Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 I think that is one of the hardest things; trying to balance work and kids with special needs. If I did not have a flexible boss (who happens to be Dylan's Godfather) I would have been fired long ago, for all the time I take off for appts, when he is feeling off etc. Even so, I know that a lot of Dylan's learned helplessness happened after I increased my hours from 24 - 32/ week. I am always feeling like I haven't gotten my hours in for work and I haven't done enough with Dylan. I am sure your being home will benefit Patty, but it is a bit sad that even now as an adult it still requires that you not work. Kim L > I have decided to make a few changes in our lives. Patty continues to sit > here at home. She got turned down for a transportation program in MA because > we > didn't have a doctor's note... It is complicated. Without this ride she > can't get to medical appointments, or any where! The MA commission for the > Blind > is going to try to fix that, but they should have done it in the first place. > I work in the city and leave at 5:45 to get home at 5:15. And still Patty > sits. The squeeky wheel gets the greese and I haven't been that. I have been > just too tired to fight. Not much longer though! > I took a day off and went to social security with her. They never > changed her address. Wouldn't you believe they finally did which means a > change in > SSI of over $300 more a month! That is still far below the standard of living > but who the heck cares. > Then I also got her a MA Identification card and a transit pass. > I also took another day off to take her to a vocational program in MA. > This lady is great. But the point is I had to drive Patty there or she would > have had to wait longer. So I have put in my resignation. I think it is > almost abusive for us to have her sit here with little to do. We as a family > have > kept her busy but that shouldn't be. > My last day is going to be the 23rd! > > I have a feeling Patty's life is going to be good soon. > > Bonnie, mother to a 21 and going to be a senior at college, Patty > CHARGE 19, and wife to who is happy with my quitting because he won't > have to > do the laundry, cleaning and cooking much longer! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 I think that is one of the hardest things; trying to balance work and kids with special needs. If I did not have a flexible boss (who happens to be Dylan's Godfather) I would have been fired long ago, for all the time I take off for appts, when he is feeling off etc. Even so, I know that a lot of Dylan's learned helplessness happened after I increased my hours from 24 - 32/ week. I am always feeling like I haven't gotten my hours in for work and I haven't done enough with Dylan. I am sure your being home will benefit Patty, but it is a bit sad that even now as an adult it still requires that you not work. Kim L > I have decided to make a few changes in our lives. Patty continues to sit > here at home. She got turned down for a transportation program in MA because > we > didn't have a doctor's note... It is complicated. Without this ride she > can't get to medical appointments, or any where! The MA commission for the > Blind > is going to try to fix that, but they should have done it in the first place. > I work in the city and leave at 5:45 to get home at 5:15. And still Patty > sits. The squeeky wheel gets the greese and I haven't been that. I have been > just too tired to fight. Not much longer though! > I took a day off and went to social security with her. They never > changed her address. Wouldn't you believe they finally did which means a > change in > SSI of over $300 more a month! That is still far below the standard of living > but who the heck cares. > Then I also got her a MA Identification card and a transit pass. > I also took another day off to take her to a vocational program in MA. > This lady is great. But the point is I had to drive Patty there or she would > have had to wait longer. So I have put in my resignation. I think it is > almost abusive for us to have her sit here with little to do. We as a family > have > kept her busy but that shouldn't be. > My last day is going to be the 23rd! > > I have a feeling Patty's life is going to be good soon. > > Bonnie, mother to a 21 and going to be a senior at college, Patty > CHARGE 19, and wife to who is happy with my quitting because he won't > have to > do the laundry, cleaning and cooking much longer! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 I think that is one of the hardest things; trying to balance work and kids with special needs. If I did not have a flexible boss (who happens to be Dylan's Godfather) I would have been fired long ago, for all the time I take off for appts, when he is feeling off etc. Even so, I know that a lot of Dylan's learned helplessness happened after I increased my hours from 24 - 32/ week. I am always feeling like I haven't gotten my hours in for work and I haven't done enough with Dylan. I am sure your being home will benefit Patty, but it is a bit sad that even now as an adult it still requires that you not work. Kim L > I have decided to make a few changes in our lives. Patty continues to sit > here at home. She got turned down for a transportation program in MA because > we > didn't have a doctor's note... It is complicated. Without this ride she > can't get to medical appointments, or any where! The MA commission for the > Blind > is going to try to fix that, but they should have done it in the first place. > I work in the city and leave at 5:45 to get home at 5:15. And still Patty > sits. The squeeky wheel gets the greese and I haven't been that. I have been > just too tired to fight. Not much longer though! > I took a day off and went to social security with her. They never > changed her address. Wouldn't you believe they finally did which means a > change in > SSI of over $300 more a month! That is still far below the standard of living > but who the heck cares. > Then I also got her a MA Identification card and a transit pass. > I also took another day off to take her to a vocational program in MA. > This lady is great. But the point is I had to drive Patty there or she would > have had to wait longer. So I have put in my resignation. I think it is > almost abusive for us to have her sit here with little to do. We as a family > have > kept her busy but that shouldn't be. > My last day is going to be the 23rd! > > I have a feeling Patty's life is going to be good soon. > > Bonnie, mother to a 21 and going to be a senior at college, Patty > CHARGE 19, and wife to who is happy with my quitting because he won't > have to > do the laundry, cleaning and cooking much longer! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 It is too bad, Bonnie, that Patti cannot get the help she needs otherwise but I know she will be thrilled to hav eyou there with her. Kay Life will change soon > I have decided to make a few changes in our lives. Patty continues to sit > here at home. She got turned down for a transportation program in MA because we > didn't have a doctor's note... It is complicated. Without this ride she > can't get to medical appointments, or any where! The MA commission for the Blind > is going to try to fix that, but they should have done it in the first place. > I work in the city and leave at 5:45 to get home at 5:15. And still Patty > sits. The squeeky wheel gets the greese and I haven't been that. I have been > just too tired to fight. Not much longer though! > I took a day off and went to social security with her. They never > changed her address. Wouldn't you believe they finally did which means a change in > SSI of over $300 more a month! That is still far below the standard of living > but who the heck cares. > Then I also got her a MA Identification card and a transit pass. > I also took another day off to take her to a vocational program in MA. > This lady is great. But the point is I had to drive Patty there or she would > have had to wait longer. So I have put in my resignation. I think it is > almost abusive for us to have her sit here with little to do. We as a family have > kept her busy but that shouldn't be. > My last day is going to be the 23rd! > > I have a feeling Patty's life is going to be good soon. > > Bonnie, mother to a 21 and going to be a senior at college, Patty > CHARGE 19, and wife to who is happy with my quitting because he won't have to > do the laundry, cleaning and cooking much longer! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 It is too bad, Bonnie, that Patti cannot get the help she needs otherwise but I know she will be thrilled to hav eyou there with her. Kay Life will change soon > I have decided to make a few changes in our lives. Patty continues to sit > here at home. She got turned down for a transportation program in MA because we > didn't have a doctor's note... It is complicated. Without this ride she > can't get to medical appointments, or any where! The MA commission for the Blind > is going to try to fix that, but they should have done it in the first place. > I work in the city and leave at 5:45 to get home at 5:15. And still Patty > sits. The squeeky wheel gets the greese and I haven't been that. I have been > just too tired to fight. Not much longer though! > I took a day off and went to social security with her. They never > changed her address. Wouldn't you believe they finally did which means a change in > SSI of over $300 more a month! That is still far below the standard of living > but who the heck cares. > Then I also got her a MA Identification card and a transit pass. > I also took another day off to take her to a vocational program in MA. > This lady is great. But the point is I had to drive Patty there or she would > have had to wait longer. So I have put in my resignation. I think it is > almost abusive for us to have her sit here with little to do. We as a family have > kept her busy but that shouldn't be. > My last day is going to be the 23rd! > > I have a feeling Patty's life is going to be good soon. > > Bonnie, mother to a 21 and going to be a senior at college, Patty > CHARGE 19, and wife to who is happy with my quitting because he won't have to > do the laundry, cleaning and cooking much longer! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 Bonnie- I'm sorry you have to make these kind of decisions. It's frustrating for all of us to have to choose between a job or career and our child. I know all mom's face this decision, but it's that big DIF again (Duration, Intensity, Frequency). You wouldn't expect to be making this choice when your child is 19. I wouldn't even expect to still be facing that choice with Aubrie at 6! I'm sure it felt good to be " out on your own " for a bit. But hopefully it'll be a comfortable fit for all of you when you are back home again. I often find myself reminded that I (and our family) just can't do all of the things that regular people do because of the time and energy required to deal with CHARGE. I almost said " to deal with Aubrie " -- but it's not really her -- it's CHARGE. BTW-- We'll be at Perkins for an eval the week before Columbus Day. If you are close enough, it'd be wonderful to have a visit! Michele W Aubrie's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 Bonnie- I'm sorry you have to make these kind of decisions. It's frustrating for all of us to have to choose between a job or career and our child. I know all mom's face this decision, but it's that big DIF again (Duration, Intensity, Frequency). You wouldn't expect to be making this choice when your child is 19. I wouldn't even expect to still be facing that choice with Aubrie at 6! I'm sure it felt good to be " out on your own " for a bit. But hopefully it'll be a comfortable fit for all of you when you are back home again. I often find myself reminded that I (and our family) just can't do all of the things that regular people do because of the time and energy required to deal with CHARGE. I almost said " to deal with Aubrie " -- but it's not really her -- it's CHARGE. BTW-- We'll be at Perkins for an eval the week before Columbus Day. If you are close enough, it'd be wonderful to have a visit! Michele W Aubrie's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2004 Report Share Posted July 3, 2004 Bonnie- I'm sorry you have to make these kind of decisions. It's frustrating for all of us to have to choose between a job or career and our child. I know all mom's face this decision, but it's that big DIF again (Duration, Intensity, Frequency). You wouldn't expect to be making this choice when your child is 19. I wouldn't even expect to still be facing that choice with Aubrie at 6! I'm sure it felt good to be " out on your own " for a bit. But hopefully it'll be a comfortable fit for all of you when you are back home again. I often find myself reminded that I (and our family) just can't do all of the things that regular people do because of the time and energy required to deal with CHARGE. I almost said " to deal with Aubrie " -- but it's not really her -- it's CHARGE. BTW-- We'll be at Perkins for an eval the week before Columbus Day. If you are close enough, it'd be wonderful to have a visit! Michele W Aubrie's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 4, 2004 Report Share Posted July 4, 2004 Bonnie, Your life changes are in my prayers. Sounds like a good plan but only you would know for sure. Lynn Life will change soon I have decided to make a few changes in our lives. Patty continues to sit here at home. She got turned down for a transportation program in MA because we didn't have a doctor's note... It is complicated. Without this ride she can't get to medical appointments, or any where! The MA commission for the Blind is going to try to fix that, but they should have done it in the first place. I work in the city and leave at 5:45 to get home at 5:15. And still Patty sits. The squeeky wheel gets the greese and I haven't been that. I have been just too tired to fight. Not much longer though! I took a day off and went to social security with her. They never changed her address. Wouldn't you believe they finally did which means a change in SSI of over $300 more a month! That is still far below the standard of living but who the heck cares. Then I also got her a MA Identification card and a transit pass. I also took another day off to take her to a vocational program in MA. This lady is great. But the point is I had to drive Patty there or she would have had to wait longer. So I have put in my resignation. I think it is almost abusive for us to have her sit here with little to do. We as a family have kept her busy but that shouldn't be. My last day is going to be the 23rd! I have a feeling Patty's life is going to be good soon. Bonnie, mother to a 21 and going to be a senior at college, Patty CHARGE 19, and wife to who is happy with my quitting because he won't have to do the laundry, cleaning and cooking much longer! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 4, 2004 Report Share Posted July 4, 2004 My mind has gone blank. When is Columbus Day? I'd love to meet another CHARGE parent - you would be my first! comes home for August and goes back to Perkins after Labor Day. Will you be staying in a guest house? Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Martha, How is it that you have not met the other parents??? I am shocked and embarrassed!! For as often as you are, there are parents of the other CHARGE kids here all the time. PLease let me arrange this for you--Oh my gosh, I cannot believe it!!! Let me know when you are arriving to get Kate and I'll see what I can do. In the meantime, I am glad that things are moving ahead with you regarding Kate's transition--I am assuming that you are using Sue Summersby and will let people know what you need. I am off to get my things together for school tomorrow. And to spend some time with your long-legged girl tomorrow in the testing room. pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Martha, How is it that you have not met the other parents??? I am shocked and embarrassed!! For as often as you are, there are parents of the other CHARGE kids here all the time. PLease let me arrange this for you--Oh my gosh, I cannot believe it!!! Let me know when you are arriving to get Kate and I'll see what I can do. In the meantime, I am glad that things are moving ahead with you regarding Kate's transition--I am assuming that you are using Sue Summersby and will let people know what you need. I am off to get my things together for school tomorrow. And to spend some time with your long-legged girl tomorrow in the testing room. pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Pam: It was so good to see your post. I've just realized that Andy and I have met Will's mother (however briefly - and the two kiddos aren't that similar), but that's it. I would love to connect with parents not just on the CHARGE list. We get in on the evening of the 19th and don't leave until the 23rd (because of differing fares). 's IEP is on the 21st at 1:00 your time, I think. I assume that you'll be seeing in the testing room for the eval. I'd forgotten all about that! As things wind down for the year, I think Andy and I just get more and more forgetful - or more odd; that's more likely! Sharon Streett is still researching comp ed for and will make up her mind prior to the IEP. Please let know. I don't know what the legal issues are, but Andy and I remembered today that the district and state let go for many months without even offering a program. This is when we had K. at home, and Sharon provided her psychologist, etc. On a brighter note, our extremely neurotic Airedale who has always declined to climb our stairs, has suddenly decided to do so when it thunders. Alas, the year old " puppy " joins him and also joins us in our bed. We've laughed and laughed --- lord only knows how will handle the change...Life in the midwest is peculiar. In New Orleans, my brother put his St. Bernard (wouldn't cross doorways) on Prozac. Here, we just laugh. Umm. I wonder if OCD just runs in family dogs and is transmitted to the rest of us... Can't wait to see everyone! Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Pam: It was so good to see your post. I've just realized that Andy and I have met Will's mother (however briefly - and the two kiddos aren't that similar), but that's it. I would love to connect with parents not just on the CHARGE list. We get in on the evening of the 19th and don't leave until the 23rd (because of differing fares). 's IEP is on the 21st at 1:00 your time, I think. I assume that you'll be seeing in the testing room for the eval. I'd forgotten all about that! As things wind down for the year, I think Andy and I just get more and more forgetful - or more odd; that's more likely! Sharon Streett is still researching comp ed for and will make up her mind prior to the IEP. Please let know. I don't know what the legal issues are, but Andy and I remembered today that the district and state let go for many months without even offering a program. This is when we had K. at home, and Sharon provided her psychologist, etc. On a brighter note, our extremely neurotic Airedale who has always declined to climb our stairs, has suddenly decided to do so when it thunders. Alas, the year old " puppy " joins him and also joins us in our bed. We've laughed and laughed --- lord only knows how will handle the change...Life in the midwest is peculiar. In New Orleans, my brother put his St. Bernard (wouldn't cross doorways) on Prozac. Here, we just laugh. Umm. I wonder if OCD just runs in family dogs and is transmitted to the rest of us... Can't wait to see everyone! Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 > Some of us need to think about setting up an ever-so-wonderful place for our > adult children. I just don't believe it would be impossible! Any thoughts? In Canada, the late 80's many of the children with Rubella were graduating the same year. At the residential school we did set up " off-campus " transition programs to ease the jump into adult life. At this time, many of the parents got together and petitioned the gov't for funding for adult supported living. They developed their own non-profit agency. With the initial funding they were able to buy three houses across Toronto, with 3 young adults and support staff in each house, and also were able to hire experienced staff for administration and training. Now the program continues to grow, but the houses are rented using part of the pension. Many houses do their own fundraising with the young adults to support extra living expenses for fun things. They have job placements, attend courses, go to exercises clubs, etc. with support staff. Another group of parents started a non-profit agency, where initially it was a whole apartment building, with separate units. Support was interchangable in the units, but most recieved one to one in order to access the community.The LIONS Club helped to fund the initial costs. They have since moved to a one floor facility newly built, again with the help of the LIONS Club, with ~10 little apartments, and some common areas for such things as crafts, woodworking, group meals when wanted, etc... Still other parents choose to make their own separate setting, and have more control of the program. They run administration costs and funding through a larger agency for deafblind. The individual lives in her own apartment with roommates from the University, all chosen by the parents. These students help cover the overnights, getting reduced rent, and also get paid to work some of the recreational hours to go swimming, play table pool, exercise club, etc.. There is also a one-to-one for 7-3 to help the indivudal go to community courses such as pottery, computer classes, attend job placements, and goes to the literacy course offered by CNIB. Others have opted for their children to be at home, using support staff when in the community, and still others made apartments within their home, using gov't money to help renovate. Good luck thinking about these very difficult decisions. Ann Gloyn Specialist Teacher Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Columbus Day is in October. We'll be at Perkins Oct 4-6. We'll arrive before 5pm on the 4th with the eve free. Evals on Tues. Wed is " overflow " day for anything we don't get done or discussed on Tues. We'll leave Wed pm by train. I hope to stay in guest housing. I'd love to meet you if you are able to be around then! Sounds like Pam will try to hook you up with another CHARGE family or 2 in the meantime. Take care! Michele W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Columbus Day is in October. We'll be at Perkins Oct 4-6. We'll arrive before 5pm on the 4th with the eve free. Evals on Tues. Wed is " overflow " day for anything we don't get done or discussed on Tues. We'll leave Wed pm by train. I hope to stay in guest housing. I'd love to meet you if you are able to be around then! Sounds like Pam will try to hook you up with another CHARGE family or 2 in the meantime. Take care! Michele W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Columbus Day is in October. We'll be at Perkins Oct 4-6. We'll arrive before 5pm on the 4th with the eve free. Evals on Tues. Wed is " overflow " day for anything we don't get done or discussed on Tues. We'll leave Wed pm by train. I hope to stay in guest housing. I'd love to meet you if you are able to be around then! Sounds like Pam will try to hook you up with another CHARGE family or 2 in the meantime. Take care! Michele W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 WOW!!!!! In AZ there is only one group home in the whole state. It was started by a brother for his sibling (age 50). He made the family home that he and his sister had been living in, into a group home and he moved out. Now another adult client lives there and they hire staff to come in and work with them, although training in deafblindness is an ongoing issue. Kim L > >> Some of us need to think about setting up an ever-so-wonderful place > for our >> adult children. I just don't believe it would be impossible! Any > thoughts? > > In Canada, the late 80's many of the children with Rubella were > graduating the same year. At the residential school we did set up > " off-campus " transition programs to ease the jump into adult life. At > this time, many of the parents got together and petitioned the gov't > for funding for adult supported living. They developed their own > non-profit agency. With the initial funding they were able to buy > three houses across Toronto, with 3 young adults and support staff in > each house, and also were able to hire experienced staff for > administration and training. Now the program continues to grow, but > the houses are rented using part of the pension. Many houses do their > own fundraising with the young adults to support extra living expenses > for fun things. They have job placements, attend courses, go to > exercises clubs, etc. with support staff. Another group of parents > started a non-profit agency, where initially it was a whole apartment > building, with separate units. Support was interchangable in the > units, but most recieved one to one in order to access the > community.The LIONS Club helped to fund the initial costs. They have > since moved to a one floor facility newly built, again with the help > of the LIONS Club, with ~10 little apartments, and some common areas > for such things as crafts, woodworking, group meals when wanted, > etc... Still other parents choose to make their own separate setting, > and have more control of the program. They run administration costs > and funding through a larger agency for deafblind. The individual > lives in her own apartment with roommates from the University, all > chosen by the parents. These students help cover the overnights, > getting reduced rent, and also get paid to work some of the > recreational hours to go swimming, play table pool, exercise club, > etc.. There is also a one-to-one for 7-3 to help the indivudal go to > community courses such as pottery, computer classes, attend job > placements, and goes to the literacy course offered by CNIB. > Others have opted for their children to be at home, using support > staff when in the community, and still others made apartments within > their home, using gov't money to help renovate. > Good luck thinking about these very difficult decisions. > Ann Gloyn > Specialist Teacher > Canada > > > > > Membership of this email support groups does not constitute membership in the > CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 WOW!!!!! In AZ there is only one group home in the whole state. It was started by a brother for his sibling (age 50). He made the family home that he and his sister had been living in, into a group home and he moved out. Now another adult client lives there and they hire staff to come in and work with them, although training in deafblindness is an ongoing issue. Kim L > >> Some of us need to think about setting up an ever-so-wonderful place > for our >> adult children. I just don't believe it would be impossible! Any > thoughts? > > In Canada, the late 80's many of the children with Rubella were > graduating the same year. At the residential school we did set up > " off-campus " transition programs to ease the jump into adult life. At > this time, many of the parents got together and petitioned the gov't > for funding for adult supported living. They developed their own > non-profit agency. With the initial funding they were able to buy > three houses across Toronto, with 3 young adults and support staff in > each house, and also were able to hire experienced staff for > administration and training. Now the program continues to grow, but > the houses are rented using part of the pension. Many houses do their > own fundraising with the young adults to support extra living expenses > for fun things. They have job placements, attend courses, go to > exercises clubs, etc. with support staff. Another group of parents > started a non-profit agency, where initially it was a whole apartment > building, with separate units. Support was interchangable in the > units, but most recieved one to one in order to access the > community.The LIONS Club helped to fund the initial costs. They have > since moved to a one floor facility newly built, again with the help > of the LIONS Club, with ~10 little apartments, and some common areas > for such things as crafts, woodworking, group meals when wanted, > etc... Still other parents choose to make their own separate setting, > and have more control of the program. They run administration costs > and funding through a larger agency for deafblind. The individual > lives in her own apartment with roommates from the University, all > chosen by the parents. These students help cover the overnights, > getting reduced rent, and also get paid to work some of the > recreational hours to go swimming, play table pool, exercise club, > etc.. There is also a one-to-one for 7-3 to help the indivudal go to > community courses such as pottery, computer classes, attend job > placements, and goes to the literacy course offered by CNIB. > Others have opted for their children to be at home, using support > staff when in the community, and still others made apartments within > their home, using gov't money to help renovate. > Good luck thinking about these very difficult decisions. > Ann Gloyn > Specialist Teacher > Canada > > > > > Membership of this email support groups does not constitute membership in the > CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 WOW!!!!! In AZ there is only one group home in the whole state. It was started by a brother for his sibling (age 50). He made the family home that he and his sister had been living in, into a group home and he moved out. Now another adult client lives there and they hire staff to come in and work with them, although training in deafblindness is an ongoing issue. Kim L > >> Some of us need to think about setting up an ever-so-wonderful place > for our >> adult children. I just don't believe it would be impossible! Any > thoughts? > > In Canada, the late 80's many of the children with Rubella were > graduating the same year. At the residential school we did set up > " off-campus " transition programs to ease the jump into adult life. At > this time, many of the parents got together and petitioned the gov't > for funding for adult supported living. They developed their own > non-profit agency. With the initial funding they were able to buy > three houses across Toronto, with 3 young adults and support staff in > each house, and also were able to hire experienced staff for > administration and training. Now the program continues to grow, but > the houses are rented using part of the pension. Many houses do their > own fundraising with the young adults to support extra living expenses > for fun things. They have job placements, attend courses, go to > exercises clubs, etc. with support staff. Another group of parents > started a non-profit agency, where initially it was a whole apartment > building, with separate units. Support was interchangable in the > units, but most recieved one to one in order to access the > community.The LIONS Club helped to fund the initial costs. They have > since moved to a one floor facility newly built, again with the help > of the LIONS Club, with ~10 little apartments, and some common areas > for such things as crafts, woodworking, group meals when wanted, > etc... Still other parents choose to make their own separate setting, > and have more control of the program. They run administration costs > and funding through a larger agency for deafblind. The individual > lives in her own apartment with roommates from the University, all > chosen by the parents. These students help cover the overnights, > getting reduced rent, and also get paid to work some of the > recreational hours to go swimming, play table pool, exercise club, > etc.. There is also a one-to-one for 7-3 to help the indivudal go to > community courses such as pottery, computer classes, attend job > placements, and goes to the literacy course offered by CNIB. > Others have opted for their children to be at home, using support > staff when in the community, and still others made apartments within > their home, using gov't money to help renovate. > Good luck thinking about these very difficult decisions. > Ann Gloyn > Specialist Teacher > Canada > > > > > Membership of this email support groups does not constitute membership in the > CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2004 Report Share Posted July 6, 2004 Martha, I didn't want to scare you. I think you are tons ahead of us because you have the only appropriate educational placement for our CHARGErs. Because of their vast knowledge, etc., you will be having an appropriate transition for your child. I often say Perkins is the best and I shouldn't. Really I should say they are the only " most appropriate, least restrictive... " You get the point. No one or no where else could ever do what they do. Life is scary when our children get older. But because of them she has opportunities to have a fulfilling and happy life. I know what your are feeling. Everyone gets older though and life continues to move forward no matter what we do. Our story is unique in that we also moved. We moved for Patty but we still have to get things going. Yes, I have to still battle for Patty. But I also have to work things out for our other daughter, a. I have to make sure she does her financial paperwork so she can attend college. I have to make sure she is mentally, physically and spiritually content in her life. As a mother I don't think you ever stop worrying about your children. But our CHARGE children are so often misunderstood. It is understanding I fight for. You are already ahead of the game. All you really want is for your daughter to have a life in which she is content and fulfilled no matter what her abilities/disabilities she has. And this life should be a life without her parents total involvement. How to make that happen is up to whatever her individual needs are. You will find it. I am sure. It all will work out. Take it one step at a time. And then, Just breathe! Best of luck. Bonnie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2004 Report Share Posted July 6, 2004 They prefer to call them " programs " and for some, " adult supportive-independant living " to distinguish what community living (for those with cognitive impairment) offer with " group homes " . For those with combined vision/hearing problems the " support " is more in the form of helping them get information they are missing, in order that they can follow through with their independance. It is never suppose to mean " doing-for " . It is also meant to be a community integration approach, and realistic to " giving back " to society while interacting within the community. (volunteerism) Considering they get a chunk of gov't funding plus charitable gifts that makes sense. There are a bunch of children with CHARGE around the same age in the US. Has anyone thought of approaching the CHARGE Foundation to place " service delivery " in their strategic plan for the future? " CHARGE " -centered adult support " programs " , or gov't subsidized living arrangements with continued learning programs and services specific to CHARGE. I'm not sure with US laws, you may need to be a charity rather then Foundation to do that. " DREAM PROACTIVELY!!! " Ann Gloyn DB and Spec Ed Specialist CANADA > WOW!!!!! In AZ there is only one group home in the whole state. It was > started by a brother for his sibling (age 50). He made the family home that > he and his sister had been living in, into a group home and he moved out. > Now another adult client lives there and they hire staff to come in and work > with them, although training in deafblindness is an ongoing issue. > > Kim L > > > > > > >> Some of us need to think about setting up an ever-so-wonderful place > > for our > >> adult children. I just don't believe it would be impossible! Any > > thoughts? > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2004 Report Share Posted July 6, 2004 They prefer to call them " programs " and for some, " adult supportive-independant living " to distinguish what community living (for those with cognitive impairment) offer with " group homes " . For those with combined vision/hearing problems the " support " is more in the form of helping them get information they are missing, in order that they can follow through with their independance. It is never suppose to mean " doing-for " . It is also meant to be a community integration approach, and realistic to " giving back " to society while interacting within the community. (volunteerism) Considering they get a chunk of gov't funding plus charitable gifts that makes sense. There are a bunch of children with CHARGE around the same age in the US. Has anyone thought of approaching the CHARGE Foundation to place " service delivery " in their strategic plan for the future? " CHARGE " -centered adult support " programs " , or gov't subsidized living arrangements with continued learning programs and services specific to CHARGE. I'm not sure with US laws, you may need to be a charity rather then Foundation to do that. " DREAM PROACTIVELY!!! " Ann Gloyn DB and Spec Ed Specialist CANADA > WOW!!!!! In AZ there is only one group home in the whole state. It was > started by a brother for his sibling (age 50). He made the family home that > he and his sister had been living in, into a group home and he moved out. > Now another adult client lives there and they hire staff to come in and work > with them, although training in deafblindness is an ongoing issue. > > Kim L > > > > > > >> Some of us need to think about setting up an ever-so-wonderful place > > for our > >> adult children. I just don't believe it would be impossible! Any > > thoughts? > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2004 Report Share Posted July 6, 2004 Ann, Thanks for that post. As soon I finish my last day at work it looks like I will be doing some research. Thanks tons. Bonnie Quote Link to comment Share on other sites More sharing options...
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