i have so many questions today for this knowledgeable group.
First, we had our daughter set to take the bus home from school today-a 10 minute ride, she carries the AED in her backpack, according to the district all bus drivers are AED trained. Short story, her 2nd grade teacher took her to the bus yesterday to meet the driver and the driver was "not nice" in fact refuses to take her. I had an "emotional" conversation with the school nurse today...who told me what an experienced, favorite bus driver this is...yada yada but she wouldn't take her...and that they then wanted to place an aide on the school bus. I suggested they switch bus drivers---and the school principal even used the analogy of kids with allergies to bee stings! They're not excluded from the "normal" bus....we were offered the "special" bus to pick her up from home and bring her home. So I now understand even more how cardiac cripples are made and how difficult it is to help kids lead as normal a life (least-restrictive environment) as possible. Any suggestions as we navigate this? Principal is wonderful...and somehow things don't get communicated to the right people. Plan today, the school principal is riding the bus with my daughter----my husband is hanging around the school "volunteering" this afternoon so that if the driver won't let my daughter on the bus, my husband can take her home.
Second, the school doesn't have an AED so my daughter brings her. They have set up an elaborate system of her checking it in a notebook in the morning and handing it to the secretary and her stopping and checking it out in the afternoon. Seems like a simple system---but for an 8 year old, it does nothing but say "hey kid with disAbility" to her and every other kid/parent/teacher in the school at least two times a day. I'm trying to help the school figure out how they can get an AED so that hers can stay in her backpack (should she be allowed to ride the bus), she would still have to carry it, but she wouldn't have to haul it out and in and check it out and in each day.
Third, I wrote a Make a Wish grant app trying to get the school an AED so that she wouldn't have to haul it out, sign it in, sign it out, haul it back in--that seems way too much for an 8-year old---, but they don't grant equipment wishes. Can anyone help me figure out how to get the school its own AED? (That doesn't solve the bus, but it would be one small step...)
Fourth we NEED to meet kids and families with HCM! My daughter hasn't yet met anyone with HCM--feels like an oddball, doesn't want "all the adults watching her every second".... Would also love to have her meet someone with an ICD--a teenager----as that might end up being the psychological option---risk surgery for the peace of mind of others....not what we want to do, when it's not an absolute---but...I am really concerned about the psychological damage of all this to her self-esteem as she gets older. She, like all HCM kids, is already the odd ball because she must limit her activities...ANYONE with kids or teenagers with HCM in the greater Seattle area who would like to meet??????
I also am so feeling for kids and families--we're a pretty well-educated family and we know how to navigate the system quite well, but if I'm this frustrated, i wonder what happens to others...with all kinds of challenges. Ugh.
Thanks for the place to vent
First, we had our daughter set to take the bus home from school today-a 10 minute ride, she carries the AED in her backpack, according to the district all bus drivers are AED trained. Short story, her 2nd grade teacher took her to the bus yesterday to meet the driver and the driver was "not nice" in fact refuses to take her. I had an "emotional" conversation with the school nurse today...who told me what an experienced, favorite bus driver this is...yada yada but she wouldn't take her...and that they then wanted to place an aide on the school bus. I suggested they switch bus drivers---and the school principal even used the analogy of kids with allergies to bee stings! They're not excluded from the "normal" bus....we were offered the "special" bus to pick her up from home and bring her home. So I now understand even more how cardiac cripples are made and how difficult it is to help kids lead as normal a life (least-restrictive environment) as possible. Any suggestions as we navigate this? Principal is wonderful...and somehow things don't get communicated to the right people. Plan today, the school principal is riding the bus with my daughter----my husband is hanging around the school "volunteering" this afternoon so that if the driver won't let my daughter on the bus, my husband can take her home.
Second, the school doesn't have an AED so my daughter brings her. They have set up an elaborate system of her checking it in a notebook in the morning and handing it to the secretary and her stopping and checking it out in the afternoon. Seems like a simple system---but for an 8 year old, it does nothing but say "hey kid with disAbility" to her and every other kid/parent/teacher in the school at least two times a day. I'm trying to help the school figure out how they can get an AED so that hers can stay in her backpack (should she be allowed to ride the bus), she would still have to carry it, but she wouldn't have to haul it out and in and check it out and in each day.
Third, I wrote a Make a Wish grant app trying to get the school an AED so that she wouldn't have to haul it out, sign it in, sign it out, haul it back in--that seems way too much for an 8-year old---, but they don't grant equipment wishes. Can anyone help me figure out how to get the school its own AED? (That doesn't solve the bus, but it would be one small step...)
Fourth we NEED to meet kids and families with HCM! My daughter hasn't yet met anyone with HCM--feels like an oddball, doesn't want "all the adults watching her every second".... Would also love to have her meet someone with an ICD--a teenager----as that might end up being the psychological option---risk surgery for the peace of mind of others....not what we want to do, when it's not an absolute---but...I am really concerned about the psychological damage of all this to her self-esteem as she gets older. She, like all HCM kids, is already the odd ball because she must limit her activities...ANYONE with kids or teenagers with HCM in the greater Seattle area who would like to meet??????
I also am so feeling for kids and families--we're a pretty well-educated family and we know how to navigate the system quite well, but if I'm this frustrated, i wonder what happens to others...with all kinds of challenges. Ugh.
Thanks for the place to vent
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