific topics he's teaching at that time, so I can narrow it down a bit. I always bring *Maddie's book* with me too, that I had done up years ago...that's a big hit with the students. One time, years ago, I was contacted by a student at a local college asking me if she could spend a day with me and Maddie. Her professor had told the students they had to come up with their own plan for learning sensitivity in relation to families dealing with disability...that was hers. We had a great day...she even went food shopping with us. She told me that day that she was studying to be a geneticist and that before spending the day with us she firmly believed that abortion was the only option for parents upon learning their child had DS. I still have the letter she wrote me afterwards, thanking me....in it she actually said *I want to be more like you*. It's the most incredible feeling knowing you've impacted someone that way. I think you'll do the same thing, Jayne. And you'll be so happy and proud of yourself, and of !!!!!! Good luck, and let us know how it went afterwards, K? Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Interesting Donna. I had the same feeling about the audiologists who I used to take deaf consumers to and then switched to because they were so good despite not knowing sign, I interpreted for him. Louise Re: I've been asked to speak... In a message dated 1/20/2006 8:32:08 A.M. Eastern Standard Time, louandy@... writes: I used to think that the SLP should know how to sign. A few years ago one of 's staff was in a SLP program and she said that learning sign language was a part of her program now. Louise, I remember when Maddie was 2 and Alison was 3, we were hanging out back with the ST at the EI program Maddie was part of......Allie, AT THREE, showed her all the signs she knew and the ST turned to me and said, " Wow, she knows more than me " . That was the final straw that made me go in and ask for another SLP to work with Maddie....LOL Jayne, I forgot...I also always bring Maddie's communication pictures that we use here at home. Donna -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Thanks Joan! You're right, I just need to show what it's like to be MOM. And it's - I don't expect you could possibly remember the millions of children's names you hear about on a daily basis. 100 hours of support?! Ohhh that's sounds heavenly. We have 0 now so even 1 would be nice! Thanks, Jayne Joan Medlen wrote: Of course you will, Jayne! Don't worry about being any expert other than that of MOM. Share with them the trials and tribulations of juggling laundry, cooking, cleaning, parenting all your kids, and trying to implement some daily teaching strategy. Let them know what that means. But most of all, share your love for your child (whose name of course escapes me). The more we can get people to see our kids and US as REAL PEOPLE with REAL concerns (like keeping a job and paying the bills rather than being the taxi to therapy), the better they will be. THEN invite them to spend 100 hours supporting your child! Think of all the free time you'd have! j --- Jayne Hickey wrote: > Thanks Carol! I hope so. > > Csvillars@... wrote: no suggestions but I > wanted say congratulations. You aregoing to help > make > a big difference especially with the new SLP's that > are going to be > graduating. WTG! > > Carol > Trishasmom > She isn't typical, She's Trisha! > If you always do what you always did, you'll always > get what you've always > gotten. > > > [Non-text portions of this message have been > removed] > > > > -------------------------------------------------- > Checkout our homepage for information, > bookmarks, and photos of our kids. Share favorite > bookmarks, ideas, and other information by including > them. Don't forget, messages are a permanent record > of the archives for our list. > http://groups.yahoo.com/group/ > -------------------------------------------- > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 Good point from Joan and I wonder how many of the SLP students are Mom's also and are juggling families and school. Maybe ask at the start to get a feel if they can relate to you to start on that level. Louise Re: I've been asked to speak... Thanks Joan! You're right, I just need to show what it's like to be MOM. And it's - I don't expect you could possibly remember the millions of children's names you hear about on a daily basis. 100 hours of support?! Ohhh that's sounds heavenly. We have 0 now so even 1 would be nice! Thanks, Jayne Joan Medlen wrote: Of course you will, Jayne! Don't worry about being any expert other than that of MOM. Share with them the trials and tribulations of juggling laundry, cooking, cleaning, parenting all your kids, and trying to implement some daily teaching strategy. Let them know what that means. But most of all, share your love for your child (whose name of course escapes me). The more we can get people to see our kids and US as REAL PEOPLE with REAL concerns (like keeping a job and paying the bills rather than being the taxi to therapy), the better they will be. THEN invite them to spend 100 hours supporting your child! Think of all the free time you'd have! j -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 ooh good idea Louise. Always good to appeal to the Mommy in everyone. LOL. thanks, Jayne Louise & Andy wrote: Good point from Joan and I wonder how many of the SLP students are Mom's also and are juggling families and school. Maybe ask at the start to get a feel if they can relate to you to start on that level. Louise Re: I've been asked to speak... Thanks Joan! You're right, I just need to show what it's like to be MOM. And it's - I don't expect you could possibly remember the millions of children's names you hear about on a daily basis. 100 hours of support?! Ohhh that's sounds heavenly. We have 0 now so even 1 would be nice! Thanks, Jayne Joan Medlen wrote: Of course you will, Jayne! Don't worry about being any expert other than that of MOM. Share with them the trials and tribulations of juggling laundry, cooking, cleaning, parenting all your kids, and trying to implement some daily teaching strategy. Let them know what that means. But most of all, share your love for your child (whose name of course escapes me). The more we can get people to see our kids and US as REAL PEOPLE with REAL concerns (like keeping a job and paying the bills rather than being the taxi to therapy), the better they will be. THEN invite them to spend 100 hours supporting your child! Think of all the free time you'd have! j -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 If I was handing out any of 's records for a class I would take a black marker on a copy to cross off any identifying name throughout the document before I made copies for the class. It is good to share but you never know where the paper will end up so for confidentiality purposes I would feel most comfortable that the name or other identifying info on all pages was masked. Louise Re: I've been asked to speak... Donna, Thank you so much for the fantastic ideas, they are truly wonderful. Tell me about " Maddie's book " . Donna I bet you are fantastic at public speaking. I know the professors are so glad they can turn to you to shed light on family life with a child with special needs and bring that reality into the classroom. Good for you. The posterboard is a great idea, I wanted to bring a lot of pics but I wasn't sure the best route. Do you make copies of the IEP, etc. to hand out to them? What a powerful feeling it must have been to have the student share her change in thinking right before your eyes - thanks to you and Maddie. That's just great. I will definately let you all know how it goes. I'm just trying to piece together the most important things to share. You all have been really helpful. Thanks, Jayne -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2006 Report Share Posted January 20, 2006 That's what I was thinking too Louise, thanks for emailing that. In answer to your other question about Emla cream. It's a cream you can put on the area to numb it before you draw the blood. I've never used it just heard about it on the different list servs. It's prescription cream the Dr. orders, I believe. I'm sure Sherry will have more info about it. Take care, Jayne Louise & Andy wrote: If I was handing out any of 's records for a class I would take a black marker on a copy to cross off any identifying name throughout the document before I made copies for the class. It is good to share but you never know where the paper will end up so for confidentiality purposes I would feel most comfortable that the name or other identifying info on all pages was masked. Louise Re: I've been asked to speak... Donna, Thank you so much for the fantastic ideas, they are truly wonderful. Tell me about " Maddie's book " . Donna I bet you are fantastic at public speaking. I know the professors are so glad they can turn to you to shed light on family life with a child with special needs and bring that reality into the classroom. Good for you. The posterboard is a great idea, I wanted to bring a lot of pics but I wasn't sure the best route. Do you make copies of the IEP, etc. to hand out to them? What a powerful feeling it must have been to have the student share her change in thinking right before your eyes - thanks to you and Maddie. That's just great. I will definately let you all know how it goes. I'm just trying to piece together the most important things to share. You all have been really helpful. Thanks, Jayne -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 -------------------------------------------------- Checkout our homepage for information, bookmarks, and photos of our kids. Share favorite bookmarks, ideas, and other information by including them. Don't forget, messages are a permanent record of the archives for our list. http://groups.yahoo.com/group/ -------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2006 Report Share Posted January 21, 2006 They have used creams like that when a grandson or granddaughter had to have blood drawn but never knew the name of the cream. Thanks. Louise RE: I've been asked to speak... That's what I was thinking too Louise, thanks for emailing that. In answer to your other question about Emla cream. It's a cream you can put on the area to numb it before you draw the blood. I've never used it just heard about it on the different list servs. It's prescription cream the Dr. orders, I believe. I'm sure Sherry will have more info about it. Take care, Jayne Louise & Andy wrote: If I was handing out any of 's records for a class I would take a black marker on a copy to cross off any identifying name throughout the document before I made copies for the class. It is good to share but you never know where the paper will end up so for confidentiality purposes I would feel most comfortable that the name or other identifying info on all pages was masked. Louise -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.375 / Virus Database: 267.14.21/235 - Release Date: 1/19/2006 Quote Link to comment Share on other sites More sharing options...
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