Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 I'm sad to read this and it makes me realize what I may have coming with my HOH 3 year old twins... I think it is a good idea to give the copied info. to the counselor. You can't have thousands of dollars of hearing equipment getting damaged by a down pour! You don't sound overbearing to me. I am a teacher by profession. You sound like a parent should sound, and the fact that you haven't gotten angrier makes me think that you will not come off as overbearing. I question why a five year old is left at a lunch table alone with other kids. Doesn't sound too structured. I wonder if they have even told the kids that age what the bathroom routine would be - kids that age need a lot of direction, handholding, adn reminding in general. I wonder what other parents of kids (not hearing impaired) that age are thinking about the camp. And yes your son will need some extra help. It goes with this. You (we) shouldn't feel bad about that. Go advocate! You sound intelligent and sensitive and I believe that you will come off just fine! Cathy > > At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. > > My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. > > Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. > > The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. > > This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. > > Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. > > Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. > > How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. > > I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. > > K > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 Oh - hugs to you. I know just how you feel. I remember when Tom was that age (5 or maybe 6 - he was in first grade) being left on the playground in the sandbox playing by himself at dusk at the after school program - grrrrrrrrr! I was so angry, I could hardly see straight. Worse is when you know he's not being included or missing stuff - it's such a sinking feeling. In reading what you gave the counsellor, I wonder if you could make it shorter. (this is of course not having seen it!) In my experience, if you give too much information to teachers, particularly ones who've not worked with HI/deaf kids before (who come with technology!) it can be overwhelming. I do a short list with each point bulleted and that's seemed to help. So for example you might do something like this: Processor: * can't get wet * when swimming, put in white container In class: * Be sure is setting next to you in circle (or wherever you like him to be) * Repeat any questions asked so he can hear etc. We found that helped with our boys a bunch! Good luck - and keep us posted? Barbara Kearns wrote: > At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. > > My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. > > Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over ! > the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. > > The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. > > This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. > > Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his! > lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just di! > dn't hear it. I bet he didn't even SEE it either. I just said, " I gu > ess he didn't hear them, " and I think she realized the problem. > > Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. > > How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. > > I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. > > K > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 , My heart goes out to you and your experience brought tears to my eyes. I wish I could give you great advice, but as my son ( also) is newly diagnosed and is just 2.5 yr old we haven't experienced any of this yet. I will say that you don't come across at all as an over-the-top mom. Until your son is old/mature enough to advocate for himself, you are going to have to do it for him. I wish the camp director were being more helpful. I think your idea of a note that you could give to the counselor is a good idea - providing it is brief. Then s/he can read it during a slow moment in the morning. Or are the counselors available right from the start, like could you arrive 15 min early and maybe get to him/her for 5 min before the chaos begins? Perhaps you could role play at home too with on how he could ask for help? Like I said, I have no experience at this and have no idea what works best, these are just ideas off the top of my head. Good luck! Sherry camp experience At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. K Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 In a message dated 6/26/2006 2:33:13 P.M. Central Standard Time, lisak555@... writes: just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. , I had a similar situation when I went to day camp for Girl Scouts. I was left out of a lot of things because I couldn't hear the change in routine or activities. Looking back, I think it would have been so helpful to have a counselor come up to me each time and summarize what was happening next, but my mom wasn't even aware of what was happening so she couldn't advocate. I can remember going through so many crafts where I didn't know what to do and constantly had to look around to figure out how to make things because I didn't hear the directions. I can also remember just moving my mouth and pretending to sing songs because again, I had no clue what the words were. I can remember nature hikes where the counselors were talking about trees and plants, but I just skipped along. Do you think you'd be able to volunteer for a day and perhaps provide some input to the counselors as you work with them? You're not asking for special treatment-- you're asking the counselors to level the playing field so your child has access to communication during his day. Putz Illinois Families for Hands & Voices _www.handsandvoices.org_ (http://www.handsandvoices.org/) _www.ilhandsandvoices.org_ (http://www.ilhandsandvoices.org/) Email: support@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 In a message dated 6/26/2006 2:33:13 P.M. Central Standard Time, lisak555@... writes: just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. , I had a similar situation when I went to day camp for Girl Scouts. I was left out of a lot of things because I couldn't hear the change in routine or activities. Looking back, I think it would have been so helpful to have a counselor come up to me each time and summarize what was happening next, but my mom wasn't even aware of what was happening so she couldn't advocate. I can remember going through so many crafts where I didn't know what to do and constantly had to look around to figure out how to make things because I didn't hear the directions. I can also remember just moving my mouth and pretending to sing songs because again, I had no clue what the words were. I can remember nature hikes where the counselors were talking about trees and plants, but I just skipped along. Do you think you'd be able to volunteer for a day and perhaps provide some input to the counselors as you work with them? You're not asking for special treatment-- you're asking the counselors to level the playing field so your child has access to communication during his day. Putz Illinois Families for Hands & Voices _www.handsandvoices.org_ (http://www.handsandvoices.org/) _www.ilhandsandvoices.org_ (http://www.ilhandsandvoices.org/) Email: support@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 In a message dated 6/26/2006 2:33:13 P.M. Central Standard Time, lisak555@... writes: just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. , I had a similar situation when I went to day camp for Girl Scouts. I was left out of a lot of things because I couldn't hear the change in routine or activities. Looking back, I think it would have been so helpful to have a counselor come up to me each time and summarize what was happening next, but my mom wasn't even aware of what was happening so she couldn't advocate. I can remember going through so many crafts where I didn't know what to do and constantly had to look around to figure out how to make things because I didn't hear the directions. I can also remember just moving my mouth and pretending to sing songs because again, I had no clue what the words were. I can remember nature hikes where the counselors were talking about trees and plants, but I just skipped along. Do you think you'd be able to volunteer for a day and perhaps provide some input to the counselors as you work with them? You're not asking for special treatment-- you're asking the counselors to level the playing field so your child has access to communication during his day. Putz Illinois Families for Hands & Voices _www.handsandvoices.org_ (http://www.handsandvoices.org/) _www.ilhandsandvoices.org_ (http://www.ilhandsandvoices.org/) Email: support@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 Yes, you should talk to the counselor and tell the director what's going on and why. You are not being overbearing, but if you think you are tell the counselor that. Hayley went to a typical day care/camp in Calif for years and while she did not have the oral/aural ability that has, I had relationships with the counselors assigned to her group. The counselors need to know that wears expensive equipment and how to take care of it. In fact, we went back last week when we were visiting (got to see Yuka on this list ) and was surprised to see one of the counselors who bonded with Hayley (and signed) back at the camp. She told me she is now an interpreter in Fresno. Don't discount the counselors because they are younger. They might have deaf kids in their classrooms. They might actually know more about it than the camp director. mary > > At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. > > My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. > > Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. > > The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. > > This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. > > Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. > > Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. > > How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. > > I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. > > K > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 , I'm sorry you've had a bad experience with summer camp. We put our 5 year old daughter in camp for the first time this summer and I was very leery. I got the blank stare on the first day when I met the teacher and gave my very brief run down of what the implant was all about. For some odd reason they perked up and listened intently when I mentioned the cost to replace a processor and how important the things that I've been explaining are. I also put a page of info together to keep in 's backpack, but positioned it as more of a troubleshooting guide. Stick with it and continue to advocate for your son. Randi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 , {Hugs} is only 6 months so I am a long way from this experience, but I am writing from the other point. I used to work in summer camps (counselor, unit head and waterfront director). I would definately call and speak with the Director again and the counselor this time. Maybe find out the counselor for next week and meet with them after the kids go home (stay 15 minutes extra) to talk with them. I wouldn't take no for an answer. They need to understand what needs to fit in and get the most out of this experience. Good luck Marni __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 wrote: You're not asking for special treatment-- you're asking the counselors to level the playing field so your child has access to communication during his day. ** Amen! may " only " have a loss in one ear, but it seems to cause more problems during summer camp/school than any other time. The kids go on *lots* of field trips, and I think it took last year's camp staff momentarily losing track of him to realize that if he's really interested in what they're supposed to be seeing/doing, he *doesn't* hear the teachers tell the group that it's time to move on. This year, I got lucky - the teacher he had for preschool is the director of staff at the summer school he's attending, and his classroom teacher's mother has unilateral hearing loss (not to the same degree as , but badly enough that I didn't have to repeat myself like I usually do). One of the agreements that we have is that when it's time for field trips, one teacher is specifically assigned to keeping tabs on and his whereabouts. She also knows that she has to keep a special eye on him when the class walks to the park that's four blocks away, since hearing oncoming traffic is a real challenge for him. I'm sure, though, that *something* will happen over the summer that will be cause for me to call the school and chat with the teacher or the director. Just remember - there's a difference between being an overbearing pain-in-the-rear, and being an advocate for your child's health and safety. What you've brought up definitely falls into the health and safety area - and if the camp director takes offense to you reinforcing the concept of your child's accessibility needs, then that would raise a red flag to me. Hugs to you, Kris Mom to (almost 8, Profound/Complete SNL, Left Ear) and Ethan (6, hearing) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2006 Report Share Posted June 26, 2006 wrote: You're not asking for special treatment-- you're asking the counselors to level the playing field so your child has access to communication during his day. ** Amen! may " only " have a loss in one ear, but it seems to cause more problems during summer camp/school than any other time. The kids go on *lots* of field trips, and I think it took last year's camp staff momentarily losing track of him to realize that if he's really interested in what they're supposed to be seeing/doing, he *doesn't* hear the teachers tell the group that it's time to move on. This year, I got lucky - the teacher he had for preschool is the director of staff at the summer school he's attending, and his classroom teacher's mother has unilateral hearing loss (not to the same degree as , but badly enough that I didn't have to repeat myself like I usually do). One of the agreements that we have is that when it's time for field trips, one teacher is specifically assigned to keeping tabs on and his whereabouts. She also knows that she has to keep a special eye on him when the class walks to the park that's four blocks away, since hearing oncoming traffic is a real challenge for him. I'm sure, though, that *something* will happen over the summer that will be cause for me to call the school and chat with the teacher or the director. Just remember - there's a difference between being an overbearing pain-in-the-rear, and being an advocate for your child's health and safety. What you've brought up definitely falls into the health and safety area - and if the camp director takes offense to you reinforcing the concept of your child's accessibility needs, then that would raise a red flag to me. Hugs to you, Kris Mom to (almost 8, Profound/Complete SNL, Left Ear) and Ethan (6, hearing) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , Stop worrying about being " that " mom. You are paying fort his camp, yes? Even if it is a free one through your town, that director is a paid professional and should be expected to do her job. And sharing information about a disabled child is part of that. Your son may be very " high functioning " and capable of holding his own, but he is still a special needs kid. The director has NOT done what she should have, what she said she would do, and there have been unacceptable incidences. Not eating lunch and not using the bathroom indicates that the kid is more confused than I'd find acceptable. I'd have a polite but pointed talk with the director again. I wouldn't try to sneak instruction to the counselors, but ask that each Monday morning, when I drop off my son, that in the midst of all that chaos, I get 10 minutes with the head counselor to explain my son's needs. I would guild this lily a bit as well and bring up safety concerns. Your son cannot follow instructions he can't hear and therefore could be hurt. This director should be taking this more seriously than she is and that is not good. You tried to handle your son's needs before camp started but it has not been given sufficient attention. 's counselors need to know that they have a D/HOH child in their group so that they can make sure they face him when speaking and make sure that he is on the same page as all the rest of the kids. It does not take a huge amount of effort to make sure your son is keeping up. Plus, like I said, this cold be a safety issue. If he can't ear instructions, he can't follow them. In that crowded lunchroom, if they were screaming out evacuation or fire drill type instructions, someone needs to know that they have to take your son's hand. You're not being " that " mother for no reason. You're being her because it is who you need to be to make sure your son is safe and has a good experience at camp. Best -- Jill Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , Stop worrying about being " that " mom. You are paying fort his camp, yes? Even if it is a free one through your town, that director is a paid professional and should be expected to do her job. And sharing information about a disabled child is part of that. Your son may be very " high functioning " and capable of holding his own, but he is still a special needs kid. The director has NOT done what she should have, what she said she would do, and there have been unacceptable incidences. Not eating lunch and not using the bathroom indicates that the kid is more confused than I'd find acceptable. I'd have a polite but pointed talk with the director again. I wouldn't try to sneak instruction to the counselors, but ask that each Monday morning, when I drop off my son, that in the midst of all that chaos, I get 10 minutes with the head counselor to explain my son's needs. I would guild this lily a bit as well and bring up safety concerns. Your son cannot follow instructions he can't hear and therefore could be hurt. This director should be taking this more seriously than she is and that is not good. You tried to handle your son's needs before camp started but it has not been given sufficient attention. 's counselors need to know that they have a D/HOH child in their group so that they can make sure they face him when speaking and make sure that he is on the same page as all the rest of the kids. It does not take a huge amount of effort to make sure your son is keeping up. Plus, like I said, this cold be a safety issue. If he can't ear instructions, he can't follow them. In that crowded lunchroom, if they were screaming out evacuation or fire drill type instructions, someone needs to know that they have to take your son's hand. You're not being " that " mother for no reason. You're being her because it is who you need to be to make sure your son is safe and has a good experience at camp. Best -- Jill Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , Stop worrying about being " that " mom. You are paying fort his camp, yes? Even if it is a free one through your town, that director is a paid professional and should be expected to do her job. And sharing information about a disabled child is part of that. Your son may be very " high functioning " and capable of holding his own, but he is still a special needs kid. The director has NOT done what she should have, what she said she would do, and there have been unacceptable incidences. Not eating lunch and not using the bathroom indicates that the kid is more confused than I'd find acceptable. I'd have a polite but pointed talk with the director again. I wouldn't try to sneak instruction to the counselors, but ask that each Monday morning, when I drop off my son, that in the midst of all that chaos, I get 10 minutes with the head counselor to explain my son's needs. I would guild this lily a bit as well and bring up safety concerns. Your son cannot follow instructions he can't hear and therefore could be hurt. This director should be taking this more seriously than she is and that is not good. You tried to handle your son's needs before camp started but it has not been given sufficient attention. 's counselors need to know that they have a D/HOH child in their group so that they can make sure they face him when speaking and make sure that he is on the same page as all the rest of the kids. It does not take a huge amount of effort to make sure your son is keeping up. Plus, like I said, this cold be a safety issue. If he can't ear instructions, he can't follow them. In that crowded lunchroom, if they were screaming out evacuation or fire drill type instructions, someone needs to know that they have to take your son's hand. You're not being " that " mother for no reason. You're being her because it is who you need to be to make sure your son is safe and has a good experience at camp. Best -- Jill Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH child. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH child. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH child. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 Oh yes - good point, - if you ask either of my kids if they hear you, they'll nod and say " yes " so you need to ask them a question that requires more than a yes or no answer as in " what is your favorite color " - that type of thing. We've found that oftentimes camp counsellors - who might not be as well trained as say, teachers - can be somewhat overwhelmed by our boys' hearing technology but most have appreciated us stepping in. IN 's case too, , I'm guessing he probably has good speech. I've found it's a mixed blessing - that because my own boys do have pretty clear speech, folks who don't know them don't realize their hearing needs... Barbara pcknott@... wrote: > LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH chi! > ld. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! > > > > > > > > All messages posted to this list are private and confidential. Each post is the intellectual property of the author and therefore subject to copyright restrictions. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 Oh yes - good point, - if you ask either of my kids if they hear you, they'll nod and say " yes " so you need to ask them a question that requires more than a yes or no answer as in " what is your favorite color " - that type of thing. We've found that oftentimes camp counsellors - who might not be as well trained as say, teachers - can be somewhat overwhelmed by our boys' hearing technology but most have appreciated us stepping in. IN 's case too, , I'm guessing he probably has good speech. I've found it's a mixed blessing - that because my own boys do have pretty clear speech, folks who don't know them don't realize their hearing needs... Barbara pcknott@... wrote: > LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH chi! > ld. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! > > > > > > > > All messages posted to this list are private and confidential. Each post is the intellectual property of the author and therefore subject to copyright restrictions. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 Oh yes - good point, - if you ask either of my kids if they hear you, they'll nod and say " yes " so you need to ask them a question that requires more than a yes or no answer as in " what is your favorite color " - that type of thing. We've found that oftentimes camp counsellors - who might not be as well trained as say, teachers - can be somewhat overwhelmed by our boys' hearing technology but most have appreciated us stepping in. IN 's case too, , I'm guessing he probably has good speech. I've found it's a mixed blessing - that because my own boys do have pretty clear speech, folks who don't know them don't realize their hearing needs... Barbara pcknott@... wrote: > LIsa, I used to do a one page thing on Maggie's hearing specifically for swimming. She swims on a team snf started at about 4 swimming in meets. I did it with lots of color and bullets and kept it simple, similar to what Barbara suggested. Used graphics even. I laminated it so it could be used over and over. Had lots of copies so if I saw a new person there I'd give them one. I used it at girl scout day and overnight camp too. One thing I always highlighted is to NOT ask her if she heard you. The answer would always be Yes. Said to have her repeat the instructions instead. Mags was 7 or 8 and had been swimming in meets for a couple of years before she realized there were 4 basic strokes, not 5. She thoought one particular drill they did a lot was an actual stroke! It does feel awful, and we were lucky that another child came along 6 or 8 years before Maggie who was deaf and whose brother's were star swimmers. So the entire team structure was used to a deaf/HOH chi! > ld. The deaf older girl lifeguarded and did part time coaching. She and Maggie became buddies. Everyone realized how deaf they both were when the entire pool had evacuated due to thunder and they were still in the middle of the pool clueless! > > > > > > > > All messages posted to this list are private and confidential. Each post is the intellectual property of the author and therefore subject to copyright restrictions. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , My son goes to a wonderful private school where they have gone out of their way to accomodate my son's needs. I never wanted to be pushy and also wanted him to learn to take care of himself, so I generally was very low key. In addition, I came late to the HL thing because he wasn't diagnosed until he was 9. When he was in 7th grade, his class went on a week long outdoor ed trip. I got a call the night they returned home from his teacher, apologizing about the hypothermia. It was a garbled story and I quickly realized that she was trying to tell her story before I heard from my son. She was concerned about him, but also about herself. The kids had done an exercise on rafts where thay had to figure out as a group how to get from one place to another. There wasn't enough raft space for everyone, so some people had to hang on to the side, taking turns sitting on the raft. I don't remember all the details at this point. My son ended up in the water the whole time because he didn't understand what was going on (no hearing aids) and didn't know how to get his needs across. After quite a while, a teacher noticed that my son was blue and they realized that of course he couldn't hear and this was the wrong thing for him to be doing. They got him out of the water and warmed him up. He thought this was a great adventure and did not want me to make a fuss, so I didn't, at the time. But I realized that I needed to take a much more proactive role in teacher education both to let my son's teachers know what was needed (and even the best, when dealing with a group don't necessarily think about my son first unless I have made a fuss) and to show him how to deal with a difficult situation. He learned to evaluate a situation for potential difficulties and to speak about problems as they arise. As much as I would like teachers to anticipate his needs, I know it's not going to happen. In general, they prefer hearing from me what to do, so they can go about doing it. They don't have the time or experience to do otherwise. For those who think I am being overprotective, I respect their opinion but choose to be a squeaky wheel. camp experience At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. K Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , My son goes to a wonderful private school where they have gone out of their way to accomodate my son's needs. I never wanted to be pushy and also wanted him to learn to take care of himself, so I generally was very low key. In addition, I came late to the HL thing because he wasn't diagnosed until he was 9. When he was in 7th grade, his class went on a week long outdoor ed trip. I got a call the night they returned home from his teacher, apologizing about the hypothermia. It was a garbled story and I quickly realized that she was trying to tell her story before I heard from my son. She was concerned about him, but also about herself. The kids had done an exercise on rafts where thay had to figure out as a group how to get from one place to another. There wasn't enough raft space for everyone, so some people had to hang on to the side, taking turns sitting on the raft. I don't remember all the details at this point. My son ended up in the water the whole time because he didn't understand what was going on (no hearing aids) and didn't know how to get his needs across. After quite a while, a teacher noticed that my son was blue and they realized that of course he couldn't hear and this was the wrong thing for him to be doing. They got him out of the water and warmed him up. He thought this was a great adventure and did not want me to make a fuss, so I didn't, at the time. But I realized that I needed to take a much more proactive role in teacher education both to let my son's teachers know what was needed (and even the best, when dealing with a group don't necessarily think about my son first unless I have made a fuss) and to show him how to deal with a difficult situation. He learned to evaluate a situation for potential difficulties and to speak about problems as they arise. As much as I would like teachers to anticipate his needs, I know it's not going to happen. In general, they prefer hearing from me what to do, so they can go about doing it. They don't have the time or experience to do otherwise. For those who think I am being overprotective, I respect their opinion but choose to be a squeaky wheel. camp experience At this moment the issue I'm concerned about it fresh in my mind. I'm typing to my listen-up friends to vent and maybe get some suggestions before I go off writing letters or phrasing things poorly to my son's camp. My son, , is 5.5 years old. He uses a CI and hearing aid. He is going to a half day summer camp program 8:30 - noon daily. Each week there are several different themed programs to choose from with varying age groups, so the campers and teachers/counselors change each week. Several weeks before camp I sent a letter of introduction to the camp director with some information about and tips for communicating with a child with a hearing loss and CI. I explained where the listening challenges would be and also detailed the precautions to take with the equipment. (water and static) In the letter I stated I would like to set up a time when I could come by and show them how to change batteries and answer any questions about or the equipment. I hadn't heard anything from the director the week before camp so I called. I had to leave a message and didn't hear back from her. I called again a couple days later. She suggested getting with me the first day of camp right after I dropped off. I realize people don't really " get it " when it comes to what they need to know. She had told me that she had read through all the information and she thought they were ready to go. I did stress gently that I thought it was important just to go over the information when she wouldn't be distracted or rushed, so I stopped by her office with the following day to show her how to change batteries. I also showed her how to readjust the earhook should it fall off and how the coil sometimes falls off. She mentioned that if anything happened the counselor would let her know and she would take care of it. I didn't push things at that point, but I really felt like the counselor should be in on this education too. I left feeling it was okay to send him down to her if there were battery issues. The first day of camp I met the counselor briefly when I dropped him off. There really wasn't time to start talking about concerns. I don't want to be that overbearing mother who expects a report everyday and wants special treatment. But I really do want to know how he's fitting in and I worry about him being lost in the shuffle. I was pleased with the first week. seemed really happy and adjusted well. His group that week was only about 5-6 kids. I think he benefitted from having a small group that allowed for more one on one and the counselor was an experienced school teacher. This was the first day of the second week so we start over with a new theme and new counselors. It's " pirate week " and apparently this is popular theme because he's got about 15 kids in his group this time. My husband dropped off and briefly chatted with the counselor but it was so busy and noisy that he really couldn't talk much. My husband got the impression that the counselor wasn't even briefed on having a child with hearing loss in the group which disappointed me. I had provided all that printed info to the director so I figured she would share that with everyone who would be working with . My husband had said something like... I guess you know that he uses a cochlear implant and a hearing aid so... and went on to explain some tips... and the counselor said, " No, I didn't know. " Grrrr... This time the counselors were young people so I'm thinking they might not be as knowlegeable about communicating with kindergarteners. Well today it really hit me how 's hearing loss can leave him out of the loop. I pick him up daily in the cafeteria where he's having lunch from 12:30. The kids are on their own at the tables and the counselors are seated at a main table in the center of the cafeteria. I have no idea what the rules or routine are for this period. But anyway, I picked up at the table and he told me, " I didn't have a lunch box today. " Well yes he did. He brought one, and I remember my husband telling me they were instructed to leave it in a cubby in the cafeteria. So I looked along the wall and there it was. So I told that yes, he did bring his lunchbox and that he put it in a cubby. He said, " But I don't know where it is. " I'm just wondering why someone wasn't looking out for him. I realize they don't have to " hold everyone's hands " but it really bothered me that had to sit there the whole time without lunch. I don't know why he didn't remember or know where his lunch was. I think he just isn't familiar with the routine and doesn't know who to turn to or ask. He's only 5 years old so I'm sure he doesn't really know how to problem solve in an unfamiliar environment. I told him that he should talk to a counselor next time he needs something, but again I think that takes a lot of assertiveness to approach the big table of counselors to express his concern. I will say something to them tomorrow. I did see the director on my way out and I asked if there was a new routine this week about where they put their lunchboxes. She told me no and explained that they leave them in the cubbies. I told her that didn't have lunch today because he didn't know where his was. She said, " Oh, they told the kids to get them in their cubbies. " And it was at that point I realized that in a noisy cafeteria with a bunch of campers buzzing around and the counselor shouting out over the chaos as to where and when to get your lunches, just didn't hear it. I bet he didn't even SEE it either. I just said, " I guess he didn't hear them, " and I think she realized the problem. Last week I picked him up on two separate occasions and he mentioned how he had to use the bathroom and he " just kept waiting and waiting. " I asked him why he didn't tell a counselor. He just didn't know what to do. I think he really needs to know what the " rules " are and the expectations. He didn't know what he was supposed to do if he needed to go to the bathroom. I also think he thinks it's like school where he is used to a very structured day and every day is the same routine, which includes bathroom breaks and not spending a lot of time chatting at lunch time. I really feel bad for him during that free lunch period because I know he can't keep up socially due to his age and the hearing challenge. How do I get them to look out for him without being that mom who is trying to tell everyone what to do? I'm so apprehensive about asking for special treatment, but at the same time I feel deserves it. He's doing great so far and isn't complaining. I'm sure he doesn't know what he's missing. I just want to give him as much access as I can, while at the same time letting him learn how to manage in these challenging circumstances. I'm thinking of writing a note to the counselor for tomorrow and including the two page info I provided for the director. There are just too many circumstances where I think they need to know how to deal. for instance it was raining today... I wondered if they would have known what to do if they were stuck in an unexpected downpour on the playground. Or what about when they go on field trips? They had two last week and I worried about the possibility of battery changes during that. I bet the counselor wouldn't have a clue. K Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , I just wanted to share with you what my experience was last year when Bobby was five and put into a regular mainstream camp. Until then he had been in school directed special need camps, but he progressed so well during the year that they said he didn't need services in the summer anymore. I was happy, and decided he could go into a Y camp instead. same as your son, tried to give them a heads up ahead of time, tried to talk to everyone, no one really took it seriously, that kind of thing. the first day I went to pick him up. Now thank God my three older kids were at the same camp, and they were supposed to be in a separate part of the camp doing older things, but at times they were all together. this was also before I knew Bobby had a hearing loss, so he was unaided and didn't hear well. Anyway, the first day my 14 year old was in tears because she had taken care of him the entire day. It started when Bobby walked into the girls' bathroom because he can't read and he probably didn't hear anyone explain anything to him, if they even did. He was told not to after all the girls ran out (I think it was a locker room) screaming. It really scared him. And my older kids were so upset they wouldn't leave him alone after that. Bottom line is that I pulled him out and didn't let him back in again. These are young kids on a summer job, and they don't have enough life experience to have any clue what these kids really need. No answers, just to tell you that I know how you feel. Trish Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2006 Report Share Posted June 27, 2006 , I just wanted to share with you what my experience was last year when Bobby was five and put into a regular mainstream camp. Until then he had been in school directed special need camps, but he progressed so well during the year that they said he didn't need services in the summer anymore. I was happy, and decided he could go into a Y camp instead. same as your son, tried to give them a heads up ahead of time, tried to talk to everyone, no one really took it seriously, that kind of thing. the first day I went to pick him up. Now thank God my three older kids were at the same camp, and they were supposed to be in a separate part of the camp doing older things, but at times they were all together. this was also before I knew Bobby had a hearing loss, so he was unaided and didn't hear well. Anyway, the first day my 14 year old was in tears because she had taken care of him the entire day. It started when Bobby walked into the girls' bathroom because he can't read and he probably didn't hear anyone explain anything to him, if they even did. He was told not to after all the girls ran out (I think it was a locker room) screaming. It really scared him. And my older kids were so upset they wouldn't leave him alone after that. Bottom line is that I pulled him out and didn't let him back in again. These are young kids on a summer job, and they don't have enough life experience to have any clue what these kids really need. No answers, just to tell you that I know how you feel. Trish Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2006 Report Share Posted June 30, 2006 In a message dated 6/30/2006 5:32:02 P.M. Eastern Daylight Time, Barbara.T.Mellert@... writes: Oh - that's so funny re: booty - my boys would have said the same thing! So am I the last one to learn about this joke? Q - why can't fifth graders see the Pirate movie? A - because it's rated arghhhhhhhhhhhhhhhhA Ah, the pirate stage, I remember it well. It was second only to the seemingly endless fascination with dinosaurs and frogs. How about this one ... Q: Where do pirates keep their buccaneers? A: Under their buckin' hats, of course. My kids loved that one because it sounded so-o-o-o-o naughty. LOL Jill Quote Link to comment Share on other sites More sharing options...
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