Guest guest Posted February 6, 2000 Report Share Posted February 6, 2000 Dr. Jim Hatton, of TeenOCD, has established and advises support groups for families in the Southern California area [especially San Diego] . Also, Dr. Grayson of the main OCD-List does the same in the Philadelphia area. Dr. Grayson hs given presentations on OCD support Groups [i attended the one at the ADAA Conference last year]. He was one of 's professors when she attended her OCD training in New Orleans. While Dr. Grayson has been able to go through the process of evolution of the groups, he maintains separate ones for those who suffer and for the loved ones of those who do. At this time the ones we have in San DIego are all inclusive. These 2 gentlemen are likely to be good resources for support groups. jim in san diego Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2000 Report Share Posted February 6, 2000 Hi Robin, I think a support group for parents is a great idea. I also would like to talk to others face to face about some of the things that effect the whole family when your child has OCD. The closest I have ever come to doing this was when my son went to a support group and all the other kids parents would be in the waiting room together. We started talking while we were waiting and I looked forward to it every week. After the support group for the kids ended (it was only for 12 weeks), we all drifted apart. I really miss it. Good luck with starting one in your area. Noelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2000 Report Share Posted February 6, 2000 Robin, Good for you! There is not a support group in my area either and I would like to get one started too. and Kathy... any suggestions?? Take care! mary from La. Jay and Robin Tzucker wrote: > From: Jay and Robin Tzucker <rjtzuckr@...> > > HI All, > I have a question (several, actually). > > 1. Does anyone here attend a support group for parents of kids with OCD? > If you do and you have any info you could share regarding how it > started, how it is moderated / run, frequency, etc. I would appreciate > it. > > 2. Is it realistic to think of starting a support group? I love this > mailing list, but there are times I would like to just sit down with > some of you, enjoy a cup of tea and actually talk face to face. Since > that isn't practical <g> I have been trying to find options locally. > Unfortunately, the closest one meets once a month and is in Seattle, > which isn't quite as convenient as I would like it to be. > > The other night, while attending a girl scout overnight, I spent some > early morning time chatting with another leader...and somewhere in the > course of this conversation it came out that both of our daughters have > OCD! While sharing stories (and boy, do some of these kids share similar > traits!) it really struck me how important it was to be able to talk to > other parents openly and honestly about our kids. I would imagine there > are enough kids with OCD in our area alone to make a support group work. > > If anyone has experience in starting one and how one goes about that > process please let me know. I know that some groups have a trained > moderator (therapist, for example) but if that isn't possible I wonder > if it is ok just to offer support...and acknowledge upfront that we are > parents, not trained professionals, that we would not presume to tell > parents what they " should " do, but we could point them in the direction > of the professionals who could. > > What do you all think? > > Robin > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2000 Report Share Posted February 6, 2000 Hi Jay and Robin, I was just like you ,wanted to sit face to face and talk to someone.The closest support group was 2 1/2 hours away. I start with my doctor,told her to give my name out to any parent with a child with OCD, or if they would let me have theirs. I met a lady who daughter had ocd ,the first night we talked for a hour(we both were crying). It was so wonderful to talk to someone who new what pain I was going through.We have become very good friends. We started a support that meets once a month. We put up papers at all the dr.office and in the news paper in her town and mine.I'm very open about things,and have found that people find it very easy to talk with me.I can't believe how many people suffer in secret.My wish would be that everyone suffering from cod would come out all at once!! We would see allot of people we know! At our meetings we talk and support one other,and share information.This last time we had DR. Collie .He just finished he's first book on OCD. Good Luck ,Beth in IN. support groups > From: Jay and Robin Tzucker <rjtzuckr@...> > > HI All, > I have a question (several, actually). > > 1. Does anyone here attend a support group for parents of kids with OCD? > If you do and you have any info you could share regarding how it > started, how it is moderated / run, frequency, etc. I would appreciate > it. > > 2. Is it realistic to think of starting a support group? I love this > mailing list, but there are times I would like to just sit down with > some of you, enjoy a cup of tea and actually talk face to face. Since > that isn't practical <g> I have been trying to find options locally. > Unfortunately, the closest one meets once a month and is in Seattle, > which isn't quite as convenient as I would like it to be. > > The other night, while attending a girl scout overnight, I spent some > early morning time chatting with another leader...and somewhere in the > course of this conversation it came out that both of our daughters have > OCD! While sharing stories (and boy, do some of these kids share similar > traits!) it really struck me how important it was to be able to talk to > other parents openly and honestly about our kids. I would imagine there > are enough kids with OCD in our area alone to make a support group work. > > If anyone has experience in starting one and how one goes about that > process please let me know. I know that some groups have a trained > moderator (therapist, for example) but if that isn't possible I wonder > if it is ok just to offer support...and acknowledge upfront that we are > parents, not trained professionals, that we would not presume to tell > parents what they " should " do, but we could point them in the direction > of the professionals who could. > > What do you all think? > > Robin > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2000 Report Share Posted February 6, 2000 Hi Beth: How was Dr. Collie? I am reading his OCD book - in between many others - right now. Good job with starting your group, a great idea to share the load with another mom. Take care, aloha, Kathy (H) kathyh@... At 09:49 PM 02/06/2000 -0500, you wrote: >From: " Wayt " <rwwayt@...> > >Hi Jay and Robin, I was just like you ,wanted to sit face to face and talk >to someone.The closest support group was 2 1/2 hours away. I start with my >doctor,told her to give my name out to any parent with a child with OCD, or >if they would let me have theirs. I met a lady who daughter had ocd ,the >first night we talked for a hour(we both were crying). It was so wonderful >to talk to someone who new what pain I was going through.We have become very >good friends. We started a support that meets once a month. We put up papers >at all the dr.office and in the news paper in her town and mine.I'm very >open about things,and have found that people find it very easy to talk with >me.I can't believe how many people suffer in secret.My wish would be that >everyone suffering from cod would come out all at once!! We would see allot >of people we know! At our meetings we talk and support one other,and share >information.This last time we had DR. Collie .He just finished he's >first book on OCD. > Good Luck ,Beth in IN. support groups > > >> From: Jay and Robin Tzucker <rjtzuckr@...> >> >> HI All, >> I have a question (several, actually). >> >> 1. Does anyone here attend a support group for parents of kids with OCD? >> If you do and you have any info you could share regarding how it >> started, how it is moderated / run, frequency, etc. I would appreciate >> it. >> >> 2. Is it realistic to think of starting a support group? I love this >> mailing list, but there are times I would like to just sit down with >> some of you, enjoy a cup of tea and actually talk face to face. Since >> that isn't practical <g> I have been trying to find options locally. >> Unfortunately, the closest one meets once a month and is in Seattle, >> which isn't quite as convenient as I would like it to be. >> >> The other night, while attending a girl scout overnight, I spent some >> early morning time chatting with another leader...and somewhere in the >> course of this conversation it came out that both of our daughters have >> OCD! While sharing stories (and boy, do some of these kids share similar >> traits!) it really struck me how important it was to be able to talk to >> other parents openly and honestly about our kids. I would imagine there >> are enough kids with OCD in our area alone to make a support group work. >> >> If anyone has experience in starting one and how one goes about that >> process please let me know. I know that some groups have a trained >> moderator (therapist, for example) but if that isn't possible I wonder >> if it is ok just to offer support...and acknowledge upfront that we are >> parents, not trained professionals, that we would not presume to tell >> parents what they " should " do, but we could point them in the direction >> of the professionals who could. >> >> What do you all think? >> >> Robin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2000 Report Share Posted February 7, 2000 Hi Robin: I participate in a support group for parents of children with mental illness. Our group got started through our local NAMI chapter. The chapter president is a parent of two boys with bipolar disorder. We sent flyers to schools, churches, libraries, doctors' offices, etc. We meet twice a month at a local community mental health agency. One of their social workers is available to us for support. We are still a small group, so have not done any educational programming. Instead we share where each of us is and offer mutual support. One thing that is important, is not to let one person dominate the group with their issues. We are hoping that we can get some newspaper coverage during mental health month and green ribbon childhood depression day. I think it is important to have at least a loose affiliation with an established group such as NAMI or another community health agency. It lends some credibility to what you are trying to do. Jule in Cleveland Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2000 Report Share Posted February 7, 2000 Hi Kathy, Dr. Collie is a very nice man.He's the first Dr. we took e to when she had just turned 4.I didn't stay that long with him because at that time I was in denial.A year later when things came back allot worse I thought I 'd go for the meds. Than when things got real bad ,Dr. Collie wasn't sure about the nudity problem.He thought a women would be better for e. He did work with her somewhat.I talked with him several times on the phone. I haven't read his book yet, let me know what you think. He has a support group for people with ocd ,and allot of people with ocd started to come to our parents group.I thought if they could met him they would go over to his group.Some of the mother found it hard to be open and vent with them there ,we didn't want to hurt anyone.( it's hard for these poor people with ocd already they don't need to see how hard it is for the parents) or do they????? support groups > > > > > >> From: Jay and Robin Tzucker <rjtzuckr@...> > >> > >> HI All, > >> I have a question (several, actually). > >> > >> 1. Does anyone here attend a support group for parents of kids with OCD? > >> If you do and you have any info you could share regarding how it > >> started, how it is moderated / run, frequency, etc. I would appreciate > >> it. > >> > >> 2. Is it realistic to think of starting a support group? I love this > >> mailing list, but there are times I would like to just sit down with > >> some of you, enjoy a cup of tea and actually talk face to face. Since > >> that isn't practical <g> I have been trying to find options locally. > >> Unfortunately, the closest one meets once a month and is in Seattle, > >> which isn't quite as convenient as I would like it to be. > >> > >> The other night, while attending a girl scout overnight, I spent some > >> early morning time chatting with another leader...and somewhere in the > >> course of this conversation it came out that both of our daughters have > >> OCD! While sharing stories (and boy, do some of these kids share similar > >> traits!) it really struck me how important it was to be able to talk to > >> other parents openly and honestly about our kids. I would imagine there > >> are enough kids with OCD in our area alone to make a support group work. > >> > >> If anyone has experience in starting one and how one goes about that > >> process please let me know. I know that some groups have a trained > >> moderator (therapist, for example) but if that isn't possible I wonder > >> if it is ok just to offer support...and acknowledge upfront that we are > >> parents, not trained professionals, that we would not presume to tell > >> parents what they " should " do, but we could point them in the direction > >> of the professionals who could. > >> > >> What do you all think? > >> > >> Robin > > > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2000 Report Share Posted February 7, 2000 I am a teenager interested in starting a support group for OCD here in Phoenix, Arizona. If anyone is interested, and wants to help, e-mail me. I would really like to meet other kids with OCD, and be able to talk to someone who understands, rather than a therapist, when I am having a bad day. I think that starting a support group is a great idea! There are so many people suffering out there, and this suffering is unnecessary. -Liz Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2000 Report Share Posted February 7, 2000 Hi Beth: Thanks for the heads up o Dr. Collie. I am still reading his book which to me is very different from any other OCD book I have read. I think mixed groups of family members and OCD sufferers can be effective if managed well, it is probably easier to have two separate groups though to allow people to talk freely without worrying about hurting someone's feelings. Often when an OCD sufferer realizes how their disorder affects those they love, it can help them to push through their fear and fight for recovery. Sometimes it can overwhelm them with guilt and resentment. In general this is an issue which needs to be addressed during their recovery, doing it in a group format may not be most helpful for everyone but may be very effective for some. Good luck, aloha, Kathy (H) kathyh@... At 12:09 PM 02/07/2000 -0500, you wrote: >From: " Wayt " <rwwayt@...> > >Hi Kathy, Dr. Collie is a very nice man.He's the first Dr. we took e to >when she had just turned 4.I didn't stay that long with him because at that >time I was in denial.A year later when things came back allot worse I >thought I 'd go for the meds. Than when things got real bad ,Dr. Collie >wasn't sure about the nudity problem.He thought a women would be better for >e. He did work with her somewhat.I talked with him several times on the >phone. I haven't read his book yet, let me know what you think. He has a >support group for people with ocd ,and allot of people with ocd started to >come to our parents group.I thought if they could met him they would go over >to his group.Some of the mother found it hard to be open and vent with them >there ,we didn't want to hurt anyone.( it's hard for these poor people with >ocd already they don't need to see how hard it is for the parents) or do >they????? > support groups >> > >> > >> >> From: Jay and Robin Tzucker <rjtzuckr@...> >> >> >> >> HI All, >> >> I have a question (several, actually). >> >> >> >> 1. Does anyone here attend a support group for parents of kids with >OCD? >> >> If you do and you have any info you could share regarding how it >> >> started, how it is moderated / run, frequency, etc. I would appreciate >> >> it. >> >> >> >> 2. Is it realistic to think of starting a support group? I love this >> >> mailing list, but there are times I would like to just sit down with >> >> some of you, enjoy a cup of tea and actually talk face to face. Since >> >> that isn't practical <g> I have been trying to find options locally. >> >> Unfortunately, the closest one meets once a month and is in Seattle, >> >> which isn't quite as convenient as I would like it to be. >> >> >> >> The other night, while attending a girl scout overnight, I spent some >> >> early morning time chatting with another leader...and somewhere in the >> >> course of this conversation it came out that both of our daughters have >> >> OCD! While sharing stories (and boy, do some of these kids share >similar >> >> traits!) it really struck me how important it was to be able to talk to >> >> other parents openly and honestly about our kids. I would imagine there >> >> are enough kids with OCD in our area alone to make a support group >work. >> >> >> >> If anyone has experience in starting one and how one goes about that >> >> process please let me know. I know that some groups have a trained >> >> moderator (therapist, for example) but if that isn't possible I wonder >> >> if it is ok just to offer support...and acknowledge upfront that we are >> >> parents, not trained professionals, that we would not presume to tell >> >> parents what they " should " do, but we could point them in the direction >> >> of the professionals who could. >> >> >> >> What do you all think? >> >> >> >> Robin >subscribe OCD-L your name. >The archives for the OCD and >Parenting List may be accessed by going to > . >Enter your email address and password. >Click on the highlighted list name and then click on index. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2000 Report Share Posted February 7, 2000 Liz make sure to check out local resources via www.ocfoundation.org www.ocdhelp.org Suggest you join the TeenOCD List to see if any of the other over 200 members [i think] are in your area. Also, the List advisor Dr. Jim Hatton [dr.hat@...] is a master in OCD including support groups. Also, a new advisor/contributor to the TeenOCD List named is one who has started an OCD support group which just celebrated its 2nd anniversay. Good idea--best of luck!!!!!! jim in san diego jjmcf@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2001 Report Share Posted June 14, 2001 Have them contact Kathi at NVIC about being put in the vaccineinjuries egroup. Sandy ALL INFORMATION, DATA, AND MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR LEGAL ADVICE. THE DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH YOUR HEALTH CARE PROVIDER. Support Groups I just learned of someone who lost their child due to the second round of vaccines. They are asking if anyone knows of any online support groups for parents who have lost a child due to vaccines. Anybody know? So many children have lost their lives - there must be support groups somewhere. Kathleen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2001 Report Share Posted June 14, 2001 Thanks Sandy, I let her know about the NVIC group. I also advised her of your site and your quest for vaccine damage experiences. Kathleen In a message dated 6/14/2001 6:43:42 PM Central Daylight Time, sandym@... writes: > Have them contact Kathi at NVIC about being put in the > vaccineinjuries egroup. Sandy > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2001 Report Share Posted July 30, 2001 You are right, Rick, 36 years ago there was nothing. I did go to a mother's group with ARC, but the kids had various problems. I always went home feeling very lucky. But aside from that it was every parent for him/herself. No school, no financial aid, no therapy. We found Montessori school for when he was 3, and we learned how to do therapy in a program we had to travel a distance for, but most parents didn't do that. It was a lot different. Jessie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2001 Report Share Posted July 30, 2001 You are right, Rick, 36 years ago there was nothing. I did go to a mother's group with ARC, but the kids had various problems. I always went home feeling very lucky. But aside from that it was every parent for him/herself. No school, no financial aid, no therapy. We found Montessori school for when he was 3, and we learned how to do therapy in a program we had to travel a distance for, but most parents didn't do that. It was a lot different. Jessie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2001 Report Share Posted July 31, 2001 I think it was mentioned earlier in the list that parents flocked to the casual get-togethers to chat and compare stories, and not too many made the monthly meetings. I can understand that. We went to a support group in Ohio when the boys were born, and we really needed to hear that everything was going to be fine, you know, that ds wasn't a death sentence, whatever. The doctors were very grim, so we were hoping to become more comfortable with ds, and went looking to other parents. Well, the first meeting, all we did was listen to members fight about committees, and nothing about ds. The second meeting was a speaker from a later in life care facility. I guess you could say we were not impressed. What makes this list and the chat's so popular is we talk about the everyday things, and if we NEED questions answered, we have them...I think most of all, we are looking for friendship with people in the same place we are, not a bunch of do this and do that's. So if you want to increase membership attendance, go for the informal, and give up the speakers. Have a coffee and doughnuts night, or something. That's what we need... Just a little input from a mom who was looking for it, and couldn't find it, until I discovered the Internet! Beth Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2001 Report Share Posted July 31, 2001 I think it was mentioned earlier in the list that parents flocked to the casual get-togethers to chat and compare stories, and not too many made the monthly meetings. I can understand that. We went to a support group in Ohio when the boys were born, and we really needed to hear that everything was going to be fine, you know, that ds wasn't a death sentence, whatever. The doctors were very grim, so we were hoping to become more comfortable with ds, and went looking to other parents. Well, the first meeting, all we did was listen to members fight about committees, and nothing about ds. The second meeting was a speaker from a later in life care facility. I guess you could say we were not impressed. What makes this list and the chat's so popular is we talk about the everyday things, and if we NEED questions answered, we have them...I think most of all, we are looking for friendship with people in the same place we are, not a bunch of do this and do that's. So if you want to increase membership attendance, go for the informal, and give up the speakers. Have a coffee and doughnuts night, or something. That's what we need... Just a little input from a mom who was looking for it, and couldn't find it, until I discovered the Internet! Beth Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2001 Report Share Posted July 31, 2001 I'm in the process of starting a support group for adult adoptees in Northern Virginia. I was shocked to see how many showed up for the first meeting. We had a terrible storm that evening and I thought no one would come. For the next meeting, I made a survey to see what the group wanted. I'm not an adoptee, but a social worker who searches for birthparents and help facilitate reunions (and I can't believe I get paid to do this!). My goal (and hope) is for a leader to emerge and I can act as a liaison. We are working on pamphlets right now. So far, only those I have worked with have been invited. Once we get further off the ground, we'll open it up to anyone in Northern VA. Many similar support groups include birthparents as well. Our group decided not to include them at this time. So far, my group is not in it for the food, either. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2001 Report Share Posted July 31, 2001 I'm in the process of starting a support group for adult adoptees in Northern Virginia. I was shocked to see how many showed up for the first meeting. We had a terrible storm that evening and I thought no one would come. For the next meeting, I made a survey to see what the group wanted. I'm not an adoptee, but a social worker who searches for birthparents and help facilitate reunions (and I can't believe I get paid to do this!). My goal (and hope) is for a leader to emerge and I can act as a liaison. We are working on pamphlets right now. So far, only those I have worked with have been invited. Once we get further off the ground, we'll open it up to anyone in Northern VA. Many similar support groups include birthparents as well. Our group decided not to include them at this time. So far, my group is not in it for the food, either. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2001 Report Share Posted August 1, 2001 Hi, First of all I really want to say how helpful and fun this group really is. Some of my sentiments have already been expressed by other members. Like you're always here for us day or night on a holiday or weekend. The advice is great and the info is also great. I do miss the actual talking and I try to put in everyone's accent when i read something from them. So I think that meeting you most at the Suaree (oh she's on that again!), really helps put names to faces and people and it really helps. OK, as far as people groups not on the 'puter, when amanda was in EI/preschool, we had a great parent support group and it wasnt exclusive to kids with DS, but different disabilities of the kids that went to her school. When I lived in Florida for 7 miserable months, Ralph and I started our own very successful support group. We did everything together - had Thanksgiving, decorated for Christmas, had picnics. It was great. But then the elementary school years began. I lost my support group from preschool and nothing could replace it. There is an awesome DS group called Project Hope. I know most of the parents from the DS circles that we've been in including the streets. Yes I did say the streets. i know a lot of people who have either stopped me on the street or i have stopped them and given our number on a napkin or anything we could find. The parents from Project Hope have been bugging me and Ralph to come to their meetings which meet once a month. but you know, we dont have time, we're tired, blah blah. well, one day I met one of the moms on the street (again) and she said, " You must come to this meeting it's at the penthouse! " So ralph and i went out of curiosity to check out the penthouse. WOW!!!!!! Were we glad we went to that meeting! The penthouse (someone's house) was breathtaking!!!! The people in Project Hope are very nice. Lots of old timers who dont understand inclusion but are fasinated by it and a few babies, that me and ralph love. So yes, I do have a people to people group and I will be seeing them all soon at the Buddy Walk on Sept 30. One more thing. I also go to a Mother's group for all kids with disabilites. we are very informal and meet 2x a month. Usually at a coffee shop. we get to go out every now and then for mexican food too. The leader of the group wrote a grant and got money to fund it. But it usually is about food. food always gets people to come! Oh, Ralph is very resentful of that group. But I will save that for another time! ~ mom to 10 1/2 DS and jesse 7 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2001 Report Share Posted August 1, 2001 Hi, First of all I really want to say how helpful and fun this group really is. Some of my sentiments have already been expressed by other members. Like you're always here for us day or night on a holiday or weekend. The advice is great and the info is also great. I do miss the actual talking and I try to put in everyone's accent when i read something from them. So I think that meeting you most at the Suaree (oh she's on that again!), really helps put names to faces and people and it really helps. OK, as far as people groups not on the 'puter, when amanda was in EI/preschool, we had a great parent support group and it wasnt exclusive to kids with DS, but different disabilities of the kids that went to her school. When I lived in Florida for 7 miserable months, Ralph and I started our own very successful support group. We did everything together - had Thanksgiving, decorated for Christmas, had picnics. It was great. But then the elementary school years began. I lost my support group from preschool and nothing could replace it. There is an awesome DS group called Project Hope. I know most of the parents from the DS circles that we've been in including the streets. Yes I did say the streets. i know a lot of people who have either stopped me on the street or i have stopped them and given our number on a napkin or anything we could find. The parents from Project Hope have been bugging me and Ralph to come to their meetings which meet once a month. but you know, we dont have time, we're tired, blah blah. well, one day I met one of the moms on the street (again) and she said, " You must come to this meeting it's at the penthouse! " So ralph and i went out of curiosity to check out the penthouse. WOW!!!!!! Were we glad we went to that meeting! The penthouse (someone's house) was breathtaking!!!! The people in Project Hope are very nice. Lots of old timers who dont understand inclusion but are fasinated by it and a few babies, that me and ralph love. So yes, I do have a people to people group and I will be seeing them all soon at the Buddy Walk on Sept 30. One more thing. I also go to a Mother's group for all kids with disabilites. we are very informal and meet 2x a month. Usually at a coffee shop. we get to go out every now and then for mexican food too. The leader of the group wrote a grant and got money to fund it. But it usually is about food. food always gets people to come! Oh, Ralph is very resentful of that group. But I will save that for another time! ~ mom to 10 1/2 DS and jesse 7 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2003 Report Share Posted November 5, 2003 I was just working on topic ideas too. I am starting to lead the support group next week. I'm thinking of keeping the topics very short and focused to allow time for members to interact and share. EX's protein: why it's important and how to get it. Calcium. How much & what kind. Fluids. Invite psychologist. Invite bariatric surgeon for Q & A. Any ideas other have would be appreciated! , MS, RD, CDE > support groups > > Hi, > > I am looking for some good topics for my support group. Evidently > the person who ran the support group before me had topics each > month. Any ideas or info for topics would be greatly apprciated. > > Thanks > Tomiello Rd > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2003 Report Share Posted November 5, 2003 We've had good luck with inviting a plastic surgeon to talk about what they do with bariatric patients, these meetings are usually well attended. Also, at least once a year, someone comes to speak aobut exercise. >>> .@... 11/05/03 09:27AM >>> I was just working on topic ideas too. I am starting to lead the support group next week. I'm thinking of keeping the topics very short and focused to allow time for members to interact and share. EX's protein: why it's important and how to get it. Calcium. How much & what kind. Fluids. Invite psychologist. Invite bariatric surgeon for Q & A. Any ideas other have would be appreciated! , MS, RD, CDE > support groups > > Hi, > > I am looking for some good topics for my support group. Evidently > the person who ran the support group before me had topics each > month. Any ideas or info for topics would be greatly apprciated. > > Thanks > Tomiello Rd > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2006 Report Share Posted March 9, 2006 Does anyone have some good topics that they use for support groups? We are trying to re-format our program and offer more educational support at the beginning of our groups. Thanks in advance. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2006 Report Share Posted March 9, 2006 Our support group loves when our team psychologist, plastic surgeon or exercise physiologist talk. They also love cooking demonstrations and recipe modification. Grocery store tours are a big hit too. -----Original Message-----From: [mailto: ] On Behalf Of Sent: Thursday, March 09, 2006 2:35 PM Subject: re: support groups Does anyone have some good topics that they use for support groups? We are trying to re-format our program and offer more educational support at the beginning of our groups. Thanks in advance. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2006 Report Share Posted March 10, 2006 ,] We have a schedule made out for the rest of the year. Our topics range from Exercise, Body Image and Sexuality, Obesity in Children, Reconstructive Surgery, Self esteem and Addicition, Long term Weight Management, Holiday Planning, Vacation and Travel Planning, Holiday Planning. We have had great response so far. We also revamped our program this year. Hope this helps! Strakowski, MS,RD,LD Bariatric Dietitian Mount Carmel Health System Columbus, Ohio From: [mailto: ] On Behalf Of Sent: Thursday, March 09, 2006 3:35 PM To: Subject: re: support groups Does anyone have some good topics that they use for support groups? We are trying to re-format our program and offer more educational support at the beginning of our groups. Thanks in advance. ============================================================================== "This electronic message transmission contains confidential or privileged information from Mount Carmel . The information is intended for use by the individual or entity named above. If you are not the intended recipient, be aware that any disclosure, copying, distribution or use of the contents of this information is prohibited. If you have received this electronic transmission in error, please notify us immediately by telephone (614-234-8700) or by electronic mail (exchange@...)." ============================================================================== Quote Link to comment Share on other sites More sharing options...
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